# Comparative genomics of blood and faecal E. coli and K. pneumoniae isolates from neonates with bloodstream infections in Tanzania

**Authors:** Richard N. Goodman, Sabrina J. Moyo, Ilinca Memelis, Aakash Khanijau, Joel Manyahi, Upendo O. Kibwana, Said Aboud, Bjørn Blomberg, Nina Langeland, Adam P. Roberts

PMC · DOI: 10.1038/s42003-025-09008-5 · 2025-11-18

## TL;DR

This study compares bacteria from the blood and gut of newborns in Tanzania to understand how gut bacteria can cause bloodstream infections.

## Contribution

The study provides evidence of translocation of E. coli and K. pneumoniae from the gut to the bloodstream in neonates with bloodstream infections.

## Key findings

- Highly related pairs of E. coli and K. pneumoniae were found in blood and faecal isolates from the same neonates.
- Key virulence genes and mutations were identified in strains associated with bloodstream infections.
- The findings suggest translocation from the gastrointestinal tract to the bloodstream is a common pathway for infection.

## Abstract

Bloodstream infections (BSIs) are a major cause of hospitalisation and death for children under the age of five in sub-Saharan Africa, with Gram-negative bacteria such as Klebsiella pneumoniae and Escherichia coli among the most common causative agents. These bacteria usually colonise the human gastrointestinal (GI) tract, which has been identified as a reservoir for invasive infections into extra-intestinal environments such as the urinary tract and bloodstream. In this study we used comparative genomics to compare hybrid genome assemblies of blood and faecal bacterial isolates taken from the same patients (all neonates under 19 days old) to determine if the BSI associated isolates and the GI tract associated isolates were related. Multiple pairs of highly related E. coli and K. pneumoniae were found, suggesting that translocation between the GI tract and the bloodstream occurred in multiple cases of BSI. We also highlight key virulence genes and acquired mutations that are indicative of pathogenic strains capable of BSI. These findings expand our understanding of the Gram-negative bacteria involved in BSI pathogenicity and could help guide targeted interventions to prevent future BSI infections in neonates.

Genomic comparison of E. coli and K. pneumoniae isolated from faeces and blood of the same neonatal patients revealed highly related pairs, suggesting translocation between the gastrointestinal tract and the bloodstream occurred in multiple patients.

## Linked entities

- **Species:** Escherichia coli (taxon 562), Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Diseases:** BSI infections (MESH:D007239), BSIs (MESH:D018805), death (MESH:D003643)
- **Species:** Homo sapiens (human, species) [taxon 9606], Klebsiella pneumoniae (species) [taxon 573], Escherichia coli (E. coli, species) [taxon 562]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12627497/full.md

---
Source: https://tomesphere.com/paper/PMC12627497