Abstract
The surface composition of bacteria is important in interactions with the host [6, 11, 50] and with antibiotics [7, 8]. The surface is altered by the growth environment [6, 16, 50] so that bacteria become typical of it. Thus bacteria grown in vitro and in vivo reflect both genotypic and phenotypic changes [6, 14, 20, 51]. More attention to in vivo characteristics would enhance understanding of infectious processes, and in vitro design should account for this. We report on batch-culture conditions that approximate to in vivo conditions and that alter surface hydrophobicity (SH).
This work was partly supported by grants from the Medical Research Council and the Cystic Fibrosis Research Trust. PAGD was supported by a grant from the Science and Engineering Research Council.
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References
Absolom DR, Lamberti FV, Policova Z, Zingg W, van Oss CJ, Neumann AW (1983) Surface thermodynamics of bacterial adhesion. Appl Environ Microbiol 46:90–97
Anwar H, Brown MRW, Day A, Weller PH (1984) Outer membrane antigens of mucoid Pseudomonas aeruginosa isolated directly from the sputum of a cystic fibrosis patient. FEMS Microbiol Lett 24:235–239
Anwar H, Shand GH, Ward KH, Brown MRW, Alpar KE, Gowar J (1985) Antibody response to acute Pseudomonas aeruginosa infection in a burn wound. FEMS Microbiol Lett 29:225–230
Atkinson BA, Amaral L (1982) Sublethal concentrations of antibiotics, effects on bacteria and the immune system. CRC Crit Rev Microbiol 9:101–138
Bergeron RJ, Elliott GT, Kline SJ, Ramphal R, St. James III L (1983) Bacteriostatic and fungistatic action of catecholamide iron chelators. Antimicrob Agents Chemother 24:725–730
Brown MRW, Williams P (1985) The influence of environment on envelope properties affecting survival of bacteria in infections. Ann Rev Microbiol 39:527–556
Brown MRW, Williams P (1985) Influence of substrate limitation and growth phase on sensitivity to antimicrobial agents. J Antimicrob Chemother 15 [Supp A]:7–14
Brown MRW, Gilbert P, Klemperer RMM (1979) Influence of the bacterial cell envelope on combined antibiotic action. In: Williams JD (ed) Antibiotic interactions. Academic London, pp 72–76
Brown MRW, Anwar H, Lambert PA (1984) Evidence that mucoid Pseudomonas aeruginosa in the cystic fibrosis lung grows under iron-restricted conditions. FEMS Microbiol Lett 21:113–117
Busscher HJ, Weerkamp AH, van der Mei HC, van Pelt AWJ, de Jong HP, Arends J (1984) Measurement of the surface free energy of bacterial cell surfaces and its relevance for adhesion. Appl Environ Microbiol 48:980–983
Costerton JW, Marrie TJ (1983) The role of the bacterial glycocalyx in resistance to antimicrobial agents. In: Easmon CSF, Jeljaszewicz J, Brown MRW, Lambert PA (eds) Medical microbiology, vol 3. Academic, London, pp 63–85
Cowan ST, Steel KJ (1974) Identification of medical bacteria, 2nd edn. Cambridge University Press, Cambridge
Cowart RE, Marquadt MP, Foster BC (1980) The removal of iron and other trace elements from a complex bacteriological medium. Microbios Lett 13:117–122
Dalhoff A (1985) Differences between bacteria grown in vitro and in vivo. J Antimicrob Chemother 15 [Suppl A]:175–195
Dossett JH, Kronvall G, Williams RC Jr, Quie PG (1969) Antiphagocytic effects of staphylococcal protein A. J Immunol 103:1405–1410
Ellwood DC, Tempest DW (1972) Effects of environment on bacterial wall content and composition. Adv Microb Physiol 7:83–117
England E (1986) Hydrophobic interaction chromatography. Lab Pract January:64–67
Fung DYC, Petrishko DT (1973) Capillary tube catalase test. Appl Microbiol 26:631–632
Galdiero F, Romano-Carratelli C, Folgore A, Nuzzo I (1983) Phagocytosis in diabetic subjects: increase in hydrophobicity of granulocyte cytoplasmic membrane. Experentia 39:1041–1042
Gemmell CG (1985) In vivo consequences of the interaction between antibiotic-damaged pathogens and host animal defences. In: Adam D, Hahn H, Opferkuch W (eds) The influence of antibiotics on the host-parasite relationship. II. Springer, Berlin Heidelberg New York, pp 259–266
Gilbert P, Brown MRW (1978) Influence of growth rate on the gross cellular composition of Pseudomonas aeruginosa and its resistance to 3- and 4-chlorophenol. J Bacteriol 133:1066–1072
