Vance Russell E, Zhu Jun, Mekalanos John J
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Infect Immun. 2003 May;71(5):2571-6. doi: 10.1128/IAI.71.5.2571-2576.2003.
Vibrio cholerae normally inhabits aquatic habitats but can cause a severe diarrheal illness in humans. Its arsenal of virulence factors includes a secreted hemagglutinin (HA) protease. An HA protease-deficient mutant of V. cholerae was isolated and designated E7946 mpc. E7946 mpc was found to contain a point mutation in the luxO quorum-sensing regulator. In accordance with this finding, E7946 mpc exhibits a defect in quorum sensing. The mutant luxO allele [luxO(Con)] produces a protein with a leucine-to-glutamine substitution at amino acid 104. Transfer of the luxO(Con) allele to an otherwise wild-type background was sufficient to eliminate HA protease expression; conversely, deletion of luxO(Con) from E7946 mpc restored protease activity. We demonstrate that LuxO(Con) constitutively represses the transcription of hapR, an essential positive regulator of HA protease. Interestingly, strains harboring luxO(Con) form enhanced biofilms, and enhanced biofilm formation does not appear to be dependent on reduced HA protease expression. Taken together, the results confirm the role of LuxO as a central "switch" that coordinately regulates virulence-related phenotypes such as protease production and biofilm formation.
霍乱弧菌通常栖息于水生环境,但可在人类中引起严重的腹泻疾病。其毒力因子库包括一种分泌型血凝素(HA)蛋白酶。分离出一株霍乱弧菌HA蛋白酶缺陷型突变体,并命名为E7946 mpc。发现E7946 mpc在群体感应调节因子luxO中存在一个点突变。基于这一发现,E7946 mpc在群体感应方面表现出缺陷。突变的luxO等位基因[luxO(Con)]产生一种在第104位氨基酸处由亮氨酸替换为谷氨酰胺的蛋白质。将luxO(Con)等位基因转移到其他野生型背景中足以消除HA蛋白酶的表达;相反,从E7946 mpc中删除luxO(Con)可恢复蛋白酶活性。我们证明,LuxO(Con)组成性地抑制hapR的转录,hapR是HA蛋白酶的一种重要的正调节因子。有趣的是,携带luxO(Con)的菌株形成增强的生物膜,且增强的生物膜形成似乎不依赖于HA蛋白酶表达的降低。综上所述,这些结果证实了LuxO作为一个核心“开关”的作用,它可协调调节与毒力相关的表型,如蛋白酶产生和生物膜形成。