This application is a re-submission of a revised application in response to two NIH program announcements: PA-98-070, """"""""Research on Microbial Biofilms,' and PA-97-073, 'Mucosal Immunity in Pathogenesis/Prevention of Human Disease."""""""" The goal of the proposed work is to use otorrhea as a model system to increase understanding of the interplay between the host mucosa and a community of bacteria termed a mucosal biofilm. The investigators argue that a complete understanding of this interplay can only be gained by comprehensively evaluating the gene expression patterns (expressomes) of both organisms simultaneously. Advances in gene expression detection technology have been made possible by the convergence of three technologies: 1. Advancements in robotic instrumentation for the preparation of arrayed, addressable libraries, 2. Automated imaging technology for simultaneously comparing the expression levels of thousands of genes, 3. and Programs which permit visualization of huge amounts of data in an easily understood format. The investigators hypothesize that Pseudomonas aeruginosa (PA) biofilms play an important role in acute otorrhea and chronic suppurative otitis media (CSOM) and that the expressomes of the pathogen and host undergo progressive changes during the establishment of an infection. The investigators also theorize that mucosal biofilms interact with """"""""implant"""""""" PA biofilms that form on tympanostomy tubes causing changes in species composition, and that biofilm-resistant ventilation tubes may be effective in reducing post-tympanostomy otorrhea. The investigators seek to develop a comprehensive picture of the changes and interactions of the expressomes of Ps. aeruginosa and the host mucosa during the development of a biofilm. This will be accomplished using state-of-the-art gene expression technology to characterize specimens obtained from two complementary animal models (the chinchilla model for acute otorrhea and the cynomolgus monkey model for chronic otorrhea). Gene expression changes will be correlated with changes in protein expression and with phenotypic characters. This proposal combines the expertise of three major centers, the Center for Genomic Sciences (which developed the paradigm of otitis as a biofilm disease), the Center for Biofilm Engineering (an NSF Engineering Center), and Children's Hospital of Pittsburgh.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC004173-03
Application #
6516217
Study Section
Special Emphasis Panel (ZRG1-IFCN-8 (05))
Program Officer
Watson, Bracie
Project Start
2000-07-01
Project End
2003-11-30
Budget Start
2002-07-01
Budget End
2003-11-30
Support Year
3
Fiscal Year
2002
Total Cost
$1,015,183
Indirect Cost
Name
Allegheny-Singer Research Institute
Department
Type
DUNS #
033098401
City
Pittsburgh
State
PA
Country
United States
Zip Code
15212
Swearingen, Matthew C; Mehta, Ajeet; Mehta, Amar et al. (2016) A novel technique using potassium permanganate and reflectance confocal microscopy to image biofilm extracellular polymeric matrix reveals non-eDNA networks in Pseudomonas aeruginosa biofilms. Pathog Dis 74:ftv104
Rudkjøbing, Vibeke Børsholt; Thomsen, Trine Rolighed; Xu, Yijuan et al. (2016) Comparing culture and molecular methods for the identification of microorganisms involved in necrotizing soft tissue infections. BMC Infect Dis 16:652
Ahmed, Azad; Earl, Josh; Retchless, Adam et al. (2012) Comparative genomic analyses of 17 clinical isolates of Gardnerella vaginalis provide evidence of multiple genetically isolated clades consistent with subspeciation into genovars. J Bacteriol 194:3922-37
Hu, Fen Z; Eutsey, Rory; Ahmed, Azad et al. (2012) In vivo capsular switch in Streptococcus pneumoniae--analysis by whole genome sequencing. PLoS One 7:e47983
Nistico, L; Kreft, R; Gieseke, A et al. (2011) Adenoid reservoir for pathogenic biofilm bacteria. J Clin Microbiol 49:1411-20
Boissy, Robert; Ahmed, Azad; Janto, Benjamin et al. (2011) Comparative supragenomic analyses among the pathogens Staphylococcus aureus, Streptococcus pneumoniae, and Haemophilus influenzae using a modification of the finite supragenome model. BMC Genomics 12:187
Davie, Jeremiah J; Earl, Josh; de Vries, Stefan P W et al. (2011) Comparative analysis and supragenome modeling of twelve Moraxella catarrhalis clinical isolates. BMC Genomics 12:70
Hiller, N Luisa; Eutsey, Rory A; Powell, Evan et al. (2011) Differences in genotype and virulence among four multidrug-resistant Streptococcus pneumoniae isolates belonging to the PMEN1 clone. PLoS One 6:e28850
Folsom, James P; Richards, Lee; Pitts, Betsey et al. (2010) Physiology of Pseudomonas aeruginosa in biofilms as revealed by transcriptome analysis. BMC Microbiol 10:294
Donati, Claudio; Hiller, N Luisa; Tettelin, Hervé et al. (2010) Structure and dynamics of the pan-genome of Streptococcus pneumoniae and closely related species. Genome Biol 11:R107

Showing the most recent 10 out of 50 publications