Gillman CF, Bernstein JM, van Oss CJ (1976) Decreased phagocytosis associated with increased surface hydrophobicity of neutrophils of children with chronic infections. Fed Proc 35:227
Gladstone GP, Glencross JG (1960) Growth and toxin production of Staphylococci in cellophane sacs in vivo. Br J Exp Pathol 41:313:333
Griffiths E (1983) Availability of iron and survival of bacteria in infection. In: Easmon CSF, Jeljaszewicz J, Brown MRW, Lambert PA (eds) Medical microbiology, vol 3. Academic, London, pp 153–177
Jonsson P, Wadstrom T (1983) High surface hydrophobicity of Staphylococcus aureus as revealed by hydrophobic interaction chromatography. Curr Microbiol 8:347–353
Kadurugamuwa JL, Anwar H, Brown MRW, Shand GH, Ward KH (1987) Media for study of growth kinetics and envelope properties of iron-deprived bacteria. J Clin Microbiol 25:849–855
Kefford B, Kjelleberg S, Marshall KC (1982) Bacterial scavenging: utilisation of fatty acids localised at a solid/liquid interface. Arch Microbiol 133:257–260
Kjelleberg S, Humphrey BA, Marshall KC (1983) Initial stages of starvation and activity of bacteria at surfaces. Appl Environ Microbiol 46:978–984
Lam C, Georgopoulos A, Laber G, Schutze E (1984) Therapeutic relevance of penicillin-induced hypersensitivity of Staphylococcus aureus to killing by polymorphonuclear leukocytes. Antimicrob Agents Chemother 26:149–154
Lam C, Turnowsky F, Schwarzinger E, Neruda W (1984) Bacteria recovered without subculture from infected human urines expressed iron-regulated outer membrane proteins. FEMS Microbiol Lett 24:255–259
Ljungh A, Hjerten S, Wadstrom T (1985) High surface hydrophobicity of autoaggregating Staphylococcus aureus strains isolated from human infections studied with the salt aggregation test. Infect Immun 47:522–526
Lorian V (1980) Effects of subminimum inhibitory concentrations of antibiotics on bacteria. In: Lorian V (ed) Antibiotics in laboratory medicine. Williams and Wilkins, Baltimore, pp 342–408
Magnusson K-E, Kilhstrom E, Norquist A, Davies J, Normark S (1979) Effect of iron on surface charge and hydrophobicity of Neisseria gonorrhoeae. Infect Immun 26:402–407
Magnusson K-E, Dahlgren C, Maluszynska GM, Kihlstrom E, Skogh T, Stendahl O, Soderlund G, Ohman L, Walan A (1985) Non-specific and specific recognition mechanisms of bacterial and mammalian cell membranes. J Disp Sci Technol 6:69–89
Malmqvist T (1983) Bacterial hydrophobicity measured as partition of palmitic acid between the two immiscible phases of cell surface and buffer. Acta Pathol Microbiol Immunol Scand [B] 91:69–73
Marcelis JH, den Daas-Slagt HJ, Hoogkamp-Korstanje JAA (1978) Iron requirement and chelator production of Staphylococci, Streptococcus faecalis and Enterobacteriaceae. Antonie van Leeuwenhoek 44:257–267
Maskell JP (1980) The functional interchangeability of enterobacterial and staphylococcal iron chelators. Antonie van Leeuwenhoek 46:343–351
Miles AA, Khimji PL (1975) Enterobacterial chelators of iron: their occurrence, detection and relation to pathogenicity. J Med Microbiol 8:477–490
Miller RD, Fung DYC (1973) Amino acid requirements for the production of enterotoxin B by Staphylococcus aureus S-6 in a chemically defined medium. Appl Microbiol 25:800–806
Miorner H, Myhre E, Bjork L, Kronvall G (1980) Effect of specific binding of human albumen, fibrinogen and immunoglobulin G on surface characteristics of bacterial strains as revealed by partition experiments in polymer phase systems. Infect Immun 29:879–885
Miorner H, Albertsson P-A, Kronvall G (1982) Isoelectric points and surface hydrophobicity of gram-positive cocci as determined by cross-partition and hydrophobic affinity partition in aqueous two phase systems. Infect Immun 36:227–234
Mozes N, Rouxhet PG (1987) Methods for measuring hydrophobicity of microorganisms. J Microbiol Methods 6:99–112
Mudd EBH, Mudd S (1933) The process of phagocytosis. The agreement between direct observation and deductions from theory. J Gen Physiol 16:625–636
Neilands JB (1981) Microbial iron compounds. Annu Rev Biochem 50:715–731
Neilands JB (1982) Microbial envelope proteins related to iron. Annu Rev Microbiol 36:285–309
Reeves DS, Phillips I, Williams JD, Wise R (1978) Laboratory methods in antimicrobial chemotherapy. Churchill Livingstone, London
