[go: up one dir, main page]

 
 
Sign in to use this feature.

Years

Between: -

Subjects

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Journals

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Article Types

Countries / Regions

remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline
remove_circle_outline

Search Results (14,812)

Search Parameters:
Keywords = CAT

Order results
Result details
Results per page
Select all
Export citation of selected articles as:
16 pages, 1499 KiB  
Article
Biological Mechanisms of Aflatoxin B1-Induced Bile Metabolism Abnormalities in Ducklings
by Yihong Chu, Aimei Yu, Huanbin Wang, Shahid Ali Rajput, Qianqian Yu and Desheng Qi
Animals 2024, 14(20), 2996; https://doi.org/10.3390/ani14202996 (registering DOI) - 17 Oct 2024
Viewed by 146
Abstract
This study investigated the effects and biological mechanisms of aflatoxin B1 (AFB1) on the health and bile metabolism of ducklings. Forty-eight 1-day-old ducklings were randomly assigned to two groups, with six replicates per group. The control group was fed a [...] Read more.
This study investigated the effects and biological mechanisms of aflatoxin B1 (AFB1) on the health and bile metabolism of ducklings. Forty-eight 1-day-old ducklings were randomly assigned to two groups, with six replicates per group. The control group was fed a basic diet, while the AFB1 group received a diet containing 90 µg/kg of AFB1. The experiment lasted for 2 weeks. The results showed that 90 µg/kg AFB1 caused abnormal bile metabolism; damaged liver cell nuclei and mitochondria; and significantly decreased body weight, average daily weight gain, and levels of albumin, total protein, cholesterol, total superoxide dismutase, glutathione peroxidase, and glutathione. It also significantly increased feed conversion efficiency, along with alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, total bile acids, and malondialdehyde levels. In the liver, the expression levels of CYP7A1, SCD, and other genes were significantly upregulated, while BSEP, FASN, HMGCR, CAT, and other genes were significantly downregulated. In conclusion, AFB1 causes abnormal bile metabolism and impairs the overall health and liver function of ducklings. Its mechanism of action may involve changes in gene expression related to bile acid metabolism, lipid metabolism, oxidative damage, and cancer pathways. Full article
(This article belongs to the Special Issue Animal Poisoning Related to Pathology and Toxicology)
Show Figures

Figure 1

Figure 1
<p>Effect of AFB<sub>1</sub> on liver health and tissue structure. (<b>A</b>) Effect of AFB<sub>1</sub> on the appearance of the liver. (<b>B</b>) H&amp;E staining of liver tissue (200×). (<b>C</b>) Oil Red O staining of liver tissue (200×). (<b>D</b>) Analysis of the ultrastructure of liver cell nuclei and mitochondria (10,000×). Red arrow: cell nucleus; green arrow: mitochondria.</p>
Full article ">Figure 2
<p>Liver transcriptome sequencing analysis results. (<b>A</b>) Differential gene expression status. (<b>B</b>) GO enrichment analysis of differentially expressed genes. (<b>C</b>) KEGG enrichment analysis of differentially expressed genes. (<b>D</b>) qPCR results (<span class="html-italic">n</span> = 6), <sup>a,b</sup> columns with different owercase letters indicated significant differences between the compared groups (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 3
<p>Biological mechanism of AFB<sub>1</sub>-induced abnormal bile metabolism in duckling liver.</p>
Full article ">
13 pages, 889 KiB  
Article
Antiretroviral Therapy with Ritonavir-Boosted Atazanavir- and Lopinavir-Containing Regimens Correlates with Diminished HIV-1 Neutralization
by Eloisa Yuste, Horacio Gil, Felipe Garcia and Victor Sanchez-Merino
Vaccines 2024, 12(10), 1176; https://doi.org/10.3390/vaccines12101176 (registering DOI) - 17 Oct 2024
Viewed by 229
Abstract
Background/Objectives: The impact of virion maturation on neutralizing antibody responses in HIV treatment is not fully understood. This study examines whether antiretroviral regimens (ART) with boosted protease inhibitors (b-PI), which increase exposure to immature virions, affect neutralization capacity compared to Non-b-PI regimens. Methods: [...] Read more.
Background/Objectives: The impact of virion maturation on neutralizing antibody responses in HIV treatment is not fully understood. This study examines whether antiretroviral regimens (ART) with boosted protease inhibitors (b-PI), which increase exposure to immature virions, affect neutralization capacity compared to Non-b-PI regimens. Methods: Neutralization activity was assessed in 45 HIV-infected individuals on b-PI regimens and 56 on Non-b-PI regimens, adjusting for factors like infection duration, ART initiation, and immune markers. Individuals on b-PI regimens had significantly lower neutralization scores [mean: 6.1, 95% Confidence Interval (CI): 5.3–6.9] than those on Non-b-PI regimens (mean: 8.9, 95% CI: 8.0–9.9; p < 0.0001). This difference was not explained by infection duration or CD4+ counts. CD4+/CD8+ ratios were positively associated with neutralization, while b-PI use was negatively associated. A regression model indicated that b-PI use significantly predicted lower neutralization scores (beta = −0.30, p = 0.049). Conclusions: These findings suggest that exposure to immature virions via b-PI use reduces neutralizing antibody responses, highlighting the importance of virion maturation in antibody induction. ART regimens promoting exposure to mature virions may enhance neutralization, with potential implications for HIV vaccine design. Further research is needed to explore implications for HIV vaccine design, especially using virus-like particles. Full article
Show Figures

