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比较接种三种市售 PRRS 活病毒疫苗后 PRRSV-1 攻毒后的病毒血症和鼻腔排毒。

Comparison of viraemia and nasal shedding after PRRSV-1 challenge following vaccination with three commercially available PRRS modified live virus vaccines.

机构信息

Zoetis UK Ltd, Birchwood Building, Springfield Drive, Leatherhead KT22 7LP, United Kingdom.

Zoetis Manufacturing and Research Spain S.L., Carretera Camprodon s/n, Finca La Riba, Vall de Bianya, 17813 Girona, Spain.

出版信息

Res Vet Sci. 2024 Nov;180:105416. doi: 10.1016/j.rvsc.2024.105416. Epub 2024 Sep 13.

Abstract

The effectiveness of three Porcine Reproductive and Respiratory Syndrome (PRRS) Modified Live Virus (MLV) vaccines against PRRSV viraemia and nasal shedding following experimental challenge was compared. The study comprised a negative control (T01), and three treatment groups (T02, T03 and T04) each vaccinated with a single dose of a commercial PRRS MLV vaccine, given in accordance with the vaccine's Summary of Product Characteristics (SPC). Pigs aged 21 days were vaccinated (day 0), challenged intranasally (day 28) with heterologous PRRSV-1-1 strain Olot/91, then monitored for PRRSV viraemia and nasal shedding for 12 days. After challenge, pigs were viraemic on fewer days in group T04 (0.67) than groups T01 (0.91), T02 (0.81) and T03 (0.97) (P < 0.0296). From day 34, inclusive, serum PRRSV titres were lower in group T04 than negative controls (P ≤ 0.0001) and groups T02 and T03 (P ≤ 0.0047); serum PRRSV titre Area Under the Curve (AUC) for group T04 (42.34) was lower than in T01 (65.49), T02 (60.67) and T03 (67.38) (P < 0.0100); pigs exhibited nasal shedding on fewer days in group T04 (0.40) than T01 (0.78), T02 (0.64) and T03 (0.56) (P < 0.0101); and nasal shedding AUC for group T04 (8.52) was lower than in groups T01 (23.59, P < 0.0001) and T02 (19.37, P = 0.0001). The ability of PRRS MLV vaccines to reduce the duration of viraemia and nasal shedding after intranasal challenge with a heterologous PRRSV-1-1 strain differ significantly.

摘要

比较了三种猪繁殖与呼吸综合征(PRRS)活疫苗(MLV)对实验性攻毒后 PRRSV 血症和鼻拭子脱落的效果。该研究包括一个阴性对照(T01)和三个治疗组(T02、T03 和 T04),每组均按疫苗的产品特性摘要(SPC)单次接种商业 PRRS MLV 疫苗。21 日龄仔猪接种(第 0 天),第 28 天经鼻腔感染异源 PRRSV-1-1 株 Olot/91,然后监测 12 天 PRRSV 血症和鼻拭子脱落情况。攻毒后,T04 组的病毒血症天数(0.67 天)少于 T01 组(0.91 天)、T02 组(0.81 天)和 T03 组(0.97 天)(P<0.0296)。从第 34 天开始,T04 组的血清 PRRSV 滴度低于阴性对照(P≤0.0001)和 T02 组和 T03 组(P≤0.0047);T04 组的血清 PRRSV 曲线下面积(AUC)(42.34)低于 T01 组(65.49)、T02 组(60.67)和 T03 组(67.38)(P<0.0100);T04 组的鼻拭子脱落天数(0.40 天)少于 T01 组(0.78 天)、T02 组(0.64 天)和 T03 组(0.56 天)(P<0.0101);T04 组的鼻拭子脱落 AUC(8.52)低于 T01 组(23.59,P<0.0001)和 T02 组(19.37,P=0.0001)。PRRS MLV 疫苗在经鼻腔接种异源 PRRSV-1-1 株后,降低病毒血症和鼻拭子脱落持续时间的能力有显著差异。

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