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Abstract

Vol.64 No.3 May 2016

The mechanism of vancomycin resistance in VISA andthe role of reverse antibiotic (RA)

Keiichi Hiramatsu1), Yuhu Morimoto1), Tadashi Baba1), Takashi Sasaki2), Tomomi Hishinuma2), Yuki Katayama2), Miki Matsuo2), Kyoko Kuwahara2), Yuki Uehara3) and Masayuki Igarashi4)

1)Research Center for Infection Control Science, Graduate School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, Japan
2)Department of Microbiology, Faculty of Medicine, Juntendo University
3)Infection Control Science, Graduate School of Medicine, Juntendo University
4)Institute of Microbial Chemistry

Abstract

Anti-bacterial chemotherapy of the last century has greatly contributed to the welfare and prolongation human life by conquering the threat of bacterial infection. However, in 21st century, we started to notice the rise of antimicrobial resistance in the pathogenic bacteria causing infection refractory to chemotherapy. That trend suppressed the motivation of pharmaceutical companies to develop new antimicrobial agents. However, it is important to regard the resistance emergence is an inevitable result since resistance has been a phenomenon existent since much before the rise of humans on the earth. Given this, it is necessary for us to raise antimicrobials against antibiotic-resistant pathogens. We re-discovered a natural antibacterial substance called nybomycin by screening the soil bacterial culture, which exhibited potent antimicrobial activity against quinolone-resistant bacteria but poor activity against quinolone-susceptible bacteria. Although at a very low frequency, bacteria do produce nybomycin-resistant mutants. However, we found that the resistant mutants carried a reverse mutation in a codon of gyrA gene encoding DNA gyrase subunit A, which cured the bacteria of quinolone resistance. We designated nybomycin reverse antibiotic(RA). We expect that this discovery of new genre of antibiotic class in nature would lead to revitalization of chemotherapy.

Key word

MRSA, multi-drug resistance, reverse antibiotic, coevolution

Received

September 15, 2015

Accepted

February 29, 2016

Jpn. J. Chemother. 64 (3): 503-512, 2016