624
Views
34
CrossRef citations to date
0
Altmetric
Reviews

Use of bacteriophages in the treatment of Pseudomonas aeruginosa infections

Pages 909-915 | Published online: 10 Jan 2014

References

  • Alkawash MA, Soothill JS, Schiller NL. Alginate lyase enhances antibiotic killing of mucoid Pseudomonas aeruginosa in biofilms. APMIS 114, 131–138 (2006).
  • Twort F. An investigation of ultra-microscopic viruses. Lancet 2, 1241–1243 (1915).
  • D’Herelle F. [On an invisible microbe antagonistic to dysentery bacilli.] Comptes. Rendus. Acad. Sci. 165, 373–375 (1917).
  • Asheshov IN, Wilson J, Topley WWC. The effect of an anti-vi bacteriophage on typhoid infection in mice. Lancet 1, 319–320 (1937).
  • Boyd JSK, Portnoy B. Bacteriophage therapy in bacillary dysentery. Trans R. Soc. Trop. Med. Hyg. 37, 243–262 (1944).
  • Soothill JS. Use of Bacteriophage in the Treatment of Infections. MD thesis. University of London, (1993).
  • Dubos RJ, Hookey Straus J, Pierce C. The multiplication of bacteriophage in vivo and its protective effect against an experimental infection with Shigella dysenteriae. J. Exp. Med. 78, 161–168 (1943).
  • Smith HW, Huggins MB. Successful treatment of experimental Escherichia coli infections in mice using phage: its general superiority over antibiotics. J. Gen. Microbiol. 128, 307–318 (1982).
  • Smith HW, Huggins MB. Effectiveness of phages in treating experimental Escherichia coli diarrhoea in calves, piglets and lambs. J. Gen. Microbiol. 129, 2659–2675 (1983).
  • Bertoye A, Gaillard L, Courtieu AL. Adapted bacteriophages in the treatment of infections caused by antibiotic-resistant microorganisms. J. Med. Lyon 40, 465–471 (1959).
  • Bertoye A, Courtieu AL. Treatment of infections caused by pyocyanic bacilli with bacteriophages adapted by selection. J. Med. Lyon 41, 739–751 (1960).
  • Witoszka M, Strumillo B. Attempted treatment of infected wounds with bacteriophage. Pol. Przegl. Chir. 35, 1054–1056 (1963).
  • Slopek S, Durlakowa I, Weber-Dabrowska B, Kucharewicz-Krukowska A, Dabrowski M, Bisikiewicz R. Results of bacteriophage treatment of suppurative bacterial infections. II. Detailed evaluation of the results. Arch. Immunol. Ther. Exp. (Warsz) 31, 293–327 (1983).
  • Slopek S, Kucharewicz-Krukowska A, Weber-Dabrowska B, Dabrowski M. Results of bacteriophage treatment of suppurative bacterial infections. IV. Evaluation of the results obtained in 370 cases. Arch. Immunol. Ther. Exp. (Warsz) 33, 219–240 (1985).
  • Hassan HS, El-Tahan A, Massoud B, Gomaa R. Bacteriophage therapy of pseudomonas burn wound sepsis. Ann. Medit. Burn Club 3, 262–264 (1990).
  • Kochetkova VA, Mamontov AS, Moskovtseva RL et al. Phagotherapy of postoperative suppurative-inflammatory complications in patients with neoplasms. Sov. Med. 6, 23–26 (1989).
  • Perepanova TS, Darbeeva OS, Kotliarova GA et al. The efficacy of bacteriophage preparations in treating inflammatory urologic diseases. Urol. Nefrol. (Mosk). 5, 14–17 (1995).
  • Soothill JS, Lawrence JC, Ayliffe GAJ. The efficacy of phages in the prevention of the destruction of pig skin in vitro by Pseudomonas aeruginosa. Med. Sci. Res. 16, 1287–1288 (1988).
