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Role of respiratory system microbiota in development of lung cancer and clinical application 呼吸系统微生物群在肺癌发病中的作用及临床应用
IF 23.7
iMeta Pub Date : 2024-08-25 DOI: 10.1002/imt2.232
Bowen Li, Daoyun Wang, Chengye Zhang, Yadong Wang, Zhicheng Huang, Libing Yang, Huaxia Yang, Naixin Liang, Shanqing Li, Zhihua Liu
{"title":"Role of respiratory system microbiota in development of lung cancer and clinical application","authors":"Bowen Li,&nbsp;Daoyun Wang,&nbsp;Chengye Zhang,&nbsp;Yadong Wang,&nbsp;Zhicheng Huang,&nbsp;Libing Yang,&nbsp;Huaxia Yang,&nbsp;Naixin Liang,&nbsp;Shanqing Li,&nbsp;Zhihua Liu","doi":"10.1002/imt2.232","DOIUrl":"https://doi.org/10.1002/imt2.232","url":null,"abstract":"<p>Microbes play a significant role in human tumor development and profoundly impact treatment efficacy, particularly in immunotherapy. The respiratory tract extensively interacts with the external environment and possesses a mucosal immune system. This prompts consideration of the relationship between respiratory microbiota and lung cancer. Advancements in culture-independent techniques have revealed unique communities within the lower respiratory tract. Here, we provide an overview of the respiratory microbiota composition, dysbiosis characteristics in lung cancer patients, and microbiota profiles within lung cancer. We delve into how the lung microbiota contributes to lung cancer onset and progression through direct functions, sustained immune activation, and immunosuppressive mechanisms. Furthermore, we emphasize the clinical utility of respiratory microbiota in prognosis and treatment optimization for lung cancer.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 5","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.232","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142451248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dietary therapies interlinking with gut microbes toward human health: Past, present, and future 饮食疗法与肠道微生物相互关联,促进人类健康:过去、现在和未来
IF 23.7
iMeta Pub Date : 2024-08-10 DOI: 10.1002/imt2.230
Jiali Chen, Jiaqiang Luo, Sjaak Pouwels, Beijinni Li, Bian Wu, Tamer N. Abdelbaki, Jayashree Arcot, Wah Yang
{"title":"Dietary therapies interlinking with gut microbes toward human health: Past, present, and future","authors":"Jiali Chen,&nbsp;Jiaqiang Luo,&nbsp;Sjaak Pouwels,&nbsp;Beijinni Li,&nbsp;Bian Wu,&nbsp;Tamer N. Abdelbaki,&nbsp;Jayashree Arcot,&nbsp;Wah Yang","doi":"10.1002/imt2.230","DOIUrl":"https://doi.org/10.1002/imt2.230","url":null,"abstract":"<p>Overview of personalized dietary therapies. This flow chart exhibits the future prospect for integrating human microbiome and bio-medical research to revolutionize the precise personalized dietary therapies. With the development of artificial intelligence (AI), incorporating database may achieve personalized dietary therapies with high precision.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 5","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.230","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142451182","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
tigeR: Tumor immunotherapy gene expression data analysis R package tigeR:肿瘤免疫疗法基因表达数据分析 R 软件包
IF 23.7
iMeta Pub Date : 2024-08-06 DOI: 10.1002/imt2.229
Yihao Chen, Li-Na He, Yuanzhe Zhang, Jingru Gong, Shuangbin Xu, Yuelong Shu, Di Zhang, Guangchuang Yu, Zhixiang Zuo
{"title":"tigeR: Tumor immunotherapy gene expression data analysis R package","authors":"Yihao Chen,&nbsp;Li-Na He,&nbsp;Yuanzhe Zhang,&nbsp;Jingru Gong,&nbsp;Shuangbin Xu,&nbsp;Yuelong Shu,&nbsp;Di Zhang,&nbsp;Guangchuang Yu,&nbsp;Zhixiang Zuo","doi":"10.1002/imt2.229","DOIUrl":"https://doi.org/10.1002/imt2.229","url":null,"abstract":"<p>Immunotherapy shows great promise for treating advanced cancers, but its effectiveness varies widely among different patients and cancer types. Identifying biomarkers and developing robust predictive models to discern which patients are most likely to benefit from immunotherapy is of great importance. In this context, we have developed the tumor immunotherapy gene expression R package (tigeR 1.0) to address the