Lipopolysaccharide (LPS) is the major component of the surface of Gram-negative bacteria and its polysaccharide portion is situated at the outermost region. We investigated the relationship between the polysaccharide portion of LPS and biofilm formation using a series of Escherichia coli mutants defective in genes earlier shown to affect the LPS sugar compositions. Biofilm formation by a deep rough LPS mutant, the hldE strain, was strongly enhanced in comparison with the parental strain and other LPS mutants. The hldE strain also showed a phenotype of increased auto-aggregation and stronger cell surface hydrophobicity compared to the wild-type. Similar results were obtained with another deep rough LPS mutant, the waaC strain whose LPS showed same molecular mass as that of the hldE strain. Confocal laser scanning microscopy (CLSM) analysis and biofilm formation assay using DNase I revealed that biofilm formation by the hldE strain was dependent on extracellular DNA. Furthermore, a loss of flagella and an increase in amount of outer membrane vesicles in case of the hldE strain were also observed by transmission electron microscopy and atomic force microscopy, respectively. In addition, we demonstrated that a mutation in the hldE locus, which alters the LPS structure, caused changes in both expression and properties of several surface bacterial factors involved in biofilm formation and virulence. We suggest that the implication of these results should be considered in the context of biofilm formation on abiotic surfaces, which is frequently associated with nosocominal infections such as the catheter-associated infections.
References
[1]
O'Toole G, Kaplan HB, Kolter R (2000) Biofilm formation as microbial development. Annu Rev Microbiol 54: 49–79.
[2]
Beloin C, Roux A, Ghigo JM (2008) Escherichia coli biofilms. Curr Top Microbiol Immunol 322: 249–289.
Costerton JW, Stewart PS, Greenberg EP (1999) Bacterial biofilms: a common cause of persistent infections. Science 284: 1318–1322.
[5]
Danese PN, Pratt LA, Kolter R (2000) Exopolysaccharide production is required for development of Escherichia coli K-12 biofilm architecture. J Bacteriol 182: 3593–3596.
[6]
Whitchurch CB, Tolker-Nielsen T, Ragas PC, Mattick JS (2002) Extracellular DNA required for bacterial biofilm formation. Science 295: 1487.
[7]
Petersen FC, Tao L, Scheie AA (2005) DNA binding-uptake system: a link between cell-to-cell communication and biofilm formation. J Bacteriol 187: 4392–4400.
[8]
Rice KC, Mann EE, Endres JL, Weiss EC, Cassat JE, et al. (2007) The cidA murein hydrolase regulator contributes to DNA release and biofilm development in Staphylococcus aureus. Proc Natl Acad Sci U S A 104: 8113–8118.
[9]
Lappann M, Claus H, van Alen T, Harmsen M, Elias J, et al.. (2010) A dual role of extracellular DNA during biofilm formation of Neisseria meningitidis. Mol Microbiol.
[10]
Harmsen M, Lappann M, Knochel S, Molin S (2010) Role of extracellular DNA during biofilm formation by Listeria monocytogenes. Appl Environ Microbiol 76: 2271–2279.
[11]
Das T, Sharma PK, Busscher HJ, van der Mei HC, Krom BP (2010) Role of extracellular DNA in initial bacterial adhesion and surface aggregation. Appl Environ Microbiol 76: 3405–3408.
[12]
Tetz VV, Tetz GV (2010) Effect of extracellular DNA destruction by DNase I on characteristics of forming biofilms. DNA Cell Biol 29: 399–405.
[13]
Lindhout T, Lau PC, Brewer D, Lam JS (2009) Truncation in the core oligosaccharide of lipopolysaccharide affects flagella-mediated motility in Pseudomonas aeruginosa PAO1 via modulation of cell surface attachment. Microbiology 155: 3449–3460.
[14]
Nakao R (2009) Polysaccharide of Gram-negative periodontopathic bacteria. In: Ullrich M, editor. Bacterial polysaccharides, current innovations and future trends. Caister Academic Press: 129–142.
[15]
Bouchet V, Hood DW, Li J, Brisson JR, Randle GA, et al. (2003) Host-derived sialic acid is incorporated into Haemophilus influenzae lipopolysaccharide and is a major virulence factor in experimental otitis media. Proc Natl Acad Sci U S A 100: 8898–8903.
[16]
Camprubi S, Merino S, Benedi VJ, Tomas JM (1993) The role of the O-antigen lipopolysaccharide and capsule on an experimental Klebsiella pneumoniae infection of the rat urinary tract. FEMS Microbiol Lett 111: 9–13.
[17]
Camprubi S, Merino S, Guillot JF, Tomas JM (1993) The role of the O-antigen lipopolysaccharide on the colonization in vivo of the germfree chicken gut by Klebsiella pneumoniae. Microb Pathog 14: 433–440.
[18]
Harvill ET, Preston A, Cotter PA, Allen AG, Maskell DJ, et al. (2000) Multiple roles for Bordetella lipopolysaccharide molecules during respiratory tract infection. Infect Immun 68: 6720–6728.
