Boyanova Lyudmila, Markovska Rumyana, Mitov Ivan
Department of Medical Microbiology, Medical University of Sofia, Zdrave Street 2, 1431 Sofia, Bulgaria.
Department of Medical Microbiology, Medical University of Sofia, Zdrave Street 2, 1431 Sofia, Bulgaria.
Anaerobe. 2016 Dec;42:145-151. doi: 10.1016/j.anaerobe.2016.10.007. Epub 2016 Oct 15.
This review focuses on the virulence arsenal of the most pathogenic species among Gram positive anaerobic cocci, Finegoldia magna according to recently published data from 2012 to 2016. Virulence factors like sortase dependent pili and F. magna adhesion factor (FAF) facilitate the start of the infection. Albumin binding protein (PAB) enhances F. magna survival. FAF, subtilisin-like extracellular serine protease (SufA) and superantigen protein L protect the bacteria from factors of innate defense system. SufA, capsule and tissue-destroying enzymes provide a deep penetration or spread of the infections and the protein L is associated with infection severity. Biofilm production results in infection chronification and complicated treatment as well as to persistence of multi-species biofilms. Resistance rates to quinolones (13.0->70%) and clindamycin (0-40.0%) are important, and resistance to penicillins (<4%), chloramphenicol (7.0%) and metronidazole (<7%) has been reported. F. magna should not be overlooked when present in monoinfections or mixed infections in humans.
根据2012年至2016年最近发表的数据,本综述聚焦于革兰氏阳性厌氧球菌中致病性最强的物种——巨大芬戈尔德菌的毒力武器库。诸如分选酶依赖性菌毛和巨大芬戈尔德菌黏附因子(FAF)等毒力因子促进感染的起始。白蛋白结合蛋白(PAB)提高巨大芬戈尔德菌的存活率。FAF、枯草杆菌蛋白酶样细胞外丝氨酸蛋白酶(SufA)和超抗原蛋白L保护细菌免受先天性防御系统因子的影响。SufA、荚膜和组织破坏酶可使感染深入渗透或扩散,而蛋白L与感染严重程度相关。生物膜的产生导致感染慢性化和治疗复杂化,以及多物种生物膜的持续存在。对喹诺酮类药物(13.0%->70%)和克林霉素(0-40.0%)的耐药率很重要,并且已报道对青霉素(<4%)、氯霉素(7.0%)和甲硝唑(<7%)的耐药情况。当巨大芬戈尔德菌存在于人类的单一感染或混合感染中时,不应被忽视。