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Diagnostic assays and sampling protocols for the detection of Batrachochytrium dendrobatidis

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What this work says

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

inferredcites →https://doi.org/10.1016/s0006-3207(00)00132-4openalex-snapshot

Evidence of a chytrid fungus infection involved in the decline of the common midwife toad (Alytes obstetricans) in protected areas of central Spain

inferredcites →https://doi.org/10.1016/s0958-1669(98)80082-7openalex-snapshot

Advances in quantitative PCR technology: 5′ nuclease assays

inferredcites →https://doi.org/10.1038/431403aopenalex-snapshot

Ethics and amphibians

inferredcites →https://doi.org/10.1046/j.1523-1739.1999.97185.xopenalex-snapshot

Mass Mortality and Population Declines of Anurans at an Upland Site in Western Panama

inferredcites →https://doi.org/10.1101/gr.6.10.986openalex-snapshot

Real time quantitative PCR.

inferredcites →https://doi.org/10.1111/j.0021-8901.2004.00919.xopenalex-snapshot

Clarifying the effect of toe clipping on frogs with Bayesian statistics

inferredcites →https://doi.org/10.1111/j.1523-1739.2005.00217.xopenalex-snapshot

Inconclusiveness of Chytridiomycosis as the Agent in Widespread Frog Declines

inferredcites →https://doi.org/10.1111/j.1523-1739.2005.00255.xopenalex-snapshot

The Novel and Endemic Pathogen Hypotheses: Competing Explanations for the Origin of Emerging Infectious Diseases of Wildlife

inferredcites →https://doi.org/10.1111/j.1749-6632.2002.tb04400.xopenalex-snapshot

Epizootiology of Sixty‐Four Amphibian Morbidity and Mortality Events in the USA, 1996‐2001

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.287.5452.443openalex-snapshot

Emerging Infectious Diseases of Wildlife-- Threats to Biodiversity and Human Health

inferredcites →https://doi.org/10.1177/104063879901100219openalex-snapshot

Cutaneous Chytridiomycosis in Poison Dart Frogs ( Dendrobates spp.) and White's Tree Frogs ( Litoria Caerulea )

inferredcites →https://doi.org/10.1643/0045-8511(2001)001[0945:ocitmy]2.0.co;2openalex-snapshot

Oral Chytridiomycosis in the Mountain Yellow-Legged Frog (Rana muscosa)

inferredcites →https://doi.org/10.1670/0022-1511(2003)037[0116:pdotjt]2.0.co;2openalex-snapshot

Population Decline of the Jambato Toad Atelopus ignescens (Anura: Bufonidae) in the Andes of Ecuador

inferredcites →https://doi.org/10.3201/eid0506.990601openalex-snapshot

Emerging Infectious Diseases and Amphibian Population Declines

inferredcites →https://doi.org/10.3201/eid0908.030145openalex-snapshot

Survival ofBatrachochytrium dendrobatidisin Water: Quarantine and Disease Control Implications

inferredcites →https://doi.org/10.3201/eid1012.030804openalex-snapshot

Origin of the Amphibian Chytrid Fungus

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/dao061085openalex-snapshot

Co-localisation of Batrachochytrium dendrobatidis and keratin for enhanced diagnosis of chytridiomycosis in frogs

inferredcites →https://doi.org/10.3354/dao068051openalex-snapshot

Life cycle stages of the amphibian chytrid Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.3354/dao068065openalex-snapshot

Distribution of Batrachochytrium dendrobatidis and pathology in the skin of green tree frogs Litoria caerulea with severe chytridiomycosis

inferredcites →https://doi.org/10.3354/dao071141openalex-snapshot

Techniques for detecting chytridiomycosis in wild frogs: comparing histology with real-time Taqman PCR

inferredcites →https://doi.org/10.7589/0090-3558-38.1.206openalex-snapshot

Chytridiomycosis in Native Arizona Frogs

inferredcites →https://doi.org/10.7589/0090-3558-39.3.742openalex-snapshot

Use of Immunohistochemistry to Diagnose Chytridiomycosis in Dyeing Poison Dart Frogs (Dendrobates tinctorius)

inferredcites →https://doi.org/10.7589/0090-3558-40.3.420openalex-snapshot

A DNA-BASED ASSAY IDENTIFIES BATRACHOCHYTRIUM DENDROBATIDIS IN AMPHIBIANS

What points at this work

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

inferred← citeshttps://doi.org/10.11646/zootaxa.3887.4.4zenodo-depositor-declared

A new species of Psychrophrynella (Anura: Craugastoridae) from the Cordillera Real, Department La Paz, Bolivia

inferred← citeshttps://doi.org/10.11646/zootaxa.4273.3.4zenodo-depositor-declared

Four new species of terrestrial-breeding frogs of the genus Phrynopus (Anura: Terrarana: Craugastoridae) from Río Abiseo National Park, Peru

inferred← citeshttps://doi.org/10.11646/zootaxa.4363.3.2zenodo-depositor-declared

A new species of Microkayla (Anura: Craugastoridae: Holoadeninae) from Department La Paz, Bolivia

inferred← citeshttps://doi.org/10.2139/ssrn.4803698openalex-extracted

Historical Evidence and the Global Frog Trade Suggest a New Hypothesis Regarding the Origin and Spread of a Chytrid Fungus Lineage

inferred← citeshttps://doi.org/10.3897/neobiota.102.150311zenodo-depositor-declared

