Centcinc Coworking, C, Montserrat de Casanovas 105, 08032 Barcelona, Spain.
Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University, 1800 Christensen Drive, Ames, IA 50011, USA.
Viruses. 2020 Jul 23;12(8):789. doi: 10.3390/v12080789.
The efficacy of the combined administration of a porcine reproductive and respiratory syndrome (PRRS) modified live virus (MLV) vaccine and a porcine parvovirus 1 (PPV1) subunit vaccine in gilts was addressed in two experiments. Experiment A aimed to establish a 4-week onset of immunity (OOI). Gilts were randomly distributed in three treatment groups: non-vaccinated control animals (group 1), animals vaccinated with the combined vaccine (group 2), and a third group that consisted of animals vaccinated with the PRRS MLV vaccine alone (group 3). Four weeks after the first vaccination, gilts were challenged with a heterologous PRRS virus 1 (PRRSV1) and euthanized three weeks after. Besides this, experiment B pursued a 17-week duration of immunity (DOI). In this case, gilts were distributed in the same treatment groups, but for the third group, which consisted of non-vaccinated, non-challenged animals were used instead. For the DOI assessment, gilts were artificially inseminated 4 weeks after the first vaccination, challenged at day 90 of gestation, and followed up, together with their offspring, until day 20 post-farrowing. Serology and viremia post-challenge were determined in gilts from both experiments, while farrowing and piglet performance were only evaluated in experiment B. Overall, the combined vaccine helped to protect gilts from viremia post-challenge and, consequently, to prevent PRRS clinical symptoms and diminish the proportion of piglets infected congenitally or early in life. The combined vaccine also elicited a significant improvement in piglet survival rate and growth performance until weaning. The present results reveal efficacy and lack of interference of the mixed use of the tested vaccines against PRRSV1 infection, with at least 4-week OOI and 17-week DOI.
本研究旨在评估猪繁殖与呼吸综合征(PRRS)灭活疫苗和猪细小病毒 1 型(PPV1)亚单位疫苗联合免疫后备母猪的效果。实验 A 的目的是确定 4 周免疫起始期(OOI)。后备母猪随机分为 3 个处理组:未免疫对照组(第 1 组)、联合疫苗免疫组(第 2 组)和 PRRS 灭活疫苗免疫组(第 3 组)。首免后 4 周,所有后备母猪均用异源 PRRS 病毒 1 型(PRRSV1)攻毒,3 周后扑杀。此外,实验 B 旨在确定 17 周免疫持续期(DOI)。后备母猪分组与实验 A 相同,但第 3 组为未免疫、未攻毒的母猪。DOI 评估时,所有后备母猪在首免后 4 周进行人工授精,妊娠 90 天攻毒,随后与仔猪一起观察至产后 20 天。实验 A 和 B 均检测了攻毒后备母猪的血清学和病毒血症,仅实验 B 评估了产仔和仔猪性能。总的来说,联合疫苗能有效保护后备母猪免受攻毒后病毒血症的影响,从而预防 PRRS 临床症状,并减少仔猪先天感染或早期感染的比例。联合疫苗还显著提高了仔猪的成活率和断奶前的生长性能。本研究结果表明,联合使用两种疫苗可有效预防 PRRSV1 感染,具有至少 4 周 OOI 和 17 周 DOI。