Grimm Dorothee, Tilly Kit, Byram Rebecca, Stewart Philip E, Krum Jonathan G, Bueschel Dawn M, Schwan Tom G, Policastro Paul F, Elias Abdallah F, Rosa Patricia A
Laboratory of Human Bacterial Pathogenesis, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 South Fourth Street, Hamilton, MT 59840, USA.
Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):3142-7. doi: 10.1073/pnas.0306845101. Epub 2004 Feb 17.
Environmentally responsive synthesis of surface proteins represents a hallmark of the infectious cycle of the Lyme disease agent, Borrelia burgdorferi. Here we created and analyzed a B. burgdorferi mutant lacking outer-surface protein C (OspC), an abundant Osp that spirochetes normally synthesize in the tick vector during the blood meal and down-regulate after transmission to the mammal. We demonstrate that B. burgdorferi strictly requires OspC to infect mice but not to localize or migrate appropriately in the tick. The induction of a spirochetal virulence factor preceding the time and host in which it is required demonstrates a developmental sequence for transmission of this arthropod-borne pathogen.
环境响应性表面蛋白的合成是莱姆病病原体伯氏疏螺旋体感染周期的一个标志。在这里,我们构建并分析了一种缺乏外表面蛋白C(OspC)的伯氏疏螺旋体突变体,OspC是一种丰富的外表面蛋白,螺旋体通常在蜱虫吸食血液期间于蜱虫载体中合成,并在传播至哺乳动物后下调表达。我们证明,伯氏疏螺旋体感染小鼠严格需要OspC,但在蜱虫中正常定位或迁移则不需要。在需要该螺旋体毒力因子的时间和宿主之前诱导该因子,证明了这种节肢动物传播病原体传播的发育顺序。