Mapping the northernmost transnational non-native population of Xenopus laevis using pooled eDNA sampling

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/10.3897/zookeys.1187.104536zenodo-depositor-declared

A new cryptic species of terrestrial breeding frog of the Pristimantis danae Group (Anura, Strabomantidae) from montane forests in Ayacucho, Peru

inferred← citeshttps://doi.org/10.1002/aah.10041openalex-snapshot

Concurrent Infection of Batrachochytrium dendrobatidis and Ranavirus among Native Amphibians from Northeastern Oklahoma, USA

inferred← citeshttps://doi.org/10.1002/aah.10119openalex-snapshot

Nephroblastoma in a Common Mudpuppy Necturus maculosus simultaneously Present with a Mollicute Bacterium of the Genus Acholeplasma

inferred← citeshttps://doi.org/10.1002/aah.10231openalex-snapshot

Chytridiomycosis in a colony of hellbenders Cryptobranchus alleganiensis

inferred← citeshttps://doi.org/10.1002/aqc.3653openalex-snapshot

Improving breed‐and‐release programmes in the face of a threatening pathogen, Batrachochytrium dendrobatidis

inferred← citeshttps://doi.org/10.1002/bit.28592openalex-snapshot

Using eDNA to survey amphibians: Methods, applications, and challenges

inferred← citeshttps://doi.org/10.1002/eap.1607openalex-snapshot

A pesticide paradox: fungicides indirectly increase fungal infections

inferred← citeshttps://doi.org/10.1002/eap.1792openalex-snapshot

Eco‐evolutionary rescue promotes host–pathogen coexistence

inferred← citeshttps://doi.org/10.1002/eap.2256openalex-snapshot

Host contribution to parasite persistence is consistent between parasites and over time, but varies spatially

inferred← citeshttps://doi.org/10.1002/eap.2724openalex-snapshot

Recovered frog populations coexist with endemic Batrachochytrium dendrobatidis despite load‐dependent mortality

inferred← citeshttps://doi.org/10.1002/ece3.1199openalex-snapshot

Experimental evolution alters the rate and temporal pattern of population growth in Batrachochytrium dendrobatidis, a lethal fungal pathogen of amphibians

inferred← citeshttps://doi.org/10.1002/ece3.3309openalex-snapshot

Prevalence and genetic diversity of Batrachochytrium dendrobatidis in Central African island and continental amphibian communities

inferred← citeshttps://doi.org/10.1002/ece3.3468openalex-snapshot

Rapid extirpation of a North American frog coincides with an increase in fungal pathogen prevalence: Historical analysis and implications for reintroduction

inferred← citeshttps://doi.org/10.1002/ece3.3616openalex-snapshot

Design‐ and model‐based recommendations for detecting and quantifying an amphibian pathogen in environmental samples

inferred← citeshttps://doi.org/10.1002/ece3.70294openalex-snapshot

Optimising recovery of DNA from minimally invasive sampling methods: Efficacy of buccal swabs, preservation strategy and DNA extraction approaches for amphibian studies

inferred← citeshttps://doi.org/10.1002/ece3.72350openalex-snapshot

Do I Sound Sick? Condition‐Dependent Advertisement Signals in Naturally Infected Frogs

inferred← citeshttps://doi.org/10.1002/ece3.72873openalex-snapshot

Monitoring the Prevalence and Distribution of Chytrid Fungus ( Batrachochytrium dendrobatidis ) in the Kihansi Spray Toad ( Nectophrynoides asperginis ) Population in the Kihansi Gorge Spray Wetlands, Tanzania

inferred← citeshttps://doi.org/10.1002/ece3.73201openalex-snapshot

Differential Susceptibility May Not Drive Chytridiomycosis Related Declines in Multi‐Host Amphibian Communities

inferred← citeshttps://doi.org/10.1002/ece3.73250openalex-snapshot

Host Genus and Habitat Use Shape the Distribution of Batrachochytrium dendrobatidis Lineages in a Hyper‐Diverse Tropical Amphibian Community

inferred← citeshttps://doi.org/10.1002/ece3.73944openalex-snapshot

Physiological and Skin Microbiome Divergence Among Closely Related Anurans Co‐Occurring in Agricultural Wetlands

inferred← citeshttps://doi.org/10.1002/ece3.7594openalex-snapshot

Geography, Host Genetics, and Cross‐Domain Microbial Networks Structure the Skin Microbiota of Fragmented Brazilian Atlantic Forest Frog Populations

inferred← citeshttps://doi.org/10.1002/ece3.7779openalex-snapshot

Exposure to a fungal pathogen increases the critical thermal minimum of two frog species

inferred← citeshttps://doi.org/10.1002/ecm.70001openalex-snapshot

Pan‐amphibia distribution of the fungal parasite Batrachochytrium dendrobatidis varies with species and temperature

inferred← citeshttps://doi.org/10.1002/eco.2395openalex-snapshot

Seasonal drought and its effects on frog population dynamics and amphibian disease in intermittent streams

inferred← citeshttps://doi.org/10.1002/ecs2.1740openalex-snapshot

Extreme drought, host density, sex, and bullfrogs influence fungal pathogen infection in a declining lotic amphibian

inferred← citeshttps://doi.org/10.1002/ecs2.2499openalex-snapshot

Disease and climate effects on individuals drive post‐reintroduction population dynamics of an endangered amphibian

inferred← citeshttps://doi.org/10.1002/ecs2.2892openalex-snapshot

Effects of latitudinal, seasonal, and daily temperature variations on chytrid fungal infections in a North American frog

