Bacteriology Division, United States Army Medical Research Institute of Infectious Diseases , Frederick, Maryland, USA.
Virulence. 2020 Dec;11(1):1041-1058. doi: 10.1080/21505594.2020.1806675.
Burkholderia pseudomallei: is the etiological agent of the disease melioidosis and is a Tier 1 select agent. It survives and replicates inside phagocytic cells by escaping from the endocytic vacuole, replicating in the cytosol, spreading to other cells via actin polymerization and promoting the fusion of infected and uninfected host cells to form multinucleated giant cells. In this study, we utilized a proteomics approach to identify bacterial proteins produced inside RAW264.7 murine macrophages and host proteins produced in response to infection. Cells infected with strain K96243 were lysed and the lysate proteins digested and analyzed using nanoflow reversed-phase liquid chromatography and tandem mass spectrometry. Approximately 160 bacterial proteins were identified in the infected macrophages, including BimA, TssA, TssB, Hcp1 and TssM. Several previously uncharacterized proteins were also identified, including BPSS1996 and BPSL2748. Mutations were constructed in the genes encoding these novel proteins and their relative virulence was assessed in BALB/c mice. The 50% lethal dose for the mutant was approximately 55-fold higher than that of the wild type, suggesting that BPSS1996 is required for full virulence. Sera from -infected animals reacted with BPSS1996 and it was found to localize to the bacterial surface using indirect immunofluorescence. Finally, we identified 274 host proteins that were exclusively present or absent in infected RAW264.7 cells, including chemokines and cytokines involved in controlling the initial stages of infection.
是类鼻疽病的病原体,也是一级选择剂。它通过从吞噬细胞的内吞小泡中逃逸,在细胞质中复制,通过肌动蛋白聚合在细胞间扩散,并促进感染和未感染宿主细胞的融合,从而在吞噬细胞中存活和复制,形成多核巨细胞。在这项研究中,我们利用蛋白质组学方法来鉴定 RAW264.7 鼠巨噬细胞内产生的细菌蛋白和宿主对感染的反应产生的蛋白。用 菌株 K96243 感染细胞,裂解细胞并使用纳流反相液相色谱和串联质谱分析裂解物蛋白。在感染的巨噬细胞中鉴定出约 160 种细菌蛋白,包括 BimA、TssA、TssB、Hcp1 和 TssM。还鉴定出几个以前未被表征的 蛋白,包括 BPSS1996 和 BPSL2748。构建了这些新蛋白编码基因的突变体,并在 BALB/c 小鼠中评估了它们的相对毒力。突变体的 50%致死剂量比野生型高约 55 倍,表明 BPSS1996 是完全毒力所必需的。感染动物的血清与 BPSS1996 反应,通过间接免疫荧光发现它定位于细菌表面。最后,我们鉴定了 274 种仅存在于感染 RAW264.7 细胞或不存在于感染 RAW264.7 细胞中的宿主蛋白,包括参与控制感染初始阶段的趋化因子和细胞因子。