Department of Microbiology, Immunology, and Infectious Diseases, College of Medicine & Medical Sciences, Arabian Gulf University, Manama, Bahrain.
Department of Pathology, Microbiology Section, Salmaniya Medical Complex, Manama, Bahrain.
Front Cell Infect Microbiol. 2022 Oct 11;12:1033305. doi: 10.3389/fcimb.2022.1033305. eCollection 2022.
The prevalence of Carbapenem-resistant (CRKP) is currently increasing worldwide, prompting WHO to classify it as an urgent public health threat. CRKP is considered a difficult to treat organism owing to limited therapeutic options. In this study, a total of 24 CRKP clinical isolates were randomly collected from Salmaniya Medical Complex, Bahrain. Bacterial identification and antibiotic susceptibility testing were performed, on MALDI-TOF and VITEK-2 compact, respectively. The isolates were screened for carbapenem resistance markers ( and ) and plasmid-mediated quinolone resistance genes (, and ) by monoplex PCR. On the other hand, only colistin-resistant isolates (n=12) were screened for MCR-1, MCR-2 and MCR-3 genes by monoplex PCR. Moreover, the Genetic environment of , integrons analysis, and molecular characterization of plasmids was also performed. Antibiotic susceptibility revealed that all the isolates (100%) were resistant to ceftolozane/tazobactam, piperacillin/tazobactam, 96% resistant to ceftazidime, trimethoprim/sulfamethoxazole, 92% resistant to meropenem, gentamicin and cefepime, 88% resistant to ciprofloxacin, imipenem, and 37% resistant to amikacin. Ceftazidime/avibactam showed the least resistance (12%). 75% (n=12/16) were resistant to colistin and 44% (n=7/16) showed intermediate susceptibility to tigecycline. The detection of resistant determinants showed that the majority (95.8%) of CRKP harbored , followed by (91.6%) (45.8%), and (41.6%). Sequencing of the amplicons revealed the presence of . Alarmingly, 100% of isolates showed the presence of . These predominant genes were distributed in various combinations wherein the majority were + + + (n =10, 41.7%), + + + (n=8, 33.3%), among others. In conclusion, the resistance rate to most antibiotics is very high in our region, including colistin and tigecycline, and the genetic environment of CRKP is complex with the carriage of multiple resistance markers. Resistance to ceftazidime/avibactam is uncommon and hence can be used as a valuable option for empirical therapy. Molecular data on resistance markers and the genetic environment of CRKP is lacking from this geographical region; this would be the first report addressing the subject matter. Surveillance and strict infection control strategies should be reinforced in clinical settings to curb the emergence and spread of such isolates.
碳青霉烯类耐药(CRKP)的流行率目前在全球范围内呈上升趋势,促使世界卫生组织将其列为紧急公共卫生威胁。由于治疗选择有限,CRKP 被认为是一种难以治疗的病原体。在这项研究中,从巴林萨利曼尼亚医疗综合体随机收集了总共 24 株 CRKP 临床分离株。分别使用 MALDI-TOF 和 VITEK-2 compact 进行细菌鉴定和抗生素敏感性测试。通过单plex PCR 筛选碳青霉烯类耐药标志物(和)和质粒介导的喹诺酮类耐药基因(、和)。另一方面,仅对 12 株耐粘菌素的分离株(n=12)进行单plex PCR 筛选 MCR-1、MCR-2 和 MCR-3 基因。此外,还进行了 基因的遗传环境、整合子分析和质粒的分子特征分析。抗生素敏感性试验表明,所有分离株(100%)均对头孢洛扎/他唑巴坦、哌拉西林/他唑巴坦、头孢他啶、复方磺胺甲噁唑、美罗培南、庆大霉素和头孢吡肟具有耐药性,96%对头孢唑肟耐药,92%对环丙沙星、亚胺培南耐药,37%对阿米卡星耐药。头孢他啶/阿维巴坦的耐药性最低(12%)。75%(n=12/16)对粘菌素耐药,44%(n=7/16)对替加环素中介敏感。耐药决定因素的检测表明,大多数 CRKP(95.8%)携带 ,其次是 (91.6%) (45.8%)和 (41.6%)。 扩增子的测序显示存在 。令人震惊的是,100%的分离株均存在 。这些主要基因分布在各种组合中,其中大多数为 + + + (n=10,41.7%), + + + (n=8,33.3%)等。总之,我们地区对大多数抗生素(包括粘菌素和替加环素)的耐药率非常高,CRKP 的遗传环境复杂,携带多种耐药标志物。头孢他啶/阿维巴坦的耐药性不常见,因此可作为经验性治疗的有价值选择。该地理区域缺乏关于耐药标志物和 CRKP 遗传环境的分子数据;这将是首次对此主题进行的报告。应在临床环境中加强对耐药标志物和 CRKP 遗传环境的监测和严格的感染控制策略,以遏制此类分离株的出现和传播。