inferred← citeshttps://doi.org/10.1002/ecs2.3010openalex-snapshot

Tick parasitism as a cost of sexual selection and male parental care in a Neotropical frog

inferred← citeshttps://doi.org/10.1002/ecs2.3169openalex-snapshot

Torrent frogs have fewer macroparasites but higher rates of chytrid infection in landscapes with smaller forest cover

inferred← citeshttps://doi.org/10.1002/ecs2.4158openalex-snapshot

Seasonality of host immunity in a tropical disease system

inferred← citeshttps://doi.org/10.1002/ecs2.4224openalex-snapshot

Localized carry‐over effects of pond drying on survival, growth, and pathogen defenses in amphibians

inferred← citeshttps://doi.org/10.1002/ecs2.4294openalex-snapshot

To treat or not to treat? Experimental pathogen exposure, treatment, and release of a threatened amphibian

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/10.1002/ecs2.70365openalex-snapshot

Impacts of sequential and simultaneous coinfection by major amphibian pathogens on disease outcomes

inferred← citeshttps://doi.org/10.1002/ecs2.70447openalex-snapshot

Environmental watering elevates chytrid infection probability in frogs

inferred← citeshttps://doi.org/10.1002/ecs2.70794openalex-snapshot

Differential skin microbiomes and disease outcomes in sympatric hosts despite similar infection burdens

inferred← citeshttps://doi.org/10.1002/ecy.3759openalex-snapshot

Once a reservoir, always a reservoir? Seasonality affects the pathogen maintenance potential of amphibian hosts

inferred← citeshttps://doi.org/10.1002/edn3.86openalex-snapshot

Using environmental DNA for detection of Batrachochytrium salamandrivorans in natural water

inferred← citeshttps://doi.org/10.1002/etc.2419openalex-snapshot

The interactive effects of chytrid fungus, pesticides, and exposure timing on gray treefrog (Hyla versicolor) larvae

inferred← citeshttps://doi.org/10.1002/jez.2427openalex-snapshot

Preparing for invasion: Assessing risk of infection by chytrid fungi in southeastern plethodontid salamanders

inferred← citeshttps://doi.org/10.1002/jez.2497openalex-snapshot

Infection with Batrachochytrium dendrobatidis reduces salamander capacity to mount a cell‐mediated immune response

inferred← citeshttps://doi.org/10.1002/jez.2581openalex-snapshot

Does the thermal mismatch hypothesis predict disease outcomes in different morphs of a terrestrial salamander?

inferred← citeshttps://doi.org/10.1002/jez.70061openalex-snapshot

Ophidiomycosis Prevalence and Disease Ecology in a Natrix tessellata (Laurenti, 1768) Population From Northern Italy

inferred← citeshttps://doi.org/10.1002/jwmg.1031openalex-snapshot

Factors limiting early life stage survival and growth during endangered Wyoming toad reintroductions

inferred← citeshttps://doi.org/10.1002/jwmg.21118openalex-snapshot

Influence of demography and environment on persistence in toad populations

inferred← citeshttps://doi.org/10.1002/zoo.21122openalex-snapshot

Chironomidae bloodworms larvae as aquatic amphibian food

inferred← citeshttps://doi.org/10.1007/978-3-319-27288-7_4openalex-snapshot

Monitoring Essential Biodiversity Variables at the Species Level

inferred← citeshttps://doi.org/10.1007/978-3-319-72093-7_14openalex-snapshot

Chytridiomycosis

inferred← citeshttps://doi.org/10.1007/s00027-026-01287-2openalex-snapshot

Drivers of aquatic zoosporic parasites in natural and artificial environments

inferred← citeshttps://doi.org/10.1007/s00248-015-0653-0openalex-snapshot

Microbiome Variation Across Amphibian Skin Regions: Implications for Chytridiomycosis Mitigation Efforts

inferred← citeshttps://doi.org/10.1007/s00248-016-0916-4openalex-snapshot

Greater Species Richness of Bacterial Skin Symbionts Better Suppresses the Amphibian Fungal Pathogen Batrachochytrium Dendrobatidis

inferred← citeshttps://doi.org/10.1007/s00248-017-1034-7openalex-snapshot

Skin Bacterial Community Reorganization Following Metamorphosis of the Fire-Bellied Toad (Bombina orientalis)

inferred← citeshttps://doi.org/10.1007/s00248-018-1288-8openalex-snapshot

The Influence of Habitat and Phylogeny on the Skin Microbiome of Amphibians in Guatemala and Mexico

inferred← citeshttps://doi.org/10.1007/s00248-019-01372-0openalex-snapshot

Ecological Correlates of Large-Scale Turnover in the Dominant Members of Pseudacris crucifer Skin Bacterial Communities

inferred← citeshttps://doi.org/10.1007/s00248-021-01706-xopenalex-snapshot

Inhibition of Batrachochytrium dendrobatidis Infection by Skin Bacterial Communities in Wild Amphibian Populations

inferred← citeshttps://doi.org/10.1007/s00248-021-01897-3openalex-snapshot

Habitat Disturbance Linked with Host Microbiome Dispersion and Bd Dynamics in Temperate Amphibians

inferred← citeshttps://doi.org/10.1007/s00248-022-02049-xopenalex-snapshot

Factors Influencing Bacterial and Fungal Skin Communities of Montane Salamanders of Central Mexico

