Rashid Fairuz Abdul, Suhaila Che Hussin Nurzam, Anuar Nurul Fathiyah Zaipul, Sahlan Noraziah, Palanisamy Navindra Kumari, Mohd Nor Fadzilah
Microbiology Unit, Department of Pathology, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia.
Department of Medical Microbiology & Parasitology, Faculty of Medicine, Universiti Teknologi MARA, Jalan Hospital, Selangor, Malaysia.
Microbiol Spectr. 2025 Sep 22:e0055325. doi: 10.1128/spectrum.00553-25.
Knowledge gap on the susceptibility of novel β-lactam agents (cefiderocol, ceftazidime-avibactam, imipenem-cilastatin-relebectam, and aztreonam) against carbapenem-resistant Enterobacterales (CRE) has been recognized. This study aimed to genotypically characterize CRE isolates and investigate the novel β-lactam activity against CRE. CRE is defined as Enterobacterales that is phenotypically non-susceptible to any carbapenems, including imipenem, meropenem, and ertapenem. A total of 154 CRE isolates were collected from two tertiary centers in Malaysia from October 2023 to May 2024. Carbapenemase-producing genes (, , , , and ,) were detected using PCR. Susceptibility to β-lactams was determined using disc diffusion. Of 154 CRE isolates, 102 (66.2%) were carbapenemase-producing carbapenem-resistant Enterobacterales (CP-CRE). (76/102; 74.5%), (17/102; 16.7%), & (8/102; 7.8%), and & (1/102; 1.0%) were identified among the CP-CRE isolates. The proportion of CRE isolates that exhibited susceptibility towards cefiderocol, ceftazidime-avibactam, and imipenem-cilastatin-relebactam was 86.4% (133/154), 41.6% (64/154), and 26.0% (40/154), respectively. Among -harboring isolates, cefiderocol (57/76; 75.0%) demonstrated superior activity compared with ceftazidime-avibactam (3/76; 3.9%) and imipenem-cilastatin-relebectam (1/76; 1.3%). Among isolates harboring , cefiderocol, ceftazidime-avibactam, and imipenem-cilastatin-relebectam demonstrated 100% (17/17), 70.6% (12/17), and 17.6% (3/17) susceptibility, respectively. Nine isolates that harbored two genes (eight + , one + ) demonstrated 100% susceptibility to cefiderocol but 100% resistance to ceftazidime-avibactam and imipenem-cilastatin-relebectam. The ceftazidime-avibactam plus aztreonam combination achieved 100% susceptibility in isolates harboring metallo-β-lactamases-producing genes; (76/76; 100%), + (8/8; 100%), and + (1/1; 100%). was the most prevalent gene causing CRE. Cefiderocol has the greatest activity compared with other investigated β-lactams.IMPORTANCECarbapenem-resistant Enterobacterales (CRE) has been recognized as a priority and public health concern requiring urgent attention for the development of effective antimicrobial resistance (AMR) prevention and control strategies. Differentiating between carbapenemase-producing CRE (CP-CRE) and non-CP-CRE, along with identifying carbapenemase-producing genes, is essential for guiding targeted antibiotic therapy. Among novel β-lactam agents, cefiderocol and the combination of ceftazidime-avibactam and aztreonam have shown promising activity against -producing CRE, supporting precision medicine approaches. Nevertheless, our study observed the emergence of cefiderocol resistance in isolates without prior drug exposure, highlighting a potential challenge in combating AMR.
新型β-内酰胺类药物(头孢地尔、头孢他啶-阿维巴坦、亚胺培南-西司他丁-瑞来巴坦和氨曲南)对耐碳青霉烯类肠杆菌科细菌(CRE)的敏感性方面存在知识空白已得到认可。本研究旨在对CRE分离株进行基因分型,并研究新型β-内酰胺类药物对CRE的活性。CRE被定义为对任何碳青霉烯类药物(包括亚胺培南、美罗培南和厄他培南)表型不敏感的肠杆菌科细菌。2023年10月至2024年5月期间,从马来西亚的两个三级中心共收集了154株CRE分离株。使用聚合酶链反应(PCR)检测产碳青霉烯酶基因(blaKPC、blaNDM、blaVIM、blaIMP和blaOXA-48)。使用纸片扩散法测定对β-内酰胺类药物的敏感性。在154株CRE分离株中,102株(66.2%)是产碳青霉烯酶的耐碳青霉烯类肠杆菌科细菌(CP-CRE)。在CP-CRE分离株中鉴定出blaKPC(76/102;74.5%)、blaNDM(17/102;16.7%)、blaVIM&blaIMP(8/102;7.8%)和blaOXA-48&blaNDM(1/102;1.0%)。对头孢地尔、头孢他啶-阿维巴坦和亚胺培南-西司他丁-瑞来巴坦表现出敏感性的CRE分离株比例分别为86.4%(133/154)、41.6%(64/154)和26.0%(40/154)。在携带blaKPC的分离株中,头孢地尔(57/76;75.0%)相比头孢他啶-阿维巴坦(3/76;3.9%)和亚胺培南-西司他丁-瑞来巴坦(1/76;1.3%)表现出更好的活性。在携带blaNDM的分离株中,头孢地尔、头孢他啶-阿维巴坦和亚胺培南-西司他丁-瑞来巴坦的敏感性分别为100%(17/17)、70.6%(12/17)和17.6%(3/17)。9株携带两种基因(8株blaKPC+blaNDM,1株blaVIM+blaNDM)的分离株对头孢地尔表现出100%的敏感性,但对头孢他啶-阿维巴坦和亚胺培南-西司他丁-瑞来巴坦表现出100%的耐药性。头孢他啶-阿维巴坦联合氨曲南在携带产金属β-内酰胺酶基因的分离株中达到了100%的敏感性;blaNDM(76/76;100%)、blaVIM+blaNDM(8/8;100%)和blaIMP+blaNDM(1/1;100%)。blaKPC是导致CRE的最常见基因。与其他研究的β-内酰胺类药物相比,头孢地尔具有最大的活性。重要性耐碳青霉烯类肠杆菌科细菌(CRE)已被视为一个优先事项和公共卫生问题,需要紧急关注以制定有效的抗菌药物耐药性(AMR)预防和控制策略。区分产碳青霉烯酶的CRE(CP-CRE)和非CP-CRE,以及鉴定产碳青霉烯酶基因,对于指导有针对性的抗生素治疗至关重要。在新型β-内酰胺类药物中,头孢地尔以及头孢他啶-阿维巴坦与氨曲南的联合用药已显示出对产blaKPC的CRE有前景的活性,支持精准医学方法。然而,我们的研究观察到在未接触过药物的分离株中出现了头孢地尔耐药性,凸显了对抗AMR的一个潜在挑战。