Caron J, Scott J R
Department of Microbiology and Immunology, Emory University Health Sciences Center, Atlanta, Georgia 30322.
Infect Immun. 1990 Apr;58(4):874-8. doi: 10.1128/iai.58.4.874-878.1990.
Colonization factor antigens (CFA) are needed for adherence of human enterotoxigenic Escherichia coli (ETEC) strains to their hosts. The CFA/II antigens, CS1 and CS2, which are found in some ETEC strains, require the plasmid-encoded gene rns for expression (J. Caron, L. M. Coffield, and J. R. Scott, Proc. Natl. Acad. Sci. USA 86:963-967, 1989). Other ETEC strains express CFA/I, whose synthesis and assembly require genes on two unlinked regions (regions 1 and 2) of a plasmid (G. A. Willshaw, H. R. Smith, and B. Rowe, FEMS Microbiol. Lett. 16:101-106, 1983). We report that CFA/I region 2 DNA can substitute for rns to cause expression of CS1 and CS2. The cfaR gene in region 2 is defined by a mutation abolishing both expression of CFA/I and complementation of a rns mutant for expression of CS1 or CS2. In a strain containing only region 1, complementation for expression of CFA/I by a plasmid containing rns+ is inefficient but is adequate to cause hemagglutination by the CFA/I adhesin.
定居因子抗原(CFA)是人类产肠毒素大肠杆菌(ETEC)菌株黏附于宿主所必需的。在一些ETEC菌株中发现的CFA/II抗原,即CS1和CS2,其表达需要质粒编码的基因rns(J. 卡隆、L. M. 科菲尔德和J. R. 斯科特,《美国国家科学院院刊》86:963 - 967, 1989年)。其他ETEC菌株表达CFA/I,其合成和组装需要质粒上两个不连锁区域(区域1和区域2)的基因(G. A. 威尔肖、H. R. 史密斯和B. 罗,《FEMS微生物学快报》16:101 - 106, 1983年)。我们报道CFA/I区域2的DNA可以替代rns来促使CS1和CS2的表达。区域2中的cfaR基因由一个突变定义,该突变既消除了CFA/I的表达,也消除了rns突变体中CS1或CS2表达的互补作用。在仅含有区域1的菌株中,含有rns⁺的质粒对CFA/I表达的互补作用效率低下,但足以使CFA/I黏附素引起血细胞凝集。