Rapid differentiation of mycobacteria by simplex real-time PCR with melting temperature calling analysis

被引:1
作者
Lin, L. [1 ]
Yin, X. [2 ]
Wang, Q. [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Lab Med, Guangzhou 510515, Guangdong, Peoples R China
[2] Southern Med Univ, Affiliated Hosp 5, Clin Lab, Guangzhou 510515, Guangdong, Peoples R China
关键词
differentiation; Mycobacterium tuberculosis complex; nontuberculous mycobacteria; real-time PCR; rpoB gene; POLYMERASE GENE RPOB; NONTUBERCULOUS MYCOBACTERIA; TUBERCULOSIS COMPLEX; IDENTIFICATION; DIAGNOSTICS; MULTIPLEX;
D O I
10.1111/jam.12884
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
AimsThis study aimed to develop a rapid, simple and cost-effective method for the differentiation of Mycobacterium species. Methods and ResultsA total of 80 clinical mycobacterial isolates belonging to 12 different species and 16 reference strains of 16 different species were differentiated by the simplex real-time PCR coupled with melting temperature calling analysis. By comparing their melting profiles with those of the reference strains, all clinical mycobacterial isolates were differentiated as Mycobacterium tuberculosis complex or nontuberculous mycobacteria, and the latter were further divided into five groups. In comparison with 16S-23S internal transcribed spacer sequencing method as the gold standard method, both sensitivity and specificity of the assay were 100% when it was used for the differentiation between Myco.tuberculosis complex and nontuberculous mycobacteria. ConclusionsThe simplex real-time PCR coupled with melting temperature calling analysis could be an alternative method for the differentiation between Myco.tuberculosis complex and nontuberculous mycobacteria. Significance and Impact of the StudyRapid differentiation of mycobacteria could shorten the diagnostic time of mycobacterial diseases. It is also helpful for achieving optimal therapy and appropriate patient management.
引用
收藏
页码:853 / 858
页数:6
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