Identification of biofilm proteins in non-typeable Haemophilus Influenzae

被引:60
作者
Gallaher, Timothy K.
Wu, Siva
Webster, Paul
Aguilera, Rodrigo
机构
[1] Univ So Calif, Sch Pharm, Proteom Core Facil, Los Angeles, CA 90033 USA
[2] House Ear Res Inst, Ahmanson Adv Electron Microscopy & Imaging Ctr, Los Angeles, CA 90057 USA
关键词
D O I
10.1186/1471-2180-6-65
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Non-typeable Haemophilus influenzae biofilm formation is implicated in a number of chronic infections including otitis media, sinusitis and bronchitis. Biofilm structure includes cells and secreted extracellular matrix that is "slimy" and believed to contribute to the antibiotic resistant properties of biofilm bacteria. Components of biofilm extracellular matrix are largely unknown. In order to identify such biofilm proteins an ex-vivo biofilm of a non-typeable Haemophilus influenzae isolate, originally from an otitis media patent, was produced by on-filter growth. Extracellular matrix fraction was subjected to proteomic analysis via LC-MS/MS to identify proteins. Results: 265 proteins were identified in the extracellular matrix sample. The identified proteins were analyzed for COG grouping and predicted cellular location via the TMHMM and SignalP predictive algorithms. The most over-represented COG groups identified compared to their frequency in the Haemophilus influenzae genome were cell motility and secretion (group N) followed by ribosomal proteins of group J. A number of hypothetical or un-characterized proteins were observed, as well as proteins previously implicated in biofilm function. Conclusion: This study represents an initial approach to identifying and cataloguing numerous proteins associated with biofilm structure. The approach can be applied to biofilms of other bacteria to look for commonalities of expression and obtained information on biofilm protein expression can be used in multidisciplinary approaches to further understand biofilm structure and function.
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页数:9
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共 41 条
[1]  
[Anonymous], BIOFILMS, DOI DOI 10.1017/S1479050504001425
[2]   Defining the role of the Escherichia coli chaperone SecB using comparative proteomics [J].
Baars, L ;
Ytterberg, AJ ;
Drew, D ;
Wagner, S ;
Thilo, C ;
van Wijk, KJ ;
de Gier, JW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (15) :10024-10034
[3]   Hha, YbaJ, and OmpA regulate Escherichia coli K12 biofilm formation and conjugation plasmids abolish motility [J].
Barrios, AFG ;
Zuo, RJ ;
Ren, DC ;
Wood, TK .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 93 (01) :188-200
[4]   Non-classical protein secretion in bacteria [J].
Bendtsen, JD ;
Kiemer, L ;
Fausboll, A ;
Brunak, S .
BMC MICROBIOLOGY, 2005, 5 (1)
[5]   Improved prediction of signal peptides: SignalP 3.0 [J].
Bendtsen, JD ;
Nielsen, H ;
von Heijne, G ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (04) :783-795
[6]   Outer membrane protein P6 of nontypeable Haemophilus influenzae is a potent and selective inducer of human macrophage proinflammatory cytokines [J].
Berenson, CS ;
Murphy, TF ;
Wrona, CT ;
Sethi, S .
INFECTION AND IMMUNITY, 2005, 73 (05) :2728-2735
[7]   Identification and characterization of the Escherichia coli stress protein UP12, a putative in vivo substrate of GroEL [J].
Bochkareva, ES ;
Girshovich, AS ;
Bibi, E .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (12) :3032-3040
[8]   Arginine or nitrate enhances antibiotic susceptibility of Pseudomonas aeruginosa in biofilms [J].
Borriello, G ;
Richards, L ;
Ehrlich, GD ;
Stewart, PS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (01) :382-384
[9]   Biofilms:: the matrix revisited [J].
Branda, SS ;
Vik, Å ;
Friedman, L ;
Kolter, R .
TRENDS IN MICROBIOLOGY, 2005, 13 (01) :20-26
[10]   Genes involved in formation of structured multicellular communities by Bacillus subtilis [J].
Branda, SS ;
González-Pastor, JE ;
Dervyn, E ;
Ehrlich, SD ;
Losick, R ;
Kolter, R .
JOURNAL OF BACTERIOLOGY, 2004, 186 (12) :3970-3979