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首页> 外文期刊>Aquatic Microbial Ecology >Flow cytometric enumeration of marine viral populations at low abundances
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Flow cytometric enumeration of marine viral populations at low abundances

机译:低丰度海洋病毒种群的流式细胞计数

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ABSTRACT: Flow cytometric enumeration has advanced our ability to analyze aquatic virus samples and thereby our understanding of the ecological role viruses play in the oceans. However, low virus abundances are underestimated using the current flow cytometry (FCM) protocol. Our results revealed that low dilutions (30-fold) not only decreased the total virus count but also limited the ability to differentiate between virus clusters. Here we report a simple and efficient method optimization for improving virus counts and optical resolution at low abundances. Raising the pH of the Tris-EDTA (TE) buffer to 8.2 successfully countered the effect of insufficient buffering capacity at low dilutions, which is caused by the higher proportion of acidic glutaraldehyde fixative in the final sample. The higher buffer pH did not interfere with virus counts at higher dilutions. We therefore recommend amendment of the standard FCM aquatic virus enumeration protocol using a TE buffer with pH 8.2 as a simple and efficient improvement.
机译:摘要:流式细胞仪枚举提高了我们分析水生病毒样品的能力,因此我们了解了病毒在海洋中的生态作用。但是,使用当前的流式细胞仪(FCM)协议低估了病毒的低丰度。我们的结果表明,低稀释度(<30倍)不仅减少了病毒总数,而且限制了区分病毒簇的能力。在这里,我们报告了一种简单有效的方法优化方法,用于在低丰度条件下提高病毒计数和光学分辨率。将Tris-EDTA(TE)缓冲液的pH值提高到8.2,成功地抵消了低稀释度时缓冲能力不足的影响,这是由于最终样品中酸性戊二醛固定剂的比例较高所致。较高的缓冲液pH值不会在较高稀释度时干扰病毒计数。因此,我们建议使用pH 8.2的TE缓冲液修改标准FCM水生病毒枚举规程,以实现简单有效的改进。

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