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20 pages, 4065 KiB  
Article
Laundry Isolate Delftia sp. UBM14 Capable of Biodegrading Industrially Relevant Aminophosphonates
by Ramona Riedel, Karsten Meißner, Arne Kaschubowski, Dirk Benndorf, Marion Martienssen and Burga Braun
Microorganisms 2024, 12(8), 1664; https://doi.org/10.3390/microorganisms12081664 - 13 Aug 2024
Abstract
Phosphonates such as ethylenediaminetetra (methylenephosphonic acid) (EDTMP) and aminotris (methylenephosphonic acid) (ATMP) are used every day in water treatment processes or in household products. Their consumption is still increasing, regardless of the debates on their environmental impact. Here, the microbial characterisation and determination [...] Read more.
Phosphonates such as ethylenediaminetetra (methylenephosphonic acid) (EDTMP) and aminotris (methylenephosphonic acid) (ATMP) are used every day in water treatment processes or in household products. Their consumption is still increasing, regardless of the debates on their environmental impact. Here, the microbial characterisation and determination of the biodegradation potential of selected industrially relevant phosphonates for the isolate Delftia sp. UMB14 is reported. The opportunistic strain was isolated from a biofilm that was derived from a conventional washing machine using conventional detergents containing phosphonates. In antimicrobial susceptibility testing, the strain was only susceptible to sulfonamide, tetracycline, and chloramphenicol. Physiological and biochemical characteristics were determined using the BIOLOG EcoPlate assay. Most importantly, the strain was shown to convert D-malic acid and D-mannitol, as confirmed for strains of Delftia lacustris, and thus the new isolate could be closely related. Biodegradation tests with different phosphonates showed that the strain preferentially degrades ATMP and EDTMP but does not degrade glyphosate (GS) and amino (methylphosphonic acid) (AMPA). A specific gene amplification confirmed the presence of phnX (phosphonoacetaldehyde hydrolase) and the absence of PhnJ (the gene for the core component of C–P lyase). The presence of PhnCDE is strongly suggested for the strain, as it is common in Delftia lacustris species. Full article
(This article belongs to the Section Environmental Microbiology)
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Figure 1

Figure 1
<p>Chemical structures of the phosphonates used in the degradation tests.</p>
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<p>Biodegradation test of selected phosphonates with strain <span class="html-italic">Delftia</span> sp. UMB14. The phosphonates were dosed at 20 mgP L<sup>−1</sup> to ensure comparability, except of HEDP, to prevent the precipitation of the latter. (<b>A1</b>,<b>A2</b>) ATMP. (<b>B1</b>,<b>B2</b>) EDTMP. (<b>C1</b>,<b>C2</b>) IDMP. (<b>D1</b>,<b>D2</b>) HEDP. (<b>E1</b>,<b>E2</b>) DTPMP. (<b>F1</b>,<b>F2</b>) GS. (<b>G1,G2</b>) AMPA. (<b>H1</b>,<b>H2</b>) Positive control KH<sub>2</sub>PO<sub>4</sub>. The optical density was measured at 660 nm.</p>
Full article ">Figure 2 Cont.
<p>Biodegradation test of selected phosphonates with strain <span class="html-italic">Delftia</span> sp. UMB14. The phosphonates were dosed at 20 mgP L<sup>−1</sup> to ensure comparability, except of HEDP, to prevent the precipitation of the latter. (<b>A1</b>,<b>A2</b>) ATMP. (<b>B1</b>,<b>B2</b>) EDTMP. (<b>C1</b>,<b>C2</b>) IDMP. (<b>D1</b>,<b>D2</b>) HEDP. (<b>E1</b>,<b>E2</b>) DTPMP. (<b>F1</b>,<b>F2</b>) GS. (<b>G1,G2</b>) AMPA. (<b>H1</b>,<b>H2</b>) Positive control KH<sub>2</sub>PO<sub>4</sub>. The optical density was measured at 660 nm.</p>
Full article ">Figure 3
<p>Growth test with strain <span class="html-italic">Delftia</span> sp. UMB14 and different sole phosphorus sources. (<b>A</b>) KH<sub>2</sub>PO<sub>4</sub> as sole P source. (<b>B</b>) ATMP as sole P source. (<b>C</b>) HEDP as sole P source. Test was running in triplicates for each test condition. The optical density was measured at 660 nm.</p>
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<p>Adaptation test with inocula with preconditioned bacteria either grown on ATMP or EDTMP. (<b>A</b>) Growth test on different phosphonates with pre-inoculated bacteria on ATMP as P source. (<b>B</b>) Growth test on different phosphonates with pre-inoculated bacteria on EDTMP as P source. The optical density was measured at 660 nm.</p>
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13 pages, 1104 KiB  
Article
Effects of SGLT2-Inhibitors on Comprehensive Geriatric Assessment, Biomarkers of Oxidative Stress, and Platelet Activation in Elderly Diabetic Patients with Heart Failure with Preserved Ejection Fraction
by Marcello Magurno, Velia Cassano, Francesco Maruca, Carlo Alberto Pastura, Marcello Divino, Federica Fazio, Giandomenico Severini, Elvira Clausi, Giuseppe Armentaro, Sofia Miceli, Raffaele Maio, Egidio Imbalzano, Francesco Andreozzi, Marta Letizia Hribal and Angela Sciacqua
Int. J. Mol. Sci. 2024, 25(16), 8811; https://doi.org/10.3390/ijms25168811 (registering DOI) - 13 Aug 2024
Abstract
Background: Heart failure (HF) with preserved ejection fraction (HFpEF) represents a major comorbidity in the elderly and is associated with cognitive impairment (CoI) and type 2 diabetes mellitus (T2DM). In this context, there is an increase in oxidative stress and platelet activation biomarkers. [...] Read more.
Background: Heart failure (HF) with preserved ejection fraction (HFpEF) represents a major comorbidity in the elderly and is associated with cognitive impairment (CoI) and type 2 diabetes mellitus (T2DM). In this context, there is an increase in oxidative stress and platelet activation biomarkers. The aim of this study was to evaluate the effects of 6 months’ treatment with SGLT2i on functional, mood-related, and cognitive aspects, assessed by performing a comprehensive geriatric assessment (CGA), and on oxidative stress and platelet activation biomarkers, in a cohort of HFpEF elderly patients with T2DM. We recruited 150 elderly outpatients (mean age 75.8 ± 7.4 years). Results: At six-month follow-up, there was a significant improvement in MMSE (p < 0.0001), MoCA (p < 0.0001), GDS score (p < 0.0001), and SPPB (p < 0.0001). Moreover, we observed a significant reduction in Nox-2 (p < 0.0001), 8-Isoprostane (p < 0.0001), Sp-Selectin (p < 0.0001), and Gp-VI (p < 0.0001). Considering ΔMMSE as the dependent variable, ΔE/e’, ΔNox-2, ΔHOMA, Δ8-Isoprostane, and ΔUricemia were associated for 59.6% with ΔMMSE. When ΔMoCA was considered as the dependent variable, ΔHOMA, ΔE/e’, Δ8-Isoprostane, ΔNox-2 and ΔUricemia were associated for 59.2%. Considering ΔGDS as the dependent variable, ΔHOMA, ΔNox-2, Δ8-Isoprostane, and ΔUricemia were associated with 41.6% of ΔGDS variation. Finally, ΔHOMA was the main predictor of ΔSPPB, which was associated with 21.3% with ΔSPPB, Δ8-Isoprostane, ΔNox-2, ΔE/e’, and ΔUricemia added another 24.1%. Conclusion: The use of SGLT2i in elderly patients with T2DM and HFpEF significantly contributes to improving CGA scales and biomarkers of OS and PA. Full article
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Figure 1

Figure 1
<p>Changes in oxidative stress biomarkers and platelet activation biomarkers between baseline and follow-up. Abbreviations: Nox-2: NAPDH Oxidase 2.</p>
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<p>Changes in echocardiographic parameters between baseline and follow-up. Abbreviations: LAVI: left atrial volume index, E/e’: between wave E and wave e’ (reliable estimate of changes in end-diastolic blood pressure); s-PAP: systolic pulmonary arterial pressure; GLS: global longitudinal strain.</p>
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<p>Changes in cognitive and functional parameters between baseline and follow-up. Abbreviations: MMSE: Mini-Mental state examination; MoCA: Montreal cognitive assessment; GDS: Geriatric Depression Scale; SPPB: short performance physical battery.</p>
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21 pages, 3438 KiB  
Review
Insights and Considerations in Development and Performance Evaluation of Generative Adversarial Networks (GANs): What Radiologists Need to Know
by Jeong Taek Yoon, Kyung Mi Lee, Jang-Hoon Oh, Hyug-Gi Kim and Ji Won Jeong
Diagnostics 2024, 14(16), 1756; https://doi.org/10.3390/diagnostics14161756 - 13 Aug 2024
Viewed by 151
Abstract
The rapid development of deep learning in medical imaging has significantly enhanced the capabilities of artificial intelligence while simultaneously introducing challenges, including the need for vast amounts of training data and the labor-intensive tasks of labeling and segmentation. Generative adversarial networks (GANs) have [...] Read more.
The rapid development of deep learning in medical imaging has significantly enhanced the capabilities of artificial intelligence while simultaneously introducing challenges, including the need for vast amounts of training data and the labor-intensive tasks of labeling and segmentation. Generative adversarial networks (GANs) have emerged as a solution, offering synthetic image generation for data augmentation and streamlining medical image processing tasks through models such as cGAN, CycleGAN, and StyleGAN. These innovations not only improve the efficiency of image augmentation, reconstruction, and segmentation, but also pave the way for unsupervised anomaly detection, markedly reducing the reliance on labeled datasets. Our investigation into GANs in medical imaging addresses their varied architectures, the considerations for selecting appropriate GAN models, and the nuances of model training and performance evaluation. This paper aims to provide radiologists who are new to GAN technology with a thorough understanding, guiding them through the practical application and evaluation of GANs in brain imaging with two illustrative examples using CycleGAN and pixel2style2pixel (pSp)-combined StyleGAN. It offers a comprehensive exploration of the transformative potential of GANs in medical imaging research. Ultimately, this paper strives to equip radiologists with the knowledge to effectively utilize GANs, encouraging further research and application within the field. Full article
(This article belongs to the Section Machine Learning and Artificial Intelligence in Diagnostics)
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Figure 1

Figure 1
<p>A schematic diagram of various generative adversarial networks (GANs). In a basic GAN structure (<b>A</b>), and imposing conditions on both the generator and discriminator in a conditional GAN (cGAN) (<b>B</b>). Pix2pix (<b>C</b>) uses a paired image set, whereas cycle-consistent GAN (CycleGAN) (<b>D</b>) performs image translation between two domains using unpaired images. StyleGAN (<b>E</b>) utilizes a mapping network to transform the input Vector Z into an intermediate Vector W before inputting it into the generator.</p>
Full article ">Figure 1 Cont.
