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TaqMan real-time polymerase chain reaction for detection of Ophidiomyces ophiodiicola, the fungus associated with snake fungal disease
by
Griffin, Kathryn M
, Bohuski, Elizabeth
, Blehert, David S
, Lorch, Jeffrey M
in
Animals
/ Base Sequence
/ Biotechnology industry
/ Chrysosporium
/ Chrysosporium - genetics
/ Chrysosporium - isolation & purification
/ DNA, Fungal - genetics
/ fungi
/ Genetic aspects
/ genome
/ Health aspects
/ histology
/ intergenic DNA
/ internal transcribed spacers
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Medicine, Experimental
/ Methodology
/ Methodology Article
/ Mycology
/ North America
/ quantitative polymerase chain reaction
/ Real-Time Polymerase Chain Reaction - methods
/ Sensitivity and Specificity
/ Skin
/ skin lesions
/ Snakes
/ Snakes - microbiology
/ transcription (genetics)
/ Transgenics
/ Veterinary Medicine/Veterinary Science
/ Zoology
2015
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TaqMan real-time polymerase chain reaction for detection of Ophidiomyces ophiodiicola, the fungus associated with snake fungal disease
by
Griffin, Kathryn M
, Bohuski, Elizabeth
, Blehert, David S
, Lorch, Jeffrey M
in
Animals
/ Base Sequence
/ Biotechnology industry
/ Chrysosporium
/ Chrysosporium - genetics
/ Chrysosporium - isolation & purification
/ DNA, Fungal - genetics
/ fungi
/ Genetic aspects
/ genome
/ Health aspects
/ histology
/ intergenic DNA
/ internal transcribed spacers
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Medicine, Experimental
/ Methodology
/ Methodology Article
/ Mycology
/ North America
/ quantitative polymerase chain reaction
/ Real-Time Polymerase Chain Reaction - methods
/ Sensitivity and Specificity
/ Skin
/ skin lesions
/ Snakes
/ Snakes - microbiology
/ transcription (genetics)
/ Transgenics
/ Veterinary Medicine/Veterinary Science
/ Zoology
2015
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TaqMan real-time polymerase chain reaction for detection of Ophidiomyces ophiodiicola, the fungus associated with snake fungal disease
by
Griffin, Kathryn M
, Bohuski, Elizabeth
, Blehert, David S
, Lorch, Jeffrey M
in
Animals
/ Base Sequence
/ Biotechnology industry
/ Chrysosporium
/ Chrysosporium - genetics
/ Chrysosporium - isolation & purification
/ DNA, Fungal - genetics
/ fungi
/ Genetic aspects
/ genome
/ Health aspects
/ histology
/ intergenic DNA
/ internal transcribed spacers
/ Medical research
/ Medicine
/ Medicine & Public Health
/ Medicine, Experimental
/ Methodology
/ Methodology Article
/ Mycology
/ North America
/ quantitative polymerase chain reaction
/ Real-Time Polymerase Chain Reaction - methods
/ Sensitivity and Specificity
/ Skin
/ skin lesions
/ Snakes
/ Snakes - microbiology
/ transcription (genetics)
/ Transgenics
/ Veterinary Medicine/Veterinary Science
/ Zoology
2015
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TaqMan real-time polymerase chain reaction for detection of Ophidiomyces ophiodiicola, the fungus associated with snake fungal disease
Journal Article
TaqMan real-time polymerase chain reaction for detection of Ophidiomyces ophiodiicola, the fungus associated with snake fungal disease
2015
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Overview
Background
Fungal skin infections associated with
Ophidiomyces ophiodiicola
, a member of the
Chrysosporium
anamorph of
Nannizziopsis vriesii
(CANV) complex, have been linked to an increasing number of cases of snake fungal disease (SFD) in captive snakes around the world and in wild snake populations in eastern North America. The emergence of SFD in both captive and wild situations has led to an increased need for tools to better diagnose and study the disease.
Results
We developed two TaqMan real-time polymerase chain reaction (PCR) assays to rapidly detect
O. ophiodiicola
in clinical samples. One assay targets the internal transcribed spacer region (ITS) of the fungal genome while the other targets the more variable intergenic spacer region (IGS). The PCR assays were qualified using skin samples collected from 50 snakes for which
O. ophiodiicola
had been previously detected by culture, 20 snakes with gross skin lesions suggestive of SFD but which were culture-negative for
O. ophiodiicola
, and 16 snakes with no clinical signs of infection. Both assays performed equivalently and proved to be more sensitive than traditional culture methods, detecting
O. ophiodiicola
in 98% of the culture-positive samples and in 40% of the culture-negative snakes that had clinical signs of SFD. In addition, the assays did not cross-react with a panel of 28 fungal species that are closely related to
O. ophiodiicola
or that commonly occur on the skin of snakes. The assays did, however, indicate that some asymptomatic snakes (~6%) may harbor low levels of the fungus, and that PCR should be paired with histology when a definitive diagnosis is required.
Conclusions
These assays represent the first published methods to detect
O. ophiodiicola
by real-time PCR. The ITS assay has great utility for assisting with SFD diagnoses whereas the IGS assay offers a valuable tool for research-based applications.
Publisher
BioMed Central,BioMed Central Ltd
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