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

Author:

Doan Thuy12,Liu Zijun2,Sié Ali3,Dah Clarisse3,Bountogo Mamadou3,Ouattara Mamadou3,Coulibaly Boubacar3,Kiemde Dramane3,Zonou Guillaume3,Nebie Eric3,Brogdon Jessica1,Lebas Elodie1,Hinterwirth Armin1,Zhong Lina1,Chen Cindi1,Zhou Zhaoxia1,Porco Travis124,Arnold Benjamin F.14,Oldenburg Catherine E.145,Lietman Thomas M.1245

Affiliation:

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

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

3. Centre de Recherche en Santé de Nouna, Nouna, Burkina Faso;

4. Department of Epidemiology and Biostatistics, University of California, San Francisco, California;

5. Institute for Global Health Sciences, University of California, San Francisco, California

Abstract

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.

Publisher

American Society of Tropical Medicine and Hygiene

Reference13 articles.

1. Azithromycin to reduce childhood mortality in sub-Saharan Africa;Keenan,2018

2. Longer-term assessment of azithromycin for reducing childhood mortality in Africa;Keenan,2019

3. Trachoma;Solomon,2022

4. Antimicrobial resistance following mass azithromycin distribution for trachoma: a systematic review;O’Brien,2019

5. Macrolide and nonmacrolide resistance with mass azithromycin distribution;Doan,2020

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