Department of Fishery Microbiology, College of Fisheries, Karnataka Veterinary, Animal and Fisheries Sciences University, Mangalore, India.
FEMS Microbiol Lett. 2010 Jun;307(2):151-7. doi: 10.1111/j.1574-6968.2010.01974.x.
Thermostable direct hemolysin-related hemolysin encoded by the trh gene is considered a major virulence factor in the pathogenesis of Vibrio parahaemolyticus infections. In this study, we report the presence of a trh homolog in three clinical isolates of Aeromonas veronii biovar veronii. The presence of a trh homolog in these strains of A. veronii was confirmed by PCR, followed by cloning, sequencing and colony hybridization using a digoxigenin-labelled probe. DNA sequence analysis revealed that the A. veronii trh gene had an identity of 99% and 84% to the trh1 and trh2 genes of V. parahaemolyticus, respectively. However, the expression of a trh-like gene in A. veronii could not be detected by reverse transcription PCR. Hence, the role of the gene product in the virulence of A. veronii strains is not clear. Further, these A. veronii isolates were negative for the ure gene encoding urease and the transposase gene by PCR. These genes are part of the trh gene cluster in V. parahaemolyticus. However, the presence of a trh homolog in a pathogen other than V. parahaemolyticus points to the fact that detection of the trh gene in stool samples, seafood enrichments or environmental samples does not always imply that trh-carrying V. parahaemolyticus are present.
由 trh 基因编码的耐热直接溶血素相关溶血素被认为是副溶血性弧菌感染发病机制中的主要毒力因子。在本研究中,我们报告了三种临床分离的嗜水气单胞菌 veronii 生物型 veronii 中存在 trh 同源物。这些气单胞菌菌株中 trh 同源物的存在通过 PCR 确认,然后通过克隆、测序和使用地高辛标记探针进行菌落杂交进行确认。DNA 序列分析表明,A. veronii 的 trh 基因与副溶血性弧菌的 trh1 和 trh2 基因分别具有 99%和 84%的同一性。然而,无法通过逆转录 PCR 检测到 A. veronii 中 trh 样基因的表达。因此,该基因产物在气单胞菌菌株毒力中的作用尚不清楚。此外,这些 A. veronii 分离株通过 PCR 对编码脲酶的 ure 基因和转座酶基因呈阴性。这些基因是副溶血性弧菌 trh 基因簇的一部分。然而,除副溶血性弧菌以外的病原体中存在 trh 同源物这一事实表明,在粪便样本、海鲜富集物或环境样本中检测到 trh 基因并不总是意味着携带 trh 的副溶血性弧菌存在。