<p>A schematic diagram of various generative adversarial networks (GANs). In a basic GAN structure (<b>A</b>), and imposing conditions on both the generator and discriminator in a conditional GAN (cGAN) (<b>B</b>). Pix2pix (<b>C</b>) uses a paired image set, whereas cycle-consistent GAN (CycleGAN) (<b>D</b>) performs image translation between two domains using unpaired images. StyleGAN (<b>E</b>) utilizes a mapping network to transform the input Vector Z into an intermediate Vector W before inputting it into the generator.</p>
Full article ">Figure 2
<p>Paired and unpaired image sets. Brain tumor image sets in preconstrast and postcontrast T1-weighted images. Paired image sets are on the <b>right</b> and unpaired image sets are on the <b>left</b>. Paired images require identical conditions, whereas unpaired images can handle images under different conditions.</p>
Full article ">Figure 3
<p>Schematic diagram of a CycleGAN-based generation model. The <b>top row</b> shows GENERATOR<sub>DN</sub>, which creates a virtual normal diffusion weighted image (DWI) from a real DWI image of acute infarction. GENERATOR<sub>ND</sub> creates a virtual acute infarction from a virtual normal image. In the <b>below</b> is DISCRIMINATOR<sub>N</sub>, which distinguishes between virtual normal images and real normal images. These two networks compete with each other to make the reconstructed images more realistic and to distinguish between real and reconstructed images, resulting in the generation of high-quality images.</p>
Full article ">Figure 4
<p>Examples of the synthesized images from the test datasets of GENERTOR<sub>ND</sub> and GENERTOR<sub>DN</sub>. (<b>A</b>) The first column (x) shows the real normal images when given as input. The second column (G<sub>ND</sub>(x)) shows the synthesized acute infarction images. The third column (x − G<sub>ND</sub>(x)) shows the subtraction between the real normal images and the synthesized acute infarction images, which highlights the lesions. (<b>B</b>) The first column (x) shows the real normal images when given as input. The second column (G<sub>DN</sub>(x)) shows the synthesized normal images. The third column (x − G<sub>DN</sub>(x)) shows the subtraction between the real acute infarction images and the synthesized normal images, which highlights the lesions.</p>
Full article ">Figure 5
<p>A schematic diagram of the image processing and generation of the pixel2style2pixel (pSp)-encoder-combined StyleGAN generator. Image processing was performed by segmentation of the thick vessels that were relevant to the evaluation following angle augmentation by rotating the image by five degrees each time. Red, green, and blue (RGB) color augmentation of the processed black background image was performed with red for the bright areas and blue for the dark areas. Training each processed black background and the color augmentation images was conducted using a style pSp encoder and GAN generator.</p>
Full article ">Figure 6
<p>Examples of the StyleGAN generated images from the test datasets of processed time of flight-magnetic resonance angiography (TOF-MRA) maximal intensity projection (MIP) images of normal patients. For three patients of the test datasets, input images and output images were paired and arranged in rows, and vertical +90 degrees, right-rotated horizontal −45 degrees rotation, and horizontal −30 degrees rotation images were arranged in columns.</p>
Full article ">Figure 7
<p>Input and synthetic images of stenosis, occlusion, and aneurysm on StyleGAN. (<b>A</b>) Synthetic black background and color augmentation images of 4 mm-sized left posterior communicating artery aneurysm (arrows) at the angle of horizontal 160 degrees and 230 degrees. (<b>B</b>) Synthetic black background and color augmentation images of 4 mm-sized basilar top aneurysm and occlusion of right proximal M1 segment and right distal vertebral artery (VA) (arrows) at the angle of vertical 30 degrees. (<b>C</b>) Synthetic color augmentation images of stenosis and occlusion of intracranial arteries at the angle of vertical 35 degrees; occlusion of right proximal M1 segment and right distal VA and mild stenosis of left distal M1 segment (arrows).</p>
Full article ">Figure 8
<p>Training saturation of pSp-encoder-combined StyleGAN generator. The cosine similarity between the input and output data embedded in the pSp framework was calculated and expressed as one-test loss. As the number of processed data increased, the one-test loss showed saturation; when the number of color augmentation training data exceeded 170,000, the one-test loss reached 0.93.</p>
Full article ">Figure 9
<p>Examples of outer margin blurring/irregularity and consistency of the vessel diameter and separability of the course of adjacent vessels for the qualitative evaluations of radiologists. (<b>A</b>) Examples images of outer margin blurring and irregularity in right distal internal carotid artery (ICA), from input to a mild, moderate, and severe degree. (<b>B</b>) Examples images of the consistency of the vessel diameter in the right M1 segment, from input to a mild, moderate, and severe degree. (<b>C</b>) Examples images of the separability of the course of adjacent or intersected vessels in both ICAs at a horizontal −45 degree, both possible and impossible.</p>
Full article ">Figure 9 Cont.
<p>Examples of outer margin blurring/irregularity and consistency of the vessel diameter and separability of the course of adjacent vessels for the qualitative evaluations of radiologists. (<b>A</b>) Examples images of outer margin blurring and irregularity in right distal internal carotid artery (ICA), from input to a mild, moderate, and severe degree. (<b>B</b>) Examples images of the consistency of the vessel diameter in the right M1 segment, from input to a mild, moderate, and severe degree. (<b>C</b>) Examples images of the separability of the course of adjacent or intersected vessels in both ICAs at a horizontal −45 degree, both possible and impossible.</p>
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21 pages, 6189 KiB  
Article
Characterization of the Serine Protease TlSP1 from Trichoderma longibrachiatum T6 and Its Function in the Control of Heterodera avenae in Wheat
by Xiujuan Wang, Shuwu Zhang and Bingliang Xu
J. Fungi 2024, 10(8), 569; https://doi.org/10.3390/jof10080569 - 12 Aug 2024
Viewed by 267
Abstract
Serine protease is an extracellular protease secreted by biocontrol fungi that can effectively control nematode diseases by degrading nematode eggshells and enhancing plant resistance. Trichoderma longibrachiatum T6, an important biocontrol fungus, has been demonstrated to effectively parasitize and degrade Heterodera avenae cysts, eggs, [...] Read more.
Serine protease is an extracellular protease secreted by biocontrol fungi that can effectively control nematode diseases by degrading nematode eggshells and enhancing plant resistance. Trichoderma longibrachiatum T6, an important biocontrol fungus, has been demonstrated to effectively parasitize and degrade Heterodera avenae cysts, eggs, and second-stage juveniles (J2s). However, the genes that encoding serine protease and their functions in T. longibrachiatum T6 have not been thoroughly investigated. In this study, we successfully cloned and sequenced the serine protease gene TlSP1 in T. longibrachiatum T6. Our results revealed that the expression level of the TlSP1 gene was induced and significantly increased in T. longibrachiatum T6 after inoculation with H. avenae cysts. The full-length sequence of the coding region (CDS) of TlSP1 gene was 1230 bp and encoded a protein consisting of 409 amino acids. Upon the transformation of the TlSP1 gene into Pichia pastoris X33, the purified recombinant TlSP1 protein exhibited optimal activity at a temperature of 50 °C and pH 8.0. Following 4–10-day of treatment with the purified recombinant TlSP1 protein, the eggshells and content were dissolved and exuded. The number of nematodes invading wheat roots was reduced by 38.43% in the group treated with both TlSP1 and eggs on one side (P1+N) compared to the control group, while the number of nematodes invading wheat roots was reduced by 30.4% in the TlSP1 and eggs two-sided treatment group (P1/N). Furthermore, both the P1+N and P1/N treatments significantly upregulated genes associated with defense enzymes (TaPAL, TaCAT, TaSOD, and TaPOD), genes involved in the lignin synthesis pathway (TaC4H, Ta4CL2, TaCAD1, and TaCAD12), and salicylic acid (SA)-responsive genes (TaNPR1, TaPR1, and TaPR2) and led to the high expression of jasmonic acid (JA)-responsive genes (TaPR4, TaOPR3, and TaAOS2). This study has highlighted the significant role of the TlSP1 gene in facilitating H. avenae eggshells’ dissolution, preventing nematode invasion in the host plant, and boosting plant resistance in wheat. Full article
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Figure 1
<p>Schematic diagram of TlSP1-induced resistance to cyst nematodes in wheat studied in the split-root system.</p>
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<p>Multiple sequence alignment and phylogenetic analysis. (<b>A</b>) Multiple sequence alignment of TlSP1 with other species’ SPs. Thick solid lines and arrows represent highly conserved structural domains and the triad of Asp (D), His (H), and Ser (S) residues. The dark shaded areas indicate 100% sequence similarity, and the light blue shaded areas represent sequence similarity greater than 50%. (<b>B</b>) Phylogenetic tree of TlSP1 constructed using the neighbor-joining (NJ) method. Lp, <span class="html-italic">Lecanicillium psalliotae</span>. Al, <span class="html-italic">Akanthomyces lecanii</span>. Pl, <span class="html-italic">Purpureocillium lilacinum</span>. Ma, <span class="html-italic">Metarhizium anisopliae</span>. Pc, <span class="html-italic">Pochonia chlamydosporia</span>. Th, <span class="html-italic">T. harzianum</span>. Tv, <span class="html-italic">T. virens</span>. Tl, <span class="html-italic">T. longibrachiatum</span>. Am, <span class="html-italic">Arthrobotrys microscaphoides</span>. Oo, <span class="html-italic">Orbilia oligospora</span>. (Bootstrap = 1000).</p>
Full article ">Figure 3
