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The specificity of PCR-based protocols for detection of Erwinia amylovora

机译:基于PCR的协议检测支链淀粉欧文氏菌的特异性

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摘要

An evaluation of seven published conventional PCR protocols used for the detection of Erwinia amylovora has shown that six out of the seven protocols tested were not specific for all strains of E. amylovora. A collection of 40 genetically diverse strains of E. amylovora and 55 geographically diverse bacteria that are closely related or share the same ecological niche as E. amylovora were used to test the seven PCR protocols. All bacteria were tested for virulence by inoculation of immature pear fruit and for cultural characteristics on selective media. Only one PCR protocol, Taylor et al. (2001), was specific for all strains of E. amylovora and was able to differentiate E. amylovora from all other bacteria tested. Diagnostic laboratories may need to review their testing procedures in light of these findings.
机译:对用于检测解淀粉欧文氏菌的七个公开的常规PCR方案的评估显示,所测试的七个方案中有六个不是对所有链霉菌都特异的。收集了40种不同基因的淀粉链球菌菌株和55种地理上多样的细菌,它们与淀粉链球菌密切相关或具有相同的生态位,用于测试这7种PCR方案。通过接种未成熟的梨果来测试所有细菌的毒性,并在选择性培养基上测试其培养特性。 Taylor等仅一种PCR方案。 (2001年),是针对所有的链霉菌菌株,并能够区分从所有其他细菌测试的链霉菌。诊断实验室可能需要根据这些发现来审查其测试程序。

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