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Antimicrobial activity and mode of action of terpene linalyl anthranilate against carbapenemase-producing Klebsiella pneumoniae 被引量:2
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作者 Shun-Kai Yang Khatijah Yusoff +3 位作者 Mokrish Ajat Wai-Sum Yap Swee-Hua Erin Lim Kok-Song Lai 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2021年第2期210-219,共10页
Mining of plant-derived antimicrobials is the major focus at current to counter antibiotic resistance. This study was conducted to characterize the antimicrobial activity and mode of action of linalyl anthranilate(LNA... Mining of plant-derived antimicrobials is the major focus at current to counter antibiotic resistance. This study was conducted to characterize the antimicrobial activity and mode of action of linalyl anthranilate(LNA) against carbapenemase-producing Klebsiella pneumoniae(KPC-KP). LNA alone exhibited bactericidal activity at 2.5%(V/V), and in combination with meropenem(MPM) at 1.25%(V/V). Comparative proteomic analysis showed a significant reduction in the number of cytoplasmic and membrane proteins,indicating membrane damage in LNA-treated KPC-KP cells. Up-regulation of oxidative stress regulator proteins and down-regulation of oxidative stress-sensitive proteins indicated oxidative stress. Zeta potential measurement and outer membrane permeability assay revealed that LNA increases both bacterial surface charge and membrane permeability. Ethidium bromide influx/efflux assay showed increased uptake of ethidium bromide in LNA-treated cells, inferring membrane damage. Furthermore, intracellular leakage of nucleic acid and proteins was detected upon LNA treatment. Scanning and transmission electron microscopies again revealed the breakage of bacterial membrane and loss of intracellular materials. LNA was found to induce oxidative stress by generating reactive oxygen species(ROS) that initiate lipid peroxidation and damage the bacterial membrane. In conclusion, LNA generates ROS, initiates lipid peroxidation, and damages the bacterial membrane, resulting in intracellular leakage and eventually killing the KPC-KP cells. 展开更多
关键词 Comparative proteomic kpc-kp Linalyl anthranilate Membrane damage ROS
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产KPC-2型碳青霉烯酶肺炎克雷伯菌耐药致泌尿系感染机制分析 被引量:1
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作者 刘拥荣 余亚敏 +3 位作者 李丽君 卢胜男 罗文婷 贺立飞 《晓庄学院学报(医学版)》 2020年第5期51-54,共4页
目的:研究宁乡市人民医院产KPC-2型碳青霉烯酶肺炎克雷伯菌致泌尿系感染的潜在机制。方法:对产KPC-2型碳青霉烯酶的病例进行筛选入组,分离菌株后,利用聚合酶链反应(PCR)对其进行荚膜血清型基因及毒力基因的检测,采用体外验证的方式确定... 目的:研究宁乡市人民医院产KPC-2型碳青霉烯酶肺炎克雷伯菌致泌尿系感染的潜在机制。方法:对产KPC-2型碳青霉烯酶的病例进行筛选入组,分离菌株后,利用聚合酶链反应(PCR)对其进行荚膜血清型基因及毒力基因的检测,采用体外验证的方式确定菌株在小鼠体内的高毒力性。结果:收集2018年4月~2019年4月宁乡市人民医院CRKP致泌尿系感染的病例35名,其中12株产KPC-2酶,毒力荚膜血清型检出3例,分别为K2型2例,K1型1例,K1携带2种毒力基因:rmpA、magA(K1),K2携带3种毒力基因:magA(K1)、rmpA、mrkD。据产KPC-2酶肺炎克雷伯菌感染的小鼠死亡率结果,与未检出毒力基因的CRKP对比,注入K1及K2型菌株的小鼠死亡率于第7天死亡率更高,且K2型菌株较K1型菌株感染致小鼠死亡更快。结论:宁乡市人民医院产KPC-2碳青霉烯酶的CRKP可能在携带更多毒力基因从而造成更强毒力的高毒力荚膜血清型如K1、K2型中产生。 展开更多
关键词 KPC-2碳青霉烯酶 肺炎克雷伯菌 耐药机制
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