Evidence map›Paper›PMID 41989089›Full record

ArticleJournal of travel medicine2026

Rapid whole-genome sequencing of Plasmodium DNA from cryptic malaria cases in UK travellers provides insights into infection origins, transmission and antimalarial resistance.

Mark K I Tan, Nina Billows, Debbie Nolder, Sophie Moss, Jody E Phelan, Joseph Thorpe, Jonathan L Edgeworth, Colin J Sutherland, Peter L Chiodini, Susana Campino and 1 more

Abstract read
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Article in Journal of travel medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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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.

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Mark K I TanFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.
Nina BillowsFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.ORCID 0000-0002-3786-6911
Debbie NolderFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.
Sophie MossFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.
Jody E PhelanFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.
Joseph ThorpeFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.ORCID 0009-0006-5860-0182
Jonathan L EdgeworthDepartment of Infectious Diseases, King's College London, St Thomas' Street, London SE1 9RT, UK.
Colin J SutherlandFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.ORCID 0000-0003-1592-6407
Peter L ChiodiniUK Health Security Agency (UKHSA) Malaria Reference Laboratory, LSHTM, Keppel Street, Camden, London WC1E 7HT, UK.
Susana CampinoFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.ORCID 0000-0003-1403-6138
Taane G ClarkFaculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine (LSHTM), Keppel Street, Camden, London WC1E 7HT, UK.ORCID 0000-0001-8985-9265

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe UK reports approximately 2000 imported malaria cases annually, necessitating effective surveillance to determine infection sources and transmission routes, inform strategies for prevention and detect molecular markers of drug resistance that may compromise treatment outcomes. Defined by their unclear route of infection, cryptic malaria cases pose a particular challenge for malaria surveillance because they may signify undetected localized transmission or malaria re-introduction and therefore necessitate additional public health resources and epidemiological investigations. Here, we demonstrate the utility of near-real-time whole-genome sequencing (WGS) in providing high genomic resolution and detailed molecular characterization to help resolve cryptic malaria cases in the UK.

methodsPlasmodium DNA (9 isolates) sourced from clinical blood samples underwent WGS using either Illumina or Oxford Nanopore Technologies (ONT) platforms. Sequence data were rapidly analysed with Malaria-Profiler, which performs read mapping, variant calling, quality control, drug resistance prediction and artificial intelligence (AI)-based geographic origin inference using a reference database of more than 15 000 isolate genomes. Plasmodium ovale spp. and P. falciparum infections identified among family members were further analysed to assess parasite relatedness using identity-by-descent and multiplicity of infection approaches to investigate transmission clusters.

resultsUsing a combination of Illumina and ONT WGS platforms alongside Malaria-Profiler, we rapidly profiled parasites from four cryptic P. falciparum malaria cases in the UK, identifying drug resistance markers and predicting geographic origins through AI-based methods. We also applied WGS to family-related clusters of P. ovale spp. and P. falciparum cases, confirming (sub)species identities and enabling fine-scale transmission cluster analysis.

conclusionsThis study highlights the power of real-time WGS and AI-enhanced tools for high-resolution malaria genomic surveillance. By enabling rapid characterization of cryptic and imported cases, this approach supports timely public health responses, including targeted epidemiological investigations and, where appropriate, the de-escalation of entomological surveillance. In doing so, this approach helps sustain malaria elimination in non-endemic settings.

Indexed as

DNA, ProtozoanDrug ResistanceMalariaPlasmodiumPlasmodium falciparumPlasmodium ovaleTravelWhole Genome SequencingAntimalarialsGenome, ProtozoanHumansUnited KingdomAntimalarialsDNA, Protozoancryptic malariadrug resistancegeographic originsmalaria profilingPlasmodium parasitestransmissionwhole-genome sequencing

Identifiers

PMID41989089
PMCPMC13318844

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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.