Nederbragt Alexander J, Balasingham Anusha, Sirevåg Reidun, Utkilen Hans, Jakobsen Kjetill S, Anderson-Glenna Mary J
University of Oslo, Department of Biology, Centre for Ecological and Evolutionary Synthesis, P.O. Box 1066 Blindern, N-0316 Oslo, Norway.
J Microbiol Methods. 2008 May;73(2):111-7. doi: 10.1016/j.mimet.2008.02.007. Epub 2008 Feb 23.
Several methods for typing of Legionella pneumophila exist, one of which is an 8-locus variable-number of tandem repeats analysis (MLVA). This method is based on separating and sizing amplified VNTR PCR products by agarose gel electrophoresis. In the present work, the existing L. pneumophila MLVA-8 assay is adapted to capillary electrophoresis. The assay was multiplexed by using multiple fluorescent labeling dyes and tested on a panel of L. pneumophila strains with known genotypes. The results from the capillary electrophoresis-based assay are shown to be equivalent to, and in a few cases more sensitive than, the gel-based genotyping assay. The assay presented here allows for a swift, automated and precise typing of L. pneumophila from patient or environmental samples and represents an improvement over the current gel-based method.
嗜肺军团菌有多种分型方法,其中之一是8个基因座的可变数目串联重复序列分析(MLVA)。该方法基于通过琼脂糖凝胶电泳分离和测定扩增的VNTR PCR产物的大小。在本研究中,现有的嗜肺军团菌MLVA-8检测方法被调整用于毛细管电泳。该检测方法通过使用多种荧光标记染料进行多重检测,并在一组已知基因型的嗜肺军团菌菌株上进行测试。基于毛细管电泳的检测结果显示与基于凝胶的基因分型检测相当,在少数情况下甚至更灵敏。本文介绍的检测方法能够快速、自动且精确地对来自患者或环境样本的嗜肺军团菌进行分型,是对当前基于凝胶的方法的一种改进。