Journal of Animal Science and Biotechnology最新文献

{"title":"Mechanisms of high-glucose-induced mitochondrial damage and glycolipid accumulation in largemouth bass","authors":"Zhihong Liao, Xuanshu He, Xingyu Gu, Tao Ye, Anqi Chen, Yucai Guo, Wei Zhao, Jin Niu","doi":"10.1186/s40104-025-01261-2","DOIUrl":"https://doi.org/10.1186/s40104-025-01261-2","url":null,"abstract":"The carnivorous fish, largemouth bass (Micropterus salmoides), has difficulty metabolizing dietary carbohydrates, frequently resulting in issues with energy metabolism and fatty liver disease. Nevertheless, the molecular mechanisms involved are still not fully understood. The results of high-carbohydrate (HC) diets and high-glucose (HG) treatments in largemouth bass hepatocytes showed that high-glucose causes liver damage and glycolipid accumulation. High-glucose promoted the lipogenesis process by activating AMPK/ACC/SREBP-1 pathway and reduced bile acid synthesis by downregulating cholesterol 7-hydroxylase (cyp7a1) and sterol 12-hydroxylase (cyp8b1). Concurrently, HG treatments also caused mitochondrial fission and damage by increasing the expression of dynamin-related protein 1 (Drp1), leading to impaired mitochondria accumulation and mitochondria-dependent apoptosis via the p38 MAPK/Bcl-2/Casp3 pathway. Additionally, HG treatments decreased Sirt1 expression and relocated it from the nucleus to the cytoplasm, where it interacts with autophagosomes and lysosomes, inhibiting Pink1/Parkin-mediated mitophagy. This also led to the cytoplasmic translocation of Pink1 and its co-localization with Sirt1, indicating that Sirt1 regulates high glucose-induced metabolic stress by inhibiting the Pink1/Parkin mitophagy pathway. In summary, HG treatment induces mitochondrial damage and glycolipid accumulation in largemouth bass through mechanisms involving AMPK/SREBP1/ACC1-mediated lipogenesis, bile acid metabolism, Sirt-mediated mitophagy, and p38 MAPK/Bcl-2/Casp3-activated apoptosis. ","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"25 1","pages":"132"},"PeriodicalIF":7.0,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145289270","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Effects of dietary L-glutamate and L-aspartate supplementation on growth performance, severity of diarrhea, intestinal barrier integrity, and fecal microbiota of weaned piglets challenged with F18 enterotoxigenic Escherichia coli","authors":"Supatirada Wongchanla, Kunal Dixit, Sangwoo Park, Kwangwook Kim, Shuhan Sun, Maria Marco, Steven B. Palomares, Alejandra Mejia-Caballero, Sahana Mohan, Xunde Li, Xiaojing Li, Yanhong Liu","doi":"10.1186/s40104-025-01266-x","DOIUrl":"https://doi.org/10.1186/s40104-025-01266-x","url":null,"abstract":"L-Glutamate and L-aspartate are functional amino acids that play pivotal roles in the cellular metabolic pathways of swine enterocytes. Therefore, this study aimed to investigate the effects of dietary L-glutamate and L-aspartate on growth performance, diarrhea severity, intestinal barrier integrity, and fecal microbiota of weaned piglets challenged with F18 enterotoxigenic Escherichia coli (ETEC). Weaned piglets were randomly assigned to seven dietary treatments, including unchallenged and ETEC-challenged controls, amino acid-supplemented groups, and an antibiotic control, to assess their responses to ETEC challenge. Supplementation with 1% L-glutamate or 2% L-aspartate enhanced growth performance, with significantly greater (P < 0.05) average daily weight gain and gain-to-feed ratio compared with the positive control group from d 0 to d 5 post-inoculation. Pigs fed with 1% or 2% L-aspartate had reduced (P < 0.05) diarrhea severity in ETEC-challenged pigs compared with the positive control group. The 1% L-aspartate supplementation also supported intestinal structure by increasing (P < 0.05) duodenal villi height and ileal villi width compared with carbadox supplementation. Additionally, 1% L-glutamate supplementation significantly improved (P < 0.05) resilience in ETEC-challenged pigs by reducing fecal shedding of β-hemolysin-producing bacteria compared with the positive control group on d 14 post-inoculation. Moreover, 1% L-aspartate supplementation promoted intestinal barrier integrity by significantly up-regulated (P < 0.05) the expression of ileal OCDN and ileal ZO-1 compared with the positive control group on d 14 post-inoculation. Interestingly, 2% L-aspartate supplementation altered the intestinal mucosa by down-regulating (P < 0.05) the expression of jejunal CLDN-1, while up-regulating (P < 0.05) the expression of ileal CLDN-1 compared with the negative control group on d 14 post-inoculation. Furthermore, L-glutamate supplementation significantly changed proportions of Firmicutes and Bacteroidota and showed the trend for enrichment in beneficial bacterial genera such as Bifidobacterium and Megasphaera in ETEC-infected pigs by d 14 post-inoculation. Supplementation with L-glutamate or L-aspartate promoted growth performance, supported gut health, and enhanced disease resistance in weaned pigs challenged with F18 ETEC. During the weaning period, L-glutamate or L-aspartate could potentially be considered conditionally essential amino acids, helping to alleviate weaning complications and reduce the need for antibiotic use in swine farming.","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"1 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145188846","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Proinflammatory polarization of adipose tissue macrophages in cows with subclinical ketosis constitutes a critical driver of adipose tissue remodeling and inflammation","authors":"Bichen Zhao, Ming Li, Huijing Zhang, Renxu Chang, Jingyi Wang, Wanli Zhao, Yue Yang, Muhammad Usman, Juan J. Loor, Chuang Xu","doi":"10.1186/s40104-025-01252-3","DOIUrl":"https://doi.org/10.1186/s40104-025-01252-3","url":null,"abstract":"Sustained lipolysis exacerbates subclinical ketosis (SCK) in dairy cows and is associated with inflammation and adipose tissue macrophage (ATM) infiltration. While ATM involvement in adipose homeostasis and inflammation in early lactation is recognized, a comprehensive exploration of ATM polarization phenotypes in SCK cows is lacking. This study aimed to characterize ATM polarization and its link to lipolysis and inflammation in SCK cows. Subcutaneous adipose tissue samples were obtained from dairy cows to analyze protein expression and gene profiles. Compared with healthy cows, SCK cows had higher serum BHBA and NEFA, smaller adipocytes, and increased expression of lipolytic enzymes (LIPE, ATGL), indicating enhanced lipolysis. Decreased levels of FASN, PPARγ, p-SMAD3, and TGFβ suggested impaired adipogenesis. Inflammatory markers (TNF-α, IFN-γ, TLR4, Caspase1) and NFκB signaling activity were elevated. ATM infiltration was supported by increased CD9, CD68, TREM2, and CXCL1 expression. Protein abundance of M1 polarization markers (iNOS, CD86 and CCL2) in ATMs were associated with greater levels of NOS2, IL1B, CD86 and CCL2 mRNA expression in SCK cows; fluorescence intensity of NOS2 and CD86 also was elevated, alongside a higher proportion of CD68+/CD86+ immunopositive cells within adipose tissue. ELISA further quantified increased concentrations of IL-1β and CCL2. Conversely, the abundance of ATM M2 polarization markers, including CD206, IL-10, KLF4, and Arg1, at both the protein and mRNA levels demonstrated a decline. Meanwhile, the proportion of CD68+/CD206+ immune response cells was relatively low in SCK cows. Overall, the present study indicated an augmented macrophage presence within adipose tissue during subclinical ketosis, with a predominance of pro-inflammatory macrophages (M1 ATM). This observation suggested a vicious cycle wherein macrophage infiltration and pro-inflammatory polarization coincide with enhanced lipolysis and an amplified inflammatory cascade.","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"53 