Persistence of Multidrug-Resistant Acinetobacter baumannii Isolates Harboring blaOXA-23 and bap for 5 Years
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The emergence and dissemination of carbapenemase-producing Acinetobacter baumannii isolates have been reported worldwide, and A. baumannii isolates harboring blaOXA-23 are often resistant to various antimicrobial agents. Antimicrobial resistance can be particularly strong for biofilm-forming A. baumannii isolates. We investigated the genetic basis for carbapenem resistance and biofilm-forming ability of multidrug-resistant (MDR) clinical isolates. Ninetytwo MDR A. baumannii isolates were collected from one university hospital located in the Chungcheong area of Korea over a 5-year period. Multiplex PCR and DNA sequencing were performed to characterize carbapenemase and bap genes. Clonal characteristics were analyzed using REP-PCR. In addition, imaging and quantification of biofilms were performed using a crystal violet assay. All 92 MDR A. baumannii isolates involved in our study contained the blaOXA-23 and bap genes. The average absorbance of biomass in Bap-producing strains was much greater than that in non-Bap-producing strains. In our study, only three REP-PCR types were found, and the isolates showing type A or type B were found more than 60 times among unique patients during the 5 years of surveillance. These results suggest that the isolates have persisted and colonized for 5 years, and biofilm formation ability has been responsible for their persistence and colonization.
Abstract
The emergence and dissemination of carbapenemase-producing Acinetobacter baumannii isolates have been reported worldwide, and A. baumannii isolates harboring blaOXA-23 are often resistant to various antimicrobial agents. Antimicrobial resistance can be particularly strong for biofilm-forming A. baumannii isolates. We investigated the genetic basis for carbapenem resistance and biofilm-forming ability of multidrug-resistant (MDR) clinical isolates. Ninetytwo MDR A. baumannii isolates were collected from one university hospital located in the Chungcheong area of Korea over a 5-year period. Multiplex PCR and DNA sequencing were performed to characterize carbapenemase and bap genes. Clonal characteristics were analyzed using REP-PCR. In addition, imaging and quantification of biofilms were performed using a crystal violet assay. All 92 MDR A. baumannii isolates involved in our study contained the blaOXA-23 and bap genes. The average absorbance of biomass in Bap-producing strains was much greater than that in non-Bap-producing strains. In our study, only three REP-PCR types were found, and the isolates showing type A or type B were found more than 60 times among unique patients during the 5 years of surveillance. These results suggest that the isolates have persisted and colonized for 5 years, and biofilm formation ability has been responsible for their persistence and colonization.
참고문헌 (24)
- Bou G, "PCR-based DNA fingerprinting (REP-PCR, AP-PCR) and pulsed-field gel electrophoresis characterization of a nosocomial outbreak caused by imipenem- and meropenem-resistant Acinetobacter baumannii", Clin. Microbiol. Infect, 6, pp.635~643 (2000)
- Brossard KA, "The Acinetobacter baumannii biofilm-associated protein plays a role in adherence to human epithelial cells", Infect. Immun, 80, pp.228~233 (2012)
- Clinical and Laboratory Standards Institute, "Performance standards for antimicrobial susceptibility testing; 21st informational supplement. M100-S21", CLSI, ~ (2011)
- Coelho J, "Occurrence of OXA-58-like carbapenemases in Acinetobacter spp. collected over 10 years in three continents", Antimicrob. Agents Chemother, 50, pp.756~758 (2006)
- Donlan RM, "Biofilms: survival mechanisms of clinically relevant microorganisms", Clin. Microbiol. Rev, 15, pp.167~193 (2002)
- Ellington MJ, "Multiplex PCR for rapid detection of genes encoding acquired metallo-beta-lactamases", J. Antimicrob. Chemother, 59, pp.321~322 (2007)
- Girlich D, "First isolation of the blaOXA-23 carbapenemase gene from an environmental Acinetobacter baumannii isolate", Antimicrob. Agents Chemother, 54, pp.578~579 (2010)
- Goh HM, "Molecular analysis of the Acinetobacter baumannii biofilm-associated protein", Appl. Environ. Microbiol, 79, pp.6535~6543 (2013)
- Gundi VA, "Validation of partial rpoB gene sequence analysis for the identification of clinically important and emerging Acinetobacter species", Microbiology, 155, pp.2333~2341 (2009)
- Hall-Stoodley L, "Bacterial biofilms: from the natural environment to infectious diseases", Nat. Rev. Microbiol, 2, pp.95~108 (2004)
- Hall-Stoodley L, "Biofilm formation and dispersal and the transmission of human pathogens", Trends Microbiol, 13, pp.7~10 (2005)
- Jean SS, "High burden of antimicrobial resistance in Asia", Int. J. Antimicrob. Agents, 37, pp.291~295 (2011)
- 구선회, "Genetic Basis of Multidrug-resistant Acinetobacter baumannii Clinical Isolates from Three University Hospitals in Chungcheong Province, Korea", Annals of Laboratory Medicine, 30(5), pp.498~506 (2010), 대한진단검사의학회
- Loehfelm TW, "Identification and characterization of an Acinetobacter baumannii biofilmassociated protein", J. Bacteriol, 190, pp.1036~1044 (2008)
- Luo TL, "Association of blaOXA-23 and bap with the persistence of Acinetobacter baumannii within a major healthcare system", Front. Microbiol, 12, pp.182~ (2015)
- Martí S, "Biofilm formation at the solid-liquid and air-liquid interfaces by Acinetobacter species", BMC Res. Notes, 11, pp.4~5 (2011)
- O’Toole GA, "Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis", Mol. Microbiol, 28, pp.449~461 (1998)
- Poirel L, "Carbapenemases:molecular diversity and clinical consequences", Future Microbiol, 2, pp.501~512 (2007)
- Poirel L, "Multiplex PCR for detection of acquired carbapenemase genes", Diagn. Microbiol. Infect. Dis, 70, pp.119~123 (2011)
- Pour NK, "Biofilm formation by Acinetobacter baumannii strains isolated from urinary tract infection and urinary catheters", FEMS Immunol. Med. Microbiol, 62, pp.328~338 (2011)
- 성지연, "Antimicrobial Resistance Determinants in Imipenem-nonsusceptible Acinetobacter calcoaceticus-baumannii Complex Isolated in Daejeon, Korea", Annals of Laboratory Medicine, 31(4), pp.265~270 (2011), 대한진단검사의학회
- Vidal R, "Effect of imipenem and sulbactam on sessile cells of Acinetobacter baumannii growing in biofilm", Microbios, 91, pp.79~87 (1997)
- Van Looveren M, "Antimicrobial resistance of Acinetobacter spp. in Europe", Clin. Microbiol. Infect, 10, pp.684~704 (2004)
- Woodford N, "Multiplex PCR for genes encoding prevalent OXA carbapenemases in Acinetobacter spp", Int. J. Antimicrob. Agents, 27, pp.351~353 (2006)
