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Seasonal variation in the prevalence of a fungal pathogen and unexpected clearance from infection in a susceptible frog species

https://doi.org/10.3354/dao03628
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ece3.980openalex-snapshot
Evaluating monitoring methods to guide adaptive management of a threatened amphibian ( L itoria aurea )
inferredcites →https://doi.org/10.1007/s003600050072openalex-snapshot
Changes in selected aspects of immune function in the leopard frog, Rana pipiens , associated with exposure to cold
inferredcites →https://doi.org/10.1007/s00442-005-0228-8openalex-snapshot
Population trends associated with skin peptide defenses against chytridiomycosis in Australian frogs
inferredcites →https://doi.org/10.1007/s00442-016-3607-4openalex-snapshot
Susceptibility to disease varies with ontogeny and immunocompetence in a threatened amphibian
inferredcites →https://doi.org/10.1007/s00442-017-3866-8openalex-snapshot
Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
inferredcites →https://doi.org/10.1007/s10393-006-0027-7openalex-snapshot
Survivorship in Wild Frogs Infected with Chytridiomycosis
inferredcites →https://doi.org/10.1007/s10393-007-0093-5openalex-snapshot
Spread of Chytridiomycosis Has Caused the Rapid Global Decline and Extinction of Frogs
inferredcites →https://doi.org/10.1007/s10393-009-0228-yopenalex-snapshot
Chytridiomycosis, Amphibian Extinctions, and Lessons for the Prevention of Future Panzootics
inferredcites →https://doi.org/10.1007/s10393-017-1240-2openalex-snapshot
Batrachochytrium dendrobatidis and the Decline and Survival of the Relict Leopard Frog
inferredcites →https://doi.org/10.1007/s10393-019-01446-yopenalex-snapshot
Population-Level Resistance to Chytridiomycosis is Life-Stage Dependent in an Imperiled Anuran
inferredcites →https://doi.org/10.1007/s13157-010-0029-7openalex-snapshot
Rapid Turnover in Site Occupancy of a Pond-breeding Frog Demonstrates the Need for Landscape-level Management
inferredcites →https://doi.org/10.1016/j.biocon.2011.03.018openalex-snapshot
Disease dynamics vary spatially and temporally in a North American amphibian
inferredcites →https://doi.org/10.1016/j.biocon.2013.12.034openalex-snapshot
Decline and re-expansion of an amphibian with high prevalence of chytrid fungus
inferredcites →https://doi.org/10.1016/j.biocon.2014.11.032openalex-snapshot
Low impact of chytridiomycosis on frog recruitment enables persistence in refuges despite high adult mortality
inferredcites →https://doi.org/10.1016/j.dci.2014.09.003openalex-snapshot
Development of antimicrobial peptide defenses of southern leopard frogs, Rana sphenocephala, against the pathogenic chytrid fungus, Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1016/j.tree.2009.07.011openalex-snapshot
The ecology and impact of chytridiomycosis: an emerging disease of amphibians
inferredcites →https://doi.org/10.1016/s0145-305x(01)00088-xopenalex-snapshot
Activity of antimicrobial skin peptides from ranid frogs against Batrachochytrium dendrobatidis, the chytrid fungus associated with global amphibian declines
inferredcites →https://doi.org/10.1016/s0169-5347(00)89050-3openalex-snapshot
Detecting disease and parasite threats to endangered species and ecosystems
inferredcites →https://doi.org/10.1038/nature13491openalex-snapshot
Amphibians acquire resistance to live and dead fungus overcoming fungal immunosuppression
inferredcites →https://doi.org/10.1038/s41598-017-03605-zopenalex-snapshot
Skin sloughing in susceptible and resistant amphibians regulates infection with a fungal pathogen
inferredcites →https://doi.org/10.1071/wr15223openalex-snapshot
The role of non-declining amphibian species as alternative hosts for Batrachochytrium dendrobatidis in an amphibian community
inferredcites →https://doi.org/10.1073/pnas.0912886107openalex-snapshot
Enzootic and epizootic dynamics of the chytrid fungal pathogen of amphibians
inferredcites →https://doi.org/10.1073/pnas.1106893108openalex-snapshot
MHC genotypes associate with resistance to a frog-killing fungus
inferredcites →https://doi.org/10.1073/pnas.1600983113openalex-snapshot
Large-scale recovery of an endangered amphibian despite ongoing exposure to multiple stressors
inferredcites →https://doi.org/10.1080/00275514.1999.12061011openalex-snapshot
Batrachochytrium dendrobatidis gen. et sp. nov., a chytrid pathogenic to amphibians
inferredcites →https://doi.org/10.1080/15572536.2005.11832990openalex-snapshot
Physiology ofBatrachochytrium dendrobatidis, a chytrid pathogen of amphibians
