Evidence map›Paper›PMID 32243630›Full record

ArticleMolecular ecology2020

Ecological and evolutionary drivers of haemoplasma infection and bacterial genotype sharing in a Neotropical bat community.

Daniel J Becker, Kelly A Speer, Alexis M Brown, M Brock Fenton, Alex D Washburne, Sonia Altizer, Daniel G Streicker, Raina K Plowright, Vladimir E Chizhikov, Nancy B Simmons and 1 more

Abstract read
In one paragraph

Article in Molecular ecology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

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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

11 authors.

Daniel J BeckerDepartment of Biology, Indiana University, Bloomington, IN, USA.ORCID 0000-0003-4315-8628
Kelly A SpeerRichard Gilder Graduate School, American Museum of Natural History, New York, NY, USA.ORCID 0000-0002-8775-7254
Alexis M BrownDepartment of Ecology and Evolution, Stony Brook University, Stony Brook, NY, USA.ORCID 0000-0003-4258-0501
M Brock FentonDepartment of Biology, Western University, London, ON, Canada.
Alex D WashburneDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT, USA.ORCID 0000-0002-6174-0526
Sonia AltizerCenter for the Ecology of Infectious Disease, University of Georgia, Athens, GA, USA.ORCID 0000-0001-9966-2773
Daniel G StreickerOdum School of Ecology, University of Georgia, Athens, GA, USA.ORCID 0000-0001-7475-2705
Raina K PlowrightDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT, USA.ORCID 0000-0002-3338-6590
Vladimir E ChizhikovCenter for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USA.
Nancy B SimmonsRichard Gilder Graduate School, American Museum of Natural History, New York, NY, USA.ORCID 0000-0001-8807-7499
Dmitriy V VolokhovCenter for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USA.ORCID 0000-0003-3363-8361

Funding

Research Core (Developmental Research Project Program)P20GM103474 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI Jeffrey Good · 2012 to 2026
$60.0M
Pilot Grants ProgramP30GM110732 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI QUINN, MARK T · 2014 to 2018
$5.4M
Medical Research Council MC_UU_12014/8NIGMS NIH HHS P20 GM103474NIGMS NIH HHS P30 GM110732Wellcome TrustWellcome Trust 102507/Z/13/Z
6 · The paper itself

Abstract

Most emerging pathogens can infect multiple species, underlining the importance of understanding the ecological and evolutionary factors that allow some hosts to harbour greater infection prevalence and share pathogens with other species. However, our understanding of pathogen jumps is based primarily around viruses, despite bacteria accounting for the greatest proportion of zoonoses. Because bacterial pathogens in bats (order Chiroptera) can have conservation and human health consequences, studies that examine the ecological and evolutionary drivers of bacterial prevalence and barriers to pathogen sharing are crucially needed. Here were studied haemotropic Mycoplasma spp. (i.e., haemoplasmas) across a species-rich bat community in Belize over two years. Across 469 bats spanning 33 species, half of individuals and two-thirds of species were haemoplasma positive. Infection prevalence was higher for males and for species with larger body mass and colony sizes. Haemoplasmas displayed high genetic diversity (21 novel genotypes) and strong host specificity. Evolutionary patterns supported codivergence of bats and bacterial genotypes alongside phylogenetically constrained host shifts. Bat species centrality to the network of shared haemoplasma genotypes was phylogenetically clustered and unrelated to prevalence, further suggesting rare-but detectable-bacterial sharing between species. Our study highlights the importance of using fine phylogenetic scales when assessing host specificity and suggests phylogenetic similarity may play a key role in host shifts not only for viruses but also for bacteria. Such work more broadly contributes to increasing efforts to understand cross-species transmission and the epidemiological consequences of bacterial pathogens.

Indexed as

ChiropteraAnimalsBacteriaBelizeGenotypeHumansMalePhylogeny16S rRNAbacterial zoonosiscophylogenyhost shiftshost specificityMycoplasmaparasite sharing

Identifiers

PMID32243630
PMCPMC8299350

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.