<p>Analysis of the expression patterns of <span class="html-italic">TlSP1</span> gene. Data presented are means ± SD and columns labeled with different letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Identification of positive clone strains of <span class="html-italic">TlSP1</span> transformed into <span class="html-italic">P. pastoris</span> X33 and determination of protease activity at different times during fermentation of pPICZαA-<span class="html-italic">TlSP1</span>/X33 and purification of recombinant TlSP1 protein. (<b>A</b>) +: Positive control is pPICZαA-<span class="html-italic">TlSP1</span> recombinant vector; −: negative control is wild <span class="html-italic">P. pastoris</span> X33. 1: the PCR products of positive clones from <span class="html-italic">P. pastoris</span> X33 that have been transformed with the <span class="html-italic">TlSP1</span> gene. M: DL5000 DNA marker. (<b>B</b>) Protease activity at different fermentation times and (<b>C</b>) purification of recombinant TlSP1 protein, where M represents protein markers, 1 represents the recombinant protein crude enzyme solution sample, 2 represents the effluent sample, 3 represents 20 mM imidazole eluent, and 4 represents 500 mM imidazole eluent.</p>
Full article ">Figure 5
<p>Effect of temperature and pH on enzyme activity of recombinant TlSP1 protein. (<b>A</b>) Optimal temperature, (<b>B</b>) thermal stability, (<b>C</b>) optimal pH, and (<b>D</b>) pH stability of TlSP1 protein.</p>
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<p>(<b>A</b>) Effect of substrate specificity and (<b>B</b>,<b>C</b>) kinetic parameters of TlSP1 enzyme activity. S: substrate concentration. V: enzyme-catalysed reaction rate.</p>
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<p>Morphological observation of eggs treated with recombinant TlSP1 protein. (<b>A1</b>–<b>A4</b>) represent eggs after treatment with sterile water at 4, 6, 8, and 10 days, respectively. (<b>B1</b>–<b>B4</b>) represent eggs after treatment with PBS at 4, 6, 8, and 10 days, respectively. (<b>C1</b>–<b>C4</b>) represent eggs after treatment with recombinant TlSP1 protein at 4, 6, 8, and 10 days, respectively. Bar: 20 μm.</p>
Full article ">Figure 8
<p>Effect of TlSP1 on callose accumulation and allergic reactions in wheat, depicted in photomicrographs. (<b>A1</b>–<b>A3</b>) illustrate callus accumulation, under 200× magnification: (<b>A1</b>) sterile water, (<b>A2</b>) PBS, (<b>A3</b>) TlSP1. Bar: 20 μm. (<b>B1</b>–<b>B3</b>) depict allergic reactions, under 40× magnification: (<b>B1</b>) sterile water, (<b>B2</b>) PBS, (<b>B3</b>) TlSP1. Bar: 500 μm.</p>
Full article ">Figure 9
<p>TlSP1 effect on wheat growth using the split-root method. (<b>A</b>) Shoot fresh and dry weights; (<b>B</b>) root fresh and dry weights. Different lowercase letters indicate significant differences at <span class="html-italic">p</span> &lt; 0.05. Treatments are listed in <a href="#jof-10-00569-f001" class="html-fig">Figure 1</a>.</p>
Full article ">Figure 10
<p>Effect of TlSP1 on nematode invasion. Data are presented as the means ± SD of three biological replicates. Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). Treatments are listed in <a href="#jof-10-00569-f001" class="html-fig">Figure 1</a>.</p>
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<p>Effect of TlSP1 on (<b>A</b>) <span class="html-italic">TaPAL</span>, (<b>B</b>) <span class="html-italic">TaCAT</span>, (<b>C</b>) <span class="html-italic">TaSOD</span>, and (<b>D</b>) <span class="html-italic">TaPOD</span> relative expression at different days after treatment. Data are presented as the means ± SD of three biological replicates. Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). Treatments are listed in <a href="#jof-10-00569-f001" class="html-fig">Figure 1</a>.</p>
Full article ">Figure 12
<p>Effect of TlSP1 on (<b>A</b>) <span class="html-italic">TaC4H</span>, (<b>B</b>) <span class="html-italic">Ta4CL2</span>, (<b>C</b>) <span class="html-italic">TaCAD1</span>, and (<b>D</b>) <span class="html-italic">TaCAD12</span> relative expression at different days after treatment. Data are presented as the means ± SD of three biological replicates. Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). Treatments are listed in <a href="#jof-10-00569-f001" class="html-fig">Figure 1</a>.</p>
Full article ">Figure 13
<p>Effect of TlSP1 on (<b>A</b>) <span class="html-italic">TaNPR1</span>, (<b>B</b>) <span class="html-italic">TaPR1</span>, and (<b>C</b>) <span class="html-italic">TaPR2</span> genes of SA pathway. Data are presented as the means ± SD of three biological replicates. Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). Treatments are listed in <a href="#jof-10-00569-f001" class="html-fig">Figure 1</a>.</p>
Full article ">Figure 14
<p>Effect of TlSP1 on (<b>A</b>) <span class="html-italic">TaPR4</span>, (<b>B</b>) <span class="html-italic">TaAOS2</span>, and (<b>C</b>) <span class="html-italic">TaOPR3</span> genes of JA pathway. Data are presented as the means ± SD of three biological replicates. Different letters above the bars indicate significant differences (<span class="html-italic">p</span> &lt; 0.05). Treatments are listed in <a href="#jof-10-00569-f001" class="html-fig">Figure 1</a>.</p>
Full article ">
11 pages, 1893 KiB  
Article
Unique Jurassic Ovaries Shed a New Light on the Nature of Carpels
by Qiang Fu, Jie Sun, Shaolin Zheng and Xin Wang
Plants 2024, 13(16), 2239; https://doi.org/10.3390/plants13162239 - 12 Aug 2024
Viewed by 157
Abstract
Enclosed ovules are a reproductive feature restricted to angiosperms. Although this feature can be used as a criterion for identifying fossil angiosperms, how ovules are enclosed and the nature of the placenta are still foci of debates. A reason underlying these controversies is [...] Read more.
Enclosed ovules are a reproductive feature restricted to angiosperms. Although this feature can be used as a criterion for identifying fossil angiosperms, how ovules are enclosed and the nature of the placenta are still foci of debates. A reason underlying these controversies is the lack of reproductive organ fossils shedding light on these issues. These controversies hinder a clear understanding of angiosperm evolution and systematics. Here, we report a new fossil ovary, Xenofructus dabuensis gen. et sp. nov, from the Middle Jurassic of Liaoning, China. Our fossil clearly demonstrates the existence of ovules in Xenofructus that has a free central placentation. This new feature implies that a placenta in angiosperm gynoecia is homologous to an ovule/seed-bearing axis, and free central placentation is one of the early developed placentations. This discovery is apparently at odds with the current understanding of placentation and its evolution. Apparently, the understanding of angiosperms and their gynoecia should be updated with newly available palaeobotanical data. Full article
(This article belongs to the Special Issue Inflorescence Architecture and Development in Plants)
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<p><span class="html-italic">Xenofructus dabuensis</span> gen. et sp. nov and its details. Specimen number KP10-18A. (<b>a</b>). Holotype, showing the profile of Ovary A and its seeds/ovules exposed after the foreground ovary is removed. Scale bar = 1 mm. (<b>b</b>). Ovary B and its internal ovules partially exposed and partially covered by the broken ovary wall. Scale bar = 1 mm. (<b>c</b>). Detailed view of the black rectangle in (<b>b</b>), showing three ovules (s) of variable shapes and ovary wall (upper right) covering other ovules. Scale bar = 1 mm. (<b>d</b>). Detailed view of the rectangle in (<b>a</b>), showing robust abaxial margin (between the triangles) of the ovary. Scale bar = 1 mm. (<b>e</b>). Broken ovary wall (upper right) and exposed internal of the ovary (lower left), and the boundary in between (triangles), enlarged from the white rectangle in (<b>b</b>). Scale bar = 0.5 mm. (<b>f</b>). A sickle-shaped ovule with a distal invagination (possible micropyle, triangle), enlarged from the rectangle in (<b>c</b>). Scale bar = 1 mm. (<b>g</b>). A micro-CT rendering of the specimen showing two ovaries parallel deployed on the surface of the specimen. (<b>h</b>–<b>j</b>). Serial sections of Ovary B, showing the ovule-bearing placenta (triangles) independent from both margins of the ovary. Scale bar = 2 mm.</p>
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<p>Sketches of two <span class="html-italic">Xenofructus</span> ovaries. The ovary outline is in black, while the seed outline is in red. (<b>a</b>). The ovary in <a href="#plants-13-02239-f001" class="html-fig">Figure 1</a>a. (<b>b</b>). The ovary in <a href="#plants-13-02239-f001" class="html-fig">Figure 1</a>b.</p>
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<p>Several representatives of early angiosperms, showing variable placentations in the fruits/ovaries of early angiosperms. Seeds (S)/ovules (O) are inserted either along the adaxial (AD), abaxial (AB), or both margins of a fruit/ovary, or are basally fixed in a fruit/ovary. 1. <span class="html-italic">Archaefructus</span>, according to Wang and Zheng [<a href="#B19-plants-13-02239" class="html-bibr">19</a>]; 2. <span class="html-italic">Xenofructus</span>; 3. <span class="html-italic">Qingganninginfructus</span>, according to Han et.al. [<a href="#B36-plants-13-02239" class="html-bibr">36</a>]; 4. <span class="html-italic">Gansufructus</span>, according to Du et al. [<a href="#B57-plants-13-02239" class="html-bibr">57</a>]; 5. <span class="html-italic">Sinocarpus</span>, according to Leng and Friis [<a href="#B55-plants-13-02239" class="html-bibr">55</a>]; 6. <span class="html-italic">Archaeanthus</span>, according to Wang [<a href="#B20-plants-13-02239" class="html-bibr">20</a>].</p>
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15 pages, 3796 KiB  
Article
Coprological Survey of Helminths in Reindeer (Rangifer tarandus) in 50 Selected Zoos and Menageries in Russia
by Olga A. Loginova, Svetlana V. Akulova, Dmitry N. Egorov, Natalia S. Egorova, Sergei E. Spiridonov, Iuliia K. Plotnikova, Larisa M. Belova, Yuriy E. Kuznetsov, Daria I. Chuprak, Anna A. Krutikova, Iuliia V. Vasilkova, Diana A. Gelashvili, Yuri A. Shchepanovsky, Ivan A. Mizin, Danila V. Panchenko, Mikhail G. Bondar and Taras P. Sipko
J. Zool. Bot. Gard. 2024, 5(3), 492-506; https://doi.org/10.3390/jzbg5030033 (registering DOI) - 12 Aug 2024
Viewed by 203
Abstract
Zoo conditions are unique for reindeer, since domestic reindeer are not kept in captive facilities like cattle. In the zoo, reindeer are usually surrounded by many different animals that they would never encounter naturally. Thus, they might be infected with new helminths. Numerous [...] Read more.
