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11 pages, 9938 KiB  
Article
Mechanical and Lattice Thermal Properties of Si-Ge Lateral Heterostructures
by Liuhuan Zhao, Lei Huang, Ke Wang, Weihua Mu, Qiong Wu, Zhen Ma and Kai Ren
Molecules 2024, 29(16), 3823; https://doi.org/10.3390/molecules29163823 (registering DOI) - 12 Aug 2024
Abstract
Two-dimensional (2D) materials have drawn extensive attention due to their exceptional characteristics and potential uses in electronics and energy storage. This investigation employs simulations using molecular dynamics to examine the mechanical and thermal transport attributes of the 2D silicene–germanene (Si-Ge) lateral heterostructure. The [...] Read more.
Two-dimensional (2D) materials have drawn extensive attention due to their exceptional characteristics and potential uses in electronics and energy storage. This investigation employs simulations using molecular dynamics to examine the mechanical and thermal transport attributes of the 2D silicene–germanene (Si-Ge) lateral heterostructure. The pre-existing cracks of the Si-Ge lateral heterostructure are addressed with external strain. Then, the effect of vacancy defects and temperature on the mechanical attributes is also investigated. By manipulating temperature and incorporating vacancy defects and pre-fabricated cracks, the mechanical behaviors of the Si-Ge heterostructure can be significantly modulated. In order to investigate the heat transport performance of the Si-Ge lateral heterostructure, a non-equilibrium molecular dynamics approach is employed. The efficient phonon average free path is obtained as 136.09 nm and 194.34 nm, respectively, in the Si-Ge heterostructure with a zigzag and armchair interface. Our results present the design and application of thermal management devices based on the Si-Ge lateral heterostructure. Full article
(This article belongs to the Special Issue Novel Two-Dimensional Energy-Environmental Materials)
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Figure 1

Figure 1
<p>(<b>a</b>) The comprehensive construction of the Si-Ge lateral heterostructure constructed by (<b>c</b>) zigzag and armchair (<b>b</b>) configurations.</p>
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<p>(<b>a</b>,<b>b</b>) The atomic stress contour of the initial cracking and (<b>c</b>,<b>d</b>) stress–strain behavior of the Si-Ge heterostructure with (<b>a</b>,<b>c</b>) armchair and (<b>b</b>,<b>d</b>) zigzag interfaces under external uniaxial strain. (<b>e</b>) The fracture strain and (<b>f</b>) fracture strength of the pure silicene, germanene, and Si-Ge heterostructures.</p>
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<p>(<b>a</b>) The structure of the pre-cracked heterostructure, the tunable (<b>b</b>) fracture strength and (<b>c</b>) fracture strain of the Si-Ge heterostructure with different pre-cracked structures.</p>
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<p>(<b>a</b>) The structure of the pre-cracked heterostructure. The tunable (<b>b</b>) fracture strength and (<b>c</b>) fracture strain of the Si-Ge heterostructure with different vacancy densities.</p>
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<p>(<b>a</b>) The schematic models of pure silicene, germanene, and the lateral heterostructure used in NEMD simulations. (<b>b</b>) The obtained temperature distribution along the heat flux orientation of the system simulated.</p>
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<p>The relationship between (<b>a</b>) thermal conductivity and sample length, and (<b>b</b>) inverse thermal conductivity and inverse sample length of silicene, germanene, and the lateral heterostructure.</p>
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15 pages, 537 KiB  
Article
Cardiovascular Risk Factors as Predictors of Nutritional Status in Older Mexican Adults
by Dennys Alexandra Hernández-Torres, Myrna Elizabeth López-Hernández, Maria Elena Camacho-Moll, Mario Bermúdez de León, Katia Peñuelas-Urquides, Laura Adiene González-Escalante, Román González-Reyna, Darinka Laillete García-Leija and Brenda Leticia Escobedo-Guajardo
Nutrients 2024, 16(16), 2662; https://doi.org/10.3390/nu16162662 (registering DOI) - 12 Aug 2024
Abstract
Aging is commonly accompanied by increased cardiovascular risk and diet plays a crucial role in health condition. The aim of this study was to determine cardiovascular risk factors as predictors of nutritional risk in Mexican older adults. A cross-sectional study on Mexican patients [...] Read more.
Aging is commonly accompanied by increased cardiovascular risk and diet plays a crucial role in health condition. The aim of this study was to determine cardiovascular risk factors as predictors of nutritional risk in Mexican older adults. A cross-sectional study on Mexican patients aged ≥60 years with cardiovascular risk factors affiliated with a medical unit in Northeast Mexico was performed from July to December 2021. The nutritional risk evaluations were performed using the Mini Nutritional Assessment (MNA) questionnaire. After a multivariate analysis, the cardiovascular risk factors identified as independent predictors of risk of malnutrition were hypertriglyceridemia (adjusted OR (AOR): 1.8; 95% CI: 1.03–3.14; p = 0.04) and systolic hypertension I (AOR: 2.28; 95% CI: 1.04–5.02; p = 0.041); age over 80 years (AOR: 5.17; 95% CI: 1.83–14.65, p = 0.002) and elementary school education (AOR: 2.34; 95% CI: 1.20–4.55; p = 0.013) were also related. The cross-sectional design and single-center approach of this study limits the generalizability of the results; however, conducting timely evaluations of blood pressure, triglyceride levels, and risk of malnutrition using the MNA tool for patients aged ≥60 years could prevent illness and reduce mortality within this population group. Full article
(This article belongs to the Section Geriatric Nutrition)
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<p>Comparison among groups according to BMI for each MNA nutritional status category. Obesity is prevalent in the normal nutritional group; meanwhile, overweight is predominant in the risk group. The risk group is composed of people with malnutrition and risk of malnutrition diagnoses. χ<sup>2</sup>, chi-square test, <span class="html-italic">p</span> = 0.120.</p>
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19 pages, 10150 KiB  
Review
Photosystem I: A Paradigm for Understanding Biological Environmental Adaptation Mechanisms in Cyanobacteria and Algae
by Li-Rong Tian and Jing-Hua Chen
Int. J. Mol. Sci. 2024, 25(16), 8767; https://doi.org/10.3390/ijms25168767 (registering DOI) - 12 Aug 2024
Abstract
The process of oxygenic photosynthesis is primarily driven by two multiprotein complexes known as photosystem II (PSII) and photosystem I (PSI). PSII facilitates the light-induced reactions of water-splitting and plastoquinone reduction, while PSI functions as the light-driven plastocyanin-ferredoxin oxidoreductase. In contrast to the [...] Read more.