Figure 1

Figure 1
<p>Individual selection and stratification. Serum-purified IgGs from 364 individuals were included. b-PI: ART regimen including boosted protease inhibitor (protease inhibitor + ritonavir). Non-b-PI: ART regimen not including boosted protease inhibitor. NRTI: nucleoside analog reverse-transcriptase inhibitor; NNRTI: non-nucleoside analog reverse-transcriptase inhibitor; PI: protease inhibitor; and INSTI: integrase strand transfer inhibitor.</p>
Full article ">Figure 2
<p>Comparison of neutralizing antibody responses (neutralization scores) in individuals treated with and without boosted protease inhibitors. HIV-1 infected individuals were on treatment regimens that either included boosted protease inhibitors (b-PI) or did not (Non-b-PI). Horizontal bars in the box plots indicate the mean for each group, and the standard errors of the means (SEMs) are shown.</p>
Full article ">Figure 3
<p>Comparison of cumulative time post-infection, time to ART initiation, CD4+ and CD8+ T-cell counts, CD4+/CD8+ T-lymphocyte ratios, and nadir CD4+ T-lymphocyte counts between individuals treated with and without b-PI. (<b>a</b>) Time post-infection comparison. (<b>b</b>) Time to ART initiation comparison. (<b>c</b>) CD4+ T-cell count comparison. (<b>d</b>) CD8+ T-cell count comparison. (<b>e</b>) CD4+/CD8+ T-lymphocyte ratio comparison. (<b>f</b>) Nadir CD4+ T-lymphocyte count comparison. Horizontal bars within the box plots indicate the mean for each group, and standard errors of means (SEMs) are shown. Significance levels between groups are indicated. Mann–Whitney U tests were used for comparisons between groups. Simple comparisons were made with two-sided alpha level of 0.05.</p>
Full article ">
14 pages, 683 KiB  
Article
Fortification of Orange and Apple Juices with Ferulic Acid: Implications for Food Safety and Quality
by Maribel Abadias, Gloria Bobo, Marina Anguera, Jordi Ortiz-Solà and Ingrid Aguiló-Aguayo
Foods 2024, 13(20), 3288; https://doi.org/10.3390/foods13203288 (registering DOI) - 16 Oct 2024
Viewed by 324
Abstract
In recent years, the awareness of healthier lifestyles among consumers has driven to an increased interest in more natural, nutritious, and low-processed foods. Ferulic acid, one of the most abundant phenolic acids in plants, has demonstrated a wide spectrum of antimicrobial activities and [...] Read more.
In recent years, the awareness of healthier lifestyles among consumers has driven to an increased interest in more natural, nutritious, and low-processed foods. Ferulic acid, one of the most abundant phenolic acids in plants, has demonstrated a wide spectrum of antimicrobial activities and a range of biomedical effects, including antioxidant, antiallergic, hepatoprotective, anticarcinogenic, anti-inflammatory, and antithrombotic, among others. The objective of this work was to study the antilisterial effect of ferulic acid (FA, 1500 mg/L) on fresh, ready-to-eat orange (FOJ) and apple (FAJ) juices and evaluate its effect on product quality. The results showed that FA reduced the Listeria monocytogenes population after 9 days of storage at 4 °C, but no effect on the indigenous microbiota was observed. The titratable acidity and color significantly changed. The antioxidant capacity and total phenolic content significantly increased with the addition of FA, being at least two times greater in fortified juices. FAJ and FOJ containing FA were scored lower (6.8 and 5.7 on a 9-point hedonic scale, respectively) than their respective controls. Overall, our results demonstrated that FA treatment could be a useful strategy to maintain the safety of fresh apple and orange juices and increase the antioxidant activity and phenolic content. The potential industrial applications and health benefits of the fortification of fruit juices with FA should be further explored. Full article
(This article belongs to the Section Food Quality and Safety)
22 pages, 3701 KiB  
Article
Physiological and Transcriptomic Analyses Reveal the Role of the Antioxidant System and Jasmonic Acid (JA) Signal Transduction in Mulberry (Morus alba L.) Response to Flooding Stress
by Xuejiao Bai, He Huang, Dan Li, Fei Yang, Xinyao Cong, Siqi Wu, Wenxu Zhu, Shengjin Qin and Yibo Wen
Horticulturae 2024, 10(10), 1100; https://doi.org/10.3390/horticulturae10101100 - 16 Oct 2024
Viewed by 355
Abstract
In recent decades, the frequency of flooding has increased as a result of global climate change. Flooding has become one of the major abiotic stresses that seriously affect the growth and development of plants. Mulberry (Morus alba L.) is an important economic [...] Read more.
In recent decades, the frequency of flooding has increased as a result of global climate change. Flooding has become one of the major abiotic stresses that seriously affect the growth and development of plants. Mulberry (Morus alba L.) is an important economic tree in China. Flooding stress is among the most severe abiotic stresses that affect the production of mulberry. However, the physiological and molecular biological mechanisms of mulberry responses to flooding stress are still unclear. In the present study, reactive oxygen species (ROS) metabolism, antioxidant mechanism, and plant hormones in mulberry associated with the response to flooding stress were investigated using physiological and transcriptomic analysis methods. The results showed significant increases in the production rate of superoxide anion (O2•−) and the content of hydrogen peroxide (H2O2) in leaves on the 5th day of flooding stress. This led to membrane lipid peroxidation and elevated malondialdehyde (MDA) levels. Antioxidant enzymes such as catalase (CAT), superoxide dismutase (SOD), and peroxidase (POD) exhibited enhanced activities initially, followed by fluctuations. The ascorbic acid–glutathione (AsA-GSH) cycle played a crucial role in scavenging ROS, promoting the reduction of oxidized glutathione (GSSG) to reduced glutathione (GSH). Transcriptomic analysis revealed the up-regulation of the gene-encoding antioxidant enzymes (APX, MDHAR, GPX, GR, GST) involved in ROS scavenging and stress tolerance mechanisms. Jasmonic acid (JA) levels and the expression of JA synthesis-related genes increased significantly in mulberry leaves under flooding stress. This activation of the JA signaling pathway contributed to the plant’s adaptability to flooding conditions. Proline (Pro) and soluble sugar (SS) contents increased notably in response to flooding stress. Proline helped maintain cell turgor and protected enzymes and membranes from damage, while soluble sugars supported anaerobic respiration and energy supply. However, soluble protein (SP) content decreased, suggesting inhibition of protein synthesis. The study provides insights into mulberry’s flooding tolerance mechanisms, guiding future molecular breeding efforts. This summary captures the key findings and implications of the study on mulberry’s response to flooding stress, focusing on physiological and molecular mechanisms identified in the research. Full article
Show Figures

Figure 1

Figure 1
<p>Production rate of O<sub>2</sub><sup>•−</sup> (<b>A</b>), H<sub>2</sub>O<sub>2</sub> (<b>B</b>) and MDA content (<b>C</b>), SOD activity (<b>D</b>), POD activity (<b>E</b>), CAT activity (<b>F</b>), and heatmaps of genes expression of ROS scavenging enzymes (<b>G</b>) in mulberry (<span class="html-italic">Morus alba</span> L.) leaves under flooding stress. Note: Heat map data are derived from the gene expression data of transcriptome analysis results, which are drawn according to the normalized gene expression amount under Ctl conditions. Under different waterlogging conditions, the gene expression amount higher than the average value under Ctl conditions is marked with red, and vice versa, and the gene expression amount lower than the average value is marked with blue. The color shading indicates the degree of difference between gene expression and Ctl. The darker the color, the more significant the difference. Data are represented as means ± SD of five replicate samples. Different lowercase letters indicating significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 2
<p>Activity key enzymes, content of metabolic substance, and heatmaps of gene expression in ASA-GSH cycle in mulberry (<span class="html-italic">Morus alba</span> L.) leaves under flooding stress. The content of ascorbic acid (<b>A</b>), the content of dehydroascorbate (<b>B</b>), the ratio of the content of ascorbate to dehydroascorbate (<b>C</b>), the content of glutathione (<b>D</b>), the content of glutathiol (<b>E</b>), the ratio of the content of glutathione to glutathiol (<b>F</b>), the activity of ascorbate peroxidase (<b>G</b>), the activity of monodehydroascorbate reductase (<b>H</b>), the activity of dehydroascorbate reductase (<b>I</b>), the activity of glutathione peroxidase (<b>J</b>), the activity of glutathione reductase (<b>K</b>), the activity of glutathione S-transferase (<b>L</b>), heatmaps of the expression levels of relevant genes in the AsA-GSH cycle (<b>M</b>). APX: ascorbate peroxidase; MDHAR: monodehydroascorbate reductase; GPX: glutathione peroxidase; GR: gluathione reductase; DHAR: dehydroascorbate reductase; AsA: ascorbate; DHA: dehydroascorbate; GSH: glutathione; MDHA: monodehydroascorbate; GSSG: glutathiol. Note: Heat map data processing method is the same as above. Data are represented as means ± SD of five replicate samples. Different lowercase letters indicating significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 3
<p>Activity key enzymes and heatmaps of genes expression in Trx-Prx pathway in mulberry (<span class="html-italic">Morus alba</span> L.) leaves under flooding stress. The activity of thioredoxin reductase (<b>A</b>), the activity of peroxiredoxin (<b>B</b>), heatmaps of the expression levels of related genes in the Trx-Prx pathway (<b>C</b>). Note: Data are represented as means ± SD of five replicate samples. Different lowercase letters indicating significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 4
<p>JA content and heatmaps of gene expression in JA synthesis and JA signal in mulberry (<span class="html-italic">Morus alba</span> L.) leaves under flooding stress. The content of JA (<b>A</b>), heatmaps of the expression levels of related genes in JA synthesis and JA signal (<b>B</b>). Note: Data are represented as means ± SD of five replicate samples. Different lowercase letters indicating significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 5
<p>Proline content (<b>A</b>), soluble sugar content (<b>B</b>), and soluble protein content (<b>C</b>) in mulberry (<span class="html-italic">Morus alba</span> L.) leaves under flooding stress. Note: Data are represented as means ± SD of five replicate samples. Different lowercase letters indicating significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 6
<p>RT-qPCR verified transcript expression levels of DEGs in mulberry (<span class="html-italic">Morus alba</span> L.) leaves under flooding stress. Data are represented as means ± SD of five replicate samples. Different lowercase letters indicating significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">
15 pages, 949 KiB  
Article
Regional Variations in and Key Predictors of Feline Tumor Malignancy: A Decade-Long Retrospective Study in Korea
by Byung-Joon Seung, Min-Kyung Bae and Jung-Hyang Sur
Animals 2024, 14(20), 2989; https://doi.org/10.3390/ani14202989 - 16 Oct 2024
Viewed by 218
Abstract
Feline cancer is increasingly recognized as a major cause of mortality, yet data on tumor prevalence and behavior in cats, particularly in non-Western regions, remain limited. This study analyzed a decade of feline tumor data in Korea from 2012 to 2022, focusing on [...] Read more.
Feline cancer is increasingly recognized as a major cause of mortality, yet data on tumor prevalence and behavior in cats, particularly in non-Western regions, remain limited. This study analyzed a decade of feline tumor data in Korea from 2012 to 2022, focusing on age, breed, and anatomical location as predictors of malignancy. Data were collected from 683 cats, with regression analysis applied to determine significant associations. Older cats exhibited a markedly higher risk of malignancy, particularly in mast cell and mammary tumors. Tumors in the mammary gland and alimentary tract had malignancy rates exceeding 90%, underscoring the need for early detection in these regions. Interestingly, squamous cell carcinoma was rare in the skin, in stark contrast to Western studies, likely reflecting differences in environmental exposure. While breed was not a statistically significant predictor, certain breeds, including Persians and Russian Blues, showed a higher frequency of malignancy. These findings highlight the importance of regional tumor research in cats and the need for larger, multicenter datasets that incorporate environmental, genetic, and lifestyle factors. Understanding these influences will help refine veterinary care and improve cancer treatment outcomes in feline populations. Full article
(This article belongs to the Section Companion Animals)
Show Figures

