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冷诱导的不可培养创伤弧菌核酸的原位分析。

In situ analysis of nucleic acids in cold-induced nonculturable Vibrio vulnificus.

作者信息

Weichart D, McDougald D, Jacobs D, Kjelleberg S

机构信息

School of Microbiology and Immunology, University of New South Wales, Sydney, Australia.

出版信息

Appl Environ Microbiol. 1997 Jul;63(7):2754-8. doi: 10.1128/aem.63.7.2754-2758.1997.

Abstract

Low-temperature-induced nonculturable cells of the human pathogenic bacterium Vibrio vulnificus retained significant amounts of nucleic acids for more than 5 months. Upon permeabilization of fixed cells, however, an increasing number of cold-incubated cells released the nucleic acids. This indicates substantial degradation of DNA and RNA in nonculturable cells prior to fixation. Treatment of permeabilized cells with DNase and RNase allowed differential staining of DNA and RNA with the nucleic acid dye 4',6-diamidino-2-phenylindole (DAPI). Epifluorescence microscopy revealed that the could-induced nonculturable populations of V. vulnificus are highly heterogeneous with regard to their nucleic acid content. The fraction of nonculturable cells which maintained DNA and RNA structures decreased gradually during cold incubation. After 5 months at 5 degrees C, less than 0.05% of the cells could be observed to retain DNA and RNA. In parallel with the loss of nucleic acids, an increase in the concentrations of UV-absorbing material in the culture supernatants was observed in nonculturable-cell suspensions. It is hypothesized that there are two phases of the formation of nonculturable cells of V. vulnificus: the first involves a loss of culturability with maintenance of cellular integrity and intact RNA and DNA (and thus possibly viability), and the second is typified by a gradual degradation of nucleic acids, the products of which partly remain inside the cells and partly diffuse into the extracellular space. A small number of nonculturable cells, however, retain DNA and RNA, and thus may be viable despite having reduced culturability.

摘要

人类致病细菌创伤弧菌经低温诱导形成的不可培养细胞在5个多月的时间里保留了大量核酸。然而,固定细胞经通透处理后,越来越多经低温培养的细胞释放出核酸。这表明在固定之前,不可培养细胞中的DNA和RNA已大量降解。用DNA酶和RNA酶处理通透细胞后,可用核酸染料4',6-二脒基-2-苯基吲哚(DAPI)对DNA和RNA进行差异染色。落射荧光显微镜观察显示,创伤弧菌经低温诱导形成的不可培养群体在核酸含量方面具有高度异质性。在低温培养过程中,维持DNA和RNA结构的不可培养细胞比例逐渐下降。在5℃下培养5个月后,可观察到只有不到0.05%的细胞保留DNA和RNA。与核酸损失同时,在不可培养细胞悬液的培养上清液中观察到吸光物质浓度增加。据推测,创伤弧菌不可培养细胞的形成有两个阶段:第一阶段是失去可培养性,但细胞完整性以及RNA和DNA保持完整(因此可能仍具有活力),第二阶段的特征是核酸逐渐降解,其产物部分保留在细胞内,部分扩散到细胞外空间。然而,少数不可培养细胞保留了DNA和RNA,因此尽管可培养性降低,但仍可能具有活力。

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