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10 pages, 4026 KiB  
Communication
Molecular Characterization of a Clade 2.3.4.4b H5N1 High Pathogenicity Avian Influenza Virus from a 2022 Outbreak in Layer Chickens in the Philippines
by Zyne Baybay, Andrew Montecillo, Airish Pantua, Milagros Mananggit, Generoso Rene Romo, Esmeraldo San Pedro, Homer Pantua and Christina Lora Leyson
Pathogens 2024, 13(10), 844; https://doi.org/10.3390/pathogens13100844 - 28 Sep 2024
Viewed by 551
Abstract
H5 subtype high-pathogenicity avian influenza (HPAI) viruses continue to devastate the poultry industry and threaten food security and public health. The first outbreak of H5 HPAI in the Philippines was reported in 2017. Since then, H5 HPAI outbreaks have been reported in 2020, [...] Read more.
H5 subtype high-pathogenicity avian influenza (HPAI) viruses continue to devastate the poultry industry and threaten food security and public health. The first outbreak of H5 HPAI in the Philippines was reported in 2017. Since then, H5 HPAI outbreaks have been reported in 2020, 2022, and 2023. Here, we report the first publicly available complete whole-genome sequence of an H5N1 high-pathogenicity avian influenza virus from a case in Central Luzon. Samples were collected from a flock of layer chickens exhibiting signs of lethargy, droopy wings, and ecchymotic hemorrhages in trachea with excessive mucus exudates. A high mortality rate of 96–100% was observed within the week. Days prior to the high mortality event, migratory birds were observed around the chicken farm. Lungs, spleen, cloacal swabs, and oropharyngeal–tracheal swabs were taken from two chickens from this flock. These samples were positive in quantitative RT-PCR assays for influenza matrix and H5 hemagglutinin (HA) genes. To further characterize the virus, the same samples were subjected to whole-virus-genome amplification and sequencing using the Oxford Nanopore method with mean coverages of 19,190 and 2984, respectively. A phylogenetic analysis of the HA genes revealed that the H5N1 HPAI virus from Central Luzon belongs to the Goose/Guangdong lineage clade 2.3.4.4b viruses. Other segments also have high sequence identity and the same genetic lineages as other clade 2.3.4.4b viruses from Asia. Collectively, these data indicate that wild migratory birds are the likely source of H5N1 viruses from the 2022 outbreaks in the Philippines. Thus, biosecurity practices and surveillance for HPAI viruses in both domestic and wild birds should be increased to prevent and mitigate HPAI outbreaks. Full article
(This article belongs to the Special Issue Pathogenesis, Epidemiology, and Control of Animal Influenza Viruses)
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<p>H5 phylogeny reveals that the HA genes from a virus detected in Central Luzon, Philippines belong to the Gs/Gd clade 2.3.4.4b. A/chicken/Philippines/BA-PTY/2022|H5N1 and A/chicken/Philippines/BA-MHN/2022|H5N1 are indicated by a black arrow and red dot. All hemagglutinin (HA) sequences from the H5 clade 2.3.4.4/b/c/e/g/h from avian hosts and from any location were downloaded from GISAID Database. After removal of sequences with duplicated strain names, the dataset was down-sampled at 98% threshold using CD-HIT version 4.8.1. to obtain another dataset of 104 sequences. This dataset and the HA sequences obtained from the HPAIV samples from Central Luzon, Philippines were aligned using MAFFT v7.407 and maximum likelihood trees were created using RaxML-ng v1.2.1.</p>
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<p>Viruses detected from Central Luzon, Philippines belong to group G2c viruses across all segments. A/chicken/Philippines/BA-PTY/2022|H5N1 (PTY) and A/chicken/Philippines/BA-MHN/2022|H5N1 (MHN) are indicated by a black arrow and red dot. Avian influenza virus sequences were downloaded from GISAID and subsequently down-sampled with CD-HIT. Phylogenetic trees were generated using RaxML-ng v1.2.1 with alignments made using MAFFT v7.407. For simplicity, only branches showing PTY and MHN are shown. The complete phylogenetic trees are shown in <a href="#app1-pathogens-13-00844" class="html-app">Supplementary Figure S1</a>. (<b>A</b>) PB2, (<b>B</b>) PB1, (<b>C</b>) PA, (<b>D</b>) HA, (<b>E</b>) NP, (<b>F</b>) NA, (<b>G</b>) M, (<b>H</b>) NS.</p>
Full article ">Figure 2 Cont.
<p>Viruses detected from Central Luzon, Philippines belong to group G2c viruses across all segments. A/chicken/Philippines/BA-PTY/2022|H5N1 (PTY) and A/chicken/Philippines/BA-MHN/2022|H5N1 (MHN) are indicated by a black arrow and red dot. Avian influenza virus sequences were downloaded from GISAID and subsequently down-sampled with CD-HIT. Phylogenetic trees were generated using RaxML-ng v1.2.1 with alignments made using MAFFT v7.407. For simplicity, only branches showing PTY and MHN are shown. The complete phylogenetic trees are shown in <a href="#app1-pathogens-13-00844" class="html-app">Supplementary Figure S1</a>. (<b>A</b>) PB2, (<b>B</b>) PB1, (<b>C</b>) PA, (<b>D</b>) HA, (<b>E</b>) NP, (<b>F</b>) NA, (<b>G</b>) M, (<b>H</b>) NS.</p>
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<p>Viruses detected from Central Luzon, Philippines belong to group G2c viruses across all segments. A/chicken/Philippines/BA-PTY/2022|H5N1 (PTY) and A/chicken/Philippines/BA-MHN/2022|H5N1 (MHN) are indicated by a black arrow and red dot. Avian influenza virus sequences were downloaded from GISAID and subsequently down-sampled with CD-HIT. Phylogenetic trees were generated using RaxML-ng v1.2.1 with alignments made using MAFFT v7.407. For simplicity, only branches showing PTY and MHN are shown. The complete phylogenetic trees are shown in <a href="#app1-pathogens-13-00844" class="html-app">Supplementary Figure S1</a>. (<b>A</b>) PB2, (<b>B</b>) PB1, (<b>C</b>) PA, (<b>D</b>) HA, (<b>E</b>) NP, (<b>F</b>) NA, (<b>G</b>) M, (<b>H</b>) NS.</p>
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12 pages, 6804 KiB  
Article
Haematological and Biochemical Alterations in Pekin Ducks Affected by Short Beak and Dwarfism Syndrome: An Analytical Study
by Barbara Szczepankiewicz, Jarosław Popiel, Stanisław Graczyk, Rafał Ciaputa, Kamila Bobrek and Andrzej Gaweł
Appl. Sci. 2024, 14(19), 8637; https://doi.org/10.3390/app14198637 - 25 Sep 2024
Viewed by 368
Abstract
Short beak and dwarfism syndrome (SBDS), characterised by growth retardation and short beak, is a contagious disease of ducks, caused by goose parvovirus (GPV). This study aimed to compare morphology and biochemistry data obtained from 4-week-old Pekin ducks naturally infected with parvovirus causing [...] Read more.
