Gut microbiome diversity and composition in individuals with and without extended-spectrum β-lactamase-producing Enterobacterales carriage: a matched case–control study in infectious diseases department

马车 医学 生物 人口 内科学 微生物学 环境卫生 病理
作者
Anders Boyd,Mariam El Dani,Roula Ajrouche,Vanessa Démontant,Justine Cheval,Karine Lacombe,Guillaume Cosson,Christophe Rodriguez,Jean–Michel Pawlotsky,Paul‐Louis Woerther,Laure Surgers
出处
期刊:Clinical Microbiology and Infection [Elsevier BV]
卷期号:30 (9): 1154-1163 被引量:4
标识
DOI:10.1016/j.cmi.2024.03.016
摘要

Objective Little is known on the effect of gut microbial and Extended-Spectrum β-Lactamase-Producing Enterobacterales (ESBL-E) carriage, particularly in the general population. The aim of this study was to identify microbiota signatures uniquely correlated with ESBL-E carriage. Methods We conducted a case-control study among individuals seeking care at the Sexual Health Clinic or Department of Infectious and Tropical Diseases at Saint-Antoine Hospital, Paris, France. Using coarsened exact matching, 176 participants with ESBL-carriage (i.e., cases) were matched 1:1 to those without ESBL-carriage (i.e., controls) based on sexual group, ESBL-E prevalence of countries traveled in <12 months, number of sexual partners in <6 months, geographic origin, and any antibiotic use in <6 months. 16S rRNA gene amplicon sequencing was used to generate differential abundances at the genus level and measures of α- and β-diversity. Results Participants were mostly men (83.2%, n=293/352) and had a median age of 33 years (IQR=27-44). Nine genera were found associated with ESBL-E carriage (Figure 2C): Proteus (p<0.0001), Carnobacterium (p<0.0001), Enterorhabdus (p=0.0079), Catonella (p=0.017), Dermacoccus (p=0.017), Escherichia/Shigella (p=0.021), Kocuria (p=0.023), Bacillus (p=0.040), and Filifactor (p=0.043); however, differences were no longer significant after Benjamini-Hochberg correction (q>0.05). There were no differences between those with versus without ESBL-E carriage in measures of α-diversity (Shannon Diversity Index, p=0.49; Simpson Diversity Index, p=0.54; and Chao1 Richness Estimator, p=0.16) or β-diversity (Bray-Curtis dissimilarity index, p=0.42). Conclusion In this large carefully controlled study, there is lacking evidence that gut microbial composition and diversity is any different between individuals with and without ESBL-E carriage.
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