DETERMINATION OF BOVINE ROTAVIRUS-G AND P-SEROTYPES BY POLYMERASE CHAIN-REACTION

被引:84
作者
ISEGAWA, Y
NAKAGOMI, O
NAKAGOMI, T
ISHIDA, S
UESUGI, S
UEDA, S
机构
[1] AKITA UNIV,SCH MED,DEPT MICROBIOL,AKITA 010,JAPAN
[2] OSAKA UNIV,MICROBIAL DIS RES INST,DEPT PREVENT MED,SUITA 560,JAPAN
[3] AKITA UNIV,SCH MED,DEPT LAB MED,AKITA 010,JAPAN
关键词
ROTAVIRUS; PCR; DIAGNOSTICS; G-SEROTYPE; P-SEROTYPE;
D O I
10.1006/mcpr.1993.1041
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Among bovine rotaviruses there are two major G serotypes (G6 and G10) and three P serotypes (P1, P5, and P11, each of which is defined on the basis of the VP4 antigenic specificity of NCDV, UK and KK-3, respectively). The nucleotide sequence of a P11 gene (KK-3) was determined. The predicted KK-3 VP4 contained 772 amino-acids and showed 96% amino-acid identity with B223 VP4, an American prototype of P11 bovine rotavirus. Comparative analysis of the genes determining the G and P serotypes of bovine rotaviruses allowed us to develop polymerase chain reaction (PCR)-based assays which distinguished two G serotypes and three P serotypes commonly found in bovine rotaviruses. For determination of G serotypes, a 1013 bp fragment of the VP7 gene was first reverse-transcribed and then amplified with a pair of generic primers. In a second PCR amplification, the 5′ generic primer and two different typing primers (either G6- or G10-specific) were used to generate fragments whose sizes served to identify the G serotype. Similarly, for determination of P serotypes, an 864 bp fragment of the VP4 gene was first reverse-transcribed and then amplified with another pair of generic primers. In a second PCR amplification, the 5′ generic primer and three different typing primers, each one specific to one of the three P serotypes, were used to generate fragments whose sizes served to identify the P serotype. These assays were able to identify the G and P serotype of six reference bovine rotavirus strains. © 1993 Academic Press, Limited.
引用
收藏
页码:277 / 284
页数:8
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