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霍乱弧菌O1型埃尔托溶血素的氨基末端结构域在古典生物型菌株中表达且具有细胞毒性。

Amino-terminal domain of the El Tor haemolysin of Vibrio cholerae O1 is expressed in classical strains and is cytotoxic.

作者信息

Alm R A, Mayrhofer G, Kotlarski I, Manning P A

机构信息

Department of Microbiology and Immunology, University of Adelaide, SA.

出版信息

Vaccine. 1991 Aug;9(8):588-94. doi: 10.1016/0264-410x(91)90247-4.

Abstract

Previous studies have shown that the classical isolates of Vibrio cholerae possess an 11 bp deletion in the structural gene for the El Tor haemolysin leading to the production of a 27 kDa non-haemolytic truncated product HlyA* compared to the 82 kDa haemolysin, HlyA. These studies were designed to assess whether this truncated product had any biological activity. A KmR cartridge was introduced into the hlyA gene effectively eliminating the haemolysin. This was recombined into the chromosome of a variety of strains and isogenic pairs were examined in a number of systems. These studies suggest that the haemolytic (cytolytic) domain of HlyA resides at the C-terminus and that the N-terminus, which is conserved as HlyA* in classical strains, possesses enterotoxic (cytotoxic) activity. Experiments with the cholera-toxinless vaccine candidate JBK70 and its hlyA::KmR mutant suggest that HlyA* may be responsible for the residual diarrhoea observed in cholera-toxinless vaccine strains.

摘要

先前的研究表明,霍乱弧菌的经典菌株在埃尔托溶血素的结构基因中存在11 bp的缺失,导致产生一种27 kDa的非溶血截短产物HlyA*,而与之相比,溶血素HlyA的大小为82 kDa。这些研究旨在评估这种截短产物是否具有任何生物学活性。将一个卡那霉素抗性盒导入hlyA基因,有效地消除了溶血素。将其重组到多种菌株的染色体中,并在多个系统中检查同基因对。这些研究表明,HlyA的溶血(细胞溶解)结构域位于C端,而在经典菌株中作为HlyA保守的N端具有肠毒素(细胞毒素)活性。对霍乱毒素缺失疫苗候选株JBK70及其hlyA::KmR突变体进行的实验表明,HlyA可能是霍乱毒素缺失疫苗株中观察到的残留腹泻的原因。

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