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在海水分批培养中评估浮游病毒对古菌和细菌群落丰富度的影响。

Impact of virioplankton on archaeal and bacterial community richness as assessed in seawater batch cultures.

作者信息

Winter Christian, Smit Arjan, Herndl Gerhard J, Weinbauer Markus G

机构信息

Department of Biological Oceanography, Royal Netherlands Institute for Sea Research, Texel, The Netherlands.

出版信息

Appl Environ Microbiol. 2004 Feb;70(2):804-13. doi: 10.1128/AEM.70.2.804-813.2004.

Abstract

During cruises in the tropical Atlantic Ocean (January to February 2000) and the southern North Sea (December 2000), experiments were conducted to monitor the impact of virioplankton on archaeal and bacterial community richness. Prokaryotic cells equivalent to 10 to 100% of the in situ abundance were inoculated into virus-free seawater, and viruses equivalent to 35 to 360% of the in situ abundance were added. Batch cultures with microwave-inactivated viruses and without viruses served as controls. The apparent richness of archaeal and bacterial communities was determined by terminal restriction fragment length polymorphism (T-RFLP) analysis of PCR-amplified 16S rRNA gene fragments. Although the estimated richness of the prokaryotic communities generally was greatly reduced within the first 24 h of incubation due to confinement, the effects of virus amendment were detected at the level of individual operational taxonomic units (OTUs) in the T-RFLP patterns of both groups, Archaea and Bacteria. One group of OTUs was detected in the control samples but was absent from the virus-treated samples. This negative response of OTUs to virus amendment probably was caused by viral lysis. Additionally, we found OTUs not responding to the amendments, and several OTUs exhibited variable responses to the addition of inactive or active viruses. Therefore, we conclude that individual members of pelagic archaeal and bacterial communities can be differently affected by the presence of virioplankton.

摘要

在2000年1月至2月对热带大西洋以及2000年12月对北海南部的巡航考察期间,开展了实验以监测浮游病毒对古菌和细菌群落丰富度的影响。将相当于原位丰度10%至100%的原核细胞接种到无病毒海水中,并添加相当于原位丰度35%至360%的病毒。以经微波灭活病毒的批次培养物和无病毒的批次培养物作为对照。通过对PCR扩增的16S rRNA基因片段进行末端限制性片段长度多态性(T-RFLP)分析来确定古菌和细菌群落的表观丰富度。尽管由于受限,原核生物群落的估计丰富度在培养的最初24小时内通常大幅降低,但在古菌和细菌两组的T-RFLP图谱中,在单个操作分类单元(OTU)水平上检测到了病毒添加的影响。在对照样品中检测到一组OTU,但在病毒处理的样品中不存在。OTU对病毒添加的这种负面反应可能是由病毒裂解引起的。此外,我们发现一些OTU对添加物没有反应,并且有几个OTU对添加灭活或活性病毒表现出不同的反应。因此,我们得出结论,浮游古菌和细菌群落的个体成员受浮游病毒存在的影响可能不同。

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