  • Soothill JS. Bacteriophage prevents destruction of skin grafts by Pseudomonas aeruginosa. Burns 20, 209–211 (1994).
  • Soothill JS. Treatment of experimental infections of mice using bacteriophages. J. Med. Microbiol. 37, 258–261 (1992).
  • Soothill JS, Morton DB, Ahmad A. The HID50 (Hypothermia Inducing Dose 50): an alternative to the LD50 for measurement of bacterial virulence. Int. J. Exp. Pathol. 73, 95–98 (1992).
  • Wang J, Hu B, Xu M, et al. Use of bacteriophage in the treatment of experimental animal bacteremia from imipenem-resistant Pseudomonas aeruginosa. Int. J. Mol. Med. 17, 309–317 (2006).
  • Vinodkumar CS, Kalsurmath S, Neelagund YF. Utility of lytic bacteriophage in the treatment of multidrug-resistant Pseudomonas aeruginosa septicemia in mice. Indian J. Pathol. Microbiol. 51, 360–366 (2008).
  • Heo YJ, Lee YR, Jung HH, Lee J, Ko G, Cho YH. Antibacterial efficacy of phages against Pseudomonas aeruginosa infections in mice and Drosophila melanogaster. Antimicrob. Agents Chemother. 53, 2469–2474 (2009).
  • Tiwari BR, Kim S, Rahman M, Kim J. Antibacterial efficacy of lytic Pseudomonas bacteriophage in normal and neutropenic mice models. J. Microbiol. 49, 994–999 (2011).
  • Watanabe R, Matsumoto T, Sano G et al. Efficacy of bacteriophage therapy against gut-derived sepsis caused by Pseudomonas aeruginosa in mice. Antimicrob. Agents Chemother. 51, 446–452 (2007).
  • Mc Vay CS, Velásquez M, Fralick JA. Phage therapy of Pseudomonas aeruginosa infection in a mouse burn wound model. Antimicrob. Agents Chemother. 51, 1934–1938. (2007).
  • Hall AR, De Vos D, Friman VP, Pirnay JP, Buckling A. Effects of sequential and simultaneous applications of bacteriophages on populations of Pseudomonas aeruginosa in vitro and in wax moth larvae. Appl. Environ. Microbiol. 78, 5646–5652 (2012).
  • Debarbieux L, Leduc D, Maura D et al. Bacteriophages can treat and prevent Pseudomonas aeruginosa lung infections. J. Infect. Dis. 201, 1096–1104 (2010).
  • Morello E, Saussereau E, Maura D, Huerre M, Touqui L, Debarbieux L. Pulmonary bacteriophage therapy on Pseudomonas aeruginosa cystic fibrosis strains: first steps towards treatment and prevention. PLoS ONE 6, e1 6963. (2011).
  • Alemayehu D, Casey PG, McAuliffe O et al. Bacteriophages φMR299–2 and φNH-4 can eliminate Pseudomonas aeruginosa in the murine lung and on cystic fibrosis lung airway cells. MBio 3(2), e00029-e00012 (2012).
  • Hagens S, Habel A, Von Ahsen U, Von Gabain A, Bläsi U. Therapy of experimental Pseudomonas infections with a nonreplicating genetically modified phage. Antimicrob. Agents Chemother. 48, 3817–3822 (2004).
  • Marza JA, Soothill JS, Boydell P, Collyns TA. Multiplication of therapeutically administered bacteriophages in Pseudomonas aeruginosa infected patients. Burns 32, 644–646 (2006).
  • Hawkins C, Harper D, Burch D, Anggård E, Soothill J. Topical treatment of Pseudomonas aeruginosa otitis of dogs with a bacteriophage mixture: A before/after clinical trial. Vet. Microbiol. 15, 309–313 (2010).
