Evidence map›Paper›PMID 42870688›Full record

ArticleMolecular ecology2026

Overcoming Detection Lag in a Cryptic Panzootic: Chytrid Invasion Linked to Historically Enigmatic Amphibian Declines in the Brazilian Atlantic Forest.

Jack L Boyette, Tamilie Carvalho, David Rodriguez, Wesley J Neely, Daniel Medina, Renato A Martins, Robert J Ossiboff, Zaira Gomez, William C Vuyk, Shannon M Buttimer and 7 more

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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jack L BoyetteDepartment of Biology, The Pennsylvania State University, University Park, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-6182-2505
Tamilie CarvalhoDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan, USA.ORCID https://orcid.org/0000-0001-7300-2777
David RodriguezDepartment of Biology, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0000-0003-0239-0498
Wesley J NeelyDepartment of Biology, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0000-0003-4563-5248
Daniel MedinaThe School for Field Studies, Center for Tropical Island Biodiversity Studies, Bocas del Toro, Panama.ORCID https://orcid.org/0000-0002-5217-6353
Renato A MartinsDepartment of Biodiversity, Aquaculture Center (CAUNESP), and CBioClima, I.B., Universidade Estadual Paulista, Rio Claro, SP, Brazil.ORCID https://orcid.org/0000-0002-8733-290X
Robert J OssiboffDepartment of Comparative, Diagnostic, and Population Medicine, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.ORCID https://orcid.org/0000-0001-6951-6070
Zaira GomezDepartment of Comparative, Diagnostic, and Population Medicine, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.
William C VuykDepartment of Anthropology, The Pennsylvania State University, University Park, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-9461-4788
Shannon M ButtimerDepartment of Biology, The Pennsylvania State University, University Park, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-4128-5482
Karen A Paniagua TorresDepartment of Biology, The Pennsylvania State University, University Park, Pennsylvania, USA.ORCID https://orcid.org/0009-0000-8010-6419
Ananda Brito de AssisDepartamento de Biodiversidade, Instituto de Biociências, Universidade Estadual de São Paulo, Rio Claro, SP, Brazil.ORCID https://orcid.org/0000-0001-8172-9386
Carlos A NavasDepartamento de Fisiologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, SP, Brazil.ORCID https://orcid.org/0000-0002-9859-0568
Carly R Muletz-WolzCenter for Conservation Genomics, Smithsonian's National Zoo and Conservation Biology Institute, Smithsonian Institution, Washington, DC, USA.ORCID https://orcid.org/0000-0001-5047-9601
Michael G CampanaCenter for Conservation Genomics, Smithsonian's National Zoo and Conservation Biology Institute, Smithsonian Institution, Washington, DC, USA.ORCID https://orcid.org/0000-0003-0461-6462
Corinne L Richards-ZawackiDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-4212-041X
C Guilherme BeckerDepartment of Biology, The Pennsylvania State University, University Park, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-5122-8238

Funding

National Science Foundation BII-2120084National Science Foundation DEB-2227340National Science Foundation DEB-2413542National Science Foundation DGE-1255832National Science Foundation IOS-2131060Smithsonian Institution
6 · The paper itself

Abstract

As human activity accelerates the spread of pathogens and other invasive species, reconstructing the cryptic early dynamics of undetected invasions has become a central challenge in disease ecology and invasion biology. Here, we leverage museum specimens to reconstruct the invasion of Batrachochytrium dendrobatidis (Bd), a fungal panzootic driving global amphibian biodiversity loss, across historically enigmatic declines in the Brazilian Atlantic Forest. Two hypotheses have been proposed to explain Bd's historical dynamics in this region: long-term enzootic persistence versus recent epizootic invasion coinciding with declines. Using molecular screening, histopathology, and genotyping of museum and modern specimens, we find no evidence of Bd infection prior to the decline, followed by widespread infection immediately thereafter. Only the global panzootic lineage (Bd-GPL) was detected during the first year of post-decline sampling, implicating its invasion in driving regional losses. Infection prevalence varied among species following the decline, likely reflecting species-specific interactions between baseline susceptibility and ecological exposure risk. Contemporary host populations exhibit more uniform prevalence regardless of decline history, consistent with the evolution of pathogen tolerance under enzootic conditions. Together, these results provide the first site-specific evidence linking Bd-GPL invasion to enigmatic amphibian declines in Brazil and demonstrate the power of museum collections for resolving detection lag dynamics in emerging infectious diseases.

Indexed as

AmphibiansBatrachochytriumChytridiomycotaIntroduced SpeciesAnimalsBiodiversityBrazilForestsGenotypeamphibianschytridiomycosisinfectious diseasemuseum collections

Identifiers

PMID42870688
PMCPMC13662623

What OpenQuestion holds

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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.