inferred← citeshttps://doi.org/10.1007/s00248-025-02671-5openalex-snapshot

Imprints of Land Use History on the Cutaneous Microbiota of Mexican Cloud Forest Salamanders

inferred← citeshttps://doi.org/10.1007/s00251-022-01252-xopenalex-snapshot

Habitat fragmentation in the Brazilian Atlantic Forest is associated with erosion of frog immunogenetic diversity and increased fungal infections

inferred← citeshttps://doi.org/10.1007/s00265-021-03057-6openalex-snapshot

Social group size influences pathogen transmission in salamanders

inferred← citeshttps://doi.org/10.1007/s00265-024-03529-5openalex-snapshot

Infection by a fungal pathogen and mating behavior in Pacific treefrogs: a test of the Hamilton-Zuk hypothesis

inferred← citeshttps://doi.org/10.1007/s00442-015-3422-3openalex-snapshot

Infection dynamics in frog populations with different histories of decline caused by a deadly disease

inferred← citeshttps://doi.org/10.1007/s00442-018-4167-6openalex-snapshot

Beyond the swab: ecosystem sampling to understand the persistence of an amphibian pathogen

inferred← citeshttps://doi.org/10.1007/s00442-020-04646-4openalex-snapshot

Assessing amphibian disease risk across tropical streams while accounting for imperfect pathogen detection

inferred← citeshttps://doi.org/10.1007/s00442-020-04743-4openalex-snapshot

Evaluating environmental DNA as a tool for detecting an amphibian pathogen using an optimized extraction method

inferred← citeshttps://doi.org/10.1007/s00442-023-05406-wopenalex-snapshot

Limited impact of chytridiomycosis on juvenile frogs in a recovered species

inferred← citeshttps://doi.org/10.1007/s00442-023-05489-5openalex-snapshot

Body size mediates latitudinal population differences in the response to chytrid fungus infection in two amphibians

inferred← citeshttps://doi.org/10.1007/s00442-024-05604-0openalex-snapshot

Centrifugation is an effective and inexpensive way to determine Batrachochytrium dendrobatidis quantity in water samples with low turbidity

inferred← citeshttps://doi.org/10.1007/s10344-014-0800-9openalex-snapshot

Detection of Batrachochytrium dendrobatidis in amphibians inhabiting cloud forests and coffee agroecosystems in central Veracruz, Mexico

inferred← citeshttps://doi.org/10.1007/s10393-008-0190-0openalex-snapshot

Chytridiomycosis and Amphibian Population Declines Continue to Spread Eastward in Panama

inferred← citeshttps://doi.org/10.1007/s10393-009-0228-yopenalex-snapshot

Chytridiomycosis, Amphibian Extinctions, and Lessons for the Prevention of Future Panzootics

inferred← citeshttps://doi.org/10.1007/s10393-009-0229-xopenalex-snapshot

Detection of Batrachochytrium dendrobatidis in Endemic Salamander Species from Central Texas

inferred← citeshttps://doi.org/10.1007/s10393-009-0232-2openalex-snapshot

Fatal Chytridiomycosis in the Tyrrhenian Painted Frog

inferred← citeshttps://doi.org/10.1007/s10393-009-0271-8openalex-snapshot

Chytrid Blinders: What Other Disease Risks to Amphibians Are We Missing?

inferred← citeshttps://doi.org/10.1007/s10393-010-0307-0openalex-snapshot

First Evidence of Batrachochytrium dendrobatidis in China: Discovery of Chytridiomycosis in Introduced American Bullfrogs and Native Amphibians in the Yunnan Province, China

inferred← citeshttps://doi.org/10.1007/s10393-010-0327-9openalex-snapshot

Persistence with Chytridiomycosis Does Not Assure Survival of Direct-developing Frogs

inferred← citeshttps://doi.org/10.1007/s10393-010-0350-xopenalex-snapshot

Immmunological Clearance of Batrachochytrium dendrobatidis Infection at a Pathogen-optimal Temperature in the Hylid Frog Hypsiboas crepitans

inferred← citeshttps://doi.org/10.1007/s10393-010-0358-2openalex-snapshot

What Drives Chytrid Infections in Newt Populations? Associations with Substrate, Temperature, and Shade

inferred← citeshttps://doi.org/10.1007/s10393-010-0364-4openalex-snapshot

High Prevalence of the Amphibian Chytrid Pathogen in Gabon

inferred← citeshttps://doi.org/10.1007/s10393-010-0634-1openalex-snapshot

Ubiquity of the Pathogenic Chytrid Fungus, Batrachochytrium dendrobatidis, in Anuran Communities in Panamá

inferred← citeshttps://doi.org/10.1007/s10393-011-0685-yopenalex-snapshot

First Record of Batrachochytrium dendrobatidis Infecting Four Frog Families from Peninsular Malaysia

inferred← citeshttps://doi.org/10.1007/s10393-011-0704-zopenalex-snapshot

Detection of Batrachochytrium dendrobatidis in Mexican Bolitoglossine Salamanders Using an Optimal Sampling Protocol

inferred← citeshttps://doi.org/10.1007/s10393-013-0824-8openalex-snapshot

Amphibian Chytrid Prevalence in an Amphibian Community in Arid Australia

inferred← citeshttps://doi.org/10.1007/s10393-013-0831-9openalex-snapshot

Batrachochytrium dendrobatidis Infection and Lethal Chytridiomycosis in Caecilian Amphibians (Gymnophiona)