  • Wright A, Hawkins CH, Anggård EE, Harper DR. A controlled clinical trial of a therapeutic bacteriophage preparation in chronic otitis due to antibiotic-resistant Pseudomonas aeruginosa; a preliminary report of efficacy. Clin. Otolaryngol. 34, 349–357 (2009).
  • Weber-Dabrowska B, Dabrowski M, Slopek S. Studies on bacteriophage penetration in patients subjected to phage therapy. Arch. Immunol. Ther. Exp. (Warsz) 35, 563–568 (1987).
  • Hildebrand GJ, Wolochow H. Translocation of bacteriophage across the intestinal wall of the rat. Proc. Soc. Exp. Biol. Med. 109, 183–185 (1962).
  • Park BH. An enzyme produced by a phage-host cell system. I. The properties of a Klebsiella phage.Virology 2, 711–718 (1956).
  • Bartell PF, Lam GK, Orr TE. Purification and properties of polysaccharide depolymerase associated with phage-infected Pseudomonas aeruginosa. J. Biol. Chem. 10(243), 2077–2080 (1968).
  • Ghani M. The Effect of Antibiotics and Bacteriophages on Biofilms of Pseudomonas Aeruginosa. PhD Thesis. University of Manchester, UK (1996).
  • Hanlon GW, Denyer SP, Olliff CJ, Ibrahim LJ. Reduction in exopolysaccharide viscosity as an aid to bacteriophage penetration through Pseudomonas aeruginosa biofilms. Appl. Environ. Microbiol. 67, 2746–2753 (2001).
  • Glonti T, Chanishvili N, Taylor PW. Bacteriophage-derived enzyme that depolymerizes the alginic acid capsule associated with cystic fibrosis isolates of Pseudomonas aeruginosa. J. Appl. Microbiol. 108, 695–702 (2010).
  • Bayer AS, Park S, Ramos MC, Nast CC, Eftekhar F, Schiller NL. Effects of alginase on the natural history and antibiotic therapy of experimental endocarditis caused by mucoid Pseudomonas aeruginosa. Infect. Immun. 60, 3979–3985 (1992).
  • Ghani M, Soothill JS. Rapid, continuous propagation of bacteriophage in biofilms. Infect. Dis. Rev. 1, 30–31 (1999).
  • Doolittle MM, Cooney JJ, Caldwell DE. Tracing the interaction of bacteriophage with bacterial biofilms using fluorescent and chromogenic probes. J. Ind. Microbiol. 16, 331–341. (1996).
  • Fu W, Forster T, Mayer O, Curtin JJ, Lehman SM, Donlan RM. Bacteriophage cocktail for the prevention of biofilm formation by Pseudomonas aeruginosa on catheters in an in vitro model system. Antimicrob. Agents Chemother. 54, 397–404 (2010).
  • Kim S, Rahman M, Seol SY, Yoon SS, Kim J. Pseudomonas aeruginosa bacteriophage PA1Ø requires type IV pili for infection and shows broad bactericidal and biofilm removal activities. Appl. Environ. Microbiol. 78, 6380–6385 (2012).
  • Zhang Y, Hu Z. Combined treatment of Pseudomonas aeruginosa biofilms with bacteriophages and chlorine. Biotechnol. Bioeng. 110, 286–295 (2013).
  • Budzik JM, Rosche WA, Rietsch A, O'Toole GA. Isolation and characterization of a generalized transducing phage for Pseudomonas aeruginosa strains PAO1 and PA14. J. Bacteriol. 186, 3270–3273 (2004).
  • Zegans ME, Wagner JC, Cady KC, Murphy DM, Hammond JH, O'Toole GA. Interaction between bacteriophage DMS3 and host CRISPR region inhibits group behaviors of Pseudomonas aeruginosa. J. Bacteriol. 191, 210–219 (2009).
  • Ochs HD, Davis SD, Wedgwood RJ. Immunologic responses to bacteriophage phi-X 174 in immunodeficiency diseases. J. Clin. Invest. 50, 2559–2568 (1971).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.