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首页> 外文期刊>Viruses >Evaluation of the Cross-Protective Efficacy of a Chimeric Porcine Reproductive and Respiratory Syndrome Virus Constructed Based on Two Field Strains
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Evaluation of the Cross-Protective Efficacy of a Chimeric Porcine Reproductive and Respiratory Syndrome Virus Constructed Based on Two Field Strains

机译:基于两个野毒株构建的嵌合猪繁殖与呼吸综合征病毒的交叉防护功效评价

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摘要

One of the major hurdles to porcine reproductive and respiratory syndrome (PRRS) vaccinology is the limited or no cross-protection conferred by current vaccines. To overcome this challenge, a PRRS chimeric virus (CV) was constructed using an FL12-based cDNA infectious clone in which open reading frames (ORFs) 3–4 and ORFs 5–6 were replaced with the two Korean field isolates K08-1054 and K07-2273,respectively. This virus was evaluated as a vaccine candidate to provide simultaneous protection against two genetically distinct PRRS virus (PRRSV) strains. Thirty PRRS-negative three-week-old pigs were divided into five groups and vaccinated with CV, K08-1054, K07-2273, VR-2332, or a mock inoculum. At 25 days post-vaccination (dpv), the pigs in each group were divided further into two groups and challenged with either K08-1054 or K07-2273. All of the pigs were observed until 42 dpv and were euthanized for pathological evaluation. Overall, the CV-vaccinated group exhibited higher levels of tumor necrosis factor-alpha (TNF-α), interferon-gamma (IFN-γ), and interleukin-12 (IL-12) expression and of serum virus-neutralizing antibodies compared with the other groups after vaccination and also demonstrated better protection levels against both viruses compared with the challenge control group. Based on these results, it was concluded that CV might be an effective vaccine model that can confer a broader range of cross-protection to various PRRSV strains.
机译:猪生殖和呼吸综合症(PRRS)疫苗学的主要障碍之一是当前疫苗所赋予的交叉保护作用有限或没有交叉保护作用。为克服这一挑战,使用基于FL12的cDNA感染性克隆构建了PRRS嵌合病毒(CV),其中,开放阅读框3–4和ORF 5–6被两个韩国大田分离株K08-1054和分别为K07-2273。该病毒被评估为候选疫苗,可同时针对两种遗传上不同的PRRS病毒(PRRSV)株提供保护。将30头PRRS阴性的三周龄猪分为五组,并用CV,K08-1054,K07-2273,VR-2332或模拟接种疫苗接种。接种后25天(dpv),将每组猪进一步分为两组,并用K08-1054或K07-2273攻击。观察所有猪直到42 dpv,并对其实施安乐死进行病理评估。总体而言,与Cv疫苗接种组相比,肿瘤坏死因子-α(TNF-α),干扰素-γ(IFN-γ)和白细胞介素12(IL-12)的表达水平更高,血清中和病毒的抗体的水平高于接种疫苗后,其他组也显示出比攻击对照组更好的针对两种病毒的保护水平。根据这些结果,可以得出结论,CV可能是一种有效的疫苗模型,可以为各种PRRSV菌株提供更广泛的交叉保护。

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