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Applied and Environmental Microbiology, July 2009, p. 4913-4918, Vol. 75, No. 14
0099-2240/09/$08.00+0 doi:10.1128/AEM.00246-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

School of Marine and Atmospheric Sciences, Stony Brook University, Stony Brook, New York 11794-5000
Received 1 February 2009/ Accepted 15 May 2009
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.
Published ahead of print on 22 May 2009.
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