inferredcites →https://doi.org/10.1093/femsle/fnw111openalex-snapshot
Low disease-causing threshold in a frog species susceptible to chytridiomycosis
inferredcites →https://doi.org/10.1111/1365-2435.12194openalex-snapshot
Temporal patterns in immunity, infection load and disease susceptibility: understanding the drivers of host responses in the amphibian‐chytrid fungus system
inferredcites →https://doi.org/10.1111/aec.12080openalex-snapshot
Six-year demographic study reveals threat of stochastic extinction for remnant populations of a threatened amphibian
inferredcites →https://doi.org/10.1111/aec.12256openalex-snapshot
Winter microhabitat selection of a threatened pond amphibian in constructed urban wetlands
inferredcites →https://doi.org/10.1111/cobi.12073openalex-snapshot
Chytridiomycosis and Seasonal Mortality of Tropical Stream‐Associated Frogs 15 Years after Introduction of Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1111/cobi.12402openalex-snapshot
Effects of pond salinization on survival rate of amphibian hosts infected with the chytrid fungus
inferredcites →https://doi.org/10.1111/geb.12022openalex-snapshot
A high‐resolution bioclimate map of the world: a unifying framework for global biodiversity research and monitoring
inferredcites →https://doi.org/10.1111/j.1365-2435.2006.01159.xopenalex-snapshot
Negative effects of changing temperature on amphibian immunity under field conditions
inferredcites →https://doi.org/10.1111/j.1365-2656.2007.01256.xopenalex-snapshot
Quantifying the disease transmission function: effects of density onBatrachochytrium dendrobatidistransmission in the mountain yellow‐legged frogRana muscosa
inferredcites →https://doi.org/10.1111/j.1442-9993.2012.02452.xopenalex-snapshot
Life stage specific variation in the occupancy of ponds by L itoria aurea, a threatened amphibian
inferredcites →https://doi.org/10.1111/j.1469-1795.2010.00407.xopenalex-snapshot
Host species determines whether infection load increases beyond disease‐causing thresholds following exposure to the amphibian chytrid fungus
inferredcites →https://doi.org/10.1111/j.1469-7998.2006.00220.xopenalex-snapshot
Large‐scale seasonal variation in the prevalence and severity of chytridiomycosis
inferredcites →https://doi.org/10.1111/j.1523-1739.2005.004403.xopenalex-snapshot
Ecology of Chytridiomycosis in Rainforest Stream Frog Assemblages of Tropical Queensland
inferredcites →https://doi.org/10.1111/j.1523-1739.2007.00777.xopenalex-snapshot
Latitudinal Variation in the Prevalence and Intensity of Chytrid ( Batrachochytrium dendrobatidis ) Infection in Eastern Australia
inferredcites →https://doi.org/10.1111/j.1523-1739.2011.01728.xopenalex-snapshot
Environmental Refuge from Disease‐Driven Amphibian Extinction
inferredcites →https://doi.org/10.1111/j.1751-0813.2004.tb11137.xopenalex-snapshot
Effect of season and temperature on mortality in amphibians due to chytridiomycosis
inferredcites →https://doi.org/10.1111/jzo.12773openalex-snapshot
Chytrid fungus dynamics and infections associated with movement distances in a red‐listed amphibian
inferredcites →https://doi.org/10.1126/science.1103538openalex-snapshot
Status and Trends of Amphibian Declines and Extinctions Worldwide
inferredcites →https://doi.org/10.1126/science.1176765openalex-snapshot
Pathogenesis of Chytridiomycosis, a Cause of Catastrophic Amphibian Declines
inferredcites →https://doi.org/10.1126/science.1243316openalex-snapshot
The Invasive Chytrid Fungus of Amphibians Paralyzes Lymphocyte Responses
inferredcites →https://doi.org/10.1126/science.aav0379openalex-snapshot
Amphibian fungal panzootic causes catastrophic and ongoing loss of biodiversity
inferredcites →https://doi.org/10.1128/iai.00402-10openalex-snapshot
Immune Defenses againstBatrachochytrium dendrobatidis, a Fungus Linked to Global Amphibian Declines, in the South African Clawed Frog,Xenopus laevis
inferredcites →https://doi.org/10.1128/iai.02231-14openalex-snapshot
Inhibition of Local Immune Responses by the Frog-Killing Fungus Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1163/017353710x518405openalex-snapshot
Comparing three body condition indices in amphibians: a case study of yellow-bellied toad Bombina variegata
inferredcites →https://doi.org/10.1177/0049124104268644openalex-snapshot
Multimodel Inference
inferredcites →https://doi.org/10.1186/1472-6785-10-6openalex-snapshot
Prevalence of the pathogenic chytrid fungus, Batrachochytrium dendrobatidis, in an endangered population of northern leopard frogs, Rana pipiens
inferredcites →https://doi.org/10.1201/9780429258411openalex-snapshot
