Porcine reproductive and respiratory syndrome virus 2 (PRRSV-2) genetic diversity and occurrence of wild type and vaccine-like strains in the United States swine industry
Open Access
- 19 November 2021
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 16 (11) , e0259531
Abstract
Porcine reproductive and respiratory syndrome virus genotype 2 (PRRSV-2) genetic diversity in the U.S. was assessed using a database comprising 10 years’ worth of sequence data obtained from swine production systems routine monitoring and outbreak investigations. A total of 26,831 ORF5 PRRSV-2 sequences from 34 production systems were included in this analysis. Within group mean genetic distance (i.e. mean proportion of nucleotide differences within ORF5) per year according to herd type was calculated for all PRRSV-2 sequences. The percent nucleotide difference between each sequence and the ORF5 sequences from four commercially available PRRSV-2 vaccines (Ingelvac PRRS MLV, Ingelvac PRRS ATP, Fostera PRRS, and Prevacent PRRS) within the same lineage over time was used to classify sequences in wild-type or vaccine-like. The mean ORF5 genetic distance fluctuated from 0.09 to 0.13, being generally smaller in years in which there was a relative higher frequency of dominant lineage. Vaccine-like sequences comprised about one fourth of sequences obtained through routine monitoring of PRRS. We found that lineage 5 sequences were mostly Ingelvac PRRS MLV-like. Lineage 8 sequences up to 2011 were 62.9% Ingelvac PRRS ATP-like while the remaining were wild-type viruses. From 2012 onwards, 51.9% of lineage 8 sequences were Ingelvac PRRS ATP-like, 45.0% were Fostera PRRS-like, and only 3.2% were wild-type. For lineage 1 sequences, 0.1% and 1.7% of the sequences were Prevacent PRRS-like in 2009–2018 and 2019, respectively. These results suggest that repeated introductions of vaccine-like viruses through use of modified live vaccines might decrease within-lineage viral diversity as vaccine-like strains become more prevalent. Overall, this compilation of private data from routine monitoring provides valuable information on PRRSV viral diversity.Keywords
Funding Information
- Swine Health Information Center (19-235 SHIC)
- Swine Health Information Center (19-235 SHIC)
- Swine Health Information Center (19-235 SHIC)
- Swine Health Information Center (19-235 SHIC)
- NIFA-NSF-NIH (2019-67015-29918)
- NIFA-NSF-NIH (2019-67015-29918)
This publication has 33 references indexed in Scilit:
- Significance of genetic variation of PRRSV ORF5 in virus neutralization and molecular determinants corresponding to cross neutralization among PRRS virusesVeterinary Microbiology, 2013
- Porcine reproductive and respiratory syndrome virus vaccines: Immunogenicity, efficacy and safety aspectsWorld Journal of Virology, 2012
- Phylogeny-Based Evolutionary, Demographical, and Geographical Dissection of North American Type 2 Porcine Reproductive and Respiratory Syndrome VirusesJournal of Virology, 2010
- The role of porcine reproductive and respiratory syndrome (PRRS) virus structural and non-structural proteins in virus pathogenesisAnimal Health Research Reviews, 2010
- Impact of a modified-live porcine reproductive and respiratory syndrome virus vaccine intervention on a population of pigs infected with a heterologous isolateVaccine, 2007
- Instability of the Restriction Fragment Length Polymorphism Pattern of Open Reading Frame 5 of Porcine Reproductive and Respiratory Syndrome Virus during Sequential Pig-to-Pig PassagesJournal of Clinical Microbiology, 2004
- Genetic variation in porcine reproductive and respiratory syndrome virus isolates in the midwestern United StatesJournal of General Virology, 1996
- Characterization of Swine Infertility and Respiratory Syndrome (SIRS) Virus (Isolate ATCC VR-2332)Journal of Veterinary Diagnostic Investigation, 1992
- Mystery swine disease in the Netherlands: The isolation of Lelystad virusVeterinary Quarterly, 1991
- Recommendations of the coronavirus study group for the nomenclature of the structural proteins, mRNAs, and genes of coronavirusesVirology, 1990