Schade AL (1963) Significance of serum iron for the growth, biological characteristics and metabolism of Staphylococcus aureus. Biochem Z 338:140–148
Schade AL, Myers NH, Reinhart RW (1968) Carbohydrate metabolism and production of diffusible active substances by Staphylococcus aureus grown in serum at iron levels in excess of siderophilin iron-saturation and below. J Gen Microbiol 52:253–260
Shand GH, Anwar H, Kadurugamuwa J, Brown MRW, Silverman SH, Melling J (1985) In vivo evidence that bacteria in urinary tract infection grow under iron-restricted conditions. Infect Immun 48:35–39
Smith H (1977) Microbial surfaces in relation to pathogenicity. Bacteriol Rev 41:475–500
Smith H (1980) The effect of environmental conditions in vivo and in vitro on the determinants of microbial pathogenicity. In: Smith H, Skehel JJ, Turner MJ (eds) The molecular basis of microbial pathogenicity. Chemie, Dahlem, pp 159–172
Stendhal O (1983) The physiochemical basis of surface interaction between bacteria and phagocytic cells. In: Easmon CSF, Jeljaszewicz J, Brown MRW, Lambert PA (eds) Medical microbiology, vol 3. Academic, London, pp 137–152
Tempest DW, Wouters JM (1981) Properties and performance of microorganisms in chemostat culture. Enzyme Microb Technol 3:283–290
Theodore TS, Schade AL (1965) Growth of Staphylococcus aureus in media of restricted and unrestricted inorganic iron availability. J Gen Microbiol 39:75–83
Theodore TS, Schade AL (1965) Carbohydrate metabolism of iron-rich and iron-poor Staphylococcus aureus. J Gen Microbiol 40:385–395
Tufano MA, Romano-Carratelli C, Sommese L, Bentivoglio C, Galdiero F (1985) Modifications of surface properties in some enteropathogenic serogroups of Escherichia coli. Microbiologica 8:181–190
Turnowsky F, Brown MRW, Anwar H, Lambert PA (1983) Effect of iron limitation of growth rate on the binding of penicillin G to the penicillin binding proteins of mucoid and non-mucoid strains of Pseudomonas aeruginosa. FEMS Microbiol Lett 17:243–245
van Loosdrecht MCM, Lyklema J, Norde W, Schraa G, Zehnder AJB (1987) The role of bacterial cell wall hydrophobicity in adhesion. Appl Environ Microbiol 53:1893–1897
van Loosdrecht MCM, Lyklema J, Norde W, Schraa G, Zehnder AJB (1987) Electro-phorectic mobility and hydrophobicity as a measure to predict the initial steps of bacterial adhesion. Appl Environ Microbiol 53:1898–1901
van Loosdrecht MCM, Norde W, Zehnder AJB (1987) Influence of cell surface characteristics on bacterial adhesion to solid supports. In: Neijssel OM, van der Meer RR, Luyben KCAM (eds) Proceedings of the European congress on biotechnology, vol 4. Elsevier, Amsterdam
van Oss CJ (1978) Phagocytosis as a surface phenomenon. Annu Rev Microbiol 32:19–39
van Oss CJ, Gillman CF, Neuman AW (1975) Phagocytic engulfment and cell adhesiveness. Dekker, New York
Wadstrom T, Hjerten S, Jonnson P, Tylewska S (1981) Hydrophobic surface properties of Staphylococcus aureus, Staphylococcus saprophyticus and Streptococcus pyogenes. In: Jeljaszewicz J (ed) Staphylococci and Staphylococcal infections. Fischer, Stuttgart, pp 441–447
Wadstrom T, Bjornberg S, Hjerten S (1985) Hydrophobised wound dressings in the treatment of experimental Staphylococcus aureus infections in the young pig. Acta Pathol Microbiol Immunol Scand [B] 93:359–363
Wadstrom T, Brown A, Ljungh A, Rozgonyi F, Hjerten S (1985) Comparative hydrophobicity studies of Staphylococus aureus and coagulase-negative Staphylococci in the salt aggregation test (SAT) and binding to various hydrophobic biomaterials. Abstr Annu Meeting Am Soc Microbiol 26:B48
Xiu JH, Magnusson K-E, Stendahl O, Edebo L (1983) Physiochemical surface properties and phagocytosis by polymorphonuclear leucocytes of different serogroups of Salmonella. J Gen Microbiol 129:3075–3084
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Domingue, P.A.G., Schwarzinger, E., Brown, M.R.W. (1989). Growth Rate, Iron Depletion, and a Sub-Minimal Inhibitory Concentration of Penicillin G Affect the Surface Hydrophobicity of Staphylococcus aureus . In: Gillissen, G., Opferkuch, W., Peters, G., Pulverer, G. (eds) The Influence of Antibiotics on the Host-Parasite Relationship III. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73653-7_7
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