Abstract
We developed a real-time quantitative PCR (qPCR) assay targeting the rRNA internal transcribed spacer region of the hard clam pathogen QPX. The qPCR assay was more sensitive than was histology in detecting clams with light QPX infections. QPX was detected in 4 of 43 sediment samples but in none of 40 seawater samples.
Publication types
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Evaluation Study
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Animals
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DNA Primers / genetics
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DNA, Ribosomal / chemistry
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DNA, Ribosomal / genetics
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Geologic Sediments / parasitology
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Mercenaria / parasitology*
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Molecular Sequence Data
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Parasites / classification
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Parasites / genetics
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Parasites / isolation & purification*
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Polymerase Chain Reaction / methods*
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Sensitivity and Specificity
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Sequence Analysis, DNA
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Time Factors
Substances
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DNA Primers
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DNA, Ribosomal
Associated data
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GENBANK/FJ533155
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GENBANK/FJ533156
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GENBANK/FJ533157
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GENBANK/FJ533158
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GENBANK/FJ533159
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GENBANK/FJ533160
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GENBANK/FJ533161
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GENBANK/FJ533162
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GENBANK/FJ533163