Assessment of in vitro antimicrobial activities of ceftolozane/tazobactam and ceftazidime/avibactam against carbapenem-resistant Pseudomonas aeruginosa clinical isolates.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Dalia Salem, Ahmed El-Shenawy, Heba Dahroug, Manar Zaiton, Doaa Gamal, Manal Diab
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引用次数: 0

Abstract

Background: Carbapenem resistant Pseudomonas aeruginosa (P. aeruginosa) is a global health concern that poses a challenge to treat in health care facilities. Ceftazidim/avibactam and ceftolozane/tazobactam have a potential role in treatment of multi-drug resistant phenotypes including carbapenem resistant P. aeruginosa. Therefore, we aimed to assess the in vitro antimicrobial activity of ceftazidime/avibactam and ceftolozane/tazobactam against carbapenem-resistant P. aeruginosa (CRPA) strains with different β-lactamase/carbapenemase genes.

Methods: Sixty CRPA isolates identified from clinical samples were examined for antimicrobial susceptibility including ceftazidim/avibactam and ceftolozane/tazobactam by Vitek2 compact system, and carbapenemase production by modified carbapenem inactivation method (mCIM) test and carbapenemase producing genes by polymerase chain reaction (PCR).

Results: Isolates were resistant to imipenem in 96.7% and meropenem in 88.3%. of isolates. Carbapenemase production by mCIM test was 70% compared to 73.3% by (PCR). Carbapenemase encoding genes blaNDM, blaVIM and blaOXA-48 were detected in 60%, 41.7% and 25% respectively while blaIMP and blaKPC weren't identified in this study. Among CRPA, both ceftazidim/avibactam and ceftolozane/tazobactam; were sensitive in only 11.7% of the isolates. Resistance to ceftazidim/avibactam and ceftolozane/tazobactam in isolates owning blaNDM, blaVIM, blaOXA-48 and those having combined blaNDM, blaVIM and blaOXA-48 carbapenemase resistance genes were 97.2%, 92%, 100% and 100% respectively.

Conclusion: Modified carbapenem inactivation method test gave satisfactory results and could be used as an alternative to expensive genotypic methods. Ceftazidim/avibactam and ceftolozane/tazobactam were unsuccessful against carbapenem resistant P. aeruginosa isolates carrying carbapenemase genes especially metallo-β lactamase genes. Therefore, it is essential to detect susceptibility patterns to newly introduced β-Lactam/β-Lactamase inhibitor combinations due to the emerging resistance to these therapeutics.

头孢噻嗪/他唑巴坦和头孢噻啶/阿维巴坦对耐碳青霉烯铜绿假单胞菌临床分离株的体外抗菌活性评价。
背景:耐碳青霉烯类铜绿假单胞菌(P. aeruginosa)是一个全球性的健康问题,对卫生保健机构的治疗提出了挑战。头孢他啶/阿维巴坦和头孢甲苯/他唑巴坦在治疗多重耐药表型(包括耐碳青霉烯类P. aeruginosa)中具有潜在作用。因此,本研究旨在评价头孢他啶/阿维巴坦和头孢氯氮唑/他唑巴坦对不同β-内酰胺酶/碳青霉烯酶基因的耐碳青霉烯P. aeruginosa (CRPA)菌株的体外抑菌活性。方法:采用Vitek2紧凑系统对60株临床分离的CRPA菌株进行头孢他啶/阿维巴坦和头孢甲苯/他唑巴坦的药敏检测,采用改良碳青霉烯烯酶失活法(mCIM)检测碳青霉烯酶产酶,采用聚合酶链反应(PCR)检测碳青霉烯酶产酶基因。结果:亚胺培南耐药率为96.7%,美罗培南耐药率为88.3%。隔离。mCIM法产碳青霉烯酶率为70%,PCR法为73.3%。碳青霉烯酶编码基因blaNDM、blaVIM和blaOXA-48的检出率分别为60%、41.7%和25%,blaIMP和blaKPC在本研究中未检出。在CRPA中,头孢他啶/阿维巴坦和头孢甲苯/他唑巴坦均存在;仅对11.7%的分离株敏感。含有blaNDM、blaVIM、blaOXA-48和blaNDM、blaVIM、blaOXA-48碳青霉烯酶耐药基因的分离株对头孢他啶/阿维巴坦和头孢氯氮酮/他唑巴坦的耐药率分别为97.2%、92%、100%和100%。结论:改良碳青霉烯类灭活方法试验结果满意,可替代昂贵的基因分型方法。头孢他啶/阿维巴坦和头孢甲苯/他唑巴坦对携带碳青霉烯酶基因尤其是金属β内酰胺酶基因的耐碳青霉烯类铜绿假单胞菌均不成功。因此,检测对新引入的β-内酰胺/β-内酰胺酶抑制剂组合的敏感性模式是必要的,因为这些治疗方法正在出现耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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