inferred← citeshttps://doi.org/10.1007/s10393-013-0864-0openalex-snapshot

The Absence of Zoonotic Agents in Invasive Bullfrogs (Lithobates catesbeianus) in Belgium and The Netherlands

inferred← citeshttps://doi.org/10.1007/s10393-014-0967-2openalex-snapshot

Extremely Low Prevalence of Batrachochytrium dendrobatidis in Frog Populations from Neotropical Dry Forest of Costa Rica Supports the Existence of a Climatic Refuge from Disease

inferred← citeshttps://doi.org/10.1007/s10393-016-1101-4openalex-snapshot

Prevalence and Seasonality of the Amphibian Chytrid Fungus Batrachochytrium dendrobatidis Along Widely Separated Longitudes Across the United States

inferred← citeshttps://doi.org/10.1007/s10393-016-1114-zopenalex-snapshot

Assessing the ability of swab data to determine the true burden of infection for the amphibian pathogen Batrachochytrium dendrobatidis

inferred← citeshttps://doi.org/10.1007/s10393-016-1138-4openalex-snapshot

Detection of Batrachochytrium dendrobatidis in Amphibians Imported into the UK for the Pet Trade

inferred← citeshttps://doi.org/10.1007/s10393-016-1186-9openalex-snapshot

Xenopus laevis and Emerging Amphibian Pathogens in Chile

inferred← citeshttps://doi.org/10.1007/s10393-016-1201-1openalex-snapshot

Recent Emergence of a Chytrid Fungal Pathogen in California Cascades Frogs (Rana cascadae)

inferred← citeshttps://doi.org/10.1007/s10393-018-1358-xopenalex-snapshot

External Reinfection of a Fungal Pathogen Does not Contribute to Pathogen Growth

inferred← citeshttps://doi.org/10.1007/s10393-020-01501-zopenalex-snapshot

Differences in Fungal Disease Dynamics in Co-occurring Terrestrial and Aquatic Amphibians

inferred← citeshttps://doi.org/10.1007/s10393-021-01570-8openalex-snapshot

Three Pathogens Impact Terrestrial Frogs from a High-Elevation Tropical Hotspot

inferred← citeshttps://doi.org/10.1007/s10393-021-01572-6openalex-snapshot

Sustained Ranavirus Outbreak Causes Mass Mortality and Morbidity of Imperiled Amphibians in Florida

inferred← citeshttps://doi.org/10.1007/s10393-025-01698-xopenalex-snapshot

Climatically Specialized Lineages of Batrachochytrium dendrobatidis, and its Likely Asian Origins

inferred← citeshttps://doi.org/10.1007/s10393-025-01716-yopenalex-snapshot

Community-Wide Genotyping of Batrachochytrium dendrobatidis in Ecuadorian Forests

inferred← citeshttps://doi.org/10.1007/s10393-025-01736-8openalex-snapshot

Genotypic Discrimination of Chytrid Fungus Lineages in the Amphibian Trade

inferred← citeshttps://doi.org/10.1007/s10452-019-09727-yopenalex-snapshot

Batrachochytrium dendrobatidis infection in amphibians from a high elevation habitat in the trans-Mexican volcanic belt

inferred← citeshttps://doi.org/10.1007/s10452-021-09869-yopenalex-snapshot

Effects of intrinsic and extrinsic factors on the prevalence of the fungus Batrachochytrium dendrobatidis (Chytridiomycota) in stream tadpoles in the Atlantic Forest domain

inferred← citeshttps://doi.org/10.1007/s10530-017-1390-8openalex-snapshot

Unraveling the historical prevalence of the invasive chytrid fungus in the Bolivian Andes: implications in recent amphibian declines

inferred← citeshttps://doi.org/10.1007/s10530-019-01973-3openalex-snapshot

Double trouble: co-infections of chytrid fungi will severely impact widely distributed newts

inferred← citeshttps://doi.org/10.1007/s10530-021-02536-1openalex-snapshot

Plethodontid salamanders show variable disease dynamics in response to Batrachochytrium salamandrivorans chytridiomycosis

inferred← citeshttps://doi.org/10.1007/s10531-015-0946-0openalex-snapshot

Island provides a pathogen refuge within climatically suitable area

inferred← citeshttps://doi.org/10.1007/s10531-022-02525-3openalex-snapshot

Amphibian survival compromised by long-term effects of chytrid fungus

inferred← citeshttps://doi.org/10.1007/s10531-026-03354-4openalex-snapshot

Shifting baselines in amphibian conservation: Historic survey uncovers the disease-driven collapse of a once mega-diverse community

inferred← citeshttps://doi.org/10.1007/s10592-016-0923-5openalex-snapshot

Population genetic structure of the endangered Sierra Nevada yellow-legged frog (Rana sierrae) in Yosemite National Park based on multi-locus nuclear data from swab samples

inferred← citeshttps://doi.org/10.1007/s10661-011-2378-yopenalex-snapshot

Assessment of the effects of urbanization on trace elements of toe bones

inferred← citeshttps://doi.org/10.1007/s10682-023-10247-3openalex-snapshot

High relative humidity and temperature limit disease development and mortality in golden frogs of Panama, Atelopus zeteki, infected with Batrachochytrium dendrobatidis

inferred← citeshttps://doi.org/10.1007/s10750-017-3367-0openalex-snapshot

Stream tadpoles present high prevalence but low infection loads of Batrachochytrium dendrobatidis (Chytridiomycota)