Short beak and dwarfism syndrome (SBDS), characterised by growth retardation and short beak, is a contagious disease of ducks, caused by goose parvovirus (GPV). This study aimed to compare morphology and biochemistry data obtained from 4-week-old Pekin ducks naturally infected with parvovirus causing SBDS in healthy Pekin ducks of the same age. Materials and Methods: Forty Pekin ducks (twenty infected GPV and twenty clinically healthy controls) were examined. Measurement of the beak and metatarsus and histopathological examination were conducted, and blood morphological and biochemical analyses were performed for each individual. Results: Statistically significant increases in the SBDS group were observed in white blood cells (WBCs), alkaline phosphatase (ALP), and albumin levels, while decreases were noted in non-organic phosphorus, potassium, and amylase levels. ALP in the control group was 465.70 ± 161.49, while in the SBDS group it was 353.68 ± 79.97 (p ˂ 0.006). 1,2-o-dilauryl-rac-glycero-3-glutaric acid-(6′-methylresorufin) ester (DGGR) lipase marker offered a refined gauge for pancreatic function, with established reference values for the healthy control group set at 14.95 ± 4.27 U/L. Conclusions: This study sheds light on the unique impact of GPV on the skeletal system of Pekin ducks, revealing significant insights into the mechanisms of SBDS without osteitis. Additionally, this work offers groundbreaking insights into the morphological and biochemical alterations in the blood during SBDS, establishing normative haematological and biochemical indices for Pekin ducks. It also introduces the DGGR lipase marker as a refined marker for pancreatic function for the healthy control group set at 14.95 ± 4.27 U/L. It highlights the role of ALP in ensuring proper bone growth and the need for ongoing research on its activity in the context of viral infections. Full article
(This article belongs to the Section Food Science and Technology)
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<p>Shortened beak of a duck with SBDS.</p>
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<p>Protruding tongue of a duck with SBDS.</p>
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<p>Shortened beak and metatarsus of a duck with SBDS.</p>
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13 pages, 8494 KiB  
Article
Effects of Different Photoperiods on the Transcriptome of the Ovary and Small White Follicles in Zhedong White Geese
by Tao Huang, Meina Fei, Xiaolong Zhou, Ke He, Songbai Yang and Ayong Zhao
Animals 2024, 14(18), 2747; https://doi.org/10.3390/ani14182747 - 23 Sep 2024
Viewed by 454
Abstract
Photoperiod can regulate the broodiness of geese and thus increase their egg-laying rate. The laying performance of geese is mainly determined by ovary and follicle development. To understand the effect of photoperiod on the ovary and small white follicles, sixteen 220-day-old healthy female [...] Read more.
Photoperiod can regulate the broodiness of geese and thus increase their egg-laying rate. The laying performance of geese is mainly determined by ovary and follicle development. To understand the effect of photoperiod on the ovary and small white follicles, sixteen 220-day-old healthy female Zhedong white geese were randomly divided into two groups for long photoperiods (15L:9D) and short photoperiods (9L:15D). The geese were euthanized after two months of feeding, and their ovaries and follicles were collected for transcriptome sequencing. RNA-seq analysis identified 187 and 448 differentially expressed genes in ovaries and small white follicles of different photoperiod groups, respectively. A long photoperiod promotes high expression of SPP1, C6, MZB1, GP1BA, and FCGBP genes in the ovaries, and increases the expression of SPP1, ANGPTL5, ALPL, ZP1, and CHRNA4 genes in small white follicles. Functional enrichment analysis showed that photoperiod could affect respiratory system development, smooth muscle cell proliferation in ovaries, and extracellular matrix-related function in small white follicles. WGCNA revealed 31 gene modules, of which 2 were significantly associated with ovarian weight and 17 with the number of small white follicles. Our results provide a better understanding of the molecular regulation in the photoperiod affecting goose reproduction. Full article
(This article belongs to the Section Poultry)
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<p>Volcano plot of DEGs between short-photoperiod group and long-photoperiod group. (<b>A</b>) Ovary. (<b>B</b>) Small white follicles.</p>
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<p>Pathway enrichment analysis of DEGs. (<b>A</b>) Ovary. (<b>B</b>) Small white follicles. The top 20 pathways with the most significant enrichment are displayed in the figure.</p>
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<p>Significantly enriched PPI for DEGs of different photoperiods. (<b>A</b>) Ovary. (<b>B</b>) Small white follicles. Each node represents a gene, and the thickness of the line connecting two nodes indicates the strength of the protein interaction.</p>
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<p>Weighted gene co-expression network analysis of the gene expression dataset. (<b>A</b>) Scale independence. (<b>B</b>) Mean connectivity. (<b>C</b>) Gene clustering tree. The upper part of the figure is the gene hierarchy clustering tree, and the lower part is the gene module. Different modules are represented by colors in the horizontal bar.</p>
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<p>Heatmap of the correlation between modules and traits. Each column represents a trait, and each row denotes an eigengene for a certain module. The matching correlation and <span class="html-italic">p</span> value are included in each cell. The darker the color, the higher the correlation. Red represents a positive correlation; blue represents a negative correlation.</p>
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<p>RT-qPCR validation of DEGs obtained by RNA-seq. Total RNA was extracted from the SWFs and ovaries and measured by qRT-PCR analysis. Relative expression levels were calculated according to the 2<sup>−△△Ct</sup> method using <span class="html-italic">GAPDH</span> as an internal reference gene.</p>
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21 pages, 6642 KiB  
Article
Investigating the Impact of Fasting and Refeeding on Blood Biochemical Indicators and Transcriptional Profiles in the Hypothalamus and Subcutaneous Adipose Tissue in Geese
by Yi Liu, Xianze Wang, Guangquan Li, Shufang Chen, Huiyan Jia, Jiuli Dai and Daqian He
Animals 2024, 14(18), 2746; https://doi.org/10.3390/ani14182746 - 23 Sep 2024
Viewed by 499
Abstract
Fasting and refeeding systems can cause significant short-term fluctuations in nutrient and energy levels, triggering adaptive physiological responses in animals. This study examines the effects of fasting and refeeding on blood biochemical indicators and transcriptional profiles in the hypothalamus and subcutaneous adipose tissue [...] Read more.
Fasting and refeeding systems can cause significant short-term fluctuations in nutrient and energy levels, triggering adaptive physiological responses in animals. This study examines the effects of fasting and refeeding on blood biochemical indicators and transcriptional profiles in the hypothalamus and subcutaneous adipose tissue of geese. Biochemical assays reveal that fasting significantly increases levels of free fatty acids and glucagon, while reducing concentrations of triglycerides, leptin, and insulin. Transcriptomic analyses identify a complex transcriptional response in both the hypothalamus and subcutaneous adipose tissue, affecting several metabolic pathways and key genes associated with feed intake and energy metabolism. In subcutaneous adipose tissue, fasting downregulates genes involved in fatty acid synthesis (LPL, SCD, and ACSL1) and upregulates PLIN2, a gene promoting lipid droplet degradation. Fasting affects a variety of metabolic pathways and critical genes in the hypothalamus, including Apelin, insulin, and mTOR signaling pathways. After fasting, the mRNA expression of NOG, GABRD, and IGFBP-1 genes in the hypothalamus are significantly upregulated, while proopiomelanocortin (POMC) gene expression is markedly downregulated. This study highlights the intricate biological responses to nutritional changes in geese, which adds to our understanding of energy balance and metabolic regulation in avian species. Full article
(This article belongs to the Section Animal Physiology)
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<p>Blood lipid marker concentrations of geese under fasting and refeeding conditions. (Serum free fatty acids (FFA) (<b>A</b>), triglyceride (TG) (<b>B</b>), total cholesterol (TC) (<b>C</b>), high-density lipoprotein (HDL) (<b>D</b>), low-density lipoprotein (LDL) (<b>E</b>), and very-low-density lipoprotein (VLDL) (<b>F</b>); CON: control group; Fasted: 24 h fasting; and Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6; ns &gt; 0.05, * <span class="html-italic">p</span> &lt; 0.05, and ** <span class="html-italic">p</span> &lt; 0.01).</p>
