Infection Program, Monash Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, VIC 3800, Australia.
Department of Microbiology and Immunology at the Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC 3000, Australia.
Pathog Dis. 2024 Feb 7;82. doi: 10.1093/femspd/ftae018.
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.
贝氏考克斯体是一种分布广泛的严格细胞内病原体。尽管通常无症状,但感染可引起类似流感的急性 Q 热和/或严重的慢性 Q 热。贝氏考克斯体在宿主细胞内形成一个独特的复制小生境,称为考克斯体包含的空泡(CCV),这得益于 Dot/Icm 型 IV 型分泌系统将一群细菌效应蛋白转运到宿主中。一些效应物的作用已经阐明;然而,大多数效应物的作用仍然神秘莫测,真正的效应物的清单也存在争议。本研究检查了 CBU2016,这是一种以前被指定为感染作用效应物的独特的贝氏考克斯体蛋白。我们无法验证 CBU2016 是一种易位的效应蛋白。通过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 细胞内的复制缺陷,也不会影响在 Galleria mellonella 感染模型中贝氏考克斯体的致病性。然而,CBU2016 的缺失确实导致了 HeLa 细胞中 CCV 的大小持续减小。这些结果表明,尽管 CBU2016 可能不是 Dot/Icm 效应物,但它仍然能够在感染过程中影响宿主环境。