|Rowland r, R|
Submitted to: Meeting Abstract
Publication Type: Abstract only
Publication Acceptance Date: 4/30/2007
Publication Date: 8/15/2007
Citation: Lunney, J.K., Petry, D., Johnson, R., Kuhar, D.J., Molina, R., Christopher-Hennings, J., Zimmerman, J., Rowland R, R.R. 2007. Swine immunity and genetic resistance to Porcine Reproductive and Respiratory Syndrome virus (PRRSV) infection. Interpretive Summary:
Technical Abstract: Current vaccines are only partially effective against Porcine Reproductive and Respiratory Syndrome (PRRS) virus infection because they elicit a weak immune response that is not fully protective. PRRS is the most economically significant disease facing the swine industry today, costing U.S. pork producers at least $560 million annually. Despite substantial research efforts the exact components of a protective anti-PRRSV immune response are still not known, thus we are testing alternate approaches to evaluate immunity and genetic resistance to PRRSV. We used host genomics to compare different lines of pigs and look for factors that correlated with PRRSV resistance/susceptibility. Viremia, weight change, and rectal temperature at 0, 4, 7, and 14 days post-PRRSV infection (dpi) were recorded and genetic differences detected (Petry et al., 2005). We evaluated immune gene expression in RNA from frozen lung and bronchial lymph node (BLN) tissue of the 7 highest and lowest responders per line, and from each of their control littermates, as well as serum cytokine protein levels. Genetic analyses of this data indicated that levels of interleukin-8 (IL8) may be predictive of resistance. Additionally, low (not the expected high) levels of serum interferon-gamma (IFNG) after infection may be associated with a PRRSV resistant phenotype. These data are critical for genetic association studies to fine map candidate genes and determine causative alleles of PRRSV resistance/susceptibility. Further genetic studies are required to affirm these associations. For direct immunity studies we’ve assessed immune gene expression in lung, BLN, and tonsil samples, and protein expression in serum, collected from pigs infected for over 200 days after PRRSV infection. We compared pigs that apparently cleared the viral infection in the first 28 dpi to pigs that even at 150 dpi have evidence of long term persistent PRRSV infection. Results show that there is up regulation of expression of IFNG associated T helper 1 (Th1) markers from 14 to 84 dpi; regulatory IL10 and apoptosis associated markers are also increased early. To date, however, no significant differences between persistent and non-persistent PRRSV infected pigs have been discovered in immune gene expression; serum protein expression studies are underway. We hope to reveal differential protein expression associated with PRRSV clearance. Overall, by combining these diverse approaches, we expect to develop new hypotheses about protective anti-PRRSV responses and to identify novel regulatory pathways that would stimulate PRRSV immunity. Supported by USDA ARS and NRI PRRS CAP1 funds.