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<p>Serum appetite-related factor concentrations of geese under fasting and refeeding conditions. (Serum leptin (LEP) (<b>A</b>), insulin (INS) (<b>B</b>), glucagon (GC) (<b>C</b>), and adiponectin (ADP) (<b>D</b>); CON: control group; Fasted: 24 h fasting; and Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6; ns &gt; 0.05, * <span class="html-italic">p</span> &lt; 0.05, and *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>Overview of transcriptome sequencing of the goose hypothalamus, including (<b>A</b>) a principal component analysis (PCA) conducted for each mRNA−Seq sample, (<b>B</b>) the identification of differentially upregulated and downregulated genes in each group, (<b>C</b>) a Venn diagram showing the intersection for the differentially expressed genes between groups, and (<b>D</b>) a hierarchical clustering analysis of differential gene expression (DGE), with higher expression levels represented by shades of red and lower expression levels depicted in shades of steel blue. CON: control group; Fasted: 24 h fasting; Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6.</p>
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<p>Overview of transcriptome sequencing of the goose subcutaneous fatty tissue, including (<b>A</b>) a principal component analysis (PCA) conducted for each mRNA−Seq sample, (<b>B</b>) the identification of differentially upregulated and downregulated genes in each group, (<b>C</b>) a Venn diagram showing the intersection for the differentially expressed genes between groups, and (<b>D</b>) a hierarchical clustering analysis of differential gene expression (DGE), with higher expression levels represented by shades of red and lower expression levels depicted in shades of steel blue. CON: control group; Fasted: 24 h fasting; Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6.</p>
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<p>Analysis of GO enrichment in DEGs in the hypothalamus and subcutaneous adipose tissue of geese under fasting and refeeding conditions. The GO annotation terms are divided into three main categories: biological processes (BPs), cellular components (CCs), and molecular functions (MFs). The GO classification map of the hypothalamus was generated to compare CON and Fasted (<b>A1</b>), as well as Fasted and Refed (<b>A2</b>). Additionally, the GO classification map of subcutaneous adipose tissue was generated for comparing CON and Fasted (<b>B1</b>), along with Fasted and Refed (<b>B2</b>). (CON: control group; Fasted: 24 h fasting; Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6).</p>
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<p>Top 20 enriched KEGG pathways of DEGs in the hypothalamus and subcutaneous adipose tissue of geese under fasting and refeeding conditions. Enriched KEGG pathways of the hypothalamus were generated to compare CON and Fasted (<b>A1</b>), as well as Fasted and Refed (<b>A2</b>). Additionally, enriched KEGG pathways of subcutaneous adipose tissue were generated for comparing CON and Fasted (<b>B1</b>), along with Fasted and Refed (<b>B2</b>). (CON: control group; Fasted: 24 h fasting; Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6).</p>
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<p>Volcano plot of DEGs in the hypothalamus and subcutaneous adipose tissue of geese under fasting and refeeding conditions. Upregulated and downregulated DEGs are shown as red and blue dots, respectively. Genes are marked with red arrows and abbreviations. The DEGs of the hypothalamus were generated to compare CON and Fasted (<b>A1</b>), as well as Fasted and Refed (<b>A2</b>). Additionally, the DEGs of the subcutaneous adipose tissue were generated for comparing CON and Fasted (<b>B1</b>), along with Fasted and Refed (<b>B2</b>). (CON: control group; Fasted: 24 h fasting; Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6).</p>
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<p>The expression of genes in the hypothalamus and subcutaneous adipose tissue of geese under fasting and refeeding conditions. (<b>A</b>–<b>D</b>) represent the expression trends of genes (POMC, NOG, IGFBP1, and GABRD) in the hypothalamus under fasting and refeeding conditions. (<b>E</b>–<b>H</b>) represent the expression trends of genes (POMC, NOG, IGFBP1, and GABRD) in subcutaneous adipose tissue under fasting and refeeding conditions. (CON: control group; Fasted: 24 h fasting; Refed: 24 h of fasting followed by 3 h of refeeding; <span class="html-italic">n</span> = 6; ns: <span class="html-italic">p</span> &gt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, and *** <span class="html-italic">p</span> &lt; 0.001).</p>
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<p>FISH for <span class="html-italic">POMC</span> and relative <span class="html-italic">POMC</span> expression in the ARC of goose hypothalamus during periods of fasting and refeeding. (<b>A</b>–<b>C</b>) Representative images of FISH for the <span class="html-italic">POMC</span> gene are shown, with a scale bar of 100 μm. The localization of <span class="html-italic">POMC</span> (red) is indicated by red arrows. (<b>D</b>–<b>F</b>) The higher magnification images of <span class="html-italic">POMC</span> (indicated by the white dotted box) obtained through FISH are presented, with scale bars measuring 20 μm. The localization of <span class="html-italic">POMC</span> (red) is indicated by the red arrows.</p>
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9 pages, 1531 KiB  
Review
Review of the Highly Pathogenic Avian Influenza in Argentina in 2023: Chronicle of Its Emergence and Control in Poultry
by Ariel E. Vagnozzi
Pathogens 2024, 13(9), 810; https://doi.org/10.3390/pathogens13090810 - 19 Sep 2024
Viewed by 642
Abstract
Highly pathogenic avian influenza (HPAI) is a highly contagious viral disease that represents a significant threat to poultry production worldwide. Variants of the HPAI virus (HPAIV) H5A/Goose/GuangDong/1/96 (H5 Gs/GD/96) lineage have caused five intercontinental epizootic waves, with the most recent, clade 2.3.4.4b, reaching [...] Read more.
Highly pathogenic avian influenza (HPAI) is a highly contagious viral disease that represents a significant threat to poultry production worldwide. Variants of the HPAI virus (HPAIV) H5A/Goose/GuangDong/1/96 (H5 Gs/GD/96) lineage have caused five intercontinental epizootic waves, with the most recent, clade 2.3.4.4b, reaching Argentina in February 2023. Initially detected in wild birds, the virus quickly spread to backyard and commercial poultry farms, leading to economic losses, including the loss of influenza-free status (IFS). By March/April 2023 the epidemic had peaked and vaccination was seriously considered. However, the success of strict stamping-out measures dissuaded the National Animal Health Authority (SENASA) from authorizing any vaccine. Suspected cases sharply declined by May, and the last detection in commercial poultry was reported in June. The effective control and potential eradication of HPAIV in Argentina were due to SENASA’s early detection and rapid response, supported by private companies, veterinarians, and other stakeholders. Stamping-out measures have been effective for virus elimination and reduced farm-to-farm transmission; however, as the virus of this clade may remain present in wild birds, the risk of reintroduction into poultry production is high. Therefore, maintaining continuous active surveillance will be crucial for promptly detecting any new HPAIV incursion and taking appropriate action to contain virus dissemination. Full article
(This article belongs to the Special Issue Pathogenesis, Epidemiology, and Control of Animal Influenza Viruses)
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<p>The graph shows the number of cases detected by RRT-PCR reported by SENASA from February to December 2023. The peak of detections in backyard and commercial poultry was observed in February and March. Between August and October, 18 cases in sea mammals were reported. Source: SENASA (<a href="https://qliksensebycores.senasa.gob.ar/sense/app/28a22e66-c131-434e-861d-213bab5efc80/sheet/cf22d176-442b-4856-ab37-5210007b06d1/state/analysis" target="_blank">https://qliksensebycores.senasa.gob.ar/sense/app/28a22e66-c131-434e-861d-213bab5efc80/sheet/cf22d176-442b-4856-ab37-5210007b06d1/state/analysis</a>, accessed on 13 August 2024).</p>
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<p>The graph shows the geographical distribution of the outbreaks of HPAIV H5 clade 2.3.4.4b in Argentina. (<b>A</b>) Commercial poultry cases, (<b>B</b>) backyard poultry cases, (<b>C</b>) wild-bird cases, and (<b>D</b>) sea mammal cases. More details are in <a href="#app1-pathogens-13-00810" class="html-app">Tables S1–S3</a>. Source: WAHIS WOAH [<a href="#B15-pathogens-13-00810" class="html-bibr">15</a>,<a href="#B16-pathogens-13-00810" class="html-bibr">16</a>].</p>
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19 pages, 586 KiB  
Review
Recent Occurrence, Diversity, and Candidate Vaccine Virus Selection for Pandemic H5N1: Alert Is in the Air
by Yordanka Medina-Armenteros, Daniela Cajado-Carvalho, Ricardo das Neves Oliveira, Milena Apetito Akamatsu and Paulo Lee Ho
Vaccines 2024, 12(9), 1044; https://doi.org/10.3390/vaccines12091044 - 12 Sep 2024
Viewed by 1125
Abstract
The prevalence of the highly pathogenic avian influenza virus H5N1 in wild birds that migrate all over the world has resulted in the dissemination of this virus across Asia, Europe, Africa, North and South America, the Arctic continent, and Antarctica. So far, H5N1 [...] Read more.
