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Host species vary in infection probability, sub-lethal effects and costs of immune response when exposed to an amphibian parasite
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/jtbi.1999.0982openalex-snapshot
Persistence of Tick-borne Virus in the Presence of Multiple Host Species: Tick Reservoirs and Parasite Mediated Competition
inferredcites →https://doi.org/10.1016/j.ijpara.2004.02.003openalex-snapshot
Optimal parasite infection strategies: a state-dependent approach
inferredcites →https://doi.org/10.1017/s0030605306000093openalex-snapshot
Chytrid fungus infection related to unusual mortalities of Salamandra salamandra and Bufo bufo in the Peñalara Natural Park, Spain
inferredcites →https://doi.org/10.1034/j.1600-0706.2002.960110.xopenalex-snapshot
Optimal infection strategies: should macroparasites hedge their bets?
inferredcites →https://doi.org/10.1038/38483openalex-snapshot
Trade-off between parasitoid resistance and larval competitive ability in Drosophila melanogaster
inferredcites →https://doi.org/10.1046/j.1365-2656.2003.00777.xopenalex-snapshot
The population dynamical implications of covert infections in host–microparasite interactions
inferredcites →https://doi.org/10.1046/j.1461-0248.2003.00501.xopenalex-snapshot
Parasite establishment in host communities
inferredcites →https://doi.org/10.1073/pnas.0506889103openalex-snapshot
Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community
inferredcites →https://doi.org/10.1073/pnas.1108490108openalex-snapshot
A dilution effect in the emerging amphibian pathogen Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1073/pnas.1111915108openalex-snapshot
Multiple emergences of genetically diverse amphibian-infecting chytrids include a globalized hypervirulent recombinant lineage
inferredcites →https://doi.org/10.1073/pnas.95.15.9031openalex-snapshot
Chytridiomycosis causes amphibian mortality associated with population declines in the rain forests of Australia and Central America
inferredcites →https://doi.org/10.1080/15572536.2008.11832493openalex-snapshot
Chemotaxis of the amphibian pathogenBatrachochytrium dendrobatidisand its response to a variety of attractants
inferredcites →https://doi.org/10.1086/346134openalex-snapshot
Assessing the Cost of Mounting an Immune Response
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004143openalex-snapshot
Roles of Diversifying Selection and Coordinated Evolution in the Evolution of Amphibian Antimicrobial Peptides
inferredcites →https://doi.org/10.1098/rspb.1999.0650openalex-snapshot
Cost of resistance: relationship between reduced fertility and increased resistance in a snail—schistosome host—parasite system
inferredcites →https://doi.org/10.1111/cobi.12128openalex-snapshot
Assessing Risk and Guidance on Monitoring of Batrachochytrium dendrobatidis in Europe through Identification of Taxonomic Selectivity of Infection
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00298.xopenalex-snapshot
PATTERNS OF NATURAL SELECTION ON SIZE AT METAMORPHOSIS IN WATER FROGS
inferredcites →https://doi.org/10.1111/j.1365-2435.2006.01163.xopenalex-snapshot
Immune challenge reduces reproductive output and growth in a lizard
inferredcites →https://doi.org/10.1111/j.1365-2486.2010.02272.xopenalex-snapshot
Climate change, chytridiomycosis or condition: an experimental test of amphibian survival
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.04041.xopenalex-snapshot
Proteomic and phenotypic profiling of the amphibian pathogen Batrachochytrium dendrobatidis shows that genotype is linked to virulence
inferredcites →https://doi.org/10.1111/j.1432-1033.1996.0788r.xopenalex-snapshot
Temporins, Antimicrobial Peptides from the European Red Frog Rana temporaria
inferredcites →https://doi.org/10.1111/j.1461-0248.2006.00885.xopenalex-snapshot
Effects of species diversity on disease risk
inferredcites →https://doi.org/10.1111/j.1461-0248.2008.01212.xopenalex-snapshot
Diversity and disease: community structure drives parasite transmission and host fitness
inferredcites →https://doi.org/10.1111/j.1461-0248.2009.01434.xopenalex-snapshot
Factors driving pathogenicity vs. prevalence of amphibian panzootic chytridiomycosis in Iberia
inferredcites →https://doi.org/10.1111/j.1523-1739.2011.01708.xopenalex-snapshot