Figure 1

Figure 1
<p>Distribution of benign and malignant tumors in cats. (<b>A</b>) Distribution by age, with error bars representing standard deviations (SDs) to show variability. Asterisks (****) indicate statistically significant differences between groups (<span class="html-italic">p</span> &lt; 0.0001). (<b>B</b>) Distribution by sex, illustrating differences in tumor prevalence between males and females.</p>
Full article ">Figure 2
<p>Patterns of tumor distribution by breed and anatomical location in cats. (<b>A</b>) Distribution by breed, highlighting the comparison of benign and malignant tumor cases among various cat breeds. (<b>B</b>) Distribution by anatomical location, illustrating the prevalence of tumor types in different body regions.</p>
Full article ">
16 pages, 1106 KiB  
Article
Cryoprotective Potential of Theobromine in the Improvement of the Post-Thaw Quality of Bovine Spermatozoa
by Filip Benko, Štefan Baňas, Michal Ďuračka, Miroslava Kačániová and Eva Tvrdá
Cells 2024, 13(20), 1710; https://doi.org/10.3390/cells13201710 - 16 Oct 2024
Viewed by 183
Abstract
Theobromine (TBR) is a methylxanthine known for its bronchodilatory and stimulatory effects. This research evaluated the vitality, capacitation patterns, oxidative characteristics, microbial profile and expression of capacitation-associated proteins (CatSper1/2, sodium bicarbonate cotransporter [NBC], protein kinases A [PKA] and C [PKC] and adenylate cyclase [...] Read more.
Theobromine (TBR) is a methylxanthine known for its bronchodilatory and stimulatory effects. This research evaluated the vitality, capacitation patterns, oxidative characteristics, microbial profile and expression of capacitation-associated proteins (CatSper1/2, sodium bicarbonate cotransporter [NBC], protein kinases A [PKA] and C [PKC] and adenylate cyclase 10 [ADCY10]) in cryopreserved bovine spermatozoa (n = 30) in the absence (cryopreserved control [CtrlC]) or presence of different TBR concentrations (12.5, 25, and 50 µM) in egg yolk extender. Fresh ejaculate served as a negative control (CtrlN). Significant post-thaw maintenance of the sperm motility, membrane and DNA integrity and mitochondrial activity (p < 0.001) were recorded following the administration of 25 μM and 50 μM TBR, then compared to CtrlC. All groups supplemented with TBR exhibited a significantly lower percentage of prematurely capacitated spermatozoa (p < 0.001) than CtrlC. Significantly decreased levels of global reactive oxygen species (ROS), hydrogen peroxide and hydroxyl radicals were observed in the presence of 25 μM and 50 μM TBR (p < 0.01). Western blot analysis revealed that supplementation with 50 μM TBR significantly prevented the loss of NBC and ADCY10 (p < 0.01), while all TBR doses stabilized the levels of PKC (p < 0.05 at 50 μM TBR; p < 0.001 at 12.5 μM and 25 μM TBR). In summary, we suggest that TBR is effective in protecting the spermatozoa during the cryopreservation process through its potential to stimulate energy synthesis while preventing ROS overproduction and the loss of proteins involved in the sperm activation process. Full article
(This article belongs to the Section Reproductive Cells and Development)
Show Figures

Figure 1

Figure 1
<p>Protein levels of the cation channels of sperm isoforms 1 and 2 (CatSper1 and CatSper2), sodium bicarbonate cotransporter (NBC), protein kinase A (PKA), protein kinase C (PKC) and adenylyl cyclase 10 (ADCY10) in bovine spermatozoa in fresh state and cryopreserved in the absence or presence of selected theobromine (TBR) doses, assessed by Western blotting. Original photos of the gels and blots are available as <a href="#app1-cells-13-01710" class="html-app">Supplementary Materials</a>. Created with BioRender.com (accessed on 27 August 2024).</p>
Full article ">Figure 2
<p>Graphical representation of the relative quantification of the CatSper1 (<b>a</b>), CatSper2 (<b>b</b>), NBC (<b>c</b>), PKA (<b>d</b>), PKC (<b>e</b>) and ADCY 10 (<b>f</b>) proteins in bovine spermatozoa (n = 30) in fresh state (native control (Ctrl<sub>N</sub>)) and cryopreserved in the absence (cryopreserved control (Ctrl<sub>C</sub>)) or presence of selected theobromine (TBR) doses. Mean ± S.D. * <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.</p>
Full article ">
14 pages, 11381 KiB  
Article
Cats: The New Challenge for Rabies Control in the State of Yucatan, Mexico
by Aurea Mariana Salgado-Cardoso, José Ignacio Olave-Leyva, Ivonne Morales, Alvaro Aguilar-Setién, Irma López-Martínez and Nidia Aréchiga-Ceballos
Pathogens 2024, 13(10), 907; https://doi.org/10.3390/pathogens13100907 (registering DOI) - 16 Oct 2024
Viewed by 286
Abstract
The growing population in Yucatan has led to the expansion of construction in the Mayan jungle for tourist spaces, residential areas, and agriculture. Recently, rabies cases in cats (Felis catus) have increased in the state. This study aimed to perform antigenic [...] Read more.
The growing population in Yucatan has led to the expansion of construction in the Mayan jungle for tourist spaces, residential areas, and agriculture. Recently, rabies cases in cats (Felis catus) have increased in the state. This study aimed to perform antigenic and genetic characterization of the rabies viruses in felines and to present the spatial distribution and environmental features of the areas where these cases were reported. The ArcGIS software and R were employed to generate maps depicting the geographic locations of rabies cases in cats. A total of nine feline rabies cases occurred during the period 2003–2022. Three antigenic variants were detected: dog-related RVV1 (n = 1); vampire bat variant RVV3 (n = 1); and the canine-originated atypical variant (n = 7). Cases reported in Merida (n = 4) and Muna (n = 4) were localized to urban areas, while Cuncunul (n = 1) was rural. This study highlights the concerning resurgence of rabies infections in cats, emphasizing the looming threat of its reintroduction in dogs should vaccination rates diminish. The genetic affinity between the atypical variant and the canine virus underscores the urgent need for vigilance in maintaining high vaccination coverage across all susceptible species. Full article
(This article belongs to the Special Issue Emerging Zoonoses)
Show Figures

