Related Experiment Video
Updated: May 28, 2026

Applying Live Cell Imaging and Cryo-Electron Tomography to Resolve Spatiotemporal Features of the Legionella pneumophila Dot/Icm Secretion System
Published on: March 10, 2020
Identification of Legionella pneumophila serogroups and other Legionella species by mip gene sequencing
Attiya Haroon1, Michio Koide, Futoshi Higa
1Department 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.
Abstract:
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.
Insights
Sequencing the macrophage infectivity potentiator (mip) gene effectively distinguishes Legionella pneumophila strains from other Legionella species. This method also differentiates serogroups within L. pneumophila, aiding in bacterial identification.
Area of Science:
- Microbiology
- Genetics
- Bacterial Pathogenesis
Background:
- The macrophage infectivity potentiator (mip) gene is crucial for intracellular survival in Legionella species.
- Accurate identification of Legionella species and serogroups is vital for clinical and epidemiological studies.
Purpose of the Study:
- To evaluate the efficacy of mip gene sequencing for differentiating Legionella species.
- To determine if mip gene sequencing can distinguish between different serogroups of Legionella pneumophila.
Main Methods:
- Genomic DNA extraction from clinical and environmental Legionella isolates and type strains.
- Polymerase Chain Reaction (PCR) amplification of the mip gene.
- Sequencing of the amplified mip gene and phylogenetic analysis.
Main Results:
- Mip gene sequencing successfully differentiated Legionella species.
- Legionella pneumophila isolates clustered into two distinct groups based on mip gene sequence similarity.
- Phylogenetic analysis showed a distinct cluster for Legionella anisa, with other species at discrete levels.
Conclusions:
- Mip gene sequencing is a reliable method for distinguishing Legionella species.
- The mip gene sequence can differentiate Legionella pneumophila serogroups, aiding in strain typing.
Related Concept Videos
Modern Molecular Taxonomy
Rapid Identification of Pathogens
Methods of Classification and Identification
Applications of Molecular Taxonomy