Differential Host Susceptibility to Batrachochytrium dendrobatidis , an Emerging Amphibian Pathogen
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01570.xopenalex-snapshot
GENETIC EROSION IN WILD POPULATIONS MAKES RESISTANCE TO A PATHOGEN MORE COSTLY
inferredcites →https://doi.org/10.1111/j.1600-0706.2008.17202.xopenalex-snapshot
Life history tradeoffs influence mortality associated with the amphibian pathogen Batrachochytrium dendrobatidis
inferredcites →https://doi.org/10.1111/j.1755-263x.2008.00015.xopenalex-snapshot
Predicting susceptibility to future declines in the world's frogs
inferredcites →https://doi.org/10.1128/aac.47.3.1157-1160.2003openalex-snapshot
Activities of Temporin Family Peptides against the Chytrid Fungus (Batrachochytrium dendrobatidis) Associated with Global Amphibian Declines
inferredcites →https://doi.org/10.1242/jeb.037721openalex-snapshot
Diversity, decoys and the dilution effect: how ecological communities affect disease risk
inferredcites →https://doi.org/10.1371/journal.pone.0004616openalex-snapshot
Evidence for Directional Selection at a Novel Major Histocompatibility Class I Marker in Wild Common Frogs (Rana temporaria) Exposed to a Viral Pathogen (Ranavirus)
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/10.1890/04-0383openalex-snapshot
FUNGAL PATHOGEN CAUSES COMPETITIVE AND DEVELOPMENTAL STRESS IN LARVAL AMPHIBIAN COMMUNITIES
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/10.2307/5220openalex-snapshot
The Effects of a Sublethal Baculovirus Infection in the Indian Meal Moth, Plodia interpunctella
inferredcites →https://doi.org/10.3201/eid1112.050306openalex-snapshot
Community Epidemiology Framework for Classifying Disease Threats
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/dao075201openalex-snapshot
Strain differences in the amphibian chytrid Batrachochytrium dendrobatidis and non-permanent, sub-lethal effects of infection
inferredcites →https://doi.org/10.3852/mycologia.100.1.1openalex-snapshot
Chemotaxis of the amphibian pathogen Batrachochytrium dendrobatidis and its response to a variety of attractants
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/ece3.11679openalex-snapshot
Potential effects of traffic noise on anuran call characteristics in Louisiana, USA during winter
inferred← citeshttps://doi.org/10.1002/ece3.70219openalex-snapshot
No sex‐dependent mortality in an amphibian upon infection with the chytrid fungus, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1002/ecs2.70458openalex-snapshot
Persistence of sub‐clinical infections caused by Batrachochytrium dendrobatidis in stream anurans in South Asia
inferred← citeshttps://doi.org/10.1002/edn3.180openalex-snapshot
The first detection of the fungal pathogen batrachochytrium dendrobatidis in Norway with no evidence of population declines for great crested and smooth newts based on modeling on traditional trapping data
inferred← citeshttps://doi.org/10.1002/edn3.283openalex-snapshot
Tracking the prevalence of a fungal pathogen, Batrachochytrium dendrobatidis (chytrid fungus), using environmental DNA
inferred← citeshttps://doi.org/10.1002/oik.12414openalex-snapshot
Ranavirus risk depends on host community characteristics more than the presence of Batrachochytrium dendrobatidis
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/s10530-016-1161-yopenalex-snapshot
Invasive North American bullfrogs transmit lethal fungus Batrachochytrium dendrobatidis infections to native amphibian host species
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/10.1016/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.ijpara.2018.11.003openalex-snapshot
Neither Diplectanum nor specific: a dramatic twist to the taxonomic framework of Diplectanum (Monogenea: Diplectanidae)
inferred← citeshttps://doi.org/10.1017/9781316479964.018openalex-snapshot
When chytrid fungus invades: integrating theory and data to understand disease-induced amphibian declines
inferred← citeshttps://doi.org/10.1038/s41598-018-35874-7openalex-snapshot
Interaction between temperature and sublethal infection with the amphibian chytrid fungus impacts a susceptible frog species
inferred← citeshttps://doi.org/10.1038/s41598-020-78196-3openalex-snapshot
