Vaginal microbial dynamics and pathogen colonization in a humanized microbiota mouse model.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2023-11-20 DOI:10.1038/s41522-023-00454-9
Marlyd E Mejia, Vicki Mercado-Evans, Jacob J Zulk, Samantha Ottinger, Korinna Ruiz, Mallory B Ballard, Stephanie W Fowler, Robert A Britton, Kathryn A Patras
{"title":"Vaginal microbial dynamics and pathogen colonization in a humanized microbiota mouse model.","authors":"Marlyd E Mejia, Vicki Mercado-Evans, Jacob J Zulk, Samantha Ottinger, Korinna Ruiz, Mallory B Ballard, Stephanie W Fowler, Robert A Britton, Kathryn A Patras","doi":"10.1038/s41522-023-00454-9","DOIUrl":null,"url":null,"abstract":"<p><p>Vaginal microbial composition is associated with differential risk of urogenital infection. Although Lactobacillus spp. are thought to confer protection against infection, the lack of in vivo models resembling the human vaginal microbiota remains a prominent barrier to mechanistic discovery. Using 16S rRNA amplicon sequencing of C57BL/6J female mice, we found that vaginal microbial composition varies within and between colonies across three vivaria. Noting vaginal microbial plasticity in conventional mice, we assessed the vaginal microbiome of humanized microbiota mice (<sup>HMb</sup>mice). Like the community structure in conventional mice, <sup>HMb</sup>mice vaginal microbiota clustered into community state types but, uniquely, <sup>HMb</sup>mice communities were frequently dominated by Lactobacillus or Enterobacteriaceae. Compared to conventional mice, <sup>HMb</sup>mice were less susceptible to uterine ascension by urogenital pathobionts group B Streptococcus (GBS) and Prevotella bivia. Although Escherichia and Lactobacillus both correlated with the absence of uterine GBS, vaginal pre-inoculation with exogenous <sup>HMb</sup>mouse-derived E. coli, but not Ligilactobacillus murinus, reduced vaginal GBS burden. Overall, <sup>HMb</sup>mice serve as a useful model to elucidate the role of endogenous microbes in conferring protection against urogenital pathogens.</p>","PeriodicalId":19370,"journal":{"name":"npj Biofilms and Microbiomes","volume":null,"pages":null},"PeriodicalIF":7.8000,"publicationDate":"2023-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661851/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"npj Biofilms and Microbiomes","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41522-023-00454-9","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Vaginal microbial composition is associated with differential risk of urogenital infection. Although Lactobacillus spp. are thought to confer protection against infection, the lack of in vivo models resembling the human vaginal microbiota remains a prominent barrier to mechanistic discovery. Using 16S rRNA amplicon sequencing of C57BL/6J female mice, we found that vaginal microbial composition varies within and between colonies across three vivaria. Noting vaginal microbial plasticity in conventional mice, we assessed the vaginal microbiome of humanized microbiota mice (HMbmice). Like the community structure in conventional mice, HMbmice vaginal microbiota clustered into community state types but, uniquely, HMbmice communities were frequently dominated by Lactobacillus or Enterobacteriaceae. Compared to conventional mice, HMbmice were less susceptible to uterine ascension by urogenital pathobionts group B Streptococcus (GBS) and Prevotella bivia. Although Escherichia and Lactobacillus both correlated with the absence of uterine GBS, vaginal pre-inoculation with exogenous HMbmouse-derived E. coli, but not Ligilactobacillus murinus, reduced vaginal GBS burden. Overall, HMbmice serve as a useful model to elucidate the role of endogenous microbes in conferring protection against urogenital pathogens.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
阴道微生物动力学和病原体定植在人源化微生物群小鼠模型。
阴道微生物组成与泌尿生殖系统感染的不同风险相关。尽管乳酸菌被认为具有抗感染的作用,但缺乏类似于人类阴道微生物群的体内模型仍然是发现其机制的一个突出障碍。通过对C57BL/6J雌性小鼠的16S rRNA扩增子测序,我们发现在3个不同的小鼠体内,阴道微生物组成在菌落内和菌落之间存在差异。注意到常规小鼠阴道微生物的可塑性,我们评估了人源化微生物群小鼠(HMbmice)的阴道微生物组。与传统小鼠的群落结构一样,HMbmice阴道微生物群聚集成不同的群落状态类型,但其独特之处在于,HMbmice的群落往往以乳杆菌或肠杆菌科为主。与常规小鼠相比,hmb小鼠对泌尿生殖道病原体B组链球菌(GBS)和bivia普氏菌(Prevotella bivia)引起的子宫上升的易感性较低。虽然大肠杆菌和乳酸菌都与子宫GBS的不存在相关,但阴道预接种外源性hmbmouse来源的大肠杆菌,而不是轻乳酸菌,减少了阴道GBS的负担。总之,HMbmice可以作为一个有用的模型来阐明内源性微生物在保护泌尿生殖系统病原体方面的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
期刊最新文献
Large-scale metagenomic assembly provide new insights into the genetic evolution of gut microbiomes in plateau ungulates. Microbial diversity and secondary metabolism potential in relation to dark alterations in Paleolithic Lascaux Cave. Combating biofilm-associated Klebsiella pneumoniae infections using a bovine microbial enzyme. Kinetics of imidazole propionate from orally delivered histidine in mice and humans. Autoinducer-2 relieves soil stress-induced dormancy of Bacillus velezensis by modulating sporulation signaling.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1