Casabona M Guillermina, Buchanan Grant, Zoltner Martin, Harkins Catriona P, Holden Matthew T G, Palmer Tracy
Division of Molecular Microbiology School of Life Sciences, University of Dundee, Dundee, UK.
School of Medicine, University of St Andrews, St Andrews, KY16 9TF, UK.
Microbiology (Reading). 2017 Dec;163(12):1851-1863. doi: 10.1099/mic.0.000580.
Type VII secretion systems (T7SS) are found in many bacteria and secrete proteins involved in virulence and bacterial competition. In the small ubiquitin-like EsaB protein has been previously implicated as having a regulatory role in the production of the EsxC substrate. Here we show that in the RN6390 strain, EsaB does not genetically regulate production of any T7 substrates or components, but is indispensable for secretion activity. Consistent with EsaB being an essential component of the T7SS, loss of either EsaB or EssC are associated with upregulation of a common set of iron acquisition genes. However, a further subset of genes were dysregulated only in the absence of EsaB. Quantitative western blotting indicates that EsaB is present at very low levels in cells. Substitution of a highly conserved threonine for alanine or arginine resulted in a loss of EsaB activity and destabilisation of the protein. Taken together our findings show that EsaB is essential for T7SS activity in RN6390.
VII型分泌系统(T7SS)存在于许多细菌中,可分泌与毒力和细菌竞争相关的蛋白质。此前已表明,小泛素样蛋白EsaB在EsxC底物的产生中具有调节作用。在此我们表明,在RN6390菌株中,EsaB在基因层面上并不调节任何T7底物或组分的产生,但对于分泌活性却是不可或缺的。与EsaB是T7SS的必需组分一致,EsaB或EssC的缺失均与一组共同的铁获取基因的上调相关。然而,仅在缺乏EsaB的情况下,另有一组基因的表达出现失调。定量蛋白质免疫印迹表明,EsaB在细胞中的含量非常低。将一个高度保守的苏氨酸替换为丙氨酸或精氨酸会导致EsaB活性丧失以及蛋白质不稳定。综合我们的研究结果表明,EsaB对于RN6390中的T7SS活性至关重要。