The prevalence of the highly pathogenic avian influenza virus H5N1 in wild birds that migrate all over the world has resulted in the dissemination of this virus across Asia, Europe, Africa, North and South America, the Arctic continent, and Antarctica. So far, H5N1 clade 2.3.4.4.b has reached an almost global distribution, with the exception of Australia and New Zealand for autochthonous cases. H5N1 clade 2.3.4.4.b, derived from the broad-host-range A/Goose/Guangdong/1/96 (H5N1) lineage, has evolved, adapted, and spread to species other than birds, with potential mammal-to-mammal transmission. Many public health agencies consider H5N1 influenza a real pandemic threat. In this sense, we analyzed H5N1 hemagglutinin sequences from recent outbreaks in animals, clinical samples, antigenic prototypes of candidate vaccine viruses, and licensed human vaccines for H5N1 with the aim of shedding light on the development of an H5N1 vaccine suitable for a pandemic response, should one occur in the near future. Full article
(This article belongs to the Special Issue Immunity to Influenza Viruses and Vaccines)
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<p>Influenza A (H5N1) lethality in humans by clade. Influenza A (H5N1) lethality in humans by clade (numbers in white). The colored sectors indicate the fraction of total cases (N = 30) in each clade: 2.3.2.1a (orange; N = 2), 2.3.2.1c (red; N = 11), 2.3.4.4b (blue; N = 15), and not reported (gray; N = 2). The percentages in each sector show the percent mortality relative to the number of cases in each clade. The period of analysis was from July 2021 to June 2024.</p>
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29 pages, 2920 KiB  
Article
Acoustic Analysis of Vowels in Australian Aboriginal English Spoken in Victoria
by Debbie Loakes and Adele Gregory
Languages 2024, 9(9), 299; https://doi.org/10.3390/languages9090299 - 12 Sep 2024
Viewed by 431
Abstract
(1) Background: Australian Aboriginal English (AAE) is a variety known to differ in various ways from the mainstream, but to date very little phonetic analysis has been carried out. This study is a description of L1 Aboriginal English in southern Australia, aiming to [...] Read more.
(1) Background: Australian Aboriginal English (AAE) is a variety known to differ in various ways from the mainstream, but to date very little phonetic analysis has been carried out. This study is a description of L1 Aboriginal English in southern Australia, aiming to comprehensively describe the acoustics of vowels, focusing in particular on vowels known to be undergoing change in Mainstream Australian English. Previous work has focused on static measures of F1/F2, and here we expand on this by adding duration analyses, as well as dynamic F1/F2 measures. (2) Methods: This paper uses acoustic-phonetic analyses to describe the vowels produced by speakers of Aboriginal Australian English from two communities in southern Australia (Mildura and Warrnambool). The focus is vowels undergoing change in the mainstream variety–the short vowels in KIT, DRESS, TRAP, STRUT, LOT, and the long vowel GOOSE; focusing on duration, and static and dynamic F1/F2. As part of this description, we analyse the data using the sociophonetic variables gender, region, and age, and also compare the Aboriginal Australian English vowels to those of Mainstream Australian English. (3) Results: On the whole, for duration, few sociophonetic differences were observed. For static F1/F2, we saw that L1 Aboriginal English vowel spaces tend to be similar to Mainstream Australian English but can be analysed as more conservative (having undergone less change) as has also been observed for L2 Aboriginal English, in particular for KIT, DRESS, and TRAP. The Aboriginal English speakers had a less peripheral vowel space than Mainstream Australian English speakers. Dynamic analyses also highlighted dialectal differences between Aboriginal and Mainstream Australian English speakers, with greater F1/F2 movement in the trajectories of vowels overall for AAE speakers, which was more evident for some vowels (TRAP, STRUT, LOT, and GOOSE). Regional differences in vowel quality between the two locations were minimal, and more evident in the dynamic analyses. (4) Conclusions: This paper further highlights how Aboriginal Australian English is uniquely different from Mainstream Australian English with respect to certain vowel differences, and it also highlights some ways in which the varieties align. The differences, i.e., a more compressed vowel space, and greater F1/F2 movement in the trajectories of short vowels for AAE speakers, are specific ways that Aboriginal Australian English and Mainstream Australian English accents are different in these communities in the southern Australian state of Victoria. Full article
(This article belongs to the Special Issue An Acoustic Analysis of Vowels)
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<p>Map of Australia (small) showing Victoria (large)—locations of the communities can be seen in relation to the capital Melbourne.</p>
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<p>Duration (ms) of AAE vowels plotted according to location (MI/WN) and gender (F/M).</p>
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<p>Duration (ms) of AAE and MAE vowels.</p>
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<p>Mean vowel values plotted in Bark according to (<b>top</b>) location (MI/WN), (<b>middle</b>) gender (F/M), and (<b>bottom</b>) age (&lt;40/&gt;40).</p>
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<p>Vowel ellipses plotted in Bark according to dialect (AAE—solid line /MAE—dotted line) with labels at the mean value.</p>
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<p>AAE vowel formant trajectories taken at five points across the vowel (bark normalized) for location, gender, and age.</p>
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<p>Vowel formant trajectories taken at five points across the vowel (bark normalized) for MAE and AAE speakers.</p>
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17 pages, 3553 KiB  
Article
Comparative Transcriptome Analysis Unveils Regulatory Factors Influencing Fatty Liver Development in Lion-Head Geese under High-Intake Feeding Compared to Normal Feeding
by Jie Kong, Ziqi Yao, Junpeng Chen, Qiqi Zhao, Tong Li, Mengyue Dong, Yuhang Bai, Yuanjia Liu, Zhenping Lin, Qingmei Xie and Xinheng Zhang
Vet. Sci. 2024, 11(8), 366; https://doi.org/10.3390/vetsci11080366 - 11 Aug 2024
Viewed by 1030
Abstract
The lion-head goose is the only large goose species in China, and it is one of the largest goose species in the world. Lion-head geese have a strong tolerance for massive energy intake and show a priority of fat accumulation in liver tissue [...] Read more.
The lion-head goose is the only large goose species in China, and it is one of the largest goose species in the world. Lion-head geese have a strong tolerance for massive energy intake and show a priority of fat accumulation in liver tissue through special feeding. Therefore, the aim of this study was to investigate the impact of high feed intake compared to normal feeding conditions on the transcriptome changes associated with fatty liver development in lion-head geese. In this study, 20 healthy adult lion-head geese were randomly assigned to a control group (CONTROL, n = 10) and high-intake-fed group (CASE, n = 10). After 38 d of treatment, all geese were sacrificed, and liver samples were collected. Three geese were randomly selected from the CONTROL and CASE groups, respectively, to perform whole-transcriptome analysis to analyze the key regulatory genes. We identified 716 differentially expressed mRNAs, 145 differentially expressed circRNAs, and 39 differentially expressed lncRNAs, including upregulated and downregulated genes. GO enrichment analysis showed that these genes were significantly enriched in molecular function. The node degree analysis and centrality metrics of the mRNA–lncRNA–circRNA triple regulatory network indicate the presence of crucial functional nodes in the network. We identified differentially expressed genes, including HSPB9, Pgk1, Hsp70, ME2, malic enzyme, HSP90, FADS1, transferrin, FABP, PKM2, Serpin2, and PKS, and we additionally confirmed the accuracy of sequencing at the RNA level. In this study, we studied for the first time the important differential genes that regulate fatty liver in high-intake feeding of the lion-head goose. In summary, these differentially expressed genes may play important roles in fatty liver development in the lion-head goose, and the functions and mechanisms should be investigated in future studies. Full article
