Characterization of the CsfC and CsfD proteins involved in the biogenesis of CS5 pili from enterotoxigenic Escherichia coli

被引:4
作者
Duthy, TG
Manning, PA
Heuzenroeder, MW [1 ]
机构
[1] Inst Med & Vet Sci, Infect Dis Labs, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Discipline Microbiol & Immunol, Dept Mol Biosci, Adelaide, SA 5005, Australia
[3] AstraZeneca R&D Boston, Waltham, MA 02451 USA
基金
英国医学研究理事会;
关键词
enterotoxigenic E coli; pili; outer membrane protein; CsfC; CsfD; minor pilin;
D O I
10.1006/mpat.2001.0452
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The region required for biosynthesis of CS5 pili consists of six csf genes, with csfA encoding the major subunit. In this study, we describe the characterization of two of the genes constituting the region, csfC and csfD, but also identify the true morphology of the CS5 pilus by high resolution electron microscopy. CsfD was shown to be essential in the initiation of CS5 pilus biogenesis, did not possess any chaperone-like activity for the major subunit, and was an integral minor component of the pilus structure. Studies on CsfD translocation across the outer membrane in Escherichia coli K-12 using a csfA mutant also showed that CsfD is likely to be the first pilin subunit assembled. A specific in-frame deletion in the csfC gene resulted in the complete absence of cell surface CS5 pili and prevented the translocation of CsfA and CsfD pilins across the outer membrane. Specific cell localization studies showed an accumulation of CsfC in the outer membranes of E. coli K-12, while complementation experiments with homologous outer membrane assembly genes from CS1 and CFA/I pili systems were unable to restore assembly of CS5 pili. The CS5 pilus was shown to be a 2 nm flexible fibrillar structure, which adopted a predominantly open helical conformation under the electron microscope.
引用
收藏
页码:115 / 129
页数:15
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