RESEARCH ASSOCIATES |
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![]() Website: http://microbiology.oregonstate.edu/michael-kent I maintain and manage the Kent Lab zebrafish facilities. This includes coordinating daily animal care, maintaining life support/water systems, and managing lab safety and animal husbandry compliance. I also assist with research related to fish disease, which currently includes several disease transmission studies in zebrafish. |
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![]() Website: https://microbiology.science.oregonstate.edu/content/julie-alexander My research interests lie in the field of disease ecology. I am fascinated by parasites that exploit multiple hosts (myxozoans in particular) during their life cycles as a means of ensuring their reproductive success. I am interested in factors that drive and determine the outcomes of host-parasite interactions, how interactions may change under different environmental contexts, and how ecological and life history variables influence host-parasite dynamics and evolution. |
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![]() Website: http://microbiology.science.oregonstate.edu/content/dr-peter-bottomley Our lab studies the nitrogen cycle in soil, and specifically the oxidation of ammonia to nitrite. This process is known as nitrification and is carried out by ammonia oxidizing archaea and bacteria (AOA and AOB). Over the past few years my work has focused primarily on developing tools to distinguish the contributions to nitrification by AOA and AOB. Using these tools I am now investigating how different environmental conditions, such as temperature and soil water content, influence the ecology, physiology, and function of the two groups of nitrifiers in soil. This work has particular significance as global climate change becomes more pronounced. Changes in soil temperature and rainfall patterns will affect the contributions of the AOA and AOB to nitrification, and may have profound effects on nitrogen balance in agricultural and forest soils and the production of greenhouse gasses. |
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![]() Website: http://sharptonlab.cgrb.oregonstate.edu/?=gaulkec A growing body of evidence has identified the gut microbiome as an important factor involved in the maintenance of gastrointestinal homeostasis. However, relatively little is known about how routine environmental exposures might influence the structure and function of these microbial communities and how these shifts might alter host physiology. My research employs high-throughput molecular and computational techniques to evaluate the impact of environmental exposures on microbial abundance, function, and host physiology. These investigations aim to (1) identify potential microbial biomarkers of environmental exposure, (2) Define microbial functions that are associated with host health, and (3) Generate testable hypotheses about how microbial communities interact with their hosts. |
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D![]() Website: https://microbiology.science.oregonstate.edu/content/sascha-hallett I find parasites fascinating organisms and have always been drawn to the aquatic environment. Thus, I am interested in parasites of marine and freshwater fish. Most of my research has focused on one phylum - the Myxozoa and I've never dissected a fish without encountering at least one of these microscopic, spore-forming, endoparasitic metazoans. Over 2000 are found in fish world-wide and most do not harm their host, but there are several that cause serious diseases (Ceratomyxa shasta, Parvicapsula minibicornis, Myxobolus cerebralis) in the Pacific Northwest of North America. My current research focuses on answering questions about these parasites so that we can make informed management decisions and reduce their impact on native fishes. |
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![]() Website: http://microbiology.science.oregonstate.edu/dr-stephen-giovannoni My research interests lie in the understanding of the factors that shape the dynamics and interactions of microbial ecosystems. I am currently investigating the diversity of marine plankton in the North Atlantic bloom and how it changes at different depths and cycle time points. |
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Dr. Karen Dierksen, Research Associate RETIRED! Website: http://microbiology.science.oregonstate.edu/content/dr-janine-trempy My research in the Trempy Lab is focused on developing new strains of lactic acid bacteria of potential interest to the food, dairy and/or pharmaceutical industries. Our original patent strain, Lactococcus lactis Ropy 352, which produces a unique exopolysaccharide, has been licensed commercially. |
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POSTDOCS |