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<p>Phenotypic changes in liver and body weight after high-intake feeding in lion-head geese. (<b>A</b>) Goose liver in the groups of high-intake feeding and normal feeding. (<b>B</b>) The weight of liver. (<b>C</b>) The size of the goose liver. (<b>D</b>) The weight of goose (** <span class="html-italic">p</span> &lt; 0.01; * <span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Overview of whole-transcriptome sequencing. (<b>A</b>) The density distribution of transcriptome was according to log10 (FPKM), original gene read counts were normalized using the FPKM method. (<b>B</b>) The 6−sample expression violin plot. (<b>C</b>) The principal component analysis (PCA) is useful for exploring the distance relationship between the 6 samples. (<b>D</b>) Pearson’s correlation matrix for mRNA, lncRNA, and circRNA profiles.</p>
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<p>Identification and analysis of mRNA, lncRNA, and circRNA associated with fatty liver. (<b>A</b>) Volcano plots of DEGs in mRNA. (<b>B</b>) Volcano plots of DEGs in lncRNA. (<b>C</b>) Volcano plots of DEGs in circRNA. Each dot in the plot represents a gene with its corresponding log2 fold change (FC) on the x-axis and <span class="html-italic">p</span>-value (log10) on the y-axis. The horizontal line indicates the significance threshold (false discovery rate &lt;5%), whereas the vertical line segregates genes with logFC &gt;1.5. Gray represents no significant difference between the two groups, red indicates the upregulated genes, and blue indicates the downregulated genes.</p>
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<p>Functional analyses of significantly enriched trends. The top 8 significant terms at the mRNA level. The size of dots shows the number of DEGs clustered in the same terms. The color of dots indicates the <span class="html-italic">p</span>-value.</p>
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<p>Construction and visualization of lncRNA–mRNA–circRNA network. (<b>A</b>) lncRNA–mRNA–circRNA network structure. (<b>B</b>) The betweenness centrality difference among lncRNAs, mRNAs, and circRNAs. (<b>C</b>) The closeness centrality difference among lncRNAs, mRNAs, and circRNAs. (<b>D</b>) The degree centrality difference among lncRNAs, mRNAs, and circRNAs. (<b>E</b>) Node degree of the lncRNAs, mRNAs, and circRNAs.</p>
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<p>Comparison and identification of differentially expressed RNAs in high-intake feeding in lion-head geese liver tissue by qRT-PCR. (<b>A</b>) The RNA-seq results revealed the upregulated genes by FPKM. (<b>B</b>) Verification of the upregulated genes by RT-qPCR. (<b>C</b>) The RNA-seq results revealed the downregulated genes by FPKM. (<b>D</b>) Verification of the downregulated genes by RT-qPCR. Log2 FC is expressed as mean ± SD. n = 3. The statistical significance of all genes reached <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; 0.01; * <span class="html-italic">p</span> &lt; 0.05).</p>
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12 pages, 2576 KiB  
Article
A Novel Application of Virus Like Particles in the Hemagglutination Inhibition Assay
by Mohamed H. El-Husseiny, Peter Pushko, Irina Tretyakova, Naglaa M. Hagag, Sara Abdel-Mawgod, Ahmed Shabaan, Neveen R. Bakry and Abdel Satar Arafa
Int. J. Mol. Sci. 2024, 25(16), 8746; https://doi.org/10.3390/ijms25168746 - 11 Aug 2024
Viewed by 920
Abstract
The hemagglutination inhibition (HI) assay is a traditional laboratory procedure for detection and quantitation of serum antibodies of hemagglutinating viruses containing the hemagglutinin (HA) gene. The current study aimed to investigate the novel use of virus like particles (VLP) as an antigen for [...] Read more.
The hemagglutination inhibition (HI) assay is a traditional laboratory procedure for detection and quantitation of serum antibodies of hemagglutinating viruses containing the hemagglutinin (HA) gene. The current study aimed to investigate the novel use of virus like particles (VLP) as an antigen for the HI assay. VLPs were prepared from a strain of H5N1 using a baculovirus expression system. The VLPs were characterized using the hemagglutination test, Sodium dodecyl-sulfate polyacrylamide gel electrophoresis (SDS-PAGE), Western blotting, and transmission electron microscopy. The comparative HI assay was performed using three different seed antigens: A/chicken/Mexico/232/94 (H5N2), A/chicken/Egypt/18-H/09(H5N1) and A/goose/Guangdong/1/1996(H5N1). The HI assay of serum antibody titrations using homologous antigens to these vaccinal seeds were compared to the VLP’s antigens for the same serum. The HI titers were logically relevant to the similarity between VLP antigens and vaccinal seeds, indicating the VLPs behave similarly to the standard HI assay which uses inactivated whole virus as an antigen. VLPs could be considered as an alternative to the HI assay antigen as they show a relatedness between the similarity with vaccinal seed and serum antibodies. Compared to typical entire H5N1 viral antigen prepared in SPF eggs that require proper inactivation to avoid any public health risk, VLPs prepared in tissue culture, plants or insect cells are a safe, inexpensive and scalable alternative to inactivated whole virus antigen. Full article
(This article belongs to the Section Molecular Microbiology)
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<p>Gel electrophoresis of the restriction enzyme digestion screening of the combined pFastBac1 vector containing the three genes (<span class="html-italic">HA, NA and M1</span>). Lane 1 indicates the 1 Kilo base (kB) ladder (500 bp, 800 bp, 1600 bp, 2000 bp, 3000 bp, 4000 bp, 5000 bp, etc.). The even No. lanes are combined pFastBac1 vectors that are undigested by restriction enzyme Tth111I and are considered the control, while the odd No. lanes are combined pFastBac1 vectors digested by restriction enzyme Tth111I. The figure shows that the colony in lane No. 3 (marked by the white arrow) is the only one that gave specific bands (5158 bp, 2211 bp, 1719 bp) with the negative control of the same colony without restriction enzyme digestion as shown in lane 2.</p>
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<p>The hemagglutination assay (HA assay) of the recombinant baculovirus yielded from passage 1 (P1) using 1% of RBCS. The figure shows the HA activity of the passage 1 harvest at 2<sup>6</sup> hemagglutination unit (HAU) titers, approximately. The two rows show HA titer for two different recombinant baculovirus candidates.</p>
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<p>Characterization of VLP-expressed proteins using SDS-PAGE and Western blot. Figure (<b>a</b>) shows the VLP proteins separated using 4–12% gradient SDS-PAGE. The protein ladder used is SeeBlue<sup>®</sup> Plus2 Pre-Stained Standard (Invitrogen). The gel shows the full-length HA protein (64 kDa) and M1 protein (30 kDa). NA protein did not appear as it was expressed less than the other influenza virus proteins. Figure (<b>b</b>) shows the Western blot of the specific band of the whole HA and M1.</p>
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<p>Characterization of VLPs using negative stain transmission electron microscopy. The micrograph shows the spherical VLPs with the spikes of HA and NA proteins protruding from its envelope and resembling the natural virus particles. The size bar indicates the size of the VLP particles. The normal size varies from 80 to 120 nm, the natural Avian Influenza virus size.</p>
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<p>Individual HI titers of the different serum antibody groups using homologous relevant vaccinal antigens (the antibodies derived from chickens vaccinated by the same antigen used in the HI assay) against the heterologous VLP antigen.</p>
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<p>Individual HI titer of serum antibodies from SPF chickens vaccinated by VLPs using the homologous relevant vaccinal antigen (VLP) against heterologous the A/chicken/Egypt/18-H/2009(H5N1) antigen.</p>
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<p>Alignment of the H5 HA1 amino acid sequences (excluding signal peptide) of the different vaccinal seeds used in this study, including the prepared VLPs’ seed. The HA1 includes the residues relevant to the epitopes in the predetermined major antigenic sites A–D. Single letter codes are shown for amino acids and colors indicate their major biochemical properties such as Red-acidic; Blue-basic.</p>
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12 pages, 4348 KiB  
Article
Low Testosterone and High Leptin Activate PPAR Signaling to Induce Adipogenesis and Promote Fat Deposition in Caponized Ganders
by Mingming Lei, Yaxin Li, Jiaying Li, Jie Liu, Zichun Dai, Rong Chen and Huanxi Zhu
Int. J. Mol. Sci. 2024, 25(16), 8686; https://doi.org/10.3390/ijms25168686 - 9 Aug 2024
Viewed by 573
Abstract
Low or insufficient testosterone levels caused by caponization promote fat deposition in animals. However, the molecular mechanism of fat deposition in caponized animals remains unclear. This study aimed to investigate the metabolomics and transcriptomic profiles of adipose tissues and study the effect of [...] Read more.
