Alm R A, Mayrhofer G, Kotlarski I, Manning P A
Department of Microbiology and Immunology, University of Adelaide, SA.
Vaccine. 1991 Aug;9(8):588-94. doi: 10.1016/0264-410x(91)90247-4.
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.
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。