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在一株大肠杆菌血清型O139.H28中通过质粒编码产生大肠杆菌表面相关抗原1(CS1)

Plasmid-encoded production of coli surface-associated antigen 1 (CS1) in a strain of Escherichia coli serotype O139.H28.

作者信息

Willshaw G A, Smith H R, McConnell M M, Gaastra W, Thomas A, Hibberd M, Rowe B

机构信息

Division of Enteric Pathogens, Central Public Health Laboratory, London, U.K.

出版信息

Microb Pathog. 1990 Jul;9(1):1-11. doi: 10.1016/0882-4010(90)90035-o.

Abstract

Production of coli surface-associated antigen 1 (CS1) by Escherichia coli strain E24377 of serotype O139.H28 was controlled by a plasmid that also encoded heat stable and heat labile enterotoxins and CS3. The presence of a regulatory sequence was detected on this plasmid by hybridization with the cfaD gene that regulates expression of colonization factor antigen I fimbriae and is at least 96% homologous with the rns sequence controlling production of CS1 or CS2 fimbriae by strains of serotype O6.H16 of appropriate biotype. A separate plasmid, pDEP20, carrying the structural genes for CS1 synthesis was identified and transformed into E. coli strain HB101 or a derivative of strain E24377 without large plasmids. Transformants carrying pDEP20 did not produce CS1 fimbrial antigen, but antigen expression was obtained when a cloned cfaD gene or a wild-type plasmid carrying the rns sequence was introduced. Transposon mutagenesis with Tn1000 identified a 3.7 kbp region of pDEP20 essential for production of CS1 fimbriae. Genes encoding production of CS1 fimbriae were cloned on a 9.9 kbp BamHI fragment and were expressed in the presence of the cfaD sequence. A strain producing both CS1 and CS2 antigens was constructed by introduction of the cloned cfaD gene into a strain of serotype O6.H16 biotype C carrying plasmid pDEP20.

摘要

血清型O139.H28的大肠杆菌菌株E24377产生的大肠杆菌表面相关抗原1(CS1)受一种质粒控制,该质粒还编码热稳定和热不稳定肠毒素以及CS3。通过与调控定居因子抗原I菌毛表达的cfaD基因杂交,在该质粒上检测到一个调控序列,该基因与控制合适生物型的血清型O6.H16菌株产生CS1或CS2菌毛的rns序列至少96%同源。鉴定出一个携带CS1合成结构基因的单独质粒pDEP20,并将其转化到大肠杆菌菌株HB101或无大质粒的E24377菌株衍生物中。携带pDEP20的转化体不产生CS1菌毛抗原,但当引入克隆的cfaD基因或携带rns序列的野生型质粒时可获得抗原表达。用Tn1000进行转座子诱变确定了pDEP20中对CS1菌毛产生至关重要的一个3.7 kbp区域。编码CS1菌毛产生的基因克隆在一个9.9 kbp的BamHI片段上,并在cfaD序列存在时表达。通过将克隆的cfaD基因引入携带质粒pDEP20的血清型O6.H16生物型C菌株中,构建了一个同时产生CS1和CS2抗原的菌株。

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