Co-detection of Helicobacter pylori and of its resistance to clarithromycin by PCR

被引:23
|
作者
Sevin, E
Lamarque, D
Delchier, JC
Soussy, CJ
Tankovic, J [1 ]
机构
[1] Hop Henri Mondor, Serv Bacteriol Virol Hyg, Creteil, France
[2] Hop Henri Mondor, Serv Hepatogastroenterol, Creteil, France
关键词
Helicobacter pylori; antibiotic resistance; macrolide antibiotic; 23S rRNA mutation; polymerase chain reaction;
D O I
10.1016/S0378-1097(98)00285-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Our aim was to develop a rapid molecular test based on polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and making it possible to detect Helicobacter pylori directly from gastric biopsy samples, and to test its susceptibility to clarithromycin. A 629-bp fragment of the 23S rRNA gene of H. pylori H. was amplified by PCR and the mutations responsible for clarithromycin resistance were detected with BsaI and BbsI restriction endonucleases. Thirty-five gastric samples were tested in parallel by standard microbiologic methods (culture and clarithromycin susceptibility testing with E-test strips) and by PCR-RFLP. The 10 culture-negative samples were also PCR-negative. Sixteen out of the 25 culture positive samples (64%) were PCR-positive. RFLP analysis could be done in 12 cases and the results were in agreement with those of the E-test: susceptibility in five cases, resistance in seven (six A2144G mutations and one A2143G mutation). (C) 1998 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:369 / 372
页数:4
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