Harvey Richard M, Trappetti Claudia, Mahdi Layla K, Wang Hui, McAllister Lauren J, Scalvini Alexandra, Paton Adrienne W, Paton James C
Research Centre for Infectious Diseases, Department of Molecular and Cellular Biology, University of Adelaide, S.A., Australia.
Research Centre for Infectious Diseases, Department of Molecular and Cellular Biology, University of Adelaide, S.A., Australia
Infect Immun. 2016 Jan 11;84(3):822-32. doi: 10.1128/IAI.01454-15.
Streptococcus pneumoniae is the leading infectious cause of death in children in the world. However, the mechanisms that drive the progression from asymptomatic colonization to disease are poorly understood. Two virulence-associated genomic accessory regions (ARs) were deleted in a highly virulent serotype 1 clinical isolate (strain 4496) and examined for their contribution to pathogenesis. Deletion of a prophage encoding a platelet-binding protein (PblB) resulted in reduced adherence, biofilm formation, reduced initial infection within the lungs, and a reduction in the number of circulating platelets in infected mice. However, the region's overall contribution to the survival of mice was not significant. In contrast, deletion of the variable region of pneumococcal pathogenicity island 1 (vPPI1) was also responsible for a reduction in adherence and biofilm formation but also reduced survival and invasion of the pleural cavity, blood, and lungs. While the 4496ΔPPI1 strain induced higher expression of the genes encoding interleukin-10 (IL-10) and CD11b in the lungs of challenged mice than the wild-type strain, very few other genes exhibited altered expression. Moreover, while the level of IL-10 protein was increased in the lungs of 4496ΔPPI1 mutant-infected mice compared to strain 4496-infected mice, the levels of gamma interferon (IFN-γ), CXCL10, CCL2, and CCL4 were not different in the two groups. However, the 4496ΔPPI1 mutant was found to be more susceptible than the wild type to phagocytic killing by a macrophage-like cell line. Therefore, our data suggest that vPPI1 may be a major contributing factor to the heightened virulence of certain serotype 1 strains, possibly by influencing resistance to phagocytic killing.
肺炎链球菌是全球儿童死亡的主要感染性病因。然而,驱动从无症状定植发展为疾病的机制却知之甚少。在一株高毒力1型临床分离株(菌株4496)中删除了两个与毒力相关的基因组辅助区域(ARs),并研究了它们对发病机制的作用。删除一个编码血小板结合蛋白(PblB)的原噬菌体导致粘附性降低、生物膜形成减少、肺部初始感染减少以及感染小鼠循环血小板数量减少。然而,该区域对小鼠存活的总体影响并不显著。相比之下,肺炎球菌致病岛1(vPPI1)可变区的缺失也导致粘附性和生物膜形成减少,但同时也降低了在胸腔、血液和肺部的存活及侵袭能力。虽然4496ΔPPI1菌株在受攻击小鼠肺部诱导的编码白细胞介素10(IL-10)和CD11b的基因表达高于野生型菌株,但很少有其他基因表现出表达改变。此外,与感染4496菌株的小鼠相比,感染4496ΔPPI1突变体的小鼠肺部IL-10蛋白水平升高,但两组中γ干扰素(IFN-γ)、CXCL10、CCL2和CCL4的水平没有差异。然而,发现4496ΔPPI1突变体比野生型更易被巨噬细胞样细胞系吞噬杀伤。因此,我们的数据表明,vPPI1可能是某些1型菌株毒力增强的主要因素,可能是通过影响对吞噬杀伤的抗性来实现的。