Chowdhury Goutam, Ramamurthy Thandavarayan, Das Bhabatosh, Ghosh Debjani, Okamoto Keinosuke, Miyoshi Shin-Ichi, Dutta Shanta, Mukhopadhyay Asish K
Division of Bacteriology, ICMR-National Institute of Cholera and Enteric Diseases, Kolkata, India.
Collaborative Research Centre of Okayama University for Infectious Diseases, ICMR-National Institute of Cholera and Enteric Diseases, Kolkata, India.
Infect Drug Resist. 2022 Jul 8;15:3631-3642. doi: 10.2147/IDR.S364526. eCollection 2022.
The multidrug resistance Enterobacteriaceae cause many serious infections resulting in prolonged hospitalization, increased treatment charges and mortality rate. In this study, we characterized -positive multidrug resistance commensal (CE) isolated from diarrheal patients in Kolkata, India.
Three CE strains were isolated from diarrheal stools, which were negative for different pathogroups of diarrheagenic (DEC). The presence of carbapenemases encoding genes and other antimicrobial resistance genes (ARGs) was detected using PCR. The genetic arrangement adjoining was investigated by plasmid genome sequencing. The genetic relatedness of the strains was determined by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) methods.
In addition to colistin, the -positive CE strains showed resistance to most of the antibiotics. Higher MICs were detected for ciprofloxacin (>32 mg/L) and imipenem (8 mg/L). Molecular typing revealed that three CE strains belonged to two different STs (ST 101 and ST 648) but they were 95% similar in the PFGE analysis. Screening for ARGs revealed that CE strains harbored , , , , , , and . In conjugation experiment, transfer frequencies ranged from 2.5×10 to 8.4x10. The gene was located on a 94-kb pNDM-TC-CE-89 type plasmid, which is highly similar to the IncFII plasmid harboring an IS26-IS30- - --IS structure.
To the best of our knowledge, this is the first report on carbapenem resistance involving the gene in CE from diarrheal patients. The circulation of gene in CE is worrisome, since it has the potential to transfer gene to other enteric pathogens.
多重耐药肠杆菌科细菌可导致许多严重感染,从而导致住院时间延长、治疗费用增加和死亡率上升。在本研究中,我们对从印度加尔各答腹泻患者中分离出的产碳青霉烯酶多重耐药共生大肠杆菌(CE)进行了特征分析。
从腹泻粪便中分离出三株CE菌株,它们对不同致病组的致泻性大肠杆菌(DEC)呈阴性。使用聚合酶链反应(PCR)检测碳青霉烯酶编码基因和其他抗菌耐药基因(ARG)的存在。通过质粒基因组测序研究与blaNDM相邻的基因排列。通过脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)方法确定菌株的遗传相关性。
除黏菌素外,产blaNDM的CE菌株对大多数抗生素均表现出耐药性。检测到环丙沙星(>32 mg/L)和亚胺培南(8 mg/L)的最低抑菌浓度(MIC)较高。分子分型显示,三株CE菌株属于两个不同的序列型(ST 101和ST 648),但在PFGE分析中它们的相似度为95%。对ARG的筛选显示,CE菌株携带blaNDM、blaCTX-M、blaTEM、tet(A)、tet(B)、aac(6’)-Ib-cr、qnrS和mcr-1。在接合实验中,转移频率范围为2.5×10⁻⁶至8.4×10⁻⁵。blaNDM基因位于一个94 kb的pNDM-TC-CE-89型质粒上,该质粒与携带IS26-IS30-blaNDM-IS1结构的IncFII质粒高度相似。
据我们所知,这是关于腹泻患者CE中产碳青霉烯酶blaNDM基因的首次报道。CE中blaNDM基因的传播令人担忧,因为它有可能将blaNDM基因转移到其他肠道病原体。