将细菌外排泵 OMPs 作为针对耐多药革兰氏阴性菌的候选疫苗。

IF 3.6 3区 医学 Q3 CELL BIOLOGY
Thaynara O Silva, Ana Carolina S Bulla, Bárbara A Teixeira, Vinnicius Machado Schelk Gomes, Thiago Raposo, Luiza S Barbosa, Manuela Leal da Silva, Lilian O Moreira, Priscilla C Olsen
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引用次数: 0

摘要

对抗菌药物产生抗药性的细菌的出现和繁殖是对全球公共卫生的严重威胁。目前的抗菌药物库正在变得过时,药物开发的速度也在下降,这凸显了投资替代方法以治疗或预防抗菌细菌引起的感染的重要性。革兰氏阴性细菌产生抗菌药耐药性的一个重要机制是外排泵的过度表达,外排泵可以从细菌中挤出多种化合物,包括抗菌药。在几种具有多重耐药性(MDR)的革兰氏阴性细菌中检测到了外排泵蛋白的过度表达,这引起了人们对这些蛋白作为抗击这些病原体潜在靶点的关注。本综述将重点讨论外排泵的外膜蛋白(OMPs)作为抗临床相关 MDR 革兰氏阴性菌潜在候选疫苗的作用,并讨论其优势和缺陷。此外,我们还将探讨外排泵 OMP 多样性的相关性以及疫苗接种对微生物群可能产生的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bacterial efflux pump OMPs as vaccine candidates against multidrug-resistant Gram-negative bacteria.

The emergence and propagation of bacteria resistant to antimicrobial drugs is a serious public health threat worldwide. The current antibacterial arsenal is becoming obsolete, and the pace of drug development is decreasing, highlighting the importance of investment in alternative approaches to treat or prevent infections caused by antimicrobial-resistant bacteria. A significant mechanism of antimicrobial resistance employed by Gram-negative bacteria is the overexpression of efflux pumps that can extrude several compounds from the bacteria, including antimicrobials. The overexpression of efflux pump proteins has been detected in several multidrug-resistant Gram-negative bacteria, drawing attention to these proteins as potential targets against these pathogens. This review will focus on the role of outer membrane proteins from efflux pumps as potential vaccine candidates against clinically relevant multidrug-resistant Gram-negative bacteria, discussing advantages and pitfalls. Additionally, we will explore the relevance of efflux pump outer membrane protein diversity and the possible impact of vaccination on microbiota.

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来源期刊
Journal of Leukocyte Biology
Journal of Leukocyte Biology 医学-免疫学
CiteScore
11.50
自引率
0.00%
发文量
358
审稿时长
2 months
期刊介绍: JLB is a peer-reviewed, academic journal published by the Society for Leukocyte Biology for its members and the community of immunobiologists. The journal publishes papers devoted to the exploration of the cellular and molecular biology of granulocytes, mononuclear phagocytes, lymphocytes, NK cells, and other cells involved in host physiology and defense/resistance against disease. Since all cells in the body can directly or indirectly contribute to the maintenance of the integrity of the organism and restoration of homeostasis through repair, JLB also considers articles involving epithelial, endothelial, fibroblastic, neural, and other somatic cell types participating in host defense. Studies covering pathophysiology, cell development, differentiation and trafficking; fundamental, translational and clinical immunology, inflammation, extracellular mediators and effector molecules; receptors, signal transduction and genes are considered relevant. Research articles and reviews that provide a novel understanding in any of these fields are given priority as well as technical advances related to leukocyte research methods.
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