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2.
Science ; 346(6209): 630-1, 2014 Oct 31.
Article in English | MEDLINE | ID: mdl-25359973

ABSTRACT

Emerging infectious diseases are reducing biodiversity on a global scale. Recently, the emergence of the chytrid fungus Batrachochytrium salamandrivorans resulted in rapid declines in populations of European fire salamanders. Here, we screened more than 5000 amphibians from across four continents and combined experimental assessment of pathogenicity with phylogenetic methods to estimate the threat that this infection poses to amphibian diversity. Results show that B. salamandrivorans is restricted to, but highly pathogenic for, salamanders and newts (Urodela). The pathogen likely originated and remained in coexistence with a clade of salamander hosts for millions of years in Asia. As a result of globalization and lack of biosecurity, it has recently been introduced into naïve European amphibian populations, where it is currently causing biodiversity loss.


Subject(s)
Chytridiomycota , Communicable Diseases, Emerging/veterinary , Endangered Species , Mycoses/veterinary , Urodela/microbiology , Animals , Biodiversity , Communicable Diseases, Emerging/microbiology , Mycoses/microbiology , Phylogeny , Urodela/classification
3.
J Clin Microbiol ; 51(12): 4173-7, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24108616

ABSTRACT

Chytridiomycosis is a lethal fungal disease contributing to declines and extinctions of amphibian species worldwide. The currently used molecular screening tests for chytridiomycosis fail to detect the recently described species Batrachochytrium salamandrivorans. In this study, we present a duplex real-time PCR that allows the simultaneous detection of B. salamandrivorans and Batrachochytrium dendrobatidis. With B. dendrobatidis- and B. salamandrivorans-specific primers and probes, detection of the two pathogens in amphibian samples is possible, with a detection limit of 0.1 genomic equivalent of zoospores of both pathogens per PCR. The developed real-time PCR shows high degrees of specificity and sensitivity, high linear correlations (r(2) > 0.995), and high amplification efficiencies (>94%) for B. dendrobatidis and B. salamandrivorans. In conclusion, the described duplex real-time PCR can be used to detect DNA of B. dendrobatidis and B. salamandrivorans with highly reproducible and reliable results.


Subject(s)
Amphibians/microbiology , Chytridiomycota/classification , Chytridiomycota/isolation & purification , Multiplex Polymerase Chain Reaction/methods , Mycoses/veterinary , Real-Time Polymerase Chain Reaction/methods , Animals , Chytridiomycota/genetics , Mycoses/diagnosis , Mycoses/microbiology , Sensitivity and Specificity
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