Characterization of virus isolates by particle-associated nucleic acid PCR.
Ontology highlight
ABSTRACT: Diagnostic virus isolation is still frequently used, particularly from respiratory tract secretions. Testing positive virus cultures for all possible viruses is time-consuming, and unexpected or unknown viruses may escape detection. Therefore, a novel random PCR approach was developed that allows sequence-independent amplification of viral nucleic acids from virus isolation-positive cultures. Selectivity for viral sequences is obtained by preferential isolation of nucleic acids that are particle associated and resistant to nucleases. Using primers with a degenerated 3' end, the isolated nucleic acids are amplified and the randomly amplified PCR products are cloned and sequenced. As proof of the concept, the PAN-PCR approach was applied to supernatants of coxsackievirus B3 and murine adenov
SUBMITTER: Stang A
PROVIDER: S-EPMC548055 | biostudies-literature | 2005 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA