Institute of Biological Sciences, Faculty of Exact and Natural Sciences, Siedlce University of Natural Sciences and Humanities, 14 Bolesława Prusa Str., 08-110, Siedlce, Poland.
Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdańsk University of Technology, 11/12 G. Narutowicza Str., 80-233, Gdańsk, Poland.
Sci Rep. 2023 Mar 17;13(1):4448. doi: 10.1038/s41598-023-31086-w.
Klebsiella pneumoniae (KP) is a nosocomial pathogen causing difficult-to-treat infections. The presence of virulence genes and antibiotic resistance of 109 KP isolates from hospitalized patients were investigated. Among them, 68.8% were multi-drug resistant (MDR) and 59.6% produced extended-spectrum beta-lactamases (ESBLs). Metallo-β-lactamases (MBLs) were produced by 22% of isolates (mainly from anus), including 16.5% of isolates producing New Delhi metallo-β-lactamase (NDM-1). The genes encoding adhesins (fimH-91.7%, mrkD-96.3%), enterobactin (entB-100%) and yersiniabactin (irp-1-88%) were frequently identified. The genes encoding salmochelin (iroD-9.2%, iroN-7.3%) and colibactin (clbA, clbB-0.9%) were identified rarely. Iron acquisition system-related kfu gene and wcaG gene involved in capsule production were identified in 6.4% and 11% of isolates, respectively. The rmpA gene associated with hypermucoviscosity was present in 6.4% of isolates. In 19.2% of isolates magA gene was detected, specific for K1 capsule serotype, while 22.9% of isolates showed K2 capsule serotype. The rmpA, iroD or iroN genes being diagnostic biomarkers for hypervirulent KP (hvKP) were detected in 16.5% of isolates. We found that 55.5% of hvKP were MDR and produced ESBLs, thus hospital KP isolates pose a serious threat to the healthcare system.
肺炎克雷伯菌(KP)是一种医院获得性病原体,可引起难以治疗的感染。本研究调查了 109 株住院患者来源的 KP 分离株的毒力基因和抗生素耐药性。其中,68.8%为多药耐药(MDR),59.6%产生超广谱β-内酰胺酶(ESBLs)。22%的分离株产生金属β-内酰胺酶(MBLs)(主要来自肛门),包括 16.5%的产生新德里金属β-内酰胺酶(NDM-1)的分离株。黏附素(fimH-91.7%,mrkD-96.3%)、enterobactin(entB-100%)和yersiniabactin(irp-1-88%)编码基因频繁检出。salmochelin(iroD-9.2%,iroN-7.3%)和 colibactin(clbA、clbB-0.9%)编码基因很少检出。6.4%和 11%的分离株分别携带铁摄取系统相关的 kfu 基因和参与荚膜产生的 wcaG 基因。与高黏液性相关的 rmpA 基因存在于 6.4%的分离株中。19.2%的分离株检测到 magA 基因,该基因特异性针对 K1 荚膜血清型,而 22.9%的分离株显示 K2 荚膜血清型。rmpA、iroD 或 iroN 基因是高毒力 KP(hvKP)的诊断生物标志物,在 16.5%的分离株中检出。我们发现,55.5%的 hvKP 为 MDR 并产生 ESBLs,因此医院 KP 分离株对医疗系统构成严重威胁。