Characterization and Molecular Analysis of Macrolide-Resistant <i>Mycoplasma pneumoniae</i> Clinical Isolates Obtained in Japan

Mayumi Matsuoka(National Institute of Infectious Diseases), Mitsuo Narita, Norio Okazaki(Kanagawa Prefectural Institute of Public Health), Hitomi Ohya(Kanagawa Prefectural Institute of Public Health), Tsutomu Yamazaki(Saitama Medical University), Kazunobu Ouchi(Kawasaki Medical School), Isao Suzuki, Tomoaki Andoh, Tsuyoshi Kenri(National Institute of Infectious Diseases), Yuko Sasaki(National Institute of Infectious Diseases), Atsuko Horino(National Institute of Infectious Diseases), Miharu Shintani(National Institute of Infectious Diseases), Yoshichika Arakawa(National Institute of Infectious Diseases), Tsuguo Sasaki(National Institute of Infectious Diseases)
Antimicrobial Agents and Chemotherapy
November 24, 2004
Cited by 252Open Access
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Abstract

In recent years, Mycoplasma pneumoniae strains that are clinically resistant to macrolide antibiotics have occasionally been encountered in Japan. Of 76 strains of M. pneumoniae isolated in three different areas in Japan during 2000 to 2003, 13 strains were erythromycin (ERY) resistant. Of these 13 strains, 12 were highly ERY resistant (MIC, > or =256 microg/ml) and 1 was weakly resistant (MIC, 8 microg/ml). Nucleotide sequencing of domains II and V of 23S rRNA and ribosomal proteins L4 and L22, which are associated with ERY resistance, showed that 10 strains had an A-to-G transition at position 2063 (corresponding to 2058 in Escherichia coli numbering), 1 strain showed A-to-C transversion at position 2063, 1 strain showed an A-to-G transition at position 2064, and the weakly ERY-resistant strain showed C-to-G transversion at position 2617 (corresponding to 2611 in E. coli numbering) of domain V. Domain II and ribosomal proteins L4 and L22 were not involved in the ERY resistance of these clinical M. pneumoniae strains. In addition, by using our established restriction fragment length polymorphism technique to detect point mutations of PCR products for domain V of the 23S rRNA gene of M. pneumoniae, we found that 23 (24%) of 94 PCR-positive oral samples taken from children with respiratory infections showed A2063G mutation. These results suggest that ERY-resistant M. pneumoniae infection is not unusual in Japan.


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