increasing need for effective tools to explore biomarkers and construct predictive models. tigeR encompasses four distinct yet closely interconnected modules. The Biomarker Evaluation module enables researchers to evaluate whether the biomarkers of interest are associated with immunotherapy response via built-in or custom immunotherapy gene expression data. The Tumor Microenvironment Deconvolution module integrates 10 open-source algorithms to obtain the proportions of different cell types within the tumor microenvironment, facilitating the investigation of the association between immune cell populations and immunotherapy response. The Prediction Model Construction module equips users with the ability to construct sophisticated prediction models using a range of built-in machine-learning algorithms. The Response Prediction module predicts the immunotherapy response for the patients from gene expression data using our pretrained machine learning models or public gene expression signatures. By providing these diverse functionalities, tigeR aims to simplify the process of analyzing immunotherapy gene expression data, thus making it accessible to researchers without advanced programming skills. The source code and example for the tigeR project can be accessed at http://github.com/YuLab-SMU/tigeR.</p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 5","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.229","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142451210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
OmicShare tools: A zero-code interactive online platform for biological data analysis and visualization OmicShare 工具:用于生物数据分析和可视化的零代码交互式在线平台
IF 23.7
iMeta Pub Date : 2024-08-01 DOI: 10.1002/imt2.228
Hongyan Mu, Jianzhou Chen, Wenjie Huang, Gui Huang, Meiying Deng, Shimiao Hong, Peng Ai, Chuan Gao, Huangkai Zhou
{"title":"OmicShare tools: A zero-code interactive online platform for biological data analysis and visualization","authors":"Hongyan Mu,&nbsp;Jianzhou Chen,&nbsp;Wenjie Huang,&nbsp;Gui Huang,&nbsp;Meiying Deng,&nbsp;Shimiao Hong,&nbsp;Peng Ai,&nbsp;Chuan Gao,&nbsp;Huangkai Zhou","doi":"10.1002/imt2.228","DOIUrl":"https://doi.org/10.1002/imt2.228","url":null,"abstract":"<p>The OmicShare tools platform is a user-friendly online resource for data analysis and visualization, encompassing 161 bioinformatic tools. Users can easily track the progress of projects in real-time through an overview interface. The platform has a powerful interactive graphics engine that allows for the custom-tailored modification of charts generated from analyses. The visually appealing charts produced by OmicShare improve data interpretability and meet the requirements for publication. It has been acknowledged in over 4000 publications and is available in https://www.omicshare.com/tools/.\u0000\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 5","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.228","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142449033","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single-cell landscape revealed immune characteristics associated with disease phases in brucellosis patients 单细胞图谱揭示了布鲁氏菌病患者与疾病阶段相关的免疫特征
IF 23.7
iMeta Pub Date : 2024-07-23 DOI: 10.1002/imt2.226
Yi Wang, Siyuan Yang, Bing Han, Xiufang Du, Huali Sun, Yufeng Du, Yinli Liu, Panpan Lu, Jinyu Di, Laurence Don Wai Luu, Xiao Lv, Songnian Hu, Linghang Wang, Rongmeng Jiang
{"title":"Single-cell landscape revealed immune characteristics associated with disease phases in brucellosis patients","authors":"Yi Wang,&nbsp;Siyuan Yang,&nbsp;Bing Han,&nbsp;Xiufang Du,&nbsp;Huali Sun,&nbsp;Yufeng Du,&nbsp;Yinli Liu,&nbsp;Panpan Lu,&nbsp;Jinyu Di,&nbsp;Laurence Don Wai Luu,&nbsp;Xiao Lv,&nbsp;Songnian Hu,&nbsp;Linghang Wang,&nbsp;Rongmeng Jiang","doi":"10.1002/imt2.226","DOIUrl":"10.1002/imt2.226","url":null,"abstract":"<p>A comprehensive immune landscape for <i>Brucella</i> infection is crucial for developing new treatments for brucellosis. Here, we utilized single-cell RNA sequencing (scRNA-seq) of 290,369 cells from 35 individuals, including 29 brucellosis patients from acute (<i>n</i> = 