Pharmacology and Toxicology, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
Vascular Biology Center, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.
Toxins (Basel). 2020 Apr 2;12(4):223. doi: 10.3390/toxins12040223.
Bacterial toxins play a key role in the pathogenesis of lung disease. Based on their structural and functional properties, they employ various strategies to modulate lung barrier function and to impair host defense in order to promote infection. Although in general, these toxins target common cellular signaling pathways and host compartments, toxin- and cell-specific effects have also been reported. Toxins can affect resident pulmonary cells involved in alveolar fluid clearance (AFC) and barrier function through impairing vectorial Na transport and through cytoskeletal collapse, as such, destroying cell-cell adhesions. The resulting loss of alveolar-capillary barrier integrity and fluid clearance capacity will induce capillary leak and foster edema formation, which will in turn impair gas exchange and endanger the survival of the host. Toxins modulate or neutralize protective host cell mechanisms of both the innate and adaptive immunity response during chronic infection. In particular, toxins can either recruit or kill central players of the lung's innate immune responses to pathogenic attacks, i.e., alveolar macrophages (AMs) and neutrophils. Pulmonary disorders resulting from these toxin actions include, e.g., acute lung injury (ALI), the acute respiratory syndrome (ARDS), and severe pneumonia. When acute infection converts to persistence, i.e., colonization and chronic infection, lung diseases, such as bronchitis, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF) can arise. The aim of this review is to discuss the impact of bacterial toxins in the lungs and the resulting outcomes for pathogenesis, their roles in promoting bacterial dissemination, and bacterial survival in disease progression.
细菌毒素在肺部疾病的发病机制中起着关键作用。基于它们的结构和功能特性,它们采用各种策略来调节肺屏障功能,并损害宿主防御,以促进感染。尽管总的来说,这些毒素针对的是常见的细胞信号通路和宿主隔室,但也有报道称毒素和细胞特异性的效应。毒素可以通过损害向量 Na 转运和细胞骨架崩溃,从而影响参与肺泡液清除(AFC)和屏障功能的驻留肺细胞,从而破坏细胞-细胞间的粘附。由此导致的肺泡毛细血管屏障完整性和液体清除能力的丧失将引起毛细血管渗漏并促进水肿形成,这反过来又会损害气体交换并危及宿主的生存。毒素在慢性感染期间调节或中和先天和适应性免疫反应的保护性宿主细胞机制。特别是,毒素可以招募或杀死肺部先天免疫反应的关键参与者,即肺泡巨噬细胞(AMs)和中性粒细胞。这些毒素作用引起的肺部疾病包括急性肺损伤(ALI)、急性呼吸窘迫综合征(ARDS)和严重肺炎。当急性感染转变为持续存在,即定植和慢性感染时,可能会出现支气管疾病,如支气管炎、慢性阻塞性肺疾病(COPD)和囊性纤维化(CF)。本综述的目的是讨论细菌毒素在肺部的作用及其对发病机制的影响,它们在促进细菌传播和细菌在疾病进展中的存活中的作用。