PMID- 26963101 OWN - NLM STAT- MEDLINE DCOM- 20160801 LR - 20190219 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 11 IP - 3 DP - 2016 TI - Pathologic Evaluation of Type 2 Porcine Reproductive and Respiratory Syndrome Virus Infection at the Maternal-Fetal Interface of Late Gestation Pregnant Gilts. PG - e0151198 LID - 10.1371/journal.pone.0151198 [doi] LID - e0151198 AB - The pathogenesis of fetal death caused by porcine reproductive and respiratory syndrome virus (PRRSV) remains unclear. The objective of this study was to improve our understanding of the pathogenesis by assessing potential relationships between specific histopathological lesions and PRRSV RNA concentration in the fetuses and the maternal-fetal interface. Pregnant gilts were inoculated with PRRSV (n = 114) or sham inoculated (n = 19) at 85+/-1 days of gestation. Dams and their litters were humanely euthanized and necropsied 21 days later. PRRSV RNA concentration was measured by qRT-PCR in the maternal-fetal interface and fetal thymus (n = 1391). Presence of fetal lesions was positively related to PRRSV RNA concentration in the maternal-fetal interface and fetal thymus (P<0.05 for both), but not to the distribution or severity of vasculitis, or the severity of endometrial inflammation. The presence of fetal and umbilical lesions was associated with greater odds of meconium staining (P<0.05 for both). The distribution and severity of vasculitis in endometrium were not significantly related to PRRSV RNA concentration in maternal-fetal interface or fetal thymus. Endometrial inflammation severity was positively related to distribution and severity of vasculitis in endometrium (P<0.001 for both). Conclusions from this study suggest that type 2 PRRSV infection in pregnant gilts induces significant histopathological lesions at maternal-fetal interface, but they are not associated with presence of PRRSV in the maternal-fetal interface at 21 days post infection. Conversely, fetal pathological lesions are associated with presence of PRRSV in the maternal-fetal interface and fetal thymus, and meconium staining is significantly associated with the presence of both fetal and umbilical lesions observed 21 days post infection. FAU - Novakovic, Predrag AU - Novakovic P AD - Department of Veterinary Pathology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, Canada. FAU - Harding, John C S AU - Harding JC AD - Department of Large Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, Canada. FAU - Al-Dissi, Ahmad N AU - Al-Dissi AN AD - Department of Veterinary Pathology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, Canada. FAU - Ladinig, Andrea AU - Ladinig A AD - Department of Large Animal Clinical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, Canada. AD - University Clinic for Swine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine Vienna, Vienna, Austria. FAU - Detmer, Susan E AU - Detmer SE AD - Department of Veterinary Pathology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, Canada. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20160310 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (RNA, Viral) SB - IM MH - Animals MH - Endometriosis/metabolism/pathology/virology MH - Female MH - Fetus/embryology/pathology/virology MH - Placenta/*metabolism/pathology/*virology MH - Porcine Reproductive and Respiratory Syndrome/*metabolism/pathology MH - Porcine respiratory and reproductive syndrome virus/*metabolism MH - Pregnancy MH - Pregnancy Complications, Infectious/*metabolism/pathology/*virology MH - RNA, Viral/*metabolism MH - Swine/metabolism/virology MH - Thymus Gland/embryology/pathology/virology MH - Vasculitis/metabolism/pathology/virology PMC - PMC4786155 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2016/03/11 06:00 MHDA- 2016/08/02 06:00 PMCR- 2016/03/10 CRDT- 2016/03/11 06:00 PHST- 2015/11/27 00:00 [received] PHST- 2016/02/24 00:00 [accepted] PHST- 2016/03/11 06:00 [entrez] PHST- 2016/03/11 06:00 [pubmed] PHST- 2016/08/02 06:00 [medline] PHST- 2016/03/10 00:00 [pmc-release] AID - PONE-D-15-51777 [pii] AID - 10.1371/journal.pone.0151198 [doi] PST - epublish SO - PLoS One. 2016 Mar 10;11(3):e0151198. doi: 10.1371/journal.pone.0151198. eCollection 2016.