This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Bacteriophages are important conduits for horizontal gene exchange among bacteria and are directly responsible for the virulence of many bacterial pathogens. Phage-encoded virulence factors include the shiga toxins in pathogenic strains of Escherichia coli and the cholera toxin in Vibrio cholerae. Bacteriophages can drive the emergence of new pathogenic bacterial strains through the horizontal transfer of virulence factors and thus an understanding of phage genome evolution has important public health implications. This research project will examine the population genetics and genome evolution of bacteriophages. We will test the hypothesis that much of the genetic diversity within bacteriophage populations and communities can be attributed to recent horizontal genetic exchange events among phages and between phages and bacteria. A natural community of aquatic bacteriophages will be used to address questions about phage genome evolution and the frequency of horizontal gene transfer within populations and communities of aquatic bacteriophages.
The specific aims of this research are to: (1) Assess the frequency of horizontal gene transfer events and its influences on bacteriophage genome organization and evolution, (2) Examine the population genetics/genomics of specific bacteriophages to determine the extent to which bacteriophages in the same population carry different alleles of laterally transferred host-derived genes, (3) Analyze the composition and distribution of non-viral, non-host genetic material carried in bacteriophage genomes, and (4) Train undergraduate students in the key molecular genetic techniques used in biomedical research. Students will gain experience in scientific communication, laboratory techniques, use of instrumentation, and bioinformatics as they complete individual projects.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR016457-11
Application #
8360081
Study Section
Special Emphasis Panel (ZRR1-RI-4 (01))
Project Start
2011-05-01
Project End
2012-04-30
Budget Start
2011-05-01
Budget End
2012-04-30
Support Year
11
Fiscal Year
2011
Total Cost
$59,464
Indirect Cost
Name
University of Rhode Island
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
144017188
City
Kingston
State
RI
Country
United States
Zip Code
02881
Taylor, David L; Calabrese, Nicholas M (2018) Mercury content of blue crabs (Callinectes sapidus) from southern New England coastal habitats: Contamination in an emergent fishery and risks to human consumers. Mar Pollut Bull 126:166-178
Chen, Xiaodi; Hovanesian, Virginia; Naqvi, Syed et al. (2018) Systemic infusions of anti-interleukin-1? neutralizing antibodies reduce short-term brain injury after cerebral ischemia in the ovine fetus. Brain Behav Immun 67:24-35
Paquin, Karissa L; Howlett, Niall G (2018) Understanding the Histone DNA Repair Code: H4K20me2 Makes Its Mark. Mol Cancer Res 16:1335-1345
Hahn, Mark E; Karchner, Sibel I; Merson, Rebeka R (2017) Diversity as Opportunity: Insights from 600 Million Years of AHR Evolution. Curr Opin Toxicol 2:58-71
Preiss, Matthew R; Cournoyer, Eily; Paquin, Karissa L et al. (2017) Tuning the Multifunctionality of Iron Oxide Nanoparticles Using Self-Assembled Mixed Lipid Layers. Bioconjug Chem 28:2729-2736
Tiwari, Rakesh K; Brown, Alex; Sadeghiani, Neda et al. (2017) Design, Synthesis, and Evaluation of Dasatinib-Amino Acid and Dasatinib-Fatty Acid Conjugates as Protein Tyrosine Kinase Inhibitors. ChemMedChem 12:86-99
Shimpi, Prajakta C; More, Vijay R; Paranjpe, Maneesha et al. (2017) Hepatic Lipid Accumulation and Nrf2 Expression following Perinatal and Peripubertal Exposure to Bisphenol A in a Mouse Model of Nonalcoholic Liver Disease. Environ Health Perspect 125:087005
Malloy, Thomas E; Kinney, Lorin (2017) Implications for the Self Determine Benevolence and Self-Protection in Intergroup Relations. Self Identity 16:171-193
Vierra, David A; Garzon, Jada L; Rego, Meghan A et al. (2017) Modulation of the Fanconi anemia pathway via chemically induced changes in chromatin structure. Oncotarget 8:76443-76457
Wan, Jerry; Lin, Fuquan; Zhang, Wei et al. (2017) Novel approaches to vitiligo treatment via modulation of mTOR and NF-?B pathways in human skin melanocytes. Int J Biol Sci 13:391-400

Showing the most recent 10 out of 376 publications