Zoo conditions are unique for reindeer, since domestic reindeer are not kept in captive facilities like cattle. In the zoo, reindeer are usually surrounded by many different animals that they would never encounter naturally. Thus, they might be infected with new helminths. Numerous petting zoos raise concerns about the safety of tactile interactions for human visitors. Our study is the first large-scale one. Qualitative and quantitative fecal analyses were carried out for 233 reindeer distributed over 50 Russian zoos according to the National Standard of the Russian Federation (GOST R 54627-2011) Ruminant animals—Methods of Laboratory Helminthological Diagnostics. Where possible, DNA analyses of helminths were performed targeting internal transcribed spacer region. As a result, F. hepatica, Paramphistomum sp., Moniezia sp. (including M. expansa), gastrointestinal strongylids (including Nematodirus spp.), Dictyocaulus sp., E. rangiferi, Trichuris sp., and Capillaria sp. were found in 106 (45%) zoo reindeer. All these helminths were previously reported in reindeer and pose no direct danger for humans. The intensity of invasions was mostly low. Fecal examination might be considered as an indirect method for mange diagnostics, as Chorioptes and Demodex mites were found in reindeer fecal samples. The latter may represent a novel species of mite specific for reindeer. Full article
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<p>Diagnostic stages of helminths obtained from feces of zoo reindeer. (<b>A</b>) <span class="html-italic">Fasciola hepatica</span> egg; (<b>B</b>) <span class="html-italic">Moniezia expansa</span> egg; (<b>C</b>) <span class="html-italic">Nematodirus</span> sp. egg at late stage of embryonic development; (<b>D</b>) rounded strongyle-type egg; (<b>E</b>) <span class="html-italic">Trichuris</span> sp. egg; (<b>F</b>) <span class="html-italic">Paramphistomum</span> sp. egg; (<b>G</b>) <span class="html-italic">Moniezia</span> sp. egg; (<b>H</b>) <span class="html-italic">Nematodirus</span> sp. egg at early stage of embryonic development; (<b>I</b>) elongated strongyle-type egg; (<b>J</b>) <span class="html-italic">Capillaria</span> sp. egg; (<b>K</b>) <span class="html-italic">Dictyocaulus</span> sp. L1; (<b>L</b>) <span class="html-italic">Elaphostrongylus rangiferi</span> L1. Bright field microscopy, 400× magnification. Scale bar equals 50 μm.</p>
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<p>Prevalence rates (%) of helminths found in feces of zoo reindeer.</p>
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<p>Map of Russia indicating the zoos. Insert on the right represents magnified area marked with a rectangle. Numbers correspond to the zoo ID numbers in <a href="#jzbg-05-00033-t0A1" class="html-table">Table A1</a>.</p>
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<p>Mites of reindeer. (<b>A</b>) <span class="html-italic">Demodex</span> sp. obtained from the feces of a reindeer from zoo #12; (<b>B</b>) egg of mite at early developmental stage obtained from the feces of a reindeer from zoo #30; (<b>C</b>) egg of mite at late developmental stage obtained from the feces of a reindeer from zoo #48; (<b>D</b>) <span class="html-italic">Chorioptes</span> sp. obtained from the feces of a reindeer from zoo #40; (<b>E</b>) manifestation of mange caused by mites in a reindeer from zoo #30 (furless patches in the front leg and chest are shown); photo courtesy: Kristina Zabarina. Light micrographs were made via bright field microscopy, 400× magnification. Scale bar equals 50 μm.</p>
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16 pages, 21584 KiB  
Article
PSAT1 Promotes Metastasis via p-AKT/SP1/ITGA2 Axis in Estrogen Receptor-Negative Breast Cancer Cell
by Xingda Zhang, Siyu Wang, Wei Li, Jianyu Wang, Yajie Gong, Quanrun Chen, Shihan Cao, Da Pang and Song Gao
Biomolecules 2024, 14(8), 990; https://doi.org/10.3390/biom14080990 (registering DOI) - 12 Aug 2024
Viewed by 183
Abstract
Background: Accumulating evidence indicates that PSAT1 not only reprogrammed metabolic function but also exhibits “moonlighting” functions in promoting tumor malignancy. However, the underlying molecular mechanisms of PSAT1 promoting ER-negative breast cancer cell migration need further investigation. Methods: Briefly, the PSAT1 and ITGA2 expression [...] Read more.
Background: Accumulating evidence indicates that PSAT1 not only reprogrammed metabolic function but also exhibits “moonlighting” functions in promoting tumor malignancy. However, the underlying molecular mechanisms of PSAT1 promoting ER-negative breast cancer cell migration need further investigation. Methods: Briefly, the PSAT1 and ITGA2 expression in cells and tissues was detected using qRT-PCR, immunofluorescence staining and western blot assay. The effect of PSAT1 and ITGA2 was verified both in vitro and in vivo. RNA-seq analysis explored a series of differently expressed genes. The regulation between SP1 and ITGA2 was investigated by ChIP analysis. Results: We reported PSAT1 was highly expressed in ER-breast cancer tissues and tumor cells and positively correlated with metastasis. Moreover, RNA-seq analysis explored a series of differently expressed genes, including ITGA2, in PSAT1 overexpressed cells. Mechanistically, PSAT1 facilitated breast cancer metastasis via the p-AKT/SP1/ITGA2 axis. We further elucidated that PSAT1 promoted the entry of SP1 into the nucleus through the upregulation of p-AKT and confirmed ITGA2 is a target of SP1. In addition, enhanced cell migration was remarkably reversed by ITGA2 depletion or p-AKT inhibitor treatment. Conclusion: This study clarified the mechanism of PSAT1 in promoting ER-negative breast cancer metastasis, which may provide mechanistic clues for attenuating breast cancer metastasis. Full article
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<p>PSAT1 overexpressed in ER negative breast cancer with lymph node metastasis. (<b>A</b>) Expression profile of PSAT1 in primary breast cancer tissues (<span class="html-italic">n</span> = 1113) compared with normal breast tissues (<span class="html-italic">n</span> = 113) (TCGA). (<b>B</b>) Expression profile of PSAT1 in ER− breast cancer tissues (<span class="html-italic">n</span> = 238) compared with ER+ tissues (<span class="html-italic">n</span> = 808) (TCGA). (<b>C</b>) Representative images of PSAT1 immunohistochemical staining in breast cancer samples; scale bar, 100 µm. (<b>D</b>) Quantification of positive or negative PSAT1 expression in ER− or ER+ BC samples by Chi-square test. Quantification of positive or negative PSAT1 expression in ER− (<b>E</b>) and ER+ (<b>F</b>) BC samples with corresponding LN status by Chi-square test. TCGA = The Cancer Genome Atlas; ER− = ER negative; ER+ = ER positive; lymph node = LN; BC = breast cancer. * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001, ns: no significance.</p>
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<p>PSAT1 knockdown prevented metastasis of ER-negative breast cancer cells. Western blot (<b>A</b>) and qRT-PCR assay (<b>B</b>) showed PSAT1 knockdown and overexpression in BT-549 and HCC1937 cells infected with PSAT1 lentivirus (PSAT1-KD1, PSAT1-KD2 and PSAT1-OE) or control (PSAT1-NC and PSAT1-CON). The values of the PSAT1-NC and PSAT1-CON groups were normalized to 1. (<b>C</b>,<b>F</b>) Image and quantification of adhesion assay, transwell migration, and invasion assays in BT-549 and HCC-1937 cells. The cell numbers of PSAT1-NC and PSAT1-CON group were normalized to 1; scale bar for adhesion assay 200 µm and for transwell migration and invasion assay 100 µm. The wound healing assay revealed PSAT1 knockdown inhibited cell metastasis in BT-549 (<b>D</b>) and HCC1937 (<b>E</b>) cellsThe wound healing assay revealed PSAT1 overexpression promoted cell metastasis in BT-549 (<b>G</b>) and HCC1937 (<b>H</b>) cells; scale bar, 200 µm. Statistical analysis was performed using unpaired two-tailed Student <span class="html-italic">t</span>-test. For (<b>C</b>–<b>H</b>), the results are expressed as the mean ± SD; <span class="html-italic">n</span> = 3. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>PSAT1 promoted metastasis of ER-negative breast cancer cells in mouse model. Western blot (<b>A</b>) and qRT-PCR (<b>B</b>) were used to analyze PSAT1 expression in PSAT1-knockdown (PSAT1-KD1, PSAT1-KD2) or control (PSAT1-NC) 4T1 cells and PSAT1-overexpression (PSAT1-OE) or vector (PSAT1-CON) 4T1 cells. The adhesion assays, transwell migration assays, or invasion assays (<b>B</b>) showed the cellular transfer ability of the indicated cells. The number of PSAT1-NC or PSAT1-CON cells were normalized to 1. Scale bar for adhesion assays were 200 µm and for transwell migration assays or invasion assays were 100 µm. Images and quantification of BALB/C mice tail vein injection lung metastasis mode with PSAT1 knockdown (<b>C</b>) and PSAT1 overexpression (<b>D</b>) 4T1 cells. The quantification was analyzed using Student’s <span class="html-italic">t</span>-test for comparisons. For (<b>B</b>), the results are expressed as the mean ± SD; <span class="html-italic">n</span> = 3. Lung tissues were resected from mice at 27 days. Lung metastases were counted. (<span class="html-italic">n</span> = 5). ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001.</p>
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<p>PSAT1 promoted metastasis of ER-negative breast cancer cells through upregulation of ITGA2 (<b>A</b>). The volcano maps of all samples. Red dots mean the signal value of up-regulated genes (<span class="html-italic">n</span> = 1276), and blue ones indicate the signal value of down-regulated genes (<span class="html-italic">n</span> = 535) (<b>B</b>). Bubble map of KEGG enrichment analysis for DEGs (<b>C</b>). qRT-PCR is used to validation in the indicated BT-549 cells. The PSAT1 ITGA2 expression was analyzed with western blot (<b>D</b>) and qRT-PCR (<b>E</b>) in the indicated cells. The values of the PSAT1-NC and PSAT1-CON groups were normalized to 1 (<b>F</b>). Immunofluorescence staining showed PSAT1 knockdown reduced ITGA2 expression, but PSAT1 overexpression promoted ITGA2 expression. Scale bar, 50 µm (<b>G</b>). Immunoblot assay of PSAT1 and ITGA2 protein levels in PSAT1-CON, PSAT1-OE, PSAT1-OE+siNC, and PSAT1-OE+siITGA2. The adhesion assay (<b>H</b>) and transwell migration assay (<b>I</b>) of BT-549 cells with PSAT1-CON, PSAT1-OE, PSAT1-OE+siNC, and PSAT1-OE+siITGA2. The cell numbers of PSAT1-CON groups were normalized to 1. Scale bar, 100 µm (<b>J</b>). Wound healing assay showed that silencing ITGA2 abrogates cell metastasis due to PSAT1 overexpression. Scale bar, 200, µm. Statistical analysis was performed with unpaired two-tailed Student <span class="html-italic">t</span>-test. For (<b>H</b>–<b>J</b>), the results are expressed as the mean ± SD; <span class="html-italic">n</span> = 3. #ITGA2 level compared to PSAT1-NC or PSAT1-CON. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001, ### <span class="html-italic">p</span> &lt; 0.001, #### <span class="html-italic">p</span> &lt; 0.0001, ns: no significance. DEGs: differentially expressed genes.</p>
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<p>PSAT1 upregulated ITGA2 expression through transcription factors SP1 (<b>A</b>). Western blot was performed to analyze the expression of SP1 in nucleus and cytoplasm of indicated cells (<b>B</b>). Schematic representation of the predicated SP1 binding site within the ITGA2 promotor (<b>C</b>). Binding of SP1 to the ITGA2 promoter region in vitro was assessed using ChIP with anti-SP1 or anti-IgG antibodies in BT-549 cells. Input DNA purified by ChIP assay were measured using qRT-PCR. The results of IgG were normalized to 1 (<b>D</b>). Western blot was used to show PSAT1 and ITGA2 protein levels in PSAT1-CON, PSAT1-OE, PSAT1-OE+DMSO, and PSAT1-OE+MIT (<b>E</b>). qRT-PCR quantification of the indicated mRNAs in BT-549 cells (<b>F</b>). Wound healing assay showed that silencing SP1 abrogates cell metastasis caused by PSAT1 overexpression. Scale bar, 200 µm. The adhesion assay (<b>G</b>) and transwell migration assay (h) of BT-549 cells with PSAT1-CON, PSAT1-OE, PSAT1-OE+DMSO, and PSAT1-OE+MIT. Scale bar, 100 µm. Statistical analysis was performed with unpaired two-tailed Student <span class="html-italic">t</span>-test. For (<b>D</b>–<b>H</b>), treated with MIT (40 μM) for 24 h. For (<b>F</b>–<b>H</b>), the results are expressed as the mean ± SD; <span class="html-italic">n</span> = 3. For <span class="html-italic">p</span> values in e *PSAT1 level compared to PSAT1-CON; #ITGA2 level compared to PSAT1-CON; ^ITGA2 level compared to PSAT1-OE+DMSO. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001, ### <span class="html-italic">p</span> &lt; 0.001, #### <span class="html-italic">p</span> &lt; 0.0001, ^^^ <span class="html-italic">p</span> &lt; 0.001, ns: no significance.</p>