The process of oxygenic photosynthesis is primarily driven by two multiprotein complexes known as photosystem II (PSII) and photosystem I (PSI). PSII facilitates the light-induced reactions of water-splitting and plastoquinone reduction, while PSI functions as the light-driven plastocyanin-ferredoxin oxidoreductase. In contrast to the highly conserved structure of PSII among all oxygen-evolving photosynthetic organisms, the structures of PSI exhibit remarkable variations, especially for photosynthetic organisms that grow in special environments. In this review, we make a concise overview of the recent investigations of PSI from photosynthetic microorganisms including prokaryotic cyanobacteria and eukaryotic algae from the perspective of structural biology. All known PSI complexes contain a highly conserved heterodimeric core; however, their pigment compositions and peripheral light-harvesting proteins are substantially flexible. This structural plasticity of PSI reveals the dynamic adaptation to environmental changes for photosynthetic organisms. Full article
(This article belongs to the Special Issue New Insights into Photosystem I)
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Figure 1
<p>Structural diversity of cyanobacterial PSI. (<b>a</b>,<b>b</b>) The monomeric (PDB ID: 6LU1) and trimeric (PDB ID: 1JB0) PSI complexes from <span class="html-italic">T. elongatus</span> share similar subunit components; however, the PSI monomer lacks two peripheral subunits, PsaK and PsaX, which are colored in red. (<b>c</b>) The tetrameric PSI is mainly observed in heterocyst-forming cyanobacteria. A PSI tetramer (PDB ID: 6JEO) in <span class="html-italic">Anabaena</span> sp. PCC 7120 is organized with two PSI dimers with a <span class="html-italic">C</span>2 symmetry, forming two different interfaces (marked in dashed red and blue lines) between the neighboring PSI monomers.</p>
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<p>Two structures of cyanobacterial PSI–IsiA complexes under iron-deficiency condition. (<b>a</b>) The mesophilic cyanobacterium <span class="html-italic">Synechocystis</span> sp. PCC 6803 forms PSI3–IsiA18 supercomplex (PDB ID: 6K33) with three-fold rotational symmetry. (<b>b</b>) The monomer–PSI–IsiA6 complex of <span class="html-italic">Anabaena</span> sp. PCC 7120 (PDB ID: 7Y3F) associates six IsiA subunits. The C-terminal PsaL-like domain of IsiA2-1 occupies the corresponding position of PsaL in the <span class="html-italic">Anabaena</span> PSI tetramer.</p>
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<p>Structure and the cofactor arrangement along the electron transfer chain (ETC) of <span class="html-italic">A. marina</span> PSI monomer (PDB ID: 7DWQ). (<b>a</b>) The protein subunits are colored respectively, and the missing subunit PsaK is marked with dashed circle. (<b>b</b>) The cofactors of P<sub>740</sub>, A<sub>cc</sub>, A<sub>0</sub>, and A<sub>1</sub> of the ETC are arranged in two separated branches (branch A and branch B). Phylloquinones and Fe4S4 clusters are labeled as PhyQ, F<sub>X</sub>, F<sub>A</sub>, and F<sub>B</sub>, respectively. Uniquely, the Chls of A<sub>0</sub> in <span class="html-italic">A. marina</span> PSI are identified as two pheophytins <span class="html-italic">a</span>, instead of the typical Chls <span class="html-italic">a</span> in other cyanobacterial PSI complexes [<a href="#B53-ijms-25-08767" class="html-bibr">53</a>].</p>
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<p>Structural variations of <span class="html-italic">C. reinhardtii</span> PSI–LHCI complexes. (<b>a</b>) The structures of <span class="html-italic">C. reinhardtii</span> PSI–LHCI complexes binding with eight and ten Lhca subunits. The antenna subunits are distributed as three belts: two crescent-shaped belts including one inner belt and one outer belt which are associated to one side of the PSI core (PDB ID: 6JO6), and an additional small belt made up of the Lhca2 and Lhca9 heterodimer on the opposite side (PDB ID: 6JO5). (<b>b</b>) During the state transitions (state 2), phosphorylated LHCIIs dissociate from PSII and migrate to PSI, forming the PSI–LHCI–LHCII supercomplex (PDB ID: 7D0J). (<b>c</b>) Under low light and anoxic conditions, PSI–LHCI dimer is formed from two PSI–LHCI monomers that are arranged in a “head-to-head” manner. The PsaH and Lhca2 subunits are absent; instead, two Lhca9 subunits interact with the subunits of PsaI, PsaL, PsaG from two PSI–LHCI monomers (PDB ID: 7ZQD).</p>
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<p>Comparison of the PSI–LHCI complexes from different red algae. (<b>a</b>,<b>b</b>) <span class="html-italic">C. merolae</span> contains two different forms of PSI–LHCI complexes, with one binding three Lhcr subunits (PDB ID: 5ZGH) and the other one binding five Lhcr subunits (PDB ID: 5ZGB). (<b>c</b>) <span class="html-italic">Porphyridium purpureum</span> PSI–LHCI associates seven LHCI subunits and one chlorophyll <span class="html-italic">a</span>/<span class="html-italic">b</span>-binding-like protein (RedCAP) (PDB ID: 7Y5E). (<b>d</b>) <span class="html-italic">Cyanidium caldarium</span> PSI–LHCI complex contains five LHCI subunits which are distributed as two separated clusters (PDB ID: 8WEY).</p>
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<p>Structures of PSI–LHCI complexes from green algae <span class="html-italic">D. salina</span> (<b>a</b>,<b>b</b>) (PDB ID: 6QPH, 6SL5) and <span class="html-italic">C. ohadii</span> (PDB ID: 6ZZY) (<b>c</b>).</p>
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<p>Subunit organization and pigment network of diatom <span class="html-italic">C. gracilis</span> PSI–FCPI complexes (PDB ID: 6LY5).</p>
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<p>Structure of PSI tetramer from <span class="html-italic">Cyanophora paradoxa</span> (PDB ID: 7DR2).</p>
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<p>Structures of PSI–ACPI supercomplexes from cryptophyte <span class="html-italic">C. placoidea</span> (PDB ID: 7Y7B).</p>
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<p>Structures and organizations of PSI-AcpPCI supercomplexes with 13 (<b>a</b>) and 14 (<b>b</b>) AcpPCIs from symbiotic dinoflagellate in <span class="html-italic">Symbiodinium</span>.</p>
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20 pages, 1175 KiB  
Review
Optogenetic Brain–Computer Interfaces
by Feifang Tang, Feiyang Yan, Yushan Zhong, Jinqian Li, Hui Gong and Xiangning Li
Bioengineering 2024, 11(8), 821; https://doi.org/10.3390/bioengineering11080821 (registering DOI) - 12 Aug 2024
Abstract
The brain–computer interface (BCI) is one of the most powerful tools in neuroscience and generally includes a recording system, a processor system, and a stimulation system. Optogenetics has the advantages of bidirectional regulation, high spatiotemporal resolution, and cell-specific regulation, which expands the application [...] Read more.
The brain–computer interface (BCI) is one of the most powerful tools in neuroscience and generally includes a recording system, a processor system, and a stimulation system. Optogenetics has the advantages of bidirectional regulation, high spatiotemporal resolution, and cell-specific regulation, which expands the application scenarios of BCIs. In recent years, optogenetic BCIs have become widely used in the lab with the development of materials and software. The systems were designed to be more integrated, lightweight, biocompatible, and power efficient, as were the wireless transmission and chip-level embedded BCIs. The software is also constantly improving, with better real-time performance and accuracy and lower power consumption. On the other hand, as a cutting-edge technology spanning multidisciplinary fields including molecular biology, neuroscience, material engineering, and information processing, optogenetic BCIs have great application potential in neural decoding, enhancing brain function, and treating neural diseases. Here, we review the development and application of optogenetic BCIs. In the future, combined with other functional imaging techniques such as near-infrared spectroscopy (fNIRS) and functional magnetic resonance imaging (fMRI), optogenetic BCIs can modulate the function of specific circuits, facilitate neurological rehabilitation, assist perception, establish a brain-to-brain interface, and be applied in wider application scenarios. Full article
(This article belongs to the Section Biomedical Engineering and Biomaterials)
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<p>(<b>a</b>) Upper half: mechanism of ChR2. When irradiated with blue light, ion channels open, leading to sodium inward flow, causing depolarization. Lower half: NpHR mechanism. When irradiated with yellow light, the ion channel opens, leading to chloride ion inward flow, resulting in hyperpolarization. (<b>b</b>) Upper half: open-loop system. The output is generated directly through the processing and stimulation systems with no feedback control. Lower half: closed-loop system. Outputs are generated through the processing system, the stimulation system, and the recording system, using the recording system as a feedback control to modulate the outputs. (<b>c</b>) Frame diagram of the EEG-based optogenetic BCI. The recording system reads signals from the animal’s brain through electrodes, performs a series of pre-processing, and then transfers the data to the processing system. The processing system analyzes and decodes the signal read by the recording system and encodes the signal according to the analysis results. After the encoding is completed, the stimulus system is controlled to output the signal. The stimulus system gives corresponding optogenetic stimulation to the animal according to the encoding of the processing system.</p>
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<p>Examples of optogenetic BCI applications. In an example of enhancing cognitive function, optogenetic stimulation of firing inhibition on the troughs of endogenous theta rhythms in the mouse hippocampus increased the probability of correct selection when the mice were in the retrieval arm [<a href="#B90-bioengineering-11-00821" class="html-bibr">90</a>]. In an example of neurotherapy, detecting the onset of epilepsy and providing optogenetic stimulation can be effective in alleviating it [<a href="#B8-bioengineering-11-00821" class="html-bibr">8</a>]. In an assisted perception example, the primary somatosensory cortex (vS1) was given light stimulus feedback along with a water reward, while the mouse controlled the primary motor cortex (vM1) firing rate within a certain range, that is, mouse-specific whisker movement [<a href="#B101-bioengineering-11-00821" class="html-bibr">101</a>]. After training, the mouse’s licking behavior relied on the feedback of artificial light stimulation provided in vS1, which proved that the light stimulation made the mice feel that they were in contact with the virtual stick that provided water. In a brain–computer–brain interface example, calcium imaging signals related to locomotion velocity in the brainstem nuclei (NI) of autonomously moving mice were used to encode optogenetic stimuli in controlled mice, modulating their locomotor patterns so that they closely mimicked the movements of the active locomotor mice [<a href="#B102-bioengineering-11-00821" class="html-bibr">102</a>]. Blue arrows indicate brain-machine information flow and pink arrows indicate machine-brain information flow.</p>
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<p>(<b>a</b>) Future development trends. (<b>b</b>) Spatial and temporal resolutions of different neural interface technologies.</p>
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16 pages, 15526 KiB  
Article
Identification of Pathogen Causing Bulb Rot in Fritillaria taipaiensis P. Y. Li and Establishment of Detection Methods
by Shijie Wang, Keke Chen, Jiaqi Guo, Panwang Zhang, Yuchen Li, Zhenghao Xu, Langjun Cui and Yi Qiang
Plants 2024, 13(16), 2236; https://doi.org/10.3390/plants13162236 (registering DOI) - 12 Aug 2024
Abstract
Fritillaria taipaiensis P. Y. Li (F. taipaiensis) is a traditional Chinese herbal medicine that has been used for over two millennia to treat cough and expectoration. However, the increasing cultivation of F. taipaiensis has led to the spread of bulb rot [...] Read more.
