共 19 条
The detection of human sapoviruses with universal and genogroup-specific primers
被引:93
作者:

Okada, M.
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机构:
Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan

Yamashita, Y.
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机构:
Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan

Oseto, M.
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Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan

Shinozaki, K.
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Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan
机构:
[1] Chiba Prefectural Inst Publ Hlth, Div Virol, Chuo Ku, Chiba 2608715, Japan
关键词:
D O I:
10.1007/s00705-006-0820-1
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Sapovirus (SV) causes gastroenteritis in humans and comprises genetically divergent viruses. A nested reverse transcription-polymerase chain reaction (RT-PCR) targeting the capsid-protein-coding region was developed using universal and genogroup-specific primer sets. The universal primers were capable of detecting human SV genogroups I, II, IV and V. Genetic analysis of the amplified products enabled us to phylogenetically determine the genotypes of the viruses. In addition, genogroup-specific primers that amplified different lengths of the amplicon depending on the genogroup were developed. These genogroup-specific primers were also used as inner primers for the nested PCR. These two simple RT-PCR methods are powerful tools for both detection and epidemiological studies of human SV.
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页码:2503 / 2509
页数:7
相关论文
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