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<p>PSAT1 promoted metastasis of ER-negative breast cancer cells by p-AKT/SP1/ITGA2 axis (<b>A</b>). Western blot was performed to analyze the expression of PSAT1 and AKT/p-AKT in the indicated cells (<b>B</b>). PSAT1 overexpression cell treated with PI3K-AKT pathway inhibitor. Then the expression of P-AKT and ITGA2 were tested (<b>C</b>). Western blot was used to show PSAT1, SP1, and ITGA2 protein levels in PSAT1-CON, PSAT1-OE, PSAT1-OE+DMSO, and PSAT1-OE+LY294002 (<b>D</b>). qRT-PCR quantification of the indicated mRNAs in BT-549 cells (<b>E</b>). The adhesion assay and transwell migration assay of BT-549 cells showed that silencing p-AKT pathway abrogates cell metastasis caused by PSAT1 overexpression. Statistical analysis was performed using unpaired two-tailed Student <span class="html-italic">t</span>-test (<b>F</b>). Proposed model for PSAT1 promotes estrogen receptor negative breast cancer cell metastasis via p-AKT/SP1/ITGA2 pathway. For (<b>C</b>–<b>E</b>), treated with LY294002 (10 μM) for 1 h. For (<b>E</b>), the results are expressed as the mean ± SD; <span class="html-italic">n</span> = 3. For <span class="html-italic">p</span> values in e *PSAT1 level compared to PSAT1-CON; #ITGA2 level compared to PSAT1-CON; ^ITGA2 level compared to PSAT1-OE+DMSO. ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001, **** <span class="html-italic">p</span> &lt; 0.0001, #### <span class="html-italic">p</span> &lt; 0.0001, ^^^^ <span class="html-italic">p</span> &lt; 0.0001, ns: no significance.</p>
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10 pages, 227 KiB  
Article
Perinatal Outcomes of Singleton, Twin and Triplet Gestations after Oocyte Donation: A Retrospective, Population-Based Cohort Analysis
by Or Eliner, Roni Rahav Koren, Hila Shalev Ram, Mattan Levi, Einat Haikin Herzberger, Amir Wiser and Netanella Miller
Children 2024, 11(8), 962; https://doi.org/10.3390/children11080962 (registering DOI) - 10 Aug 2024
Viewed by 167
Abstract
Background/Objectives: Although high live birth rates are associated with oocyte donation (OD), these pregnancies are associated with increased obstetric and perinatal risks. This study evaluated maternal and neonatal risks after OD compared to in vitro fertilization (IVF) with autologous oocytes, and to spontaneous [...] Read more.
Background/Objectives: Although high live birth rates are associated with oocyte donation (OD), these pregnancies are associated with increased obstetric and perinatal risks. This study evaluated maternal and neonatal risks after OD compared to in vitro fertilization (IVF) with autologous oocytes, and to spontaneous pregnancies (SPs), among singletons, twins and triplets. Methods: A retrospective, large, population-based cohort study was conducted based on electronic data from Maccabi Healthcare Services. A total of 469,134 pregnancies were grouped according to the mode of conception. The main outcome measures were preterm birth (PTB), small for gestational age (SGA) and pregnancy-induced hypertension (PIH). The data were analyzed separately for singletons, twins and triplets. Results: The mean maternal age was older in the OD group compared with the IVF and SP groups (singletons: 39.7 ± 4.1 vs. 34.5 ± 4.8 and 31.7 ± 5.3 years; twins: 39 ± 4.6 vs. 32.6 ± 4.4 and 31.2 ± 5.1 years; and triplets: 35.6 ± 2.5 vs. 32 ± 3.9 and 29.7 ± 5 years). The mean gestational age was younger among the OD group compared to the SP group (singletons: 37.5 ± 3 vs. 39 ± 2 p = 0.001, and twins: 35 ± 3 vs. 36 ± 2.5 p = 0.001). Higher rates of PTB < 37, PTB < 34 and PTB < 28 weeks were found among OD singletons. Multivariable logistic regressions for PTB < 37 weeks and SGA in singletons demonstrated that OD and IVF are significant risk factors (OR = 4.1, 95%CI = 3.3–5.2; OR = 4.3, 95%CI = 4.1–4.6; OR = 1.9, 95%CI = 1.3–2.6; OR = 2.2, 95%CI = 2–2.4, respectively). Significantly higher rates of PIH were demonstrated among the OD vs. IVF and SP groups in singleton (4.3% vs. 1.7% and 0.7%) and in twin pregnancies (7.5% vs. 4.3% and 3.4%). Conclusions: OD pregnancies are at increased risk for PTB, SGA and PIH. Full article
(This article belongs to the Section Pediatric Neonatology)
13 pages, 1666 KiB  
Article
Fruit Variation in Yellow-Fleshed Actinidia (Actinidia chinensis Planch) Plants Grown in Southern Italy as a Function of Shoot Type
by Antonio Dattola, Antonella Accardo, Rocco Zappia and Gregorio Antonio Maria Gullo
Agriculture 2024, 14(8), 1335; https://doi.org/10.3390/agriculture14081335 - 10 Aug 2024
Viewed by 236
Abstract
One of the goals of modern orcharding is to produce a high volume of fruits with uniform size, organoleptic parameters, and health characteristics. The aim of this work was to study various shoot types and their prevailing positions along the cane and to [...] Read more.
One of the goals of modern orcharding is to produce a high volume of fruits with uniform size, organoleptic parameters, and health characteristics. The aim of this work was to study various shoot types and their prevailing positions along the cane and to identify how shoot type can influence the quality of fruit from the Actinidia tree. The experiment was conducted over a two-year period in a commercial orchard of Actinidia chinensis, cv. Gold 3. The shoots along the cane were classified as follows: spur shoots (SPs), terminated shoots (TEs), non-terminated shoots (NTs), and cut non-terminated shoots (CNTs). The data were statistically processed using ANOVA and Principal Component Analysis (ACP). Four different categories of fruit were obtained from the four shoot types, and their various attributes were compared. The prevailing category (comprising 55% of the studied fruits) was TEs, which are characterised by a higher soluble solid content, sweetness, and excellent health characteristics, as well as the reduced hardness of their pulp, which would support the hypothesis that harvesting could be brought forward. The second most common category (comprising 19% of total fruit) with the lowest soluble solid content, but a high antioxidant capacity, was that which was detached from the CNTs, while 13% of the fruit was produced from NTs, which had the lowest health value but good sweetness perception. Finally, the category with the lowest fruit percentage over the total fruit harvested (10%) was SPs, which are characterised by their smaller size. It has yet to be determined what the performance of each category will be post-harvest; whether it is possible to assign the quality categories while harvesting the fruit or to differentiate the harvest time accordingly remains subject to debate. Full article
(This article belongs to the Section Crop Production)
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<p>Biplot with centroid and variable vectors on F1 and F2 planes.</p>
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<p>Three-dimensional representation of latent variables discriminated according to shoot type.</p>
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<p>Thermo-pluviometric regime of the 2022–2023 biennium of the area of interest.</p>
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20 pages, 7530 KiB  
Article
Coastal Almond-Leaved Pear (Pyrus spinosa) Seedlings’ Responses to Saline Stress Alleviated by Formulated L-Methionine and Bacterial Exogenous Soil Application
by Helen Kalorizou, Paschalis Giannoulis, Stefanos Leontopoulos, Charalambos Angelakis and Maria Sorovigka
Horticulturae 2024, 10(8), 849; https://doi.org/10.3390/horticulturae10080849 (registering DOI) - 10 Aug 2024
Viewed by 291
Abstract
Coastal Pyrus spinosa seedlings were tested for their developmental, chlorophyll content and antioxidant performance under soil saline conditions where bacterial and l-methionine exogenous treatments were applied as potential saline alleviation stress schemes. Scaling up saline stress, the number of formed lateral shoots was [...] Read more.
Coastal Pyrus spinosa seedlings were tested for their developmental, chlorophyll content and antioxidant performance under soil saline conditions where bacterial and l-methionine exogenous treatments were applied as potential saline alleviation stress schemes. Scaling up saline stress, the number of formed lateral shoots was reduced in all treatments. Medium salt stress (75 mM NaCl) demonstrated a rather unified decline in shoot fresh weight values, which became toxic at 100 mM NaCl, with up to 89.1% shoot fresh weight losses, in comparison to unchallenged status. Both exogenous applications increased root/shoot ratio, providing developmental boost for root growth. Total chlorophyll content values (May–July) did not differ among non-stressed plantlets independently of exogenous treatment. All experimental plantlet lines increased their antioxidant activity on scaled up soil NaCl enrichment. Νo differences in root orientation and their angle frequencies were observed while soil saline exposure took place. In brief, spring–summer exposure of P. spinosa plantlets under 100 mM NaCl saline stress can be manageable, achieving higher root/shoot ratio values, upregulating leaf antioxidant activity and optimizing root growth upon bacterial and l-methionine supplementation. However, many of the examined parameters were found to be not extensively different between exogenously treated plantlets and non-supplemented ones, suggesting a potential role of intergenerational and transgenerational stress memory. Full article
(This article belongs to the Section Biotic and Abiotic Stress)
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<p><span class="html-italic">P. spinosa</span> seedlings: (<b>A</b>) Non-salt-treated plantlets, and (<b>B</b>–<b>D</b>) plantlets treated with 50 mM, 75 mM and 100 mM NaCl soil stress, respectively. From each section in left to right direction, non-stimulatory supplementation, amino acid- and microbial-supplemented plantlet lines.</p>
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<p>Total phenolic content (mg GAE/g d.w.) in <span class="html-italic">P. spinosa</span> seedlings upon saline soil stress. The different letters indicate a significant (<span class="html-italic">p</span> &lt; 0.05) difference; first letter demonstrates differences between exogenous treatments and the second one among salt stress levels. Data are presented as the mean ± SE of five replicates.</p>
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<p>Antioxidant activity (%) found on <span class="html-italic">P. spinosa</span> leaves upon saline soil stress. The different letters indicate a significant (<span class="html-italic">p</span> &lt; 0.05) difference; first letter demonstrates differences between exogenous treatments and the second one among salt stress levels. Data are presented as the mean ± SE of five replicates.</p>
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<p>Roots of <span class="html-italic">P. spinosa</span> seedlings without amino acid or microbial supplementation: (<b>A</b>) Non-salt-treated plantlets, and (<b>B</b>–<b>D</b>) plantlets treated with 50 mM, 75 mM and 100 mM NaCl soil stress, respectively.</p>
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<p>Roots of <span class="html-italic">P. spinosa</span> seedlings with amino acid supplementation: (<b>A</b>) Non-salt-treated plantlets, and (<b>B</b>–<b>D</b>) plantlets treated with 50 mM, 75 mM and 100 mM NaCl soil stress, respectively.</p>
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<p>Roots of <span class="html-italic">P. spinosa</span> seedlings with microbial supplementation: (<b>A</b>) Non-salt-treated plantlets, and (<b>B</b>–<b>D</b>) plantlets treated with 50 mM, 75 mM and 100 mM NaCl soil stress, respectively.</p>
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16 pages, 13049 KiB  
Article
Image Databases with Features Augmented with Singular-Point Shapes to Enhance Machine Learning
by Nikolay Metodiev Sirakov and Adam Bowden
Electronics 2024, 13(16), 3150; https://doi.org/10.3390/electronics13163150 - 9 Aug 2024
Viewed by 333
Abstract
The main objective of this paper is to present a repository of image databases whose features are augmented with embedded vector field (VF) features. The repository is designed to provide the user with image databases that enhance machine learning (ML) classification. Also, six [...] Read more.
