bioRxivMicrobiologyPreprint
Faecal carriage of ESBL-producing Escherichia coli in a remote region of Niger
H. Jacquier, B. Assao, F. Chau, O. Guindo, B. Condamine, M. Magnan, A. Bridier-Nahmias, N. Sayingoza-Makombe, A. Moumouni, A.-L. Page, C. Langendorf, M. Coldiron, E. Denamur, V. de Lastours
Abstract
ObjectiveWhole genome sequencing (WGS) of extended-spectrum {beta}-lactamase-producing Escherichia coli (ESBL-E. coli) in developing countries is lacking. Here we describe the population structure and molecular characteristics of ESBL-E. coli faecal isolates in rural Southern Niger. MethodsStools of 383 healthy participants were collected among which 92.4% were ESBL-E. coli carriers; 90 of these ESBL-E. coli containing stools (109 ESBL-E. coli isolates) were further analysed by WGS, using short- and long-reads. ResultsMost isolates belonged to the commensalism-adapted phylogroup A (83.5%), with high clonal diversity. The blaCTX-M-15 gene was the major ESBL determinant (98.1%), chromosome-integrated in approximately 50% of cases, in multiple integration sites. When plasmid-borne, blaCTX-M-15 was found in IncF (57.4%) and IncY plasmids (26.2%). Closely related plasmids were found in different genetic backgrounds. Genomic environment analysis of blaCTX-M-15 in closely related strains argued for mobilisation between plasmids or from plasmid to chromosome. ConclusionsMassive prevalence of community faecal carriage of CTX-M-15-producing E. coli was observed in a rural region of Niger due to the spread of highly diverse A phylogroup commensalism-adapted clones, with frequent chromosomal integration of blaCTX-M-15. Plasmid spread was also observed. These data suggest a risk of sustainable implementation of ESBL in community faecal carriage.
- organism: E. coli
- assay: whole-genome sequencing
- research focus: cell type annotation
- approach: experimental assay
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