Nocker Andreas, Camper Anne K
Center for Biofilm Engineering, Montana State University, Bozeman, MT 59717, USA.
FEMS Microbiol Lett. 2009 Feb;291(2):137-42. doi: 10.1111/j.1574-6968.2008.01429.x. Epub 2008 Nov 21.
This article elaborates on possible future directions for microbial viability assessment using nucleic acid-modifying compounds in combination with DNA- (and potentially RNA-) amplification technologies. Bacteria were traditionally considered viable when they could be cultured, whereas today's viability concept is based on the presence of some form of metabolic activity, responsiveness, RNA transcripts that tend to degrade rapidly after cell death, or of an intact membrane. The latter criterion was the focus of recent approaches to limit detection to intact cells using ethidium monoazide or propidium monoazide. Membrane integrity must, however, be considered as a very conservative criterion for microbial viability. The new concept presented here aims at limiting nucleic acid-based detection to cells with an active metabolism, which might be a more appropriate viability criterion. To selectively detect only cells with metabolic and respiratory activity (while excluding inactive dead cells from detection), we suggest the use of 'activity-labile compounds'. In addition to their potential usefulness for viability assessment, these new compounds could also be beneficial for selectively amplifying nucleic acids of cells that have metabolic activities of interest. This preferential detection of microorganisms with certain metabolic capabilities is referred to as 'molecular enrichment' in distinction to 'growth enrichment'.
本文阐述了使用核酸修饰化合物结合DNA(以及潜在的RNA)扩增技术进行微生物活力评估的未来可能方向。传统上,当细菌能够培养时就被认为是有活力的,而如今的活力概念基于某种形式的代谢活性、反应能力、细胞死亡后往往迅速降解的RNA转录本或完整的细胞膜。后一个标准是最近使用单叠氮化乙锭或单叠氮化丙锭将检测限制在完整细胞上的方法的重点。然而,膜完整性必须被视为微生物活力的一个非常保守的标准。这里提出的新概念旨在将基于核酸的检测限制在具有活跃代谢的细胞上,这可能是一个更合适的活力标准。为了仅选择性地检测具有代谢和呼吸活性的细胞(同时排除无活性的死细胞),我们建议使用“活性不稳定化合物”。除了它们对活力评估的潜在用途外,这些新化合物还可能有利于选择性地扩增具有感兴趣代谢活性的细胞的核酸。这种对具有特定代谢能力的微生物的优先检测与“生长富集”不同,被称为“分子富集”。