破坏与适应:婴儿肠道微生物群对SARS-CoV-2感染的动态反应

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Li-Ting Zhu, Lei Zhao, Yue Zhu, Xue-Li Xu, Jing-Jing Lin, Yi-Fang Duan, Lu Long, Yang-Yu Wu, Wen-Juan Xu, Jing-Yu Chen, Yu-Han Yin, Alex Ujong Obeten, Qiansheng Huang
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引用次数: 0

摘要

背景:婴儿肠道微生物群对感染的反应显著破坏了宿主内微生物群的自然进化过程。在这里,我们收集了受严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)影响的16个月的婴儿肠道微生物群纵向队列。然后,我们开发了一种多标准方法来识别在环境干扰下驱动社区动态的核心交互网络,我们将其称为保守变交互群(cviggroup)。结果:cviggroup在精确定位与扰动相关的稀疏集方面显示出显著的优势,正如我们自己和公开可用的数据集所验证的那样。利用牛津纳米孔技术,我们发现该群体通过增强可移动遗传元件的移动性,包括增强双精氨酸易位途径以响应增加的毒力因素,从而促进了生态系统对环境破坏的适应。此外,cviggroup是生态系统健康的有效指标。肠道菌群适应的时间尺度超过了10个月。cviggroup的成员,如拟杆菌(Bacteroides thetaiotaomicron)和粪杆菌(Faecalibacterium),表现出不同程度的基因组结构变异,这有助于引导群落走向新的稳定状态,而不是回到原来的结构。结论:总的来说,cviggroup提供了肠道微生物群对环境干扰的适应性反应的快照。婴儿感染COVID-19后肠道微生物群的破坏和随后的适应强调了在大流行后时代背景下重新评估参考标准的必要性。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disruption and adaptation: infant gut microbiota's dynamic response to SARS-CoV-2 infection.

Background: The responses of the infant gut microbiota to infection significantly disrupt the natural intrahost evolutionary processes of the microbiome. Here, we collected a 16-month longitudinal cohort of infant gut microbiomes affected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Then, we developed a multicriteria approach to identify core interaction network driving community dynamics under environmental disturbances, which we termed the Conserved Variated Interaction Group (CVIgroup).

Results: The CVIgroup showed significant advantages on pinpointing a sparse set associated with the disturbances, as validated both our own and publicly available datasets. Leveraging the Oxford Nanopore Technology, we found this group facilitates the ecosystem's adaptation to environmental disruptions by enhancing the mobility of mobile genetic elements, including the reinforcement of the twin-arginine translocation pathway in response to increased virulence factors. Furthermore, the CVIgroup serves as an effective indicator of ecosystem health. The timescale for the gut microbiota's adaptation extends beyond 10 months. Members of the CVIgroup, such as Bacteroides thetaiotaomicron and Faecalibacterium, exhibit varying degrees of genomic structural variants, which contribute to guiding the community toward a new stable state rather than returning to its original configuration.

Conclusions: Collectively, the CVIgroup offers a snapshot of the gut microbiota's adaptive response to environmental disturbances. The disruption and subsequent adaptation of the gut microbiota in infants after COVID-19 infection underscores the necessity of re-evaluating reference standards in the context of the post-pandemic era. Video Abstract.

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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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