Demczuk Walter, Martin Irene, Peterson Shelley, Bharat Amrita, Van Domselaar Gary, Graham Morag, Lefebvre Brigitte, Allen Vanessa, Hoang Linda, Tyrrell Greg, Horsman Greg, Wylie John, Haldane David, Archibald Chris, Wong Tom, Unemo Magnus, Mulvey Michael R
Bacteriology and Enteric Diseases Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
Science Technology Cores and Services Division, National Microbiology Laboratory, Public Health Agency of Canada, and Department of Medical Microbiology, University of Manitoba, Winnipeg, Manitoba, Canada.
J Clin Microbiol. 2016 May;54(5):1304-13. doi: 10.1128/JCM.03195-15. Epub 2016 Mar 2.
The emergence of Neisseria gonorrhoeae strains with decreased susceptibility to cephalosporins and azithromycin (AZM) resistance (AZM(r)) represents a public health threat of untreatable gonorrhea infections. Genomic epidemiology through whole-genome sequencing was used to describe the emergence, dissemination, and spread of AZM(r) strains. The genomes of 213 AZM(r) and 23 AZM-susceptible N. gonorrhoeae isolates collected in Canada from 1989 to 2014 were sequenced. Core single nucleotide polymorphism (SNP) phylogenomic analysis resolved 246 isolates into 13 lineages. High-level AZM(r) (MICs ≥ 256 μg/ml) was found in 5 phylogenetically diverse isolates, all of which possessed the A2059G mutation (Escherichia coli numbering) in all four 23S rRNA alleles. One isolate with high-level AZM(r) collected in 2009 concurrently had decreased susceptibility to ceftriaxone (MIC = 0.125 μg/ml). An increase in the number of 23S rRNA alleles with the C2611T mutations (E. coli numbering) conferred low to moderate levels of AZM(r) (MICs = 2 to 4 and 8 to 32 μg/ml, respectively). Low-level AZM(r) was also associated with mtrR promoter mutations, including the -35A deletion and the presence of Neisseria meningitidis-like sequences. Geographic and temporal phylogenetic clustering indicates that emergent AZM(r) strains arise independently and can then rapidly expand clonally in a region through local sexual networks.
对头孢菌素敏感性降低且具有阿奇霉素耐药性(AZM(r))的淋病奈瑟菌菌株的出现,代表了无法治疗的淋病感染对公共卫生的威胁。通过全基因组测序的基因组流行病学方法被用于描述AZM(r)菌株的出现、传播和扩散情况。对1989年至2014年在加拿大收集的213株AZM(r)淋病奈瑟菌分离株和23株对AZM敏感的分离株进行了基因组测序。核心单核苷酸多态性(SNP)系统发育基因组分析将246株分离株分为13个谱系。在5株系统发育不同的分离株中发现了高水平的AZM(r)(最低抑菌浓度≥256μg/ml),所有这些分离株的4个23S rRNA等位基因均具有A2059G突变(大肠杆菌编号)。2009年收集的1株高水平AZM(r)分离株同时对头孢曲松的敏感性降低(最低抑菌浓度=0.125μg/ml)。具有C2611T突变(大肠杆菌编号)的23S rRNA等位基因数量增加,导致低至中等水平的AZM(r)(最低抑菌浓度分别为2至4μg/ml和8至32μg/ml)。低水平的AZM(r)也与mtrR启动子突变有关,包括-35A缺失和脑膜炎奈瑟菌样序列的存在。地理和时间系统发育聚类表明,新出现的AZM(r)菌株是独立出现的,然后可以通过当地的性网络在一个地区迅速进行克隆性扩张。