The main objective of this paper is to present a repository of image databases whose features are augmented with embedded vector field (VF) features. The repository is designed to provide the user with image databases that enhance machine learning (ML) classification. Also, six VFs are provided, and the user can embed them into her/his own image database with the help of software named ELPAC. Three of the VFs generate real-shaped singular points (SPs): springing, sinking, and saddle. The other three VFs generate seven kinds of SPs, which include the real-shaped SPs and four complex-shaped SPs: repelling and attracting (out and in) spirals and clockwise and counterclockwise orbits (centers). Using the repository, this work defines the locations of the SPs according to the image objects and the mappings between the SPs’ shapes if separate VFs are embedded into the same image. Next, this paper produces recommendations for the user on how to select the most appropriate VF to be embedded in an image database so that the augmented SP shapes enhance ML classification. Examples of images with embedded VFs are shown in the text to illustrate, support, and validate the theoretical conclusions. Thus, the contributions of this paper are the derivation of the SP locations in an image; mappings between the SPs of different VFs; and the definition of an imprint of an image and an image database in a VF. The advantage of classifying an image database with an embedded VF is that the new database enhances and improves the ML classification statistics, which motivates the design of the repository so that it contains image features augmented with VF features. Full article
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<p>The SP shapes are cropped from a synthetic image where the VF is embedded: (<b>a</b>) <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </msub> </semantics></math>—sinking-shaped SP; (<b>b</b>) <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </msub> </semantics></math>—springing-shaped SP; (<b>c</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>—saddle-shaped SP.</p>
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<p>The SP shapes are cropped from a COIL100 [<a href="#B11-electronics-13-03150" class="html-bibr">11</a>] image where the VF <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </msub> </semantics></math> has been embedded: (<b>a</b>) shows a spiral-out (repelling)-shaped SP; (<b>b</b>) presents a clockwise orbit SP.</p>
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<p>A malignant skin lesion image from [<a href="#B21-electronics-13-03150" class="html-bibr">21</a>].</p>
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<p>Parts (<b>a</b>,<b>c</b>,<b>e</b>,<b>g</b>,<b>i</b>,<b>k</b>) show the six VFs <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> <mo>,</mo> <mo>∇</mo> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> <mo>,</mo> <mo>∇</mo> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> <mo>,</mo> <msub> <mi>v</mi> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </msub> <mo>,</mo> <msub> <mi>v</mi> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </msub> <mo>,</mo> <msub> <mi>v</mi> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> </msub> </mrow> </semantics></math> embedded into the skin lesion image shown in <a href="#electronics-13-03150-f003" class="html-fig">Figure 3</a>. The remaining parts (<b>b</b>,<b>d</b>,<b>f</b>,<b>h</b>,<b>j</b>,<b>l</b>) show the imprints of the skin lesion in the six VFs, respectively.</p>
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<p>(<b>a</b>) A synthetic object. The upper row shows zooms of the lower branch of the object in (<b>a</b>) with embedded VFs: (<b>b</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </mrow> </semantics></math>; (<b>c</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>; (<b>d</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>. The lower row shows zooms of the core part of the object in (<b>a</b>) with embedded VFs: (<b>e</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </mrow> </semantics></math>; (<b>f</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>; (<b>g</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>.</p>
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<p>An overall view of the object in <a href="#electronics-13-03150-f005" class="html-fig">Figure 5</a>a with embedded VFs: (<b>a</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </mrow> </semantics></math>; (<b>b</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>; (<b>c</b>) <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>.</p>
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<p>The object in <a href="#electronics-13-03150-f005" class="html-fig">Figure 5</a>a with embedded VFs: <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </msub> </semantics></math> in the left column, parts (<b>a</b>,<b>d</b>,<b>g</b>); <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </msub> </semantics></math> in the middle column, parts (<b>b</b>,<b>e</b>,<b>h</b>); <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> </msub> </semantics></math> in the right column, parts (<b>c</b>,<b>f</b>,<b>i</b>).</p>
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<p>The mappings between the CPs of <math display="inline"><semantics> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </semantics></math>, <math display="inline"><semantics> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </semantics></math>, and <math display="inline"><semantics> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> </semantics></math> and the SPs of the six VFs derived from the three functions, as well as the mappings between the SPs of the VFs.</p>
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<p>Examples of ISIC 2018 and ISIC2020 images with embedded VFs.</p>
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<p>Examples of COIL100 images with embedded VFs. From left to right: <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>, <math display="inline"><semantics> <mrow> <mo>∇</mo> <mover accent="true"> <mi>ψ</mi> <mo>^</mo> </mover> </mrow> </semantics></math>, <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>u</mi> <mo>^</mo> </mover> </msub> </semantics></math>, and <math display="inline"><semantics> <msub> <mi>v</mi> <mover accent="true"> <mi>ϕ</mi> <mo>^</mo> </mover> </msub> </semantics></math>.</p>
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<p>Examples of YALE face database images with embedded VFs.</p>
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<p>The GUI of ELPAC software [<a href="#B14-electronics-13-03150" class="html-bibr">14</a>]. The drop-down list below “Vector Field Generation” shows the list of VFs that can be embedded in an image.</p>
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14 pages, 3698 KiB  
Article
Biological Control Potential of Bacillus subtilis Isolate 1JN2 against Fusarium Wilt on Cucumber
by Wei Yang, Lan Wang, Xiao Li, Haixia Yan, Beibei Zhong, Xinru Du, Qi Guo, Tingting He and Yuming Luo
Horticulturae 2024, 10(8), 843; https://doi.org/10.3390/horticulturae10080843 - 9 Aug 2024
Viewed by 248
Abstract
Cucumber is one of the top ten vegetables globally and is widely cultivated worldwide. However, Fusarium wilt, caused by Fusarium oxysporum f. sp. Cucumerinum, is one of the most serious soil-borne diseases in cucumber cultivation, causing significant economic losses. Biological control has [...] Read more.
Cucumber is one of the top ten vegetables globally and is widely cultivated worldwide. However, Fusarium wilt, caused by Fusarium oxysporum f. sp. Cucumerinum, is one of the most serious soil-borne diseases in cucumber cultivation, causing significant economic losses. Biological control has great potential in the prevention of cucumber wilt disease, but the mechanism involved still needs further research. In this study, biocontrol isolate Bacillus subtilis 1JN2, which was isolated in our previous work, was evaluated in field conditions against Fusarium wilt, and the rhizosphere fungal diversity was analyzed. The results indicated that the biocontrol efficacy of B. subtilis 1JN2 reached 58.5% compared with the blank control, and the population density of F. oxysporum in the rhizosphere decreased from 495 copies/g of soil before inoculation to 20 copies/g 14 days after treatment. High-throughput sequencing demonstrated that after an inoculation of 1JN2, the populations that decreased significantly include the genera of Olpidium and Pseudallescheria, from more than 20% to less than 8%. And the most increased population belonged to the family Chaetomiaceae, from 6.82% to 18.77%, 12.39%, 44.41%, and 19.41% at the four sample time points after treatment. In addition, soil-related enzyme activities, including catalase, soil dehydrogenase, alkaline phosphatase, and polyphenol oxidase, were analyzed before and after treatment with 1JN2. The results indicated that all the enzyme activities showed an upward trend following inoculation. These findings demonstrate the potential of using B. subtilis 1JN2 as a biocontrol agent for controlling Fusarium wilt in cucumber. Full article
(This article belongs to the Special Issue Plant Disease Management and Pathogens Control in Horticulture)
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<p>The population density of <span class="html-italic">Fusarium oxysporum</span> f. sp. <span class="html-italic">cucumerinum</span> (FOC) in the rhizosphere soil of cucumber after treatment with <span class="html-italic">Bacillus subtilis</span> 1JN2. Values are means and standard deviations of three replicates.</p>
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<p>Trend of changes at the genus level of cucumber rhizosphere fungi at different time points after the treatment of field soil with the biocontrol agent <span class="html-italic">Bacillus subtilis</span> 1JN2. PLS-DA = Partial Least Squares Discriminant Analysis.</p>
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<p>Analysis of the rhizo-fungal community of cucumber after treatment with <span class="html-italic">Bacillus subtilis</span> 1JN2. (<b>A</b>) Circos analysis at the phyla level; (<b>B</b>) Circos analysis at the genus level; (<b>C</b>–<b>G</b>) analysis at the genus level by sampling time point. In (<b>A</b>,<b>B</b>), J1–J3, J4–6, J7–J9, J10–J12, and J13–J15 represent three repetitions of each sampling time point, respectively. The small semicircle (left half-circle) represents the composition of species in the sample. The color of the outer color band represents which group it comes from, the color of the inner color band represents the species, and the length represents the relative abundance of the species in the corresponding sample. The large semicircle (right half-circle) represents the distribution ratio of species in different samples at the taxonomic level, with the outer color band representing the species, the inner color band representing different groups, and the length representing the distribution ratio of the sample in a certain species.</p>
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<p>Analysis of the rhizo-fungal community of cucumber after treatment with <span class="html-italic">Bacillus subtilis</span> 1JN2. (<b>A</b>) Circos analysis at the phyla level; (<b>B</b>) Circos analysis at the genus level; (<b>C</b>–<b>G</b>) analysis at the genus level by sampling time point. In (<b>A</b>,<b>B</b>), J1–J3, J4–6, J7–J9, J10–J12, and J13–J15 represent three repetitions of each sampling time point, respectively. The small semicircle (left half-circle) represents the composition of species in the sample. The color of the outer color band represents which group it comes from, the color of the inner color band represents the species, and the length represents the relative abundance of the species in the corresponding sample. The large semicircle (right half-circle) represents the distribution ratio of species in different samples at the taxonomic level, with the outer color band representing the species, the inner color band representing different groups, and the length representing the distribution ratio of the sample in a certain species.</p>
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<p>Analysis of the rhizo-fungal community of cucumber after treatment with <span class="html-italic">Bacillus subtilis</span> 1JN2. (<b>A</b>) Circos analysis at the phyla level; (<b>B</b>) Circos analysis at the genus level; (<b>C</b>–<b>G</b>) analysis at the genus level by sampling time point. In (<b>A</b>,<b>B</b>), J1–J3, J4–6, J7–J9, J10–J12, and J13–J15 represent three repetitions of each sampling time point, respectively. The small semicircle (left half-circle) represents the composition of species in the sample. The color of the outer color band represents which group it comes from, the color of the inner color band represents the species, and the length represents the relative abundance of the species in the corresponding sample. The large semicircle (right half-circle) represents the distribution ratio of species in different samples at the taxonomic level, with the outer color band representing the species, the inner color band representing different groups, and the length representing the distribution ratio of the sample in a certain species.</p>
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<p>Rhizosphere soil enzyme activities of cucumber after treatment with <span class="html-italic">Bacillus subtilis</span> 1JN2. Values are means of standard deviations of three replicates.</p>
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14 pages, 5253 KiB  
Article
Mapping and Candidate Gene Analysis of an All-Stage Stem Rust Resistance Gene in Durum Wheat Landrace PI 94701
by Hongyu Li, Kairong Li, Hongna Li, Chen Yang, Geetha Perera, Guiping Wang, Shikai Lyu, Lei Hua, Shams ur Rehman, Yazhou Zhang, Michael Ayliffe, Haitao Yu and Shisheng Chen
Plants 2024, 13(16), 2197; https://doi.org/10.3390/plants13162197 - 8 Aug 2024
Viewed by 333
Abstract
Puccinia graminis f. sp. tritici (Pgt), the causal agent of wheat stem rust, poses a significant threat to global wheat production. Genetic resistance offers a cost-effective and sustainable solution. The durum wheat landrace PI 94701 was previously hypothesized to carry two stem [...] Read more.
