Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
about
Seasonal pattern of Batrachochytrium dendrobatidis infection and mortality in Lithobates areolatus: affirmation of Vredenburg's "10,000 zoospore rule"Is chytridiomycosis an emerging infectious disease in Asia?Using "Omics" and Integrated Multi-Omics Approaches to Guide Probiotic Selection to Mitigate Chytridiomycosis and Other Emerging Infectious DiseasesViolacein: Properties and Production of a Versatile Bacterial PigmentPathogenic chytrid fungus Batrachochytrium dendrobatidis, but not B. salamandrivorans, detected on eastern hellbendersSeasonal and ontogenetic variation of skin microbial communities and relationships to natural disease dynamics in declining amphibiansA horizon scan of global conservation issues for 2014The rise of pathogens: predation as a factor driving the evolution of human pathogens in the environmentBacterial-fungal interactions: hyphens between agricultural, clinical, environmental, and food microbiologistsMitigating amphibian disease: strategies to maintain wild populations and control chytridiomycosisHigh quality draft genome sequence of Janthinobacterium psychrotolerans sp. nov., isolated from a frozen freshwater pondEmerging fungal threats to animal, plant and ecosystem healthBridging taxonomic and disciplinary divides in infectious disease.Disease and the dynamics of extinction.Deciphering microbial landscapes of fish eggs to mitigate emerging diseasesSkin sloughing in susceptible and resistant amphibians regulates infection with a fungal pathogen.Path analyses of cross-sectional and longitudinal data suggest that variability in natural communities of blood-associated parasites is derived from host characteristics and not interspecific interactionsCo-habiting amphibian species harbor unique skin bacterial communities in wild populations.Long-term monitoring of tropical alpine habitat change, Andean anurans, and chytrid fungus in the Cordillera Vilcanota, Peru: Results from a decade of study.Cutaneous bacteria of the redback salamander prevent morbidity associated with a lethal disease.Within- and among-population variation in chytridiomycosis-induced mortality in the toad Alytes obstetricans.Inhibition of Batrachochytrium dendrobatidis Caused by Bacteria Isolated from the Skin of Boreal Toads, Anaxyrus (Bufo) boreas boreas, from Grand Teton National Park, Wyoming, USA.Chytrid fungus infection in zebrafish demonstrates that the pathogen can parasitize non-amphibian vertebrate hosts.Evolutionary history and functional characterization of the amphibian xenosensor CAR.The impact of conservation on the status of the world's vertebrates.Cool temperatures reduce antifungal activity of symbiotic bacteria of threatened amphibians--implications for disease management and patterns of decline.Coincident mass extirpation of neotropical amphibians with the emergence of the infectious fungal pathogen Batrachochytrium dendrobatidisMuseum collections: Mining the past to manage the future.Motile zoospores of Batrachochytrium dendrobatidis move away from antifungal metabolites produced by amphibian skin bacteria.Unexpected rarity of the pathogen Batrachochytrium dendrobatidis in Appalachian Plethodon Salamanders: 1957-2011.Interactions between amphibians' symbiotic bacteria cause the production of emergent anti-fungal metabolites.Variations in the expressed antimicrobial peptide repertoire of northern leopard frog (Rana pipiens) populations suggest intraspecies differences in resistance to pathogens.Immune defenses against Batrachochytrium dendrobatidis, a fungus linked to global amphibian declines, in the South African clawed frog, Xenopus laevis.Ecophysiology meets conservation: understanding the role of disease in amphibian population declines.Microbiota of healthy corals are active against fungi in a light-dependent mannerSurviving chytridiomycosis: differential anti-Batrachochytrium dendrobatidis activity in bacterial isolates from three lowland species of Atelopus.The amphibian chytrid fungus, Batrachochytrium dendrobatidis, in fully aquatic salamanders from Southeastern North America.Tolerance of fungal infection in European water frogs exposed to Batrachochytrium dendrobatidis after experimental reduction of innate immune defenses.Microbiome Variation Across Amphibian Skin Regions: Implications for Chytridiomycosis Mitigation Efforts.Eco-Evo-Devo: developmental symbiosis and developmental plasticity as evolutionary agents.
