The 94th Annual Meeting of Japanese Society for Bacteriology

Presentation information

On-demand Presentation

6 Virulence Factors and Biophylaxis

[ODP6B] b. Toxins, Effectors, and Bioactive Substances

[ODP-154] Functional analysis of mycobacterial protein PE_PGRS30

○Kazunori Matsumura1, Satoshi Takaki1, Teruo Kirikae2 (1Dept. Immune Reg., Inst., NCGM, 2Dept. Microbiol., Sch. Med., Juntendo Univ.)

Mycobacterium tuberculosis infects macrophages and subsequently induces their cell death. We report here that Mycobacterial protein PE_PGRS30, belonging to proline-glutamate (PE) and polymorphic GC-rich sequence (PGRS) family, induces apoptosis in murine macrophage-like RAW264.7 cells via interacting a host protein, prohibitin (PHB) 2. Ectopic expression of PE_PGRS30 induced apoptosis in RAW264.7 cells. Those cells showed phenotypes of apoptosis; condensed and fragmented nuclei, dissipation of mitochondrial membrane potential, and caspase-3. A pull down assay identified PHB2 as a target of PE_PGRS30. Immunoprecipitations and in vitro binding assays revealed that the PGRS domain of PE_PGRS30 interacted with PHB2 via a region including a putative mitochondria localization signal. PE_PGRS30 were detected in culture supernatants of M. tuberculosis Erdman strain. Recombinant PGRS domain of PE_PGRS30 induced apoptosis in RAW264.7 cells. The long-isoforms of OPA1 decreased in RAW264.7 cells treated with the PGRS domain, whereas the short-isoforms increased in the cells. ATP5B puncta, the marker of mitophagy, increased in the RAW264.7 after treatment with the PGRS domain. These results indicate that PE_PGRS30 induces apoptosis through interfering PHB2 functions in macrophages.