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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)

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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.

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