Puccinia graminis f. sp. tritici (Pgt), the causal agent of wheat stem rust, poses a significant threat to global wheat production. Genetic resistance offers a cost-effective and sustainable solution. The durum wheat landrace PI 94701 was previously hypothesized to carry two stem rust resistance (Sr) genes, but their chromosomal locations were unknown. In this study, we mapped and characterized an all-stage Sr gene in PI 94701, temporarily designated as SrPI94701. In seedling tests, SrPI94701 was effective against all six Pgt races tested. Using a large segregating population, we mapped SrPI94701 on chromosome arm 5BL within a 0.17-cM region flanked by markers pku69124 and pku69228, corresponding to 1.04 and 2.15 Mb genomic regions in the Svevo and Chinese Spring reference genomes. Within the candidate region, eight genes exhibited differential expression between the Pgt-inoculated resistant and susceptible plants. Among them, two nucleotide-binding leucine-rich repeat (NLR) genes, TraesCS5B03G1334700 and TraesCS5B03G1335100, showed high polymorphism between the parental lines and were upregulated in Pgt-inoculated resistant plants. However, the flanking and completely linked markers developed in this study could not accurately predict the presence of SrPI94701 in a survey of 104 wheat accessions. SrPI94701 is a promising resource for enhancing stem rust resistance in wheat breeding programs. Full article
(This article belongs to the Special Issue Mining and Mapping of Disease-Resistant Genes in Wheat)
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<p>Infection types of PI 94701 and Rusty in response to <span class="html-italic">Pgt</span> races. Six <span class="html-italic">Pgt</span> races (BCCBC, 34MTGSM, 34C3RTGQM, 21C3CTTTM, 34MKGQM, and 34C3RKGQM) were used in this study, and their avirulence/virulence profiles are detailed in <a href="#app1-plants-13-02197" class="html-app">Table S1</a>. Plants were grown in growth chambers at 22–24 °C with 16 h light/8 h dark. Seedlings at the three-leaf stage were challenged with a urediniospore/talc suspension using the shaking-off method [<a href="#B29-plants-13-02197" class="html-bibr">29</a>]. RP, resistant parent; SP, susceptible parent; R, resistant; S, susceptible; CK, plants without inoculation.</p>
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<p>BSR-Seq analysis of <span class="html-italic">SrPI94701</span>. (<b>A</b>) Δ(SNP-index) was calculated for each SNP across all chromosomes. (<b>B</b>) Δ(SNP-index) were specifically calculated for each SNP on chromosome 5B. SNP-index plotting was conducted following a previously established protocol [<a href="#B30-plants-13-02197" class="html-bibr">30</a>]. SNP index values in the resistant and susceptible pools were calculated using a custom Perl script, and the Δ(SNP-index) = |(SNP-index of the resistant pool) − (SNP-index of the susceptible pool)| was determined for each SNP. Sliding window analysis was applied to ΔSNP-index plots with a 5 Mb window size and a 50 kb increment. A total of 160 SNPs within the genomic region spanning from 673.5 to 699.9 Mb (Svevo Rel.1.0; <a href="#app1-plants-13-02197" class="html-app">Table S2</a>) on chromosome arm 5BL showed significant association with the phenotype. The mapping region is highlighted by red arrows.</p>
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<p>Genetic maps for <span class="html-italic">SrPI94701</span>. (<b>A</b>) Genetic mapping of the resistance locus on chromosome arm 5BL by BSR-seq. The gray rectangle indicates the genomic region spanning from 673.5 to 699.9 Mb (Svevo Rel.1.0). (<b>B</b>) Genetic map for <span class="html-italic">SrPI94701</span> based on 143 F<sub>2:3</sub> families from the PI 94701 × Rusty cross and 14 PCR markers. The values to the left of the markers indicate the genetic distances in centimorgans (cM). (<b>C</b>) High-density map based on 1151 F<sub>2</sub> plants and seven molecular markers. The values to the left of the markers indicate the genetic distances in centimorgans (cM). (<b>D</b>) Colinear genomic region on chromosome 5B of Svevo (Rel.v1.0). The values to the left of the genes indicate their physical locations in megabases (Mb). Genetic maps were constructed using the software MapChart v2.2 [<a href="#B31-plants-13-02197" class="html-bibr">31</a>].</p>
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<p>Genotypes of F<sub>2</sub> plants derived from the PI 94701 × Rusty cross. F<sub>2</sub> plants genotyped with (<b>A</b>) CAPS marker <span class="html-italic">pku69124</span> (digested with SspI); (<b>B</b>) CAPS marker <span class="html-italic">pku69187</span> (BbvCI); (<b>C</b>) CAPS marker <span class="html-italic">pku69211</span> (HpyCH4IV); (<b>D</b>) CAPS marker <span class="html-italic">pku69227</span> (PvuII); (<b>E</b>) CAPS marker <span class="html-italic">pku69228</span> (Hpy188III); and (<b>F</b>) CAPS marker <span class="html-italic">pku69231</span> (BtgI). PCR products were separated on agarose gels and stained directly with ethidium bromide. RP, resistant parent PI 94701; SP, susceptible parent Rusty; A, band corresponds to the resistant allele; B, band corresponds to the susceptible allele; H, heterozygous; M, DNA ladder.</p>
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<p>A heat map illustrating the differentially expressed genes (DEGs) within the candidate region of <span class="html-italic">SrPI94701</span>. DEGs between homozygous resistant plants (R32-1, R32-2, and R32-3; R) and homozygous susceptible plants (S73-1, S73-2, and S73-3; S) were identified from RNA-seq analysis of <span class="html-italic">Pgt</span>-inoculated RNA samples from R32 and S73. The heatmap was generated using the pheatmap <span class="html-italic">R</span> package. Leaves from S73 and R32 inoculated with race 34MKGQM were sampled at 6 days post-inoculation (dpi). Each genotype was evaluated using three independent biological replicates.</p>
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22 pages, 10671 KiB  
Article
A New Species of Brachynemurus Hagen in the B. versutus Subgroup (Neuroptera, Myrmeleontidae, Brachynemurini) from the Sonoran Province, Mexico
by Yesenia Marquez-López, Eder Leonardo Chávez-Valdez, Leon Gustavo de Miranda Tavares and Atilano Contreras-Ramos
Taxonomy 2024, 4(3), 587-608; https://doi.org/10.3390/taxonomy4030029 - 8 Aug 2024
Viewed by 203
Abstract
Brachynemurus bowlesi, sp. n. is a newly discovered myrmeleontid from the Sonoran Province, the northernmost subtropical region of Mexico. The new species fits within the Brachynemurus versutus subgroup, which now includes five species, all of them occurring in Mexico and the central and [...] Read more.
