Evidence map›Paper›PMID 42435377›Full record

ArticleMolecular ecology2026

Longitudinal Impacts of Forest Loss on Bartonella and Hemotropic Mycoplasma Dynamics in Vampire Bats Within a Fragmented Habitat.

Lauren R Lock, Kristin E Dyer, Dmitriy V Volokhov, Anni Yang, M Brock Fenton, Nancy B Simmons, Daniel J Becker

Abstract read
In one paragraph

Article in Molecular ecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Lauren R LockSchool of Biological Sciences, University of Oklahoma, Norman, Oklahoma, USA.ORCID https://orcid.org/0009-0003-1731-1235
Kristin E DyerSchool of Biological Sciences, University of Oklahoma, Norman, Oklahoma, USA.
Dmitriy V VolokhovCenter for Biologics Evaluation & Research, U.S. Food & Drug Administration, Silver Spring, Maryland, USA.ORCID https://orcid.org/0000-0003-3363-8361
Anni YangDepartment of Geography and Environmental Sustainability, University of Oklahoma, Norman, Oklahoma, USA.ORCID https://orcid.org/0000-0002-9535-2193
M Brock FentonDepartment of Biology, Western University, London, Canada.
Nancy B SimmonsDivision of Vertebrate Zoology, Department of Mammalogy, American Museum of Natural History, New York, New York, USA.
Daniel J BeckerSchool of Biological Sciences, University of Oklahoma, Norman, Oklahoma, USA.ORCID https://orcid.org/0000-0003-4315-8628

Funding

Achievement Rewards for College Scientists FoundationAmerican Museum of Natural HistoryAmerican Society of MammalogistsEdward Mallinckrodt, Jr. FoundationExplorers ClubNational Geographic Society NGS-55503R-19National Science Foundation DEB 1601052National Science Foundation DEB 2508535Research Corporation for Scientific Advancement 58-3022-0-005University of Oklahoma Libraries
6 · The paper itself

Abstract

Habitat fragmentation can negatively impact wildlife, including increasing infectious disease risk. We assessed spatiotemporal changes in pathogen dynamics in vampire bats (Desmodus rotundus) in response to habitat fragmentation using general linear mixed models to investigate the influence of site, year, and tree cover on Bartonella spp. and hemotropic Mycoplasma spp. (hemoplasmas) infection risk in bats in one large and one small forest fragment in Belize across seven years. While Bartonella infections were more likely in the final years of the study regardless of site, hemoplasma infection likelihood was not significantly different across years or sites. Bartonella infections were associated with increased forest loss in the large fragment only, whereas hemoplasma infections were not associated with forest loss. The effects of site, year, and forest loss on infection likelihood varied by pathogen genotype despite low model explanatory power. Neither site nor year was associated with bartonellae, but one genotype was positively associated with tree cover. Two hemoplasmas were influenced by year with differing trends: one genotype was negatively associated with tree loss across sites, while another was positively associated with forest loss at the small fragment only. Both pathogens were similarly influenced by bat demographics and showed instances of infection status and genotype switching. Our work suggests that the effects of habitat fragmentation on infection risk depend on both the pathogen and specific genotype, complicating expectations of how environmental change affects wildlife disease dynamics. Efforts to mitigate infectious disease impacts in fragmented systems should be tailored to specific pathogens of concern.

Indexed as

BartonellaChiropteraEcosystemForestsMycoplasmaAnimalsBartonella InfectionsGenotypeMycoplasma InfectionsbartonellaeDesmodus rotundushemoplasmasland‐use change

Identifiers

PMID42435377
PMCPMC13355873

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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.