A rapid identification scheme for Helicobacter pylori and other species of Helicobacter based on 23S rRNA gene polymorphisms

被引:20
作者
Hurtado, A [1 ]
Owen, RJ [1 ]
机构
[1] CENT PUBL HLTH LAB,LAB ENTER PATHOGENS,HELICOBACTER REFERENCE UNIT,LONDON NW9 5HT,ENGLAND
关键词
identification; Helicobacter species; 23S rRNA; PCR; RFLPs;
D O I
10.1016/S0723-2020(97)80069-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Restriction fragment length polymorphism (RFLP) analysis of a similar to 2.6-kbp PCR-amplified DNA fragment of the 23S (large subunit) ribosomal RNA gene was performed on 92 strains selected to represent 12 species of Helicobacter as well as ''Flexispira rappini'' and Wolinella succinogenes. The amplicon was digested with four restriction endonucleases (HaeIII, HpaII, CfoI and Hinfl). The PCR-RFLP profiles obtained from the type strains were used to build an identification scheme which was then assessed using available field strains. The scheme is based on the use of HaeIII as first choice enzyme, combined with HpaII for confirmation purposes, and in some particular cases with CfoI and Hinfl to increase discrimination. The proposed scheme is useful for differentiation of Helicobacter species from each other and has the potential of being expanded to include the increasing number of new Helicobacter species being described. Therefore, it can be a valuable tool for routine identification when used in combination with relevant phenotypic tests.
引用
收藏
页码:222 / 231
页数:10
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