Brachynemurus bowlesi, sp. n. is a newly discovered myrmeleontid from the Sonoran Province, the northernmost subtropical region of Mexico. The new species fits within the Brachynemurus versutus subgroup, which now includes five species, all of them occurring in Mexico and the central and western United States. The new species may be identified by characteristics of the internal male genitalia, especially by a roof-like mediuncus, as well as the basal part of the 10th gonostyli, with paired processes in an acute angle and a shield-like expansion more evident in the dorsocaudal view. The formerly proposed synonymy of Brachynemurus mexicanus Banks, under B. versutus (Walker), is herein reinstated and supported. Full article
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<p><span class="html-italic">Brachynemurus bowlesi</span>, sp. n. and the new species name recipient. (<b>A</b>) Dr. David Bowles (<b>left</b>) in the Symposium of Neuropterology held in Mexico City in 2015, in the company of Dr. Oliver S. Flint, Jr.† (†—deceased) (<b>right</b>). (<b>B</b>) Habitus. (<b>C</b>) Head, thorax, and first abdominal segments in lateral view. (<b>D</b>) Head, frontal. (<b>E</b>) Head and pronotum, dorsal. (<b>B</b>–<b>E</b>) Male holotype.</p>
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<p>Wings of <span class="html-italic">Brachynemurus bowlesi</span>, sp. n. (<b>A</b>) Forewing. (<b>B</b>) Hindwing. (<b>C</b>) Venation of forewing. (<b>D</b>) Venation of hindwing. Abbreviations: A, anal vein; bR, bifurcation of radio; bCu, bifurcation of cubitus; Cu, cubitus vein; CuA, cubitus anterior; CuP, cubitus posterior; Gr, gradates crossveins; HyC, hypostigmatic cell; M, media; MA, media anterior; MP, media posterior; PsCr, presectoral crossveins; PoA, posterior area; R, radius; RA, radius anterior; Rg, rhegma; RP, radius posterior; Sc, subcostal.</p>
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<p>Male genital structures of <span class="html-italic">Brachynemurus bowlesi</span>, sp. n. (<b>A</b>) Male external genitalia, lateral view. (<b>B</b>) Male external genitalia, dorsal view. (<b>C</b>) Male external genitalia, ventral view. (<b>D</b>–<b>I</b>) The 10th gonocoxite—10th gonostylus complex: (<b>D</b>) Closed state, ventrocaudal view. (<b>E</b>) Closed state, lateral view. (<b>F</b>) Closed state, dorsal view. (<b>G</b>) Closed state, ventral view. (<b>H</b>) Everted state, ventrocaudal view. (<b>I</b>) Everted state, lateral view. Abbreviations. Ap, apodeme; bp, basal part; dp, distal part; ggc, 10th gonocoxite—10th gonostylus complex; gst, gonostylus; gx, gonocoxite; ihy, hypandrium internum; med, mediuncus; plt, pelta; pvl, posterior ventral lobe; stn, sternum; ter, tergite.</p>
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<p>Distribution map and habitat of <span class="html-italic">Brachynemurus versutus</span> subgroup. (<b>A</b>) Specimen records from Colección Nacional de Insectos, Instituto de Biología, UNAM. (<b>B</b>) Vegetation in Rancho Agua Nueva, Álamos, Sonora, Mexico. (<b>C</b>) <span class="html-italic">Brachynemurus bowlesi,</span> sp. n., male on light trap.</p>
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<p>Maps of <span class="html-italic">Brachynemurs versutus</span> subgroup. (<b>A</b>) Elevation map; star, holotype locality; circles, specimens from CNIN, UNAM; rhombus, records from GBIF database and bibliography. (<b>B</b>) Distribution based on GBIF and bibliographic records.</p>
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<p>Heads in frontal view. (<b>A</b>) <span class="html-italic">Brachynemurus divisus</span>. (<b>B</b>) <span class="html-italic">Brachynemurus elongatus</span>. (<b>C</b>) <span class="html-italic">Brachynemnurus hubbardii</span>. (<b>D</b>) <span class="html-italic">Brachynemurus versutus</span>.</p>
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<p>Vertex, pronotum, and thorax in dorsal view. (<b>A</b>) <span class="html-italic">Brachynemurus divisus</span>. (<b>B</b>) <span class="html-italic">Brachynemurus elongatus</span>. (<b>C</b>) <span class="html-italic">Brachynemnurus hubbardii</span>. (<b>D</b>) <span class="html-italic">Brachynemurus versutus</span>.</p>
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<p>Specimens in lateral view. (<b>A</b>) <span class="html-italic">Brachynemurus divisus</span>. (<b>B</b>) <span class="html-italic">Brachynemurus elongatus</span>. (<b>C</b>) <span class="html-italic">Brachynemnurus hubbardii</span>. (<b>D</b>) <span class="html-italic">Brachynemurus versutus</span>, forewing and hindwing. (<b>E</b>) <span class="html-italic">Brachynemurus divisus</span>. (<b>F</b>) <span class="html-italic">Brachynemurus elongatus</span>. (<b>G</b>) <span class="html-italic">Brachynemurus hubbardii</span>. (<b>H</b>) <span class="html-italic">Brachynemurus versutus</span>. Abbreviations: bR, bifurcation of radius; bCu, bifurcation of cubitus; Gr, gradates crossveins; HyC, hypostigmatic cell; PsCr, presectoral crossveins; PoA, posterior area; Rg, rhegma; scale bar in (<b>E</b>–<b>H</b>) = 0.5 mm.</p>
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<p><span class="html-italic">Brachynemurus versutus</span> subgroup external genitalia. (<b>A</b>–<b>C</b>) <span class="html-italic">Brachynemurus divisus</span>. (<b>D</b>–<b>F</b>) <span class="html-italic">Brachynemurus elongatus</span>. (<b>G</b>–<b>I</b>) <span class="html-italic">Brachynemurus hubbardii</span>. (<b>J</b>–<b>L</b>) <span class="html-italic">Brachynemurus versutus</span>. Abbreviations. ggc, 10th gonocoxite—10th gonostylus complex; pvl, posteroventral lobe; stn, sternum; ter, tergite.</p>
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<p><span class="html-italic">Brachynemurus versutus</span> subgroup 10th gonocoxite—10th gonostylus complex. (<b>A</b>,<b>B</b>) <span class="html-italic">Brachynemurus divisus</span>. (<b>C</b>,<b>D</b>) <span class="html-italic">Brachynemurus elongatus</span>. (<b>E</b>,<b>F</b>) <span class="html-italic">Brachynemurus hubbardii</span>. (<b>G</b>,<b>H</b>) <span class="html-italic">Brachynemurus versutus</span>. Abbreviations. Ap, apodeme; bp, basal part; dp, distal part; ggc, 10th gonocoxite—10th gonostylus complex; gst, gonostylus; gx, gonocoxite; ihy, hypandrium internum; med, mediuncus; plt, pelta; pvl, posterior ventral lobe.</p>
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<p>Type specimens. (<b>A</b>) <span class="html-italic">Brachynemurus versutus</span> (Walker), holotype male from the Natural History Museum of London (photographs under CC-BY-4.0 license). (<b>B</b>) <span class="html-italic">Brachynemurus mexicanus</span> Banks, lectotype female from the Museum of Comparative Zoology (photographs under Museum of Comparative Zoology, Harvard University; © President and Fellows of Harvard College license).</p>
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12 pages, 3814 KiB  
Article
Alteration of Photosynthetic and Antioxidant Gene Expression in Sugarcane Infected by Multiple Mosaic Viruses
by Intan Ria Neliana, Wardatus Soleha, Suherman, Nurmalasari Darsono, Rikno Harmoko, Widhi Dyah Sawitri and Bambang Sugiharto
Int. J. Plant Biol. 2024, 15(3), 757-768; https://doi.org/10.3390/ijpb15030055 - 8 Aug 2024
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Abstract
Sugarcane mosaic virus (SCMV), sugarcane streak mosaic virus (SCSMV), and sorghum mosaic virus (SrMV) are the causative pathogens of mosaic disease. This study aimed to identify mosaic virus infection and its impact on photosynthetic and antioxidant gene expression in eight commercial sugarcane cultivars [...] Read more.
Sugarcane mosaic virus (SCMV), sugarcane streak mosaic virus (SCSMV), and sorghum mosaic virus (SrMV) are the causative pathogens of mosaic disease. This study aimed to identify mosaic virus infection and its impact on photosynthetic and antioxidant gene expression in eight commercial sugarcane cultivars grown on sugarcane plantations in East Java, Indonesia. The disease incidence and severity were observed in symptomatic leave samples, and then the virus was identified. A high incidence and severity of mosaic symptoms were observed in the PS881 and NX04 cultivars compared with the other cultivars. RT-PCR analysis detected SCSMV infection in all cultivars; double infections with SCSMV and SCMV in the PS881, PS882, and Cening cultivars; and triple infections with SCSMV, SCMV, and SrMV in the PS881 cultivar. Ascorbate peroxidase (Apx) expression was upregulated in all virus-infected cultivars and significantly increased in the triple-infected PS881 cultivar. However, catalase (Cat) expression was only slightly increased in the PS881 cultivar. The chlorophyll content was reduced, and the PsaA gene was downregulated in all cultivars. The expression of PsaA, RbcS, and Sps was significantly suppressed in the triple-infected PS881 cultivar. Moreover, the downregulation of both the RbcS and Pepc genes was concomitant with that of their protein levels. Full article
(This article belongs to the Topic Microbe-Induced Abiotic Stress Alleviation in Plants)
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Figure 1

Figure 1
<p>Percentage of mosaic disease incidence (<b>A</b>) and severity (<b>B</b>) observed on the leaves of eight sugarcane cultivars grown in the field at four locations in East Java, Indonesia: Lumajang, Jember, Bondowoso, and Kediri.</p>
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<p>RT-PCR analysis of mosaic virus coat protein genes and mosaic symptom pattern variations in field-grown sugarcane. RT-PCR was conducted with RNA isolated from infected leaves of eight sugarcane cultivars and using specific primers for SCSMV (<b>A</b>), SCMV (<b>B</b>), and SrMV (<b>C</b>). The image presents the RT-PCR products from five infected samples of each sugarcane cultivar among the 61 positive mosaic virus infection samples. M, 1 kb DNA ladder (Thermo Fisher Scientific, Massachusetts, USA); C: control, non-symptomatic sugarcane. Red asterisk indicates positive CP-SCMV DNA. (<b>D</b>) Variation of mosaic symptoms intensity in the leaves of sugarcane varieties infected by SCSMV (single), SCSMV-SCMV (double), and SCSMV-SCMV-SrMV (triple) compared to non-symptomatic healthy leaf (control).</p>
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<p>Phylogenetic analysis of SCSMV (<b>A</b>), SCMV (<b>B</b>), and SrMV (<b>C</b>) based on the CP nucleotide sequences along with the neighbor-joining (NJ) method with 1000 bootstrap replicates. SCYLV: Sugarcane yellow leaf virus was selected as outgroup. Sequence clusters according to the geographical origin of the virus isolates, such as Thailand (KP987832.1) for SCSMV; USA (MT725538.1) and Germany (X98168.1) for SCMV; and Argentina (EU189037.1), USA (EF078962.1), and China (DQ227695.1) for SrMV.</p>
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<p>Expression of <span class="html-italic">Apx</span> and <span class="html-italic">Cat</span> gene in response to mosaic virus infection in sugarcane leaves. Relative expression of the <span class="html-italic">Apx</span> gene under single infection (<b>A</b>) and the <span class="html-italic">Cat</span> and <span class="html-italic">Apx</span> genes under single, double, and triple infection (<b>B</b>). The expression of <span class="html-italic">Cat</span> and <span class="html-italic">Apx</span> in the control, single, double, and triple infection samples was determined using the PS881 sugarcane cultivar. β-tubulin was used as the reference gene. Values are reported as the means ± SD of three biological replicates. Asterisk (*) denotes statically significant differences at <span class="html-italic">t</span>-test: <span class="html-italic">p</span> ≤ 0.05.</p>
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<p>Chlorophyll content and gene expression of photosynthetic-related in response to mosaic virus infection in sugarcane leaves. Total chlorophyll content (<b>A</b>) and PsaA expression (<b>B</b>) were determined in single-infection sugarcane leaves. Expression of the <span class="html-italic">PsaA</span>, <span class="html-italic">RbcS</span>, <span class="html-italic">Pepc</span>, and <span class="html-italic">Sps</span> genes (<b>C</b>) and levels of PEPC and Rubisco proteins (<b>D</b>) were determined in the control and single-, double-, and triple-infection PS881 leaves. Values represent the means ± SD of three biological replicates. Asterisk (*) denotes statically significant differences at <span class="html-italic">t</span>-test: <span class="html-italic">p</span> ≤ 0.05. Inset shows the PEPC and Rubisco large subunit (RbcL) and small subunit (RbcS) proteins detected by immunoblot analysis. C, S, D, and T represent the control and single, double, and triple infections, respectively. The intensities of the protein bands were quantitively expressed using ImageJ free software version 1.54h.</p>
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