Figure 1

Figure 1
<p>Time series of laboratory-confirmed rabies cases in cats in the state of Yucatan, from 2003 to 2022.</p>
Full article ">Figure 2
<p>Phylogenetic reconstruction of the nine positive rabies cases in cats in Yucatan. The analysis was based on a dataset of 45 RABV partial nucleoprotein sequences belonging to terrestrial mammals and bats of the Americas. The neighbor-joining analysis was carried out using the evolutionary model Kimura 2P + G. ♦ Black diamonds indicate RABV isolated from cats in Yucatan.</p>
Full article ">Figure 3
<p>Geographic distribution of cat rabies cases (n = 9) in Yucatan at the municipality level, overlaid with population size. Rabies cases in cats are represented by the green triangles.</p>
Full article ">Figure 4
<p>Maps of the changes in vegetation for 2001 and 2021. Panel (<b>A</b>): year 2001. Panel (<b>B</b>): Year 2021. Purple triangles show the georeferencing of the rabies cases registered in cats since 2003 in Yucatan, Mexico. (Modified from INEGI [<a href="#B36-pathogens-13-00907" class="html-bibr">36</a>,<a href="#B37-pathogens-13-00907" class="html-bibr">37</a>]) DATUM WGS84 geographic coordinates.</p>
Full article ">
16 pages, 1808 KiB  
Review
Molecular Factors Involved in the Pathogenesis of Pyometra in Domestic Cats (Felis catus)
by Acácia Eduarda de Jesus Nascimento, Luciano Cardoso Santos and Juneo Freitas Silva
Animals 2024, 14(20), 2987; https://doi.org/10.3390/ani14202987 - 16 Oct 2024
Viewed by 291
Abstract
Pyometra is a major reproductive disorder affecting female cats. Characterized by the accumulation of purulent exudate in the uterus, it can lead to severe and potentially fatal complications. This pathology primarily occurs in adult cats during diestrus, but can also affect younger felines, [...] Read more.
Pyometra is a major reproductive disorder affecting female cats. Characterized by the accumulation of purulent exudate in the uterus, it can lead to severe and potentially fatal complications. This pathology primarily occurs in adult cats during diestrus, but can also affect younger felines, often due to inappropriate administration of hormonal medications. While the etiopathogenesis of pyometra is better understood in bitches, few studies have addressed the molecular factors involved in feline pyometra. Therefore, this review aims to provide an up-to-date and comprehensive discussion of pyometra in cats, focusing on the regulation of molecular factors described in this species, including hormonal, redox, immunological, and growth factors. Understanding the regulation of these factors in pyometra is crucial for elucidating its pathogenesis in domestic cats and for improving diagnosis and identifying novel therapeutic approaches. Full article
Show Figures

Figure 1

Figure 1
<p>Schematic representation of the domestic cat estrous cycle and pyometra development. (<b>a</b>) Reproductive cycle of cats. The cycle begins with proestrus, followed by estrus, characterized by male receptivity and elevated E2 levels. Without ovulatory stimulus or spontaneous ovulation (1), cats return to proestrus, potentially experiencing brief interestrus or anestrus periods. In ovulatory cycles (2 and 3), fertilization may occur, resulting in pregnancy (2), lasting 63–65 days; without fertilization (3), cats enter diestrus, a luteal phase. Post-pregnancy and lactation, or after diestrus, cats return to proestrus through interestrus intervals or seasonal anestrus. (<b>b</b>) Hormonal factors favoring bacterial proliferation and pyometra development. During proestrus and estrus, increased E2 causes uterine sensitization and cervical opening, while in diestrus, increased P4 results in uterine relaxation, increased glandular secretion, anti-inflammatory action, and cervical closure. (<b>c</b>) Photomicrographs of uterus with grade 3 pyometra. Lower magnification: uterine cross-section showing glandular hyperplasia and ectasia (arrows) and interstitial inflammatory infiltrate (arrowhead) with pus accumulation in the uterine lumen (asterisk). Higher magnification (inset): glandular (asterisk) and interstitial (arrow) infiltration of neutrophils, lymphocytes, and macrophages. E2, estradiol; P4, progesterone; scale bar = 100 μm.</p>
Full article ">Figure 2
<p>Plasma and uterine modulation of molecular factors involved in the occurrence of pyometra in domestic cats. P4, progesterone; PR, progesterone receptor; ERα, estrogen receptor α; Kiss1, kisspeptin; kiss1r, kisspeptin receptor; VEGF, vascular endothelial growth factor; flk-1, tyrosine kinase receptor 1; PLGF, placental growth factor; CRP, C-reactive protein; SAA, serum amyloid A protein; IL-6, interleukin 6; MIF, macrophage migration inhibitory factor; IL-10, interleukin 10; MDA, malondialdehyde; 8-OHdG, 8-hydroxy-2′-deoxyguanosine; SOD, superoxide dismutase; CAT, catalase; GPx, glutathione peroxidase; TAC, total antioxidant capacity; FRAP, ferric reducing ability of plasma; CUPRAC, cupric reducing antioxidant capacity; TEAC, trolox equivalent antioxidant capacity. Upward arrows (↑) indicate an increase in expression or activity of the respective factors, while downward arrows (↓) indicate a decrease.</p>
Full article ">
15 pages, 4033 KiB  
Article
NaCl Stress Stimulates Phenolics Biosynthesis and Antioxidant System Enhancement of Quinoa Germinated after Magnetic Field Pretreatment
by Shufang Wang, Xuejiao Zhang, Yiting Wang, Jirong Wu, Yin-Won Lee, Jianhong Xu and Runqiang Yang
Foods 2024, 13(20), 3278; https://doi.org/10.3390/foods13203278 - 16 Oct 2024
Viewed by 308
Abstract
Our previous study showed that magnetic field pretreatment promoted germination and phenolic enrichment in quinoa. In this study, we further investigated the effects of NaCl stress on the growth and phenolic synthesis of germinated quinoa after magnetic field pretreatment (MGQ). The results showed [...] Read more.
Our previous study showed that magnetic field pretreatment promoted germination and phenolic enrichment in quinoa. In this study, we further investigated the effects of NaCl stress on the growth and phenolic synthesis of germinated quinoa after magnetic field pretreatment (MGQ). The results showed that NaCl stress inhibited the growth of MGQ, reduced the moisture content and weight of a single plant, but increased the fresh/dry weight. The higher the NaCl concentration, the more obvious the inhibition effect. In addition, NaCl stress inhibited the hydrolysis of MGQ starch, protein, and fat but increased the ash content. Moreover, lower concentrations (50 and 100 mM) of NaCl stress increased the content of MGQ flavonoids and other phenolic compounds. This was due to the fact that NaCl stress further increased the enzyme activities of PAL, C4H, 4CL, CHS, CHI, and CHR and up-regulated the gene expression of the above enzymes. NaCl stress at 50 and 100 mM increased the DPPH and ABTS scavenging capacity of MGQ and increased the activities of antioxidant enzymes, including SOD, POD, CAT, APX, and GSH-Px, further enhancing the antioxidant system. Furthermore, principal component analysis showed that NaCl stress at 100 mM had the greatest combined effect on MGQ. Taken together, NaCl stress inhibited the growth of MGQ, but appropriate concentrations of NaCl stress, especially 100 mM, helped to further increase the phenolic content of MGQ and enhance its antioxidant system. Full article
Show Figures