[19]
Nesper J, Lauriano CM, Klose KE, Kapfhammer D, Kraiss A, et al. (2001) Characterization of Vibrio cholerae O1 El tor galU and galE mutants: influence on lipopolysaccharide structure, colonization, and biofilm formation. Infect Immun 69: 435–445.
[20]
Nevola JJ, Stocker BA, Laux DC, Cohen PS (1985) Colonization of the mouse intestine by an avirulent Salmonella typhimurium strain and its lipopolysaccharide-defective mutants. Infect Immun 50: 152–159.
[21]
Nevola JJ, Laux DC, Cohen PS (1987) In vivo colonization of the mouse large intestine and in vitro penetration of intestinal mucus by an avirulent smooth strain of Salmonella typhimurium and its lipopolysaccharide-deficient mutant. Infect Immun 55: 2884–2890.
[22]
Hoshino K, Takeuchi O, Kawai T, Sanjo H, Ogawa T, et al. (1999) Cutting edge: Toll-like receptor 4 (TLR4)-deficient mice are hyporesponsive to lipopolysaccharide: evidence for TLR4 as the Lps gene product. J Immunol 162: 3749–3752.
[23]
Poltorak A, He X, Smirnova I, Liu MY, Van Huffel C, et al. (1998) Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science 282: 2085–2088.
[24]
Russell JA (2006) Management of sepsis. N Engl J Med 355: 1699–1713.
[25]
Raetz CR, Whitfield C (2002) Lipopolysaccharide endotoxins. Annu Rev Biochem 71: 635–700.
[26]
Bahrami S, Yao YM, Leichtfried G, Redl H, Schlag G, et al. (1997) Monoclonal antibody to endotoxin attenuates hemorrhage-induced lung injury and mortality in rats. Crit Care Med 25: 1030–1036.
[27]
Di Padova FE, Brade H, Barclay GR, Poxton IR, Liehl E, et al. (1993) A broadly cross-protective monoclonal antibody binding to Escherichia coli and Salmonella lipopolysaccharides. Infect Immun 61: 3863–3872.
[28]
Bennett-Guerrero E, McIntosh TJ, Barclay GR, Snyder DS, Gibbs RJ, et al. (2000) Preparation and preclinical evaluation of a novel liposomal complete-core lipopolysaccharide vaccine. Infect Immun 68: 6202–6208.
[29]
Dissanayake DR, Wijewardana TG, Gunawardena GA, Poxton IR (2010) Potential use of a liposome-encapsulated mixture of lipopolysaccharide core types (R1, R2, R3 and R4) of Escherichia coli in controlling colisepticaemia in chickens. J Med Microbiol 59: 100–107.
[30]
Desroy N, Moreau F, Briet S, Le Fralliec G, Floquet S, et al. (2009) Towards Gram-negative antivirulence drugs: new inhibitors of HldE kinase. Bioorg Med Chem 17: 1276–1289.
[31]
Moreau F, Desroy N, Genevard JM, Vongsouthi V, Gerusz V, et al. (2008) Discovery of new Gram-negative antivirulence drugs: structure and properties of novel E. coli WaaC inhibitors. Bioorg Med Chem Lett 18: 4022–4026.
[32]
Valvano MA, Marolda CL, Bittner M, Glaskin-Clay M, Simon TL, et al. (2000) The rfaE gene from Escherichia coli encodes a bifunctional protein involved in biosynthesis of the lipopolysaccharide core precursor ADP-L-glycero-D-manno-heptose. J Bacteriol 182: 488–497.
[33]
Moller AK, Leatham MP, Conway T, Nuijten PJ, de Haan LA, et al. (2003) An Escherichia coli MG1655 lipopolysaccharide deep-rough core mutant grows and survives in mouse cecal mucus but fails to colonize the mouse large intestine. Infect Immun 71: 2142–2152.
[34]
Nagy G, Dobrindt U, Grozdanov L, Hacker J, Emody L (2005) Transcriptional regulation through RfaH contributes to intestinal colonization by Escherichia coli. FEMS Microbiol Lett 244: 173–180.
[35]
Kong Q, Yang J, Liu Q, Alamuri P, Roland KL, et al. (2011) Effect of deletion of genes involved in lipopolysaccharide core and O-antigen synthesis on virulence and immunogenicity of Salmonella enterica serovar typhimurium. Infect Immun 79: 4227–4239.
[36]
Schooling SR, Beveridge TJ (2006) Membrane vesicles: an overlooked component of the matrices of biofilms. J Bacteriol 188: 5945–5957.
[37]
Renelli M, Matias V, Lo RY, Beveridge TJ (2004) DNA-containing membrane vesicles of Pseudomonas aeruginosa PAO1 and their genetic transformation potential. Microbiology 150: 2161–2169.
[38]
Galanos C, Luderitz O, Westphal O (1969) A new method for the extraction of R lipopolysaccharides. Eur J Biochem 9: 245–249.
