Comparison of nucleic acid hybridization and nucleic acid amplification using conserved sequences from the 5' noncoding region for detection of bovine viral diarrhea virus

Author:

Ridpath J F1,Bolin S R1,Katz J1

Affiliation:

1. Virology Cattle Research, USDA Agricultural Research Service, Ames, Iowa.

Abstract

Primers and probes derived from conserved sequences located in the 5' noncoding region of pestiviruses were evaluated for detection of bovine viral diarrhea virus. With these reagents, hybridization and polymerase chain reaction tests detected 62 of 90 and 90 of 90 bovine viral diarrhea virus isolates, respectively. A quick lysis method for preparing RNA for use in polymerase chain reaction amplification also was evaluated.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference35 articles.

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4. Monoclonal antibodies with neutralizing activity segregate isolates of bovine viral diarrhea virus into groups;Bolin S. R.;Arch. Virol.,1988

5. Specific sequence amplification of bovine virus diarrhea virus (BVDV) and hog cholera virus and sequencing of BVDV nucleic acid;Boye M.;Vet. Microbiol.,1991

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