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Microbial grazers may aid in controlling infections caused by aquatic zoosporic fungi

https://doi.org/10.1101/2020.02.03.931857

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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/bies.950140113openalex-snapshot

Chemosensory behaviour of Tetrahymena

inferredcites →https://doi.org/10.1002/ece3.777openalex-snapshot

Daphnia predation on the amphibian chytrid fungus and its impacts on disease risk in tadpoles

inferredcites →https://doi.org/10.1007/978-3-642-73086-3openalex-snapshot

Paramecium

inferredcites →https://doi.org/10.1007/978-90-481-2801-3_10openalex-snapshot

The “Tetrahymena pyriformis” complex of cryptic species

inferredcites →https://doi.org/10.1007/978-94-009-1583-1_50openalex-snapshot

Influence of the filamentous cyanobacterium Planktothrix agardhii on population growth and reproductive pattern of the rotifer Brachionus calyciflorus

inferredcites →https://doi.org/10.1007/bf00170069openalex-snapshot

Monoxenic and mixed cultures of the small metazoa Philodina erythrophthalma and Aeolosoma hemprichi isolated from a waste-water treatment process

inferredcites →https://doi.org/10.1007/bf00344893openalex-snapshot

The dependence of reproductive rate on cell size and temperature in freshwater ciliated protozoa

inferredcites →https://doi.org/10.1007/bf00348052openalex-snapshot

Maximum growth rate, size and commonness in a community of bactivorous ciliates

inferredcites →https://doi.org/10.1007/bf02011594openalex-snapshot

Survival of ciliate protozoa under starvation conditions and at low bacterial levels

inferredcites →https://doi.org/10.1007/s00248-003-9000-yopenalex-snapshot

Determining Parameters of the Numerical Response

inferredcites →https://doi.org/10.1007/s10531-011-0147-4openalex-snapshot

Predation by zooplankton on Batrachochytrium dendrobatidis: biological control of the deadly amphibian chytrid fungus?

inferredcites →https://doi.org/10.1016/j.biocon.2015.12.041openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.cub.2013.11.032openalex-snapshot

Microscopic Aquatic Predators Strongly Affect Infection Dynamics of a Globally Emerged Pathogen

inferredcites →https://doi.org/10.1016/j.ejop.2012.08.001openalex-snapshot

Systematics and species-specific response to pH of Oxytricha acidotolerans sp. nov. and Urosomoida sp. (Ciliophora, Hypotricha) from acid mining lakes

inferredcites →https://doi.org/10.1016/j.mib.2016.03.016openalex-snapshot

Aquatic fungi: targeting the forgotten in microbial ecology

inferredcites →https://doi.org/10.1016/j.protis.2010.04.001openalex-snapshot

The Filter-Feeding Ciliates Colpidium striatum and Tetrahymena pyriformis Display Selective Feeding Behaviours in the Presence of Mixed, Equally-Sized, Bacterial Prey

inferredcites →https://doi.org/10.1016/j.protis.2015.02.003openalex-snapshot

Restructuring Fundamental Predator-Prey Models by Recognising Prey-Dependent Conversion Efficiency and Mortality Rates

inferredcites →https://doi.org/10.1016/j.pt.2019.04.003openalex-snapshot

Biological Concepts for the Control of Aquatic Zoosporic Diseases

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/10.1073/pnas.0912886107openalex-snapshot

Enzootic and epizootic dynamics of the chytrid fungal pathogen of amphibians

inferredcites →https://doi.org/10.1086/705381openalex-snapshot

False Exclusion: A Case to Embed Predator Performance in Classical Population Models

inferredcites →https://doi.org/10.1093/labmed/15.2.109openalex-snapshot

Use of Calcofluor White in Clinical Mycology

inferredcites →https://doi.org/10.1098/rsbl.2015.0874openalex-snapshot

Successful elimination of a lethal wildlife infectious disease in nature

inferredcites →https://doi.org/10.1098/rspb.2007.1356openalex-snapshot

Persistence of the emerging pathogen Batrachochytrium dendrobatidis outside the amphibian host greatly increases the probability of host extinction

inferredcites →https://doi.org/10.1098/rspb.2013.2783openalex-snapshot

Assessing host extinction risk following exposure to Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.1098/rstb.2016.0207openalex-snapshot

Mitigating amphibian chytridiomycoses in nature

inferredcites →https://doi.org/10.1111/avj.12337openalex-snapshot

Mortality in northern corroboree frog tadpoles (Pseudophryne pengilleyi) associated with Tetrahymena‐like infection

inferredcites →https://doi.org/10.1111/ecog.02378openalex-snapshot

Spatial extinction or persistence: landscape‐temperature interactions perturb predator–prey dynamics

inferredcites →https://doi.org/10.1111/ele.13239openalex-snapshot

Impacts of thermal mismatches on chytrid fungus Batrachochytrium dendrobatidis prevalence are moderated by life stage, body size, elevation and latitude

inferredcites →https://doi.org/10.1111/fwb.12685openalex-snapshot

Effects of nutrient supplementation on host‐pathogen dynamics of the amphibian chytrid fungus: a community approach

inferredcites →https://doi.org/10.1111/j.1365-2427.2011.02731.xopenalex-snapshot

Daphnia in tadpole mesocosms: trophic links and interactions with Batrachochytrium dendrobatidis