Figure 1

Figure 1
<p>Effects of NaCl stress on the sprout length (<b>A</b>), germination percentage (<b>B</b>), single plant weight (<b>C</b>), moisture content (<b>D</b>), and fresh weight/dry weight (<b>E</b>) of germinated quinoa after magnetic field pretreatment. Values are expressed as mean ± SD. Lowercase letters represent significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 2
<p>Effects of NaCl stress on the starch (<b>A</b>), reducing sugar (<b>B</b>), soluble protein (<b>C</b>), free amino acid (<b>D</b>), crude fat (<b>E</b>), and ash (<b>F</b>) content of germinated quinoa after magnetic field pretreatment. Values are expressed as mean ± SD. Lowercase letters represent significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 3
<p>Effects of NaCl stress on the phenolics (<b>A</b>) and flavonoids (<b>B</b>) content of germinated quinoa after magnetic field pretreatment. Values are expressed as mean ± SD. Lowercase letters represent significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 4
<p>Effects of NaCl stress on the activities of PAL (<b>A</b>), C4H (<b>B</b>), 4CL (<b>C</b>), CHS (<b>D</b>), CHR (<b>E</b>), and CHI (<b>F</b>) of germinated quinoa after magnetic field pretreatment. Values are expressed as mean ± SD. Lowercase letters represent significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 5
<p>Effects of NaCl stress on the gene expression of <span class="html-italic">PAL</span> (<b>A</b>), <span class="html-italic">C4H</span> (<b>B</b>), <span class="html-italic">4CLs</span> (<b>C</b>), <span class="html-italic">CHS</span> (<b>D</b>), <span class="html-italic">CHR</span> (<b>E</b>), and <span class="html-italic">CHIs</span> (<b>F</b>) of germinated quinoa after magnetic field pretreatment. Values are expressed as mean ± SD. Lowercase letters represent significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 6
<p>Effects of NaCl stress on the scavenging capacity of DPPH (<b>A</b>) and ABTS (<b>B</b>) of germinated quinoa after magnetic field pretreatment. Values are expressed as mean ± SD. Lowercase letters represent significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 7
<p>Effects of NaCl stress on the antioxidative enzyme activity of SOD (<b>A</b>), POD (<b>B</b>), CAT (<b>C</b>), APX (<b>D</b>), and GSH-Px (<b>E</b>) of germinated quinoa after magnetic field pretreatment. Values are expressed as mean ± SD. Lowercase letters represent significant differences among treatments (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 8
<p>A comprehensive evaluation of the effects of various NaCl concentrations on germinated quinoa following pretreatment with a magnetic field (<b>A</b>). Rotated component matrix of principal component analysis (<b>B</b>). Indicators of significant differences under NaCl stress (<b>C</b>). Correlation analysis of indices of germinated quinoa after magnetic field pretreatment under different NaCl concentrations (<b>D</b>).</p>
Full article ">
22 pages, 3502 KiB  
Article
Transcriptome Analysis Reveals Immune and Antioxidant Defense Mechanisms in the Eriocheir japonica sinensis after Exposure to Ammonia
by Xi-Rong Zhu, Ye Jin, Xue Zhang, Qiu-Ning Liu and Bo-Ping Tang
Animals 2024, 14(20), 2981; https://doi.org/10.3390/ani14202981 - 16 Oct 2024
Viewed by 215
Abstract
As a key species in freshwater aquaculture, Eriocheir japonica sinensis was subjected to ammonia stress to assess its impact on the hepatopancreas. A total of 4007 differentially expressed genes (DEGs) were identified between control and treatment groups, comprising 1838 upregulated and 2169 downregulated [...] Read more.
As a key species in freshwater aquaculture, Eriocheir japonica sinensis was subjected to ammonia stress to assess its impact on the hepatopancreas. A total of 4007 differentially expressed genes (DEGs) were identified between control and treatment groups, comprising 1838 upregulated and 2169 downregulated genes. Following exposure to 300 mg/L of ammonia, the oxidative phosphorylation pathway was activated, while the lysosomal pathway was suppressed, thereby influencing immune functions. Thirteen DEGs from these pathways were further validated via qRT-PCR, revealing gene expression changes of one- to two-fold. Both acid phosphatase (ACP) and alkaline phosphatase (AKP) levels in the hepatopancreas and hemolymph initially increased and then decreased, indicating a disruption in immune functionality. Additionally, alanine transaminase (ALT) and triglyceride (TG) levels were measured, alongside catalase (CAT) activity, total antioxidant capacity (T-AOC), and malondialdehyde (MDA) content, all of which showed an upward trend, signifying oxidative stress and tissue damage. These results offer critical insights into the antioxidant and immune mechanisms of E. j. sinensis in ammonia-enriched environments. Full article
(This article belongs to the Section Animal Genetics and Genomics)
Show Figures

Figure 1

Figure 1
<p>HE staining of hepatopancreatic tissue structure of <span class="html-italic">E. j. sinensis</span> under ammonia stress. (<b>A</b>), control group; (<b>B</b>), medium-concentration stress group (300 mg/L); Bm, basement membrane; Bc, secretory cell; Ec, embryonic cell; Va, vacuole; Lu, lumen.</p>
Full article ">Figure 2
<p>Effects of ammonia stress on non-specific enzyme activity in <span class="html-italic">E. j. sinensis</span>. (<b>A</b>) AKP in hepatopancreas; (<b>B</b>) ACP in hepatopancreas; (<b>C</b>) CAT in hepatopancreas; (<b>D</b>) MDA in hepatopancreas; (<b>E</b>) ALT in hepatopancreas; (<b>F</b>) TG in hepatopancreas. Different letters (a, b, c, d) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 3
<p>Results of cell apoptosis detection. Arrows represent apoptotic cells.</p>
Full article ">Figure 4
<p>Effect of ammonia stress on non-specific enzyme activity in <span class="html-italic">E. j. sinensis</span>. (<b>A</b>) AKP in hemolymph; (<b>B</b>) ACP in hemolymph; (<b>C</b>) hemocyanin content; (<b>D</b>) CAT in hemolymph; (<b>E</b>) T-AOC in hemolymph; (<b>F</b>) MDA in hemolymph. Different letters (a, b, c, d) indicate significant differences (<span class="html-italic">p</span> &lt; 0.05).</p>
Full article ">Figure 5
<p>Volcano plot of differentially expressed genes (DEGs) from the transcriptomes of the control and treatment groups. For each unigene, the ratio of expression levels was plotted against the -log error rate. The <span class="html-italic">x</span>-axis represents the fold-change between the 300 mg/L ammonia and PBS control groups, and the <span class="html-italic">y</span>-axis indicates the significance of differential expression. Gray dots indicate genes with no significant difference, while red and blue dots indicate upregulated and downregulated unigenes, respectively (q-value &lt; 0.05 and |log<sub>2</sub> (fold-change)| &gt; 1).</p>
Full article ">Figure 6
<p>DEG enrichment analysis: (<b>A</b>) GO classification of unigenes from the hepatopancreas transcriptome of <span class="html-italic">E. j. sinensis</span>. Each annotated sequence is assigned to at least one GO term under the categories of biological process, cellular component, or molecular function. (<b>B</b>) KEGG pathway analysis of DEGs in <span class="html-italic">E. j. sinensis</span> hepatopancreas.</p>
Full article ">Figure 7
<p>KEGG enrichment bubble diagram (<b>A</b>) and GSEA results (<b>B</b>,<b>C</b>) of DEG analysis.</p>
Full article ">Figure 8
<p>(<b>A</b>) Oxidative phosphorylation pathway; (<b>B</b>) Lysosome pathway.</p>
Full article ">Figure 9
<p>Validation of RNA-seq data by qRT-PCR. (<b>A</b>) Relative expression profiles of seven selected oxidative phosphorylation pathway genes in the hepatopancreas after ammonia stress compared to the control group. (<b>B</b>) Relative expression profiles of six immune-related genes in the hepatopancreas after ammonia stress. Statistical significance: * <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.</p>
Full article ">
13 pages, 860 KiB  
Article
Measurement of New Biomarkers of Immunity and Welfare in Colostrum and Milk of Pigs: Analytical Validation and Changes During Lactation
by María Botía, Damián Escribano, Eva Mainau, Alberto Muñoz-Prieto and José J. Cerón
Biology 2024, 13(10), 829; https://doi.org/10.3390/biology13100829 (registering DOI) - 16 Oct 2024
Viewed by 248
Abstract
Colostrum is a mammary secretion released from the time of farrowing to 36 h post-farrowing. After this time and during all the rest of lactation, the mammary secretion is considered milk. The objectives of this study were: (1) to perform an analytical validation [...] Read more.
Colostrum is a mammary secretion released from the time of farrowing to 36 h post-farrowing. After this time and during all the rest of lactation, the mammary secretion is considered milk. The objectives of this study were: (1) to perform an analytical validation in the colostrum and milk of sows of assays for four analytes related to immunity: total ADA (tADA) and its isoenzymes (ADA1 and ADA2), myeloperoxidase (Mpx), calprotectin, and calgranulin, and two analytes related to welfare: cortisol and alpha-amylase. (2) To evaluate the changes in these analytes during lactation (3) To assess the correlations between these new analytes, as well as with IgG and IgA. In the analytical validation, all the assays were precise and accurate. When changes during lactation were evaluated, the concentration of tADA and ADA2 was found to be higher in colostrum than in milk (p < 0.02), while the activity of Mpx was observed to be higher in mature milk than in colostrum (p < 0.03). Furthermore, cortisol and alpha-amylase activity were found to be higher in colostrum compared to mature milk (p < 0.04 and p < 0.0001, respectively). Regarding the relation between analytes, alpha-amylase showed a significant correlation with both IgG and IgA and calprotectin was correlated with calgranulin and Mpx. Further studies should be performed to elucidate the possible practical application of the analytes evaluated in this study as biomarkers of colostrum and milk in sows. Full article
Show Figures

