Human Biology Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N, Seattle, WA 98109, United States.
Curr Opin Microbiol. 2020 Apr;54:11-17. doi: 10.1016/j.mib.2019.12.002. Epub 2020 Jan 31.
A genetic screen for colonization factors of the human stomach pathogen Helicobacter pylori took a surprising turn with the discovery that some colonization mutants had lost helical cell morphology. Further pursuit of direct morphology screens revealed a large H. pylori 'shapesome' complex consisting of peptidoglycan modification and precursor synthesis enzymes, a cytoskeletal element and putative scaffold or regulatory proteins that promote enhanced asymmetric cell wall growth. Functional characterization of H. pylori shape mutants indicates multiple roles for cell shape during colonization of mucosal surfaces. Conservation of both the molecular constituents of the H. pylori cell shape program and a newly appreciated enrichment of this morphotype at mucosal surface suggests that helical organisms may be particularly well poised to exploit host perturbations to become pathogens.
一项针对人类胃部病原体幽门螺杆菌定植因子的基因筛选出现了惊人的转折,发现一些定植突变体失去了螺旋细胞形态。进一步进行直接形态筛选揭示了一个由肽聚糖修饰和前体合成酶、细胞骨架成分和假定支架或调节蛋白组成的大型幽门螺杆菌“形态复合物”,这些蛋白促进增强的不对称细胞壁生长。对幽门螺杆菌形态突变体的功能表征表明,在黏膜表面定植过程中,细胞形态发挥了多种作用。幽门螺杆菌细胞形态程序的分子成分的保守性,以及这种形态型在黏膜表面的新的富集,表明螺旋生物可能特别适合利用宿主的扰动成为病原体。