2019 年耐碳青霉烯类大肠埃希菌和肺炎克雷伯菌的抗生素敏感性模式

Ibrahim Mohammed Hussaini , Ahmed Babagida Suleiman , Olayeni Stephen Olonitola , Rukayat Avosuahi Oyi
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摘要

全球范围内耐碳青霉烯类细菌感染率的上升使治疗院内感染成为一项挑战。这是因为除了碳青霉烯酶基因外,耐碳青霉烯类细菌还携带多种耐药基因。本研究旨在确定对碳青霉烯类耐药的大肠埃希菌和肺炎克雷伯菌分离株的耐药模式。通过柯比鲍尔(Kirby Bauer)技术筛选了之前分离到的对碳青霉烯类耐药的大肠埃希菌和肺炎克雷伯菌,以确定它们对头孢曲松、三甲氧苄青霉素-磺胺甲恶唑、强力霉素、阿米卡星、庆大霉素、萘啶酸、氯霉素、可乐定、替加环素和磷霉素的敏感性。采用 EUCAST 和 CLSI 断点来解释抑菌区。分离菌株对头孢曲松(100.00%)、三甲双氨苄-磺胺甲噁唑(100.00%)和强力霉素(83.33%)的耐药性较高。据观察,三分之二的分离物(66.67%)对阿米卡星敏感,33.33%的分离物对庆大霉素和萘啶酸敏感。16.67% 的分离菌株对氯霉素和可乐定敏感,而所有筛选出的分离菌株(100.0%)都对磷霉素和替加环素敏感。在携带碳青霉烯酶基因(blaNDM、blaOXA 或两者)的分离物中,观察到较高的抗生素耐药率。耐碳青霉烯酶分离物的 MAR 指数介于 0.46 和 0.82 之间。因此,筛选出的所有分离菌株都对多种抗生素具有耐药性,即 MDR 分离菌株。总之,耐碳青霉烯类抗生素的分离物对多种抗生素具有耐药性,但对替加环素、磷霉素和阿米卡星敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibiotic susceptibility pattern of carbapenem resistant Escherichia coli and Klebsiella pneumoniae, 2019
The rise in the prevalence of carbapenem resistant bacteria worldwide has made the treatment of nosocomial infections challenging. This is because carbapenem resistant bacteria harbor multiple resistance genes aside the carbapenemase genes. This study was conducted to determine the susceptibility pattern of carbapenem resistant isolates of Escherichia coli and Klebsiella pneumoniae. Previously isolated and characterized carbapenem resistant E. coli and K. pneumoniae were screened for their susceptibility to ceftriaxone, trimethoprim-sulphamethoxazole, doxycycline, amikacin, gentamicin, nalidixic acid, chloramphenicol, colistin, tigecycline and fosfomycin by the Kirby Bauer technique. EUCAST and CLSI breakpoints were used to interpret the zones of inhibition. High level of resistance was observed among the isolates to ceftriaxone (100.00 %), trimethoprim-sulphamethoxazole (100.00 %) and doxycycline (83.33 %). Two-third of the isolates (66.67 %) were observed to be susceptible to amikacin, while 33.33 % of the isolates were gentamicin and nalidixic acid susceptible. Susceptibility to chloramphenicol and colistin was recorded in 16.67 % of the isolates while all the screened isolates (100.0 %) were susceptible to fosfomycin and tigecycline. A higher antibiotic resistance rate was observed among isolates habouring carbapenemase genes (blaNDM, blaOXA or both). The MAR indices of the carbapenem resistant isolates ranged between 0.46 and 0.82. So also, all the isolates screened were observed to be resistant to multiple antibiotics, hence MDR isolates. In conclusion, the carbapenem resistant isolates were resistant to multiple antibiotics but were however susceptible to tigecycline, fosfomycin and amikacin.
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