10), sub-acute (<i>n</i> = 9), and chronic (<i>n</i> = 10) phases as well as six healthy donors. Enzyme-linked immunosorbent assays were applied for validation within this cohort. <i>Brucella</i> infection caused a significant change in the composition of peripheral immune cells and inflammation was a key feature of brucellosis. Acute patients are characterized by potential cytokine storms resulting from systemic upregulation of <i>S100A8</i>/<i>A9</i>, primarily due to classical monocytes. Cytokine storm may be mediated by activating S100A8/A9-TLR4-MyD88 signaling pathway. Moreover, monocytic myeloid-derived suppressor cells were the probable contributors to immune paralysis in acute patients. Chronic patients are characterized by a dysregulated Th1 response, marked by reduced expression of IFN-γ and Th1 signatures as well as a high exhausted state. Additionally, <i>Brucella</i> infection can suppress apoptosis in myeloid cells (e.g., mDCs, classical monocytes), inhibit antigen presentation in professional antigen-presenting cells (APCs; e.g., mDC) and nonprofessional APCs (e.g., monocytes), and induce exhaustion in CD8<sup>+</sup> T/NK cells, potentially resulting in the establishment of chronic infection. Overall, our study systemically deciphered the coordinated immune responses of <i>Brucella</i> at different phases of the infection, which facilitated a full understanding of the immunopathogenesis of brucellosis and may aid the development of new effective therapeutic strategies, especially for those with chronic infection.</p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 4","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.226","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141812274","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Efficient and easy-to-use capturing three-dimensional metagenome interactions with GutHi-C 利用 GutHi-C 高效、易用地捕捉三维元基因组相互作用
IF 23.7
iMeta Pub Date : 2024-07-22 DOI: 10.1002/imt2.227
Yu-Xi Lu, Jin-Bao Yang, Chen-Ying Li, Yun-Han Tian, Rong-Rong Chang, Da-Shuai Kong, Shu-Lin Yang, Yan-Fang Wang, Yu-Bo Zhang, Xiu-Sheng Zhu, Wei-Hua Pan, Si-Yuan Kong
{"title":"Efficient and easy-to-use capturing three-dimensional metagenome interactions with GutHi-C","authors":"Yu-Xi Lu,&nbsp;Jin-Bao Yang,&nbsp;Chen-Ying Li,&nbsp;Yun-Han Tian,&nbsp;Rong-Rong Chang,&nbsp;Da-Shuai Kong,&nbsp;Shu-Lin Yang,&nbsp;Yan-Fang Wang,&nbsp;Yu-Bo Zhang,&nbsp;Xiu-Sheng Zhu,&nbsp;Wei-Hua Pan,&nbsp;Si-Yuan Kong","doi":"10.1002/imt2.227","DOIUrl":"10.1002/imt2.227","url":null,"abstract":"<p>Hi-C can obtain three-dimensional chromatin structure information and is widely used for genome assembly. We constructed the GutHi-C technology. As shown in the graphical abstract, it is a highly efficient and quick-to-operate method and can be widely used for human, livestock, and poultry gut microorganisms. It provides a reference for the Hi-C methodology of the microbial metagenome. DPBS, Dulbecco's phosphate-buffered saline; Hi-C, high-through chromatin conformation capture; LB, Luria-Bertani; NGS, next-generation sequencing; PCR, polymerase chain reaction; QC, quality control.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 5","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.227","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141815430","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Intestinal microbiota by angiotensin receptor blocker therapy exerts protective effects against hypertensive damages 血管紧张素受体阻滞剂疗法的肠道微生物群对高血压损害具有保护作用
IF 23.7
iMeta Pub Date : 2024-07-18 DOI: 10.1002/imt2.222
Jing Li, Si-Yuan Wang, Kai-Xin Yan, Pan Wang, Jie Jiao, Yi-Dan Wang, Mu-Lei Chen, Ying Dong, Jiu-Chang Zhong
