Wu Chia-wei, Schmoller Shelly K, Bannantine John P, Eckstein Torsten M, Inamine Julia M, Livesey Michael, Albrecht Ralph, Talaat Adel M
The Laboratory of Bacterial Genomics, Department of Pathobiological Sciences, University of Wisconsin-Madison, 1656 Linden Drive, Madison, WI 53706-1581, USA.
Microb Pathog. 2009 Apr;46(4):222-30. doi: 10.1016/j.micpath.2009.01.010. Epub 2009 Feb 5.
Biofilm formation by pathogenic bacteria plays a key role in their pathogenesis. Previously, the pstA gene was shown to be involved in the virulence of Mycobacterium avium subspecies paratuberculosis (M. ap), the causative agent of Johne's disease in cattle and a potential risk factor for Crohn's disease. Scanning electron microscopy and colonization levels of the M. ap mutant indicated that the pstA gene significantly contributes to the ability of M. ap to form biofilms. Digital measurements taken during electron microscopy identified a unique morphology for the DeltapstA mutant, which consisted of significantly shorter bacilli than the wild type. Analysis of the lipid profiles of the mycobacterial strains identified a novel lipopeptide that was present in the cell wall extracts of wild-type M. ap, but missing from the DeltapstA mutant. Interestingly, the calf infection model suggested that pstA contributes to intestinal invasion of M. ap. Furthermore, immunoblot analysis of peptides encoded by pstA identified a specific and significant level of immunogenicity. Taken together, our analysis revealed a novel cell wall component that could contribute to biofilm formation and to the virulence and immunogenicity of M. ap. Molecular tools to better control M. ap infections could be developed utilizing the presented findings.
病原菌形成生物膜在其致病过程中起着关键作用。此前研究表明,pstA基因与副结核分枝杆菌(M. ap)的毒力有关,副结核分枝杆菌是牛约翰氏病的病原体,也是克罗恩病的潜在风险因素。扫描电子显微镜观察和M. ap突变体的定植水平表明,pstA基因对M. ap形成生物膜的能力有显著贡献。电子显微镜观察期间进行的数字测量确定了DeltapstA突变体的独特形态,其杆菌明显比野生型短。对分枝杆菌菌株脂质谱的分析鉴定出一种新型脂肽,它存在于野生型M. ap的细胞壁提取物中,但在DeltapstA突变体中缺失。有趣的是,犊牛感染模型表明pstA有助于M. ap的肠道侵袭。此外,对pstA编码肽的免疫印迹分析确定了特定且显著的免疫原性水平。综上所述,我们的分析揭示了一种新型细胞壁成分,它可能有助于生物膜形成以及M. ap的毒力和免疫原性。利用本研究结果可开发出更好控制M. ap感染的分子工具。