Stahl Martin, Frirdich Emilisa, Vermeulen Jenny, Badayeva Yuliya, Li Xiaoxia, Vallance Bruce A, Gaynor Erin C
Division of Gastroenterology, BC's Children's Hospital, the Child and Family Research Institute and the University of British Columbia, Vancouver, British Columbia, Canada.
Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Infect Immun. 2016 Nov 18;84(12):3399-3407. doi: 10.1128/IAI.00751-16. Print 2016 Dec.
Campylobacter jejuni is a helix-shaped enteric bacterial pathogen and a common cause of gastroenteritis. We recently developed a mouse model for this human pathogen utilizing the SIGIRR-deficient mouse strain, which exhibits significant intestinal inflammation in response to intestinal C. jejuni infection. In the current study, this mouse model was used to define whether C. jejuni's characteristic helical shape plays a role in its ability to colonize and elicit inflammation in the mouse intestine. Mice were infected with the previously characterized straight-rod Δpgp1 and Δpgp2 mutant strains, along with a newly characterized curved-rod Δ1228 mutant strain. We also compared the resultant infections and pathology to those elicited by the helix-shaped wild-type C. jejuni and complemented strains. Despite displaying wild-type colonization of the intestinal lumen, the straight-rod Δpgp1 and Δpgp2 mutants were essentially nonpathogenic, while all strains with a curved or helical shape retained their expected virulence. Furthermore, analysis of C. jejuni localization within the ceca of infected mice determined that the primary difference between the rod-shaped, nonpathogenic mutants and the helix-shaped, pathogenic strains was the ability to colonize intestinal crypts. Rod-shaped mutants appeared unable to colonize intestinal crypts due to an inability to pass through the intestinal mucus layer to directly contact the epithelium. Together, these results support a critical role for C. jejuni's helical morphology in enabling it to traverse and colonize the mucus-filled intestinal crypts of their host, a necessary step required to trigger intestinal inflammation in response to C. jejuni.
空肠弯曲菌是一种螺旋状肠道细菌病原体,是肠胃炎的常见病因。我们最近利用缺乏SIGIRR的小鼠品系开发了一种针对这种人类病原体的小鼠模型,该品系在受到肠道空肠弯曲菌感染时会表现出明显的肠道炎症。在当前的研究中,这个小鼠模型被用于确定空肠弯曲菌特有的螺旋形状是否在其定殖于小鼠肠道并引发炎症的能力中发挥作用。用先前已鉴定的直杆状Δpgp1和Δpgp2突变菌株以及新鉴定的弯杆状Δ1228突变菌株感染小鼠。我们还将由此产生的感染和病理情况与螺旋状野生型空肠弯曲菌和互补菌株所引发的情况进行了比较。尽管直杆状的Δpgp1和Δpgp2突变体在肠腔中表现出野生型定殖,但它们基本上无致病性,而所有具有弯曲或螺旋形状的菌株都保留了预期的毒力。此外,对感染小鼠盲肠内空肠弯曲菌定位的分析确定,杆状非致病突变体与螺旋状致病菌株之间的主要差异在于定殖于肠道隐窝的能力。杆状突变体似乎无法定殖于肠道隐窝,因为它们无法穿过肠道黏液层直接接触上皮细胞。总之,这些结果支持空肠弯曲菌的螺旋形态在使其能够穿过并定殖于宿主充满黏液的肠道隐窝中发挥关键作用,这是触发对空肠弯曲菌的肠道炎症反应所需的必要步骤。