

@article {13763,
	title = {Development of a quantitative {PCR} assay for the quantitation of bovine polyomavirus as a microbial source-tracking tool},
	journal = {Journal of Virological Methods},
	volume = {163},
	number = {2},
	year = {2010},
	abstract = {Adenoviruses and polyomaviruses are two distinct DNA viral families that are excreted in high concentrations and distributed in human and animal populations. Targeting specific virus included in these families has proved to be a promising and useful tool for tracing specifically sources of environmental contamination. In this study, a quantitative PCR assay that is specific for bovine polyomaviruses was developed and used to determine the excretion level and concentration of bovine polyomaviruses in urine and environmental samples, including urban sewage, slaughterhouse sewage, and river water. A set of primers and a TaqMan probe were designed to target a 77-bp region of the bovine polyomavirus VP1 gene, and the conditions of the reaction were optimized. A detection limit was established at 1-10 genome copies per test tube. The assay was specific and produced negative results when samples containing human or porcine fecal contamination were analyzed. This is, to our knowledge, the first description of bovine polyomaviruses excreted in bovine urine samples (mean values of 104 GC/l). Bovine polyomaviruses were also detected and quantified in slaughterhouse wastewater and river waters, which shows the spread of these viruses in many environmental samples containing contamination of bovine origin. The procedure described in this paper provides a quantitative source-tracking tool for the analysis of bovine polyomaviruses as indicators of the presence of bovine contamination in environmental samples. {\textcopyright} 2009 Elsevier B.V. All rights reserved.},
	doi = {10.1016/j.jviromet.2009.10.029},
	author = {Hundesa, A. and Bofill-Mas, S. and Maluquer de Motes, C. and Rodriguez-Manzano, J. and Bach, A. and Casas, M. and Girones, R.}
}
