Virulence regulation of cel-EIIB protein mediated PTS system in Streptococcus agalactiae in Nile tilapia
文献类型: 外文期刊
作者: Xu, Jun 1 ; Xie, Yun-Dan 3 ; Liu, Ling 1 ; Guo, Song 1 ; Su, You-Lu 2 ; Li, An-Xing 1 ;
作者机构: 1.Sun Yat Sen Univ, State Key Lab Biocontrol, Guangdong Prov Key Lab Aquat Econ Anim, Guangzhou, Guangdong, Peoples R China
2.Chinese Acad Fishery Sci, South China Sea Fisheries Res Inst, Minist Agr, Key Lab South China Sea Fishery Resources Exploit, Guangzhou, Guangdong, Peoples R China
3.Tianjin Agr Univ, Coll Fisheries, Tianjin, Peoples R China
关键词: biofilm formation; cel-EIIB protein; colonization; Streptococcus agalactiae; virulence regulation
期刊名称:JOURNAL OF FISH DISEASES ( 影响因子:2.767; 五年影响因子:2.689 )
ISSN: 0140-7775
年卷期: 2019 年 42 卷 1 期
页码:
收录情况: SCI
摘要: Streptococcus agalactiae is a major pathogen of tilapia causing significant economic losses for the global aquatic industry yearly. To elucidate the role of cel-EIIB protein-mediated phosphotransferase systems (PTS) in the virulence regulation of S. agalactiae, cel-EIIB gene deletion in a virulent strain THN0901 was achieved by homologous recombination. The cellobiose utilization of ocel-EIIB strain was significantly decreased relative to S.a.THN0901 strain incubating in LB with 10 mg/ml cellobiose (p < 0.05). The biofilm formation ability of ocel-EIIB strain was also significantly decreased when cultured in BHI medium (p < 0.05). Under a lower infection dose, the accumulative mortality of tilapia caused by ocel-EIIB strain was dramatically decreased (20%), of which S.a.THN0901 strain and ocel-EIIB::i strain were 53.33% and 50%, respectively. The competition experience using tilapia model indicated the invasion and colonization ability of ocel-EIIB strain was significantly weaker than that of S.a.THN0901 strain (p < 0.05). Compared to ocel-EIIB::i strain, the mRNA expression of csrS, csrR, rgfA, rgfC, bgrR and bgrS was significantly downregulated in ocel-EIIB strain (p < 0.05). In conclusion, cel-EIIB protein-mediated cel-PTS not only contributes to biofilm formation and virulence regulation, but also plays an important role in the invasion and colonization of S. agalactiae.
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