Single infection with Batrachochytrium dendrobatidis or Ranavirus does not increase probability of co-infection in a montane community of amphibians
inferred← citeshttps://doi.org/10.1038/srep30772openalex-snapshot
Dynamics and genetics of a disease-driven species decline to near extinction: lessons for conservation
inferred← citeshttps://doi.org/10.1086/720638openalex-snapshot
Host Identity Matters—Up to a Point: The Community Context of Batrachochytrium dendrobatidis Transmission
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.001.0001openalex-snapshot
Evolutionary Parasitology
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.002.0006openalex-snapshot
List of common acronyms
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0001openalex-snapshot
Parasites and their significance
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0002openalex-snapshot
The study of evolutionary parasitology
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0003openalex-snapshot
The diversity and natural history of parasites
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0004openalex-snapshot
The natural history of defences
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0005openalex-snapshot
Ecological immunology
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0006openalex-snapshot
Parasites, immunity, and sexual selection
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0008openalex-snapshot
Parasite immune evasion and manipulation of host phenotype
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0009openalex-snapshot
Transmission, infection, and pathogenesis
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0010openalex-snapshot
Host–parasite genetics
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0011openalex-snapshot
Between-host dynamics (Epidemiology)
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0012openalex-snapshot
Within-host dynamics and evolution
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0013openalex-snapshot
Virulence evolution
inferred← citeshttps://doi.org/10.1093/oso/9780198832140.003.0014openalex-snapshot
Host–parasite co-evolution
inferred← citeshttps://doi.org/10.1098/rsos.170910openalex-snapshot
Gene expression differs in susceptible and resistant amphibians exposed to Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1098/rspb.2024.1157openalex-snapshot
Archival mitogenomes identify invasion by the Batrachochytrium dendrobatidis CAPE lineage caused an African amphibian extinction in the wild
inferred← citeshttps://doi.org/10.1098/rstb.2015.0454openalex-snapshot
Climate forcing of an emerging pathogenic fungus across a montane multi-host community
inferred← citeshttps://doi.org/10.1098/rstb.2016.0090openalex-snapshot
Host species exploitation and discrimination by animal parasites
inferred← citeshttps://doi.org/10.1101/2021.07.16.452656openalex-snapshot
Body size mediates latitudinal population differences in response to Bd infection in two amphibian species
inferred← citeshttps://doi.org/10.1101/2023.08.25.554788openalex-snapshot
Infection with the chytrid fungus ( Batrachochytrium dendrobatidis ) may distort sex ratio via sex reversal but not sex-dependent mortality in a common Eurasian amphibian
inferred← citeshttps://doi.org/10.1101/2025.06.18.660433openalex-snapshot
Host species composition, not priority effects, determines infection risk in multihost-multiparasite amphibian communities
inferred← citeshttps://doi.org/10.1101/290239openalex-snapshot
Host Diet Influences Lethal and Sublethal Responses of Hosts to Amphibian Pathogen Exposure
inferred← citeshttps://doi.org/10.1111/1365-2435.13038openalex-snapshot
Routine habitat switching alters the likelihood and persistence of infection with a pathogenic parasite
inferred← citeshttps://doi.org/10.1111/btp.13186openalex-snapshot
Chytrid prevalence and infection intensity in treefrogs from three environments with different degrees of conservation in Mexico
inferred← citeshttps://doi.org/10.1111/ele.12814openalex-snapshot
Resistance, tolerance and environmental transmission dynamics determine host extinction risk in a load‐dependent amphibian disease
inferred← citeshttps://doi.org/10.1111/ele.13621openalex-snapshot
Mechanisms underlying host persistence following amphibian disease emergence determine appropriate management strategies
