Evidence map›Paper›PMID 30873523›Full record

ArticleIntegrative and comparative biology2019

Leukocyte Profiles Reflect Geographic Range Limits in a Widespread Neotropical Bat.

Daniel J Becker, Cecilia Nachtmann, Hernan D Argibay, Germán Botto, Marina Escalera-Zamudio, Jorge E Carrera, Carlos Tello, Erik Winiarski, Alex D Greenwood, Maria L Méndez-Ojeda and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Integrative and comparative biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
14.3field-weighted citation impact, top 1% of its field
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  9. Comparative staining ofVeterinary world · 2022
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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

17 authors at 11 institutions in 8 countries.

Daniel J BeckerOdum School of Ecology, University of Georgia, Athens, GA 30602, USA.
Cecilia NachtmannOdum School of Ecology, University of Georgia, Athens, GA 30602, USA.
Hernan D ArgibayDepartamento de Ecología, Genética y Evolución, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires C1428EGA, Argentina.
Germán BottoDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT 59715, USA.
Marina Escalera-ZamudioDepartment of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research, Berlin 10315, Germany.
Jorge E CarreraFacultad de Ciencias, Universidad Nacional de Piura, Piura 20009, Peru.
Carlos TelloAssociation for the Conservation and Development of Natural Resources, Lima 15037, Peru.
Erik WiniarskiDepartamento de Histología, Facultad de Medicina, Universidad de la República, Montevideo 11800, Uruguay.
Alex D GreenwoodDepartment of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research, Berlin 10315, Germany.
Maria L Méndez-OjedaFacultad de Medicina Veterinaria y Zootecnia, Universidad Veracruzana, Veracruz 91710, Mexico.
Elizabeth Loza-RubioCentro Nacional de Investigación Disciplinaria en Microbiología Animal, Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias, Mexico City 05110, Mexico.
Anne LavergneLaboratoire des Interactions Virus-Hôtes, Institut Pasteur de la Guyane, Cayenne, French Guiana F-97300, France.
Benoit de ThoisyLaboratoire des Interactions Virus-Hôtes, Institut Pasteur de la Guyane, Cayenne, French Guiana F-97300, France.
Gábor Á CzirjákDepartment of Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research, Berlin 10315, Germany.
Raina K PlowrightDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT 59715, USA.
Sonia AltizerOdum School of Ecology, University of Georgia, Athens, GA 30602, USA.
Daniel G StreickerOdum School of Ecology, University of Georgia, Athens, GA 30602, USA.
University of Georgia · USInstitut Pasteur de la Guyane · GFLeibniz Institute for Zoo and Wildlife Research · DEUniversidad de la República de Uruguay · UYCONAPAC · PEInstituto Nacional de Investigaciones Forestales Agrícolas y Pecuarias · MXMontana State University · USUniversidad de Buenos Aires · ARUniversidad Nacional de Piura · PEUniversidad Veracruzana · MXUniversity of Oxford · GB

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

Quantifying how the environment shapes host immune defense is important for understanding which wild populations may be more susceptible or resistant to pathogens. Spatial variation in parasite risk, food and predator abundance, and abiotic conditions can each affect immunity, and these factors can also manifest at both local and biogeographic scales. Yet identifying predictors and the spatial scale of their effects is limited by the rarity of studies that measure immunity across many populations of broadly distributed species. We analyzed leukocyte profiles from 39 wild populations of the common vampire bat (Desmodus rotundus) across its wide geographic range throughout the Neotropics. White blood cell differentials varied spatially, with proportions of neutrophils and lymphocytes varying up to six-fold across sites. Leukocyte profiles were spatially autocorrelated at small and very large distances, suggesting that local environment and large-scale biogeographic factors influence cellular immunity. Generalized additive models showed that bat populations closer to the northern and southern limits of the species range had more neutrophils, monocytes, and basophils, but fewer lymphocytes and eosinophils, than bats sampled at the core of their distribution. Habitats with access to more livestock also showed similar patterns in leukocyte profiles, but large-scale patterns were partly confounded by time between capture and sampling across sites. Our findings suggest that populations at the edge of their range experience physiologically limiting conditions that predict higher chronic stress and greater investment in cellular innate immunity. High food abundance in livestock-dense habitats may exacerbate such conditions by increasing bat density or diet homogenization, although future spatially and temporally coordinated field studies with common protocols are needed to limit sampling artifacts. Systematically assessing immune function and response over space will elucidate how environmental conditions influence traits relevant to epidemiology and help predict disease risks with anthropogenic disturbance, land conversion, and climate change.

Indexed as

Animal DistributionEcosystemImmunity, InnateAnimalsChiropteraLeukocytes

Identifiers

PMID30873523
PMCPMC6907035
OpenAlexW2922163893

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.