Low or insufficient testosterone levels caused by caponization promote fat deposition in animals. However, the molecular mechanism of fat deposition in caponized animals remains unclear. This study aimed to investigate the metabolomics and transcriptomic profiles of adipose tissues and study the effect of testosterone and leptin on the proliferation of adipocytes. We observed a significant enlargement in the areas of adipocytes in the abdominal fat tissues in capon, as well as increased luciferase activity of the serum leptin and a sharp decrease in the serum testosterone in caponized gander. Metabolomics and transcriptomic results revealed differentially expressed genes and differentially expressed metabolites with enhanced PARR signal pathway. The mRNA levels of peroxisome proliferators-activated receptor γ, fatty acid synthase, and suppressor of cytokine signaling 3 in goose primary pre-adipocytes were significantly upregulated with high leptin treatment and decreased significantly with increasing testosterone dose. Hence, reduced testosterone and increased leptin levels after caponization possibly promoted adipocytes proliferation and abdominal fat deposition by altering the expression of PPAR pathway related genes in caponized ganders. This study provides a new direction for the mechanism through which testosterone regulates the biological function of leptin and fat deposition in male animals. Full article
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<p>Changes of AF rate, area of adipocytes, testosterone, and LEP between caponized (Capon) and intact (Cont) geese at 45 days after caponization. (<b>A</b>) AF weight. (<b>B</b>) Percentage of AF. (<b>C</b>) Area of adipocytes on H&amp;E-stained sections. (<b>D</b>) Luciferase activity of goose serum LEP in HEK-293 cell line stably expressing the chicken LEPR. (<b>E</b>) Representative images of AF tissues and H&amp;E-stained sections of the tissues (×40). Data are means ± SD (n = 10); *, <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>
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<p>Effect of caponization on the global transcriptomic profiles of AF tissues. (<b>A</b>) Heatmap of samples from the control and caponized groups of geese. (<b>B</b>) Volcano plots showing significant DEGs in the AF of the control and caponized groups. Red and blue dots represent the upregulated and downregulated DEGs in caponization geese (n = 3), respectively. (<b>C</b>) The top 15 significantly enriched GO pathways for the DEGs. (<b>D</b>) The top 15 significantly enriched KEGG pathways for the DEGs. (<b>E</b>) Heatmap of the DEGs related to fat metabolism. (<b>F</b>) The expression of eight genes using RT-PCR. **, <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Effect of caponization on the global metabolomic profiles in AF tissues. POS, positive ion mode; NEG, negative ion mode. (<b>A</b>,<b>B</b>) OPLS-DA scores showing significant differences between the caponized and control groups. (<b>C</b>,<b>D</b>) Heatmap analysis of the DEMs between the two groups. (<b>E</b>) Significantly altered metabolic pathways. The size and color of each circle represent the pathway rich factor and <span class="html-italic">p</span>-value, respectively.</p>
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<p>Integrated enrichment analysis of DEMs and DEGs. (<b>A</b>) Heatmap of the DEMs and DEGs. Gene names are shown in italics, and metabolite names are shown in normal font. The color of the squares in the graph represents correlation, with darker colors indicating stronger correlation. *, <span class="html-italic">p</span> &lt; 0.05. (<b>B</b>) KEGG pathway enrichment of DEMs and DEGs and pathway detail. (<b>C</b>) Variations in metabolites that have an obvious relationship with the DEGs in AF tissue. Metabolome composition and fat metabolism gene expression in both groups of geese (derived from AF metabolome and RNA-Seq transcriptomic data, respectively) that were related to the 18 significant DEMs using Mantel test. Edge width corresponds to the Mantel’s r statistic for the corresponding distance correlations, and edge color indicates the statistical significance. The color gradient indicates the Pearson’s correlation coefficient. (<b>D</b>) DEGs related to trans-cinnamate and alpha-dimorphic acid. The metabolites are shown as yellow circles. Blue squares represent genes.</p>
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<p>The effect of LEP and testosterone on proliferation of goose primary pre-adipocytes. (<b>A</b>) adipocytes were treated with 100 ng/mL of LEP or 10, 50, 100, and 150 ng/·mL of testosterone for 24 h. (<b>B</b>) cell viability was assayed by CCK-8. Different letters above the bars denote significant differences (a,b: <span class="html-italic">p</span> &lt; 0.05; b,c: <span class="html-italic">p</span> &lt; 0.05; a–c: <span class="html-italic">p</span> &lt; 0.01).</p>
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<p>The mRNA expressions of the four genes of adipocytes treated with LEP and testosterone. <span class="html-italic">SOCS3</span> (<b>A</b>), <span class="html-italic">RXRG</span> (<b>B</b>), <span class="html-italic">FASN</span> (<b>C</b>), and <span class="html-italic">PPARγ</span> (<b>D</b>) mRNA levels were examined in pre-adipocytes with LEP (L; 100 ng/mL) with and without testosterone (T; 10, 100, and 150 ng/mL) treatment for 24 h. Different letters above the bars denote significant differences (a,b: <span class="html-italic">p</span> &lt; 0.05; b,c: <span class="html-italic">p</span> &lt; 0.05; a–c: <span class="html-italic">p</span> &lt; 0.01).</p>
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13 pages, 2139 KiB  
Article
Analysis of the Mitochondrial COI Gene and Genetic Diversity of Endangered Goose Breeds
by Hao Wu, Shangzong Qi, Suyu Fan, Haoyu Li, Yu Zhang, Yang Zhang, Qi Xu and Guohong Chen
Genes 2024, 15(8), 1037; https://doi.org/10.3390/genes15081037 - 6 Aug 2024
Viewed by 688
Abstract
The mitochondrial cytochrome c oxidase subunit I (COI) genes of six endangered goose breeds (Xupu, Yangjiang, Yan, Wuzong, Baizi, and Lingxian) were sequenced and compared to assess the genetic diversity of endangered goose breeds. By constructing phylogenetic trees and evolutionary maps [...] Read more.
The mitochondrial cytochrome c oxidase subunit I (COI) genes of six endangered goose breeds (Xupu, Yangjiang, Yan, Wuzong, Baizi, and Lingxian) were sequenced and compared to assess the genetic diversity of endangered goose breeds. By constructing phylogenetic trees and evolutionary maps of genetic relationships, the affinities and degrees of genetic variations among the six different breeds were revealed. A total of 92 polymorphic sites were detected in the 741 bp sequence of the mtDNA COI gene after shear correction, and the GC content of the processed sequence (51.11%) was higher than that of the AT content (48.89%). The polymorphic loci within the populations of five of the six breeds (Xupu, Yangjiang, Yan, Baizi, and Lingxian) were more than 10, the haplotype diversity > 0.5, and the nucleotide diversity (Pi) > 0.005, with the Baizi geese being the exception. A total of 35 haplotypes were detected based on nucleotide variation among sequences, and the goose breed haplotypes showed a central star-shaped dispersion; the FST values were −0.03781 to 0.02645, The greatest genetic differentiation (FST = 0.02645) was observed in Yan and Wuzong breeds. The most frequent genetic exchange (Nm > 15.00) was between the Wuzong and Yangjiang geese. An analysis of molecular variance showed that the population genetic variation mainly came from within the population; the base mismatch differential distribution analysis of the goose breeds and the Tajima’s D and Fu’s Fs neutral detection of the historical occurrence dynamics of their populations were negative (p > 0.10). The distribution curve of the base mismatches showed a multimodal peak, which indicated that the population tended to be stabilised. These results provide important genetic information for the conservation and management of endangered goose breeds and a scientific basis for the development of effective conservation strategies. Full article
(This article belongs to the Special Issue Mitochondrial DNA Replication and Transcription)
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<p>Goose breeds used in the study.</p>
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<p>Design of the primers.</p>
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<p>Example of standard pattern obtained for the analysis of the PCR products on 1% agarose gel electrophoresis.</p>
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<p>Median-joining network diagram constructed based on <span class="html-italic">COI</span> gene haplotypes. Each circle represents a unique haplotype, the colour represents endangered geese of different breeds, and the size of the circle is proportional to the number of isolates contained. The lines (shaded markers) on the branches indicate the location of the mutation, with one line for each mutation.</p>
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<p>Distribution of variable loci based on haplotype control of the mtDNA <span class="html-italic">COI</span> gene. Note: “*” indicates base-identical sequences; “-” indicates a base deletion.</p>
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<p>MEGA11 phylogeny (maximum-likelihood) map, constructed on the basis of mtDNA <span class="html-italic">COI</span> sequences from the six breeds of geese.</p>
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<p>Distribution of base difference mismatches in the mt <span class="html-italic">COI</span> gene sequence of endangered goose breeds.</p>
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24 pages, 11891 KiB  
Article
Research on a Method for Classifying Bolt Corrosion Based on an Acoustic Emission Sensor System
by Shuyi Di, Yin Wu and Yanyi Liu
Sensors 2024, 24(15), 5047; https://doi.org/10.3390/s24155047 - 4 Aug 2024
Viewed by 747
Abstract
High-strength bolts play a crucial role in ultra-high-pressure equipment such as bridges and railway tracks. Effective monitoring of bolt conditions is of paramount importance for common fault repair and accident prevention. This paper aims to detect and classify bolt corrosion levels accurately. We [...] Read more.
