摘要
应用PCR扩增15个幽门螺杆菌分离株的DNA,扩增产物经琼脂糖凝胶电泳均显示一条298bp的区带,而12株与幽门螺杆菌相关的肠道杆菌都不能扩增出该片段。PCR可检出少至100个幽门螺杆菌细胞,并能检出胃粘膜活检标本中的此菌,全部实验可在5小时内完成。
A polymerase chain reaction(PCR )assay for
the specific detection of H elicobacter pylori was developed by us-ing primers based on the
nucleotide sequences of a species-specific antigen of H. pylori.The PCR assay amplified
a298-nucleotide-pair product which was analyzed by agarose gel electrophoresis.PCR detected
all 15 H. pylori iso-lates tested,and did not amplify sequences in several closely related
species.The PCR test was able to detect asfew as 100 H.pylori cells.H. pylori in fresh gastric
biopsy specimens was detected successfully in five hours byPCR. Therefore PCR is a
rapid,sensitive and specific method for the detection of H.pylori.
出处
《中华微生物学和免疫学杂志》
CAS
CSCD
北大核心
1994年第4期280-281,共2页
Chinese Journal of Microbiology and Immunology
基金
军队青年基金
关键词
幽门螺杆菌
聚合酶链反应
胃粘膜
H elicobacter
pylori
PCR
Gastric biopsy specimens