Charon Nyles W, Goldstein Stuart F, Marko Michael, Hsieh Chyongere, Gebhardt Linda L, Motaleb M Abdul, Wolgemuth Charles W, Limberger Ronald J, Rowe Nancy
Department of Microbiology, Immunology and Cell Biology, Robert C. Byrd Health Sciences Center, West Virginia University, Morgantown, West Virginia 26506-9177, USA.
J Bacteriol. 2009 Jan;191(2):600-7. doi: 10.1128/JB.01288-08. Epub 2008 Nov 14.
Electron cryotomography was used to analyze the structure of the Lyme disease spirochete, Borrelia burgdorferi. This methodology offers a new means for studying the native architecture of bacteria by eliminating the chemical fixing, dehydration, and staining steps of conventional electron microscopy. Using electron cryotomography, we noted that membrane blebs formed at the ends of the cells. These blebs may be precursors to vesicles that are released from cells grown in vivo and in vitro. We found that the periplasmic space of B. burgdorferi was quite narrow (16.0 nm) compared to those of Escherichia coli and Pseudomonas aeruginosa. However, in the vicinity of the periplasmic flagella, this space was considerably wider (42.3 nm). In contrast to previous results, the periplasmic flagella did not form a bundle but rather formed a tight-fitting ribbon that wraps around the protoplasmic cell cylinder in a right-handed sense. We show how the ribbon configuration of the assembled periplasmic flagella is more advantageous than a bundle for both swimming and forming the flat-wave morphology. Previous results indicate that B. burgdorferi motility is dependent on the rotation of the periplasmic flagella in generating backward-moving waves along the length of the cell. This swimming requires that the rotation of the flagella exerts force on the cell cylinder. Accordingly, a ribbon is more beneficial than a bundle, as this configuration allows each periplasmic flagellum to have direct contact with the cell cylinder in order to exert that force, and it minimizes interference between the rotating filaments.
电子冷冻断层扫描技术被用于分析莱姆病螺旋体——伯氏疏螺旋体的结构。这种方法通过省去传统电子显微镜中的化学固定、脱水和染色步骤,为研究细菌的天然结构提供了一种新手段。利用电子冷冻断层扫描技术,我们注意到细胞末端形成了膜泡。这些膜泡可能是在体内和体外生长的细胞释放出的囊泡的前体。我们发现,与大肠杆菌和铜绿假单胞菌相比,伯氏疏螺旋体的周质空间相当狭窄(16.0纳米)。然而,在周质鞭毛附近,这个空间要宽得多(42.3纳米)。与之前的结果相反,周质鞭毛并没有形成束状,而是形成了一条紧密贴合的带状结构,以右手螺旋的方式缠绕在原生质细胞圆柱体周围。我们展示了组装好的周质鞭毛的带状结构在游动和形成平波形态方面如何比束状结构更具优势。之前的结果表明,伯氏疏螺旋体的运动性取决于周质鞭毛的旋转,从而在细胞长度方向上产生向后移动的波。这种游动要求鞭毛的旋转对细胞圆柱体施加力。因此,带状结构比束状结构更有利,因为这种结构使每个周质鞭毛都能直接与细胞圆柱体接触以施加该力,并且它能使旋转的细丝之间的干扰最小化。