Ingelvac PRRSandreg的疗效观察抗异源猪繁殖与呼吸综合征病毒攻毒的改良病毒活疫苗

A. Patterson, G. Haiwick, J. Hermann, B. Fergen, Kenneth Wakel, W. Chittick, R. Philips
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引用次数: 2

摘要

猪繁殖与呼吸综合征(PRRS)是由猪繁殖与呼吸综合征病毒(PRRSV)引起的一种以猪繁殖衰竭、呼吸系统疾病和体重减轻为特征的传染病。两项随机、盲法疫苗挑战研究评估了Ingelvac PRRS®修饰活病毒(MLV)疫苗保护猪免受强毒异源PRRSV分离株、限制性片段长度多态性(RFLP) 1-3-4和1-7-4的影响。在单独的攻毒研究中,猪在第0天接种了Ingelvac PRRS MLV或安慰剂“攻毒对照”,并在第28天接种了PRRSV 1-3-4或1-7-4。在1-3-4攻击研究中,接种了Ingelvac PRRS MLV的猪表现出显著降低的中位病毒血症(28-42天的曲线下面积[AUC28-42];P<0.0001)。接种疫苗的猪平均日增重(ADWG)显著高于未接种疫苗的对照组(P<0.0001)。在第42天,接种疫苗的猪的最小二乘平均肺病变评分显著低于未接种疫苗的对照组(P<0.001)。攻毒控制组的死亡率(61%)显著高于Ingelvac PRRS MLV组(15%;P < 0.01)。在1-7-4攻毒研究中,Ingelvac PRRS MLV与攻毒对照组相比,AUC28-42病毒血症水平显著降低(P=0.031)。在第29天和第42天,Ingelvac PRRS MLV组的直肠中位温度显著低于挑战对照组(P<0.01)。与未接种Ingelvac PRRS MLV的对照组相比,接种Ingelvac PRRS MLV的猪在攻毒期的ADWG显著高于未接种疫苗的猪(P<0.05),第42天肺病变最小二乘平均评分显著低于未接种疫苗的猪(P<0.05)。这些数据表明,Ingelvac PRRS MLV提供了针对两种相对较新的、毒性特别强的PRRSV野毒株的异源保护,这两种毒株在美国引起了越来越多的感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Ingelvac PRRSandreg; Modified Live Virus Vaccine against Heterologous Porcine Reproductive and Respiratory Syndrome Virus Challenges
Porcine reproductive and respiratory syndrome (PRRS) is an infectious disease caused by the PRRS virus (PRRSV) and characterized by reproductive failure, respiratory disease and weight loss in swine. Two randomized, blinded vaccination-challenge studies evaluated the efficacy of Ingelvac PRRS® modified live virus (MLV) vaccine in protecting pigs from the virulent heterologous PRRSV isolates, restriction fragment length polymorphism (RFLP) 1-3-4 and 1-7-4. In separate challenge studies, pigs were vaccinated on Day 0 with Ingelvac PRRS MLV or placebo ‘challenge control’ and challenged on Day 28 with PRRSV 1-3-4 or 1-7-4. In the 1-3-4 challenge study, pigs vaccinated with Ingelvac PRRS MLV demonstrated significantly lower median viraemia (area-under-the-curve for Day 28–42 [AUC28–42]; P<0.0001) compared with unvaccinated controls. Vaccinated pigs also had significantly higher average daily weight gain (ADWG) than unvaccinated controls (P<0.0001). At Day 42, vaccinated pigs had significantly lower least square mean lung lesion scores than unvaccinated controls (P<0.001). Mortality was significantly higher with challenge control (61%) than with Ingelvac PRRS MLV (15%; P<0.01). In the 1-7-4 challenge study, significantly lower AUC28–42 viraemia levels were observed with Ingelvac PRRS MLV compared with challenge control (P=0.031). Median rectal temperatures were significantly lower with Ingelvac PRRS MLV than with challenge controls at Days 29 and 42 (P<0.01 for both). Pigs vaccinated with Ingelvac PRRS MLV had significantly higher ADWG during the challenge phase (P<0.05) and significantly lower least square mean lung lesion scores at Day 42 compared with unvaccinated controls (P<0.05). These data indicate that Ingelvac PRRS MLV provides heterologous protection against two relatively new and particularly virulent PRRSV field strains responsible for a growing number of infections in the US.
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