Ponnusamy Duraisamy, Kozlova Elena V, Sha Jian, Erova Tatiana E, Azar Sasha R, Fitts Eric C, Kirtley Michelle L, Tiner Bethany L, Andersson Jourdan A, Grim Christopher J, Isom Richard P, Hasan Nur A, Colwell Rita R, Chopra Ashok K
Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555;
Center for Food Safety and Applied Nutrition, Office of Applied Research and Safety Assessment, Food and Drug Administration, Laurel, MD 20708;
Proc Natl Acad Sci U S A. 2016 Jan 19;113(3):722-7. doi: 10.1073/pnas.1523817113. Epub 2016 Jan 5.
Necrotizing fasciitis (NF) caused by flesh-eating bacteria is associated with high case fatality. In an earlier study, we reported infection of an immunocompetent individual with multiple strains of Aeromonas hydrophila (NF1-NF4), the latter three constituted a clonal group whereas NF1 was phylogenetically distinct. To understand the complex interactions of these strains in NF pathophysiology, a mouse model was used, whereby either single or mixed A. hydrophila strains were injected intramuscularly. NF2, which harbors exotoxin A (exoA) gene, was highly virulent when injected alone, but its virulence was attenuated in the presence of NF1 (exoA-minus). NF1 alone, although not lethal to animals, became highly virulent when combined with NF2, its virulence augmented by cis-exoA expression when injected alone in mice. Based on metagenomics and microbiological analyses, it was found that, in mixed infection, NF1 selectively disseminated to mouse peripheral organs, whereas the other strains (NF2, NF3, and NF4) were confined to the injection site and eventually cleared. In vitro studies showed NF2 to be more effectively phagocytized and killed by macrophages than NF1. NF1 inhibited growth of NF2 on solid media, but ExoA of NF2 augmented virulence of NF1 and the presence of NF1 facilitated clearance of NF2 from animals either by enhanced priming of host immune system or direct killing via a contact-dependent mechanism.
由食肉细菌引起的坏死性筋膜炎(NF)与高病死率相关。在早期的一项研究中,我们报告了一例免疫功能正常的个体感染了多株嗜水气单胞菌(NF1 - NF4),后三株构成一个克隆群,而NF1在系统发育上是不同的。为了了解这些菌株在NF病理生理学中的复杂相互作用,使用了小鼠模型,通过肌肉注射单株或混合的嗜水气单胞菌菌株。携带外毒素A(exoA)基因的NF2单独注射时具有高毒力,但在NF1(不含exoA)存在时其毒力减弱。单独的NF1虽然对动物不致命,但与NF2联合时变得具有高毒力,其单独注射到小鼠体内时通过顺式exoA表达增强毒力。基于宏基因组学和微生物学分析,发现在混合感染中,NF1选择性地扩散到小鼠外周器官,而其他菌株(NF2、NF3和NF4)局限于注射部位并最终被清除。体外研究表明巨噬细胞对NF2的吞噬和杀伤作用比对NF1更有效。NF1在固体培养基上抑制NF2的生长,但NF2的ExoA增强了NF1的毒力,并且NF1的存在通过增强宿主免疫系统的启动或通过接触依赖性机制直接杀伤促进了NF2从动物体内的清除。