Althaferi Rawan Saad, Alfouzan Wadha Ahmed, Mustafa Abu Salim
Department of Microbiology, Faculty of Medicine, Kuwait University, Kuwait City 13110, Kuwait.
Microbiology Unit, Department of Laboratory Medicine, Farwaniya Hospital, Ministry of Health, Farwaniya 80000, Kuwait.
Antibiotics (Basel). 2025 May 24;14(6):539. doi: 10.3390/antibiotics14060539.
The World Health Organization has recognized as a multidrug-resistant bacterium that presents public health concerns. This study aimed to evaluate the prevalence of MDR isolates along with their susceptibility profiles and determine the genetic basis of resistance. A total of 100 isolates were cultured on MacConkey agar with various specimens from patients admitted to ICUs and wards. Species identification was performed for each isolate using the VITEK 2 system. Each isolate was tested for susceptibility to specific antibiotics by the broth microdilution method. The resistance genes were detected by molecular methods, i.e., PCR and Sangar sequencing. Among the 100 isolates tested phenotypically, 33 MDR isolates were detected. The aminoglycoside group of antibiotics showed the least resistance against , with increasing resistance to carbapenems and ciprofloxacin. The most prevalent detected genes responsible for resistance were , , , and . DNA sequencing results for the MDR isolates showed that 14 isolates had Thr-83> Ile mutation in , and 12 isolates had Ser-87>Leu mutation in genes. We conclude that the low rates of resistance to certain antibiotics, such as amikacin and piperacillin-tazobactam, seem encouraging to be effective for the treatment of infections. Furthermore, the prominent mechanisms of resistance to fluoroquinolones in clinical strains of include mutations in and genes. These findings highlight the necessity of molecular diagnostics in guiding therapy and the potential need for broader surveillance.
世界卫生组织已将其认定为一种引起公共卫生关注的多重耐药细菌。本研究旨在评估多重耐药菌株的流行情况及其药敏谱,并确定耐药的遗传基础。从入住重症监护病房(ICU)和普通病房的患者的各种标本中,共培养出100株该细菌,并接种于麦康凯琼脂培养基上。使用VITEK 2系统对每株分离菌进行菌种鉴定。采用肉汤微量稀释法检测每株分离菌对特定抗生素的敏感性。通过分子方法(即聚合酶链反应(PCR)和桑格测序)检测耐药基因。在100株经表型检测的分离菌中,检测到33株多重耐药菌株。氨基糖苷类抗生素对该细菌的耐药性最低,对碳青霉烯类和环丙沙星的耐药性则有所增加。检测到的最常见的耐药基因是[具体基因1]、[具体基因2]、[具体基因3]和[具体基因4]。多重耐药菌株的DNA测序结果显示,14株在[基因名称1]中有Thr-83>Ile突变,12株在[基因名称2]中有Ser-87>Leu突变。我们得出结论,对某些抗生素(如阿米卡星和哌拉西林-他唑巴坦)的低耐药率似乎令人鼓舞,对治疗该细菌感染有效。此外,该细菌临床菌株对氟喹诺酮类药物的主要耐药机制包括[基因名称1]和[基因名称2]的突变。这些发现凸显了分子诊断在指导治疗中的必要性以及更广泛监测的潜在需求。