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145182874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Integrated mRNA-seq and miRNA-seq analysis reveals miR-210a-5p regulates uterine aging in laying hens by targeting the RASL11B/Raf/MAPK pathway","authors":"Xiyu Zhao, Xinyan Li, Wenxin Zhang, Mingyue Gao, Conghao Zhong, Boxuan Zhang, Congjiao Sun, Yao Zhang, Shunshun Han, Huadong Yin","doi":"10.1186/s40104-025-01257-y","DOIUrl":"https://doi.org/10.1186/s40104-025-01257-y","url":null,"abstract":"Uterine aging is a key factor contributing to the deterioration of egg quality and reproductive performance in laying hens. Despite its importance, the molecular mechanisms underlying uterine aging remain poorly defined. This study aimed to characterize gene expression and regulatory changes associated with uterine aging in hens at different life stages. Transcriptomic Analysis of uterine tissue from hens aged 350, 500, And 700 d revealed dynamic changes in gene expression patterns during aging. A significant upregulation of genes involved in cellular senescence was observed, including increased expression of the p53 signaling pathway And markers associated with inflammation And cell cycle arrest. The most notable changes occurred between 350 And 500 d of age, suggesting this as a critical window for the onset of uterine aging. MicroRNA sequencing identified miR-210a-5p as significantly reduced with age. Target prediction and experimental validation showed that miR-210a-5p directly suppresses the expression of RASL11B, a Ras-like small GTPase that activates the MAPK signaling pathway. In primary uterine epithelial cells, reduced miR-210a-5p levels led to elevated RASL11B expression, increased activation of B-Raf, MEK, and ERK proteins, and enhanced expression of aging-related genes and inflammatory factors. In contrast, overexpression of miR-210a-5p or inhibition of the MAPK pathway delayed senescence and reduced inflammatory signaling. RASL11B overexpression was sufficient to induce aging phenotypes, confirming its central role in promoting uterine cellular aging. This study identifies a novel regulatory pathway in which miR-210a-5p modulates uterine aging through the RASL11B-MAPK signaling cascade. The findings provide mechanistic insight into age-related reproductive decline in hens and suggest that targeting this pathway may offer new strategies for maintaining uterine function and extending reproductive lifespan in poultry.","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"8 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145116178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Depot-dependent effects of subclinical ketosis on visceral and subcutaneous adipose tissue transcriptional cellular diversity in dairy cows","authors":"Hunter Ford, Clarissa Strieder-Barboza","doi":"10.1186/s40104-025-01265-y","DOIUrl":"https://doi.org/10.1186/s40104-025-01265-y","url":null,"abstract":"Adipose tissue plays a central role in regulating whole-body metabolic health, facilitated by the variety of cell types and their wide-ranging functions. In addition, depot-specific differences in adipose tissue have been shown to play important roles in different disease states including obesity, diabetes, and metabolic dysfunction in human and animal models. For early postpartum dairy cattle, metabolic dysfunction, triggered by a negative energy balance, is often manifested as subclinical ketosis (SCK). However, the role that subcutaneous (SAT) and visceral (VAT) adipose tissue depots, and their diverse cellular compositions, play in the response to subclinical ketosis conditions is unclear. Flank SAT and omental VAT were collected via laparotomy from five non-ketotic (NK; BHB ≤ 0.8 mmol/L) and five subclinical ketosis (SCK; 1.4 mmol/L < BHB ≤ 2.6 mmol/L) multiparous cows during early lactation. Following collection, nuclei were isolated from the tissue and subjected to single-nuclei RNA sequencing in order to investigate