Debowski Aleksandra W, Walton Senta M, Chua Eng-Guan, Tay Alfred Chin-Yen, Liao Tingting, Lamichhane Binit, Himbeck Robyn, Stubbs Keith A, Marshall Barry J, Fulurija Alma, Benghezal Mohammed
Helicobacter pylori Research Laboratory, Marshall Centre for Infectious Disease Research and Training, School of Biomedical Sciences, University of Western Australia, Nedlands, Western Australia, Australia.
Ondek Pty. Ltd., Marshall Centre for Infectious Disease Research and Training, School of Biomedical Sciences, University of Western Australia, Nedlands, Western Australia, Australia.
PLoS Pathog. 2017 Jun 23;13(6):e1006464. doi: 10.1371/journal.ppat.1006464. eCollection 2017 Jun.
Helicobacter pylori infection causes chronic active gastritis that after many years of infection can develop into peptic ulceration or gastric adenocarcinoma. The bacterium is highly adapted to surviving in the gastric environment and a key adaptation is the virulence factor urease. Although widely postulated, the requirement of urease expression for persistent infection has not been elucidated experimentally as conventional urease knockout mutants are incapable of colonization. To overcome this constraint, conditional H. pylori urease mutants were constructed by adapting the tetracycline inducible expression system that enabled changing the urease phenotype of the bacteria during established infection. Through tight regulation we demonstrate that urease expression is not only required for establishing initial colonization but also for maintaining chronic infection. Furthermore, successful isolation of tet-escape mutants from a late infection time point revealed the strong selective pressure on this gastric pathogen to continuously express urease in order to maintain chronic infection. In addition to mutations in the conditional gene expression system, escape mutants were found to harbor changes in other genes including the alternative RNA polymerase sigma factor, fliA, highlighting the genetic plasticity of H. pylori to adapt to a changing niche. The tet-system described here opens up opportunities to studying genes involved in the chronic stage of H. pylori infection to gain insight into bacterial mechanisms promoting immune escape and life-long infection. Furthermore, this genetic tool also allows for a new avenue of inquiry into understanding the importance of various virulence determinants in a changing biological environment when the bacterium is put under duress.
幽门螺杆菌感染会引发慢性活动性胃炎,在多年感染后可能发展为消化性溃疡或胃腺癌。这种细菌高度适应在胃部环境中生存,一个关键的适应性因素是毒力因子尿素酶。尽管有广泛的推测,但由于传统的尿素酶基因敲除突变体无法定殖,尿素酶表达对于持续感染的必要性尚未通过实验阐明。为了克服这一限制,通过采用四环素诱导表达系统构建了条件性幽门螺杆菌尿素酶突变体,该系统能够在已建立的感染过程中改变细菌的尿素酶表型。通过严格调控,我们证明尿素酶表达不仅对于建立初始定殖是必需的,而且对于维持慢性感染也是必需的。此外,从感染后期成功分离出四环素逃逸突变体,揭示了这种胃部病原体为维持慢性感染而持续表达尿素酶所面临的强大选择压力。除了条件性基因表达系统中的突变外,还发现逃逸突变体在其他基因中存在变化,包括替代RNA聚合酶西格玛因子fliA,这突出了幽门螺杆菌适应不断变化的生态位的遗传可塑性。本文所述的四环素系统为研究参与幽门螺杆菌感染慢性阶段的基因提供了机会,以深入了解细菌促进免疫逃逸和终身感染的机制。此外,这种遗传工具还为在细菌处于胁迫状态下不断变化的生物环境中理解各种毒力决定因素的重要性开辟了一条新的研究途径。