Figure 1

Figure 1
<p>Changes in tADA (<b>A</b>), ADA1 (<b>B</b>), ADA2 (<b>C</b>), S100A12 (<b>D</b>), S100A8/A9 (<b>E</b>) and Mpx (<b>F</b>) in colostrum/milk samples obtained at one day (T1), nine days (T9) and twenty days (T20) after farrowing. Asterisks indicate significant differences (** <span class="html-italic">p</span> ≤ 0.01; * <span class="html-italic">p</span> ≤ 0.05).</p>
Full article ">Figure 2
<p>Changes in alpha-amylase (<b>A</b>) and cortisol (<b>B</b>) concentrations in colostrum/milk samples obtained at one day (T1), nine days (T9) and twenty days (T20) after farrowing. Asterisks indicate significant differences (*** <span class="html-italic">p</span> ≤ 0.001; * <span class="html-italic">p</span> ≤ 0.05).</p>
Full article ">
12 pages, 2764 KiB  
Article
Proximal Co-Translation Facilitates Detection of Weak Protein-Protein Interactions
by Alina Kordonsky, Matan Gabay, Aurelia Rosinoff, Reut Avishid, Amir Flornetin, Noam Deouell, Taimaa Abd Alkhaleq, Noa Efron, Shoham Milshtein, Julia M. Shifman, Maayan Gal and Gali Prag
Int. J. Mol. Sci. 2024, 25(20), 11099; https://doi.org/10.3390/ijms252011099 (registering DOI) - 16 Oct 2024
Viewed by 179
Abstract
Ubiquitin (Ub) signals are recognized and decoded into cellular responses by Ub-receptors, proteins that tether the Ub-binding domain(s) (UBDs) with response elements. Typically, UBDs bind mono-Ub in highly dynamic and weak affinity manners, presenting challenges in identifying and characterizing their binding interfaces. Here, [...] Read more.
Ubiquitin (Ub) signals are recognized and decoded into cellular responses by Ub-receptors, proteins that tether the Ub-binding domain(s) (UBDs) with response elements. Typically, UBDs bind mono-Ub in highly dynamic and weak affinity manners, presenting challenges in identifying and characterizing their binding interfaces. Here, we report the development of a new approach to facilitate the detection of these weak interactions using split-reporter systems where two interacting proteins are proximally co-translated from a single mRNA. This proximity significantly enhances the readout signals of weak protein–protein interactions (PPIs). We harnessed this system to characterize the ultra-weak UBD and ENTH (Epsin N-terminal Homology) and discovered that the yeast Ent1-ENTH domain contains two Ub-binding patches. One is similar to a previously characterized patch on STAM1(signal-transducing adaptor molecule)-VHS (Vps27, Hrs, and STAM), and the other was predicted by AlphaFold. Using a split-CAT selection system that co-translates Ub and ENTH in combination with mutagenesis, we assessed and confirmed the existence of a novel binding patch around residue F53 on ENTH. Co-translation in the split-CAT system provides an effective tool for studying weak PPIs and offers new insights into Ub-receptor interactions. Full article
Show Figures

Figure 1

Figure 1
<p>Proximal co-translation from a single mRNA facilitates the detection of PPI. (<b>A</b>) In the polycistronic system, two proteins of interest (A and B) are encoded on the same plasmid under the same promoter. The two proteins are co-translated from the same mRNA, bringing them into close proximity and facilitating binding despite even weak affinity. This system minimizes the distance the two proteins need to diffuse to bind to each other. In contrast, when the two proteins are encoded on separate plasmids, each is transcribed and translated independently at different locations within the cell, reducing the likelihood of interaction due to their spatial separation. (<b>B</b>) Genetic selection system for testing binding affinity. The folding and activity of reporter proteins depend on the interaction between two proteins of interest (Prey and Bait), each fused to one of the split reporter protein fragments.</p>
Full article ">Figure 2
<p>Detection of weak PPIs in proximal co-translation versus separated translation systems. We employed co-translation systems to study weak protein–protein interactions. In all plots, pink represents co-translation systems, and blue represents separated translation systems. (<b>A</b>) N-CAT-ENTH and C-CAT-Ub selective growth in 10 μg/mL chloramphenicol media. (<b>B</b>) Same as in (<b>A</b>), but the split-CAT reporter was replaced with split-DHFR, and growth in minimal selective media was supplemented with 2.5 μg/mL trimethoprim. (<b>C</b>) Rpn10 and Ub fused with the split-CAT fragments, showing selective growth in 12 μg/mL chloramphenicol media (<b>D</b>) PLK4 and DCAF1 selective growth in 16 μg/mL chloramphenicol media using split-CAT. Quantification of the growth was calculated by the integration of the sigmoidal curves. The relative integral values are presented as bar charts.</p>
Full article ">Figure 3
<p>Homology-based structural model of ENTH:Ub. The complex structure of STAM1-VHS:Ub (PDB: 3LDZ) was superimposed on the structure of the yeast Ent1-ENTH domain (PDB: 5LOZ). (<b>A</b>) The alignment of the structures of VHS and ENTH suggests the binding patch of Ub on the ENTH surface. (<b>B</b>) Zoom-in view of the binding interface, showing the residues on the Ub-I44 patch. (<b>C</b>) Heatmap summarizing the relative growth efficiency of the indicated point mutants. The <span class="html-italic">E. coli</span> growth assay was performed on selective media with 10 μg/mL chloramphenicol. Growth efficiency compared to the WT Ub, measured by quantification of the spot’s growth over 24 h, integrating the sigmoidal growth curves. Red represents weaker binding, blue represents stronger binding, and the wild-type residues at each position are framed in black.</p>
Full article ">Figure 4
<p>ENTH possesses two Ub-binding patches. (<b>A</b>) Overlap of the AlphaFold2 model (Ub in orange, ENTH in blue) with the homology-based model (Ub in yellow, ENTH in light blue). (<b>B</b>) Zoom-in view of the ENTH:Ub interaction, highlighting the importance of F53 and A50. (<b>C</b>) Growth curves of wild-type ENTH and the indicated mutants in the co-translation system. (<b>D</b>) Bar-plot showing the relative cumulative growth based on the integrated growth curves.</p>
Full article ">
15 pages, 1641 KiB  
Article
Expression of Myeloperoxidase in Patient-Derived Endothelial Colony-Forming Cells—Associations with Coronary Artery Disease and Mitochondrial Function
by Weiqian Eugene Lee, Elijah Genetzakis, Giannie Barsha, Joshua Vescovi, Carmen Mifsud, Stephen T. Vernon, Tung Viet Nguyen, Michael P. Gray, Stuart M. Grieve and Gemma A. Figtree
Biomolecules 2024, 14(10), 1308; https://doi.org/10.3390/biom14101308 (registering DOI) - 16 Oct 2024
Viewed by 294
Abstract
Background and Aims: Myeloperoxidase (MPO) plays a critical role in the innate immune response and has been suggested to be a surrogate marker of oxidative stress and inflammation, with elevated levels implicated in cardiovascular diseases, such as atherosclerosis and heart failure, as well [...] Read more.
Background and Aims: Myeloperoxidase (MPO) plays a critical role in the innate immune response and has been suggested to be a surrogate marker of oxidative stress and inflammation, with elevated levels implicated in cardiovascular diseases, such as atherosclerosis and heart failure, as well as in conditions like rheumatoid arthritis and cancer. While MPO is well-known in leukocytes, its expression and function in human endothelial cells remain unclear. This study investigates MPO expression in patient-derived endothelial colony-forming cells (ECFCs) and its potential association with CAD and mitochondrial function. Methods: ECFCs were cultured from the peripheral blood of 93 BioHEART-CT patients. MPO expression and associated functions were examined using qRT-PCR, immunochemistry, flow cytometry, and MPO activity assays. CAD presence was defined using CT coronary angiography (CACS > 0). Results: We report MPO presence in patient-derived ECFCs for the first time. MPO protein expression occurred in 70.7% of samples (n = 41) which had nuclear co-localisation, an atypical observation given its conventional localisation in the granules of neutrophils and monocytes. This suggests potential alternative roles for MPO in nuclear processes. MPO mRNA expression was detected in 66.23% of samples (n = 77). CAD patients had a lower proportion of MPO-positive ECFCs compared to non-CAD controls (57.45% vs. 80%, p = 0.04), a difference that persisted in the statin-naïve sub-cohort (53.85% vs. 84.62%, p = 0.02). Non-CAD patients with MPO expression showed upregulated mitochondrial-antioxidant genes (AIFM2, TXNRD1, CAT, PRDX3, PRDX6). In contrast, CAD patients with MPO gene expression had heightened mROS production and mitochondrial mass and decreased mitochondrial function compared to that of CAD patients without MPO gene expression. Conclusions: MPO is present in the nucleus of ECFCs. In non-CAD ECFCs, MPO expression is linked to upregulated mitochondrial-antioxidant genes, whereas in CAD ECFCs, it is associated with greater mitochondrial dysfunction. Full article
Show Figures