inferred← citeshttps://doi.org/10.1007/s10750-018-3614-zopenalex-snapshot

Host–pathogen dynamics among the invasive American bullfrog (Lithobates catesbeianus) and chytrid fungus (Batrachochytrium dendrobatidis)

inferred← citeshttps://doi.org/10.1007/s10750-020-04339-2openalex-snapshot

High temporal and individual variation in the prevalence and intensity of chytrid infection in the southernmost Leaf Frog of the genus Pithecopus (Anura, Phyllomedusidae)

inferred← citeshttps://doi.org/10.1007/s10750-026-06301-0openalex-snapshot

Farming-associated variation in chytrid infection and shedding dynamics in invasive American bullfrogs

inferred← citeshttps://doi.org/10.1007/s11259-023-10129-7openalex-snapshot

Pilot survey reveals ophidiomycosis in dice snakes Natrix tessellata from Lake Garda, Italy

inferred← citeshttps://doi.org/10.1007/s11356-015-4566-8openalex-snapshot

The effects of a fungicide and chytrid fungus on anuran larvae in aquatic mesocosms

inferred← citeshttps://doi.org/10.1007/s12026-025-09599-5openalex-snapshot

Amphibian cellular immune response to chytridiomycosis at metamorphic climax

inferred← citeshttps://doi.org/10.1007/s12210-017-0640-0openalex-snapshot

Validation and cost-effectiveness of an alternative method to quantify Batrachochytrium dendrobatidis infection in amphibian samples using real-time PCR

inferred← citeshttps://doi.org/10.1007/s12686-024-01375-1openalex-snapshot

From jaguars to pathogens: simultaneous genetic detection of diverse taxa across biodiversity hotspots in the U.S. arid southwest

inferred← citeshttps://doi.org/10.1007/s12686-026-01436-7openalex-snapshot

Refining ranavirus surveillance: evaluating non-lethal sampling of larval amphibians

inferred← citeshttps://doi.org/10.1016/b978-1-4377-1986-4.00028-7openalex-snapshot

Diagnosis and Control of Amphibian Chytridiomycosis

inferred← citeshttps://doi.org/10.1016/b978-1-4557-0893-2.00022-3openalex-snapshot

Chytridiomycosis

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2016.05.009openalex-snapshot

Insights From Genomics Into Spatial and Temporal Variation in Batrachochytrium dendrobatidis

inferred← citeshttps://doi.org/10.1016/j.anbehav.2021.01.007openalex-snapshot

Disease influences male advertisement and mating outcomes in a critically endangered amphibian

inferred← citeshttps://doi.org/10.1016/j.biocon.2008.03.011openalex-snapshot

Distribution and environmental limitations of an amphibian pathogen in the Rocky Mountains, USA

inferred← citeshttps://doi.org/10.1016/j.biocon.2008.08.009openalex-snapshot

Widespread occurrence of an emerging pathogen in amphibian communities of the Venezuelan Andes

inferred← citeshttps://doi.org/10.1016/j.biocon.2009.02.007openalex-snapshot

Magnitude of the US trade in amphibians and presence of Batrachochytrium dendrobatidis and ranavirus infection in imported North American bullfrogs (Rana catesbeiana)

inferred← citeshttps://doi.org/10.1016/j.biocon.2011.03.018openalex-snapshot

Disease dynamics vary spatially and temporally in a North American amphibian

inferred← citeshttps://doi.org/10.1016/j.biocon.2011.08.008openalex-snapshot

Factors related to the distribution and prevalence of the fungal pathogen Batrachochytrium dendrobatidis in Rana cascadae and other amphibians in the Klamath Mountains

inferred← citeshttps://doi.org/10.1016/j.biocon.2011.12.003openalex-snapshot

Amphibian-killing fungus loses genetic diversity as it spreads across the New World

inferred← citeshttps://doi.org/10.1016/j.biocon.2012.11.023openalex-snapshot

High prevalence of infection in tadpoles increases vulnerability to fungal pathogen in high-Andean amphibians

inferred← citeshttps://doi.org/10.1016/j.biocon.2013.12.034openalex-snapshot

Decline and re-expansion of an amphibian with high prevalence of chytrid fungus

inferred← citeshttps://doi.org/10.1016/j.biocon.2014.05.029openalex-snapshot

The effect of captivity on the cutaneous bacterial community of the critically endangered Panamanian golden frog (Atelopus zeteki)

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1016/j.biocon.2015.01.034openalex-snapshot

Chytrid fungus infections in laboratory and introduced Xenopus laevis populations: assessing the risks for U.K. native amphibians

inferred← citeshttps://doi.org/10.1016/j.biocon.2015.04.007openalex-snapshot

Skin bacteria provide early protection for newly metamorphosed southern leopard frogs (Rana sphenocephala) against the frog-killing fungus, Batrachochytrium dendrobatidis

inferred← citeshttps://doi.org/10.1016/j.biocon.2015.08.039openalex-snapshot

Reconstructing historical and contemporary disease dynamics: A case study using the California slender salamander

inferred← citeshttps://doi.org/10.1016/j.biocon.2015.12.041openalex-snapshot

In-situ itraconazole treatment improves survival rate during an amphibian chytridiomycosis epidemic

inferred← citeshttps://doi.org/10.1016/j.biocon.2019.05.017openalex-snapshot

Effect of amphibian chytrid fungus (Batrachochytrium dendrobatidis) on apparent survival of frogs and toads in the western USA