the transcriptional cellular heterogeneity. Distinct clusters of adipocytes (AD), adipose stem/progenitor cells (ASPC), immune cells (IMC), endothelial cells (EC), and pericyte/smooth muscle cells (PE/SMC) were identified in both adipose depots, with a greater abundance of ASPC in SAT compared to VAT. In addition, we identified a VAT-specific AD subtype characterized by higher expression of progenitor-like marker genes. While the abundance of none of the identified cell subtypes were different between SCK and NK, underlying transcriptional changes provided insight into potential effects of SCK. In general, SCK was associated with pro-lipogenic, anti-inflammatory, and pro-angiogenic transcriptional changes, possibly indicating a greater capacity for homeostatic responsiveness in SAT under conditions of enhanced negative energy balance. In contrast, SCK appeared to promote transcriptional changes indicative of impaired adipogenesis, impaired angiogenesis, and increased inflammation in VAT. Uniquely, our study presents novel insight into the cellular heterogeneity of adipose tissue in dairy cattle with subclinical ketosis. Furthering our understanding of the role of adipose tissue in response to this form of metabolic challenge has the potential to enhance efforts aimed at limiting the incidence and impact of subclinical ketosis and improving the health and productivity of dairy cattle.","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"18 1","pages":"128"},"PeriodicalIF":7.0,"publicationDate":"2025-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145093583","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"HIF1A regulates follicular atresia through O-GlcNAcylation-mediated VEZF1/ET-1/FOXO1/BAX signaling in porcine granulosa cells","authors":"Aiwen Jiang, Jialong Li, Luyao Wang, Yi Liu, Zhengchang Wu, Haifei Wang, Shenglong Wu, Wenbin Bao","doi":"10.1186/s40104-025-01263-0","DOIUrl":"https://doi.org/10.1186/s40104-025-01263-0","url":null,"abstract":"Hypoxic stimuli induce follicular atresia by regulating granulosa cell (GC) apoptosis. Notably, mature follicles can still develop and ovulate under hypoxic conditions, highlighting the importance of the hypoxic adaptation in ovarian follicular selection. To date, the role and mechanism of hypoxia‐inducible factor 1 subunit alpha (HIF1A)-mediated hypoxic responses in follicular atresia are unclear. This study aimed to investigate whether and how HIF1A regulates follicular atresia via the modulation of O-linked N-acetylglucosamine (O-GlcNAc) protein modification (O-GlcNAcylation). Our findings revealed that HIF1A was highly expressed in pig ovaries. Compared with that in healthy follicles, its expression was significantly downregulated in atretic follicles. Under hypoxic conditions, pharmacological inhibition or siRNA-mediated knockdown of HIF1A increased porcine GC apoptosis. Mechanistically, HIF1A knockdown Suppressed O-GlcNAc transferase degradation, leading to increased global O-GlcNAcylation. Using 4D label-free quantitative proteomics, we identified 53 O-GlcNAcylated proteins. Importantly, O-GlcNAcylation stabilized vascular endothelial zinc finger 1 (VEZF1), and HIF1A knockdown upregulated VEZF1 protein levels by promoting O-GlcNAcylation. The HIF1A-VEZF1 axis modulates forkhead box O1 (FOXO1) expression by regulating endothelin-1. As a transcription factor, FOXO1 directly binds to the Bcl-2 associated X (BAX) promoter, activating its transcription and ultimately inducing porcine GC apoptosis and follicular atresia. Overall, our study elucidates a novel molecular mechanism by which HIF1A deficiency modulates follicular atresia through O-GlcNAcylation-mediated VEZF1 expression. These results not only clarify the molecular mechanism of ovarian follicular development under hypoxic conditions but also offer potential targets for improving follicular selection efficiency in pig breeding.","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"73 