Department of Molecular Microbiology, Washington University School of Medicine St Louis, St. Louis, MO, 63110-1093, United States.
Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15219, United States.
Sci Rep. 2018 Sep 24;8(1):14254. doi: 10.1038/s41598-018-32558-0.
To achieve maximum fitness, pathogens must balance growth with tissue damage, coordinating metabolism and virulence factor expression. In the gram-positive bacterium Streptococcus pyogenes, the DNA-binding transcriptional regulator Carbon Catabolite Protein A (CcpA) is a master regulator of both carbon catabolite repression and virulence, suggesting it coordinates growth/damage balance. To examine this, two murine models were used to compare the virulence of a mutant lacking CcpA with a mutant expressing CcpA locked into its high-affinity DNA-binding conformation (CcpA). In models of acute soft tissue infection and of long-term asymptomatic mucosal colonization, both CcpA mutants displayed altered virulence, albeit with distinct growth/damage profiles. Loss of CcpA resulted in a diminished ability to grow in tissue, leading to less damage and early clearance. In contrast, constitutive DNA-binding activity uncoupled the growth/damage relationship, such that high tissue burdens and extended time of carriage were achieved, despite reduced tissue damage. These data demonstrate that growth/damage balance can be actively controlled by the pathogen and implicate CcpA as a master regulator of this relationship. This suggests a model where the topology of the S. pyogenes virulence network has evolved to couple carbon source selection with growth/damage balance, which may differentially influence pathogenesis at distinct tissues.
为了实现最佳的健康状态,病原体必须在生长和组织损伤之间取得平衡,协调新陈代谢和毒力因子的表达。在革兰氏阳性菌酿脓链球菌中,DNA 结合转录调节因子碳分解代谢物阻遏物蛋白 A(CcpA)是碳分解代谢物阻遏和毒力的主要调节因子,这表明它协调了生长/损伤平衡。为了研究这一点,使用了两种小鼠模型来比较缺乏 CcpA 的突变体和表达 CcpA 的突变体(CcpA 锁定在其高亲和力 DNA 结合构象)的毒力。在急性软组织感染和长期无症状黏膜定植的模型中,两种 CcpA 突变体的毒力都发生了改变,尽管它们的生长/损伤特征不同。CcpA 的缺失导致在组织中生长能力下降,从而导致较少的损伤和早期清除。相比之下,组成型 DNA 结合活性使生长/损伤关系脱耦,尽管组织损伤减少,但仍能达到高组织负担和延长的携带时间。这些数据表明,病原体可以主动控制生长/损伤平衡,并表明 CcpA 是这种关系的主要调节因子。这表明了一个模型,其中酿脓链球菌毒力网络的拓扑结构已经进化为将碳源选择与生长/损伤平衡相耦合,这可能会对不同组织的发病机制产生不同的影响。