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Volume 17, Number 1—January 2011

Letter

Ceftriaxone-Resistant Neisseria gonorrhoeae, Japan

Makoto OhnishiComments to Author , Takeshi Saika, Shinji Hoshina, Kazuhiro Iwasaku, Shu-ichi Nakayama, Haruo Watanabe, and Jo Kitawaki
Author affiliations: Author affiliations: National Institute of Infectious Diseases, Tokyo, Japan (M. Ohnishi, S. Nakayama, H. Watanabe); Mitsubishi Chemical Medience Corporation, Tokyo (T. Saika); Hoshina Clinic, Kyoto, Japan (S. Hoshina); Kyoto Prefectural University of Medicine, Kyoto (K. Iwasaku, J. Kitawaki)

Main Article

Figure

Pulsed-field gel electrophoresis patterns of ceftriaxone-resistant Neisseria gonorrhoeae strain H041 and other multilocus sequence typing (MLST) ST7363 and ST1901 strains. SpeI-digested genomic DNA from ceftriaxone-resistant N. gonorrhoeae H041, 3 of the MLST ST7363 strains and 4 of the MLST ST1901 strains were analyzed by pulsed-field gel electrophoresis. A lambda ladder standard (Bio-Rad, Hercules, CA, USA) was used as a molecular size marker.

Figure. Pulsed-field gel electrophoresis patterns of ceftriaxone-resistant Neisseria gonorrhoeae strain H041 and other multilocus sequence typing (MLST) ST7363 and ST1901 strains. SpeI-digested genomic DNA from ceftriaxone-resistant N. gonorrhoeae H041, 3 of the MLST ST7363 strains and 4 of the MLST ST1901 strains were analyzed by pulsed-field gel electrophoresis. A lambda ladder standard (Bio-Rad, Hercules, CA, USA) was used as a molecular size marker.

Main Article

The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.

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