{"title":"Intestinal microbiota by angiotensin receptor blocker therapy exerts protective effects against hypertensive damages","authors":"Jing Li,&nbsp;Si-Yuan Wang,&nbsp;Kai-Xin Yan,&nbsp;Pan Wang,&nbsp;Jie Jiao,&nbsp;Yi-Dan Wang,&nbsp;Mu-Lei Chen,&nbsp;Ying Dong,&nbsp;Jiu-Chang Zhong","doi":"10.1002/imt2.222","DOIUrl":"10.1002/imt2.222","url":null,"abstract":"<p>Dysbiosis of the gut microbiota has been implicated in hypertension, and drug–host–microbiome interactions have drawn considerable attention. However, the influence of angiotensin receptor blocker (ARB)-shaped gut microbiota on the host is not fully understood. In this work, we assessed the alterations of blood pressure (BP), vasculatures, and intestines following ARB-modified gut microbiome treatment and evaluated the changes in the intestinal transcriptome and serum metabolome in hypertensive rats. Hypertensive patients with well-controlled BP under ARB therapy were recruited as human donors, spontaneously hypertensive rats (SHRs) receiving normal saline or valsartan were considered animal donors, and SHRs were regarded as recipients. Histological and immunofluorescence staining was used to assess the aorta and small intestine, and 16S rRNA amplicon sequencing was performed to examine gut bacteria. Transcriptome and metabonomic analyses were conducted to determine the intestinal transcriptome and serum metabolome, respectively. Notably, ARB-modified fecal microbiota transplantation (FMT), results in marked decreases in systolic BP levels, collagen deposition and reactive oxygen species accumulation in the vasculature, and alleviated intestinal structure impairments in SHRs. These changes were linked with the reconstruction of the gut microbiota in SHR recipients post-FMT, especially with a decreased abundance of <i>Lactobacillus</i>, <i>Aggregatibacter</i>, and <i>Desulfovibrio</i>. Moreover, ARB-treated microbes contributed to increased intestinal <i>Ciart</i>, <i>Per1</i>, <i>Per2</i>, <i>Per3</i>, and <i>Cipc</i> gene levels and decreased <i>Nfil3</i> and <i>Arntl</i> expression were detected in response to ARB-treated microbes. More importantly, circulating metabolites were dramatically reduced in ARB-FMT rats, including 6beta-Hydroxytestosterone and Thromboxane B2. In conclusion, ARB-modified gut microbiota exerts protective roles in vascular remodeling and injury, metabolic abnormality and intestinal dysfunctions, suggesting a pivotal role in mitigating hypertension and providing insights into the cross-talk between antihypertensive medicines and the gut microbiome.</p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 4","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.222","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141825005","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Deciphering functional groups of rumen microbiome and their underlying potentially causal relationships in shaping host traits 破译瘤胃微生物组的功能群及其在塑造宿主性状方面的潜在因果关系
IF 23.7
iMeta Pub Date : 2024-07-15 DOI: 10.1002/imt2.225
Ming-Yuan Xue, Yun-Yi Xie, Xin-Wei Zang, Yi-Fan Zhong, Xiao-Jiao Ma, Hui-Zeng Sun, Jian-Xin Liu
{"title":"Deciphering functional groups of rumen microbiome and their underlying potentially causal relationships in shaping host traits","authors":"Ming-Yuan Xue,&nbsp;Yun-Yi Xie,&nbsp;Xin-Wei Zang,&nbsp;Yi-Fan Zhong,&nbsp;Xiao-Jiao Ma,&nbsp;Hui-Zeng Sun,&nbsp;Jian-Xin Liu","doi":"10.1002/imt2.225","DOIUrl":"10.1002/imt2.225","url":null,"abstract":"<p>Over the years, microbiome research has achieved tremendous advancements driven by culture-independent meta-omics approaches. Despite extensive research, our understanding of the functional roles and causal effects of the microbiome on phenotypes remains limited. In this study, we focused on the rumen metaproteome, combining it with metatranscriptome and metabolome data to accurately identify the active functional distributions of rumen microorganisms and specific functional groups that influence feed efficiency. By integrating host genetics data, we established the potentially causal relationships between microbes-proteins/metabolites-phenotype, and identified specific patterns in which functional groups of rumen microorganisms influence host feed efficiency. We found a causal link between <i>Selenomonas bovis</i> and rumen carbohydrate metabolism, potentially mediated by bacterial chemotaxis and a two-component regulatory system, impacting feed utilization efficiency of dairy cows. Our study on the nutrient utilization functional groups in the rumen of high-feed-efficiency dairy cows, along with the identification of key microbiota functional proteins and their potentially causal relationships, will help move from correlation to causation in rumen microbiome research. This will ultimately enable precise regulation of the rumen microbiota for optimized ruminant production.