Mycoplasmas are important pathogens with usually strict natural host tropism and poorly understood virulence mechanisms. The broad objective of this work is increased understanding of mycoplasmal host-range and virulence determinants through comparison of conserved and variable features of mycoplasmal genomes. Comparative genomics is a new alternative to the usual tools of molecular biology to elucidate the genetic bases of mycoplasmosis. Mycoplasma alligatoris merits priority in that effort because in some hosts it causes hyperacute lethal disease, but it is merely commensal in others.
The specific aims are to assemble a draft map of the M. alligatoris genome by alignment with that of closely-related Mycoplasma pulmonis, and to identify candidate genes involved in host tropism and virulence. The working draft will be assembled by using automated high-throughput sequence assembly methods. Sequence alignments will be validated by comparative synteny and PCR-based gap closure. Coding sequences will be identified by interpolated Markov models trained with mycoplasmal sequences and cataloged according to their public database matches. Candidate host-range genes may be recognized by overall similarity to known adhesins or by signature ligand-binding motifs. Virulence factors may include homologs to cell-surface or secreted hydrolytic enzymes of other mollicutes, or to pathogenic determinants present in other bacteria. The sequences of homologs whose known biological roles or predicted properties are consistent with host cell-surface ligand-binding or the pathogenic effects of M. alligatoris will be characterized in detail. The data will be integrated in a representation of the complement of adhesion, transport, and metabolic pathways of M. alligatoris validated by the biologically well-documented metabolic map of the mollicutes. The ease of PCR-based cloning and the accessibility of bioinformatics software make this an ideal project to engage undergraduate students in innovative biomedical research.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15HG002389-01A1
Application #
6504644
Study Section
Bacteriology and Mycology Subcommittee 2 (BM)
Program Officer
Good, Peter J
Project Start
2002-09-30
Project End
2006-09-29
Budget Start
2002-09-30
Budget End
2006-09-29
Support Year
1
Fiscal Year
2002
Total Cost
$145,208
Indirect Cost
Name
University of Florida
Department
Pathology
Type
Schools of Veterinary Medicine
DUNS #
073130411
City
Gainesville
State
FL
Country
United States
Zip Code
32611
Brown, D R; Farmerie, W G; May, M et al. (2011) Genome sequences of Mycoplasma alligatoris A21JP2T and Mycoplasma crocodyli MP145T. J Bacteriol 193:2892-3
Brown, Daniel R; Whitcomb, Robert F; Bradbury, Janet M (2007) Revised minimal standards for description of new species of the class Mollicutes (division Tenericutes). Int J Syst Evol Microbiol 57:2703-19
Hunt, Marguerite E; Brown, Daniel R (2007) Role of sialidase in Mycoplasma alligatoris-induced pulmonary fibroblast apoptosis. Vet Microbiol 121:73-82
May, Meghan; Kleven, Stanley H; Brown, Daniel R (2007) Sialidase activity in Mycoplasma synoviae. Avian Dis 51:829-33
Hunt, M E; Brown, D R (2005) Mycoplasma alligatoris infection promotes CD95 (FasR) expression and apoptosis of primary cardiac fibroblasts. Clin Diagn Lab Immunol 12:1370-7
Brown, D R; Zacher, L A; Farmerie, W G (2004) Spreading factors of Mycoplasma alligatoris, a flesh-eating mycoplasma. J Bacteriol 186:3922-7