Department of Marine Biology, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria.
Appl Environ Microbiol. 2010 Oct;76(20):6724-32. doi: 10.1128/AEM.00531-10. Epub 2010 Aug 20.
The study site located in the Mediterranean Sea was visited eight times in 2005 and 2006 to collect samples from the epipelagic (5 m), mesopelagic (200 m, 600 m), and bathypelagic (1,000 m, 2,000 m) zones. Randomly amplified polymorphic DNA PCR (RAPD-PCR) analysis was used to obtain fingerprints from microbial and viral size fractions using two different primers each. Depending on the primer used, the number of bands in the water column varied between 12 to 24 and 6 to 19 for the microbial size fraction and between 16 to 26 and 8 to 22 for the viral size fraction. The majority of sequences from the microbial fraction was related to Alphaproteobacteria, Cyanobacteria, Gammaproteobacteria, Firmicutes, and Eukaryota. Only 9% of sequences obtained from the viral fraction were of identifiable viral origin; however, 76% of sequences had no close relatives in the nr database of GenBank. Only 20.1% of complete phage genomes tested in silico resulted in potential RAPD-PCR products, and only 12% of these were targeted by both primers. Also, in silico analysis indicated that RAPD-PCR profiles obtained by the two different primers are largely representative of two different subsets of the viral community. Also, correlation analyses and Mantel tests indicate that the links between changes in the microbial and viral community were strongest in the bathypelagic. Thus, these results suggest a strong codevelopment of virus and host communities in deep waters. The data also indicate that virus communities in the bathypelagic zone can exhibit substantial temporal dynamics.
该研究地点位于地中海,在 2005 年和 2006 年期间,共 8 次前往该地点,采集从表水层(5 米)、中层(200 米、600 米)和深海层(1000 米、2000 米)采集样本。使用两种不同的引物,通过随机扩增多态性 DNA PCR(RAPD-PCR)分析从微生物和病毒大小分数中获得指纹。根据使用的引物,水柱中的带数在微生物大小分数中从 12 到 24 不等,从 6 到 19 不等,在病毒大小分数中从 16 到 26 不等,从 8 到 22 不等。微生物部分的大多数序列与α变形菌门、蓝细菌、γ变形菌门、Firmicutes 和真核生物有关。仅从病毒部分获得的 9%序列具有可识别的病毒来源;然而,76%的序列在 GenBank 的 nr 数据库中没有密切相关的序列。仅在计算机上测试的 20.1%完整噬菌体基因组产生潜在的 RAPD-PCR 产物,并且只有 12%的产物被两个引物靶向。此外,计算机分析表明,两种不同引物获得的 RAPD-PCR 图谱在很大程度上代表了病毒群落的两个不同子集。此外,相关分析和 Mantel 检验表明,在深海层中,微生物和病毒群落之间的变化联系最强。因此,这些结果表明,在深水中,病毒和宿主群落的发展具有很强的相关性。这些数据还表明,深海区的病毒群落可能具有显著的时间动态。