Fritillaria taipaiensis P. Y. Li (F. taipaiensis) is a traditional Chinese herbal medicine that has been used for over two millennia to treat cough and expectoration. However, the increasing cultivation of F. taipaiensis has led to the spread of bulb rot diseases. In this study, pathogens were isolated from rotten F. taipaiensis bulbs. Through molecular identification, pathogenicity testing, morphological assessment, and microscopy, Fusarium solani was identified as the pathogen causing bulb rot in F. taipaiensis. The colonization of F. solani in the bulbs was investigated through microscopic observation. The rapid and accurate detection of this pathogen will contribute to better disease monitoring and control. Loop-mediated isothermal amplification (LAMP) and qPCR methods were established to quickly and specifically identify this pathogen. These results provide valuable insights for further research on the prediction, rapid detection, and effective prevention and control of bulb rot in F. taipaiensis. Full article
(This article belongs to the Collection Plant Disease Diagnostics and Surveillance in Plant Protection)
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Figure 1
<p>The morphological characteristics of FTA1. (<b>A</b>) The FTA1 phenotype following a 5-day culture period on potato dextrose agar (PDA). (<b>B</b>) The hyphal morphology of FTA1. (<b>C</b>) The morphological characteristics of FTA1’s microconidia, macroconidia, and conidia. Scale bar: 25 μm.</p>
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<p>Maximum likelihood phylogenetic tree constructed using the concatenated sequence data (ITS, <span class="html-italic">EF-1α</span>, and <span class="html-italic">ACT</span>) from FTA1 and the related <span class="html-italic">Fusarium</span> species. Bootstrap support values for maximum likelihood greater than 70% are indicated.</p>
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<p>Symptoms of <span class="html-italic">F. taipaiensis</span> inoculated with FTA1. (<b>A</b>–<b>C</b>) No symptoms of <span class="html-italic">F. taipaiensis</span> artificial infection with potato dextrose broth (PDB). The arrow points to the location where PDB was inoculated. (<b>D</b>–<b>F</b>) Distinct brown disease spots appeared after artificial inoculation with FTA1. The arrow points to the location where FTA1 was inoculated. Scale bar: 1 cm.</p>
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<p>Observation of the longitudinal anatomical structure of healthy bulbs and diseased bulbs after artificial inoculation with FTA1, utilizing Safranin O-Fast Green staining. (<b>A</b>) Diseased bulb; the arrow points to the location of the FTA1 spore suspension inoculation. (<b>B</b>) Partial magnified view of the diseased bulb. (<b>C</b>) Healthy bulb treated with PDB. (<b>D</b>) Partial magnified view of the healthy bulb. Scale bar: 100 μm.</p>
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<p>Scanning electron microscope (SEM) micro-observations of different stages of bulb rot disease in <span class="html-italic">F. taipaiensis</span>. (<b>A</b>) Surface of a healthy bulb. (<b>B</b>) Magnified image of the healthy bulb surface. (<b>C</b>) Bulb surface 6 h after inoculation. (<b>D</b>) Conidia began to germinate on the bulb surface 6 h after inoculation. (<b>E</b>) Bulb surface 12 h after inoculation. (<b>F</b>) Conidia germinated on the bulb surface, forming short hyphae 12 h after inoculation. (<b>G</b>) Infection cushions and a lobate appressorium formed on the surface of the bulb 1 day after inoculation. (<b>H</b>) A hyphal network formed on the surface of the bulb 2 days after inoculation. (<b>I</b>) A dense hyphal network formed on the surface of the bulb 3–4 days after inoculation. Scale bar: (<b>A</b>–<b>H</b>): 10 μm, (<b>I</b>): 100 μm. Abbreviations: <b>FS</b>, foot structure; <b>IC</b>, infection cushion; <b>LA</b>, lobate appressorium; <b>IH</b>, infection hypha; <b>RH</b>, runner hypha; <b>S</b>, septum.</p>
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<p>(<b>A</b>), (<b>a</b>–<b>c</b>) Symptoms of <span class="html-italic">F. taipaiensis</span> plants at 7, 14, and 21 days after treatment with PDB, and (<b>d</b>–<b>f</b>) local symptoms of <span class="html-italic">F. taipaiensis</span> bulbs at 21 days after treatment with PDB. (<b>B</b>), (<b>a</b>–<b>c</b>) Symptoms of <span class="html-italic">F. taipaiensis</span> plants at 7, 14, and 21 days post-inoculation with FTA1. (<b>d</b>–<b>f</b>) Local symptoms of <span class="html-italic">F. taipaiensis</span> bulbs at 21 days post-inoculation with FTA1. Scale bar: 1 cm.</p>
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<p>Specificity testing of LAMP and qPCR primers designed for <span class="html-italic">F. solani</span>. (<b>A</b>) LAMP primer set for <span class="html-italic">F. solani</span>. Lane M: DNA marker 2 k; Lanes 1 to 16: ddH<sub>2</sub>O, <span class="html-italic">F. solani</span>, <span class="html-italic">F. avenaceum</span>, <span class="html-italic">F. oxysporum</span>, <span class="html-italic">F. proliferatum</span>, <span class="html-italic">F. redolens</span>, <span class="html-italic">F. graminearum</span>, <span class="html-italic">F. culmorum</span>, <span class="html-italic">F. moniliforme</span>, <span class="html-italic">Alternaria alternata</span>, <span class="html-italic">Botrytis cinerea</span>, <span class="html-italic">A. fumigatus</span>, <span class="html-italic">A. tubingensis</span>, <span class="html-italic">A. flavus</span>, <span class="html-italic">A. westerdijkiae</span>, and <span class="html-italic">Mucor circinelloides</span>. (<b>B</b>) Amplification curve for qPCR primer specificity detection. (<b>C</b>) Melting peaks for qPCR primer specificity detection.</p>
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<p>Sensitivity test of LAMP and qPCR primers designed for <span class="html-italic">F. solani</span>. (<b>A</b>) LAMP primer set for <span class="html-italic">F. solani</span>. Lane M: DNA marker 2 k; Lanes 1 to 8: 10 ng/µL, 1 ng/µL, 100 pg/µL, 10 pg/µL, 1 pg/µL, 100 fg/µL, 10 fg/µL, and 1 fg/uL. (<b>B</b>) Standard curve of specific qPCR for <span class="html-italic">F. solani</span>. (<b>C</b>) Amplification curves for qPCR primer sensitivity detection. (<b>D</b>) Melting peaks for qPCR primer sensitivity detection.</p>
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<p>Application of the LAMP assay for the detection of <span class="html-italic">F. solani</span> in 48 bulbs of <span class="html-italic">F. taipaiensis</span>. Samples emitting bright green fluorescence were evaluated as positive, while non-fluorescing samples were evaluated as negative.</p>
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12 pages, 5096 KiB  
Article
Theoretical Analysis of Superior Photodegradation of Methylene Blue by Cerium Oxide/Reduced Graphene Oxide vs. Graphene
by Nguyen Hoang Hao, Phung Thi Lan, Nguyen Ngoc Ha, Le Minh Cam and Nguyen Thi Thu Ha
Molecules 2024, 29(16), 3821; https://doi.org/10.3390/molecules29163821 (registering DOI) - 12 Aug 2024
Abstract
Density functional theory and a semi-empirical quantum chemical approach were used to evaluate the photocatalytic efficiency of ceria (CeO2) combined with reduced graphene oxide (rGO) and graphene (GP) for degrading methylene blue (MB). Two main aspects were examined: the adsorption ability [...] Read more.
