Evidence map›Paper›PMID 42139514›Full record

ArticleThe Journal of infectious diseases2026

Genetic Evidence of Cross-Border Plasmodium vivax Spread in a Malaria Pre-elimination Region of South Asia.

Anjana Rai, Edwin Sutanto, Prakash Ghimire, Sonam Wangchuk, Tobgyel Drukpa, Mohammad Shafiul Alam, Najia Ghanchi, Awab Gulam Rahim, Angela Rumaseb, Hidayat Trimarsanto and 14 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

24 authors.

Anjana RaiGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.ORCID 0009-0005-9299-5715
Edwin SutantoGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.ORCID 0000-0002-2997-4648
Prakash GhimireCentral Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.ORCID 0000-0003-2503-412X
Sonam WangchukPublic Health Laboratory, Department of Public Health, Ministry of Health, Thimphu, Bhutan.
Tobgyel DrukpaPublic Health Laboratory, Department of Public Health, Ministry of Health, Thimphu, Bhutan.
Mohammad Shafiul AlamInfectious Diseases Division, International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR,B), Dhaka, Bangladesh.ORCID 0000-0001-8330-5499
Najia GhanchiDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Awab Gulam RahimDepartment of Public and Global Health, Afghan International Islamic University, Kabul, Afghanistan.
Angela RumasebGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.
Hidayat TrimarsantoGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.
Kian Soon HoonGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.
Nabaraj AdhikariCentral Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Sanjib AdhikariCentral Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.ORCID 0000-0002-5874-2547
Megha Raj BanjaraCentral Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.ORCID 0000-0002-5024-6127
Komal Raj RijalCentral Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.ORCID 0000-0001-6281-8236
Roshan NepalCentral Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Ramesh Sharma RegmiCentral Department of Microbiology, Tribhuvan University, Kirtipur, Kathmandu, Nepal.ORCID 0000-0003-3412-6165
Bushra QurashiDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Shan-E-Zehra ZaidiDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Mohammad Asim BegDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Benedikt LeyGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.ORCID 0000-0002-5734-0845
Ric N PriceGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.ORCID 0000-0003-2000-2874
Kamala ThriemerGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.ORCID 0000-0001-7536-7497
Sarah AuburnGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territory, Australia.ORCID 0000-0002-4638-536X

Funding

Australian Centre for Research Excellence in Malaria Elimination 1134989Bill & Melinda Gates Foundation INV-043618MenziesNational Health and Medical Research Council of Australia GNT2025377
6 · The paper itself

Abstract

backgroundPlasmodium vivax is the predominant cause of malaria in South Asia. P. vivax cases have fallen over the past decade, but cross-border transmission remains a major challenge to elimination. Genetic data can generate valuable insights into transmission; however, until now, only low-resolution data have been available from Nepal, Bhutan and Bangladesh. We piloted high-resolution genotyping using a new microhaplotype (multiallelic) assay to monitor P. vivax transmission across borders.

methodsGenotyping was conducted using the 93-microhaplotype vivaxGEN panel on P. vivax parasites collected from patients enrolled in clinical trials in Bangladesh, Bhutan, and Nepal between 2013 and 2023. These data were compared with open-access microhaplotype and genomic data derived from Afghanistan, India, and Pakistan between 2014 and 2024. Complexity and relatedness (identity by descent [IBD]) were determined within and between countries.

resultsHigh-quality genotyping data were generated for Nepal (n = 19), Bhutan (n = 27), and Bangladesh (n = 35); comparative data were sourced from Afghanistan (n = 159), India (n = 24), and Pakistan (n = 213). High-complexity infections were observed in 27.04% (43/159) of isolates from Afghanistan, 16.43% (35/213) from Pakistan, and 28.57% (10/35) from Bangladesh. Low prevalence of high-complexity infections was observed in Bhutan (3.70%; 1/27) and Nepal (5.26%; 1/19), suggesting lower superinfection or co-infection. Country-wide IBD analyses revealed 3 genetic clusters partitioning Bangladesh and Bhutan (partial) from the remaining countries. There were 2 subpopulations in Bhutan, which separated local and cross-border imported cases.

conclusionsOur results highlight the use of regional high-resolution genetic data to enhance monitoring of transmission intensity and cross-border importations.

Indexed as

Malaria, VivaxPlasmodium vivaxAfghanistanBhutanGenetic VariationGenotypeHumansNepalSouth Asian Peoplecross-border transmissiongenotypingmalariaPlasmodium vivax; population structureSouth Asia

Identifiers

PMID42139514
PMCPMC13600386

What OpenQuestion holds

Textmetadata
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.