# Exploring the Genetic Diversity, Virulence and Antimicrobial Resistance of Diarrhoeagenic Escherichia coli From Southern Africa Using Whole‐Genome Data

**Authors:** Josphat Gichure, Tina Hald, Elna Buys

PMC · DOI: 10.1002/puh2.70098 · Public Health Challenges · 2025-08-12

## TL;DR

This study uses whole-genome sequencing to explore the genetic diversity, virulence, and antibiotic resistance of Escherichia coli causing diarrhea in Southern Africa, revealing regional transmission patterns and public health risks.

## Contribution

The study provides new insights into DEC genetic diversity and antimicrobial resistance patterns in Southern Africa, highlighting region-specific lineages and horizontal gene transfer.

## Key findings

- Region-specific DEC lineages were identified, with clustering based on geography, sample niche, and pathovar.
- Common virulence genes included eae (63.97%), LT (25.00%), and Stx1 (15.44%), with inverse associations between LT and eae.
- High resistance to sulfamethoxazole (55.9%), β-lactamases (54.4%), and streptomycin (55.1%) was observed, suggesting horizontal gene transfer.

## Abstract

Introduction: Previous studies, including our research, provide critical insights on the contamination of food, water and environment in the Southern African Development Community (SADC) with diarrhoeagenic Escherichia coli (DEC). This study used whole‐genome sequencing to investigate the genetic diversity, virulence‐associated factors and antimicrobial resistance (AMR) patterns of DEC isolated from children under 5 years old and food sources in Maputo and compared these findings with publicly available DEC genome assemblies from the Southern Africa region.

Methods: Whole‐genome sequence data from 11 DEC isolates from food, children under 5 and water sources in Maputo, Mozambique, were analysed alongside 125 publicly available DEC genomic assemblies from the SADC region. The latter were retrieved from the EnteroBase database (http://enterobase.warwick.ac.uk) and included isolates previously collected from food, animals and environmental sources. Genomic analyses were performed using the online pipelines provided by the Centre for Genomic Epidemiology (CGE), Denmark. Unsupervised hierarchical clustering was applied to visualize patterns in genetic diversity, AMR, virulence‐associated genes and plasmid content using the R software.

Results: Clustering based on single nucleotide polymorphism (SNP) and core genome multilocus sequence typing (cgMLST) alleles revealed associations based on geographic locations, sample niche, pathovar and O:H antigen, pointing to evolutionary relatedness between the clades with principal coordinate analysis uncovering this accounted for 27.55% of the genetic diversity. Virulence‐associated genes encoding for attaching and effacing (eae) (63.97%), heat‐labile toxin (LT) (25.00%) and Shiga toxin 1 (Stx1) (15.44%) were most abundant, with an inverse association between genes encoding for the presence of LT and eae. Resistance to folate pathway antagonists (sulfamethoxazole—55.9%), β‐lactamases (amoxicillin, ampicillin and piperacillin—all 54.4%) and aminoglycoside (streptomycin—55.1%) was most abundant.

Conclusions: The study revealed region‐specific lineages, evidence of horizontal gene transfer and the clustering patterns suggest both localized and cross‐border transmission. The study provides insightful evidence on DEC transmission patterns associated with antimicrobial and disinfectant resistance and associated virulence factors.

Whole genome insights into diarrhoeagenic Escherichia coli (DEC) strains from Southern Africa

→ Study focus: Comparative genomics of DEC strains isolated from food, clinical and environmental sources in Southern Africa.

Key Findings:

1. High genetic diversity

→ Region‐specific distribution system observed from association trends between strains from similar geographic locations, sample niche, pathovar and O:H antigen, pointing to evolutionary relatedness between the clades.

2. Virulence gene profiles

→ Virulence‐associated genes encoding for attaching and effacing (eae) (63.97%), heat‐labile toxin (LT) (25.00%) and Shiga toxin 1 (Stx1) (15.44%) were most abundant.

3. Antimicrobial resistance (AMR)

→ Resistance to folate pathway antagonists (sulfamethoxazole—55.9%), β‐lactamases (amoxicillin, ampicillin and piperacillin—all 54.4%) and aminoglycoside (streptomycin—55.1%) were most abundant.

→ Antimicrobial resistance patterns among the DEC strains suggest horizontal gene transfer within similar geographical locations in Southern Africa.

Regional relevance:

→ Highlights the public health risk posed by DEC in food systems and human populations across the Southern African Development Community (SADC) region.

## Linked entities

- **Genes:** eae (T3SS intimin) [NCBI Gene 915471], LTA (lymphotoxin alpha) [NCBI Gene 4049], STX1A (syntaxin 1A) [NCBI Gene 6804]
- **Chemicals:** sulfamethoxazole (PubChem CID 5329), amoxicillin (PubChem CID 33613), ampicillin (PubChem CID 6249), piperacillin (PubChem CID 43672), streptomycin (PubChem CID 5297)
- **Diseases:** diarrhea (MONDO:0001673)
- **Species:** Escherichia coli (taxon 562)

## Full-text entities

- **Diseases:** DEC (MESH:D004927)
- **Chemicals:** streptomycin (MESH:D013307), piperacillin (MESH:D010878), -lactamases (-), amoxicillin (MESH:D000658), folate (MESH:D005492), sulfamethoxazole (MESH:D013420), ampicillin (MESH:D000667), aminoglycoside (MESH:D000617)

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12342054/full.md

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Source: https://tomesphere.com/paper/PMC12342054