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A bovine viral diarrhea virus type 1a strain in China: isolation, identification, and experimental infection in calves

机译:中国的牛1a型病毒性腹泻病毒株:牛犊的分离,鉴定和实验感染

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Background Bovine viral diarrhea virus (BVDV) is one of the most important pathogens in cattle. Previously, BVDV sub-genotypes of 1b, 1c, 1d, and 1?m were detected in China. However, isolation of BVDV type 1a from cattle has not been reported in China. In 2010, twenty nasal swabs and blood samples were collected from the cattle suspected BVDV infection in Henan province, China. A BVDV isolate was isolated using cell culture, and the pathogenesis of the virus isolate was studied. Methods Virus isolation was performed on MDBK cells. The virus identification was conducted by RT-PCR, neutralization test and immunofluorescence assay. In order to determine the genotype of the newly isolated virus, the 5′ un-translated region (5′UTR) of the virus isolate was cloned, sequenced and phylogenetically analyzed. To evaluate the virulence of the virus isolate, four BVDV sero-negative calves were intranasally inoculated with the virus suspension. Rectal temperatures and clinical signs were recorded daily. Blood samples were analyzed for changes in white blood cell counts, and tissue samples were taken for histopathology analysis. Results A new isolate of bovine viral diarrhea virus (BVDV), named HN01, was isolated from the nasal swabs using MDBK cell culture. The HN01 strain caused cytopathic effect (CPE) in MDBK cell cultures after two passages. The virus specifically reacted to BVDV1-specific monoclonal antibody in an immunofluorescence assay. A fragment of 288?bp of genome from this isolate was amplified by the RT-PCR. Phylogenetic analysis of 5′UTR indicated that the virus was BVDV 1a. In the pathogenesis study, four calves experimentally infected with the BVDV strain developed depression, cough and other clinical signs. Calves showed high temperature over 40°C, and white blood cell counts dropped more than 40%. Conclusions A new subgenotype 1a strain of BVDV was firstly isolated from dairy cattle in China. The experimental infection showed that the virus was moderate pathogenic to cattle and can be used as a BVDV challenge virus to evaluate the efficacy of BVDV vaccines in the target animals.
机译:背景技术牛病毒性腹泻病毒(BVDV)是牛中最重要的病原体之一。以前,在中国检测到BVDV亚型1b,1c,1d和1?m。然而,在中国尚无从牛中分离出1a型BVDV的报道。 2010年,从中国河南省怀疑感染BVDV的牛中采集了20支鼻拭子和血液样本。使用细胞培养分离BVDV分离株,并研究病毒分离株的发病机理。方法对MDBK细胞进行病毒分离。通过RT-PCR,中和试验和免疫荧光测定法进行病毒鉴定。为了确定新分离的病毒的基因型,克隆了病毒分离物的5'非翻译区(5'UTR),对其进行了测序和系统发育分析。为了评估病毒分离物的毒性,用病毒悬液鼻内接种了四个BVDV血清阴性小牛。每天记录直肠温度和临床体征。分析血样中白细胞计数的变化,并取组织样品进行组织病理学分析。结果采用MDBK细胞培养技术从鼻拭子中分离出一种新的分离株牛病毒性腹泻病毒(BVDV),命名为HN01。在两次传代后,HN01菌株在MDBK细胞培养物中引起了细胞病变效应(CPE)。该病毒在免疫荧光测定中与BVDV1特异性单克隆抗体发生了特异性反应。通过RT-PCR扩增该分离物的288bp的基因组片段。对5'UTR的系统进化分析表明该病毒为BVDV 1a。在发病机理研究中,实验性感染BVDV株的四头犊牛出现了抑郁,咳嗽和其他临床症状。小牛的温度超过40°C,白细胞计数下降了40%以上。结论从中国奶牛中首次分离到了一种新的BVDV亚型1a菌株。实验性感染表明,该病毒对牛具有中等致病性,可以用作BVDV攻击病毒,以评估BVDV疫苗在目标动物中的功效。

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