High-strength bolts play a crucial role in ultra-high-pressure equipment such as bridges and railway tracks. Effective monitoring of bolt conditions is of paramount importance for common fault repair and accident prevention. This paper aims to detect and classify bolt corrosion levels accurately. We design and implement a bolt corrosion classification system based on a Wireless Acoustic Emission Sensor Network (WASN). Initially, WASN nodes collect high-speed acoustic emission (AE) signals from bolts. Then, the ReliefF feature selection algorithm is applied to identify the optimal feature combination. Subsequently, the Extreme Learning Machine (ELM) model is utilized for bolt corrosion classification. Additionally, to achieve high prediction accuracy, an improved goose algorithm (GOOSE) is employed to ensure the most suitable parameter combination for the ELM model. Experimental measurements were conducted on five classes of bolt corrosion levels: 0%, 25%, 50%, 75%, and 100%. The classification accuracy obtained using the proposed method was at least 98.04%. Compared to state-of-the-art classification diagnostic models, our approach exhibits superior AE signal recognition performance and stronger generalization ability to adapt to variations in working conditions. Full article
(This article belongs to the Section Physical Sensors)
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<p>Illustration of the five types of bolt samples.</p>
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<p>The framework of wireless AE node configuration.</p>
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<p>Schematic diagram of the bolt and specimen connection method: (<b>a</b>) Connection method for bolt specimens with a corrosion grade of 100%; (<b>b</b>) Connection method for bolt specimens with a corrosion grade of 0%.</p>
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<p>Diagram of the external excitation process.</p>
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<p>Diagram of AE signal acquisition process: (<b>a</b>) The AE signal acquisition process for bolt samples with corrosion levels of 25%; (<b>b</b>) The AE signal acquisition process for bolt samples with corrosion levels of 50%.</p>
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<p>Schematic diagram of AE waveforms: (<b>a</b>) AE waveforms of bolts with corrosion levels of 25%; (<b>b</b>) AE waveforms of bolts with corrosion levels of 50%.</p>
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<p>Basic conceptual framework of the classification system.</p>
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<p>Scatter plot of amplitude data. (<b>a</b>) Scatter plot of amplitude near-end data; (<b>b</b>) Scatter plot of amplitude far-end data.</p>
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<p>Scatter plot of duration data: (<b>a</b>) Scatter plot of duration near-end data; (<b>b</b>) Scatter plot of duration far-end data.</p>
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<p>Illustrates the weights of the 12 features.</p>
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<p>Relationship between the number of features and accuracy.</p>
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<p>GOOSE-ELM algorithm flowchart.</p>
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<p>Confusion matrix of GOOSE-ELM algorithm classification results.</p>
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<p>Comparison between classification results and actual classification.</p>
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<p>GOOSE-ELM algorithm ROC curve.</p>
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<p>Heatmap of the 12 features.</p>
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<p>Comparison of the four evaluation indicators.</p>
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<p>F1 test functions and convergence curves.</p>
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<p>F5 test functions and convergence curves.</p>
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<p>F8 test functions and convergence curves.</p>
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<p>F21 Test functions and convergence curves.</p>
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20 pages, 3600 KiB  
Article
Machine-Learning-Based Anomaly Detection for GOOSE in Digital Substations
by Hong Nhung-Nguyen, Mansi Girdhar, Yong-Hwa Kim and Junho Hong
Energies 2024, 17(15), 3745; https://doi.org/10.3390/en17153745 - 29 Jul 2024
Cited by 1 | Viewed by 1282
Abstract
Digital substations have adopted a high amount of information and communication technology (ICT) and cyber–physical systems (CPSs) for monitoring and control. As a result, cyber attacks on substations have been increasing and have become a major concern. An intrusion-detection system (IDS) could be [...] Read more.
Digital substations have adopted a high amount of information and communication technology (ICT) and cyber–physical systems (CPSs) for monitoring and control. As a result, cyber attacks on substations have been increasing and have become a major concern. An intrusion-detection system (IDS) could be a solution to detect and identify the abnormal behaviors of hackers. In this paper, a Deep Neural Network (DNN)-based IDS is proposed to detect malicious generic object-oriented substation event (GOOSE) communication over the process and station bus network, followed by the multiclassification of the cyber attacks. For training, both the abnormal and the normal substation networks are monitored, captured, and logged, and then the proposed algorithm is applied for distinguishing normal events from abnormal ones within the network communication packets. The designed system is implemented and tested with a real-time IEC 61850 GOOSE message dataset using two different approaches. The experimental results show that the proposed system can successfully detect intrusions with an accuracy of 98%. In addition, a comparison is performed in which the proposed IDS outperforms the support vector machine (SVM)-based IDS. Full article
(This article belongs to the Section F: Electrical Engineering)
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<p>Cyber–physical system of a digital substation.</p>
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<p>Proposed hardware in the loop (HIL) testbed.</p>
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<p>STRIDE threat model of a digital substation.</p>
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<p>Examples of tampering, spoofing, and DoS attack scenarios.</p>
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<p>Confusion matrix of DNN with input shape of 1 packet.</p>
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<p>Visualized data using t-distributed stochastic neighbor embedding (t-SNE) (<b>a</b>) with input data and (<b>b</b>) with a feature vector of last hidden layer for the DNN model.</p>
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<p>Sliding window data for proposed method with 3 packets.</p>
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<p>The confusion matrix of proposed DNN and LSTM model.</p>
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13 pages, 2510 KiB  
Article
A 16S RNA Analysis of Yangzhou Geese with Varying Body Weights: Gut Microbial Difference and Its Correlation with Body Weight Parameters
by Xinlei Xu, Suyu Fan, Hao Wu, Haoyu Li, Xiaoyu Shan, Mingfeng Wang, Yang Zhang, Qi Xu and Guohong Chen
Animals 2024, 14(14), 2042; https://doi.org/10.3390/ani14142042 - 12 Jul 2024
Viewed by 776
Abstract
China is a major goose-raising country, and the geese industry plays a significant role in animal husbandry. Therefore, goose growth performance (body weight) is a critical topic. Goose gut microbiota influences weight gain by regulating its energy metabolism and digestion. Additionally, the impact [...] Read more.
