Differentiation of non-pylori Helicobacter species based on PCR-restriction fragment length polymorphism of the 23S rRNA gene

被引:8
|
作者
Yadegar, Abbas [1 ,2 ]
Alebouyeh, Masoud [1 ,2 ]
Lawson, Andy J. [3 ]
Mirzaei, Tabassom [1 ,2 ]
Mojarad, Ehsan Nazemalhosseini [1 ,2 ]
Zali, Mohammad Reza [1 ,2 ]
机构
[1] Shahid Beheshti Univ Med Sci, Gastroenterol & Liver Dis Res Ctr, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Basic & Mol Epidemiol Gastrointestinal Disorders, Tehran, Iran
[3] Publ Hlth England, Gastrointestinal Bacteria Reference Unit, London, England
来源
关键词
Helicobacter pylori; Non-pylori Helicobacter species; Wolinella succinogenes; 23S rRNA; RFLP; RAPID IDENTIFICATION; SEQUENCE-ANALYSIS; SP-NOV; PHYLOGENETIC ANALYSIS; GASTRIC-MUCOSA; 16S; STOMACH; CAMPYLOBACTER; ARCOBACTER; DISEASES;
D O I
10.1007/s11274-014-1615-2
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
Phenotypic identification of non-pylori Helicobacter species has always been problematic and time-consuming in comparison with many other bacteria. We developed a rapid two-step identification assay based on PCR-restriction fragment length polymorphism (PCR-RFLP) analysis of the 23S rRNA gene for differentiating between non-pylori Helicobacter species. A new genus-specific primer pair based on all available complete and partial 23S rRNA sequences of Helicobacter species was designed. In silico restriction analysis of variable regions of the 23S rRNA gene suggested SmaI and HindIII endonucleases would provide a good level of differentiation. Analysis of the obtained 23S rRNA RFLP patterns divided all Helicobacter study strains into three species groups (groups A-C) and 12 unique restriction patterns. Wolinella succinogenes also gave a unique pattern. Our proposed PCR-RFLP method was found to be as a valuable tool for routine identification of non-pylori Helicobacter species from human or animal samples.
引用
收藏
页码:1909 / 1917
页数:9
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