Characterization and dynamics of intestinal microbiota in patients with Clostridioides difficile colonization and infection.

IF 2.6 4区 医学 Q3 IMMUNOLOGY Microbes and Infection Pub Date : 2024-06-08 DOI:10.1016/j.micinf.2024.105373
Yanzi Zhou, Lihua Guo, Tingting Xiao, Yunbo Chen, Tao Lv, Yuan Wang, Shuntian Zhang, Hongliu Cai, Xiaohui Chi, Xiaoyang Kong, Kai Zhou, Ping Shen, Yonghong Xiao
{"title":"Characterization and dynamics of intestinal microbiota in patients with Clostridioides difficile colonization and infection.","authors":"Yanzi Zhou, Lihua Guo, Tingting Xiao, Yunbo Chen, Tao Lv, Yuan Wang, Shuntian Zhang, Hongliu Cai, Xiaohui Chi, Xiaoyang Kong, Kai Zhou, Ping Shen, Yonghong Xiao","doi":"10.1016/j.micinf.2024.105373","DOIUrl":null,"url":null,"abstract":"<p><p>Gut microbiota dysbiosis increases the susceptibility to Clostridioides difficile infection (CDI). In this study, we monitored C. difficile colonization (CDC) patients from no CDC status (CDN) to CDC status (CDCp) and CDI patients from asymptomatic status before CDI (PRECDI), CDI status (ONCDI), to asymptomatic status after CDI (POSTCDI). Based on metagenomic sequencing, we aimed to investigate the interaction pattern between gut microbiota and C. difficile. There was no significant difference of microbiota diversity between CDN and CDCp. In CDCp, Bacteroidetes and short-chain fatty acid (SCFA)-producing bacteria increased, with a positive correlation between SCFA-producing bacteria and C. difficile colonization. Compared with PRECDI, ONCDI and POSTCDI showed a significant decrease in microbiota diversity, particularly in Bacteroidetes and SCFA-producing bacteria, with a positive correlation between opportunistic pathogen and C. difficile. Fatty acid metabolism, and amino acid biosynthesis were enriched in CDN, CDCp, and PRECDI, while bile secretion was enriched in ONCDI and POSTCDI. Microbiota and metabolic pathways interaction networks in CDN and CDCp were more complex, particularly pathways in fatty acid and bile acid metabolism. Increasing of Bacteroidetes and SCFA-producing bacteria, affecting amino acid and fatty acid metabolism, is associated with colonization resistance to C. difficile and inhibiting the development of CDI.</p>","PeriodicalId":18497,"journal":{"name":"Microbes and Infection","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2024-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbes and Infection","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.micinf.2024.105373","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Gut microbiota dysbiosis increases the susceptibility to Clostridioides difficile infection (CDI). In this study, we monitored C. difficile colonization (CDC) patients from no CDC status (CDN) to CDC status (CDCp) and CDI patients from asymptomatic status before CDI (PRECDI), CDI status (ONCDI), to asymptomatic status after CDI (POSTCDI). Based on metagenomic sequencing, we aimed to investigate the interaction pattern between gut microbiota and C. difficile. There was no significant difference of microbiota diversity between CDN and CDCp. In CDCp, Bacteroidetes and short-chain fatty acid (SCFA)-producing bacteria increased, with a positive correlation between SCFA-producing bacteria and C. difficile colonization. Compared with PRECDI, ONCDI and POSTCDI showed a significant decrease in microbiota diversity, particularly in Bacteroidetes and SCFA-producing bacteria, with a positive correlation between opportunistic pathogen and C. difficile. Fatty acid metabolism, and amino acid biosynthesis were enriched in CDN, CDCp, and PRECDI, while bile secretion was enriched in ONCDI and POSTCDI. Microbiota and metabolic pathways interaction networks in CDN and CDCp were more complex, particularly pathways in fatty acid and bile acid metabolism. Increasing of Bacteroidetes and SCFA-producing bacteria, affecting amino acid and fatty acid metabolism, is associated with colonization resistance to C. difficile and inhibiting the development of CDI.

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
艰难梭菌定植和感染患者肠道微生物群的特征和动态变化。
肠道微生物群失调会增加艰难梭菌感染(CDI)的易感性。在这项研究中,我们监测了艰难梭菌定植(CDC)患者从无 CDC 状态(CDN)到 CDC 状态(CDCp),以及 CDI 患者从 CDI 前无症状状态(PRECDI)、CDI 状态(ONCDI)到 CDI 后无症状状态(POSTCDI)。基于元基因组测序,我们旨在研究肠道微生物群与艰难梭菌之间的相互作用模式。CDN 和 CDCp 的微生物群多样性无明显差异。在 CDCp 中,类杆菌和短链脂肪酸(SCFA)产生菌增加,SCFA 产生菌与艰难梭菌定植呈正相关。与 PRECCDI 相比,ONCDI 和 POSTCDI 显示微生物群多样性显著下降,尤其是类杆菌和 SCFA 产菌,机会性病原体与艰难梭菌之间呈正相关。CDN、CDCp 和 PRECDI 中富含脂肪酸代谢和氨基酸生物合成,而 ONCDI 和 POSTCDI 中富含胆汁分泌。CDN 和 CDCp 中的微生物群与代谢途径相互作用网络更为复杂,尤其是脂肪酸和胆汁酸代谢途径。类杆菌和产生 SCFA 的细菌的增加会影响氨基酸和脂肪酸的代谢,这与艰难梭菌的定植抗性和抑制 CDI 的发展有关。
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
Microbes and Infection
Microbes and Infection 医学-病毒学
CiteScore
12.60
自引率
1.70%
发文量
90
审稿时长
40 days
期刊介绍: Microbes and Infection publishes 10 peer-reviewed issues per year in all fields of infection and immunity, covering the different levels of host-microbe interactions, and in particular: the molecular biology and cell biology of the crosstalk between hosts (human and model organisms) and microbes (viruses, bacteria, parasites and fungi), including molecular virulence and evasion mechanisms. the immune response to infection, including pathogenesis and host susceptibility. emerging human infectious diseases. systems immunology. molecular epidemiology/genetics of host pathogen interactions. microbiota and host "interactions". vaccine development, including novel strategies and adjuvants. Clinical studies, accounts of clinical trials and biomarker studies in infectious diseases are within the scope of the journal. Microbes and Infection publishes articles on human pathogens or pathogens of model systems. However, articles on other microbes can be published if they contribute to our understanding of basic mechanisms of host-pathogen interactions. Purely descriptive and preliminary studies are discouraged.
期刊最新文献
Nano-Enhanced Benzylpenicillin: Bridging Antibacterial Action with Anti-Inflammatory Potential against Antibiotic-Resistant Bacteria. TGEV nonstructural protein ORF3b upregulates the expression of SLA-DR at the transcriptional level in monocyte-derived porcine dendritic cells. Bad company? The pericardium microbiome in people investigated for tuberculous pericarditis in an HIV-prevalent setting. miRNAs Regulate the Metabolic Adaptation of Paracoccidioides brasiliensis during Copper Deprivation. Intranasal immunization with poly I:C and CpG ODN adjuvants enhances the protective efficacy against Helicobacter pylori infection in mice.
×
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