inferred← citeshttps://doi.org/10.1111/eva.12520openalex-snapshot
Amphibian species traits, evolutionary history and environment predict Batrachochytrium dendrobatidis infection patterns, but not extinction risk
inferred← citeshttps://doi.org/10.1111/jeb.13987openalex-snapshot
Challenging a host–pathogen paradigm: Susceptibility to chytridiomycosis is decoupled from genetic erosion
inferred← citeshttps://doi.org/10.1111/jzo.12773openalex-snapshot
Chytrid fungus dynamics and infections associated with movement distances in a red‐listed amphibian
inferred← citeshttps://doi.org/10.1111/jzo.12974openalex-snapshot
Metamorphic common toads keep chytrid infection under control, but at a cost
inferred← citeshttps://doi.org/10.1163/15685381-00003099openalex-snapshot
Differences in chytridiomycosis infection costs between two amphibian species from Central Europe
inferred← citeshttps://doi.org/10.1186/s12898-018-0189-5openalex-snapshot
Fungal infection has sublethal effects in a lowland subtropical amphibian population
inferred← citeshttps://doi.org/10.1186/s13568-023-01585-0openalex-snapshot
Metabolites of Xenorhabdus bacteria are potent candidates for mitigating amphibian chytridiomycosis
inferred← citeshttps://doi.org/10.1371/journal.pone.0188384openalex-snapshot
Introduced bullfrog facilitates pathogen invasion in the western United States
inferred← citeshttps://doi.org/10.1371/journal.pone.0208969openalex-snapshot
Batrachochytrium dendrobatidis infection in amphibians predates first known epizootic in Costa Rica
inferred← citeshttps://doi.org/10.1655/0018-0831-76.2.101openalex-snapshot
A Synthesis of Evidence of Drivers of Amphibian Declines
inferred← citeshttps://doi.org/10.1655/0018-0831-76.2.132openalex-snapshot
Effects of Snowpack, Temperature, and Disease on Demography in a Wild Population of Amphibians
inferred← citeshttps://doi.org/10.17520/biods.2023274openalex-snapshot
Current status and challenges on the effects of chytrid infection on amphibian populations
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4281618/v1openalex-snapshot
Climatic drivers of chytrid prevalence in the critically endangered Admirable Redbelly Toad
inferred← citeshttps://doi.org/10.33256/hj29.4189-206openalex-snapshot
Emerging infectious disease threats to European herpetofauna
inferred← citeshttps://doi.org/10.3354/dao03502openalex-snapshot
Occurrence of Batrachochytrium dendrobatidis in Sweden: higher infection prevalence in southern species
inferred← citeshttps://doi.org/10.3354/dao03599openalex-snapshot
Surveying for Batrachochytrium dendrobatidis and B. salamandrivorans in wild and captive amphibian populations in Estonia and Latvia
inferred← citeshttps://doi.org/10.3354/dao03603openalex-snapshot
Seasonal variation of Batrachochytrium dendrobatidis in a threatened anuran species from Uruguay
inferred← citeshttps://doi.org/10.3389/fevo.2018.00236openalex-snapshot
Long-Term Habitat Fragmentation Is Associated With Reduced MHC IIB Diversity and Increased Infections in Amphibian Hosts
inferred← citeshttps://doi.org/10.3389/fevo.2022.915271openalex-snapshot
Major Histocompatibility Complex Variation and Haplotype Associated Survival in Response to Experimental Infection of Two Bd-GPL Strains Along a Latitudinal Gradient
inferred← citeshttps://doi.org/10.3389/fvets.2021.732993openalex-snapshot
Direct and Latent Effects of Pathogen Exposure Across Native and Invasive Amphibian Life Stages
inferred← citeshttps://doi.org/10.3390/d10030081openalex-snapshot
Effects of Emerging Infectious Diseases on Amphibians: A Review of Experimental Studies
inferred← citeshttps://doi.org/10.3390/d13060262openalex-snapshot
Does Chytridiomycosis Affect Tree Frog Attachment?
inferred← citeshttps://doi.org/10.7589/2019-01-021openalex-snapshot
LETHAL AND SUBLETHAL AMPHIBIAN HOST RESPONSES TO BATRACHOCHYTRIUM DENDROBATIDIS EXPOSURE ARE DETERMINED BY THE ADDITIVE INFLUENCE OF HOST RESOURCE AVAILABILITY
inferred← citeshttps://doi.org/10.7717/peerj.12889openalex-snapshot
Temperature and duration of exposure drive infection intensity with the amphibian pathogen Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.7717/peerj.4698openalex-snapshot
Seasonal migrations, body temperature fluctuations, and infection dynamics in adult amphibians
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