Tan Chen, Liu Manli, Jin Meilin, Liu Jinlin, Chen Yan, Wu Tao, Fu Ting, Bei Weicheng, Chen Huanchun
College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China.
FEMS Microbiol Lett. 2008 Jan;278(1):108-14. doi: 10.1111/j.1574-6968.2007.00980.x. Epub 2007 Nov 12.
Streptococcus suis causes disease in both pigs and humans. Many virulence genes, including mrp, ef, sly, gapdh, fbps, and hyl, are shown to contribute to S. suis pathogenesis. In this study, the differential expression of the key S. suis serotype 2 virulence-associated genes was monitored 24 and 48 h after infection of HeLa cells. Gene expression was further investigated in bacteria harvested from the blood, lungs, brains, and synovia of swine 24, 48, and 72 h postintravenous infection with S. suis serotype 2. Bacterial RNA was extracted and gene expression was monitored using real-time reverse transcriptase-PCR at various time points. The results showed that after 24 h postinfection in vivo, mrp, gapdh, fbps, and hyl were highly expressed in all organs. At 48 h postinfection, ef and sly were highly expressed in the lungs and brain. At 72 h postinfection, all genes had a high level of expression in all organs. This study provides direct evidence that S. suis serotype 2 key virulence-associated genes are differentially expressed in a time-specific or an organ-specific manner in vivo. These findings also show the dynamic distribution of gene expression. Characterization of the differential expression patterns of this subset of key virulence-associated genes facilitates further study into the importance of these genes in S. suis serotype 2 pathogenesis in pigs.
猪链球菌可导致猪和人类发病。许多毒力基因,包括mrp、ef、sly、gapdh、fbps和hyl,已被证明与猪链球菌的致病机制有关。在本研究中,监测了猪链球菌2型关键毒力相关基因在感染HeLa细胞24小时和48小时后的差异表达。在用猪链球菌2型静脉感染猪后24、48和72小时,进一步研究了从猪的血液、肺、脑和滑膜中收获的细菌中的基因表达。提取细菌RNA,并在不同时间点使用实时逆转录PCR监测基因表达。结果表明,在体内感染24小时后,mrp、gapdh、fbps和hyl在所有器官中均高表达。在感染48小时时,ef和sly在肺和脑中高表达。在感染72小时时,所有基因在所有器官中均有高水平表达。本研究提供了直接证据,表明猪链球菌2型关键毒力相关基因在体内以时间特异性或器官特异性方式差异表达。这些发现还显示了基因表达的动态分布。对这一关键毒力相关基因子集的差异表达模式进行表征,有助于进一步研究这些基因在猪链球菌2型感染猪的发病机制中的重要性。