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[肺炎支原体肺炎患儿肺炎支原体耐药性与DNA载量及基因型的相关性]

[Association of drug resistance of Mycoplasma pneumoniae with DNA load and genotypes in children with Mycoplasma pneumoniae pneumonia].

作者信息

Zhang Hui-Fen, Bai Hai-Tao, Li Ji-Ming, Xie Hui, Wang Ye

机构信息

Department of Pediatrics, Xiamen Maternal and Child Health Care Hospital, Xiamen, Fujian 361003, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2017 Nov;19(11):1180-1184. doi: 10.7499/j.issn.1008-8830.2017.11.011.

Abstract

OBJECTIVE

To investigate the association of drug resistance of Mycoplasma pneumoniae (MP) with DNA load and genotypes in children with MP pneumonia.

METHODS

A total of 230 children who were hospitalized and diagnosed with MP pneumonia between January 2012 and December 2016 were enrolled. Throat swabs were collected from the 230 children, and a rapid drug sensitivity assay was used to determine the sensitivity of clinical isolates of MP to nine commonly used antibacterial agents. Quantitative real-time PCR was used to measure MP-DNA load in throat swabs. PCR sequencing was used to determine the genotype of 2063 locus of the MP 23S rRNA V domain.

RESULTS

Of the 230 children, 86 (37.4%) had genotype A in 2063 locus, 134 (58.3%) had genotype G, 8 (3.5%) had genotype C, and 2 (0.9%) had genotype T. Mutant strains (genotype G+C+T) had a significantly higher MP-DNA load than wild-type strains (genotype A) (P<0.05). The strains resistant to erythromycin, azithromycin, clarithromycin, and clindamycin had a significantly higher MP-DNA load than non-resistant strains (P<0.05). MP had a high drug resistance rate to macrolide antibiotics. More than 60% of the cases with resistance to macrolides were found to have A2063G mutations. MP was rarely resistant to quinolones (less than 2%).

CONCLUSIONS

Mutations in 2063 locus of the MP 23S rRNA V domain may result in the resistance of MP to macrolides and the change in DNA load and can be used as a basis for selecting drugs for MP.

摘要

目的

探讨肺炎支原体(MP)耐药性与MP肺炎患儿DNA载量及基因型的相关性。

方法

选取2012年1月至2016年12月期间住院并诊断为MP肺炎的230例患儿。采集这230例患儿的咽拭子,采用快速药敏试验检测MP临床分离株对9种常用抗菌药物的敏感性。采用定量实时荧光PCR检测咽拭子中MP-DNA载量。采用PCR测序法确定MP 23S rRNA V区2063位点的基因型。

结果

230例患儿中,2063位点基因型A有86例(37.4%),基因型G有134例(58.3%),基因型C有8例(3.5%),基因型T有2例(0.9%)。突变株(基因型G+C+T)的MP-DNA载量显著高于野生株(基因型A)(P<0.05)。对红霉素、阿奇霉素、克拉霉素和克林霉素耐药的菌株,其MP-DNA载量显著高于非耐药菌株(P<0.05)。MP对大环内酯类抗生素耐药率较高。超过60%的大环内酯类耐药病例存在A2063G突变。MP对喹诺酮类药物耐药率较低(低于2%)。

结论

MP 23S rRNA V区2063位点突变可能导致MP对大环内酯类药物耐药及DNA载量改变,可作为MP用药选择的依据。

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