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基于23S rRNA基因PCR-限制性片段长度多态性的非幽门螺杆菌菌种鉴别

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

作者信息

Yadegar Abbas, Alebouyeh Masoud, Lawson Andy J, Mirzaei Tabassom, Nazemalhosseini Mojarad Ehsan, Zali Mohammad Reza

机构信息

Gastroenterology and Liver Diseases Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

World J Microbiol Biotechnol. 2014 Jun;30(6):1909-17. doi: 10.1007/s11274-014-1615-2. Epub 2014 Feb 4.

Abstract

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.

摘要

与许多其他细菌相比,非幽门螺杆菌菌种的表型鉴定一直存在问题且耗时。我们基于23S rRNA基因的PCR-限制性片段长度多态性(PCR-RFLP)分析,开发了一种快速的两步鉴定方法,用于区分非幽门螺杆菌菌种。根据幽门螺杆菌菌种所有可用的完整和部分23S rRNA序列,设计了一对新的属特异性引物。对23S rRNA基因可变区的计算机模拟限制性分析表明,SmaI和HindIII核酸内切酶将提供良好的区分水平。对获得的23S rRNA RFLP模式的分析将所有幽门螺杆菌研究菌株分为三个菌种组(A - C组)和12种独特的限制性模式。琥珀酸沃林菌也给出了独特的模式。我们提出的PCR-RFLP方法被发现是从人或动物样本中常规鉴定非幽门螺杆菌菌种的有价值工具。

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