Evidence map›Paper›PMID 42726894›Full record

ArticlePLoS neglected tropical diseases2026

Vampire bats in Belize harbor multiple Trypanosoma cruzi genotypes: Implications for parasite transmission at the wildlife-domestic-human interface.

Annalise Dunsmore, Kristin E Dyer, Lauren R Lock, Weihong Tu, M Brock Fenton, Nancy B Simmons, Eric Dumonteil, Daniel J Becker, Claudia P Herrera

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Annalise DunsmoreDepartment of Tropical Medicine, Celia Scott Weatherhead School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, United States of America.
Kristin E DyerSchool of Biological Sciences, University of Oklahoma, Norman, Oklahoma, United States of America.
Lauren R LockSchool of Biological Sciences, University of Oklahoma, Norman, Oklahoma, United States of America.
Weihong TuDepartment of Tropical Medicine, Celia Scott Weatherhead School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, United States of America.
M Brock FentonDepartment of Biology, Western University, London, Ontario, Canada.
Nancy B SimmonsDepartment of Mammalogy, Division of Vertebrate Zoology, American Museum of Natural History, New York, New York, United States of America.
Eric DumonteilDepartment of Tropical Medicine, Celia Scott Weatherhead School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, United States of America.
Daniel J BeckerSchool of Biological Sciences, University of Oklahoma, Norman, Oklahoma, United States of America.
Claudia P HerreraDepartment of Tropical Medicine, Celia Scott Weatherhead School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, United States of America.ORCID https://orcid.org/0000-0002-9009-4201

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChagas disease, caused by Trypanosoma cruzi, is a neglected tropical disease with complex sylvatic and domestic transmission cycles involving vectors, mammalian hosts, and humans. The common vampire bat (Desmodus rotundus) is an obligate blood-feeding species that frequently interacts with livestock and humans, yet their role in parasite maintenance in Central America remains poorly characterized. METHODOLOGY/PRINCIPAL

findingsWe analyzed 207 blood samples from vampire bats collected at two sites in northern Belize over three years (2019, 2021, 2022). PCR screening revealed an overall T. cruzi prevalence of 41.5% and increasing infection risks over time. The amplicon-based next-generation sequencing of the parasite mini-exon locus identified 36 unique haplotypes belonging to five DTUs: TcI, TcIV, TcV, TcVI, and TcBat. TcBat was present in half of the samples sequenced. TcBat and TcVI were detected in Belize for the first time. Belizean TcBat haplotypes clustered closely with Colombian reference sequences and a subset formed a Belize-specific clade, indicating previously unrecognized TcBat diversity in the region; in contrast, Brazilian TcBat sequences were more distantly related. CONCLUSIONS/SIGNIFICANCE: Vampire bats in Belize harbor diverse T. cruzi genotypes, including DTUs with established roles in human disease. Given their obligate blood diet, frequent feeding on livestock, and occasional biting of humans, vampire bats may serve as bridge hosts linking sylvatic, domestic, and human transmission cycles. Together with a recent report of an acute human Chagas disease case in northern Belize, these results underscore the need for integrated One Health surveillance of bats, vectors, livestock, and humans to better evaluate and mitigate the risk of Chagas disease in Central America.

Indexed as

Chagas DiseaseChiropteraTrypanosoma cruziAnimalsAnimals, WildBelizeGenotypeHaplotypesHumansPhylogeny

Identifiers

PMID42726894
PMCPMC13592685

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.