Prokaryotic and viral diversity patterns in marine plankton

• Published in: Ecological Research
• Main Authors: Fuhrman, Jed A., Griffith, John F., Schwalbach, Michael S.
• Format: Article in Journal/Newspaper
• Language: English
• Published: Wiley 2002
• Subjects: Weddell; Weddell Sea
• Online Access: http://dx.doi.org/10.1046/j.1440-1703.2002.00478.x; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1440-1703.2002.00478.x; http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1440-1703.2002.00478.x/fullpdf

Prokaryotes and viruses play critical roles in marine ecosystems, where they are both highly abundant and active. Although early work on both prokaryotes and viruses revealed little of their diversity, molecular biological approaches now allow us to break apart these ‘black boxes.’ The most revealing methods have been cloning and sequencing of 16S rRNA genes, community fingerprinting (such as terminal restriction fragment length polymorphism; TRFLP), and fluorescent in situ hybridization. Viral diversity can now be analyzed by pulsed field gel electrophoresis (PFGE) of viral genomes. The present paper summarizes recent advances in bacterial and virus diversity studies, and presents examples of measurements from polar, tropical, and temperate marine waters. Terminal restriction fragment length polymorphism shows that many of the same operationally defined prokaryotic taxa are present in polar and tropical waters, but there are also some unique to each environment. By one measure, a sample from over a Philippine coral reef had about 100 operationally defined taxa, whereas one from the open tropical Atlantic had about 50 and from the icy Weddell Sea, about 60. Pulsed field gel electrophoresis of two depth profiles, to 500 m, from Southern California, measured 2 months apart, shows striking similarities in viral genome length diversity over time, and some distinct differences with depth. The euphotic zone samples had extremely similar apparent diversity, but samples from 150 m and 500 m were different. An obvious next step is to compare the bacterial and viral diversity patterns, because theory tells us they should be related.