Evidence for divergence of restriction fragment length polymorphism patterns following in vivo replication of porcine reproductive and respiratory syndrome virus

Citation
Rd. Wesley et al., Evidence for divergence of restriction fragment length polymorphism patterns following in vivo replication of porcine reproductive and respiratory syndrome virus, AM J VET RE, 60(4), 1999, pp. 463-467
Citations number
21
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
AMERICAN JOURNAL OF VETERINARY RESEARCH
ISSN journal
00029645 → ACNP
Volume
60
Issue
4
Year of publication
1999
Pages
463 - 467
Database
ISI
SICI code
0002-9645(199904)60:4<463:EFDORF>2.0.ZU;2-3
Abstract
Objective-To determine stability of the restriction fragment length polymor phism (RFLP) pattern of a porcine reproductive and respiratory syndrome vac cine virus and patterns of other viral strains as they replicate in pigs. Sample Population-Field samples of porcine reproductive and respiratory syn drome virus (PRRSV) and samples from 2 weaned pigs, 2 nursery-age pigs, and 5 gilts experimentally infected with PRRSV. Procedure-PRRSV was isolated from field samples, experimentally infected pi gs, or pigs that were in contact with experimentally infected pigs. For eac h virus, RNA was isolated from infected cells, and RFLP patterns were deter mined. Results-61% of field samples had 2-5-2 RFLP patterns characteristic of the vaccine virus, 32%.had field virus RFLP patterns, and 7% had intermediate R FLP patterns that indicated a virus with a close relationship to the vaccin e virus. Viruses isolated from experimentally infected pigs had no change i n RFLP patterns after up to 13 weeks of in vivo replication and transmissio n to contact pigs. Conclusions and Clinical Relevance-RFLP patterns distinguish the vaccine an d field strains of PRRSV; however, as the vaccine virus spreads among a swi ne population, the RFLP pattern can change to a related intermediate patter n. A glycine at residue 151 of open reading frame 5 is another marker for t he vaccine virus; this glycine is rapidly lost and eventually replaced with arginine as the vaccine virus replicates in pigs.