Diagnostic implications of concurrent inoculation with attenuated and virulent strains of porcine reproductive and respiratory syndrome virus

Citation
Wl. Mengeling et al., Diagnostic implications of concurrent inoculation with attenuated and virulent strains of porcine reproductive and respiratory syndrome virus, AM J VET RE, 60(1), 1999, pp. 119-122
Citations number
5
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
AMERICAN JOURNAL OF VETERINARY RESEARCH
ISSN journal
00029645 → ACNP
Volume
60
Issue
1
Year of publication
1999
Pages
119 - 122
Database
ISI
SICI code
0002-9645(199901)60:1<119:DIOCIW>2.0.ZU;2-2
Abstract
Objective-To determine the predominant strain of progeny virus in samples o btained from cell cultures and pigs exposed simultaneously to attenuated an d virulent strains of porcine reproductive and respiratory syndrome virus ( PRRSV). Sample population-Cell cultures and twenty 4-week-old pigs. Procedure-Cell cultures and pigs were simultaneously exposed to various rel ative concentrations of an attenuated, cell-culture-adapted vaccine strain and a virulent field strain of PRRSV. Progeny virus obtained at selected in tervals thereafter was tested to determine strain identity by use of restri ction fragment length polymorphism (RFLP) analysis. Results-Progeny virus from infected cell cultures comprised the attenuated strain, alone or in combination with the virulent strain, except when cultu res had been exposed to a large excess (> 100,000-fold) of the virulent str ain. Progeny virus from infected pigs comprised only the virulent strain re gardless of the relative concentrations of the 2 strains to which the pigs had been exposed. Conclusions-During concurrent replication in cell cultures, the attenuated strain quickly predominated. Conversely, during concurrent replication in p igs, the virulent strain quickly predominated. Clinical Relevance-it is unlikely that only an attenuated strain of PRRSV w ould be identified by RFLP testing of samples obtained from pigs concurrent ly infected with a virulent strain of PRRSV. Nevertheless, the ability of a cell-culture-adapted attenuated strain of PRRSV to predominate during cell culture passage (the first step in the current RFLP testing procedure) ind icated that, if possible, samples should be obtained from pigs that do not have a history of direct or indirect exposure to attenuated-virus vaccine.