inferred← citeshttps://doi.org/10.1016/j.biocon.2020.108521openalex-snapshot

Synergistic effects of warming and disease linked to high mortality in cool-adapted terrestrial frogs

inferred← citeshttps://doi.org/10.1016/j.biocon.2021.109088openalex-snapshot

One hundred years of infection with three global pathogens in frog populations of Florida, USA

inferred← citeshttps://doi.org/10.1016/j.biocon.2021.109246openalex-snapshot

Fungal disease cluster in tropical terrestrial frogs predicted by low rainfall

inferred← citeshttps://doi.org/10.1016/j.biocon.2021.109391openalex-snapshot

Chytrid infection dynamics in frog populations from climatically disparate regions

inferred← citeshttps://doi.org/10.1016/j.biocon.2024.110504openalex-snapshot

Historical and contemporary impacts of an invasive fungal pathogen on the Yosemite toad

inferred← citeshttps://doi.org/10.1016/j.biocon.2024.110685openalex-snapshot

Partitioning the influence of host specificity in amphibian populations threatened by multiple emerging infectious diseases

inferred← citeshttps://doi.org/10.1016/j.biocon.2024.110702openalex-snapshot

Extreme climatic events modulate chytrid infection across the landscape

inferred← citeshttps://doi.org/10.1016/j.biocon.2025.111547openalex-snapshot

Origin and global spread of an endemic chytrid fungus lineage linked to the bullfrog trade

inferred← citeshttps://doi.org/10.1016/j.cbpb.2025.111113openalex-snapshot

Fungal disease does not affect skin carotenoid concentrations in dietary-supplemented strawberry poison frogs

inferred← citeshttps://doi.org/10.1016/j.cimid.2013.07.002openalex-snapshot

Bacterial flora on Cascades frogs in the Klamath mountains of California

inferred← citeshttps://doi.org/10.1016/j.crmicr.2023.100213openalex-snapshot

Low-level pathogen infection and geographic location correlate with the skin microbiomes of Columbia spotted frogs (Rana luteiventris) in a montane landscape

inferred← citeshttps://doi.org/10.1016/j.cub.2026.09.048openalex-snapshot

The chytrid fungus threatens the last epidemiologically naive Neotropical montane amphibian biodiversity hotspot

inferred← citeshttps://doi.org/10.1016/j.cvex.2013.01.005openalex-snapshot

Selected Emerging Diseases of Amphibia

inferred← citeshttps://doi.org/10.1016/j.cvex.2013.05.009openalex-snapshot

Pathogenesis, Diagnosis, and Treatment of Amphibian Chytridiomycosis

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2012.04.006openalex-snapshot

Effects of herbicides and the chytrid fungus Batrachochytrium dendrobatidis on the health of post-metamorphic northern leopard frogs (Lithobates pipiens)

inferred← citeshttps://doi.org/10.1016/j.envres.2024.118249openalex-snapshot

Chytridiomycosis causes high amphibian mortality prior to the completion of metamorphosis

inferred← citeshttps://doi.org/10.1016/j.fbr.2008.02.001openalex-snapshot

The ecology of chytrids in aquatic ecosystems: roles in food web dynamics

inferred← citeshttps://doi.org/10.1016/j.fgb.2012.07.002openalex-snapshot

Batrachochytrium dendrobatidis zoospore secretions rapidly disturb intercellular junctions in frog skin

inferred← citeshttps://doi.org/10.1016/j.fgb.2023.103858openalex-snapshot

Sequence capture identifies fastidious chytrid fungi directly from host tissue

inferred← citeshttps://doi.org/10.1016/j.funbio.2013.01.004openalex-snapshot

Combining ethidium monoazide treatment with real-time PCR selectively quantifies viable Batrachochytrium dendrobatidis cells

inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101546openalex-snapshot

Host life stage susceptibility to the chytrid fungus in a Neotropical torrent frog

inferred← citeshttps://doi.org/10.1016/j.funeco.2015.09.014openalex-snapshot

Local phenotypic variation in amphibian-killing fungus predicts infection dynamics

inferred← citeshttps://doi.org/10.1016/j.funeco.2020.100995openalex-snapshot

Biotic and abiotic determinants of Batrachochytrium dendrobatidis infections in amphibians of the Brazilian Atlantic Forest

inferred← citeshttps://doi.org/10.1016/j.gecco.2020.e01314openalex-snapshot

Towards a food web based control strategy to mitigate an amphibian panzootic in agricultural landscapes

inferred← citeshttps://doi.org/10.1016/j.gecco.2021.e01968openalex-snapshot

High fungal pathogen loads and prevalence in Baja California amphibian communities: The importance of species, elevation, and historical context

inferred← citeshttps://doi.org/10.1016/j.gecco.2025.e03599openalex-snapshot

Reproductive habitat mismatch influences chytrid infection dynamics in a tropical amphibian community

inferred← citeshttps://doi.org/10.1016/j.gene.2014.03.051openalex-snapshot

Conservation and divergence in the frog immunome: pyrosequencing and de novo assembly of immune tissue transcriptomes

inferred← citeshttps://doi.org/10.1016/j.ijppaw.2019.12.005openalex-snapshot

Chiggers (Acariformes: Trombiculoidea) do not increase rates of infection by Batrachochytrium dendrobatidis fungus in the endemic Dwarf Mexican Treefrog Tlalocohyla smithii (Anura: Hylidae)

