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Antimicrobial Agents and Chemotherapy, May 2009, p. 2158-2159, Vol. 53, No. 5
0066-4804/09/$08.00+0     doi:10.1128/AAC.01563-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Molecular Mechanisms of Macrolide Resistance in Clinical Isolates of Mycoplasma pneumoniae from China{triangledown}

Deli Xin,1* Zuhuang Mi,2 Xu Han,3 Ling Qin,2 Jing Li,1 Tianli Wei,1 Xiaogeng Chen,1 Shaojie Ma,1 Ancun Hou,1 Gui Li,1 and Dawei Shi1

Department of Pediatrics, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China,1 Wuxi Research Institute of Genetics & Cloning Technology, Wuxi, Jiangsu 214026, China,2 Department of Pediatrics, Central Hospital of China National Petroleum Corporation, Langfang, Hebei 065000, China3

Received 24 November 2008/ Returned for modification 22 December 2008/ Accepted 22 February 2009


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ABSTRACT
 
Fifty clinical Mycoplasma pneumoniae strains were isolated from 370 children with respiratory tract infections. Four strains were susceptible to macrolides, while the other 46 (92%) were macrolide resistant. The molecular mechanism of resistance was shown to be associated with point mutations in 23S rRNA at positions 2063 and 2064.


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INTRODUCTION
 
Mycoplasma pneumoniae is a common pathogen found in respiratory tract infections of children and teenagers and is commonly treated with macrolides. In recent years, strains which are resistant to common drugs have been isolated from patients (1, 3-8). In order to evaluate the prevalence of macrolide resistance, we collected clinical samples during 2003 to 2006, cultured M. pneumoniae isolates, and screened for macrolide drug resistance. We investigated the mechanism of resistance by examining the erythromycin target site in the 23S rRNA gene of these strains.

Throat swab specimens were collected from 300 inpatient and 70 outpatient children with respiratory tract infection at the Pediatric Department of Beijing Friendship Hospital, affiliated with Capital Medical University, during June 2003 to June 2006. Modified Hayflick medium was used for the isolation and growth of M. pneumoniae. Nested PCR was carried out to verify the identity of M. pneumoniae, using primers which amplify part of the 16S rRNA gene as described previously (2). The MICs of erythromycin, azithromycin, and josamycin required to inhibit M. pneumoniae growth were determined by the microdilution method (1). A reference strain, FH, was used as a drug-sensitive control. Erythromycin resistance was defined as having a MIC of ≥32 µg/ml in accordance with the 2006 standards recommended by the CLSI (formerly NCCLS). To examine the molecular mechanisms of drug resistance, the 23S rRNA gene was amplified by nested PCR and the product was sequenced as described previously (8). The DNA sequences were compared with the sequence of M. pneumoniae M129 (GenBank accession no. X68422).

Fifty clinical M. pneumoniae strains (44 of them from inpatients) were isolated from the 370 specimens collected. Four strains were susceptible to macrolides, and the other 46 (92%) strains were macrolide resistant. MICs of resistant strains to erythromycin, azithromycin, and josamycin were higher than that of the reference strain and higher than the CLSI guidelines (especially in the case of erythromycin and azithromycin). Table 1 shows the MIC range, MIC50, and MIC90 of clinical isolate strains and the M. pneumoniae reference strain.


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  		TABLE 1. MIC range, MIC50, and MIC90 of clinical isolate strains and the M. pneumoniae reference strain

The 23S rRNA gene sequences of four susceptible strains and the reference strain FH were identical to that of the M. pneumoniae gene in GenBank (accession no. X68422). All 46 resistant strains displayed a point mutation in the 23S rRNA: 40 strains had an A-to-G transition at position 2063, 1 had an A-to-C transition at position 2063, and the other 5 showed an A-to-G transition at position 2064.

M. pneumoniae is a common pathogen associated with respiratory tract infection in children and teenagers, and macrolides are the first choice for treatment. Since their first introduction, increasing use of macrolides has given rise to increasing resistance among bacteria, but the sensitivity of M. pneumoniae to these drugs was unclear. In recent years, drug-resistant M. pneumoniae strains have been isolated from patients in a number of locations. In Japan, macrolide-resistant strains have been reported by Morozumi (3) and Matsuoka (1). In March 2005, D. Xin reported four of five M. pneumoniae strains were resistant to erythromycin in China (7, 8). Pereyre reported two macrolide-resistant strains in France (5), and Wolff reported five macrolide-resistant strains isolated in America (6). In these and our own studies, mutations at position 2063 or 2064 in domain V in the 23S rRNA gene were shown to be the predominant mutations associated with resistance.

The 44 inpatients who produced macrolide-resistant samples showed positive M. pneumoniae immunoglobulin M antibody tests around the 8th to 14th day of the illness and were diagnosed clinically as being infected with M. pneumoniae (including four cases which were complicated with pleural effusion). All of the patients had had prior treatment with macrolides before hospitalization. In this study, most of the isolates cultured were shown to be macrolide resistant in vitro and it was not possible to determine whether macrolides would have been effective in vivo. Furthermore, there were no patients infected with susceptible strains to act as a control. Further research will be needed to determine whether macrolides retain any clinical efficacy in patients shown to be harboring strains of M. pneumoniae which may be defined in vitro as macrolide resistant.


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ACKNOWLEDGMENTS
 
This work was supported in part by three grants, one each from the National Natural Science Foundation of China, the Beijing Natural Sciences Fund, and the Beijing Chinese Medicine Bureau.


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FOOTNOTES
 
* Corresponding author. Mailing address: Pediatric Department of Beijing Friendship Hospital, Capital Medical University, No. 95, Yongan Road, XuanWu District, Beijing 100050, China. Phone: 86-010-63138404. Fax: 86-010-63023261. E-mail: xindl48{at}sina.com.cn Back

{triangledown} Published ahead of print on 9 March 2009. Back


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Antimicrobial Agents and Chemotherapy, May 2009, p. 2158-2159, Vol. 53, No. 5
0066-4804/09/$08.00+0     doi:10.1128/AAC.01563-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.




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