China is a major goose-raising country, and the geese industry plays a significant role in animal husbandry. Therefore, goose growth performance (body weight) is a critical topic. Goose gut microbiota influences weight gain by regulating its energy metabolism and digestion. Additionally, the impact of cecal microbial community structure on goose growth and development, energy metabolism, and immunity has been examined. However, most studies have used different additives or feeds as variables. Improving the understanding of the dynamic changes in gut microbial communities in geese of different body weights during their growth and development and their correlation with the host’s body weight is necessary. In this study, the cecal microbiota of healthy Yangzhou geese with large (L) and small (S) body weights, all at the same age (70 days old) and under the same feeding conditions, were sequenced using 16S rRNA. The sequencing results were annotated using QIIME2 (classify-sklearn algorithm) software, and the linkET package was used to explore the correlation between intestinal microorganisms and the body weight of the Yangzhou goose (Spearman). At the phylum level, the Firmicutes/Bacteroidetes ratio in the large body weight group was approximately 20% higher than that in the small body weight group, with Bacteroidetes and Firmicutes exhibiting a highly significant negative correlation. At the genus level, Bacteroides constituted the most abundant microbial group in both groups, although the Prevotellaceae_Ga6A1_group exhibited a higher abundance in the large than the small weight group. Spearman correlation analysis and the linkET package were used to analyze the correlation between cecal microflora and production performance indicators that showed significant differences between the two groups and showed that birth weight was significantly positively correlated with Deferribacterota at the phylum level. At the genus level, leg and chest muscle weights exhibited significant positive correlations with Prevotellace-ae_Ga6A1_group, suggesting its critical role in promoting the growth and development of goose leg and chest muscles. A significant negative correlation was observed between [Ruminococ-cus]_torque and Prevotellaceae_Ga6A1_group. These findings offer a crucial theoretical foundation for the study of gastrointestinal microorganisms and provide insights into the development and formulation of poultry probiotics. Full article
(This article belongs to the Special Issue Genetics and Breeding Advances in Poultry Health and Production)
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<p>Body weight changes in groups L and S are depicted in the graph. The <span class="html-italic">x</span>-axis represents time changes (0 represents birth weight, 2, 4, 6, 8, and 10 represent weeks of age); the <span class="html-italic">y</span>-axis represents body weight changes (in grams). * indicates a difference between groups (<span class="html-italic">p</span> &lt; 0.05); * <span class="html-italic">p</span> &lt; 0.05 indicates differences; ** <span class="html-italic">p</span> &lt; 0.01 indicates significant differences; *** <span class="html-italic">p</span> &lt; 0.001 indicates extremely significant differences.</p>
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<p>Sample richness and diversity statistics. (<b>A</b>) Characteristics of sequence statistics for groups L and S. (<b>B</b>–<b>E</b>) Dilution curves. (<b>B</b>,<b>C</b>) Richness and diversity statistics for all samples, with different colors representing different samples. (<b>D</b>,<b>E</b>) Overall richness and diversity statistics for groups L and S. (<b>F</b>) Species accumulation box plot, with sample size on the <span class="html-italic">x</span>-axis and the number of characteristic sequences after sampling on the <span class="html-italic">y</span>-axis.</p>
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<p>Differences in cecal microbial diversity and composition between groups L and S. (<b>A</b>) Box plot illustrating inter-group differences in alpha diversity indices. (<b>B</b>) PCoA plot. Left: weighted UniFrac; right: unweighted UniFrac. (<b>C</b>) Relative abundance of taxa at the phylum level (top 10). (<b>D</b>) Relative abundance of taxa at the genus level (top 10). (<b>E</b>) Heatmap showing the major phyla of cecal microbiota. (<b>F</b>) Heatmap showing the major genera of the cecal microbiota. * <span class="html-italic">p</span> &lt; 0.05 indicates differences between groups L and S; ** <span class="html-italic">p</span> &lt; 0.01 indicates significant differences between groups L and S.</p>
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<p>Differences in cecal microbial diversity and composition between groups L and S. (<b>A</b>) Box plot illustrating inter-group differences in alpha diversity indices. (<b>B</b>) PCoA plot. Left: weighted UniFrac; right: unweighted UniFrac. (<b>C</b>) Relative abundance of taxa at the phylum level (top 10). (<b>D</b>) Relative abundance of taxa at the genus level (top 10). (<b>E</b>) Heatmap showing the major phyla of cecal microbiota. (<b>F</b>) Heatmap showing the major genera of the cecal microbiota. * <span class="html-italic">p</span> &lt; 0.05 indicates differences between groups L and S; ** <span class="html-italic">p</span> &lt; 0.01 indicates significant differences between groups L and S.</p>
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<p>Correlation analysis of gut microbiota and slaughter performance in Yangzhou geese. (<b>A</b>) Association analysis at the phylum level between cecal microbiota and breast muscle weight, leg muscle weight, birth weight, and weight at 70 d old in Yangzhou geese. (<b>B</b>) Association analysis at the genus level between cecal microbiota and breast muscle weight, leg muscle weight, birth weight, and weight at 70 d old in Yangzhou geese. * <span class="html-italic">p</span> &lt; 0.05 indicates differences; ** <span class="html-italic">p</span> &lt; 0.01 indicates significant differences; *** <span class="html-italic">p</span> &lt; 0.001 indicates extremely significant differences.</p>
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17 pages, 3525 KiB  
Article
Single-Sensor Global MPPT for PV System Interconnected with DC Link Using Recent Red-Tailed Hawk Algorithm
by Motab Turki Almousa, Mohamed R. Gomaa, Mostafa Ghasemi and Mohamed Louzazni
Energies 2024, 17(14), 3391; https://doi.org/10.3390/en17143391 - 10 Jul 2024
Cited by 1 | Viewed by 725
Abstract
The primary disadvantage of solar photovoltaic systems, particularly in partial shadowing conditions (PSC), is their low efficiency. A power–voltage curve with a homogenous distribution of solar irradiation often has a single maximum power point (MPP). Without a doubt, it can be extracted using [...] Read more.
The primary disadvantage of solar photovoltaic systems, particularly in partial shadowing conditions (PSC), is their low efficiency. A power–voltage curve with a homogenous distribution of solar irradiation often has a single maximum power point (MPP). Without a doubt, it can be extracted using any conventional tracker—for instance, perturb and observe. On the other hand, under PSC, the situation is entirely different since, depending on the number of distinct solar irradiation levels, the power–voltage curve has numerous MPPs (i.e., multiple local points and one global point). Conventional MPPTs can only extract the first point since they are unable to distinguish between local and global MPP. Thus, to track the global MPP, an optimized MPPT based on optimization algorithms is needed. The majority of global MPPT techniques seen in the literature call for sensors for voltage and current in addition to, occasionally, temperature and/or solar irradiance, which raises the cost of the system. Therefore, a single-sensor global MPPT based on the recent red-tailed hawk (RTH) algorithm for a PV system interconnected with a DC link operating under PSC is presented. Reducing the number of sensors leads to a decrease in the cost of a controller. To prove the superiority of the RTH, the results are compared with several metaheuristic algorithms. Three shading scenarios are considered, with the idea of changing the shading scenario to change the location of the global MPP to measure the consistency of the algorithms. The results verified the effectiveness of the suggested global MPPT based on the RTH in precisely capturing the global MPP compared with other methods. As an example, for the first shading situation, the mean PV power values varied between 6835.63 W and 5925.58 W. The RTH reaches the highest PV power of 6835.63 W flowing through particle swarm optimization (6808.64 W), whereas greylag goose optimizer achieved the smallest PV power production of 5925.58 W. Full article
(This article belongs to the Special Issue Recent Advances in Solar Cells and Photovoltaics)
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<p>Solar cell single-diode model.</p>
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<p>PV characteristics under shading: (<b>a</b>) current against voltage curve and (<b>b</b>) power against voltage curve.</p>
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<p>The three phases of the red-tailed hawk during hunting process: (<b>a</b>) high-soaring, (<b>b</b>) low-soaring, and (<b>c</b>) stopping and swooping.</p>
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<p>RTH-flowchart-based global MPPT.</p>
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<p>Schematic diagram for PV system with MPPT (* is the product).</p>
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<p>The details of shading scenarios: (<b>a</b>) power against voltage characteristics, and (<b>b</b>) current against voltage characteristics.</p>
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<p>Mean objective values: (<b>a</b>) first shadow scenario, (<b>b</b>) second shadow scenario, and (<b>c</b>) third shadow scenario.</p>
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<p>Mean objective values: (<b>a</b>) first shadow scenario, (<b>b</b>) second shadow scenario, and (<b>c</b>) third shadow scenario.</p>
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<p>Dynamic response of PV system using RTH: (<b>a</b>) PV power, (<b>b</b>) PV voltage, (<b>c</b>) PV current, and (<b>d</b>) duty cycle.</p>
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<p>ANOVA ranking: (<b>a</b>) first shadow scenario, (<b>b</b>) second shadow scenario, and (<b>c</b>) third shadow scenario.</p>
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<p>ANOVA ranking: (<b>a</b>) first shadow scenario, (<b>b</b>) second shadow scenario, and (<b>c</b>) third shadow scenario.</p>
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<p>Tukey test: (<b>a</b>) first shadow scenario, (<b>b</b>) second shadow scenario, and (<b>c</b>) third shadow scenario.</p>
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<p>Tukey test: (<b>a</b>) first shadow scenario, (<b>b</b>) second shadow scenario, and (<b>c</b>) third shadow scenario.</p>
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