Upcoming Multi-drug-Resistant and Extensively Drug-Resistant Bacteria

C. Ghazaei
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引用次数: 0

Abstract

Multi-drug-resistant (MDR) and extensively drug-resistant (XDR) bacteria are becoming a serious global health issue, which may soon become untreatable by clinicians. Since the invention of antibiotics, inappropriate consumption, non-prescribed drugs, overuse, and hoarding have caused the rapid emergence of MDR and XDR bacteria. The ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Enterobacter spp.) cause many nosocomial infections and thus escape the biocidal action of the antibiotic. Gram-positive and Gram-negative bacteria have acquired self-defense tools like ESBL (extended spectrum beta-lactamase), a mutation in porin genes, biofilm production, and many more to develop multi-drug resistance. Antimicrobial resistance (AMR) endangers patients' treatment as it causes high mortality and morbidity rates, economic loss of both patient and country, and prolonged hospital stay. To combat upcoming MDR and XDR bacteria, it is essential to design novel therapeutic techniques to eradicate such resistant bacteria via burgeoning technologies like nanoparticles, CRISPER-Cas9, genetic engineering, and synthetic biology.
即将到来的多重耐药和广泛耐药细菌
多药耐药(MDR)和广泛耐药(XDR)细菌正在成为一个严重的全球健康问题,临床医生可能很快无法治疗。自从抗生素发明以来,不适当的消费、非处方药、过度使用和囤积导致了耐多药和广泛耐药细菌的迅速出现。ESKAPE病原体(粪肠球菌、金黄色葡萄球菌、肺炎克雷伯菌、铜绿假单胞菌、鲍曼不动杆菌和肠杆菌属)会引起许多医院感染,从而逃脱抗生素的杀菌作用。革兰氏阳性菌和革兰氏阴性菌已经获得了自卫工具,如ESBL(超广谱β-内酰胺酶)、孔蛋白基因突变、生物膜产生等,从而产生多种耐药性。抗微生物耐药性(AMR)危及患者的治疗,因为它会导致高死亡率和发病率、患者和国家的经济损失以及住院时间延长。为了对抗即将出现的MDR和XDR细菌,必须设计新的治疗技术,通过纳米颗粒、CRISPER-Cas9、基因工程和合成生物学等新兴技术根除这种耐药细菌。
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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