Humphreys Sue, Rowley Gary, Stevenson Andrew, Anjum Muna F, Woodward Martin J, Gilbert Stephen, Kormanec Jan, Roberts Mark
Molecualr Bacteriology Group, Institute of Comparative Medicine, Department of Veterinary Pathology, Glasgow University Veterinary School, Glasgow G61 1QH, United Kingdom.
Infect Immun. 2004 Aug;72(8):4654-61. doi: 10.1128/IAI.72.8.4654-4661.2004.
The CpxAR (Cpx) two-component regulator controls the expression of genes in response to a variety of environmental cues. The Cpx regulator has been implicated in the virulence of several gram-negative pathogens, although a role for Cpx in vivo has not been demonstrated directly. Here we investigate whether positive or negative control of gene expression by Cpx is important for the pathogenesis of Salmonella enterica serotype Typhimurium. The Cpx signal pathway in serotype Typhimurium was disrupted by insertional inactivation of the cpxA and cpxR genes. We also constitutively activated the Cpx pathway by making an internal in-frame deletion in cpxA (a cpxA* mutation). Activation of the Cpx pathway inhibited induction of the envelope stress response pathway controlled by the alternative sigma factor sigma(E) (encoded by rpoE). Conversely, the Cpx pathway was highly up-regulated (>40-fold) in a serotype Typhimurium rpoE mutant. The cpxA* mutation, but not the cpxA or the cpxR mutation, significantly reduced the capacity of serotype Typhimurium to adhere to and invade eucaryotic cells, although intracellular replication was not affected. The cpxA and cpxA* mutations significantly impaired the ability of serotype Typhimurium to grow in vivo in mice. To our knowledge, this is the first demonstration that the Cpx system is important for a bacterial pathogen in vivo.
CpxAR(Cpx)双组分调节因子可根据多种环境信号控制基因表达。尽管尚未直接证明Cpx在体内的作用,但它已被认为与几种革兰氏阴性病原体的毒力有关。在此,我们研究Cpx对基因表达的正调控或负调控对于鼠伤寒沙门氏菌血清型的发病机制是否重要。通过插入失活cpxA和cpxR基因破坏了鼠伤寒沙门氏菌血清型中的Cpx信号通路。我们还通过在cpxA中进行内部读码框缺失(cpxA突变)来组成性激活Cpx通路。Cpx通路的激活抑制了由替代sigma因子sigma(E)(由rpoE编码)控制的包膜应激反应通路的诱导。相反,在鼠伤寒沙门氏菌rpoE突变体中,Cpx通路高度上调(>40倍)。cpxA突变而非cpxA或cpxR突变显著降低了鼠伤寒沙门氏菌血清型粘附和侵入真核细胞的能力,尽管细胞内复制不受影响。cpxA和cpxA*突变显著损害了鼠伤寒沙门氏菌血清型在小鼠体内生长的能力。据我们所知,这是首次证明Cpx系统对体内细菌病原体很重要。