Eichenberger Emily M, Thaden Joshua T
Department of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, NC 27710, USA.
Antibiotics (Basel). 2019 Apr 6;8(2):37. doi: 10.3390/antibiotics8020037.
Antibiotic resistance has increased markedly in gram-negative bacteria over the last two decades, and in many cases has been associated with increased mortality and healthcare costs. The adoption of genotyping and next generation whole genome sequencing of large sets of clinical bacterial isolates has greatly expanded our understanding of how antibiotic resistance develops and transmits among bacteria and between patients. Diverse mechanisms of resistance, including antibiotic degradation, antibiotic target modification, and modulation of permeability through the bacterial membrane have been demonstrated. These fundamental insights into the mechanisms of gram-negative antibiotic resistance have influenced the development of novel antibiotics and treatment practices in highly resistant infections. Here, we review the mechanisms and global epidemiology of antibiotic resistance in some of the most clinically important resistance phenotypes, including carbapenem resistant , extensively drug resistant (XDR) , and XDR . Understanding the resistance mechanisms and epidemiology of these pathogens is critical for the development of novel antibacterials and for individual treatment decisions, which often involve alternatives to β-lactam antibiotics.
在过去二十年中,革兰氏阴性菌的抗生素耐药性显著增加,在许多情况下,这与死亡率上升和医疗成本增加有关。对大量临床细菌分离株采用基因分型和新一代全基因组测序,极大地扩展了我们对抗生素耐药性在细菌之间以及患者之间如何产生和传播的理解。已经证实了多种耐药机制,包括抗生素降解、抗生素靶点修饰以及通过细菌膜调节通透性。这些对革兰氏阴性菌抗生素耐药机制的基本认识影响了新型抗生素的开发以及高度耐药感染的治疗实践。在这里,我们回顾了一些临床上最重要的耐药表型中抗生素耐药性的机制和全球流行病学,包括耐碳青霉烯类、广泛耐药(XDR)和XDR。了解这些病原体的耐药机制和流行病学对于新型抗菌药物的开发以及个体治疗决策至关重要,这些决策通常涉及β-内酰胺类抗生素的替代药物。