Density functional theory and a semi-empirical quantum chemical approach were used to evaluate the photocatalytic efficiency of ceria (CeO2) combined with reduced graphene oxide (rGO) and graphene (GP) for degrading methylene blue (MB). Two main aspects were examined: the adsorption ability of rGO and GP for MB, and the separation of photogenerated electrons and holes in CeO2/rGO and CeO2/GP. Our results, based on calculations of the adsorption energy, population analysis, bond strength index, and reduced density gradient, show favorable energetics for MB adsorption on both rGO and GP surfaces. The process is driven by weak, non-covalent interactions, with rGO showing better MB adsorption. A detailed analysis involving parameters like fractional occupation density, the centroid distance between molecular orbitals, and the Lewis acid index of the catalysts highlights the effective charge separation in CeO2/rGO compared to CeO2/GP. These findings are crucial for understanding photocatalytic degradation mechanisms of organic dyes and developing efficient photocatalysts. Full article
(This article belongs to the Topic Advances in Computational Materials Sciences)
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<p>Models of GP (<b>a</b>) and rGO (<b>b</b>); color codes: brown—C; ivory—H; red—O.</p>
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<p>Optimized adsorption configurations of MB on GP (<b>a</b>) and rGO (<b>b</b>); color codes: brown—C; ivory—H, yellow—Ce; red—O; green—Cl; gray—N; light yellow—S.</p>
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<p>IBSI values corresponding to the interatomic interactions between atoms of MB and atoms of rGO.</p>
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<p>Scatter graph of RDG for MB/GP (<b>a</b>) and MB/rGO (<b>b</b>) systems.</p>
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<p>RDG isosurfaces (isovalue = 0.8) of MB/GP (<b>a</b>) and MB/rGO (<b>b</b>) systems.</p>
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<p>Optimized structures of CeO<sub>2</sub>/GP (<b>a</b>) and CeO<sub>2</sub>/rGO (<b>b</b>).</p>
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<p>Frontier molecular orbitals of CeO<sub>2</sub>/GP: HOMO (<b>a</b>) and LUMO (<b>b</b>); and CeO<sub>2</sub>/rGO: HOMO (<b>c</b>) and LUMO (<b>d</b>).</p>
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<p>The FOD maps of GP, rGO, CeO<sub>2</sub>/GP, and CeO<sub>2</sub>/rGO.</p>
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10 pages, 1115 KiB  
Article
The Mitogenome of the Haecon-5 Strain of Haemonchus contortus and a Comparative Analysis of Its Nucleotide Variation with Other Laboratory Strains
by Yuanting Zheng, Neil D. Young, Jiangning Song and Robin B. Gasser
Int. J. Mol. Sci. 2024, 25(16), 8765; https://doi.org/10.3390/ijms25168765 (registering DOI) - 12 Aug 2024
Abstract
Haemonchus contortus (the barber’s pole worm)—a highly pathogenic gastric nematode of ruminants—causes significant economic losses in the livestock industry worldwide. H. contortus has become a valuable model organism for both fundamental and applied research (e.g., drug and vaccine discovery) because of the availability [...] Read more.
Haemonchus contortus (the barber’s pole worm)—a highly pathogenic gastric nematode of ruminants—causes significant economic losses in the livestock industry worldwide. H. contortus has become a valuable model organism for both fundamental and applied research (e.g., drug and vaccine discovery) because of the availability of well-defined laboratory strains (e.g., MHco3(ISE).N1 in the UK and Haecon-5 in Australia) and genomic, transcriptomic and proteomic data sets. Many recent investigations have relied heavily on the use of the chromosome-contiguous genome of MHco3(ISE).N1 in the absence of a genome for Haecon-5. However, there has been no genetic comparison of these and other strains to date. Here, we assembled and characterised the mitochondrial genome (14.1 kb) of Haecon-5 and compared it with that of MHco3(ISE).N1 and two other strains (i.e., McMaster and NZ_Hco_NP) from Australasia. We detected 276 synonymous and 25 non-synonymous single nucleotide polymorphisms (SNPs) within Haecon-5. Between the Haecon-5 and MHco3(ISE).N1 strains, we recorded 345 SNPs, 31 of which were non-synonymous and linked to fixed amino acid differences in seven protein-coding genes (nad5, nad6, nad1, atp6, nad2, cytb and nad4) between these strains. Pronounced variation (344 and 435 SNPs) was seen between Haecon-5 and each of the other two strains from Australasia. The question remains as to what impact these mitogenomic mutations might have on the biology and physiology of H. contortus, which warrants exploration. The high degree of mitogenomic variability recorded here among these strains suggests that further work should be undertaken to assess the nature and extent of the nuclear genomic variation within H. contortus. Full article
(This article belongs to the Special Issue Parasite Biology and Host-Parasite Interactions: 2nd Edition)
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Figure 1
<p>The circular mitochondrial genome of the Haecon-5 strain of <span class="html-italic">Haemonchus contortus</span> determined from a single adult male worm, with protein-coding (green), tRNA (grey) and rRNA (blue) genes, as well as non-coding regions (black), indicated (<b>A</b>). Nucleotide variability in the mitochondrial genome within a population of third-stage larvae (L3s; <span class="html-italic">n</span> = 200,000) of Haecon-5, established by a sliding window analysis of the linearised map (using a 200 bp window) (<b>B</b>). <a href="#ijms-25-08765-t002" class="html-table">Table 2</a> details the nature and extent of this variability.</p>
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<p>Nucleotide variability (<b>A</b>) and genetic distances (<b>B</b>) recorded upon pairwise comparison of the mitochondrial genomes of the Haecon-5 strain (<a href="#ijms-25-08765-f001" class="html-fig">Figure 1</a>) with the MHco3(ISE).N1, McMaster and NZ_Hco_NP strains of <span class="html-italic">Haemonchus contortus</span> (pink, yellow and blue, respectively; refs. [<a href="#B6-ijms-25-08765" class="html-bibr">6</a>,<a href="#B10-ijms-25-08765" class="html-bibr">10</a>,<a href="#B11-ijms-25-08765" class="html-bibr">11</a>]) following a sliding window analysis (200 bp window). <a href="#ijms-25-08765-t003" class="html-table">Table 3</a> details the nature and extent of this variability.</p>
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15 pages, 13437 KiB  
Article
Integrative Analysis of Transcriptomic Profiles and Physiological Responses Provide New Insights into Drought Stress Tolerance in Oil Palm (Elaeis guineensis Jacq.)
by Fernan Santiago Mejía-Alvarado, Arley Fernando Caicedo-Zambrano, David Botero-Rozo, Leonardo Araque, Cristihian Jarri Bayona-Rodríguez, Seyed Mehdi Jazayeri, Carmenza Montoya, Iván Ayala-Díaz, Rodrigo Ruiz-Romero and Hernán Mauricio Romero
Int. J. Mol. Sci. 2024, 25(16), 8761; https://doi.org/10.3390/ijms25168761 (registering DOI) - 12 Aug 2024
Abstract
Oil palm (Elaeis guineensis Jacq.) is a highly productive crop economically significant for food, cosmetics, and biofuels. Abiotic stresses such as low water availability, salt accumulation, and high temperatures severely impact oil palm growth, physiology, and yield by restricting water flux among [...] Read more.
