Department of Chemistry and Biomolecular Sciences, Centre for Chemical and Synthetic Biology, University of Ottawa, 10 Marie-Curie Private, Ottawa K1N 6N5, Canada; Life Sciences Division, National Research Council of Canada, 100 Sussex Drive, Ottawa K1A 0R6, Canada.
Health Canada, Bureau of Microbial Hazards, Ottawa K1A 0K9, Canada.
Cell Chem Biol. 2017 Aug 17;24(8):1048-1055.e3. doi: 10.1016/j.chembiol.2017.06.016. Epub 2017 Jul 27.
Pathogenic bacteria can be a major cause of illness from environmental sources as well as the consumption of contaminated products, giving rise to public health concerns globally. The surveillance of such living organisms in food and water supplies remains an important challenge in mitigating their deleterious societal effects. Here, we have developed an optimized bioorthogonal non-canonical amino acid tagging approach to the imaging, capture, and interrogation of shigatoxigenic/verotoxigenic Escherichia coli (VTEC) and Listeria that enables the distinction between living wild-type pathogenic bacteria. The approaches utilize homopropargylglycine (HPG), as well as optimized growth media, that restricts endogenous methionine biosynthesis in a variety of species of public health concern. Endogenous methionine residues are then replaced with HPG, which can then be modified using a myriad of compatible bioorthogonal reactions for tagging of exclusively live bacteria. The methods reported allow for the very rapid screening and identification of living pathogenic organisms.
病原细菌可能是环境来源以及食用受污染产品致病的主要原因,引起了全球公共卫生关注。监测食品和水源中的这些生物仍然是减轻其对社会有害影响的重要挑战。在这里,我们开发了一种优化的生物正交非天然氨基酸标记方法,用于对志贺毒素/肠毒素大肠杆菌(VTEC)和李斯特菌进行成像、捕获和检测,从而能够区分活的野生型致病菌。这些方法利用了同型丙炔基甘氨酸(HPG)和优化的生长培养基,限制了多种公共卫生关注物种中的内源性蛋氨酸生物合成。然后用 HPG 取代内源性蛋氨酸残基,然后可以使用多种相容的生物正交反应对其进行修饰,用于仅对活细菌进行标记。所报道的方法允许非常快速地筛选和鉴定活的致病生物。