Department of Surgical Sciences and Integrated Diagnostics (DISC), University of Genoa.
Microbiology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Curr Opin Infect Dis. 2023 Dec 1;36(6):537-544. doi: 10.1097/QCO.0000000000000969. Epub 2023 Sep 21.
This review provides an overview of most recent evidence about pathogenesis traits and virulence factors contributing to successful colonization or infection by P. aeruginosa , A. baumannii , S. maltophilia and B. cepacia complex, among the most clinically relevant nonfermenting Gram-negative bacteria (NFGNB).
The growing clinical importance of NFGNB as important opportunistic pathogens causing difficult-to-treat infections in a fragile patients' population in stressed by numerous studies. Identification of novel virulence factors and deciphering of their mechanisms of action have greatly furthered our understanding of NFGNB pathogenesis, revealing that each pathogen-specific armamentarium of virulence factors (adhesins, motility, capsule, biofilm, lipopolysaccharide, exotoxins, exoenzymes, secretion systems, siderophores) can be likely responsible for the difference in the pathophysiology even in the context of a similar infection site. Emerging evidence of the immunomodulatory effect of some virulence factors is also acknowledged.
NFGNB continue to be a serious global problem as cause of life-threatening opportunistic infections, owing to a highly heterogeneous content of virulence factors and their extensive number of intrinsic resistance mechanisms. Further efforts in development of novel effective antimicrobials and of alternative strategies targeting key virulence factors are warranted.
本综述概述了最近关于铜绿假单胞菌、鲍曼不动杆菌、嗜麦芽窄食单胞菌和洋葱伯克霍尔德菌等最具临床相关性的非发酵革兰阴性菌(NFGNB)成功定植或感染的发病机制特征和毒力因子的证据。
越来越多的研究表明,NFGNB 作为重要的机会性病原体,在脆弱患者群体中引起难以治疗的感染,其临床重要性不断增加。新型毒力因子的鉴定和解密其作用机制极大地促进了我们对 NFGNB 发病机制的理解,表明每个病原体特异性的毒力因子(黏附素、运动性、荚膜、生物膜、脂多糖、外毒素、外酶、分泌系统、铁载体)军备可能导致即使在相似的感染部位,其病理生理学也存在差异。一些毒力因子的免疫调节作用的新证据也得到了承认。
由于 NFGNB 具有高度异质性的毒力因子内容和广泛的内在耐药机制,它们继续成为全球严重的威胁生命的机会性感染的原因。需要进一步努力开发新型有效的抗菌药物和针对关键毒力因子的替代策略。