inferred← citeshttps://doi.org/10.1016/j.jnc.2025.126996openalex-snapshot

Chytrid fungus in threatened Brazilian amphibians: A focus on island populations

inferred← citeshttps://doi.org/10.1016/j.jviromet.2017.08.016openalex-snapshot

A quantitative-PCR based method to estimate ranavirus viral load following normalisation by reference to an ultraconserved vertebrate target

inferred← citeshttps://doi.org/10.1016/j.mimet.2012.04.021openalex-snapshot

Magnetic capture hybridization of Batrachochytrium dendrobatidis genomic DNA

inferred← citeshttps://doi.org/10.1016/j.physbeh.2025.114951openalex-snapshot

Assessing the interconnected behavioral and physiological underpinnings of amphibian responses to fungal infection

inferred← citeshttps://doi.org/10.1016/j.prevetmed.2018.10.023openalex-snapshot

Design, statistical analysis and reporting standards for test accuracy studies for infectious diseases in animals: Progress, challenges and recommendations

inferred← citeshttps://doi.org/10.1016/j.pt.2014.04.004openalex-snapshot

Policy, phylogeny, and the parasite

inferred← citeshttps://doi.org/10.1016/j.rmb.2015.07.007openalex-snapshot

First record of Batrachochytrium dendrobatidis infecting threatened populations of Tandilean Red-belly toad (Melanophryniscus aff. montevidensis) in Argentina

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2016.05.062openalex-snapshot

Potential interactions among disease, pesticides, water quality and adjacent land cover in amphibian habitats in the United States

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.170337openalex-snapshot

Estrogen contamination increases vulnerability of amphibians to the deadly chytrid fungus

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.180923openalex-snapshot

Exposure to the herbicide 2,4-D exacerbates infection outcome of a global amphibian pathogen

inferred← citeshttps://doi.org/10.1016/j.tree.2009.07.011openalex-snapshot

The ecology and impact of chytridiomycosis: an emerging disease of amphibians

inferred← citeshttps://doi.org/10.1016/j.ygcen.2013.05.012openalex-snapshot

Non-invasive monitoring of glucocorticoid physiology within highland and lowland populations of native Australian Great Barred Frog (Mixophyes fasciolatus)

inferred← citeshttps://doi.org/10.1016/j.ygcen.2019.113269openalex-snapshot

Relationships between glucocorticoids and infection with Batrachochytrium dendrobatidis in three amphibian species

inferred← citeshttps://doi.org/10.1017/s003060531300029xopenalex-snapshot

The precarious persistence of the Endangered Sierra Madre yellow-legged frog Rana muscosa in southern California, USA

inferred← citeshttps://doi.org/10.1017/s0030605323001254openalex-snapshot

Release trial of captive-bred variable harlequin frogs Atelopus varius shows that frogs disperse rapidly, are difficult to recapture and do not readily regain skin toxicity

inferred← citeshttps://doi.org/10.1017/s0031182016001943openalex-snapshot

Pathological and phylogenetic characterization ofAmphibiothecumsp. infection in an isolated amphibian (Lissotriton helveticus) population on the island of Rum (Scotland)

inferred← citeshttps://doi.org/10.1021/acs.est.0c03219openalex-snapshot

Widespread Pig Farming Practice Linked to Shifts in Skin Microbiomes and Disease in Pond-Breeding Amphibians

inferred← citeshttps://doi.org/10.1021/acs.est.3c03191openalex-snapshot

Toxicities of Legacy and Current-Use PFAS in an Anuran: Do Larval Exposures Influence Responses to a Terrestrial Pathogen Challenge?

inferred← citeshttps://doi.org/10.1021/es401725sopenalex-snapshot

Nonmonotonic and Monotonic Effects of Pesticides on the Pathogenic Fungus Batrachochytrium dendrobatidis in Culture and on Tadpoles

inferred← citeshttps://doi.org/10.1038/ismej.2014.241openalex-snapshot

Correlates of virulence in a frog-killing fungal pathogen: evidence from a California amphibian decline

inferred← citeshttps://doi.org/10.1038/nature13491openalex-snapshot

Amphibians acquire resistance to live and dead fungus overcoming fungal immunosuppression

inferred← citeshttps://doi.org/10.1038/ncomms15048openalex-snapshot

Chytrid fungus infection in zebrafish demonstrates that the pathogen can parasitize non-amphibian vertebrate hosts

inferred← citeshttps://doi.org/10.1038/s41396-018-0284-9openalex-snapshot

Microbiota and skin defense peptides may facilitate coexistence of two sympatric Andean frog species with a lethal pathogen

inferred← citeshttps://doi.org/10.1038/s41396-020-00875-wopenalex-snapshot

The amphibian microbiome exhibits poor resilience following pathogen-induced disturbance

inferred← citeshttps://doi.org/10.1038/s41467-020-19241-7openalex-snapshot

Presence of low virulence chytrid fungi could protect European amphibians from more deadly strains

inferred← citeshttps://doi.org/10.1038/s41598-017-03352-1openalex-snapshot

Emerging fungal pathogen Ophidiomyces ophiodiicola in wild European snakes

inferred← citeshttps://doi.org/10.1038/s41598-017-03605-zopenalex-snapshot

Skin sloughing in susceptible and resistant amphibians regulates infection with a fungal pathogen

inferred← citeshttps://doi.org/10.1038/s41598-017-16425-yopenalex-snapshot

Low resistance to chytridiomycosis in direct-developing amphibians

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