Lemos José A, Nascimento Marcelle M, Lin Vanessa K, Abranches Jacqueline, Burne Robert A
Department of Microbiology and Immunology and Center for Oral Biology, University of Rochester Medical Center, Rochester, New York 14642, USA.
J Bacteriol. 2008 Aug;190(15):5291-9. doi: 10.1128/JB.00288-08. Epub 2008 Jun 6.
The RelA, RelP, and RelQ enzymes are responsible for the production of the alarmone (p)ppGpp in Streptococcus mutans. A strain lacking all three synthetases (DeltarelAPQ) does not grow in minimal medium lacking the branched-chain amino acids (BCAA) leucine or valine but grows well if isoleucine is also omitted. Here, we investigated whether there was a correlation between growth in the absence of leucine and valine with (p)ppGpp pools and the activation of CodY. By using a combination of single, double, and triple mutants lacking the (p)ppGpp synthetase enzymes, we demonstrated that the ability to grow in the absence of leucine or valine required basal levels of (p)ppGpp production by RelP and RelQ. The introduction of a codY mutation into the DeltarelAPQ strain fully restored growth in medium lacking leucine or valine, revealing that the growth-defective phenotype of DeltarelAPQ was directly linked to CodY. Lowering GTP levels through the addition of decoyinine did not alleviate CodY repression or affect the expression of genes involved in BCAA biosynthesis, suggesting that S. mutans CodY is not activated by GTP. The results of phenotypic studies revealed that the codY mutant had a reduced capacity to form biofilms and that its growth was more sensitive to low pH, showing a role for CodY in two key virulence properties of S. mutans. Microarray results revealed the extent of the CodY regulon. Notably, the identification of putative CodY-binding boxes upstream of genes that were downregulated in the codY mutant indicates that CodY may also function as a transcriptional activator in S. mutans.
RelA、RelP和RelQ酶负责在变形链球菌中产生警报素(p)ppGpp。缺乏所有三种合成酶的菌株(ΔrelAPQ)在缺乏支链氨基酸(BCAA)亮氨酸或缬氨酸的基本培养基中无法生长,但如果同时省略异亮氨酸则生长良好。在此,我们研究了在缺乏亮氨酸和缬氨酸的情况下生长与(p)ppGpp库以及CodY激活之间是否存在相关性。通过使用缺乏(p)ppGpp合成酶的单突变体、双突变体和三突变体的组合,我们证明了在缺乏亮氨酸或缬氨酸的情况下生长的能力需要RelP和RelQ产生基础水平的(p)ppGpp。将codY突变引入ΔrelAPQ菌株可完全恢复其在缺乏亮氨酸或缬氨酸的培养基中的生长,这表明ΔrelAPQ的生长缺陷表型与CodY直接相关。通过添加脱氧精胍菌素降低GTP水平并不能减轻CodY的抑制作用,也不会影响参与BCAA生物合成的基因的表达,这表明变形链球菌的CodY不会被GTP激活。表型研究结果表明,codY突变体形成生物膜的能力降低,其生长对低pH更敏感,这表明CodY在变形链球菌的两个关键毒力特性中发挥作用。微阵列结果揭示了CodY调控子的范围。值得注意的是,在codY突变体中下调的基因上游鉴定出推定的CodY结合框,这表明CodY在变形链球菌中也可能作为转录激活因子发挥作用。