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.1461-0248.2009.01434.xopenalex-snapshot

Factors driving pathogenicity vs. prevalence of amphibian panzootic chytridiomycosis in Iberia

inferredcites →https://doi.org/10.1111/j.1550-7408.1969.tb02336.xopenalex-snapshot

The Effects of Temperature on Blepharisma intermedium

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.1600-0706.2009.17875.xopenalex-snapshot

Parameterising variable assimilation efficiency in predator–prey models

inferredcites →https://doi.org/10.1111/jeu.12299openalex-snapshot

Did Gause Have a Yeast Infection?

inferredcites →https://doi.org/10.1111/jeu.12642openalex-snapshot

Barcodes Reveal 48 New Species of Tetrahymena , Dexiostoma , and Glaucoma : Phylogeny, Ecology, and Biogeography of New and Established Species

inferredcites →https://doi.org/10.1126/science.71.1843.442openalex-snapshot

STOCK CULTURES OF AMEBA

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/aem.00087-16openalex-snapshot

Evaluation of Daphnid Grazing on Microscopic Zoosporic Fungi by Using Comparative Threshold Cycle Quantitative PCR

inferredcites →https://doi.org/10.1146/annurev.ento.47.091201.145240openalex-snapshot

Can Generalist Predators be Effective Biocontrol Agents?

inferredcites →https://doi.org/10.1306/74d71c6c-2b21-11d7-8648000102c1865dopenalex-snapshot

Tadpole holes; a true biogenic sedimentary structure

inferredcites →https://doi.org/10.1371/journal.pone.0035038openalex-snapshot

Waterfowl: Potential Environmental Reservoirs of the Chytrid Fungus Batrachochytrium dendrobatidis

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/10.2307/1935111openalex-snapshot

Diel Patterns of Aggregative Behavior in Tadpoles of Bufo Americanus, in Relation to Light and Temperature

inferredcites →https://doi.org/10.2307/3761981openalex-snapshot

Physiology of Batrachochytrium dendrobatidis, a Chytrid Pathogen of Amphibians

inferredcites →https://doi.org/10.3354/ame01229openalex-snapshot

Selective feeding behaviour of key free-living protists: avenues for continued study

inferredcites →https://doi.org/10.3354/ame020167openalex-snapshot

Population dynamics of the marine planktonic ciliate Strombidinopsis multiauris: its potential to control phytoplankton blooms

inferredcites →https://doi.org/10.3354/ame022057openalex-snapshot

Functional response and particle size selection of Halteria cf. grandinella, a common freshwater oligotrichous ciliate

inferredcites →https://doi.org/10.3354/ame032307openalex-snapshot

Using Q10: Can growth rates increase linearly with temperature?

inferredcites →https://doi.org/10.3354/ame040163openalex-snapshot

Numerical and functional responses of choreo- and oligotrich planktonic ciliates

inferredcites →https://doi.org/10.3354/dao01831openalex-snapshot

Quantitative PCR detection of Batrachochytrium dendrobatidis DNA from sediments and water

inferredcites →https://doi.org/10.3354/dao01850openalex-snapshot

Environmental detection of Batrachochytrium dendrobatidis in a temperate climate

inferredcites →https://doi.org/10.3354/dao02991openalex-snapshot

Dead or alive? Viability of chytrid zoospores shed from live amphibian hosts

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

Life cycle stages of the amphibian chytrid Batrachochytrium dendrobatidis

inferredcites →https://doi.org/10.3354/meps010257openalex-snapshot

The Ecological Role of Water-Column Microbes in the Sea

inferredcites →https://doi.org/10.3354/meps114175openalex-snapshot

Fitting ecological and physiological data to rectangular hyperbolae: a comparison of methods using Monte Carlo simulations

inferredcites →https://doi.org/10.3354/meps130241openalex-snapshot

Growth responses of planktonic ciliates in the genera Strobilidium and Strombidium

inferredcites →https://doi.org/10.3389/fmicb.2014.00166openalex-snapshot

Mycoloop: chytrids in aquatic food webs

inferredcites →https://doi.org/10.3389/fmicb.2014.00244openalex-snapshot

Ecological functions of zoosporic hyperparasites

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/10.3389/fmicb.2020.592286openalex-snapshot

Microbial Grazers May Aid in Controlling Infections Caused by the Aquatic Zoosporic Fungus Batrachochytrium dendrobatidis

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