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

被引:1
|
作者
Doan, Thuy [1 ,6 ]
Liu, Zijun
Sie, Ali [3 ]
Dah, Clarisse [3 ]
Bountogo, Mamadou [3 ]
Ouattara, Mamadou [3 ]
Coulibaly, Boubacar [3 ]
Kiemde, Dramane [3 ]
Zonou, Guillaume [3 ]
Nebie, Eric [3 ]
Brogdon, Jessica [1 ]
Lebas, Elodie [1 ]
Hinterwirth, Armin [1 ]
Zhong, Lina [1 ]
Chen, Cindi [1 ]
Zhou, Zhaoxia [1 ]
Porco, Travis [1 ,2 ,4 ]
Arnold, Benjamin F. [1 ,4 ]
Oldenburg, Catherine E. [1 ,4 ,5 ]
Lietman, Thomas M. [1 ,2 ,4 ,5 ]
机构
[1] Univ Calif San Francisco, Francis I Proctor Fdn, San Francisco, CA USA
[2] Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA USA
[3] Ctr Rech Sante Nouna, Nouna, Burkina Faso
[4] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA USA
[5] Univ Calif San Francisco, Inst Global Hlth Sci, San Francisco, CA USA
[6] 490 Illinois St,Floor 2, San Francisco, CA 94158 USA
来源
关键词
CHILDHOOD MORTALITY;
D O I
10.4269/ajtmh.23-0651
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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.
引用
收藏
页码:291 / 294
页数:4
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