Oil palm (Elaeis guineensis Jacq.) is a highly productive crop economically significant for food, cosmetics, and biofuels. Abiotic stresses such as low water availability, salt accumulation, and high temperatures severely impact oil palm growth, physiology, and yield by restricting water flux among soil, plants, and the environment. While drought stress’s physiological and biochemical effects on oil palm have been extensively studied, the molecular mechanisms underlying drought stress tolerance remain unclear. Under water deficit conditions, this study investigates two commercial E. guineensis cultivars, IRHO 7001 and IRHO 2501. Water deficit adversely affected the physiology of both cultivars, with IRHO 2501 being more severely impacted. After several days of water deficit, there was a 40% reduction in photosynthetic rate (A) for IRHO 7001 and a 58% decrease in IRHO 2501. Further into the drought conditions, there was a 75% reduction in A for IRHO 7001 and a 91% drop in IRHO 2501. Both cultivars reacted to the drought stress conditions by closing stomata and reducing the transpiration rate. Despite these differences, no significant variations were observed between the cultivars in stomatal conductance, transpiration, or instantaneous leaf-level water use efficiency. This indicates that IRHO 7001 is more tolerant to drought stress than IRHO 2501. A differential gene expression and network analysis was conducted to elucidate the differential responses of the cultivars. The DESeq2 algorithm identified 502 differentially expressed genes (DEGs). The gene coexpression network for IRHO 7001 comprised 274 DEGs and 46 predicted HUB genes, whereas IRHO 2501’s network included 249 DEGs and 3 HUB genes. RT-qPCR validation of 15 DEGs confirmed the RNA-Seq data. The transcriptomic profiles and gene coexpression network analysis revealed a set of DEGs and HUB genes associated with regulatory and transcriptional functions. Notably, the zinc finger protein ZAT11 and linoleate 13S-lipoxygenase 2-1 (LOX2.1) were overexpressed in IRHO 2501 but under-expressed in IRHO 7001. Additionally, phytohormone crosstalk was identified as a central component in the response and adaptation of oil palm to drought stress. Full article
(This article belongs to the Special Issue Recent Research in Plant Abiotic Stress)
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<p>Physical appearance of two oil palm cultivars, Deli × La Mé, (IRHO 7001 and IRHO 2501) in response to water deficit. Ninety-day-old palms were maintained under field capacity (well-watered) or subjected to water deprivation for three weeks (drought stress).</p>
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<p>Predawn leaf water potential (Ψleaf) of two oil palm cultivars, Deli × La Mé (IRHO 7001 and IRHO 2501), in response to water deficit. Ninety-day-old palms were maintained under field capacity (well-watered) or subjected to water deprivation until the photosynthetic rate of the IRHO 7001 cultivar dropped 40% (40%), which is considered moderate drought stress, or until it dropped 75% (75%), which is considered severe drought stress. Each box corresponds to the mean ± SD (<span class="html-italic">n</span> = 6).</p>
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<p>Physiological response of two oil palm cultivars, Deli × La Mé, IRHO 7001 (7001) and IRHO 2501 (2501) in response to water deficit. Ninety-day-old palms were maintained under field capacity (well-watered) or subjected to water deprivation until the photosynthetic rate of the IRHO 7001 cultivar dropped 40% (40%), which is considered moderate drought stress, or until it dropped 75% (75%), which is considered severe drought stress. Each box corresponds to the mean ± SD. (<span class="html-italic">n</span> = 6). (<b>A</b>). photosynthetic rate (<span class="html-italic">A</span>), (<b>B</b>). stomatal conductance (<span class="html-italic">gs</span>), (<b>C</b>). transpiration rate (E), and (<b>D</b>). instantaneous leaf-level water use efficiency (WUE).</p>
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<p>DEGs of two oil palm cultivars, Deli × La Mé, (IRHO 7001 and IRHO 2501) in response to water deficit. Ninety-day-old palms were maintained under field capacity (well-watered) or subjected to water deprivation until the photosynthetic rate of the IRHO 7001 cultivar dropped 40% (40%), which is considered moderate drought stress, or until it dropped 75% (75%), which is considered severe drought stress. (<b>A</b>) Heatmap of the RNA-Seq samples. A tendency toward red indicates under-expression, while a tendency toward blue indicates overexpression. (<b>B</b>) Unique and shared DEGs between two contrasting oil palm genotypes and drought stress conditions. The color key scale corresponds to the L2FC, tendency to blue correspond to underexpressed genes, while tendency to red indicates overexpressed.</p>
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<p>Gene coexpression networks of two oil palm cultivars, Deli × La Mé, (IRHO 7001 and IRHO 2501) in response to water deficit. (<b>A</b>) General; (<b>B</b>) IRHO 7001; and (<b>C</b>) IRHO 2501. The igraph R package was used to construct the general and specific cultivar coexpression networks under drought stress. Each node (sphere or bead-like shape) represents a gene, and groups of nodes highlighted with the same color indicate a module of genes. The black edges represent direct correlations between genes, and the red lines represent inverse correlations. The size of each node is proportional to the mean expression level of the gene represented by the node.</p>
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<p>Relative quantification of 15 genes by RT–qPCR compared against RNA-Seq in two oil palm cultivars, Deli × La Mé, (IRHO 7001 and IRHO 2501) in response to water deficit. Ninety-day-old palms were maintained under field capacity (well-watered) or subjected to water deprivation until the photosynthetic rate of the IRHO 7001 cultivar dropped 40% (40%), which is considered moderate drought stress, or until it dropped 75% (75%), which is considered severe drought stress. Yellow bars indicate the relative expression value obtained by RT-qPCR. Lite blue diamonds indicate the RNA-Seq value. (<b>A</b>) WRKY transcription factor 51; (<b>B</b>) NAC transcription factor NAM-B2-like_ NAM-B2; (<b>C</b>) beta-xylosidase alpha-L-arabinofuranosidase 2-like OsI_08964_ BXL1; (<b>D</b>) Leucine-rich repeat receptor-like serine_ At1g17230; (<b>E</b>) Calcium-binding protein CML42; (<b>F</b>) Ser/threo-protein phosphatase 6 regulatory ankyrin repeat subunit B; (<b>G</b>) Pectinesterase-like; (<b>H</b>) Pentatricopeptide repeat-containing protein_ At5g39980; (<b>I</b>) Multiple C2 and transmembrane domain-containing protein 2-like, (<b>J</b>) Non-specific lipid-transfer protein 2-like; (<b>K</b>) Transcription factor bHLH35-like isoform X1; (<b>L</b>) Mitogen-activated protein kinase kinase kinase 2-like; (<b>M</b>) Bidirectional sugar transporter SWEET14-like; (<b>N</b>) Galactinol synthase 1-like_ GOLS1; and (<b>O</b>) Xyloglucan endotransglucosylase/hydrolase protein 22-like XTH22.</p>
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<p>Phytohormone crosstalk and signal cascades of two oil palm cultivars, Deli × La Mé, (IRHO 7001 and IRHO 2501) in response to water deficit. The numbers indicate the step-by-step signaling cascade response in oil palms under drought stress. Numbers 1 and 2 indicate the stimulus and signal perception. 3 indicates signal transduction. 4, 5, and 6 indicate phytohormone metabolism and TFs activation/ inactivation. 7 and 8 indicate drought stress-induced genes and ROS metabolism balance. Gene expression levels are indicated for each cultivar, where 7001 = IRHO 7001 and 2501 = IRHO 2501. The square color corresponds to the gene expression color scale in the L2FC bar. The question mark indicates no gene expression. Arrows colors indicate flux of water (blue), ABA (green), and ROS (red) from soil or roots to leaves. The figure was partly generated using plant icon adaptations licensed and created by Guillaume Lobet (<a href="https://figshare.com/authors/Plant_Illustrations/3773596" target="_blank">https://figshare.com/authors/Plant_Illustrations/3773596</a> is licensed under CC-BY 4.0 Unported <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a>, accessed on 16 April 2024).</p>
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19 pages, 10196 KiB  
Article
A Chimeric ORF Fusion Phenotypic Reporter for Cryptococcus neoformans
by Louis S. Phillips-Rose, Chendi K. Yu, Nicholas P. West and James A. Fraser
J. Fungi 2024, 10(8), 567; https://doi.org/10.3390/jof10080567 (registering DOI) - 12 Aug 2024
Abstract
The plethora of genome sequences produced in the postgenomic age has not resolved many of our most pressing biological questions. Correlating gene expression with an interrogatable and easily observable characteristic such as the surrogate phenotype conferred by a reporter gene is a valuable [...] Read more.
