Department of Infectious, Respiratory, and Digestive Medicine, Control and Prevention of Infectious Diseases (First Department of Internal Medicine), University of the Ryukyus, 207 Uehara, Nishihara-cho, Okinawa 903-0215, Japan.
J Infect Chemother. 2012 Apr;18(2):276-81. doi: 10.1007/s10156-011-0324-0. Epub 2011 Oct 21.
The virulence factor known as the macrophage infectivity potentiator (mip) is responsible for the intracellular survival of Legionella species. In this study, we investigated the potential of the mip gene sequence to differentiate isolates of different species of Legionella and different serogroups of Legionella pneumophila. We used 35 clinical L. pneumophila isolates and one clinical isolate each of Legionella micdadei, Legionella longbeachae, and Legionella dumoffii (collected from hospitals all over Japan between 1980 and 2007). We used 19 environmental Legionella anisa isolates (collected in the Okinawa, Nara, Osaka, and Hyogo prefectures between 1987 and 2007) and two Legionella type strains. We extracted bacterial genomic DNA and amplified out the mip gene by PCR. PCR products were purified by agarose gel electrophoresis and the mip gene was then sequenced. The L. pneumophila isolates could be divided into two groups: one group was very similar to the type strain and was composed of serogroup (SG) 1 isolates only; the second group had more sequence variations and was composed of SG1 isolates as well as SG2, SG3, SG5, and SG10 isolates. Phylogenetic analysis displayed one cluster for L. anisa isolates, while other Legionella species were present at discrete levels. Our findings show that mip gene sequencing is an effective technique for differentiating L. pneumophila strains from other Legionella species.
已知毒力因子巨噬细胞感染增强因子(mip)是军团菌属物种在细胞内存活的原因。在这项研究中,我们研究了 mip 基因序列区分不同种属的军团菌和不同血清型的嗜肺军团菌的潜力。我们使用了 35 株临床嗜肺军团菌分离株和 1 株来自日本各地医院(1980 年至 2007 年收集)的军团菌米卡德亚种、军团菌长滩亚种和军团菌杜蒙德氏亚种的临床分离株。我们使用了 19 株环境军团菌安莎亚种分离株(1987 年至 2007 年在冲绳、奈良、大阪和兵库县收集)和 2 株军团菌标准株。我们提取细菌基因组 DNA 并通过 PCR 扩增 mip 基因。通过琼脂糖凝胶电泳纯化 PCR 产物,然后对 mip 基因进行测序。嗜肺军团菌分离株可分为两组:一组与标准株非常相似,仅由血清群(SG)1 分离株组成;第二组具有更多的序列变异,由 SG1 分离株以及 SG2、SG3、SG5 和 SG10 分离株组成。系统发育分析显示,安莎军团菌分离株聚类为一组,而其他军团菌种则处于离散水平。我们的研究结果表明,mip 基因测序是区分嗜肺军团菌菌株和其他军团菌种的有效技术。