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儿童单次口服阿奇霉素后肠道微生物多样性和抗菌药物耐药性的变化:一项随机安慰剂对照试验。

Gut Microbiome Diversity and Antimicrobial Resistance After a Single Dose of Oral Azithromycin in Children: A Randomized Placebo-Controlled Trial.

机构信息

Francis I. Proctor Foundation, University of California, San Francisco, California.

Department of Ophthalmology, University of California, San Francisco, California.

出版信息

Am J Trop Med Hyg. 2024 Jan 16;110(2):291-294. doi: 10.4269/ajtmh.23-0651. Print 2024 Feb 7.

DOI:10.4269/ajtmh.23-0651
PMID:38227963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10859792/
Abstract

Mass antibiotic distribution to preschool children resulted in alterations of the gut microbiome months after distribution. This individually randomized, placebo-controlled trial evaluated changes in the gut microbiome and resistome in children aged 8 days to 59 months after one dose of oral azithromycin in Burkina Faso. A total of 450 children were randomized in a 1:1 ratio to either placebo or azithromycin. Rectal samples were collected at baseline, 2 weeks, and 6 months after randomization and subjected to DNA deep sequencing. Gut microbiome diversity and normalized antimicrobial resistance determinants for different antibiotic classes were evaluated. Azithromycin decreased gut bacterial diversity (Shannon P < 0.0001; inverse Simpson P < 0.001) 2 weeks after treatment relative to placebo. Concurrently, the normalized abundance of macrolide resistance genetic determinants was 243-fold higher (95% CI: 76-fold to 776-fold, P < 0.0001). These alterations did not persist at 6 months, suggesting that disruptions were transient. Furthermore, we were unable to detect resistance changes in other antibiotic classes, indicating that co-resistance with a single course of azithromycin when treated at the individual level was unlikely.

摘要

大规模给学龄前儿童使用抗生素会导致肠道微生物组在分发后数月发生改变。本项在布基纳法索开展的、个体随机、安慰剂对照试验评估了在单次口服阿奇霉素后 8 天至 59 个月时,儿童肠道微生物组和耐药组的变化。共有 450 名儿童以 1:1 的比例随机分为安慰剂组或阿奇霉素组。在随机分组后 2 周和 6 个月时收集直肠样本,并进行 DNA 深度测序。评估了不同抗生素类别下肠道微生物组多样性和标准化抗菌药物耐药决定因素。与安慰剂相比,阿奇霉素治疗后 2 周时肠道细菌多样性降低(Shannon,P<0.0001;Inverse Simpson,P<0.001)。同时,大环内酯类耐药遗传决定因素的标准化丰度增加了 243 倍(95%CI:76 倍至 776 倍,P<0.0001)。这些变化在 6 个月时并未持续存在,提示这些破坏是短暂的。此外,我们未能检测到其他抗生素类别的耐药变化,这表明在个体水平接受单次阿奇霉素治疗时不太可能产生与单一疗程相关的共同耐药性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a5d/10859792/0cc30f5c5d18/ajtmh.23-0651f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a5d/10859792/0ebced34f6f1/ajtmh.23-0651f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a5d/10859792/0cc30f5c5d18/ajtmh.23-0651f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a5d/10859792/0ebced34f6f1/ajtmh.23-0651f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a5d/10859792/0cc30f5c5d18/ajtmh.23-0651f2.jpg

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