Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI025098-09
Application #
2062886
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Project Start
1993-09-30
Project End
1996-11-30
Budget Start
1995-09-01
Budget End
1996-11-30
Support Year
9
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Kentucky
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
832127323
City
Lexington
State
KY
Country
United States
Zip Code
40506
Bobrov, Alexander G; Kirillina, Olga; Vadyvaloo, Viveka et al. (2015) The Yersinia pestis?HmsCDE regulatory system is essential for blockage of the oriental rat flea (Xenopsylla cheopis), a classic plague vector. Environ Microbiol 17:947-59
Bobrov, Alexander G; Kirillina, Olga; Ryjenkov, Dmitri A et al. (2011) Systematic analysis of cyclic di-GMP signalling enzymes and their role in biofilm formation and virulence in Yersinia pestis. Mol Microbiol 79:533-51
Forman, Stanislav; Paulley, James T; Fetherston, Jacqueline D et al. (2010) Yersinia ironomics: comparison of iron transporters among Yersinia pestis biotypes and its nearest neighbor, Yersinia pseudotuberculosis. Biometals 23:275-94
Wortham, Brian W; Oliveira, Marcos A; Fetherston, Jacqueline D et al. (2010) Polyamines are required for the expression of key Hms proteins important for Yersinia pestis biofilm formation. Environ Microbiol 12:2034-47
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Vetter, Sara M; Eisen, Rebecca J; Schotthoefer, Anna M et al. (2010) Biofilm formation is not required for early-phase transmission of Yersinia pestis. Microbiology 156:2216-25
Bobrov, Alexander G; Perry, Robert D (2006) Yersinia pestis lacZ expresses a beta-galactosidase with low enzymatic activity. FEMS Microbiol Lett 255:43-51