The plethora of genome sequences produced in the postgenomic age has not resolved many of our most pressing biological questions. Correlating gene expression with an interrogatable and easily observable characteristic such as the surrogate phenotype conferred by a reporter gene is a valuable approach to gaining insight into gene function. Many reporters including lacZ, amdS, and the fluorescent proteins mRuby3 and mNeonGreen have been used across all manners of organisms. Described here is an investigation into the creation of a robust, synthetic, fusion reporter system for Cryptococcus neoformans that combines some of the most useful fluorophores available in this system with the versatility of the counter-selectable nature of amdS. The reporters generated include multiple composition and orientation variants, all of which were investigated for differences in expression. Evaluation of known promoters from the TEF1 and GAL7 genes was undertaken, elucidating novel expression tendencies of these biologically relevant C. neoformans regulators of transcription. Smaller than lacZ but providing multiple useful surrogate phenotypes for interrogation, the fusion ORF serves as a superior whole-cell assay compared to traditional systems. Ultimately, the work described here bolsters the array of relevant genetic tools that may be employed in furthering manipulation and understanding of the WHO fungal priority group pathogen C. neoformans. Full article
(This article belongs to the Special Issue Molecular Processes of Fungi, 2nd Edition)
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<p>Schematic overview of the bicistronic reporter construct integrating into <span class="html-italic">C. neoformans</span> Safe Haven locus. Built into the pSDMA57 plasmid backbone, engineered to be linearised using PacI endonuclease. The <span class="html-italic">amdS</span>-mRuby3 bicistronic reporter construct utilises the 5′ and 3′ flanking regions of the Safe Haven as regions of homologous recombination for integration. Expression is driven by the constitutive promoter of <span class="html-italic">TEF1</span>, which was inserted using the SwaI endonuclease site. The neomycin resistance gene (<span class="html-italic">NEO</span>) present in the plasmid backbone was used as the selectable marker to identify successful gene deletion mutants.</p>
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<p>Only the first of two ORFs is expressed in the bicistronic reporter construct. Spotting assay of <span class="html-italic">amdS</span>:mRuby3 bicistronic strain on 2% glucose YNB agar media plates supplemented as depicted. Strains individually expressing <span class="html-italic">amdS</span> or mRuby3 were used as controls. mRuby3 was excited using 535 nm light, capturing fluorescence between 565–645 nm. The wild-type control is H99O. Plates were photographed following 72 h of incubation at 30 °C.</p>
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<p>Fusing two ORFs produces reporters with multiple useful phenotypes. (<b>A</b>) Spotting assay of <span class="html-italic">amdS</span>:mRuby3 fusion strain on 2% glucose YNB agar media plates supplemented as depicted. mRuby3 was excited using 535 nm light, capturing fluorescence between 565 and 645 nm. (<b>B</b>) Spotting assay of <span class="html-italic">amdS</span>:mNeonGreen fusion strain on 2% glucose YNB agar media plates supplemented as depicted. mNeonGreen was excited using 460 nm light, capturing fluorescence between 505 and 545 nm. Strains individually expressing <span class="html-italic">amdS</span>, mRuby3 or mNeonGreen were used as controls. The wild-type control is H99O. Plates were photographed following 72 h of incubation at 30 °C.</p>
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<p>Order of ORF fusion does not affect phenotypic output for the fusion reporter when constitutively expressed using <span class="html-italic">TEF1</span><sub>(p)</sub>. (<b>A</b>) Spotting assay of mRuby3:<span class="html-italic">amdS</span> fusion strain on 2% glucose YNB agar media plates supplemented as depicted. mRuby3 was excited using 535 nm light, capturing fluorescence between 565 and 645 nm. (<b>B</b>) Spotting assay of mNeonGreen:<span class="html-italic">amdS</span> fusion strain on 2% glucose YNB agar media plates supplemented as depicted. mNeonGreen was excited using 460 nm light, capturing fluorescence between 505 and 545 nm. Strains individually expressing <span class="html-italic">amdS</span>, mRuby3 or mNeonGreen were used as controls. The wild-type control is H99O. Plates were photographed following 72 h of incubation at 30 °C.</p>
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<p>Order of ORF fusion affects fluorescence phenotype for the fusion reporter when expressed using inducible <span class="html-italic">GAL7</span><sub>(p)</sub>. Both orientations of the mRuby3 and mNeonGreen dual fusion reporters driven by <span class="html-italic">GAL7</span> promoter plated on supplemented YNB agar. Controls are wild-type H99O and the four reporter variants under the control of the constitutive <span class="html-italic">TEF1</span> promoter. Plates were photographed following 72 h of incubation at 30 °C. <span class="html-italic">C. neoformans</span> reporter strains in a spotting assay on 2% glucose, 2% glucose + 2% galactose, or 2% galactose. Strains were grown on media containing the indicated supplements. (<b>A</b>) mRuby3 was excited using 535 nm light, capturing fluorescence between 565 and 645 nm. (<b>B</b>) mNeonGreen was excited using 460 nm light, capturing fluorescence between 505 and 545 nm.</p>
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<p>Fluorescence of fusion reporters evaluates inducible promoter expression. <span class="html-italic">GAL7</span><sub>(p)</sub>-fluorophore:<span class="html-italic">amdS</span> fusion reporter strains were exposed to galactose-supplemented liquid YNB media following growth on 2% glucose. <span class="html-italic">C. neoformans</span> cells were incubated over 12 h and sampled at hourly time points for flow cytometry analysis. Relative fluorescence was calculated using maximal <span class="html-italic">TEF1</span><sub>(p)</sub>-fluorophore:<span class="html-italic">amdS</span> strains run through CytoFlexS flow cytometry machine. Cell count (histogram) was standardised (20,000 cells) and relative fluorescence was recorded and displayed for each time point. Mean fluorescent intensity (MFI) was calculated using FlowJo analysis software. Data were collected across five biological replicates. Gating methodology is detailed in <a href="#app1-jof-10-00567" class="html-app">Supplementary Figure S2</a>. (<b>A</b>) mRuby3 fluorescence was captured with a 610 ± 10 nm bandpass filter. (<b>B</b>) mNeonGreen fluorescence was captured with a 510 ± 20 nm bandpass filter.</p>
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10 pages, 237 KiB  
Article
STABILITY (Symptomatic Review during Biologic Therapy) of Inflammatory Bowel Disease Patients Receiving Infusion Therapy Improves Clinical Outcomes
by Kelli Morgan, James Morris, Qiang Cai, Phillip Kilgore, Urska Cvek, Marjan Trutschl, Katelynn T. Lofton, Meher Sindhoora Mavuram, Prerana Ramesh, Nhi Dao, Ahmed Alhaque and Jonathan Steven Alexander
Pathophysiology 2024, 31(3), 398-407; https://doi.org/10.3390/pathophysiology31030030 (registering DOI) - 12 Aug 2024
Abstract
Several studies have correlate improved patient outcomes with increased physician–patient contacts, particularly in chronic diseases. Extending this approach to inflammatory bowel disease (IBD) care presents a promising means of improving outcomes. At LSU Health Shreveport (LSUHS), a new approach called “STABILITY” (Symptomatic Review [...] Read more.
Several studies have correlate improved patient outcomes with increased physician–patient contacts, particularly in chronic diseases. Extending this approach to inflammatory bowel disease (IBD) care presents a promising means of improving outcomes. At LSU Health Shreveport (LSUHS), a new approach called “STABILITY” (Symptomatic Review during Biologic Therapy) was implemented during infusion therapy visits for IBD patients. These brief 15 min physician–patient interviews aimed to discuss the patients’ current IBD-related symptoms and evaluate the need for any changes in their treatment plan. Our goal was to remove a care gap and prevent intensifying symptoms created by missed appointments and loss of contact. To analyze the effectiveness of the STABILITY approach, a retrospective chart review was conducted on 111 IBD patients (18 with ulcerative colitis, 93 with Crohn’s disease) seen at LSUHS between 2011 and 2022. Since March 2019, STABILITY has been mandatory for all infusion therapy visits. The data collected included patients’ demographics, lab levels for biomarkers (fecal calprotectin, C-reactive protein, and erythrocyte sedimentation rates), hospitalizations, medication changes, and diagnosis dates before and after the implementation of STABILITY. Additionally, voluntary, anonymous infusion patient satisfaction surveys post-STABILITY were used to gather patient responses. In males with IBD, disease severity and hospitalizations were reduced significantly (p = 0.004 and 0.0234, respectively). In females with IBD, disease severity and hospitalizations were also reduced significantly (p = 0.0001 and 0.0072, respectively). In patients with UC and CD, there were significant improvements in disease severity (p = 0.043 and p = 0.0001, respectively), and CD hospitalizations were also improved (p = 0.0013). In males and females with UC, disease severity was marginally and significantly reduced (p = 0.0781 and p = 0.0379, respectively). In males and females with CD, disease severity was significantly reduced (p = 0.0161 and 0.0003, respectively), and CD male and female hospitalizations were also reduced significantly (p = 0.0436 and 0.013). Analyzing of survey responses, we found that the most patients reported improved IBD symptoms (56%), gained understanding of their condition (84%) and were in favor of continuing STABILITY consultations during infusion therapy (93%). To further investigate the impact of STABILITY, we conducted a comparative analysis between IBD patients undergoing STABILITY infusion therapy and LSUHS patients solely on self-injectable biologics. Our paired data analysis showed significant improvements in disease severity in female IBD patients (1.69 ± 0.13 vs. 1.41 ± 0.12, p = 0.0001) and male IBD patients (1.58 ± 0.16 vs. 1.2 ± 0.135, p = 0.004), in UC patients (1.833 ± 0.4.2 vs. 1.444, p = 0.043), in all CD patients (1.59 ± 0.11 vs. 1.29 ± 0.01, p = 0.0001), in male CD patients (1.52 ± 0.167 vs. 1.15 ± 0.15, p = 0.016), in female CD patients (1.66 ± 0.15 vs. 1.4 ± 0.13, p = 0.0003), in female UC patients (1.82 ± 0.32 vs. 1.45 ± 0.31, p = 0.0379), and marginally in male UC patients (p = 0.0781). Similarly, hospitalizations were significantly reduced in CD patients considered in aggregate (0.21 ± 0.04 vs. 0.11 ± 0.03, p = 0.0013), in male IBD patients (0.175 ± 0.06 vs. 0.05 ± 0.035, p = 0.024), in female IBD patients (0.21 ± 0.05 vs. 0.11 ± 0.04, p = 0.0072), in male CD patients (0.18 ± 0.07 vs. 0.06 ± 0.042, p = 0.0436), and in females with CD (0.23 ± 0.06 vs. 0.13 ± 0.04, p = 0.013). Although average values for fecal calprotectin, CRP, and sedimentation rate were frequently reduced after STABILITY interviews, these data did not reach statistical significance. These preliminary findings suggest that STABILITY may be effective in maintaining low disease activity or remission in IBD patients. Full article
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
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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20 pages, 20332 KiB  
Article
A Comparative Analysis on Impact of Extraction Methods on Carotenoids Composition, Antioxidants, Antidiabetes, and Antiobesity Properties in Seagrass Enhalus acoroides: In Silico and In Vitro Study
by Raymond Rubianto Tjandrawinata and Fahrul Nurkolis
Mar. Drugs 2024, 22(8), 365; https://doi.org/10.3390/md22080365 (registering DOI) - 12 Aug 2024
Abstract
Enhalus acoroides, a tropical seagrass, is known for its significant contribution to marine ecosystems and its potential health benefits due to bioactive compounds. This study aims to compare the carotenoid levels in E. acoroides using green extraction via ultrasound-assisted extraction (UAE) and [...] Read more.
