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Formation of microbial biofilm in hygienic situations: a problem of control

机译:卫生情况下微生物生物膜的形成:控制问题

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The formation of microbial biofilm presents a challenge to the establishment and maintenance of hygienic conditions in public health, the home and in industry. The use of biocides is central to the hygienic control of microbial growth. Such agents, optimised for their activity against suspended populations of cells, are spectacular in their failure to control adherent biofilm communities. To date there have been limited developments to remedy the situation. Recalcitrance of biofilm communities to anti-microbial treatments has been attributed to organisation of cells within an exopolymeric matrix. This, together with the close proximity of cells, causes reaction-diffusion limitation of the access of agent from its point of application to the deeper lying cells. These cells out-survive those on the surface of the biofilm and, if the bulk of the treatment agent is depleted or the exposure transient, will multiply and divide rapidly. Nutrients also will become depleted within the core of the developing community. This leads to the establishment of spatial gradients of growth rate and redox within the community structure. Different growth-limiting nutrients will also prevail at different points in the biofilm. These conditions provide for a plethora of phenotypes within the biofilm, each reflecting the physico-chemical micro-environment of individual cells and their proximity to neighbours. Faster-growing, more susceptible cells will generally lie on the periphery of the biofilm with slow-growing recalcitrant ones being more deeply placed. The more resistant phenotypes will survive the remainder. In both instances, at the fringes of action, selection pressures will enrich the populations with the least susceptible genotype or phenotype. Repeated chronic exposure to sub-lethal treatments might then select for a resistant population that share this resistance with third party agents. Whilst neither mechanism can provide a complete explanation of recalcitrance, together they will delay eradication of the treated population and allow other selection and regulation events to occur.
机译:微生物生物膜的形成对公共卫生,家庭和工业中卫生条件的建立和维持提出了挑战。杀菌剂的使用对于微生物生长的卫生控制至关重要。这类试剂针对悬浮细胞群的活性进行了优化,在无法控制粘附的生物膜群落方面表现出色。迄今为止,在纠正这种情况方面进展有限。生物膜群落对抗微生物治疗的顽固归因于外聚合基质内细胞的组织。这与细胞的紧密邻近性一起,导致从试剂的施用点到更深层的细胞的试剂进入的反应-扩散限制。这些细胞胜过生物膜表面上的细胞,并且,如果大部分处理剂被耗尽或暴露时间短暂,它们将迅速繁殖和分裂。在发展中社区的核心内,营养也将枯竭。这导致在社区结构内建立了增长率和氧化还原的空间梯度。不同的限制生长的营养素也将在生物膜的不同位置盛行。这些条件在生物膜内提供了许多表型,每个表型都反映了单个细胞的物理化学微环境及其与邻居的接近程度。更快生长,更易感的细胞通常将位于生物膜的外围,而生长缓慢的顽固性细胞则放置在更深的位置。更具抗性的表型将在其余部分中存活。在这两种情况下,在作用的边缘,选择压力将使最不易感的基因型或表型丰富人群。然后,反复长期暴露于亚致死作用的治疗中,可能会选择与第三方药物具有这种耐药性的耐药人群。虽然这两种机制都不能提供对顽固性的完整解释,但它们一起将延迟根除治疗人群并允许发生其他选择和调控事件。

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