</p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 4","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.225","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141647117","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Immune-enriched phyllosphere microbiome in rice panicle exhibits protective effects against rice blast and rice false smut diseases 水稻圆锥花序中免疫丰富的叶球微生物群对稻瘟病和水稻假穗病具有保护作用
IF 23.7
iMeta Pub Date : 2024-07-15 DOI: 10.1002/imt2.223
Dacheng Wang, Yingqiao Wan, Dekun Liu, Ning Wang, Jingni Wu, Qin Gu, Huijun Wu, Xuewen Gao, Yiming Wang
{"title":"Immune-enriched phyllosphere microbiome in rice panicle exhibits protective effects against rice blast and rice false smut diseases","authors":"Dacheng Wang,&nbsp;Yingqiao Wan,&nbsp;Dekun Liu,&nbsp;Ning Wang,&nbsp;Jingni Wu,&nbsp;Qin Gu,&nbsp;Huijun Wu,&nbsp;Xuewen Gao,&nbsp;Yiming Wang","doi":"10.1002/imt2.223","DOIUrl":"10.1002/imt2.223","url":null,"abstract":"<p>Activation of immune responses leads to an enrichment of beneficial microbes in rice panicle. We therefore selected the enriched operational taxonomy units (OTUs) exhibiting direct suppression effects on fungal pathogens, and established a simplified synthetic community (SynCom) which consists of three beneficial microbes. Application of this SynCom exhibits protective effect against fungal pathogen infection in rice.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 4","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.223","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141833129","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Probio-M9, a breast milk-originated probiotic, alleviates mastitis and enhances antibiotic efficacy: Insights into the gut–mammary axis 源自母乳的益生菌 Probio-M9 可缓解乳腺炎并提高抗生素疗效:洞察肠道-乳腺轴
IF 23.7
iMeta Pub Date : 2024-07-09 DOI: 10.1002/imt2.224
Jie Yu, Weicheng Li, Ruibo Xu, Xiaoye Liu, Guangqi Gao, Lai-Yu Kwok, Yongfu Chen, Zhihong Sun, Wenjun Liu, Heping Zhang
{"title":"Probio-M9, a breast milk-originated probiotic, alleviates mastitis and enhances antibiotic efficacy: Insights into the gut–mammary axis","authors":"Jie Yu,&nbsp;Weicheng Li,&nbsp;Ruibo Xu,&nbsp;Xiaoye Liu,&nbsp;Guangqi Gao,&nbsp;Lai-Yu Kwok,&nbsp;Yongfu Chen,&nbsp;Zhihong Sun,&nbsp;Wenjun Liu,&nbsp;Heping Zhang","doi":"10.1002/imt2.224","DOIUrl":"10.1002/imt2.224","url":null,"abstract":"<p>Breast milk naturally contains lactic acid bacteria, but their precise origin remains a subject of debate. In this study, we utilized a rat mastitis animal model to investigate the potential of a breast milk-derived probiotic strain, <i>Lacticaseibacillus rhamnosus</i> Probio-M9, in alleviating mastitis and enhancing the efficacy of antibiotic treatment. Through histopathological analysis of mammary tissue, we observed that Probio-M9 effectively relieved mastitis, mitigated inflammation, and improved the response to antibiotic treatment. Metagenomic analysis further revealed that Probio-M9 enhanced interactions among gut microbes, accompanied by an increase in the relative abundance of <i>Ruminococcaceae</i> and the regulation of specific genes and carbohydrate-active enzymes, subsequently impacting host immunity. Additionally, an intriguing finding was the translocation of live Probio-M9 from the gut to the mammary tissue only during bacterial mastitis and lactation, likely facilitated through lymphatic circulation. These findings advance our understanding of the intricate gut–mammary axis and provide valuable insights into the potential health benefits of probiotic interventions.\u0000\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":73342,"journal":{"name":"iMeta","volume":"3 4","pages":""},"PeriodicalIF":23.7,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/imt2.224","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141664228","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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