Emerging Pathogens Institute and Department of Environmental and Global Health, College of Public Health and Health Professions, University of Florida, Gainesville, Florida, USA.
Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
mBio. 2020 Feb 18;11(1):e03222-19. doi: 10.1128/mBio.03222-19.
Cell division is the ultimate process for the propagation of bacteria, and FtsZ is an essential protein used by nearly all bacteria for this function. belong to a small group of bacteria that lack the universal cell division protein FtsZ but still divide by binary fission. Chlamydial MreB is a member of the shape-determining MreB/Mbl family of proteins responsible for rod shape morphology in also encodes a homolog of RodZ, an MreB assembly cytoskeletal protein that links MreB to cell wall synthesis proteins. We hypothesized that MreB directs cell division in and that chlamydial MreB could replace FtsZ function for cell division in Overexpression of chlamydial in induced prominent morphological changes with production of large swollen or oval bacteria, eventually resulting in bacterial lysis. Low-level expression of chlamydial restored viability of a lethal Δ mutation in , although the bacteria lost their typical rod shape and grew as rounded cells. When FtsZ activity was inhibited by overexpression of SulA in the Δ mutant of complemented with chlamydial , spherical grew and divided. Localization studies using a fluorescent fusion chlamydial MreB protein indicated that chlamydial RodZ directs chlamydial MreB to the division septum. These results demonstrate that chlamydial MreB, in partnership with chlamydial RodZ, acts as a cell division protein. Our findings suggest that an -based mechanism allows to divide without the universal division protein FtsZ. The study of growth and cell division is complicated by its obligate intracellular nature and biphasic lifestyle. also lacks the universal division protein FtsZ. We employed the cell division system of as a surrogate to identify chlamydial cell division proteins. We demonstrate that chlamydial MreB, together with chlamydial RodZ, forms a cell division and growth complex that can replace FtsZ activity and support cell division in Chlamydial RodZ plays a major role in directing chlamydial MreB localization to the cell division site. It is likely that the evolution of chlamydial MreB and RodZ to form a functional cell division complex allowed to dispense with its FtsZ-based cell division machinery during genome reduction. Thus, MreB-RodZ represents a possible mechanism for cell division in other bacteria lacking FtsZ.
细胞分裂是细菌繁殖的最终过程,FtsZ 是几乎所有细菌用于此功能的必需蛋白质。而衣原体属于一组缺乏普遍存在的细胞分裂蛋白 FtsZ 的细菌,但仍通过二分法分裂。衣原体 MreB 是一种负责杆状形态的形状决定 MreB/Mbl 家族蛋白的成员,也编码一种 RodZ 的同源物,RodZ 是一种 MreB 组装细胞骨架蛋白,将 MreB 与细胞壁合成蛋白连接起来。我们假设 MreB 指导衣原体的细胞分裂,并且衣原体 MreB 可以替代 FtsZ 功能用于细胞分裂。在 中过表达衣原体 会导致明显的形态变化,产生大的肿胀或椭圆形细菌,最终导致细菌裂解。在致死性 Δ突变体中低水平表达衣原体 恢复了活力,尽管细菌失去了典型的杆状形状并长成圆形细胞。当通过过表达 SulA 在 Δ突变体中抑制 FtsZ 活性时,用衣原体 补充的 会生长并分裂成球形。使用荧光融合衣原体 MreB 蛋白进行定位研究表明,衣原体 RodZ 将衣原体 MreB 引导到 分裂隔膜。这些结果表明,衣原体 MreB 与衣原体 RodZ 合作,充当细胞分裂蛋白。我们的发现表明,基于 -的机制允许 无需普遍存在的分裂蛋白 FtsZ 就可以分裂。由于其专性细胞内性质和两相生活方式,对 的生长和细胞分裂的研究变得复杂。也缺乏普遍存在的分裂蛋白 FtsZ。我们利用 的细胞分裂系统作为替代物来鉴定衣原体细胞分裂蛋白。我们证明,衣原体 MreB 与衣原体 RodZ 一起形成一个细胞分裂和生长复合物,可以替代 FtsZ 活性并支持 在 中的细胞分裂。衣原体 RodZ 在指导衣原体 MreB 定位到细胞分裂位点方面起着重要作用。很可能是衣原体 MreB 和 RodZ 的进化形成了一个功能性的细胞分裂复合物,使 能够在基因组减少期间摆脱基于 FtsZ 的细胞分裂机制。因此,MreB-RodZ 代表了其他缺乏 FtsZ 的细菌进行细胞分裂的可能机制。