Isolation, Characterization and in vitro Evaluation of Specific Bacteriophages Targeting Extensive Drug Resistance Strains of Pseudomonas aeruginosa Isolated from Septic Burn Wounds
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Background: Antibiotic resistant bacteria and various infections caused by them especially extensive drug resistance (XDR) strains and worrying statistics of mortality due to these strains and also the lack of a clear vision for development and production of new effective antibiotics have made the necessity of using alternative therapies more apparent. Materials and methods: In this study, specific phages affecting the Pseudomonas aeruginosa XDR strain were extracted from hospital wastewater and their laboratory characteristics along with lysis effect on 40 XDR strains of P. aeruginosa were investigated. Results: The results indicated that three isolated phages (PaB1, PaBa2 and PaBa3) belonged to the Myoviridae and Pododoviridae families and were specific to Pseudomonas aeruginosa strains. More than 98% of phages absorbed their host in less than 10 minutes (Adsorption time <10 min) and completed their lytic cycle after 40 minutes (latent time = 40 min). Burst size of PaBa1, PaBa2 and PaBa3 was 240, 250 and 220 pfu/cell, respectively. PaBa1 lysed 62.5% of the XDR strains with the highest efficiency. The three Phage cocktail was effective against 67.5% of the studied strains. Conclusion: The results of this study indicate the significant potential of these phages for therapeutic use and prophylaxis of infections caused by this bacterium.
Abstract
Background: Antibiotic resistant bacteria and various infections caused by them especially extensive drug resistance (XDR) strains and worrying statistics of mortality due to these strains and also the lack of a clear vision for development and production of new effective antibiotics have made the necessity of using alternative therapies more apparent. Materials and methods: In this study, specific phages affecting the Pseudomonas aeruginosa XDR strain were extracted from hospital wastewater and their laboratory characteristics along with lysis effect on 40 XDR strains of P. aeruginosa were investigated. Results: The results indicated that three isolated phages (PaB1, PaBa2 and PaBa3) belonged to the Myoviridae and Pododoviridae families and were specific to Pseudomonas aeruginosa strains. More than 98% of phages absorbed their host in less than 10 minutes (Adsorption time <10 min) and completed their lytic cycle after 40 minutes (latent time = 40 min). Burst size of PaBa1, PaBa2 and PaBa3 was 240, 250 and 220 pfu/cell, respectively. PaBa1 lysed 62.5% of the XDR strains with the highest efficiency. The three Phage cocktail was effective against 67.5% of the studied strains. Conclusion: The results of this study indicate the significant potential of these phages for therapeutic use and prophylaxis of infections caused by this bacterium.
참고문헌 (40)
- Merakou C, "Progress toward the elusive Pseudomonas aeruginosa vaccine", Surg Infect(Larchmt), 19, pp.757~768 (2018)
- Thirumala R, "Diagnosis and management of infectious complications in critically ill patients with cancer", Crit Care Clin, 26, pp.59~91 (2010)
- Swathirajan CR, "Changing drug resistance profile in Pseudomonas aeruginosa infection among HIV patients from 2010-2017 : A retrospective study", J Glob Antimicrob Resist, 16, pp.274~277 (2019)
- Hosseininassab Nodoushan SA, "Distribution of the strains of multidrug-resistant, extensively drug-resistant, and pandrugresistant Pseudomonas aeruginosa isolates from burn patients", Adv Biomed Res, 6, pp.74~ (2017)
- Righi E, "Global prevalence of carbapenem resistance in neutropenic patients and association with mortality and carbapenem use : systematic review and meta-analysis", J Antimicrob Chemother, 72, pp.668~677 (2017)
- Kumari S, "Characterization of Pseudomonas aeruginosa PAO specific bacteriophages isolated from sewage samples", Am J Biomed Sci, 1, pp.91~102 (2009)
- Richards MJ, "Nosocomial infections in medical intensive care units in the United States", Crit Care Med, 27, pp.887~892 (1999)
- McVay CS, "Phage therapy of Pseudomonas aeruginosa infection in a mouse burn wound model", Antimicrob Agents Chemother, 51, pp.1934~1938 (2007)
- Nathwani D, "Clinical and economic consequences of hospital-acquired resistant and multidrug-resistant Pseudomonas aeruginosa infections : a systematic review and meta-analysis", Antimicrob Resist Infect Control, 3, pp.32~ (2014)