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145089523","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Silymarin as a feed additive in swine and poultry production: a comprehensive review","authors":"Sungbo Cho, Charles Martin Nyachoti, In Ho Kim","doi":"10.1186/s40104-025-01260-3","DOIUrl":"https://doi.org/10.1186/s40104-025-01260-3","url":null,"abstract":"The widespread ban on in‐feed antibiotics in many regions has driven the search for natural alternatives to maintain health and production efficiency in swine and poultry. Phytogenic feed additives (PFAs) derived from herbs and plant extracts have emerged as promising candidates owing to their antioxidant, anti‐inflammatory, and antimicrobial properties. Among these, silymarin—a flavonolignan complex extracted from milk thistle (Silybum marianum)—has attracted particular attention due to its hepatoprotective and growth‐promoting activities. This review summarizes the chemical characteristics and mechanisms of action of silymarin/silybin. Also, evidence from both experimental and field studies shows that silymarin improves growth performance, nutrient digestibility, gut health, and reproductive outcomes. Advances in formulation technologies, such as micellization, have been addressed for improved bioavailability of silymarin. Despite these promising results, further long-term field studies and economic evaluations are needed to fully integrate silymarin into commercial animal production systems. ","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"31 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145083662","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Correction: Effects of microbe-derived antioxidants on growth performance, hepatic oxidative stress, mitochondrial function and cell apoptosis in weaning piglets","authors":"Chengbing Yu, Yuxiao Luo, Cheng Shen, Zhen Luo, Hongcai Zhang, Jing Zhang, Weina Xu, Jianxiong Xu","doi":"10.1186/s40104-025-01277-8","DOIUrl":"https://doi.org/10.1186/s40104-025-01277-8","url":null,"abstract":"&lt;p&gt;&lt;b&gt;Correction: J Animal Sci Biotechnol 15, 128 (2024)&lt;/b&gt;&lt;/p&gt;&lt;p&gt;&lt;b&gt;https://doi.org/10.1186/s40104-024-01088-3&lt;/b&gt;&lt;/p&gt;&lt;br/&gt;&lt;p&gt;Following the publication of the original article [1], it is reported that in Fig. 4, the β-actin band in Fig. 4C was mistakenly used as the FIS1 protein band in Fig. 4B. It was merely an error in the use of the band image, and the corresponding statistical values remain correct. Importantly, this error does not affect the results and conclusion of the study.&lt;/p&gt;&lt;p&gt;Incorrect Fig. 4:&lt;/p&gt;&lt;figure&gt;&lt;figcaption&gt;&lt;b data-test=\"figure-caption-text\"&gt;Fig. 4&lt;/b&gt;&lt;/figcaption&gt;&lt;picture&gt;&lt;source srcset=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs40104-025-01277-8/MediaObjects/40104_2025_1277_Fig1_HTML.png?as=webp\" type=\"image/webp\"/&gt;&lt;img alt=\"figure 1\" aria-describedby=\"Fig1\" height=\"588\" loading=\"lazy\" src=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs40104-025-01277-8/MediaObjects/40104_2025_1277_Fig1_HTML.png\" width=\"685\"/&gt;&lt;/picture&gt;&lt;p&gt;The effects of weaning on mitochondrial function. &lt;b&gt;A&lt;/b&gt; Activity of mitochondrial respiratory chain complexes; &lt;b&gt;B&lt;/b&gt; The expression of proteins related to mitochondrial fusion and fission; &lt;b&gt;C&lt;/b&gt; The expression of proteins related to mitophagy. W0, W1, W4, W7, and W14 respectively represented 21, 22, 25, 28, and 35 days of age. Data were presented as mean ± SEM (&lt;i&gt;n&lt;/i&gt; = 6). Values with different letters differ significantly (&lt;i&gt;P&lt;/i&gt; &lt; 0.05). MRC I: Mitochondrial respiratory chain complex I; MRC III: Mitochondrial respiratory chain complex III; MRC IV: Mitochondrial respiratory chain complex IV; DRP1: Dynamin-related protein 1; MFN2: Mitofusin 2; FIS1: Fission protein 1; OPA1: Optic atrophy protein 1; Pink1: PTEN induced putative kinase 