JVDI Advertisement
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pring-Akerblom, P
Right arrow Articles by Kunstyr, I
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pring-Akerblom, P
Right arrow Articles by Kunstyr, I
Journal of Veterinary Diagnostic Investigation, Vol 9, Issue 3, 232-236
Copyright © 1997 by American Association of Veterinary Laboratory Diagnosticians


Articles

Polymerase chain reaction for detection of guinea pig adenovirus

P Pring-Akerblom, K Blazek, J Schramlova, and I Kunstyr

Institute of Virology and the Central Laboratory Animal Facility, Medical School Hannover, Germany.

Lack of in vitro cultivation methods has inhibited the development of rapid, reliable diagnostic procedures for adenovirus-associated necrotizing bronchopneumonia in guinea pigs. Because polymerase chain reaction (PCR) techniques are well established for human adenoviruses, primers for the amplification of guinea pig adenovirus DNA were evaluated. The DNA for PCR was purified from the lung tissue of spontaneously infected and healthy guinea pigs. Adenovirus DNA could only be detected in the lungs of the infected animals. Subsequent sequence analysis of PCR products revealed that the guinea pig adenovirus is a distinct adenovirus.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1997 by the American Association of Veterinary Laboratory Diagnosticians, Inc.