- Clinical and Laboratory Standards Institute (CLSI), "Performance standards for antimicrobial susceptibility testing" (2020), CLSI
- Jin J, "Isolation and characterization of ZZ1, a novel lytic phage that infects Acinetobacter baumannii clinical isolates", BMC Microbiol, 12, pp.156~ (2012)
- Adams MH, "Bacteriophages" (1959), Interscience publishers
- Sambrook J, "Molecular cloning: a laboratory manual" (1989), Cold Spring Harbor Press
- Pajunen M, "Bacteriophage phiYeO3-12, specific for Yersinia enterocolitica serotype O : 3, is related to coliphages T3 and T7", J Bacteriol, 182, pp.5114~5120 (2000)
- Cao F, "Evaluation of the efficacy of a bacteriophage in the treatment of pneumonia induced by multidrug resistance Klebsiella pneumoniae in mice", BioMed Res Int, 2015, pp.752930~ (2015)
- Francki RIB, "Virology division of the international union of microbiological societies" (2012), Springer Science & Business Media
- Abat C, "Extremely and pandrug-resistant bacteria extradeaths : myth or reality?", Eur J Clin Microbiol Infect Dis, 37, pp.1687~1697 (2018)
- Shokri D, "Assessment of phage cocktails with extended host range activity against antibiotic resistant strains of Pseudomonas aeruginosa", Comp Clin Pathol, 26, pp.417~422 (2017)
- Dash M, "Antimicrobial resistance pattern of Pseudomonas aeruginosa isolated from various clinical samples in a tertiary care hospital, South Odisha, India", Saudi J Med Med Sci, 3, pp.15~19 (2014)
- Hyman P, "Phages for phage therapy: isolation, characterization, and host range breadth", Pharmaceuticals(Basel), 12, pp.35~ (2019)
- Arumugam SN, "Analysis of susceptibility patterns of Pseudomonas aeruginosa and isolation, characterization of lytic bacteriophages targeting multi drug resistant Pseudomonas aeruginosa", Biomed Pharmacol J, 11, pp.1105~1117 (2018)
- Fu X, "The mechanism of DNA ejection in the Bacillus anthracis spore-binding phage 8a revealed by cryo-electron tomography", Virology, 421, pp.141~148 (2011)
- Xia G, "Phages of Staphylococcus aureus and their impact on host evolution", Infect Genet Evol, 21, pp.593~601 (2014)
- Alimoradi F, "Isolation and identification of bacteriophage effective on carbapenemase-resistant Pseudomonas aeruginosa strains", J Adv Oral Res, 7, pp.40~44 (2016)
- Wittebole X, "A historical overview of bacteriophage therapy as an alternative to antibiotics for the treatment of bacterial pathogens", Virulence, 5, pp.226~235 (2014)
- Khairnar K, "Isolation and characterization of bacteriophages infecting nocardioforms in wastewater treatment plant", Biotechnol Res Int, 2014, pp.151952~ (2014)
- Moldovan R, "On kinetics of phage adsorption", Biophys J, 93, pp.303~315 (2007)
- Shao Y, "Bacteriophage adsorption rate and optimal lysis time", Genetics, 180, pp.471~482 (2008)
- Cooper CJ, "Adapting drug approval pathways for bacteriophage-based therapeutics", Front Microbiol, 7, pp.1209~ (2016)
- Taati Moghadam M, "How phages overcome the challenges of drug resistant bacteria in clinical infections", Infect Drug Resist, 13, pp.45~61 (2020)
- Lin DM, "Phage therapy : An alternative to antibiotics in the age of multi-drug resistance", World J Gastrointest Pharmacol Ther, 8, pp.162~173 (2017)
- Costa P, "Efficiency of single phage suspensions and phage cocktail in the inactivation of Escherichia coli and Salmonella typhimurium : An in vitro preliminary study", Microorganisms, 7, pp.94~ (2019)
- Pallavali RR, "Isolation and in vitro evaluation of bacteriophages against MDR-bacterial isolates from septic wound infections", PLoS One, 12, pp.e0179245~ (2017)
- Międzybrodzki R, "Clinical aspects of phage therapy", Adv Virus Res, 83, pp.73~121 (2012)
- Fu W, "Bacteriophage cocktail for the prevention of biofilm formation by Pseudomonas aeruginosa on catheters in an in vitro model system", Antimicrob Agents Chemother, 54, pp.397~404 (2010)
- Merabishvili M, "Quality-controlled small-scale production of a well-defined bacteriophage cocktail for use in human clinical trials", PLoS One, 4, pp.e4944~ (2009)
- Sulakvelidze A, "Bacteriophage therapy", Antimicrob Agents Chemother, 45, pp.649~659 (2001)
- Kochetkova VA, "Phagotherapy of postoperative suppurative-inflammatory complications in patients with neoplasms", Sov Med, (6), pp.23~26 (1989)
- Rose T, "Experimental phage therapy of burn wound infection : difficult first steps", Int J Burns Trauma, 4, pp.66~73 (2014)
- Fukuda K, "Pseudomonas aeruginosa keratitis in mice : effects of topical bacteriophage KPP12administration", PLoS One, 7, pp.e47742~ (2012)