Figure 1

Figure 1
<p>MPO protein expression in patient-derived ECFCs. (<b>A</b>) Representative Western blot of MPO protein expression in corresponding patient-derived ECFCs using anti-MPO antibody and anti-β-actin for loading control. (<b>B</b>) MPO protein is co-localised to the nuclei of patient-derived ECFCs. Representative immunocytochemistry images of MPO protein expression co-localised to the nucleus of patient-derived ECFCs, showing nuclei (blue) and MPO granules (red) within the cell (20× magnification). The scale bar represents 100 μM. (<b>C</b>) Representative Western blot of subcellular expression of MPO in patient-derived ECFCs at the soluble nuclear and chromatin-bound nuclear subfractions. At least three biological replicates were used. Original images can be found in <a href="#app1-biomolecules-14-01308" class="html-app">Supplementary Materials</a> file.</p>
Full article ">Figure 2
<p>CAD patients were less likely to express MPO gene, as identified by qRT-PCR. Stacked bar plots showing the association between proportion in MPO gene expression and the presence of CAD in (<b>A</b>) all patients (<span class="html-italic">n</span> = 77; No CAD = 30, CAD = 47), (<b>B</b>) male patients (<span class="html-italic">n</span> = 40; No CAD = 14, CAD = 26) and (<b>C</b>) female patients (<span class="html-italic">n</span> = 36; No CAD = 16, CAD = 20). (<b>D</b>) Statin-naïve patients (<span class="html-italic">n</span> = 54; No CAD = 27, CAD = 27), (<b>E</b>) statin-naïve male patients (<span class="html-italic">n</span> = 27; No CAD = 12, CAD = 15) and (<b>F</b>) statin-naïve female patients (<span class="html-italic">n</span> = 26; No CAD = 14, CAD = 12). Statistical association was analysed using Pearson’s chi-square test (categorial variables). Categorical measurements are shown as percentages. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
Full article ">Figure 2 Cont.
<p>CAD patients were less likely to express MPO gene, as identified by qRT-PCR. Stacked bar plots showing the association between proportion in MPO gene expression and the presence of CAD in (<b>A</b>) all patients (<span class="html-italic">n</span> = 77; No CAD = 30, CAD = 47), (<b>B</b>) male patients (<span class="html-italic">n</span> = 40; No CAD = 14, CAD = 26) and (<b>C</b>) female patients (<span class="html-italic">n</span> = 36; No CAD = 16, CAD = 20). (<b>D</b>) Statin-naïve patients (<span class="html-italic">n</span> = 54; No CAD = 27, CAD = 27), (<b>E</b>) statin-naïve male patients (<span class="html-italic">n</span> = 27; No CAD = 12, CAD = 15) and (<b>F</b>) statin-naïve female patients (<span class="html-italic">n</span> = 26; No CAD = 14, CAD = 12). Statistical association was analysed using Pearson’s chi-square test (categorial variables). Categorical measurements are shown as percentages. * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
Full article ">Figure 3
<p>MPO gene expression is associated with dysregulated mitochondrial function and dynamics. (<b>A</b>–<b>C</b>) CAD ECFCs with MPO gene expression at baseline had increased (<b>A</b>) mROS production and (<b>B</b>) mitochondrial mass and decreased (<b>C</b>) mitochondrial function. N = 8; no MPO gene expression: N = 3, MPO gene expression: N = 5. Data are represented as mean ± S.E.M. Welch’s <span class="html-italic">t</span>-test was performed.</p>
Full article ">Figure 4
<p>Antioxidant genes were upregulated with MPO gene expression in non-CAD patients. Relative fold gene expression was evaluated in ECFCs without CAD at baseline in (<b>A</b>) <span class="html-italic">AIFM2</span>, (<b>B</b>) <span class="html-italic">TXNRD1</span>, (<b>C</b>) <span class="html-italic">CAT</span>, (<b>D</b>) <span class="html-italic">PRDX3</span> and (<b>E</b>) <span class="html-italic">PRDX6</span>. Each sample was performed in triplicate. N = 30; no MPO gene expression: N = 6, MPO gene expression: N = 24. Data are represented as mean ± S.E.M. Student’s <span class="html-italic">t</span>-test was performed.</p>
Full article ">
8 pages, 494 KiB  
Article
Role of Liquid Biopsy in Progressive PSA Patients after Radical Prostatectomy
by Marcel Figueras, Lourdes Mengual, Mercedes Ingelmo-Torres, Fiorella L. Roldán, Bernat Padullés, Héctor Alfambra, Sandra Herranz, Pilar Paredes, Gary Amseian, Joel Mases, Maria J. Ribal, Laura Izquierdo and Antonio Alcaraz
Diagnostics 2024, 14(20), 2293; https://doi.org/10.3390/diagnostics14202293 (registering DOI) - 16 Oct 2024
Viewed by 228
Abstract
Background/Objectives: Currently, the prediction of disease recurrence after radical prostatectomy (RP) in localized prostate cancer (PCa) relies on clinicopathological parameters, which lack accuracy in predicting clinical outcomes. This study focused on evaluating the utility of cfDNA levels and fragmentation patterns as prognostic biomarkers [...] Read more.
Background/Objectives: Currently, the prediction of disease recurrence after radical prostatectomy (RP) in localized prostate cancer (PCa) relies on clinicopathological parameters, which lack accuracy in predicting clinical outcomes. This study focused on evaluating the utility of cfDNA levels and fragmentation patterns as prognostic biomarkers in progressive prostate-specific antigen (PSA) patients, including those with persistent PSA and biochemical recurrence (BR), after primary treatment in localized PCa patients. Methods: Twenty-nine high-risk localized PCa patients were enrolled in the study between February 2022 and May 2023. Blood samples were obtained before robotic RP. cfDNA concentration and fragment size were quantified using the Quant-it PicoGreen dsDNA Assay kit and Agilent 2200 TapeStation System, respectively. Results: The mean PSA value at diagnosis was 9.4 ng/mL. Seven patients (24.1%) had stage pT2 and 22 (75.9%) pT3. Nine patients (31%) had detectable PSA at the first PSA control six weeks after surgery, and four patients (20%) had BR during a mean follow-up of 18.4 months. No associations were found between cfDNA levels or fragmentation patterns and clinicopathological data. Although not statistically significant, patients with detectable PSA levels post-surgery exhibited higher cfDNA levels and shorter fragments compared with those with undetectable PSA. Conclusions: Our study indicated a tendency toward more fragmented cfDNA levels in PCa patients with persistent PSA. Strikingly, biochemical recurrent PCa patients exhibited similar cfDNA levels and fragmentation patterns compared to non-recurrent patients. Further studies exploring liquid biopsy-derived biomarkers in localized PCa patients are needed to elucidate their clinical utility in predicting PSA persistence. Full article
(This article belongs to the Special Issue Urologic Oncology: Biomarkers, Diagnosis, and Management)
Show Figures

