• Medientyp: E-Artikel
  • Titel: Detection and Quantification of Renibacterium Salmoninarum DNA in Salmonid Tissues by Real-Time Quantitative Polymerase Chain Reaction Analysis
  • Beteiligte: Chase, Dorothy M.; Elliott, Diane G.; Pascho, Ronald J.
  • Erschienen: SAGE Publications, 2006
  • Erschienen in: Journal of Veterinary Diagnostic Investigation
  • Sprache: Englisch
  • DOI: 10.1177/104063870601800409
  • ISSN: 1040-6387; 1943-4936
  • Schlagwörter: General Veterinary
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:p> Renibacterium salmoninarum is an important salmonid pathogen that is difficult to culture. We developed and assessed a real-time, quantitative, polymerase chain reaction (qPCR) assay for the detection and enumeration of R. salmoninarum. The qPCR is based on TaqMan technology and amplifies a 69-base pair (bp) region of the gene encoding the major soluble antigen (MSA) of R. salmoninarum. The qPCR assay consistently detected as few as 5 R. salmoninarum cells per reaction in kidney tissue. The specificity of the qPCR was confirmed by testing the DNA extracts from a panel of microorganisms that were either common fish pathogens or reported to cause false-positive reactions in the enzyme-linked immunosorbent assay (ELISA). Kidney samples from 38 juvenile Chinook salmon ( Oncorhynchus tshawytscha) in a naturally infected population were examined by real-time qPCR, a nested PCR, and ELISA, and prevalences of R. salmoninarum detected were 71, 66, and 71%, respectively. The qPCR should be a valuable tool for evaluating the R. salmoninarum infection status of salmonids. </jats:p>
  • Zugangsstatus: Freier Zugang