The gonococcal genetic island (GGI) is a 57 kb region of DNA that is found in the chromosomes of 80% of Neisseria gonorrhoeae strains and was recently identified in Neisseria meningitidis. The GGI sequence shows evidence that it was horizontally acquired from another bacterial species. It is flanked by a 23-bp repeat, one copy of which makes up most of the dif site at the gonococcal replication terminus. The second copy of the repeat is part of an imperfect copy of the dif sequence. dif is a sequence that is recognized by the site-specific recombinase XerCD. In E. coli it has been shown that dif and XerCD facilitate the resolution of chromosomal dimers that result from homologous recombination following chromosomal replication. The identification of the GGI in N. meningitidis suggests that the GGI may be horizontally transferred between Neisseria species. ? ? This proposal describes experiments to characterize the mechanisms involved in acquisition and excision of the GGI and the phenotypes associated with acquisition of the GGI by N. meningitidis strains. Characterization of GGI loss in N. gonorrhoeae indicates that the dif sequence facilitates excision by site-specific recombination. Limited DNA sequence information on the GGI from several N. meningitidis isolates identifies type IV secretion system genes in the meningococcal isolates, but that certain putative surface components exist in variant forms. These data suggest that the type IV secretion system may function differently in N. meningitidis and may be subject to immune surveillance. These studies will further characterize the gene content of the N. meningitidis GGIs and examine their effects on infection of human cells in culture. ? ? This proposal describes experiments to characterize the mechanisms involved in acquisition and excision of the GGI and the phenotypes associated with acquisition of the GGI by N. meningitidis strains. These studies will further characterize the gene content of the N. meningitidis GGIs and examine their effects on infection of human cells in culture. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI072605-01A1
Application #
7313546
Study Section
Special Emphasis Panel (ZRG1-IDM-A (90))
Program Officer
Hiltke, Thomas J
Project Start
2007-07-15
Project End
2009-06-30
Budget Start
2007-07-15
Budget End
2008-06-30
Support Year
1
Fiscal Year
2007
Total Cost
$179,990
Indirect Cost
Name
University of Wisconsin Madison
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Woodhams, Katelynn L; Chan, Jia Mun; Lenz, Jonathan D et al. (2013) Peptidoglycan fragment release from Neisseria meningitidis. Infect Immun 81:3490-8
Kohler, Petra L; Chan, Yolande A; Hackett, Kathleen T et al. (2013) Mating pair formation homologue TraG is a variable membrane protein essential for contact-independent type IV secretion of chromosomal DNA by Neisseria gonorrhoeae. J Bacteriol 195:1666-79
Woodhams, Katelynn L; Benet, Zachary L; Blonsky, Sarah E et al. (2012) Prevalence and detailed mapping of the gonococcal genetic island in Neisseria meningitidis. J Bacteriol 194:2275-85
Dominguez, Nadia M; Hackett, Kathleen T; Dillard, Joseph P (2011) XerCD-mediated site-specific recombination leads to loss of the 57-kilobase gonococcal genetic island. J Bacteriol 193:377-88
Ramsey, Meghan E; Woodhams, Katelynn L; Dillard, Joseph P (2011) The Gonococcal Genetic Island and Type IV Secretion in the Pathogenic Neisseria. Front Microbiol 2:61
Zola, Tracey A; Strange, Heather R; Dominguez, Nadia M et al. (2010) Type IV secretion machinery promotes ton-independent intracellular survival of Neisseria gonorrhoeae within cervical epithelial cells. Infect Immun 78:2429-37