20132024年上海市金山区某三级医院呼吸道感染儿童的化脓链球菌基因组特征

Genomic characteristics of Streptococcus pyogenes isolated from children with respiratory tract infections in a tertiary hospital in Jinshan District of Shanghai, 2013‒2024

  • 摘要:
    目的 分析2013—2024年上海市金山区某三级医院呼吸道感染儿童的化脓性链球菌(GAS)基因组特征,比较2020年前后的特征变化,为防控GAS感染提供科学数据。
    方法 收集2013—2024年该院分离得到自呼吸道感染儿童的GAS菌株,使用微量肉汤稀释法测定菌株对青霉素、头孢噻肟、头孢吡肟、利奈唑胺、万古霉素、美罗培南、氯霉素、氧氟沙星、左氧氟沙星、红霉素、克林霉素、四环素这12种抗菌药物的敏感性,基于全基因组测序分析多位点序列分型(MLST)、emm分型、超抗原基因携带情况、可移动遗传元件(MGE)、毒力基因携带情况和基因组的遗传进化树。
    结果 共收集和鉴定50株分离自4~14岁呼吸道感染儿童的GAS菌株,菌株对红霉素、克林霉素和四环素的耐药率分别为100.00%、100.00%和86.00%。GAS菌株存在2种emm型,emm12型占76.00%(38/50),对应ST36型;emm1型占24.00%(12/50),分别对应ST28、ST1274和new⁃1型。2020年前后的MLST型构成差异有统计学意义(P=0.015)。所有菌株均携带超抗原基因speCspeGssasmeZ。占优势的emm12型菌株主要属于CladeⅡ分支,有MGE ICE⁃emm12(携带红霉素耐药基因ermB和四环素类耐药基因tetM)和ΦHKU.vir(携带毒力基因speCssa)。emm1型菌株有MGE ICE⁃HKU488(携带红霉素耐药基因ermB和四环素类耐药基因tetM)和ΦHKU488.vir(携带毒力基因speCssa),与中国香港的菌株遗传关系密切。未发现M1UK克隆株。emm1型菌株中,ST1274型菌株新发现于2020—2024年,属于一个独立的进化分支。
    结论 上海市金山区某三级医院分离自呼吸道感染儿童的GAS菌株对红霉素、克林霉素和四环素具有较高的耐药性,建议临床治疗改用青霉素、三代头孢菌素类和氟喹诺酮类等其他抗菌药物。2020—2024年emm1型GAS菌株出现新克隆株ST1274型,未发现M1UK新克隆株。建议持续关注当地流行的GAS菌株,及早鉴定MLST分型,进而及早发现菌群内部变化和可能流行的新克隆株。

     

    Abstract:
    Objective To analyze the genomic characteristics of Streptococcus pyogenes (GAS) isolated from children with respiratory tract infections in a tertiary hospital in Jinshan District of Shanghai during 2013‒2024, to compare the changes in trend for genomic characteristics before and after 2000, and to provide scientific data for the prevention and control of GAS infections.
    Methods GAS strains isolated from children with respiratory tract infections in this hospital were collected from 2013 to 2024. Antimicrobial susceptibility of the isolated strains to 12 antibiotics, including penicillin, cefotaxime, cefepime, linezolid, vancomycin, meropenem, chloramphenicol, ofloxacin, levofloxacin, erythromycin, clindamycin, and tetracycline, was determined using broth microdilution plate method. Besides, whole genome sequencing (WGS) was used to analyze multilocus sequence type (MLST), emm typing, carriage of superantigen genes, mobile genetic element (MGE), carriage of virulence gene, and genomic phylogenetic tree of the isolated strains.
    Results A total of 50 GAS strains were collected and identified from children with respiratory tract infections aged 4‒14 years old, and the resistance rates of those isolates to erythromycin, clindamycin, and tetracycline were 100.00%, 100.00%, and 86.00%, respectively. There were two emm types in the GAS isolates; the emm12 type accounted for 76.00% (38/50), corresponding to ST36 type, and the emm1 type accounted for 24.00% (12/50), corresponding to ST28, ST1274, and new-1 types. There was a statistically significant difference in the constitution of the MLST before and after 2020 (P=0.015). All the isolates carried the superantigen genes speC, speG, ssa, and smeZ. The predominant emm12 isolates belonged to the Clade Ⅱ, carrying the mobile elements ICE-emm12 (harboring erythromycin-resistance gene ermB and tetracycline-resistance gene tetM) and ΦHKU.vir (carrying virulence genes speC and ssa). The emm1 isolates carried the mobile elements ICE-HKU488 (harboring erythromycin-resistance gene ermB and tetracycline-resistance gene tetM) and ΦHKU488.vir (carrying virulence genes speC and ssa), and had close phylogenetical relationships with isolates from Hong Kong, China. No M1UK new clone strains were found. The ST1274 isolates of emm1 were newly discovered in 2020‒2024, and belonged to a separate phylogenetic clade.
    Conclusion GAS strains isolated from children with respiratory tract infections in a tertiary hospital in Jinshan District of Shanghai exhibit a high resistance to erythromycin, clindamycin, and tetracycline. It is recommended that the clinical treatments change to use other antimicrobial drugs, such as penicillin, third-generation cephalosporins, and fluoroquinolones. During 2020‒2024, a new ST1274 clone strain is discovered in emm1 GAS isolates, without M1UK new clone strains being found. It is essential to continuously concern locally prevalent GAS strains and perform early identification of MLST types to promptly monitor the internal changes of the bacterial population and potential prevalence of new clones.

     

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