1; Parkin: E3 ubiquitin ligase; P62: Sequestosome 1; LC3B: Microtubule associated protein 1 light chain 3 beta&lt;/p&gt;&lt;span&gt;Full size image&lt;/span&gt;&lt;svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"&gt;&lt;use xlink:href=\"#icon-eds-i-chevron-right-small\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"&gt;&lt;/use&gt;&lt;/svg&gt;&lt;/figure&gt;&lt;p&gt;Correct Fig. 4:&lt;/p&gt;&lt;figure&gt;&lt;figcaption&gt;&lt;b data-test=\"figure-caption-text\"&gt;Fig. 4&lt;/b&gt;&lt;/figcaption&gt;&lt;picture&gt;&lt;source srcset=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs40104-025-01277-8/MediaObjects/40104_2025_1277_Fig2_HTML.png?as=webp\" type=\"image/webp\"/&gt;&lt;img alt=\"figure 2\" aria-describedby=\"Fig2\" height=\"592\" loading=\"lazy\" src=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs40104-025-01277-8/MediaObjects/40104_2025_1277_Fig2_HTML.png\" width=\"685\"/&gt;&lt;/picture&gt;&lt;p&gt;The effects of weaning on mitochondrial function. &lt;b&gt;A&lt;/b&gt; Activity of mitochondrial respiratory chain complexes; &lt;b&gt;B&lt;/b&gt; The expression of proteins related to mitochondrial fusion and fission; &lt;b&gt;C&lt;/b&gt; The expression of proteins related to mitophagy. W0, W1, W4, W7, and W14 respectively represented 21, 22, 25, 28, and 35 days of age. Data were presented as mean ","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"75 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145077423","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Small nucleolar RNA dysregulation and potential roles in bovine subclinical mastitis","authors":"Faith A. Omonijo, Mengqi Wang, David Gagné, Mario Laterrière, Samuel Genier, Xin Zhao, Eveline M. Ibeagha-Awemu","doi":"10.1186/s40104-025-01230-9","DOIUrl":"https://doi.org/10.1186/s40104-025-01230-9","url":null,"abstract":"Subclinical mastitis, caused by many pathogens including Staphylococcus aureus (S. aureus) and Staphylococcus chromogenes (S. chromogenes), presents a major challenge to the dairy industry due to its associated economic losses and poor milk quality. The molecular regulatory mechanisms, including the role of small nucleolar RNAs (snoRNAs), of the host response to mastitis pathogens remain unclear. Therefore, this study investigated snoRNA expression and potential roles during subclinical mastitis. Milk somatic cells from cows with naturally occurring S. aureus (n = 14) and S. chromogenes (n = 3) subclinical mastitis, and healthy cows (n = 4) were subjected to transcriptome sequencing and bioinformatics analyses. We identified 255 expressed snoRNAs including 21 differentially expressed (DE) in S. aureus-positive cows and 20 DE in S. chromogenes-positive cows. Prediction of ribosomal RNA (rRNA) modification sites found several 18S rRNA and 28S rRNA modification (pseudouridylation and 2′-O-methylation) target sites essential for ribosome function for DE snoRNAs, such as SNORA79 (18S-1319, 28S-3001), SNORA1 (18S-1496, 28S-1747), suggesting their roles in translation and immune modulation during subclinical mastitis. Correlation analysis identified DE snoRNAs-mRNAs (from the same samples) pairs with majority of the correlated mRNAs (e.g., CXCL8, IL6R, IL2, IL1R, IL18R1, STAT3, NFKB2, MYD88, VEGFA, and CD40) having immune related functions. Functional enrichment of correlated genes of snoRNAs for S. aureus-positive group (regulation of defense/immune response, leukocyte differentiation, response to cytokine, NF-κB signaling pathway, JAK-STAT signaling pathway etc.) and S. chromogenes-positive group (e.g., regulation of defense response, response to cytokine, regulation of immune response, NF-κB signaling pathway, TNF signaling pathway, and JAK-STAT signaling pathway) revealed involvement in immune and inflammatory processes. Some functional terms were common to both pathogens (e.g., NF-κB, JAK-STAT signaling, immune system processes) and suggest common regulatory mechanisms used by both pathogens to contain