Boehringer Ingelheim Veterinary Research Center GmbH & Co. KG, Bemeroder Straβe 31, 30559 Hannover, Germany.
ThinkinPig, Avda. Gómez Laguna 41, 50009 Zaragoza, Spain.
Vaccine. 2021 Jun 29;39(29):3997-4005. doi: 10.1016/j.vaccine.2021.05.042. Epub 2021 Jun 5.
Porcine parvovirosis is a common and important cause of reproductive failure in naïve dams. Even though vaccination is generally effective at preventing disease occurrence, the homology between the vaccine and challenge strains has been recently suggested to play a role in protection. Therefore, the purpose of this study was to evaluate and compare the efficacy of three currently available commercial vaccines against porcine parvovirus genotype 1 (PPV1) in an experimental model using pregnant gilts. Seventy-seven PPV1-negative gilts were included in the trial and randomly allocated to four groups. In group 1, gilts received two doses, three weeks apart, of a PPV1 subunit vaccine (ReproCyc® ParvoFLEX). Following the same scheme, gilts from group 2 received two doses of a PPV1 bivalent vaccine (ERYSENG® PARVO). In group 3, gilts received two doses, four weeks apart, of a PPV1 octavalent vaccine (Porcilis® Ery + Parvo + Lepto). Lastly, gilts from group 4 were left untreated and were used as challenge controls. All gilts were artificially inseminated three weeks after completion of vaccination. Pregnant animals were subsequently challenged around 40 days of gestation with a heterologous PPV1 strain. Foetuses were harvested at around day 90 of gestation and evaluated for their macroscopic appearance (i.e., normal, mummified, or autolytic). Along the study, safety parameters after vaccination, antibody responses against PPV1 and viremia in gilts were also measured. All the foetuses in the challenge control group were mummified, which validated the challenge model, whereas the three evaluated vaccines protected the progeny against PPV1 by preventing the appearance of clinical manifestations associated to parvovirosis. Remarkably, the PPV1 subunit vaccine induced an earlier seroconversion of gilts and was the only vaccine that could prevent viremia after challenge. This vaccine also achieved the largest average litter size accompanied with a high average proportion of clinically healthy foetuses.
猪细小病毒病是初产母猪繁殖失败的常见且重要原因。尽管疫苗接种通常可有效预防疾病发生,但疫苗株与攻毒株的同源性最近被认为在保护作用中发挥了作用。因此,本研究旨在评估和比较三种目前市售的猪细小病毒 1 型(PPV1)基因型疫苗在妊娠母猪的实验模型中的效力。试验纳入 77 头 PPV1 阴性母猪,随机分为 4 组。第 1 组母猪接受了两剂间隔 3 周的 PPV1 亚单位疫苗(ReproCyc® ParvoFLEX)。按照相同的方案,第 2 组母猪接受了两剂 PPV1 二价疫苗(ERYSENG® PARVO)。第 3 组母猪间隔 4 周接受了两剂 PPV1 八价疫苗(Porcilis® Ery + Parvo + Lepto)。最后,第 4 组母猪未进行处理,用作攻毒对照。所有母猪在疫苗接种完成后 3 周进行人工授精。妊娠母猪在大约 40 日龄时接受同源性 PPV1 攻毒。大约妊娠 90 天时采集胎儿,评估其外观(正常、木乃伊化或自溶)。在研究过程中,还测量了疫苗接种后的安全性参数、母猪对 PPV1 的抗体反应和病毒血症。攻毒对照组的所有胎儿均木乃伊化,验证了攻毒模型的有效性,而三种评估的疫苗通过预防与细小病毒病相关的临床症状的出现,保护了后代免受 PPV1 的侵害。值得注意的是,PPV1 亚单位疫苗能更早地诱导母猪血清转化,是唯一能预防攻毒后病毒血症的疫苗。该疫苗还获得了最大的平均窝产仔数,并伴有较高比例的临床健康胎儿。