Key Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China.
Sci Rep. 2018 May 2;8(1):6895. doi: 10.1038/s41598-018-25271-5.
Francisella tularensis is a facultative intracellular Gram-negative bacterium that causes the zoonotic disease tularemia. We identified the transcription elongation factor GreA as a virulence factor in our previous study, but its role was not defined. Here, we investigate the effects of the inactivation of the greA gene, generating a greA mutant of F. tularensis subsp. novicida. Inactivation of greA impaired the bacterial invasion into and growth within host cells, and subsequently virulence in mouse infection model. A transcriptomic analysis (RNA-Seq) showed that the loss of GreA caused the differential expression of 196 bacterial genes, 77 of which were identified as virulence factors in previous studies. To confirm that GreA regulates the expression of virulence factors involved in cell invasion by Francisella, FTN_1186 (pepO) and FTN_1551 (ampD) gene mutants were generated. The ampD deletion mutant showed reduced invasiveness into host cells. These results strongly suggest that GreA plays an important role in the pathogenesis of Francisella by affecting the expression of virulence genes and provide new insights into the complex regulation of Francisella infection.
土拉弗朗西斯菌是一种兼性细胞内革兰氏阴性细菌,可引起人畜共患的土拉热。在我们之前的研究中,我们将转录延伸因子 GreA 鉴定为一种毒力因子,但它的作用尚未确定。在这里,我们研究了缺失 greA 基因的影响,从而生成了弗氏土拉弗朗西斯菌亚种 novicida 的 greA 突变体。greA 的失活削弱了细菌对宿主细胞的入侵和生长能力,进而降低了在小鼠感染模型中的毒力。转录组分析(RNA-Seq)显示,GreA 的缺失导致 196 个细菌基因的差异表达,其中 77 个基因在之前的研究中被鉴定为毒力因子。为了证实 GreA 通过调节细胞入侵相关的毒力因子的表达来调控土拉弗朗西斯菌,我们生成了 FTN_1186(pepO)和 FTN_1551(ampD)基因缺失突变体。ampD 缺失突变体对宿主细胞的入侵能力降低。这些结果强烈表明,GreA 通过影响毒力基因的表达在弗朗西斯菌的发病机制中发挥重要作用,并为弗朗西斯菌感染的复杂调控提供了新的见解。