犬细小病毒的聚合酶链反应检测及基因组分析。

T Hirasawa, K Yono, K Mikazuki
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引用次数: 17

摘要

研究了犬细小病毒2型(CPV-2)在日本犬中的流行率和病毒株间的基因组变异。采用在CPV-2的NS和VP1/VP2基因上设计的双巢引物对,建立了两步聚合酶链反应,用于检测粪便样本中的病毒基因组。1993年至1995年期间从腹泻家犬身上获得的74个样本进行了聚合酶链反应试验。病毒阳性率为54.1%,表明CPV-2仍与日本犬的许多急性感染性腹泻病例有关。对阳性样品的VP1/VP2基因进行限制性片段长度多态性(RFLP)分析和核苷酸测序。样品的RFLP模式与1991年分离的CPV-2菌株(TDKet-91-42)几乎相同,但与20世纪70年代末和80年代分离的CPV-2菌株的RFLP模式不同。结果表明,一种新的CPV-2基因型在20世纪90年代初出现并在日本犬中传播。
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Detection and genomic analysis of canine parvovirus by the polymerase chain reaction.

Prevalence of canine parvovirus type 2 (CPV-2) in Japanese dogs and genomic variations among the virus strains were examined. Two-step polymerase chain reaction with double-nested primer pairs designed in the NS and VP1/VP2 genes of CPV-2 was developed for the detection of the viral genome in faecal samples. A total of 74 samples obtained from diarrhoeal house dogs between 1993 and 1995 were tested by the PCR. The virus-positive rate was 54.1%, showing that CPV-2 is still involved in many cases of acute infectious diarrhoea in Japanese dogs. The VP1/VP2 gene of the positive samples was subjected to restriction fragment length polymorphism (RFLP) analysis and nucleotide sequencing. RFLP patterns of the samples were almost identical to those of one CPV-2 strain (TDKet-91-42) isolated in 1991, but different from those of the CPV-2 in the late 1970s and 1980s. The results suggest that a new genotype of CPV-2 appeared and spread among Japanese dogs in the early 1990s.

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