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从腹泻粪便中分离出的人类大肠杆菌菌株中编码CS31A的自我传递性R质粒。

Self-transmissible R plasmids encoding CS31A among human Escherichia coli strains isolated from diarrheal stools.

作者信息

Jallat C, Darfeuille-Michaud A, Girardeau J P, Rich C, Joly B

机构信息

Laboratoire de Bactériologie, Faculté de Pharmacie, Clermont-Ferrand, France.

出版信息

Infect Immun. 1994 Jul;62(7):2865-73. doi: 10.1128/iai.62.7.2865-2873.1994.

Abstract

The CS31A antigen was first described for septicemic and enterotoxigenic bovine E. coli strains. In our study, of 597 human Escherichia coli strains isolated from diarrheagenic stools of hospitalized patients, 30 (5%) hybridized with the CS31A DNA probe. These CS31A-positive E. coli strains diffusely adhered to Caco-2 and/or HEp-2 cells and produced a major surface protein of either 30 or 30.5 kDa according to the strain. These proteins were antigenically related to the two forms of the CS31A antigen, namely, CS31A-L and CS31A-H. Genes encoding CS31A were located on 140-kb conjugative R plasmids. E. coli transconjugants expressed major surface proteins similar to those of the wild-type strains and adhered to Caco-2 and/or HEp-2 cells. An association of CS31A and another adhesive factor of the Dr family was found in 70% of wild-type strains, since 21 strains hybridized with the diffuse adhesion DNA probe corresponding to the accessory gene (daaC) of the F1845 adhesin. Comparison of the restriction patterns of the 140-kb R plasmids of the CS31A-positive E. coli strains showed these plasmids to be similar. Hybridization experiments indicated that the genes encoding CS31A and resistance to penicillin were located together on either of two 20- or 27-kb EcoRI restriction fragments in four E. coli strains. We reported a similar linkage between these genes in Klebsiella pneumoniae strains which produced CF29K, a CS31A-like antigen. These results suggest a horizontal transfer between E. coli and K. pneumoniae strains.

摘要

CS31A抗原最初是在败血性和产肠毒素的牛源大肠杆菌菌株中被描述的。在我们的研究中,从住院患者腹泻性粪便中分离出的597株人源大肠杆菌菌株中,有30株(5%)与CS31A DNA探针杂交。这些CS31A阳性大肠杆菌菌株能扩散性黏附于Caco-2和/或HEp-2细胞,并根据菌株不同产生一种分子量为30或30.5 kDa的主要表面蛋白。这些蛋白在抗原性上与CS31A抗原的两种形式,即CS31A-L和CS31A-H相关。编码CS31A的基因位于140 kb的接合性R质粒上。大肠杆菌转接合子表达的主要表面蛋白与野生型菌株相似,并能黏附于Caco-2和/或HEp-2细胞。在70%的野生型菌株中发现CS31A与Dr家族的另一种黏附因子有关联,因为有21株与对应于F1845黏附素辅助基因(daaC)的扩散性黏附DNA探针杂交。对CS31A阳性大肠杆菌菌株的140 kb R质粒的限制性酶切图谱比较显示这些质粒相似。杂交实验表明,在四株大肠杆菌菌株中,编码CS31A的基因和对青霉素的抗性基因共同位于两个20 kb或27 kb的EcoRI限制性片段中的任意一个上。我们曾报道在产生CF29K(一种CS31A样抗原)的肺炎克雷伯菌菌株中这些基因之间存在类似的连锁关系。这些结果提示大肠杆菌和肺炎克雷伯菌菌株之间存在水平转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cfa/302893/c6fa03a11243/iai00007-0226-a.jpg

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