University of Vienna, Department of Ecogenomics and Systems Biology, Archaeal Biology and Ecogenomics Division, Althanstrasse 14, 1090 Vienna, Austria.
Bacterial Cell Biology and Physiology Swammerdam Institute for Life Sciences, University of Amsterdam, De Boelelaan 1108, 1081 Amsterdam, the Netherlands.
Curr Biol. 2018 Apr 2;28(7):1039-1051.e5. doi: 10.1016/j.cub.2018.02.028. Epub 2018 Mar 22.
To determine the fundamentals of cell growth, we must extend cell biological studies to non-model organisms. Here, we investigated the growth modes of the only two rods known to widen instead of elongating, Candidatus Thiosymbion oneisti and Thiosymbion hypermnestrae. These bacteria are attached by one pole to the surface of their respective nematode hosts. By incubating live Ca. T. oneisti and T. hypermnestrae with a peptidoglycan metabolic probe, we observed that the insertion of new cell wall starts at the poles and proceeds inward, concomitantly with FtsZ-based membrane constriction. Remarkably, in Ca. T. hypermnestrae, the proximal, animal-attached pole grows before the distal, free pole, indicating that the peptidoglycan synthesis machinery is host oriented. Immunostaining of the symbionts with an antibody against the actin homolog MreB revealed that it was arranged medially-that is, parallel to the cell long axis-throughout the symbiont life cycle. Given that depolymerization of MreB abolished newly synthesized peptidoglycan insertion and impaired divisome assembly, we conclude that MreB function is required for symbiont widening and division. In conclusion, our data invoke a reassessment of the localization and function of the bacterial actin homolog.
为了确定细胞生长的基本原理,我们必须将细胞生物学研究扩展到非模式生物。在这里,我们研究了仅有的两种已知会变宽而不是变长的杆状细菌的生长方式,即 Candidatus Thiosymbion oneisti 和 Thiosymbion hypermnestrae。这些细菌通过一个极附着在各自的线虫宿主的表面上。通过用肽聚糖代谢探针孵育活的 Ca. T. oneisti 和 T. hypermnestrae,我们观察到新细胞壁的插入从极开始并向内推进,同时伴随着基于 FtsZ 的膜收缩。值得注意的是,在 Ca. T. hypermnestrae 中,近端、附着动物的极在远端、自由的极之前生长,这表明肽聚糖合成机制是宿主定向的。用针对肌动蛋白同源物 MreB 的抗体对共生体进行免疫染色表明,在共生体的整个生命周期中,它都排列在中央 - 即与细胞长轴平行。鉴于 MreB 的解聚会破坏新合成的肽聚糖插入并损害分裂体组装,我们得出结论,MreB 的功能对于共生体的变宽和分裂是必需的。总之,我们的数据引发了对细菌肌动蛋白同源物的定位和功能的重新评估。