Whole-genome sequencing reveals inter-household networks of gut-colonising ESBL-producing Escherichia coli in two rural Malawian districts

Abstract Infection with extended-spectrum beta-lactamase-producing Escherichia coli (ESBL-Ec) is a global health concern that disproportionately affects sub-Saharan Africa. Gut mucosal colonisation is thought to precede invasive infection. Understanding ESBL-Ec colonisation and transmission across communities is therefore essential. Here, we investigate the genomic epidemiology and spatial structure of 159 gut-colonising ESBL-Ec isolates from the faeces of 211 people in two rural Malawian villages using longitudinal sampling (2023–24), whole-genome sequencing and household mapping. Colonisation prevalence rose from 34.1% (95% CI: 27.8–41.0) to 54.2% (95% CI: 46.0–62.3) over one year. Isolates belonged to 33 sequence types (STs), most commonly ST38 and ST131, harbouring 46 distinct antimicrobial resistance gene types. Fifteen strains were identified in ≥3 households that were typically separated by short geographic distances ( < 400 m). Of 190 pairwise comparisons between same-strain isolates from different households sampled concurrently within villages, 88.9% differed by ≤10 single nucleotide polymorphisms, consistent with multi-household involvement in community transmission networks. Lineage-specific ST38 and ST131 network analyses linked rural isolates to urban Malawian isolates collected within the last decade. Our findings provide a transferable framework for inferring ESBL-Ec flow in community settings and highlight the need for One Health surveillance and improved sanitation infrastructure to limit transmission.

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Publication Details

Journal
Nature Communications
Published
2026-10-14
DOI
https://doi.org/10.1038/s41467-026-78449-1
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
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0.00

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article

Whole-genome sequencing reveals inter-household networks of gut-colonising ESBL-producing Escherichia coli in two rural Malawian districts

Nicholas Feasey, David Lally, Ellie Allman, Joseph M. Lewis et al.
Nature Communications
Antibiotic Resistance in Bacteria
article

Whole-genome sequencing reveals inter-household networks of gut-colonising ESBL-producing Escherichia coli in two rural Malawian districts

Nicholas Feasey, David Lally, Ellie Allman, Joseph M. Lewis, Adam Paul Roberts, Peter Makaula, Janelisa Musaya, Patrick Musicha, Angus M. O’Ferrall, J. Russell Stothard, Sekeleghe Amos Kayuni, Claire S. Waddington, Richard N. Goodman, Sabrina John Moyo, Gladys Namacha
article en

Abstract

Abstract Infection with extended-spectrum beta-lactamase-producing Escherichia coli (ESBL-Ec) is a global health concern that disproportionately affects sub-Saharan Africa. Gut mucosal colonisation is thought to precede invasive infection. Understanding ESBL-Ec colonisation and transmission across communities is therefore essential. Here, we investigate the genomic epidemiology and spatial structure of 159 gut-colonising ESBL-Ec isolates from the faeces of 211 people in two rural Malawian villages using longitudinal sampling (2023–24), whole-genome sequencing and household mapping. Colonisation prevalence rose from 34.1% (95% CI: 27.8–41.0) to 54.2% (95% CI: 46.0–62.3) over one year. Isolates belonged to 33 sequence types (STs), most commonly ST38 and ST131, harbouring 46 distinct antimicrobial resistance gene types. Fifteen strains were identified in ≥3 households that were typically separated by short geographic distances ( < 400 m). Of 190 pairwise comparisons between same-strain isolates from different households sampled concurrently within villages, 88.9% differed by ≤10 single nucleotide polymorphisms, consistent with multi-household involvement in community transmission networks. Lineage-specific ST38 and ST131 network analyses linked rural isolates to urban Malawian isolates collected within the last decade. Our findings provide a transferable framework for inferring ESBL-Ec flow in community settings and highlight the need for One Health surveillance and improved sanitation infrastructure to limit transmission.

Nature Communications
University of Malawi (MW), University of St Andrews (GB), Liverpool School of Tropical Medicine (GB), Kamuzu Central Hospital (MW), Wellcome Sanger Institute (GB), Queen Elizabeth Central Hospital (MW), Kamuzu University of Health Sciences (MW)
Wellcome Trust, Medical Research Council
Good health and well-being
Openalex Percentile: Top 23%
Antibiotic Resistance in Bacteria
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