揭示耐万古霉素肠球菌诱发脓毒性腹膜炎小鼠模型中宿主-病原体的动态变化。

IF 5.5 1区 农林科学 Q1 IMMUNOLOGY
Virulence Pub Date : 2024-12-01 Epub Date: 2024-07-01 DOI:10.1080/21505594.2024.2367659
Xin Yuan, Xiaolin Song, Xi Zhang, Lingfei Hu, Dongsheng Zhou, Jianlong Zhang, Chenxi Dai
{"title":"揭示耐万古霉素肠球菌诱发脓毒性腹膜炎小鼠模型中宿主-病原体的动态变化。","authors":"Xin Yuan, Xiaolin Song, Xi Zhang, Lingfei Hu, Dongsheng Zhou, Jianlong Zhang, Chenxi Dai","doi":"10.1080/21505594.2024.2367659","DOIUrl":null,"url":null,"abstract":"<p><p>Vancomycin-resistant <i>Enterococcus faecium</i> (<i>E. faecium</i>) infection is associated with higher mortality rates. Previous studies have emphasized the importance of innate immune cells and signalling pathways in clearing <i>E. faecium</i>, but a comprehensive analysis of host-pathogen interactions is lacking. Here, we investigated the interplay of host and <i>E. faecium</i> in a murine model of septic peritonitis. Following injection with a sublethal dose, we observed significantly increased murine sepsis score and histological score, decreased weight and bacterial burden, neutrophils and macrophages infiltration, and comprehensive activation of cytokine-mediated signalling pathway. In mice receiving a lethal dose, hypothermia significantly improved survival, reduced bacterial burden, cytokines, and CD86 expression of MHC-II<sup>+</sup> recruited macrophages compared to the normothermia group. A mathematical model constructed by observational data from 80 animals, recapitulated the host-pathogen interplay, and further verified the benefits of hypothermia. These findings indicate that <i>E. faecium</i> triggers a severe activation of cytokine-mediated signalling pathway, and hypothermia can improve outcomes by reducing bacterial burden and inflammation.</p>","PeriodicalId":23747,"journal":{"name":"Virulence","volume":null,"pages":null},"PeriodicalIF":5.5000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11221476/pdf/","citationCount":"0","resultStr":"{\"title\":\"Unraveling host-pathogen dynamics in a murine Model of septic peritonitis induced by vancomycin-resistant <i>Enterococcus faecium</i>.\",\"authors\":\"Xin Yuan, Xiaolin Song, Xi Zhang, Lingfei Hu, Dongsheng Zhou, Jianlong Zhang, Chenxi Dai\",\"doi\":\"10.1080/21505594.2024.2367659\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Vancomycin-resistant <i>Enterococcus faecium</i> (<i>E. faecium</i>) infection is associated with higher mortality rates. Previous studies have emphasized the importance of innate immune cells and signalling pathways in clearing <i>E. faecium</i>, but a comprehensive analysis of host-pathogen interactions is lacking. Here, we investigated the interplay of host and <i>E. faecium</i> in a murine model of septic peritonitis. Following injection with a sublethal dose, we observed significantly increased murine sepsis score and histological score, decreased weight and bacterial burden, neutrophils and macrophages infiltration, and comprehensive activation of cytokine-mediated signalling pathway. In mice receiving a lethal dose, hypothermia significantly improved survival, reduced bacterial burden, cytokines, and CD86 expression of MHC-II<sup>+</sup> recruited macrophages compared to the normothermia group. A mathematical model constructed by observational data from 80 animals, recapitulated the host-pathogen interplay, and further verified the benefits of hypothermia. These findings indicate that <i>E. faecium</i> triggers a severe activation of cytokine-mediated signalling pathway, and hypothermia can improve outcomes by reducing bacterial burden and inflammation.</p>\",\"PeriodicalId\":23747,\"journal\":{\"name\":\"Virulence\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11221476/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virulence\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1080/21505594.2024.2367659\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/1 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virulence","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/21505594.2024.2367659","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/1 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

耐万古霉素的粪肠球菌(E. faecium)感染与较高的死亡率有关。以前的研究强调了先天性免疫细胞和信号通路在清除粪肠球菌中的重要性,但缺乏对宿主与病原体相互作用的全面分析。在这里,我们研究了脓毒性腹膜炎小鼠模型中宿主与粪大肠杆菌的相互作用。注射亚致死剂量后,我们观察到小鼠脓毒症评分和组织学评分显著增加,体重和细菌负荷、中性粒细胞和巨噬细胞浸润减少,细胞因子介导的信号通路全面激活。与正常体温组相比,接受致死剂量的小鼠低体温可显著提高存活率,减少细菌负荷、细胞因子和 MHC-II+ 募集巨噬细胞的 CD86 表达。根据 80 只动物的观察数据建立的数学模型再现了宿主与病原体之间的相互作用,并进一步验证了低体温的益处。这些研究结果表明,粪肠球菌会引发细胞因子介导的信号通路的严重激活,而低体温可以通过减少细菌负担和炎症来改善预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unraveling host-pathogen dynamics in a murine Model of septic peritonitis induced by vancomycin-resistant Enterococcus faecium.

Vancomycin-resistant Enterococcus faecium (E. faecium) infection is associated with higher mortality rates. Previous studies have emphasized the importance of innate immune cells and signalling pathways in clearing E. faecium, but a comprehensive analysis of host-pathogen interactions is lacking. Here, we investigated the interplay of host and E. faecium in a murine model of septic peritonitis. Following injection with a sublethal dose, we observed significantly increased murine sepsis score and histological score, decreased weight and bacterial burden, neutrophils and macrophages infiltration, and comprehensive activation of cytokine-mediated signalling pathway. In mice receiving a lethal dose, hypothermia significantly improved survival, reduced bacterial burden, cytokines, and CD86 expression of MHC-II+ recruited macrophages compared to the normothermia group. A mathematical model constructed by observational data from 80 animals, recapitulated the host-pathogen interplay, and further verified the benefits of hypothermia. These findings indicate that E. faecium triggers a severe activation of cytokine-mediated signalling pathway, and hypothermia can improve outcomes by reducing bacterial burden and inflammation.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Virulence
Virulence IMMUNOLOGY-MICROBIOLOGY
CiteScore
9.20
自引率
1.90%
发文量
123
审稿时长
6-12 weeks
期刊介绍: Virulence is a fully open access peer-reviewed journal. All articles will (if accepted) be available for anyone to read anywhere, at any time immediately on publication. Virulence is the first international peer-reviewed journal of its kind to focus exclusively on microbial pathogenicity, the infection process and host-pathogen interactions. To address the new infectious challenges, emerging infectious agents and antimicrobial resistance, there is a clear need for interdisciplinary research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信