Evidence map›Paper›PMID 41734917›Full record

ArticleBMJ open2026

ALARUM: Active One Health surveillance in LMICs to monitor and predict Antimicrobial Resistance Using Metagenomics - a cross-sectional study protocol.

Marianne A B van der Sande, Daniel Valia, Caroline Tigoi, Nicole Stoesser, Linda Stamm, Andrea Marten, Bram Riems, Robert Musyimi, Yougbare Sibidou, Anita C Schurch and 9 more

Abstract read
In one paragraph

Article in BMJ open, 2026. 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
–field-weighted citation impact
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

19 authors.

Marianne A B van der SandeGlobal Public Health and Bioethics, Julius Center, University Medical Centre Utrecht, Utrecht, The Netherlands M.A.B.vanderSande@umcutrecht.nl.ORCID http://orcid.org/0000-0002-4778-6739
Daniel ValiaDirection Régionale du Centre-Ouest/Clinical Research Unit of Nanoro, Institut de Recherche en Sciences de la Santé, Ouagadougou, Burkina Faso.
Caroline TigoiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Nicole StoesserModernising Medical Microbiology, University of Oxford Nuffield Department of Medicine, Oxford, UK.
Linda StammPaediatric Research Centre, University Children's Hospital Basel, Basel, Switzerland.
Andrea MartenPaediatric Research Centre, University Children's Hospital Basel, Basel, Switzerland.ORCID http://orcid.org/0009-0008-3853-1276
Bram RiemsInstitute of Tropical Medicine Department of Public Health, Antwerp, Belgium.
Robert MusyimiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Yougbare SibidouDirection Régionale du Centre-Ouest/Clinical Research Unit of Nanoro, Institut de Recherche en Sciences de la Santé, Ouagadougou, Burkina Faso.
Anita C SchurchDepartment Medical Microbiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Eric W TiendrebeogoDirection Régionale du Centre-Ouest/Clinical Research Unit of Nanoro, Institut de Recherche en Sciences de la Santé, Ouagadougou, Burkina Faso.ORCID http://orcid.org/0009-0009-1142-0864
Shalton MwaringaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Malte Kohns VasconcelosPaediatric Research Centre, University Children's Hospital Basel, Basel, Switzerland.
Brecht IngelbeenInstitute of Tropical Medicine Department of Public Health, Antwerp, Belgium.ORCID http://orcid.org/0000-0002-2214-6858
Halidou TintoInstitut de Recherche en Sciences de la Sante, Ouagadougou, Burkina Faso.
Julia A BielickiPaediatric Research Centre, University Children's Hospital Basel, Basel, Switzerland.
Ben S CooperNuffield Department of Medicine, Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.
James A BerkleyKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID http://orcid.org/0000-0002-1236-849X
Esther van KleefNuffield Department of Medicine, Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-3312-7185

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn rural sub-Saharan Africa (sSA), the burden of antimicrobial resistance (AMR) remains high. As AMR continues to rise, there is a strong need for practical, implementable surveillance to monitor and mitigate risks, as well as inform timely, evidence-based clinical decision-making. Emerging evidence points to possible community-level drivers, such as transmission between human, animal and environmental reservoirs as contributing factors, yet microbiological surveillance or opportunities for wastewater-based surveillance are often limited and insufficient in these settings. Therefore, alternative sustainable and affordable approaches are needed. We intend to build on the demonstrated potential of metagenomic profiling of pooled faecal material, which accurately predicted population-level AMR prevalence in invasive METHODS AND ANALYSIS: We aim to validate this metagenomic pooled approach on additional populations, and to evaluate whether AMR patterns could be similarly predicted from surveillance of community One Health reservoirs. We will assemble existing data from hospital-based microbiology diagnostic laboratories in rural Burkina Faso and Kenya, and determine to what extent community-level metagenomic data, and/or faecal material of patients on hospital admission, can predict AMR in clinical isolates. We will perform community-level surveys in eight clusters per country, randomly selecting 15 households per cluster. We will systematically sample suspected environmental AMR exposure sites in and around households (soil, drinking water, latrines, chicken faeces) and collect data on community-level antibiotic use, hygiene practices, contact with domestic animals and sanitary facilities. Samples and data will be collected twice: during the dry and during the rainy season.In addition to evaluating the accuracy of predicting resistance in clinical isolates, we will quantify community-level exposure risks. We will conduct metagenomic profiling on pooled DNA extracts from human stool samples (hospital and community-level) and from household environments. Bayesian statistical models will quantify relationships between AMR gene abundance in the environment and in human stool, and invasive bacteria identified among clinical patients, accounting for geography and seasonality. A cost-utility analysis will determine under what circumstances the use of pooled metagenomic data to inform empirical antibiotic policies would represent an efficient use of resources. ETHICS AND DISSEMINATION: The proposed surveillance protocol is developed in partnership with local communities and local and international researchers and has received ethical approval in Kenya and Burkina Faso. It will assess whether intermittent, pooled-sample metagenomics provides a viable, low-cost and practical approach for population-level AMR surveillance in settings that-like many in rural sSA-lack systematic microbiological diagnostics and where sewage systems for wastewater-based surveillance are absent. By providing an alternative to routine microbiological-based surveillance where this proves challenging to implement, this approach may help improve treatment outcomes, contribute to equity and public health. Findings will be disseminated through peer-reviewed publications and academic conferences and will contribute to the recently proposed WHO AMR surveillance strategy, which combines survey-based approaches with routine AMR surveillance.

Indexed as

Anti-Bacterial AgentsDrug Resistance, BacterialMetagenomicsOne HealthAnimalsCross-Sectional StudiesFecesHumansAnti-Bacterial Agentsantimicrobial resistancehealth demographic surveillance systemsmobile genetic elementsone health surveillancepooled metagenomicspredictionsub-Sahara Africa

Identifiers

PMID41734917
PMCPMC12933788

What OpenQuestion holds

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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.