Shen Yinfang, Cai Jiehao, Davies Mark R, Zhang Chi, Gao Kun, Qiao Dan, Jiang Haoqin, Yao Weilei, Li Yuefang, Zeng Mei, Chen Mingliang
Department of Infectious Diseases, Children's Hospital of Fudan University, Shanghai, China.
Department of Pediatrics, Jinshan Hospital, Fudan University, Shanghai, China.
Front Microbiol. 2018 Mar 23;9:542. doi: 10.3389/fmicb.2018.00542. eCollection 2018.
, also known as group A (GAS), is one of the top 10 infectious causes of death worldwide. Macrolide and tetracycline resistant GAS has emerged as a major health concern in China coinciding with an ongoing scarlet fever epidemic. Furthermore, increasing rates of fluoroquinolone (FQ) non-susceptibility within GAS from geographical regions outside of China has also been reported. Fluoroquinolones are the third most commonly prescribed antibiotic in China and is an therapeutic alternative for multi-drug resistant GAS. The purpose of this study was to investigate the epidemiological and molecular features of GAS fluoroquinolone (FQ) non-susceptibility in Shanghai, China. GAS ( = 2,258) recovered between 2011 and 2016 from children and adults were tested for FQ-non-susceptibility. Efflux phenotype and mutations in , and were investigated and genetic relationships were determined by typing, pulsed-field gel electrophoresis and phylogenetic analysis. The frequency of GAS FQ-non-susceptibility was 1.3% (30/2,258), with the phenotype more prevalent in GAS isolated from adults (14.3%) than from children (1.2%). Eighty percent (24/30) of FQ-non-susceptible isolates were also resistant to both macrolides () and tetracycline () including the GAS sequence types 12, 6, 11, and 1. Genomic fingerprinting analysis of the 30 isolates revealed that non-susceptibility may arise in various genetic backgrounds even within a single type. No efflux phenotype was observed in FQ non-susceptible isolates, and molecular analysis of the quinolone resistance-determining regions (QRDRs) identified several sequence polymorphisms in ParC and ParE, and none in GyrA and GyrB. Expansion of this analysis to 152 publically available GAS whole genome sequences from Hong Kong predicted 7.9% (12/152) of Hong Kong isolates harbored a S79F ParC mutation, of which 66.7% (8/12) were macrolide and tetracycline resistant. Phylogenetic analysis of the QRDR sequences suggested the possibility that FQ resistance may be acquired through inter-species lateral gene transfer. This study reports the emergence of macrolide, tetracycline, and fluoroquinolone multidrug-resistant clones across several GAS types including 1 and 12, warranting continual surveillance given the extensive use of fluoroquinolones in clinical use.
A群链球菌(GAS),也被称为A组链球菌,是全球十大感染性致死病因之一。在中国,随着猩红热疫情的持续,对大环内酯类和四环素耐药的GAS已成为主要的健康问题。此外,在中国以外地区也有报道称GAS对氟喹诺酮(FQ)的不敏感率在上升。氟喹诺酮类药物是中国第三大最常用的抗生素,是耐多药GAS的一种治疗选择。本研究的目的是调查中国上海GAS对氟喹诺酮(FQ)不敏感的流行病学和分子特征。对2011年至2016年间从儿童和成人中分离出的2258株GAS进行FQ不敏感性检测。研究了其外排表型以及gyrA、parC和parE基因的突变情况,并通过多位点序列分型、脉冲场凝胶电泳和系统发育分析确定了遗传关系。GAS对FQ不敏感的频率为1.3%(30/2258),该表型在从成人中分离出的GAS中(14.3%)比从儿童中分离出的GAS中(1.2%)更普遍。80%(24/30)对FQ不敏感的分离株同时对大环内酯类(ermB)和四环素(tetM)耐药,包括GAS序列类型12、6、11和1。对这30株分离株的基因组指纹分析表明,即使在单一序列类型内,不敏感性也可能出现在不同的遗传背景中。在对FQ不敏感的分离株中未观察到外排表型,对喹诺酮耐药决定区(QRDRs)的分子分析在ParC和ParE中鉴定出了几个序列多态性,而在GyrA和GyrB中未发现。将此分析扩展到来自香港的152个公开可用的GAS全基因组序列,预测7.9%(12/152)的香港分离株携带S79F ParC突变,其中66.7%(8/12)对大环内酯类和四环素耐药。对QRDR序列的系统发育分析表明,FQ耐药可能通过种间横向基因转移获得。本研究报告了包括序列类型1和12在内的几种GAS序列类型中出现了对大环内酯类、四环素类和氟喹诺酮类的多重耐药克隆,鉴于氟喹诺酮类药物在临床中的广泛使用,有必要进行持续监测。