Department of Microbiology and Immunology, University of Rochester School of Medicine and Dentistry, Rochester, New York 14642, USA.
Infect Immun. 2010 Jun;78(6):2554-70. doi: 10.1128/IAI.01073-09. Epub 2010 Apr 12.
Strain AM-19226 is a pathogenic non-O1/non-O139 serogroup Vibrio cholerae strain that does not encode the toxin-coregulated pilus or cholera toxin but instead causes disease using a type three secretion system (T3SS). Two genes within the T3SS pathogenicity island, herein named vttR(A) (locus tag A33_1664) and vttR(B) (locus tag A33_1675), are predicted to encode proteins that show similarity to the transcriptional regulator ToxR, which is found in all strains of V. cholerae. Strains with a deletion of vttR(A) or vttR(B) showed attenuated colonization in vivo, indicating that the T3SS-encoded regulatory proteins play a role in virulence. lacZ transcriptional reporter fusions to intergenic regions upstream of genes encoding the T3SS structural components identified growth in the presence of bile as a condition that modulates gene expression. Under this condition, VttR(A) and VttR(B) were necessary for maximal gene expression. In contrast, growth in bile did not substantially alter the expression of a reporter fusion to the vopF gene, which encodes an effector protein. Increased vttR(B) reporter fusion activity was observed in a DeltavttR(B) strain background, suggesting that VttR(B) may regulate its own expression. The collective results are consistent with the hypothesis that T3SS-encoded regulatory proteins are essential for pathogenesis and control the expression of selected T3SS genes.
菌株 AM-19226 是一种致病性非 O1/非 O139 血清群霍乱弧菌菌株,它不编码毒素调节菌毛或霍乱毒素,而是使用 III 型分泌系统(T3SS)引起疾病。T3SS 致病岛中的两个基因,在此命名为 vttR(A)(基因座标签 A33_1664)和 vttR(B)(基因座标签 A33_1675),预测编码与 ToxR 转录调节剂具有相似性的蛋白质,ToxR 存在于所有霍乱弧菌菌株中。vttR(A)或 vttR(B)缺失的菌株在体内定植能力减弱,表明 T3SS 编码的调节蛋白在毒力中发挥作用。与编码 T3SS 结构成分的基因间区上游的 lacZ 转录报告基因融合,鉴定出在胆汁存在的情况下生长是调节基因表达的条件。在这种条件下,VttR(A)和 VttR(B)是最大基因表达所必需的。相比之下,胆汁生长并没有实质性地改变编码效应蛋白的 vopF 基因的报告融合物的表达。在 DeltavttR(B) 菌株背景下观察到 vttR(B)报告融合物活性增加,表明 VttR(B)可能调节其自身表达。总的来说,结果与假设一致,即 T3SS 编码的调节蛋白对发病机制至关重要,并控制选定的 T3SS 基因的表达。