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Applied and Environmental Microbiology, November 2004, p. 6611-6618, Vol. 70, No. 11
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.11.6611-6618.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Real-Time PCR for Detection and Quantification of the Protistan Parasite Perkinsus marinus in Environmental Waters{dagger}

Corinne Audemard,1 Kimberly S. Reece,1 and Eugene M. Burreson1*

Virginia Institute of Marine Science, School of Marine Science, College of William and Mary, Gloucester Point, Virginia1

Received 29 March 2004/ Accepted 28 June 2004

The protistan parasite Perkinsus marinus is a severe pathogen of the oyster Crassostrea virginica along the east coast of the United States. Very few data have been collected, however, on the abundance of the parasite in environmental waters, limiting our understanding of P. marinus transmission dynamics. Real-time PCR assays with SybrGreen I as a label for detection were developed in this study for quantification of P. marinus in environmental waters with P. marinus species-specific primers and of Perkinsus spp. with Perkinsus genus-specific primers. Detection of DNA concentrations as low as the equivalent of 3.3 x 10–2 cell per 10-µl reaction mixture was obtained by targeting the multicopy internal transcribed spacer region of the genome. To obtain reliable target quantification from environmental water samples, removal of PCR inhibitors and efficient DNA recovery were two major concerns. A DNA extraction kit designed for tissues and another designed for stool samples were tested on environmental and artificial seawater (ASW) samples spiked with P. marinus cultured cells. The stool kit was significantly more efficient than the tissue kit at removing inhibitors from environmental water samples. With the stool kit, no significant difference in the quantified target concentrations was observed between the environmental and ASW samples. However, with the spiked ASW samples, the tissue kit demonstrated more efficient DNA recovery. Finally, by performing three elutions of DNA from the spin columns, which were combined prior to target quantification, variability of DNA recovery from different samples was minimized and more reliable real-time PCR quantification was accomplished.

* Corresponding author. Mailing address: Virginia Institute of Marine Science, School of Marine Science, College of William and Mary, Gloucester Point, VA 23062. Phone: (804) 684-7015. Fax: (804) 684-7796. E-mail: gene{at}vims.edu.

{dagger} This report is Virginia Institute of Marine Science contribution number 2625.

Applied and Environmental Microbiology, November 2004, p. 6611-6618, Vol. 70, No. 11
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.11.6611-6618.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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