Evidence map›Paper›PMID 37207684›Full record

ArticleThe Lancet. Microbe2023

Investigating One Health risks for human colonisation with extended spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae in Malawian households: a longitudinal cohort study.

Derek Cocker, Kondwani Chidziwisano, Madalitso Mphasa, Taonga Mwapasa, Joseph M Lewis, Barry Rowlingson, Melodie Sammarro, Winnie Bakali, Chifundo Salifu, Allan Zuza and 17 more

Open access · goldAbstract read
In one paragraph

Article in The Lancet. Microbe, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
8.8field-weighted citation impact, top 1% of its field
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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
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  3. Genomic Surveillance of ESBL-ProducingPathogens (Basel, Switzerland) · 2026
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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

27 authors at 9 institutions in 3 countries.

Derek CockerMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK. Electronic address: derek.cocker@lstmed.ac.uk.
Kondwani ChidziwisanoCentre for Water, Sanitation, Health and Appropriate Technology Development, Malawi University of Business and Applied Sciences, Blantyre, Malawi; Department of Civil and Environmental Engineering, University of Strathclyde, Glasgow, UK.
Madalitso MphasaMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Taonga MwapasaCentre for Water, Sanitation, Health and Appropriate Technology Development, Malawi University of Business and Applied Sciences, Blantyre, Malawi.
Joseph M LewisDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK; Department of Clinical Infection, Microbiology and Immunology, University of Liverpool, Liverpool, UK.
Barry RowlingsonCentre for Health Informatics Computing and Statistics, Lancaster University, Lancaster, UK.
Melodie SammarroDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK; Centre for Health Informatics Computing and Statistics, Lancaster University, Lancaster, UK.
Winnie BakaliMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Chifundo SalifuMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Allan ZuzaMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Mary CharlesMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Tamandani MandulaMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Victor MaidenMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi.
Stevie AmosCentre for Water, Sanitation, Health and Appropriate Technology Development, Malawi University of Business and Applied Sciences, Blantyre, Malawi.
Shevin T JacobGlobal Health Security Department, Infectious Disease Institute, Makerere University, Kampala, Uganda.
Henry KajumbulaDepartment of Medical Microbiology, Makerere University, Kampala, Uganda.
Lawrence MugishaCollege of Health Sciences, and College of Veterinary Medicine, Animal Resources and Biosecurity, Makerere University, Kampala, Uganda; Conservation and Ecosystem Health Alliance, Kampala, Uganda.
David MusokeDepartment of Disease Control and Environmental Health, Makerere University, Kampala, Uganda.
Rachel ByrneCentre for Drugs and Diagnostics, Liverpool School of Tropical Medicine, Liverpool, UK.
Thomas EdwardsCentre for Drugs and Diagnostics, Liverpool School of Tropical Medicine, Liverpool, UK.
Rebecca LesterDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Nicola ElvissScience Group, United Kingdom Health Security Agency, London, UK.
Adam P RobertsDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Andrew C SingerUK Centre for Ecology and Hydrology, Wallingford, UK.
Christopher JewellCentre for Health Informatics Computing and Statistics, Lancaster University, Lancaster, UK.
Tracy MorseCentre for Water, Sanitation, Health and Appropriate Technology Development, Malawi University of Business and Applied Sciences, Blantyre, Malawi; Department of Civil and Environmental Engineering, University of Strathclyde, Glasgow, UK.
Nicholas A FeaseyMalawi Liverpool Wellcome Research Programme, Kamuzu University of Health Sciences, Blantyre, Malawi; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Liverpool School of Tropical Medicine · GBKamuzu University of Health SciencesMakerere University · UGMalawi University of Business and Applied SciencesLancaster University · GBMalawi-Liverpool-Wellcome Trust Clinical Research Programme · MWUniversity of Liverpool · GBUK Centre for Ecology & Hydrology · GBUniversity of Strathclyde · GB

Funding

Medical Research Council MR/S004793/1Wellcome Trust
6 · The paper itself

Abstract

backgroundLow-income countries have high morbidity and mortality from drug-resistant infections, especially from enteric bacteria such as Escherichia coli. In these settings, sanitation infrastructure is of variable and often inadequate quality, creating risks of extended-spectrum β-lactamase (ESBL)-producing Enterobacterales transmission. We aimed to describe the prevalence, distribution, and risks of ESBL-producing Enterobacterales colonisation in sub-Saharan Africa using a One Health approach.

methodsBetween April 29, 2019, and Dec 3, 2020, we recruited 300 households in Malawi for this longitudinal cohort study: 100 each in urban, peri-urban, and rural settings. All households underwent a baseline visit and 195 were selected for longitudinal follow-up, comprising up to three additional visits over a 6 month period. Data on human health, antibiotic usage, health-seeking behaviours, structural and behavioural environmental health practices, and animal husbandry were captured alongside human, animal, and environmental samples. Microbiological processing determined the presence of ESBL-producing E coli and Klebsiella pneumoniae, and hierarchical logistic regression was performed to evaluate the risks of human ESBL-producing Enterobacterales colonisation.

findingsA paucity of environmental health infrastructure and materials for safe sanitation was identified across all sites. A total of 11 975 samples were cultured, and ESBL-producing Enterobacterales were isolated from 1190 (41·8%) of 2845 samples of human stool, 290 (29·8%) of 973 samples of animal stool, 339 (66·2%) of 512 samples of river water, and 138 (46·0%) of 300 samples of drain water. Multivariable models illustrated that human ESBL-producing E coli colonisation was associated with the wet season (adjusted odds ratio 1·66, 95% credible interval 1·38-2·00), living in urban areas (2·01, 1·26-3·24), advanced age (1·14, 1·05-1·25), and living in households where animals were observed interacting with food (1·62, 1·17-2·28) or kept inside (1·58, 1·00-2·43). Human ESBL-producing K pneumoniae colonisation was associated with the wet season (2·12, 1·63-2·76).

interpretationThere are extremely high levels of ESBL-producing Enterobacterales colonisation in humans and animals and extensive contamination of the wider environment in southern Malawi. Urbanisation and seasonality are key risks for ESBL-producing Enterobacterales colonisation, probably reflecting environmental drivers. Without adequate efforts to improve environmental health, ESBL-producing Enterobacterales transmission is likely to persist in this setting.

fundingMedical Research Council, National Institute for Health and Care Research, and Wellcome Trust. TRANSLATION: For the Chichewa translation of the abstract see Supplementary Materials section.

Indexed as

Anti-Infective AgentsEscherichia coli InfectionsKlebsiella InfectionsOne HealthAnimalsbeta-LactamasesCohort StudiesEscherichia coliHumansKlebsiella pneumoniaeLongitudinal StudiesAnti-Infective Agentsbeta-Lactamases

Identifiers

PMID37207684
PMCPMC10319635
OpenAlexW4377042569

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.