1. Highly Sensitive Quantitative PCR for the Detection and Differentiation of Pseudogymnoascus destructans and Other Pseudogymnoascus Species
- Author
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Jeffrey T. Foster, Megan M Shuey, Kevin P. Drees, Paul Keim, and Daniel L. Lindner
- Subjects
Pseudogymnoascus ,food.ingredient ,Mycology ,Real-Time Polymerase Chain Reaction ,Polymorphism, Single Nucleotide ,Sensitivity and Specificity ,Applied Microbiology and Biotechnology ,Microbiology ,Geomyces ,food ,Ascomycota ,Microbial ecology ,Pseudogymnoascus destructans ,Environmental Microbiology ,Methods ,DNA, Fungal ,Ecology ,biology ,Fungal genetics ,biology.organism_classification ,Real-time polymerase chain reaction ,North America ,Oligonucleotide Probes ,Food Science ,Biotechnology - Abstract
White-nose syndrome is a fungal disease that has decimated bat populations across eastern North America. Identification of the etiologic agent, Pseudogymnoascus destructans (formerly Geomyces destructans ), in environmental samples is essential to proposed management plans. A major challenge is the presence of closely related species, which are ubiquitous in many soils and cave sediments and often present in high abundance. We present a dual-probe real-time quantitative PCR assay capable of detecting and differentiating P. destructans from closely related fungi in environmental samples from North America. The assay, based on a single nucleotide polymorphism (SNP) specific to P. destructans , is capable of rapid low-level detection from various sampling media, including sediment, fecal samples, wing biopsy specimens, and skin swabs. This method is a highly sensitive, high-throughput method for identifying P. destructans , other Pseudogymnoascus spp., and Geomyces spp. in the environment, providing a fundamental component of research and risk assessment for addressing this disease, as well as other ecological and mycological work on related fungi.
- Published
- 2014
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