Department of Laboratory Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.
Department of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo 315010, China.
Drug Resist Updat. 2024 Sep;76:101123. doi: 10.1016/j.drup.2024.101123. Epub 2024 Jul 29.
The global dissemination of carbapenemase genes, particularly bla, poses a significant threat to public health. While research has mainly focused on strains with phenotypic resistance, the impact of silent resistance genes has been largely overlooked. This study documents the first instance of silent bla in a cluster of clonally related carbapenem-susceptible K. pneumoniae strains from a single patient. Despite initial effectiveness of carbapenem therapy, the patient experienced four recurrent lung infections over five months, indicating persistent K. pneumoniae infection. Genomic sequencing revealed all strains harbored bla on the epidemic IncX3 plasmid. A deletion within the upstream promoter region (P) of bla hindered its expression, resulting in phenotypic susceptibility to carbapenems. However, in vitro bactericidal assays and a mouse infection model showed that K. pneumoniae strains with silent bla exhibited significant tolerance to carbapenem-mediated killing. These findings demonstrate that silent bla can mediate both phenotypic susceptibility and antibiotic tolerance. In silico analysis of 1986 bla sequences showed that 1956 (98.5%) retained the original promoter P. Given that previous genomic sequencing typically targets carbapenem-resistant strains, accurately assessing the prevalence of silent bla remains challenging. This study highlights the hidden threat of silent resistance genes to clinical antimicrobial therapy and calls for enhanced clinical awareness and laboratory detection.
碳青霉烯酶基因的全球传播,尤其是 bla,对公共卫生构成了重大威胁。虽然研究主要集中在表型耐药的菌株上,但沉默耐药基因的影响在很大程度上被忽视了。本研究记录了首例来自单一患者的克隆相关碳青霉烯敏感肺炎克雷伯菌菌株中沉默 bla 的情况。尽管最初的碳青霉烯治疗有效,但该患者在五个月内经历了四次复发性肺部感染,表明持续存在肺炎克雷伯菌感染。基因组测序显示所有菌株都在流行的 IncX3 质粒上携带 bla。bla 上游启动子区域 (P) 内的缺失阻碍了其表达,导致对碳青霉烯类药物的表型敏感性。然而,体外杀菌试验和小鼠感染模型表明,携带沉默 bla 的肺炎克雷伯菌菌株对碳青霉烯类介导的杀伤具有显著的耐受性。这些发现表明,沉默 bla 可以介导表型敏感性和抗生素耐受性。对 1986 个 bla 序列的计算机分析表明,1956 个(98.5%)保留了原始启动子 P。由于以前的基因组测序通常针对耐碳青霉烯的菌株,因此准确评估沉默 bla 的流行情况仍然具有挑战性。本研究强调了沉默耐药基因对临床抗菌治疗的潜在威胁,并呼吁提高临床认识和实验室检测。