David R Thomas, Sarah E Garnish, Chen Ai Khoo, Bhavna Padmanabhan, Nichollas E Scott, Hayley J Newton
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引用次数: 0
摘要
烧伤柯西氏菌是一种分布于全球的强制性细胞内病原体。虽然通常没有症状,但感染后可引起急性Q热,并伴有流感样症状和/或严重的慢性Q热。烧伤桿菌在宿主细胞内形成一个独特的复制位点,称为含柯西氏菌空泡(CCV),由 Dot/Icm IV 型分泌系统将一系列细菌效应蛋白转运到宿主体内。一些效应蛋白的作用已被阐明,但大多数效应蛋白的作用仍是个谜,真正的效应蛋白清单也存在争议。本研究对 CBU2016 进行了研究,这是一种独特的烧伤疽杆菌蛋白,以前曾被指定为在感染中发挥作用的效应物。我们无法证实 CBU2016 是一种转运效应蛋白。通过使用靶向敲除和互补菌株,我们发现 CBU2016 的缺失不会导致 Hela、THP-1、J774 或 iBMDM 细胞或轴突培养基中的复制缺陷,也不会影响 C. burnetii 在 Galleria mellonella 感染模型中的致病性。然而,CBU2016 的缺失确实导致 HeLa 细胞中 CCVs 的大小持续减小。这些结果表明,尽管 CBU2016 可能不是 Dot/Icm 效应体,但它仍然能够在感染期间影响宿主环境。
Coxiella burnetii protein CBU2016 supports CCV expansion.
Coxiella burnetii is a globally distributed obligate intracellular pathogen. Although often asymptomatic, infections can cause acute Q fever with influenza-like symptoms and/or severe chronic Q fever. Coxiella burnetii develops a unique replicative niche within host cells called the Coxiella-containing vacuole (CCV), facilitated by the Dot/Icm type IV secretion system translocating a cohort of bacterial effector proteins into the host. The role of some effectors has been elucidated; however, the actions of the majority remain enigmatic and the list of true effectors is disputable. This study examined CBU2016, a unique C. burnetii protein previously designated as an effector with a role in infection. We were unable to validate CBU2016 as a translocated effector protein. Employing targeted knock-out and complemented strains, we found that the loss of CBU2016 did not cause a replication defect within Hela, THP-1, J774, or iBMDM cells or in axenic media, nor did it affect the pathogenicity of C. burnetii in the Galleria mellonella infection model. The absence of CBU2016 did, however, result in a consistent decrease in the size of CCVs in HeLa cells. These results suggest that although CBU2016 may not be a Dot/Icm effector, it is still able to influence the host environment during infection.
期刊介绍:
Pathogens and Disease publishes outstanding primary research on hypothesis- and discovery-driven studies on pathogens, host-pathogen interactions, host response to infection and their molecular and cellular correlates. It covers all pathogens – eukaryotes, prokaryotes, and viruses – and includes zoonotic pathogens and experimental translational applications.