A highly sensitive, non-invasive qPCR-based strategy for direct quantification ofYersinia ruckeriin fish faeces
Author:
Affiliation:
1. Institute for Marine and Antarctic Sciences; University of Tasmania; Launceston Tasmania Australia
Publisher
Wiley
Subject
Veterinary (miscalleneous),Aquatic Science
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jfd.12839/fullpdf
Reference42 articles.
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2. Use of random DNA amplification to generate specific molecular probes for hybridization tests and PCR-based diagnosis of Yersinia ruckeri;Argenton;Diseases of Aquatic Organisms,1996
3. Recovery of a new biogroup of yersinia ruckeri from diseased rainbow trout (Oncorhynchus mykiss, Walbaum);Austin;Systematic and Applied Microbiology,2003
4. Highly sensitive detection and quantification of the pathogen Yersinia ruckeri in fish tissues by using real-time PCR;Bastardo;Applied Microbiology and Biotechnology,2012
5. Rapid detection of Clostridium difficile in feces by real-time PCR;Bélanger;Journal of Clinical Microbiology,2003
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