摘要
选用与A组人类轮状病毒(HumanRotavirus,HRV)编码VP7蛋白的第9(或8)基因片段中保守序列互补的两个引物,建立检测A组HRVRNA的逆转录-聚合酶链反应(RT-PCR)技术,扩增产物片段约342bp。经检测35例无腹泻症状新生儿129份粪便标本,并与聚丙烯酰胺凝胶电泳(PAGE)方法进行比较,结果前者检出HRV核酸77份(59.69%),而后者则检出49份(37.98%),PCR结果可能比较接近新生儿排泌轮状病毒的实际情况。
The primers selected in this
study were complementary ones to the common conserved sequence of gene 9(or8 ) among A
group four rotavirus serotypes.The method of polymerase chain reaction(PCR)was used for
detec-tion of group A rotavirus nucleic acid in fecal samples.About 342 nucleotides were
amplified with them.comparingwith polyacrylamide gel electrophorsis(PAGE ).We tested 129
fecal samples of 35 cases of asymptomatic rotavirusinfection of neonates by using reverse
transcriptase-polymerase chain reaction(RT-PCR).of 129 fecal samplesfrom the 35 neonates
,77(59.69%)contained rotavirus RNA detected by RT-PCR,whereas only 49(37.98%)weredetected
for rotavirus RNA by PAGE.The result probably were colse to the actual situation of the
neonates shed-ding rotavirus.
出处
《中华微生物学和免疫学杂志》
CAS
CSCD
北大核心
1994年第1期52-57,共6页
Chinese Journal of Microbiology and Immunology
基金
军队青年科学基金
关键词
新生儿感染
聚合酶链反应
HRV
Human rotavirus
Neonatal infections
Polymerase chain
reaction
Polyacrylamide gel electrophoresis.