Evidence map›Paper›PMID 41254151›Full record

ArticleCommunications biology2025

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

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

Abstract readComparative StudyMulticenter StudyComparative Study
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Richard N GoodmanDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, UK.ORCID http://orcid.org/0009-0008-0578-789X
Sabrina J MoyoDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Ilinca MemelisDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Aakash KhanijauDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Joel ManyahiDepartment of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Upendo O KibwanaDepartment of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Said AboudDepartment of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Bjørn BlombergDepartment of Clinical Science, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0001-5647-4297
Nina LangelandDepartment of Clinical Science, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0003-0278-1616
Adam P RobertsDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, UK. Adam.Roberts@lstmed.ac.uk.ORCID http://orcid.org/0000-0002-0760-3088

Funding

Joint Programming Initiative on Antimicrobial Resistance (Joint Programming Initiative for Antimicrobial Resistance) MR/W030578/1Norges Forskningsråd (Research Council of Norway) NFR333432RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) MR/W030578/1RCUK | Medical Research Council (MRC) MR/W030578/1RCUK | Natural Environment Research Council (NERC) MR/W030578/1
6 · The paper itself

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.

Indexed as

BacteremiaBacterial TranslocationEscherichia coliEscherichia coli InfectionsKlebsiella InfectionsKlebsiella pneumoniaeCross-Sectional StudiesFecesGastrointestinal MicrobiomeGenome, BacterialGenomicsHumansInfant, NewbornProspective StudiesTanzania

Identifiers

PMID41254151
PMCPMC12627497

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.