Soliman Ahmed M, Ramadan Hazem, Shimamoto Toshi, Komatsu Tetsuya, Maruyama Fumito, Shimamoto Tadashi
Department of Microbiology and Immunology, Faculty of Pharmacy, Kafrelsheikh University, Kafr El-Sheikh 33516, Egypt.
Hygiene and Zoonoses Department, Faculty of Veterinary Medicine, Mansoura University, Mansoura 35516, Egypt.
Microorganisms. 2025 Jul 29;13(8):1769. doi: 10.3390/microorganisms13081769.
This study describes the first complete genomic sequence of an NDM-19 and QnrS11-producing multidrug-resistant (MDR) isolate collected from a fecal swab from a poultry farm in 2019 in Egypt. The was identified by PCR screening and DNA sequencing. The isolate was then subjected to antimicrobial susceptibility testing, conjugation and transformation experiments, and complete genome sequencing. The chromosome of strain M2-13-1 measures 4,738,278 bp and encodes 4557 predicted genes, with an average G + C content of 50.8%. M2-13-1 is classified under ST167, serotype O101:H5, phylogroup A, and shows an MDR phenotype, having minimum inhibitory concentrations (MICs) of 64 mg/L for both meropenem and doripenem. The genes and are present on 49,816 bp IncX3 and 113,285 bp IncFII: IncFIB plasmids, respectively. M2-13-1 harbors genes that impart resistance to sulfonamides (), trimethoprim (), β-lactams (), aminoglycosides (, , , , and ), tetracycline ((A)), and chloramphenicol (). It was susceptible to aztreonam, colistin, fosfomycin, and tigecycline. The genetic context surrounding includes IS-IS---F-1-2-IS. Hierarchical clustering of the core genome MLST (HierCC) indicated M2-13-1 clusters with global ST167 lineages, showing HC levels of 100 (HC100) core genome allelic differences. Plasmids of the IncX3 group and the insertion sequence (IS) are critical vehicles for the dissemination of and its related variants. To our knowledge, this is the first genomic report of a /IncX3-carrying isolate of animal origin globally.
本研究描述了2019年从埃及一家家禽养殖场的粪便拭子中分离出的一株产NDM-19和QnrS11的多重耐药(MDR)菌株的完整基因组序列。通过PCR筛选和DNA测序进行鉴定。然后对该分离株进行抗菌药敏试验、接合和转化实验以及全基因组测序。菌株M2-13-1的染色体长度为4,738,278 bp,编码4557个预测基因,平均G + C含量为50.8%。M2-13-1属于ST167,血清型为O101:H5,菌系为A,表现出MDR表型,美罗培南和多黏菌素B的最低抑菌浓度(MIC)均为64 mg/L。blaNDM-19和qnrS11基因分别存在于49,816 bp的IncX3质粒和113,285 bp的IncFII:IncFIB质粒上。M2-13-1含有赋予对磺胺类药物(sul1)、甲氧苄啶(dfrA12)、β-内酰胺类(blaTEM-1B、blaCTX-M-15、blaSHV-11、blaOXA-1、blaNDM-19)、氨基糖苷类(aadA2、aph(3")-Ib、aph(6)-Id、ant(3")-Ia、ant(2")-Ia)、四环素(tet(A))和氯霉素(catB3)耐药的基因。它对氨曲南、黏菌素、磷霉素和替加环素敏感。blaNDM-19周围的遗传环境包括IS26-ISCR1-blaNDM-19-F-1-2-IS26。核心基因组多位点序列分型(HierCC)的层次聚类表明M2-13-1与全球ST167谱系聚类,核心基因组等位基因差异的层次聚类(HC)水平为100(HC100)。IncX3组质粒和插入序列(IS)是blaNDM-19及其相关变体传播的关键载体。据我们所知,这是全球首例关于动物源携带blaNDM-19/IncX3分离株的基因组报告。