Bayesian Data Analysis
inferredcites →https://doi.org/10.1242/jeb.191817openalex-snapshot
Epidermal epidemic: unravelling the pathogenesis of chytridiomycosis
inferredcites →https://doi.org/10.1371/journal.pone.0056802openalex-snapshot
Mapping the Global Emergence of Batrachochytrium dendrobatidis, the Amphibian Chytrid Fungus
inferredcites →https://doi.org/10.1371/journal.pone.0073830openalex-snapshot
Variation in Thermal Performance of a Widespread Pathogen, the Amphibian Chytrid Fungus Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1643/cp-02-120r1openalex-snapshot
Pathogenicity and Transmission of Chytridiomycosis in Tiger Salamanders (Ambystoma tigrinum)
inferredcites →https://doi.org/10.1890/06-1842.1openalex-snapshot
LIFE-HISTORY TRADE-OFFS INFLUENCE DISEASE IN CHANGING CLIMATES: STRATEGIES OF AN AMPHIBIAN PATHOGEN
inferredcites →https://doi.org/10.1890/13-0389.1openalex-snapshot
Wetland characteristics influence disease risk for a threatened amphibian
inferredcites →https://doi.org/10.2193/2006-345openalex-snapshot
Chytridiomycosis Widespread in Anurans of Northeastern United States
inferredcites →https://doi.org/10.3354/cr01204openalex-snapshot
Climate classification revisited: from Köppen to Trewartha
inferredcites →https://doi.org/10.3354/dao01830openalex-snapshot
Behaviour of Australian rainforest stream frogs may affect the transmission of chytridiomycosis
inferredcites →https://doi.org/10.3354/dao02216openalex-snapshot
Batrachochytrium dendrobatidis: requirement for further isolate collection and archiving
inferredcites →https://doi.org/10.3354/dao055065openalex-snapshot
Emerging disease of amphibians cured by elevated body temperature
inferredcites →https://doi.org/10.3354/dao060141openalex-snapshot
Rapid quantitative detection of chytridiomycosis (Batrachochytrium dendrobatidis) in amphibian samples using real-time Taqman PCR assay
inferredcites →https://doi.org/10.3354/dao068051openalex-snapshot
Life cycle stages of the amphibian chytrid Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.7882/az.1996.004openalex-snapshot
The efficacy of using Passive Integrated Transponder (PIT) tags without anaesthetic in free-living frogs
inferredcites →https://doi.org/10.7882/az.2001.003openalex-snapshot
A Review of the Biology of the Green and Golden Bell Frog Litoria aurea
inferredcites →https://doi.org/10.7882/az.2008.009openalex-snapshot
Impact of a Chytrid-related mortality event on a population of the Green and Golden Bell Frog Litoria aurea

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/neobiota.104.160230zenodo-depositor-declared
Comparing sampling protocols and results to better detect the amphibian fungal parasite Batrachochytrium dendrobatidis in the wild
inferred← citeshttps://doi.org/10.1002/ece3.72053openalex-snapshot
Intestinal Nematode Infection Confers a Benefit to a Non‐Declining Frog Species, While a Fungal Parasitic Infection Has Sublethal Impacts on Reproductive Investment
inferred← citeshttps://doi.org/10.1002/ecs2.70350openalex-snapshot
Similar population dynamics before and after a chytridiomycosis outbreak in a tropical riparian amphibian species
inferred← citeshttps://doi.org/10.1007/s10530-025-03648-8openalex-snapshot
Is exposure to chytrid fungus and ranavirus higher in ponds invaded by American bullfrogs?
inferred← citeshttps://doi.org/10.1016/j.jenvman.2026.130229openalex-snapshot
Landscape forest cover is associated with reduced agrochemical exposure and improved amphibian tadpole health in agricultural drainage ditches
inferred← citeshttps://doi.org/10.1073/pnas.2423706122openalex-snapshot
Thermal mismatch models derived from occurrence data predict pathogen prevalence in frogs
inferred← citeshttps://doi.org/10.1080/09581596.2025.2474686openalex-snapshot
Seasonal patterns of infectious diseases in Riyadh Province, Saudi Arabia: a retrospective analysis
inferred← citeshttps://doi.org/10.1111/1365-2656.70282openalex-snapshot
Playing it safe at early life stages: Balancing energy allocations to maximize fitness under seasonal pathogen dynamics
inferred← citeshttps://doi.org/10.1111/csp2.70424openalex-snapshot
A simple, robust, and inexpensive design for creating thermal refugia to protect amphibians from Batrachochytrium dendrobatidis in the field
inferred← citeshttps://doi.org/10.3389/fphys.2022.1104476openalex-snapshot
Integrated analysis of transcriptome and metabolome data reveals insights for molecular mechanisms in overwintering Tibetan frogs, Nanorana parkeri
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