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一株尿路致病性大肠杆菌二半乳糖苷结合黏附素的遗传学研究

Genetics of digalactoside-binding adhesin from a uropathogenic Escherichia coli strain.

作者信息

Normark S, Lark D, Hull R, Norgren M, Båga M, O'Hanley P, Schoolnik G, Falkow S

出版信息

Infect Immun. 1983 Sep;41(3):942-9. doi: 10.1128/iai.41.3.942-949.1983.

Abstract

The uropathogenic strain Escherichia coli J96 mediates mannose-resistant hemagglutination owing to production of a digalactoside-binding adhesin. A cosmid clone from this strain has been isolated that, when harbored in E. coli K-12, expressed Pap pili and this adhesin (R. Hull et al., Infect. Immun. 33:933-938, 1981). By transposon mutagenesis and by the construction of a number of hybrid plasmid derivatives, we have demonstrated that about 8.5 kilobases of DNA is required to generate a mannose-resistant hemagglutination-positive phenotype in E. coli K-12 strain P678-54. The structural gene for the Pap pili monomer, papA, has been identified and mapped close to the promotor-proximal end of the Pap operon. Although strain P678-54 that harbored a Tn5 insertion within papA showed a mannose-resistant hemagglutination-positive phenotype, it was negative in a competitive enzyme-linked immunosorbent assay with anti-Pap pilus serum. This could mean that a Pap adhesin is encoded by a region on the Pap operon that is distinct from papA.

摘要

尿路致病性大肠杆菌J96由于产生一种双半乳糖苷结合黏附素而介导甘露糖抗性血凝反应。已从该菌株中分离出一个黏粒克隆,当它存在于大肠杆菌K-12中时,可表达P菌毛和这种黏附素(R. Hull等人,《感染与免疫》33:933-938,1981年)。通过转座子诱变和构建多种杂交质粒衍生物,我们已证明在大肠杆菌K-12菌株P678-54中产生甘露糖抗性血凝阳性表型需要约8.5千碱基的DNA。P菌毛单体的结构基因papA已被鉴定并定位在P菌毛操纵子启动子近端附近。尽管在papA内有Tn5插入的菌株P678-54表现出甘露糖抗性血凝阳性表型,但在用抗P菌毛血清进行的竞争性酶联免疫吸附试验中呈阴性。这可能意味着P黏附素由P菌毛操纵子上一个与papA不同的区域编码。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7577/264592/5f4a8457ff0c/iai00138-0078-a.jpg

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