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Enumeration and Cell Cycle Analysis of Natural Populations of Marine Picoplankton by Flow Cytometry Using the Nucleic Acid Stain SYBR Green I.利用核酸染料 SYBR Green I 通过流式细胞术对海洋微微型浮游植物自然种群进行计数和细胞周期分析。
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通过流式细胞术对培养物和自然样本中的海洋病毒进行计数。

Enumeration of marine viruses in culture and natural samples by flow cytometry.

作者信息

Marie D, Brussaard CPD, Thyrhaug R, Bratbak G, Vaulot D

机构信息

Station Biologique, CNRS, INSU and Universite Pierre et Marie Curie, 29682 Roscoff cedex, France.

出版信息

Appl Environ Microbiol. 1999 Jan;65(1):45-52. doi: 10.1128/AEM.65.1.45-52.1999.

DOI:10.1128/AEM.65.1.45-52.1999
PMID:9872758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC90981/
Abstract

Flow cytometry (FCM) was successfully used to enumerate viruses in seawater after staining with the nucleic acid-specific dye SYBR Green-I. The technique was first optimized by using the Phaeocystis lytic virus PpV-01. Then it was used to analyze natural samples from different oceanic locations. Virus samples were fixed with 0.5% glutaraldehyde and deep frozen for delayed analysis. The samples were then diluted in Tris-EDTA buffer and analyzed in the presence of SYBR Green-I. A duplicate sample was heated at 80 degreesC in the presence of detergent before analysis. Virus counts obtained by FCM were highly correlated to, although slightly higher than, those obtained by epifluorescence microscopy or by transmission electron microscopy (r = 0.937, n = 14, and r = 0.96, n = 8, respectively). Analysis of a depth profile from the Mediterranean Sea revealed that the abundance of viruses displayed the same vertical trend as that of planktonic cells. FCM permits us to distinguish between at least two and sometimes three virus populations in natural samples. Because of its speed and accuracy, FCM should prove very useful for studies of virus infection in cultures and should allow us to better understand the structure and dynamics of virus populations in natural waters.

摘要

在用核酸特异性染料SYBR Green-I染色后,流式细胞术(FCM)成功用于对海水中的病毒进行计数。该技术首先通过使用棕囊藻裂解病毒PpV-01进行优化。然后用于分析来自不同海洋位置的天然样品。病毒样品用0.5%戊二醛固定并深度冷冻以便延迟分析。然后将样品在Tris-EDTA缓冲液中稀释,并在SYBR Green-I存在的情况下进行分析。在分析之前,将一个重复样品在有去污剂存在的情况下于80℃加热。通过流式细胞术获得的病毒计数与通过落射荧光显微镜或透射电子显微镜获得的计数高度相关,尽管略高(相关系数分别为r = 0.937,n = 14和r = 0.96,n = 8)。对地中海深度剖面的分析表明,病毒丰度与浮游细胞呈现相同的垂直趋势。流式细胞术使我们能够区分天然样品中至少两个,有时是三个病毒群体。由于其速度和准确性,流式细胞术对于研究培养物中的病毒感染应该非常有用,并且应该使我们能够更好地了解天然水体中病毒群体的结构和动态。