1株犬细小病毒的分离鉴定及其生物学特性研究  

Isolation and Identification of Canine Parvovirus Strain NY130615 and Its Biologic Characterization

作　　者：卜宾 李生涛 毛倩倩[1] 唐青海[1] 唐存多[1] 焦铸锦[1] 姚伦广[1] 阚云超[1] 

机构地区：[1]南阳师范学院 南阳市兽医生物工程技术研究中心/河南省伏牛山昆虫生物学重点实验室/昆虫生物反应器河南省工程实验室,河南 南阳473061 [2]南阳农业职业学院,河南 南阳473061

出　　处：《河南农业科学》2015年第8期121-127,140,共8页Journal of Henan Agricultural Sciences

基　　金：国家自然基金青年基金项目(31101837);河南省重点科技攻关项目(142102110101);南阳师范学院引进人才专项(70640);南阳师范学院研究生创新基金项目(20141101,2014103)

摘　　要：采集一疑似犬细小病毒(CPV)患犬的粪便,采用胶体金试纸条和PCR方法对病料进行CPV检测,并应用猫肾细胞F81进行病毒分离培养,分别采用免疫过氧化物酶单层细胞染色法(IPMA)和PCR检测病毒在F81细胞中的增殖动态,采用无血清培养和有血清培养2种方法进行体外培养,IPMA测定病毒滴度。利用PCR扩增分离病毒的VP2基因,经序列测定后采用DNAStar 7.0和MEGA 5.0软件进行生物信息学分析。结果表明,胶体金试纸条检测为CPV抗原阴性,PCR检测结果为CPV核酸阳性,病料接种到F81细胞培养后出现明显细胞病变(CPE),血清学鉴定为CPV抗原阳性,将分离得到的病毒命名为CPV-NY130615。IPMA可从感染后6 h的F81细胞中检出病毒,PCR能从感染后6 h培养上清中检出CPV核酸。血清同步接种培养法培养和无血清单层接种培养法培养的第15代病毒滴度分别为1×108.06TCID50/m L和1×107.65TCID50/m L。序列测定分析表明,该毒株VP2基因开放阅读框(ORF)为1 755 bp,编码584 aa。进化分析显示,该毒株属于CPV-2a型。The faeces samples were collected from a dog suspected infected by canine parvovirus（ CPV） , CPV in the samples was detected by colloidal gold test strip and polymerase chain reaction（PCR）,then the samples were innoculated into F81 cells to isolate CPV,propagation dynamics characterization of CPV in F81 cells were determined by immunoperoxidase monolayer assay（ IPMA） and PCR,samples that cul-tured with or without serum were titrated by IPMA. VP2 gene of this virus strain was amplified by PCR and sequenced then analyzed by software DNAStar 7 . 0 and MEGA 5 . 0 . Results of colloidal gold test strip test showed CPV Ag negative in the samples,however,PCR detection results showed positive. The sample inoculated into F81 cells showed significant cytopathic effect（ CPE） . Serologic test results showed that the nbsp;culture samples were CPV Ag positive,the isolated virus strain was named CPV-NY130615. CPV Ag in the F81 cells 6 hours post infected（ hpi） with CPV-NY130615 strain was successfully detected by IPMA, as well as the culture supernant was CPV nucleotied positive detected by PCR. The fifteenth passages vi-rus titers of two different culture method,synchronization inoculated culture with serum and monolayer in-oculated culture without serum were 1 × 108. 06 TCID50/mL and 1 ×107. 65 TCID50/mL respectively. Nucle-otid sequences showed that the open reading frame of VP2 gene was 1 755 bp encoding 584 aa. Phyloge-netic analysis showed that CPV-NY130615 strain belonged to the genotype CPV-2a.

关 键 词：犬细小病毒 分离 免疫过氧化物酶单层细胞染色法 生物学特性 

分 类 号：S855.3[农业科学—临床兽医学]