PMID- 12414926 OWN - NLM STAT- MEDLINE DCOM- 20021213 LR - 20240413 IS - 0022-538X (Print) IS - 1098-5514 (Electronic) IS - 0022-538X (Linking) VI - 76 IP - 23 DP - 2002 Dec TI - Comparison of molecular and biological characteristics of a modified live porcine reproductive and respiratory syndrome virus (PRRSV) vaccine (ingelvac PRRS MLV), the parent strain of the vaccine (ATCC VR2332), ATCC VR2385, and two recent field isolates of PRRSV. PG - 11837-44 AB - The objectives of this study were to compare the molecular and biological characteristics of recent porcine reproductive and respiratory syndrome virus (PRRSV) field isolates to those of a modified live virus (MLV) PRRS vaccine and its parent strain. One hundred seventeen, 4-week-old pigs were randomly assigned to six groups. Group 1 (n = 20) served as sham-inoculated negative controls, group 2 (n = 19) was inoculated with Ingelvac PRRS MLV vaccine, group 3 (n = 20) was inoculated with the parent strain of the vaccine (ATCC VR2332), group 4 (n = 19) was inoculated with vaccine-like PRRSV field isolate 98-38803, group 5 (n = 19) was inoculated with PRRSV field isolate 98-37120, and group 6 (n = 20) was inoculated with known high-virulence PRRSV isolate ATCC VR2385. The levels of severity of gross lung lesions (0 to 100%) among the groups were significantly different at both 10 (P < 0.0001) and 28 days postinoculation (p.i.) (P = 0.002). At 10 days p.i., VR2332 (26.5% +/- 4.64%) and VR2385 (36.4% +/- 6.51%) induced gross lesions of significantly greater severity than 98-38803 (0.0% +/- 0.0%), 98-37120 (0.8% +/- 0.42%), Ingelvac PRRS MLV (0.9% +/- 0.46%), and negative controls (2.3% +/- 1.26%). At 28 days p.i., 98-37120 (17.2% +/- 6.51%) induced gross lesions of significantly greater severity than any of the other viruses. Analyses of the microscopic-interstitial-pneumonia-lesion scores (0 to 6) revealed that VR2332 (2.9 +/- 0.23) and VR2385 (3.1 +/- 0.35) induced significantly more severe lesions at 10 days p.i. At 28 days p.i., VR2385 (2.5 +/- 0.27), VR2332 (2.3 +/- 0.21), 98-38803 (2.6 +/- 0.29), and 98-37120 (3.0 +/- 0.41) induced significantly more severe lesions than Ingelvac PRRS MLV (0.7 +/- 0.17) and controls (0.7 +/- 0.15). The molecular analyses and biological characterizations suggest that the vaccine-like isolate 98-38803 (99.5% amino acid homology based on the ORF5 gene) induces microscopic pneumonia lesions similar in type to, but different in severity and time of onset from, those observed with virulent strains VR2385 and the parent strain of the vaccine. Our data strongly suggest that isolate 98-38803 is a derivative of Ingelvac PRRS MLV and that the isolate is pneumovirulent. FAU - Opriessnig, T AU - Opriessnig T AD - Department of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa 50011, USA. FAU - Halbur, P G AU - Halbur PG FAU - Yoon, K-J AU - Yoon KJ FAU - Pogranichniy, R M AU - Pogranichniy RM FAU - Harmon, K M AU - Harmon KM FAU - Evans, R AU - Evans R FAU - Key, K F AU - Key KF FAU - Pallares, F J AU - Pallares FJ FAU - Thomas, P AU - Thomas P FAU - Meng, X J AU - Meng XJ LA - eng SI - GENBANK/AF535152 PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Virol JT - Journal of virology JID - 0113724 RN - 0 (Antibodies, Viral) RN - 0 (RNA, Viral) RN - 0 (Viral Vaccines) SB - IM MH - Animals MH - Antibodies, Viral/biosynthesis MH - Lung/pathology MH - Molecular Sequence Data MH - Phylogeny MH - Porcine Reproductive and Respiratory Syndrome/*immunology/pathology/*prevention & control/virology MH - Porcine respiratory and reproductive syndrome virus/*genetics/*immunology/isolation & purification/pathogenicity MH - RNA, Viral/genetics MH - Swine MH - Viral Vaccines/*genetics MH - Virulence/genetics PMC - PMC136866 EDAT- 2002/11/05 04:00 MHDA- 2002/12/17 04:00 PMCR- 2002/12/01 CRDT- 2002/11/05 04:00 PHST- 2002/11/05 04:00 [pubmed] PHST- 2002/12/17 04:00 [medline] PHST- 2002/11/05 04:00 [entrez] PHST- 2002/12/01 00:00 [pmc-release] AID - 0725 [pii] AID - 10.1128/jvi.76.23.11837-11844.2002 [doi] PST - ppublish SO - J Virol. 2002 Dec;76(23):11837-44. doi: 10.1128/jvi.76.23.11837-11844.2002.