Jelocnik Martina, Polkinghorne Adam, Pannekoek Yvonne
Genecology Research Centre, University of the Sunshine Coast, Sippy Downs, QLD, Australia.
Department of Microbiology and Infectious Diseases, Nepean Hospital, NSW Health Pathology, Penrith, NSW, Australia.
Methods Mol Biol. 2019;2042:69-86. doi: 10.1007/978-1-4939-9694-0_7.
Developed two decades ago as a molecular method to provide definite characterization of a bacterial isolate, Multilocus Sequence Typing (MLST) is today globally adopted as a universal fine-detailed molecular typing tool and has been applied to numerous pathogenic and nonpathogenic bacterial as well eukaryotic organisms. MLST utilizes DNA sequence of several conserved housekeeping (HK) genes which are assigned an allelic number, which then collectively constitute an allelic profile or sequence type (ST), a "molecular barcode" of the interrogated bacterial strain or a eukaryotic organism. Here, we describe the principles and molecular approaches for generating MLST data for an analysis of a bacteria in the order Chlamydiales, using a Chlamydia pecorum-specific MLST scheme as an example.
多位点序列分型(MLST)是二十年前开发的一种分子方法,用于对细菌分离株进行明确的特征描述。如今,它已在全球范围内被用作通用的精细分子分型工具,并已应用于众多致病性和非致病性细菌以及真核生物。MLST利用几个保守管家(HK)基因的DNA序列,这些基因被赋予一个等位基因编号,然后共同构成一个等位基因谱或序列类型(ST),即被检测细菌菌株或真核生物的“分子条形码”。在此,我们以猪衣原体特异性MLST方案为例,描述为衣原体目细菌分析生成MLST数据的原理和分子方法。