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编码大肠杆菌定居因子抗原II(CFA/II)的质粒表达及肠毒素产生

Expression of plasmids coding for colonization factor antigen II (CFA/II) and enterotoxin production in Escherichia coli.

作者信息

Mullany P, Field A M, McConnell M M, Scotland S M, Smith H R, Rowe B

出版信息

J Gen Microbiol. 1983 Dec;129(12):3591-601. doi: 10.1099/00221287-129-12-3591.

Abstract

Two plasmids transferred from enterotoxigenic Escherichia coli (ETEC) of serotype O6. H16 and biotypes A and C coded for mannose-resistant haemagglutination (MRHA) and production of heat-stable enterotoxin (ST) and heat-labile enterotoxin (LT). Both plasmids were nonautotransferring being mobilized most efficiently by the R plasmid R100-1. They were similar in their genetic properties being incompatible with each other and plasmids of the Inc group FI. The wild-type strains produced the colonization factor antigen II (CFA/II) which was made up of different coli surface antigens (CS). The biotype A strains produced CS1 and CS3 while the biotype C strains produced CS2 and CS3. These three antigens have the ability to cause MRHA. When plasmids coding for MRHA were transferred to K12 strains, the degree of haemagglutination was markedly reduced and only CS3 was produced. When both plasmids were transferred back into biotype A strains, good MRHA was restored and the strains produced CS1 and CS3. In a biotype C strain CS2 and CS3 were formed. The production of the antigens was compared by enzyme-linked immunosorbent assay (ELISA). The strains were also examined by electron microscopy where it was found that CS1 and CS2 were fimbrial antigens while CS3 was not.

摘要

两种质粒从血清型为O6、H16以及生物型A和C的产肠毒素大肠杆菌(ETEC)中转移而来,它们编码甘露糖抗性血凝(MRHA)以及热稳定肠毒素(ST)和热不稳定肠毒素(LT)的产生。这两种质粒均不能自主转移,在R质粒R100 - 1的作用下能最有效地被动员。它们在遗传特性上相似,彼此不相容,且与Inc组FI的质粒不相容。野生型菌株产生由不同大肠杆菌表面抗原(CS)组成的定居因子抗原II(CFA/II)。生物型A菌株产生CS1和CS3,而生物型C菌株产生CS2和CS3。这三种抗原都有引起MRHA的能力。当编码MRHA的质粒转移到K12菌株时,血凝程度明显降低,且只产生CS3。当两种质粒都转回生物型A菌株时,良好的MRHA得以恢复,且菌株产生CS1和CS3。在一个生物型C菌株中形成了CS2和CS3。通过酶联免疫吸附测定(ELISA)比较抗原的产生情况。还通过电子显微镜检查这些菌株,发现CS1和CS2是菌毛抗原,而CS3不是。

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