infection. Furthermore, snoRNA-mRNA network construction identified 7 key (hub) snoRNAs each for S. aureus-positive group (SNORA66, novelsnoRNA_26_14905 (also denoted as novelSnoRNA_86), SNORD107, SNORA1, SNORA63, SNORA79, SNORA76) and S. chromogenes-positive group (SNORD18, SNORA79, SNORA46, U2-19, SNORA66, SNORD37, SNORD49) that correlated with the most protein coding genes (|r| &gt; 0.9; ≥ 30 mRNAs). Functional enrichment of correlated genes of hub snoRNAs reveals their involvement in immune related functions (75% of enriched terms) and metabolic processes (20% of enriched terms). These data suggest potential regulatory roles for the DE snoRNAs and in particular, the 14 hub snoRNAs during subclinical mastitis. This study presents the first evidence linking snoRNAs to bovine subclinical mastitis and offers new insights into the molecular mechanisms un","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"66 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145035261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Untargeted metabolomics reveals changes in boar sperm and seminal plasma metabolites associated with sexual maturity","authors":"Asmita Shrestha, Ann Helen Gaustad, Janne Beate Øiaas, Anna Nordborg, Elisabeth Kommisrud, Maren van Son, Terkel Hansen, Anne Hege Alm-Kristiansen","doi":"10.1186/s40104-025-01258-x","DOIUrl":"https://doi.org/10.1186/s40104-025-01258-x","url":null,"abstract":"Boars undergo physiological and biochemical changes in semen composition as they grow from puberty to sexual maturity. However, comprehensive metabolomic profiles of boar semen remain uncharacterised. Understanding metabolic alterations in semen during this period is important for optimising reproductive performance in breeding programs. The aim of this study was to characterise the semen metabolome as boars mature, utilising an untargeted metabolomic approach. Semen samples were collected from 15 Duroc boars at three developmental ages: ~ 7 months, 8.5 months, and 10 months. Sperm and seminal plasma were separated and analysed by hydrophilic interaction and reversed-phase liquid chromatography coupled with mass spectrometry to capture a wide range of metabolites. We identified a total of 4,491 features in boar semen, annotating 92 distinct metabolites. Amino acids, peptides and analogues constituted the most abundant components, followed by fatty acid esters. Principal component analysis (PCA) and partial least squares discriminant analysis (PLS-DA) showed a clear separation between metabolomic profiles by age groups. PERMANOVA analysis of PCA scores confirmed statistically significant differences (P < 0.05) between younger (7 months) and more mature boars (8.5 months and 10 months). Pathway analysis identified porphyrin metabolism, taurine and hypotaurine metabolism, and glycerolipid metabolism as significantly enriched pathways in sperm, while glutathione and nitrogen metabolism were prominently enriched in seminal plasma. Using linear modelling, partial Spearman correlation and random forest analyses, we identified homoisovanillic acid as a key metabolite discriminating age groups in both sperm and seminal plasma. Additionally, L-glutamic acid, decanoyl-L-carnitine and N-(1,3-Thiazol-2-yl)benzenesulfonamide emerged as important sperm metabolites, while glyceric acid, myo-inositol, glycerophosphocholine, and several other compounds were identified as critical seminal plasma metabolites. This study provides a detailed characterisation of metabolic changes in Duroc boar semen during the transition from puberty to sexual maturity. Our findings enhance the understanding of reproductive development and could inform strategies to assess sexual maturity in breeding programs.","PeriodicalId":14928,"journal":{"name":"Journal of Animal Science and Biotechnology","volume":"38 1","pages":""},"PeriodicalIF":7.0,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144930710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}