P2860
Q21560853-AA0ED5F9-76CB-4243-8A0C-0DE0F408A2F8Q21560936-CC0D5B78-E380-4E7C-94B3-E89B9768B17BQ26766432-B737A9ED-02F8-4A84-938C-A24FF397DF9CQ26784521-D5B17DFD-9F3A-47FD-8F85-F6267ABB9419Q27317430-9488586F-E784-48A7-8642-FC69DF181061Q28608034-F375193F-FBB7-4C08-A6B2-55DEEC067E93Q28660818-9387C14B-DBD0-4C27-8654-B68D0AA6C522Q28707690-AB13F858-B257-4395-9901-31AA82F294F5Q28741795-3D467336-99FE-4D5F-90E0-959F1B92F46BQ28744438-713F332F-3B48-4CCB-9264-36EF700AB1CEQ28818787-238925FD-588C-452A-8B5D-92632CF10BD4Q29616753-FC1BB201-468E-44A4-A893-4B4FB9B84755Q30427826-F4E35BEF-933F-4AE7-9AEB-E1057B44F0A8Q30564142-2F2A912F-75F2-4C63-ADEB-32534E3779C0Q30588825-3905E42D-C2F3-4D33-8509-FF5B1032237BQ30855756-D1956266-B385-4E5F-8599-42E1EB8E6141Q30988019-7A43E0B4-A700-4EC9-8458-7F3C129F3A0CQ31031570-61EC0A68-5FAF-465A-96C2-28878316409EQ31170951-7BD5E95B-F054-488B-9935-4D3975081875Q33598334-94157DB1-97A9-4272-A694-97451E4410F0Q33598517-71D418C0-C58E-4BDE-8582-C7B37FB839B5Q33603232-8EDCA439-ADCF-49EA-9C05-C93D880B6EC2Q33622011-999CF9BA-9E7E-4BF5-B98B-B94A4CA9AC45Q33636734-FDAD9661-8E36-4329-AC29-D96B8E32BFF6Q33729331-63663244-5DDC-4E93-8F8F-6DE4A729F6A9Q33774008-1A6EE656-A943-4604-A14C-E9D7766DBA16Q33890255-B6594F1D-A01D-441F-BB9C-B3F061648921Q33910796-7BA5B8FC-ED83-4008-8CCB-4EB7ECEF25BAQ33965092-0CDE7C05-DAC6-414F-A218-DF72C9F2E00EQ33989269-07CF1939-84BD-47CB-A32B-38948876B18FQ34072027-A8ADDCFE-CB0F-4B6A-A004-1193D5AE09C6Q34083065-8F881BD2-D7FC-42A8-B61A-9A6CDEBD3154Q34119464-5CC4D972-D21B-438F-BB18-0FEA2C86AB57Q34261378-36BC6547-3346-41C1-B88B-0CCDCE921097Q34361047-5F12D6BE-BB42-4251-82FD-DE05B69A626EQ34412813-382ED4FC-7694-4296-B381-DD793A206206Q34416163-6AAEE756-C1CD-452B-ACBE-99409A6FED61Q34453970-ED4E9FD2-FFF4-4D5B-9C55-757F3490A773Q34489501-81F92229-09FB-4C9A-9406-A5E2B1F97F42Q34494155-9EC9A862-9595-4644-A743-175DEB68F460
P2860
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@ast
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@en
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@nl
type
label
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@ast
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@en
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@nl
prefLabel
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@ast
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@en
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus.
@nl
P2093
P50
P356
P1433
P1476
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus
@en
P2093
Brianna A Lam
Cheryl J Briggs
Christian R Schwantes
Devon C Flaherty
Jenifer B Walke
Kevin P C Minbiole
Matthew H Becker
Reid N Harris
P2888
P304
P356
10.1038/ISMEJ.2009.27
P577
2009-03-26T00:00:00Z
P5875
P6179
1019969556