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在家庭三联体中的队列研究:肠道微生物组成和生命早期暴露对生命头两年肠道抗药基因库的影响。

A cohort study in family triads: impact of gut microbiota composition and early life exposures on intestinal resistome during the first two years of life.

机构信息

Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

Department of Computing, University of Turku, Turku, Finland.

出版信息

Gut Microbes. 2024 Jan-Dec;16(1):2383746. doi: 10.1080/19490976.2024.2383746. Epub 2024 Aug 2.

DOI:10.1080/19490976.2024.2383746
PMID:39092808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11299627/
Abstract

Antibiotic resistance genes (ARGs) are prevalent in the infant gut microbiota and make up the intestinal resistome, representing a community ARG reservoir. This study focuses on the dynamics and persistence of ARGs in the early gut microbiota, and the effect of early exposures therein. We leveraged 2,328 stool metagenomes from 475 children in the HELMi cohort and the available parental samples to study the diversity, dynamics, and intra-familial sharing of the resistome during the first two years of life. We found higher within-family similarity of the gut resistome composition and ARG load in infant-mother pairs, and between spouses, but not in father-infant pairs. Early gut microbiota composition and development correlated with the ARG load; correlated positively and negatively with the load, reflecting the typical resistance levels in these taxa. Caesarean delivered infants harbored lower ARG loads, partly reflecting the scarcity of compared to vaginally delivered. Exposure to intrapartum or post-natal antibiotics showed only modest associations with the ARG load and composition, mainly before 12 months. Our results indicate that the resistome is strongly driven by the normal development of the microbiota in early life, and suggest importance of longer evolution of ARGs over effects of recent antibiotic exposure.

摘要

抗生素耐药基因 (ARGs) 在婴儿肠道微生物群中普遍存在,构成了肠道耐药组,代表了一个社区 ARG 库。本研究关注早期肠道微生物群中 ARGs 的动态和持久性,以及其中早期暴露的影响。我们利用 HELMi 队列中 475 名儿童的 2328 个粪便宏基因组和可用的父母样本,研究了生命头两年肠道耐药组的多样性、动态和家族内共享。我们发现,在婴儿-母亲对和配偶之间,肠道耐药组组成和 ARG 负荷的家族内相似性更高,而在父亲-婴儿对中则没有。早期肠道微生物群组成和发育与 ARG 负荷相关;与 呈正相关,与 呈负相关,反映了这些分类群中典型的耐药水平。剖腹产婴儿的 ARG 负荷较低,部分原因是与阴道分娩相比, 较少。分娩期间或产后暴露于抗生素仅与 ARG 负荷和组成有适度关联,主要发生在 12 个月之前。我们的结果表明,耐药组受生命早期微生物群正常发育的强烈驱动,并表明 ARG 是经过长时间进化的,而不是最近抗生素暴露的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/635ebd870f11/KGMI_A_2383746_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/8414d740777d/KGMI_A_2383746_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/79838c85ba42/KGMI_A_2383746_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/6de3417df746/KGMI_A_2383746_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/f6d7c71a9dfb/KGMI_A_2383746_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/1a4561546f20/KGMI_A_2383746_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/635ebd870f11/KGMI_A_2383746_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/8414d740777d/KGMI_A_2383746_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/79838c85ba42/KGMI_A_2383746_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/6de3417df746/KGMI_A_2383746_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/f6d7c71a9dfb/KGMI_A_2383746_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/1a4561546f20/KGMI_A_2383746_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/11299627/635ebd870f11/KGMI_A_2383746_F0006_OC.jpg

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Paternal and induced gut microbiota seeding complement mother-to-infant transmission.父系和诱导的肠道微生物群定植补充了母婴传播。
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