[39]
Nakao R, Senpuku H, Watanabe H (2006) Porphyromonas gingivalis galE is involved in lipopolysaccharide O-antigen synthesis and biofilm formation. Infect Immun 74: 6145–6153.
[40]
Rosenberg M, Buivids IA, Ellen RP (1991) Adhesion of Actinomyces viscosus to Porphyromonas (Bacteroides) gingivalis-coated hexadecane droplets. J Bacteriol 173: 2581–2589.
[41]
Ramstedt M, Nakao R, Wai SN, Uhlin BE, Boily JF (2011) Monitoring surface chemical changes in the bacterial cell wall: multivariate analysis of cryo-x-ray photoelectron spectroscopy data. The Journal of biological chemistry 286: 12389–12396.
[42]
Leone L, Loring J, Sjoberg S, Persson P, Shchukarev A (2006) Surface characterization of the gram-positive bacteria Bacillus subtilis-an XPS study. Surface and interface analysis 38: 202–205.
[43]
Pouttu R, Westerlund-Wikstrom B, Lang H, Alsti K, Virkola R, et al. (2001) matB, a common fimbrillin gene of Escherichia coli, expressed in a genetically conserved, virulent clonal group. J Bacteriol 183: 4727–4736.
[44]
Westerlund-Wikstrom B, Tanskanen J, Virkola R, Hacker J, Lindberg M, et al. (1997) Functional expression of adhesive peptides as fusions to Escherichia coli flagellin. Protein Eng 10: 1319–1326.
[45]
Akiyama Y, Kamitani S, Kusukawa N, Ito K (1992) In vitro catalysis of oxidative folding of disulfide-bonded proteins by the Escherichia coli dsbA (ppfA) gene product. J Biol Chem 267: 22440–22445.
[46]
Beloin C, Michaelis K, Lindner K, Landini P, Hacker J, et al. (2006) The transcriptional antiterminator RfaH represses biofilm formation in Escherichia coli. J Bacteriol 188: 1316–1331.
[47]
Seper A, Fengler VH, Roier S, Wolinski H, Kohlwein SD, et al. (2011) Extracellular nucleases and extracellular DNA play important roles in Vibrio cholerae biofilm formation. Mol Microbiol 82: 1015–1037.
[48]
Schleheck D, Barraud N, Klebensberger J, Webb JS, McDougald D, et al. (2009) Pseudomonas aeruginosa PAO1 preferentially grows as aggregates in liquid batch cultures and disperses upon starvation. PLoS One 4: e5513.
[49]
Wai SN, Lindmark B, Soderblom T, Takade A, Westermark M, et al. (2003) Vesicle-mediated export and assembly of pore-forming oligomers of the enterobacterial ClyA cytotoxin. Cell 115: 25–35.
[50]
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254.
[51]
Kaplan JB, Izano EA, Gopal P, Karwacki MT, Kim S, et al.. (2012) Low Levels of beta-Lactam Antibiotics Induce Extracellular DNA Release and Biofilm Formation in Staphylococcus aureus. MBio 3.
[52]
Sambrook J, Russel DW (2001) Molecular Cloning, a labortory manual third edition. Cold Spring Harbor Labotory Press.
[53]
Cherepanov PP, Wackernagel W (1995) Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flp-catalyzed excision of the antibiotic-resistance determinant. Gene 158: 9–14.
[54]
Willetts NS, Clark AJ, Low B (1969) Genetic location of certain mutations conferring recombination deficiency in Escherichia coli. J Bacteriol 97: 244–249.
[55]
Datsenko KA, Wanner BL (2000) One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci U S A 97: 6640–6645.
[56]
Feldman MF, Marolda CL, Monteiro MA, Perry MB, Parodi AJ, et al. (1999) The activity of a putative polyisoprenol-linked sugar translocase (Wzx) involved in Escherichia coli O antigen assembly is independent of the chemical structure of the O repeat. J Biol Chem 274: 35129–35138.
[57]
Nakao R, Tashiro Y, Nomura N, Kosono S, Ochiai K, et al. (2008) Glycosylation of the OMP85 homolog of Porphyromonas gingivalis and its involvement in biofilm formation. Biochem Biophys Res Commun 365: 784–789.
[58]
Nakao R, Hasegawa H, Ochiai K, Takashiba S, Ainai A, et al. (2011) Outer membrane vesicles of Porphyromonas gingivalis elicit a mucosal immune response. PLoS One 6: e26163.
[59]
Muller-Loennies S, Lindner B, Brade H (2003) Structural analysis of oligosaccharides from lipopolysaccharide (LPS) of Escherichia coli K-12 strain W3100 reveals a link between inner and outer core LPS biosynthesis. J Biol Chem 278: 34090–34101.
[60]
Yethon JA, Heinrichs DE, Monteiro MA, Perry MB, Whitfield C (1998) Involvement of waaY, waaQ, and waaP in the modification of Escherichia coli lipopolysaccharide and their role in the formation of a stable outer membrane. J Biol Chem 273: 26310–26316.