Figure 1

Figure 1
<p>Box plots describing (<b>A</b>) cfDNA levels and (<b>B</b>) mean fragmentation patterns for PC patients with PSA detectable after surgery.</p>
Full article ">
15 pages, 20599 KiB  
Article
Ultrasound-Guided Deep Serratus Plane Block in Cat Cadavers (Felis catus): A Description of Dye and Contrast Media Distribution
by Gonzalo Polo-Paredes, Marta Soler, Francisco Gil, Francisco G. Laredo, Amalia Agut, Sara Carrillo-Flores and Eliseo Belda
Animals 2024, 14(20), 2978; https://doi.org/10.3390/ani14202978 (registering DOI) - 16 Oct 2024
Viewed by 241
Abstract
The serratus plane block is an ultrasound-guided anaesthetic technique that aims to provide analgesia to the lateral thoracic wall cranial to the 8th rib. This block can be performed in a superficial (between the latissimus dorsi and the serratus ventralis thoracis (SVT) muscles) [...] Read more.
The serratus plane block is an ultrasound-guided anaesthetic technique that aims to provide analgesia to the lateral thoracic wall cranial to the 8th rib. This block can be performed in a superficial (between the latissimus dorsi and the serratus ventralis thoracis (SVT) muscles) or deep plane (between the intercostales externi and the SVT muscles). This study aimed to assess the distribution and nerve staining of a mixture of 0.4 mL kg−1 of methylene blue and iopromide 50:50 performing a deep serratus plane (DSP) block at the level of the 5th rib. We hypothesise that this technique would be feasible and could stain the rami cutanei laterales (RCL) of the intercostales nerves cranial to the 8th rib in cat cadavers. This study was divided into two phases. Phase 1 consisted of an anatomical study of the thoracic wall (2 cadavers). Phase 2 consisted of the ultrasound-guided injection of the aforementioned mixture and the assessment of its distribution by computed tomography and anatomical dissection (12 cadavers). Contrast media spread a median of 5.5 (2.5–7.5) intercostal spaces. The dye stained a median of 3 (0–5) RCL, affecting RCL 2 (17.39%), RCL 3 (57.17%), RCL 4 (78.26%), RCL 5 (91.30%), RCL 6 (78.26%), and RCL 7 (8.70%) within the DSP. Occasionally, the rami dorsales laterales and the thoracicus longus nerve were stained. Based on these findings, the DSP block performed with a volume of 0.4 mL kg−1 of an anaesthetic could provide analgesia in the area innervated from T4 to T6. Full article
(This article belongs to the Section Veterinary Clinical Studies)
Show Figures

Figure 1

Figure 1
<p>Ultrasound probe position to perform the deep serratus plane block. The probe is positioned at the level of the acromion, transversal to the ribs. The needle is advanced “in plane” in a caudo-cranial direction. D, dorsal; V, ventral; Cr, cranial; Cd, caudal.</p>
Full article ">Figure 2
<p>Schematic representation of the ultrasound image of the lateral aspect of the thoracic wall. The rami cutanei laterales emerge from the intercostales nerves and travel laterally towards the epidermis. The ribs produce an acoustic shadowing and the endothoracic fascia (blue dotted line), parietalis (orange dotted line), and visceralis (green dotted line) pleuras are seen as a hyperechoic line. R4–R6, ribs 4–6; L, lateral; Cr, Cranial; Cd, Caudal; M, medial.</p>
Full article ">Figure 3
<p>Ultrasound imaging and execution of the deep serratus plane block. (<b>A</b>) The needle is advanced “in plane” until contact with the R5 at its caudo-lateral border. (<b>B</b>) An anechoic pocket (green asterisks) is formed after injecting the mixture of methylene blue and iopromide between the serratus ventralis thoracis muscle and the ribs/intercostales externi muscles. R5, fifth rib; R6, sixth rib; L, lateral; Cr, cranial; Cd, caudal; M, medial.</p>
Full article ">Figure 4
<p>Superficial plane of the serratus ventralis thoracis (SVT) muscle in a cat cadaver dissection. The scapula and superficial muscle layers lateral to the SVT have been lateralized. The rami cutanei laterales of the intercostales nerves are observed between the serrations of the SVT. (<b>A</b>) Anatomical visualisation. (<b>B</b>) Schematic drawing of the anatomical structures. D, dorsal; Cr, cranial; Cd, caudal; V, ventral.</p>
Full article ">Figure 5
<p>Deep plane of the serratus ventralis thoracis muscle (detached from its insertion) in a cat cadaver dissection. The rami cutanei laterales are seen emerging caudal to their respective ribs. (<b>A</b>) Anatomical visualisation. (<b>B</b>) Schematic drawing of the anatomical structures. D, dorsal; Cr, cranial; Cd, caudal; V, ventral.</p>
Full article ">Figure 6
<p>Contrast media distribution pattern of the 23 hemithoraces subjected to CT scan after performing the ultrasound-guided deep serratus plane block with 0.4 mL kg<sup>−1</sup> of a mixture of iopromide and methylene blue. Twenty-three hemithoraces are represented in purple by their respective distribution patterns. In one hemithorax (yellow square), contrast was found in the subcutaneous space. L, left hemithorax; R, right hemithorax; D, dorsal; Cr, cranial; Cd, caudal; V, ventral.</p>
Full article ">Figure 7
<p>Computed tomography transverse images of three cat cadavers after performing an ultrasound-guided deep serratus plane block. (<b>A</b>) Image at the level of the fifth thoracic vertebra. Contrast media pooled in the target area between the serratus ventralis thoracis and intercostales externi muscles. (<b>B</b>) Image at the level of the fourth thoracic vertebra. Contrast media in the right hemithorax reach the epaxial muscles. (<b>C</b>) Image at the level of the sixth thoracic vertebra showing a combination of A and B patterns. Yellow arrow, contrast media; blue arrow, scapula; D, dorsal; LL, left lateral; RL, right lateral; V, ventral.</p>
Full article ">Figure 8
<p>Diagram of the number of nerves stained after performing the deep serratus plane block with a mixture of 0.4 mL kg<sup>−1</sup> of methylene blue and iopromide 50:50 in 12 cat cadavers. One hemithorax was excluded (red cross). L, left hemithorax; R, right hemithorax; T2, T3, T4, T5, T6, T7, and T9, spinal nerves; 1–12, cats 1–12.</p>
Full article ">Figure 9
<p>Distribution of dye in the deep serratus ventralis plane after the ultrasound-guided injection of a mixture of methylene blue and iopromide 50:50. RDL, rami laterales of the rami dorsales of the spinal nerves; RCL, rami cutanei laterales of the intercostales nerves; D, dorsal; Cr, cranial; Cd, caudal; V, ventral.</p>
Full article ">
Back to TopTop