Enhalus acoroides, a tropical seagrass, is known for its significant contribution to marine ecosystems and its potential health benefits due to bioactive compounds. This study aims to compare the carotenoid levels in E. acoroides using green extraction via ultrasound-assisted extraction (UAE) and microwave-assisted extraction (MAE) and to evaluate the biological properties of these extracts against oxidative stress, diabetes, and obesity through in silico and in vitro analyses. E. acoroides samples were collected from Manado City, Indonesia, and subjected to UAE and MAE. The extracts were analyzed using UHPLC-ESI-MS/MS to identify carotenoids, including β-carotene, lutein, lycopene, β-cryptoxanthin, and zeaxanthin. In silico analysis was conducted to predict the compounds’ bioactivity, toxicity, and drug-likeness using WAY2DRUG PASS and molecular docking with CB-Dock2. The compounds C3, C4, and C7 demonstrated notable interactions, with key metabolic proteins and microRNAs, further validating their potential therapeutic benefits. In vitro assays evaluated antioxidant activities using DPPH and FRAP assays, antidiabetic properties through α-glucosidase and α-amylase inhibition, and antiobesity effects via lipase inhibition and MTT assay with 3T3-L1 cells. Results indicated that both UAE and MAE extracts exhibited significant antioxidant, antidiabetic, and antiobesity activities. MAE extracts showed higher carotenoid content and greater biological activity compared to UAE extracts. These findings suggest that E. acoroides, mainly when extracted using MAE, has promising potential as a source of natural bioactive compounds for developing marine-based antioxidant, antidiabetic, and antiobesity agents. This study supplements existing literature by providing insights into the efficient extraction methods and the therapeutic potential of E. acoroides carotenoids. Full article
(This article belongs to the Special Issue Green Extraction for Obtaining Marine Bioactive Products)
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Graphical abstract

Graphical abstract
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<p>Antioxidant activity of <span class="html-italic">E. acoroides</span>. (<b>A</b>) EC<sub>50</sub> of FRAP. (<b>C</b>) The difference in antioxidant activity in the FRAP test based on two-way ANOVA. (<b>B</b>) EC<sub>50</sub> of DPPH inhibition activity. (<b>D</b>) Different antioxidant activity in the DPPH test based on two-way ANOVA. C3, astaxanthin; C4, canthaxanthin; E-UAE: <span class="html-italic">E. acoroides</span>—ultrasound-assisted extraction; E-MAE: <span class="html-italic">E. acoroides</span>—microwave-assisted extraction.</p>
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<p>Antidiabetic potential of <span class="html-italic">E. acoroides</span> through α-glucosidase inhibition. (<b>A</b>) EC<sub>50</sub> of α- glucosidase inhibition activity. (<b>B</b>) Difference in antidiabetic activity in a-glucosidase inhibition activity based on two-way ANOVA. C3, astaxanthin; C4, canthaxanthin; E-UAE: <span class="html-italic">E. acoroides</span>—ultrasound-assisted extraction; E-MAE: <span class="html-italic">E. acoroides</span>—microwave-assisted extraction.</p>
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<p>Antiobesity potential of <span class="html-italic">E. acoroides</span> through lipase inhibition. (<b>A</b>) EC<sub>50</sub> of lipase inhibition activity. (<b>B</b>) Difference in antiobesity activity in lipase inhibition based on two-way ANOVA. C3, astaxanthin; C4, canthaxanthin; E-UAE: <span class="html-italic">E. acoroides</span>—ultrasound-assisted extraction; E-MAE: <span class="html-italic">E. acoroides</span>—microwave-assisted extraction.</p>
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<p>Difference in antiobesity activity in 3T3-L1 preadipocytes cell inhibition, based on two-way ANOVA. C3, astaxanthin; C4, canthaxanthin; E-UAE: <span class="html-italic">E. acoroides</span>—ultrasound-assisted extraction; E-MAE: <span class="html-italic">E. acoroides</span>—microwave-assisted extraction.</p>
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<p>Downregulation of microRNA-21 (<b>A</b>) and microRNA-132 (<b>B</b>). Letters (A,B) denote significant differences (<span class="html-italic">p</span> &lt; 0.05; 95% CI; one-way ANOVA). C3, astaxanthin; C4, canthaxanthin; E-UAE: <span class="html-italic">E. acoroides</span>—ultrasound-assisted extraction; E-MAE: <span class="html-italic">E. acoroides</span>—microwave-assisted extraction.</p>
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<p>Biomechanism of astaxanthin, canthaxanthin, E-UAE, and E-MAE as antioxidants, antidiabetic, and antiobesity compounds.</p>
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13 pages, 1115 KiB  
Article
An Undetected Expansion, Spread, and Burden of Chikungunya and Dengue Cocirculating Antibodies in Nigeria
by Peter Asaga Mac, Markos Tadele, Thilini Nisansala, Philomena E. Airiohuodion, Chibuzor M. Babalola and Chukwuma Anyaike
Zoonotic Dis. 2024, 4(3), 201-213; https://doi.org/10.3390/zoonoticdis4030018 (registering DOI) - 12 Aug 2024
Abstract
Chikungunya and dengue are arboviral diseases transmitted by mosquitoes that have been increasingly recognized as public health concerns in Sub-Saharan Africa. Several studies conducted in Nigeria and other West African countries have revealed the seroprevalence burden and cocirculation of antibodies against mosquito-borne infections, [...] Read more.
Chikungunya and dengue are arboviral diseases transmitted by mosquitoes that have been increasingly recognized as public health concerns in Sub-Saharan Africa. Several studies conducted in Nigeria and other West African countries have revealed the seroprevalence burden and cocirculation of antibodies against mosquito-borne infections, thereby revealing a significant burden and clinical outcome complexities that have largely gone undetected. The current research study has important implications for disease surveillance, prevention strategies, and healthcare planning in Nigeria and other Sub-Saharan countries. A cross-sectional study was conducted on 871 outpatients and pregnant women from three regions of Nigeria. CHIKV and DENV immunoblot molecular diagnostic assays were used to analyze the serum samples for the presence of arboviral antibody serological markers IgG (Mikrogen Diagnostik, Germany) with DENV nonstructural protein 1 and DENV Equad and CHIKV virus-like particles (VLPs), according to the manufacturer’s instructions. A total of 871 participants were recruited from three geographical regions in Nigeria. Among them, 17.5% (152/871) were from Abia (southern Nigeria), 34.4% (300/871) were from Kaduna (northern Nigeria), and 48.1% (419/871) were from Nasarawa (central Nigeria). The ages of the participants ranged from 0 months to 80 years, with a mean age of 36.6 years. Of the 871 subjects, 71.0% (619/871) were female, and 29.0% (252/871) were male. The overall cohort detectable antibody seropositivity against CHIKV was 64.9% (565/871), 95% CI (61.74–68.06); DENV, 44.7% (389/871), 95% CI (41.41–47.99); and CHIKV-DENV cocirculation antibodies, 31.6% (95% CI 29–35). This study highlighted the unpredictably high seroprevalence, expansion, magnitude, and undetected burden of chikungunya and dengue in Nigeria. Full article
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<p>Arbovirus study sites in Nigeria.</p>
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<p>Distribution of CHIKV, DENV, and CHIKV-DENV cocirculating antibody seropositivity in the population.</p>
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<p>Distribution of CHIKV and DENV antibody seropositivity during sampling period.</p>
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16 pages, 3696 KiB  
Article
Molecular Detection and Phylogenetic Relationships of Honey Bee-Associated Viruses in Bee Products
by Delka Salkova, Ralitsa Balkanska, Rositsa Shumkova, Stela Lazarova, Georgi Radoslavov and Peter Hristov
Vet. Sci. 2024, 11(8), 369; https://doi.org/10.3390/vetsci11080369 (registering DOI) - 12 Aug 2024
Abstract
In the last few years, the isolation and amplification of DNA or RNA from the environment (eDNA/eRNA) has proven to be an alternative and non-invasive approach for molecular identification of pathogens and pests in beekeeping. We have recently demonstrated that bee pollen and [...] Read more.
