Research

I am interested in understanding how genetic entities called species are maintained or change in unicellular organisms by studying population evolution and the survival strategy of bacteria. My research addresses fundamental questions regarding sexual reproduction in prokaryotes and molecular mechanisms that support the persistence of prokaryotic mobile DNA elements. 

Local diversification of Mycobacterium avium complex (MAC)

MAC is a group of opportunistic human pathogens belonging to the genus Mycobacteria. MAC is known to reside in nature, for example, rivers, soil, and even in shower rooms. Comparative genomics studies have revealed that MAC conducts chromosomal recombination frequently in the evolutionary time scale unlike human-adapted Mycobacterium tuberculosis, which is thought to have spread over the world largely through clonal expansion. The evolutionary pattern of free-living environmental bacterial species has been largely unknown. Using MAC population as a model of free-living bacterial species, I address how bacterial lineage emerges (bacteria speciate), and how chromosomal recombination contributes to local adaptation. I also aim to identify chromosomal loci responsible for its virulence, antibiotic resistance, and niche adaption using the bioinformatic approach to provide clues for the prevention of MAC-associated infectious diseases.

Persistence of mobile DNA

Mobile genetic elements (MGE) such as plasmids and transposons are known as major players in the spread of antibiotic resistance to human pathogens.  My current research put emphasis on clarifying the DNA strand-exchange pathway used in the transposition of a recently discovered mobile DNA group, SE (Strand-biased circularizing integrative Elements), and tracing the evolution of SEs in clinical and environmental bacterial populations.

Publications