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.
| Original language | English |
|---|---|
| Pages (from-to) | 4913-4918 |
| Number of pages | 6 |
| Journal | Applied and Environmental Microbiology |
| Volume | 75 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 2009 |
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