Literature DB >> 33505796

Genomic diversity of Escherichia coli from healthy children in rural Gambia.

Ebenezer Foster-Nyarko1,2, Nabil-Fareed Alikhan1, Usman N Ikumapayi2, Golam Sarwar2, Catherine Okoi2, Peggy-Estelle Maguiagueu Tientcheu2, Marianne Defernez1, Justin O'Grady1, Martin Antonio2,3, Mark J Pallen1,4.   

Abstract

Little is known about the genomic diversity of Escherichia coli in healthy children from sub-Saharan Africa, even though this is pertinent to understanding bacterial evolution and ecology and their role in infection. We isolated and whole-genome sequenced up to five colonies of faecal E. coli from 66 asymptomatic children aged three-to-five years in rural Gambia (n = 88 isolates from 21 positive stools). We identified 56 genotypes, with an average of 2.7 genotypes per host. These were spread over 37 seven-allele sequence types and the E. coli phylogroups A, B1, B2, C, D, E, F and Escherichia cryptic clade I. Immigration events accounted for three-quarters of the diversity within our study population, while one-quarter of variants appeared to have arisen from within-host evolution. Several isolates encode putative virulence factors commonly found in Enteropathogenic and Enteroaggregative E. coli, and 53% of the isolates encode resistance to three or more classes of antimicrobials. Thus, resident E. coli in these children may constitute reservoirs of virulence- and resistance-associated genes. Moreover, several study strains were closely related to isolates that caused disease in humans or originated from livestock. Our results suggest that within-host evolution plays a minor role in the generation of diversity compared to independent immigration and the establishment of strains among our study population. Also, this study adds significantly to the number of commensal E. coli genomes, a group that has been traditionally underrepresented in the sequencing of this species. ©2021 Foster-Nyarko et al.

Entities:  

Keywords:  Escherichia coli; Genomic diversity; Within-host evolution

Year:  2021        PMID: 33505796      PMCID: PMC7796664          DOI: 10.7717/peerj.10572

Source DB:  PubMed          Journal:  PeerJ        ISSN: 2167-8359            Impact factor:   2.984


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