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丁香假单胞菌附生菌群中总活细胞与可培养细胞的关系。

Relationship of total viable and culturable cells in epiphytic populations of Pseudomonas syringae.

作者信息

Wilson M, Lindow S E

机构信息

Department of Plant Pathology, University of California, Berkeley 94720.

出版信息

Appl Environ Microbiol. 1992 Dec;58(12):3908-13. doi: 10.1128/aem.58.12.3908-3913.1992.

Abstract

The direct viable count method, used to detect viable but nonculturable bacteria in aquatic systems, was modified to examine epiphytic populations of Pseudomonas syringae. Viable-population sizes determined from the number of cells that elongated when incubated with yeast extract and nalidixic acid were compared with those determined by the conventional plate count method. The plate count method accurately determined the number of viable cells in epiphytic P. syringae populations in a state of active growth under conditions of high relative humidity. The plate count method also accurately determined the number of viable cells in P. syringae inoculum, or a growing P. syringae population, subject to desiccation stress under conditions of low relative humidity. In epiphytic populations of P. syringae older than 80 h, however, the plate count underestimated the viable-population size by about two- to fourfold, suggesting that up to 75% of the P. syringae population was nonculturable. These nonculturable cells may have entered a starvation-survival state, induced by low nutrient availability in the phyllosphere environment. Epiphytic P. syringae populations undergoing rapid size changes due to growth and death under fluctuating environmental conditions in the field should be accurately enumerated by the plate count method. However, the possible underestimation of viable-population size under some circumstances should be considered in epidemiological studies of phytopathogenic bacteria and when genetically engineered microorganisms in terrestrial ecosystems are monitored.

摘要

用于检测水生系统中活的但不可培养细菌的直接活菌计数法,经过改良后用于检测丁香假单胞菌的附生菌种群。将在与酵母提取物和萘啶酸一起孵育时伸长的细胞数量所确定的活菌种群大小,与通过传统平板计数法确定的大小进行比较。平板计数法准确地确定了在高相对湿度条件下处于活跃生长状态的附生丁香假单胞菌种群中的活菌数量。平板计数法还准确地确定了在低相对湿度条件下遭受干燥胁迫的丁香假单胞菌接种物或正在生长的丁香假单胞菌种群中的活菌数量。然而,在超过80小时的附生丁香假单胞菌种群中,平板计数法将活菌种群大小低估了约两到四倍,这表明高达75%的丁香假单胞菌种群是不可培养的。这些不可培养的细胞可能已进入饥饿存活状态,这是由叶际环境中低养分可用性诱导的。在田间波动环境条件下由于生长和死亡而经历快速大小变化的附生丁香假单胞菌种群,应通过平板计数法准确计数。然而,在植物病原菌的流行病学研究以及监测陆地生态系统中的基因工程微生物时,应考虑在某些情况下可能低估活菌种群大小的情况。

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