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Website: https://microbiology.science.oregonstate.edu/content/dr-kimberly-halsey My research investigates the microbial cycling of volatile organic compounds (VOCs) in the oceans under both controlled laboratory and field conditions using proton-transfer-reaction time-of-flight mass spectrometry (PTR-TOF/MS). PTR-TOF/MS allows for real time detection of VOCs at trace levels, through which we can determine the production and consumption rates pf VOCs by marine plankton and explore how these change under various conditions and at different stages of the bloom cycle. |
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Website: http://microbiology.science.oregonstate.edu/content/dr-jerri-bartholomew C. shasta is a freswater parasite that is responsible for "gut rot" in salmonids. Outbreaks caused by C. shasta have devastating effects in both wild and aquaculture settings. I am using immunoprecipitation coupled with mass spec to characterize the extracellular proteome of this parasite. My goal is to have a better understanding of how C. shasta senses its host and interacts with its environment and to ultimately develop therapies to prevent or control C. shasta outbreaks. |
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Website:https://sites.google.com/site/tyrelldeweber/ I am interested in understanding the effects of human activities on river systems and fish populations to help guide management and conservation. River system alteration and pollution can result in stressful conditions and increased disease, eventually leading to widespread mortality of wild adult and juvenile fish. I am working with Dr. Michael Kent in the Microbiology Program at Oregon State University investigating causes of prespawn mortality in Spring Run Chinook salmon in the Willamette River Basin. |
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I am interested in multi-species interactions and prokaryotic physiology in environmental systems. My research focuses on bacterial cell-cell signaling (quorum sensing), nitrification, and microbial communities in soils. My previous postdoctoral work focused on the role of acyl-homoserine lactone quorum sensing in nitrifying bacteria and constraint-based modeling of nitrogen oxide fluxes during nitrification. My current research with Ryan Mueller and David Myrold is focused on protein turnover in forest soils as a bottleneck in the nitrogen cycle. |
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My research project focuses on understanding the interaction of SAR11 bacterial clade with dissolved organic matter (DOM) in the ocean. I am particularly interested in analyzing the evolutionary ‘hotspots’ within the genomes of divergent SAR11 strains in the ocean to understand how these genomic regions may play a role in shaping their metabolic capabilities and ultimately on how they break down DOM. I am also interested in evolutionary forces shaping these regions. We plan to carry out deep sequencing of single-cell genomic and metagenomic libraries that will be generated from an upcoming cruise to Bermuda as part of the BIOS-SCOPE research collaboration.
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RESEARCH ASSISTANTS |
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Fabian Martinez, Faculty Research Assistant--Now a Graduate Student in Pharmacy
The work I am doing in the Geller lab involves testing PPMOs (peptide-conjugated phophorodiamidate morpholino oligomer) against multi-drug resistant strains of pathogenic bacteria. Molecular and biotechnology techniques coupled with in-vitro/ in-vivo is being utilized to test these PPMOs. Using antisense tech as a means to neutralize essential genes to kill the bacteria. MARC Scholar; Dexamethazone protects neonatal hypoxic eschemic brain injury via L-PGDS-dependent PGD2-DP1-PERK signaling pathway. PLOS One. Loma Linda.
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Website: http://microbiology.science.oregonstate.edu/content/bruce-geller I am working on antisense effects on multi-drug resistance bacteria. Basically, synthetic nucleotide analogs are utilized to target specific antibiotic resistant genes, and the effects are tested, using molecular and cellular biotechnology and rodent models. |
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Website: http://microbiology.science.oregonstate.edu/michael-kent I have been involved with the study of the diseases of salmonids and zebrafish for the past 30 years. Currently the focus of my research has been on the impacts of the diseases of zebrafish on experimental outcomes due to non-protocol induced variation and the development of specific pathogen free fish lines to aide in alleviating this problem. I am also investigating various drug treatments and disinfectants for their potential to control zebrafish diseases. Most recently I have been working on transmitting and identifying the etiological agent causing intestinal tumors in zebrafish. In the past I have also conducted numerous field studies including studying the lifecycles and possible effects of parasites on endangered Klamath Lake suckers and determining a parasitic causation of skeletal deformities in Willamette River fishes. Most of these studies necessitate the need for a zebrafish disease facility which I maintain and manage. |
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