2010 Annual Science Report
Montana State University Reporting | SEP 2009 – AUG 2010
Viral Ecology and Evolution
Project Summary
We are interested in studying the viruses inhabiting the acidic hot springs within Yellowstone. We hypothesize that further understanding the viral dynamics, diversity, and composition will aid in the understanding of early Earth and how cellular life may have evolved.
Project Progress
Our working hypothesis is that viruses are key drivers in the evolution of present day cellular life and likely played an essential role in the evolution of early life on Earth. We propose that by understanding the diversity of viruses on present day Earth, we will be better able to reconstruct the evolution of viruses and their cellular hosts. A glaring deficiency in our knowledge of virus diversity is associated with viruses that infect hosts belonging to the domain Archaea. We have become experts in the isolation of viruses from hyperthermophilic archaeal hosts that dominate high temperature acidic environments found in hot springs within Yellowstone National Park USA and other thermal sites worldwide. Over the past year, we have expanded our search for archaeal viruses from extreme environments found in high temperature acidic environments in Yellowstone National Park. We have made two major advances over the past year. The first of which was the development of an entirely new way to detect previously unknown viruses using DNA sequences embedded in CRISPR loci within the cellular genomes. This new approach now allows us to access literally thousands of new viruses previously unknown to science. The second major advancement was the preliminary assembly of the first known archaeal RNA virus genomes. Our analysis of these genomes over the coming years will hopefully provide new insights into the evolution of RNA viruses and possibly the role that early RNA-like viruses may have played in the early evolution of life on Earth.
Publications
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Banfield, J. F., & Young, M. (2009). Variety—the Splice of Life—in Microbial Communities. Science, 326(5957), 1198–1199. doi:10.1126/science.1181501
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Snyder, J. C., & Young, M. J. (2011). Potential role of cellular ESCRT proteins in the STIV life cycle. Biochemical Society Transactions, 39(1), 107–110. doi:10.1042/bst0390107
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Snyder, J. C., Bateson, M. M., Lavin, M., & Young, M. J. (2010). Use of Cellular CRISPR (Clusters of Regularly Interspaced Short Palindromic Repeats) Spacer-Based Microarrays for Detection of Viruses in Environmental Samples. Applied and Environmental Microbiology, 76(21), 7251–7258. doi:10.1128/aem.01109-10
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PROJECT INVESTIGATORS:
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PROJECT MEMBERS:
Mark Young
Project Investigator
Jamie Snyder
Postdoc
Ben Bolduc
Doctoral Student
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RELATED OBJECTIVES:
Objective 5.1
Environment-dependent, molecular evolution in microorganisms
Objective 5.2
Co-evolution of microbial communities
Objective 5.3
Biochemical adaptation to extreme environments
Objective 6.1
Effects of environmental changes on microbial ecosystems
Objective 6.2
Adaptation and evolution of life beyond Earth