阿奇霉素治疗解脲脲原体阳性的非淋菌性尿道炎患者失败与诱导产生大环内酯类耐药有关。
Azithromycin treatment failure in Mycoplasma genitalium-positive patients with nongonococcal urethritis is associated with induced macrolide resistance.
作者信息
Jensen Jørgen S, Bradshaw Catriona S, Tabrizi Sepehr N, Fairley Christopher K, Hamasuna Ryoichi
机构信息
Mycoplasma Laboratory, Statens Serum Institut, Copenhagen, Denmark.
出版信息
Clin Infect Dis. 2008 Dec 15;47(12):1546-53. doi: 10.1086/593188.
BACKGROUND
Mycoplasma genitalium is a common cause of nongonococcal urethritis. Treatment trials have shown that doxycycline is inefficient, whereas a 5-day course of azithromycin eradicates the bacterium from 95% of infected men. The aim of the study was to establish the reason for the occasional treatment failures.
METHODS
Seven M. genitalium strains isolated from men who experienced azithromycin treatment failure were tested for in vitro susceptibility to macrolides with use of a cell culture-based method. The genetic basis for the drug resistance was established by sequencing parts of the 23S ribosomal RNA gene and the genes encoding the L4 and L22 proteins. Nine sets of specimens obtained before and after treatment from patients who experienced azithromycin treatment failure were examined with use of sequencing of polymerase chain reaction products.
RESULTS
The 7 strains that were isolated from patients who experienced treatment failure with azithromycin had minimum inhibitory concentrations >8 microg/mL for azithromycin and erythromycin. Three different mutations at positions 2058 and 2059 (Escherichia coli numbering) in region V of the 23S rRNA gene were found. Of the 9 patients with specimens obtained before and after treatment, only 2 had an initial specimen in which the mutation was present, indicating that drug resistance was induced as the result of an inappropriate dosage of azithromycin.
CONCLUSION
Development of macrolide resistance was shown to correlate with subsequent azithromycin treatment failure. The genetic basis for the drug resistance was shown to be mutations in region V of the 23S rRNA gene, which is well described in other Mollicutes. These findings raise concern about the use of single-dose azithromycin treatment of nongonococcal urethritis of unknown etiology.
背景
生殖支原体是引起非淋菌性尿道炎的常见病因。治疗试验表明,强力霉素治疗无效,而5天疗程的阿奇霉素可使95%的感染男性体内的该细菌被清除。本研究的目的是确定偶尔治疗失败的原因。
方法
采用基于细胞培养的方法,对从阿奇霉素治疗失败的男性中分离出的7株生殖支原体菌株进行大环内酯类药物的体外敏感性测试。通过对23S核糖体RNA基因以及编码L4和L22蛋白的基因部分进行测序,确定耐药的遗传基础。对9例阿奇霉素治疗失败患者治疗前后获取的标本进行聚合酶链反应产物测序检测。
结果
从阿奇霉素治疗失败患者中分离出的7株菌株对阿奇霉素和红霉素的最低抑菌浓度>8μg/mL。在23S rRNA基因V区的2058和2059位(大肠杆菌编号)发现了3种不同的突变。在9例治疗前后均有标本的患者中,只有2例初始标本存在该突变,这表明阿奇霉素用药剂量不当导致了耐药性的产生。
结论
大环内酯类耐药的出现与随后的阿奇霉素治疗失败相关。耐药的遗传基础是23S rRNA基因V区的突变,这在其他柔膜菌纲细菌中已有充分描述。这些发现引发了对单剂量阿奇霉素治疗病因不明的非淋菌性尿道炎的担忧。