Microbiology, Department of Laboratory Medicine and Genetics, Trillium Health Partners, Mississauga, Ontario, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Microbiol Spectr. 2024 May 2;12(5):e0322323. doi: 10.1128/spectrum.03223-23. Epub 2024 Mar 25.
Gram-negative metallo-β-lactamase-producing bacteria can be extremely problematic, especially when found to be extensively drug-resistant (XDR). Cefiderocol is a novel antimicrobial that has been shown to overcome most carbapenemases, with very rare resistance reported to date. Within our institution, two multidrug-resistant and one XDR strains were isolated from a patient who recently emigrated from India. Each isolate underwent whole-genome sequencing to resolve plasmids and determine phylogenetics, strain typing, and mechanisms of resistance. The XDR was ST167, harbored NDM-5, and PBP3 mutations, consistent with cefiderocol resistance. Our study suggests that the NDM region is required in conjunction with and PBP3 mutations. It is not clear why; however, our study did determine a potential novel iron-transport region unique to the cefiderocol-resistant isolate. This is the first characterized cefiderocol-resistant reported from Canada. Health centers should be on alert for this clone.IMPORTANCEThe development of cefiderocol, a novel siderophore cephalosporin, has provided additional options to the treatment of extensively drug-resistant (XDR) Gram-negative bacteria. Resistance to cefiderocol is poorly understood and only recently described. Here, we describe a case of a patient with recent travel to India harboring three isolates, one resistant and two susceptible to cefiderocol. Two isolates are highly similar genetically, allowing the mechanism of resistance to be described more closely. The importance of this manuscript contributes both globally to the understanding of cefiderocol resistance in as well as nationally as this is the first resistant case reported in Canada. This is especially concerning as cefiderocol is not currently approved in Canada. The implications of reporting emerging resistance to new antimicrobials for XDR Gram negatives are impactful to infectious disease specialists, clinical microbiologists, physicians, and public health.
产金属β-内酰胺酶的革兰氏阴性菌可能会造成严重问题,尤其是当它们被发现具有广泛耐药性(XDR)时。头孢他啶-阿维巴坦是一种新型抗菌药物,已被证明可克服大多数碳青霉烯酶,迄今为止报道的耐药性极为罕见。在我们的机构中,从最近从印度移民来的一名患者身上分离出了两株多药耐药株和一株 XDR 株。每个分离株都进行了全基因组测序,以确定质粒并确定系统发育、菌株分型和耐药机制。XDR 菌株为 ST167,携带 NDM-5 和 PBP3 突变,与头孢他啶-阿维巴坦耐药一致。我们的研究表明,NDM 区与 PBP3 突变一起是必需的。目前尚不清楚原因;然而,我们的研究确实确定了一个潜在的新型头孢他啶耐药分离株特有的铁转运区。这是加拿大首次报道的头孢他啶耐药 。卫生中心应警惕这种克隆。
重要性:头孢他啶-阿维巴坦的开发为治疗广泛耐药(XDR)革兰氏阴性菌提供了更多选择。对头孢他啶-阿维巴坦的耐药性了解甚少,最近才有所描述。在这里,我们描述了一名最近前往印度旅行的患者携带三株 分离株的情况,其中一株对头孢他啶-阿维巴坦耐药,两株敏感。两个分离株在遗传上高度相似,因此可以更详细地描述耐药机制。本研究的重要性不仅在全球范围内对 头孢他啶-阿维巴坦耐药性有了更深入的了解,而且在加拿大也具有重要意义,因为这是加拿大首例耐药病例报告。这尤其令人担忧,因为头孢他啶-阿维巴坦目前尚未在加拿大获得批准。报告新的抗微生物药物对 XDR 革兰氏阴性菌的耐药性对传染病专家、临床微生物学家、医生和公共卫生都有影响。