State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
Lett Appl Microbiol. 2012 Aug;55(2):91-8. doi: 10.1111/j.1472-765X.2012.03260.x. Epub 2012 Jun 13.
The aims of this study were to reveal the roles of the gene locus qseEGF in the pathogenesis of Edwardsiella tarda.
Genome sequencing of fish pathogen E. tarda EIB202 reveals that the gene locus qseEGF, which encodes a novel two-component system QseEF, were located in E. tarda. The transcription of qseE, qseF and qseG was firstly characterized to be cotranscribed by reverse-transcribed PCR (RT-PCR). The mutant strains ΔqseE, ΔqseF and ΔqseG were constructed with in-frame deletion strategy. Compared with the wild type, all of the mutants showed attenuated virulence and impaired intracellular survival capabilities. Deletion in qseE, qseF and qseG resulted in different effects on hemolysin production in E. tarda. qRT-PCR results indicated that QseEF played a role in regulation of secretion systems, which in turn affected the virulence of E. tarda.
The results manifested that QseEF system affected the virulence in E. tarda EIB202 by controlling the secretion system and hemolysin production. QseE, QseG and QseF in E. tarda serve for the physiological fitness and pathogenesis related to the bacterial survival in macrophage and in vivo of fish.
The present results suggested that the important role of two-component system QseEF in regulation of E. tarda pathogenesis and its potential for attenuated live vaccine construction.
本研究旨在揭示基因座 qseEGF 在迟缓爱德华氏菌发病机制中的作用。
鱼类病原体迟缓爱德华氏菌 EIB202 的基因组测序表明,编码新型双组分系统 QseEF 的基因座 qseEGF 位于迟缓爱德华氏菌中。通过反转录 PCR(RT-PCR)首次对 qseE、qseF 和 qseG 的转录进行了特征描述,证明它们是共转录的。采用框内缺失策略构建了 qseE、qseF 和 qseG 的缺失突变株。与野生型相比,所有突变株的毒力均减弱,细胞内存活能力受损。qseE、qseF 和 qseG 的缺失对迟缓爱德华氏菌溶血素的产生有不同的影响。qRT-PCR 结果表明,QseEF 在调节分泌系统中发挥作用,进而影响迟缓爱德华氏菌的毒力。
结果表明,QseEF 系统通过控制分泌系统和溶血素的产生来影响迟缓爱德华氏菌 EIB202 的毒力。迟缓爱德华氏菌中的 QseE、QseG 和 QseF 与细菌在巨噬细胞内和鱼类体内的生存相关的生理适应性和发病机制有关。
本研究结果表明,双组分系统 QseEF 在调节迟缓爱德华氏菌发病机制中的重要作用及其作为减毒活疫苗构建的潜力。