In the last few years, the isolation and amplification of DNA or RNA from the environment (eDNA/eRNA) has proven to be an alternative and non-invasive approach for molecular identification of pathogens and pests in beekeeping. We have recently demonstrated that bee pollen and bee bread represent suitable biological material for the molecular identification of viral RNA. In the present study, we extracted total RNA from different bee products (pollen, n = 25; bee bread, n = 17; and royal jelly, n = 15). All the samples were tested for the presence of six of the most common honey bee-associated viruses—Deformed wing virus (DWV), Acute bee paralysis virus (ABPV), Chronic bee paralysis virus (CBPV), Sacbrood virus (SBV), Kashmir bee virus (KBV), and Black queen cell virus (BQCV)—using a reverse transcription polymerase chain reaction (RT-PCR). We successfully detected six records of DWV (10.5%, 6/57), four of ABPV (7.0%, 4/57), three of Israeli acute paralysis virus (IAPV) (5.3%, 3/57), and two of BQCV (3.5%, 2/57). Using ABPV primers, we also successfully detected the presence of IAPV. The obtained viral sequences were analyzed for phylogenetic relationships with the highly similar sequences (megablast) available in the GenBank database. The Bulgarian DWV isolates revealed a high homology level with strains from Syria and Turkey. Moreover, we successfully detected a DWV strain B for the first time in Bulgaria. In contrast to DWV, the ABPV isolates formed a separate clade in the phylogenetic tree. BQCV was closely grouped with Russian isolates, while Bulgarian IAPV formed its own clade and included a strain from China. In conclusion, the present study demonstrated that eRNA can be successfully used for molecular detection of honey bee-associated viruses in bee products. The method can assist the monitoring of the health status of honey bee colonies at the local, regional, and even national levels. Full article
(This article belongs to the Section Veterinary Microbiology, Parasitology and Immunology)
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<p>Map of the sampling sites from different regions in Bulgaria.</p>
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<p>Map presenting the distribution of the examined positive/negative samples of honey bee-associated viruses in Bulgaria.</p>
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<p>Phylogeny of Deformed wing virus (DWV) isolates from Bulgaria and other countries. The phylogenetic tree based on alignment of the fragment of RdRp gene sequences of DWV isolates from different countries was inferred by using the maximum likelihood method and the Tamura 3-parameter model and then selecting the topology with a superior log likelihood value [<a href="#B57-vetsci-11-00369" class="html-bibr">57</a>]. The indicated branching topology was evaluated by bootstrap resampling of the sequences of 10,000 replicates. Each isolate is indicated by country of isolation and GenBank accession number. Bulgarian isolates identified by this study are presented in green and red [<a href="#B12-vetsci-11-00369" class="html-bibr">12</a>].</p>
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<p>Phylogeny of Acute bee paralysis virus (ABPV) isolates from Bulgaria and other countries. The phylogenetic tree based on alignment of the part of the replicase polyprotein gene sequences of ABPV isolates (431 bp) from different countries was inferred by using the maximum likelihood method and the Tamura 3-parameter model and then selecting the topology with a superior log likelihood value [<a href="#B57-vetsci-11-00369" class="html-bibr">57</a>]. The indicated branching topology was evaluated by bootstrap resampling of the sequences of 10 000 replicates. Each isolate is indicated by country of isolation and GenBank accession number. Bulgarian isolates identified by this study are presented in green and yellow [<a href="#B54-vetsci-11-00369" class="html-bibr">54</a>].</p>
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<p>Phylogeny of Acute bee paralysis virus (IAPV) isolates from Bulgaria and other countries. The phylogenetic tree based on alignment of the part of the replicase polyprotein gene sequences of IAPV isolates (445 bp) from different countries was inferred by using the maximum likelihood method and the Tamura 3-parameter model and then selecting the topology with a superior log likelihood value [<a href="#B57-vetsci-11-00369" class="html-bibr">57</a>]. The indicated branching topology was evaluated by bootstrap resampling of the sequences of 10 000 replicates. Each isolate is indicated by country of isolation and GenBank accession number. Bulgarian isolates identified by this study are presented in green.</p>
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<p>Phylogeny of Black queen cell virus (BQCV) isolates from Bulgaria and other countries. The phylogenetic tree based on alignment of the part of the ORF 1 gene sequences of BQCV isolates (420 bp) from different countries was inferred by using the maximum likelihood method and the Tamura 3-parameter model and then selecting the topology with a superior log likelihood value [<a href="#B57-vetsci-11-00369" class="html-bibr">57</a>]. The indicated branching topology was evaluated by bootstrap resampling of the sequences of 10,000 replicates. Each isolate is indicated by country of isolation and GenBank accession number. Bulgarian isolates identified by this study are presented in green and yellow.</p>
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<p>ABPV–IAPV nucleotide alignment of a 452 bp fragment of the RdRp gene. Asterisks (*) indicate identical nucleotide positions in the alignment. The reported sequences are part of reference viral genomes (ABPV Acc. No. NC 002548; IAPV Acc. No. NC 009025). The PCR primer regions are underlined and in bold.</p>
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15 pages, 1191 KiB  
Systematic Review
New Perspectives for Spinal Cord Stimulation in Parkinson’s Disease-Associated Gait Impairment: A Systematic Review
by Christian G. Seufert, Matthias C. Borutta, Martin Regensburger, Yining Zhao and Thomas Kinfe
Biomedicines 2024, 12(8), 1824; https://doi.org/10.3390/biomedicines12081824 (registering DOI) - 12 Aug 2024
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Abstract
Parkinson’s Disease is a neurodegenerative disorder manifesting itself as a hypokinetic movement impairment with postural instability and gait disturbance. In case of failure and/or limited response, deep brain stimulation has been established as an alternative and effective treatment modality. However, a subset of [...] Read more.
Parkinson’s Disease is a neurodegenerative disorder manifesting itself as a hypokinetic movement impairment with postural instability and gait disturbance. In case of failure and/or limited response, deep brain stimulation has been established as an alternative and effective treatment modality. However, a subset of PD patients with gait impairment represents a therapeutic challenge. A systematic review (2000–2023) was performed using PubMed, Embase, Web of Science, Scopus, and Cochrane Library databases to determine the efficacy, stimulation waveform/parameters, spine level, and outcome measures of spinal cord stimulation using different waveforms in PD patients with and without chronic pain. Spinal cord stimulation responsiveness was assessed within the pre-defined follow-up period in three groups (short-term follow-up = 0–3 months; intermediate follow-up = 3–12 months; and long-term follow-up = more than 12 months). In addition, we briefly outline alternative neurostimulation therapies and the most recent developments in closed-loop spinal cord stimulation relevant to PD. In summary, 18 publications and 70 patients from uncontrolled observational trials were included, with low-quality evidence and conflicting findings. First and foremost, the currently available data do not support the use of spinal cord stimulation to treat PD-related gait disorders but have confirmed its usefulness for PD-associated chronic pain. Full article
(This article belongs to the Special Issue Emerging Trends in Neurostimulation and Neuromodulation Research)
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<p>The PRISMA flow chart of the assessed in-human studies related to SCS for PD-associated gait disorders in Parkinson’s Disease.</p>
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<p>Schematic illustration of the effect of spinal cord stimulation on gait disturbance.</p>
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