BMC Infectious Diseases | |
Identification of vancomycin-resistant enterococci clones and inter-hospital spread during an outbreak in Taiwan | |
Liang-Kee Siu5  Lai-Chu See6  Meng-Jiun Chiou1  Shu-Huan Huang2  Hsiang-Ju Shih4  Mi-Si Wu3  Sai-Cheong Lee4  | |
[1] Department of Public Health, Chang Gung University, Kwei-Shan, Tao-Yuan, Taiwan;Department of Laboratory Medicine, Chang Gung Memorial Hospital, Keelung, Taiwan;Department of Nephrology, Chang Gung Memorial Hospital, Keelung, Chang Gung University, Kwei-Shan, Tao-Yuan, Taiwan;Division of Infectious Diseases, Chang Gung Memorial Hospital, Keelung, Chang Gung University, 222, Mai Chin Road, Kwei-Shan, Tao-Yuan, Taiwan;Division of Clinical Research, National Health Research Institute, Miaoli, Taiwan;Biostatistics Core laboratory, Molecular Medicine Research Center, Chang Gung University, Kwei-Shan, Tao-Yuan, Taiwan | |
关键词: Inter-hospital spread; Outbreak; MLST; VRE; | |
Others : 1149038 DOI : 10.1186/1471-2334-13-163 |
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received in 2012-11-04, accepted in 2013-03-26, 发布年份 2013 | |
【 摘 要 】
Background
In 2003, nosocomial infections caused by vancomycin-resistant enterococci (VRE) occurred rarely in Taiwan. Between 2003 and 2010, however, the average prevalence of vancomycin resistance among enterococci spp. increased from 2% to 16% in community hospitals and from 3% to 21% in medical centers of Taiwan. We used molecular methods to investigate the epidemiology of VRE in a tertiary teaching hospital in Taiwan.
Methods
Between February 2009 and February 2011, rectal samples and infection site specimens were collected from all inpatients in the nephrology ward after patient consent was obtained. VRE strain types were determined by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST).
Results
A total of 59 vanA gene-containing VRE isolates (1 per patient) were obtained; 24 originated from rectal sample surveillance of patients who exhibited no symptoms (22 Enterococcus faecium and 2 Enterococcus faecalis), and 35 had developed infections over 3 days after admission (32 E. faecium, 2 E. faecalis, and 1 Enterococcus durans). The 59 VRE isolates demonstrated vancomycin minimum inhibitory concentrations (MICs) of ≥256 μg/m. The MIC range for linezolid, tigecycline, and daptomycin was 0.25–1.5 μg/mL, 0.032–0.25 and 1–4 μg/mL, respectively. For 56 isolates, the MIC for teicoplanin was >8 μg/mL. The predominant types in the nephrology ward were MLST types 414, 78, and18 as well as PFGE types A, C, and D.
Conclusion
VREs are endemic in nephrology wards. MLST 414 is the most predominant strain. The increase VRE prevalence is due to cross-transmission of VRE clones ST 414,78,18 by undetected VRE carriers. Because similar VRE STs had been reported in a different hospital of Taiwan, this finding may indicate inter-hospital VRE spread in Taiwan. Active surveillance and effective infection control policies are important controlling the spread of VRE in high risk hospital zones. All endemic VRE strains are resistant to teicoplanin but are sensitive to daptomycin, linezolid, and tigecycline.
【 授权许可】
2013 Lee et al.; licensee BioMed Central Ltd.
【 预 览 】
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20150405011453464.pdf | 181KB | download |
【 参考文献 】
- [1]Padiglione A, Wolfe R, Grabsch EA: Risk factors for the new detection of vancomycin-resistant enterococci (VRE) in acute-care hospitals that employ strict infection control procedures. Antimicrob Agents Chemother 2003, 47:2492-2498.
- [2]Grayson ML, Grabsch EA, Johnson PD: Outcome of a screening program for vancomycin-resistant enterococci in a hospital in Victoria. Med J Aust 1999, 171:133-136.
- [3]Centers for Disease Control and Prevention: Guidelines for isolation precautions in hospitals. Am J Infect Control 1996, 24:24-52.
- [4]Centers for Disease Control and Prevention: Nosocomial enterococci resistant to vancomycin—United States, 1989–1993. MMWR Morb Mortal Wkly Rep 1993, 42:597-599.
- [5]Centers for Disease Control, Department of Health, Taiwan: Vancomycin-resistant enterococci. Taiwan Nosocomial Infections Surveillance Report 2003–2010. Taipei, Taiwan; 2010.
- [6]Hospital Infection Control Practices Advisory Committee (HICPAC): Recommendations for preventing the spread of vancomycin resistance. Infect Control Hosp Epidemiol 1995, 16:105-113.
- [7]Morris JG Jr, Shay DK, Hebden JN, McCarter RJ Jr, Perdue BE, Jarvis W: Enterococci resistant to multiple antimicrobial agents, including vancomycin: establishment of endemicity in a University Medical Center. Ann Intern Med 1995, 123:250-259.
- [8]Livornese LL Jr, Dias S, Samel C, Romanowski B, Taylor S, May P, Pitsakis P, Woods G, Kaye D, Levison ME: Hospital-acquired infection with vancomycin-resistant Enterococcus faecium transmitted by electronic thermometers. Ann Intern Med 1992, 117:112-116.
- [9]Montecalvo MA, Horowitz H, Gedris C, Carbonaro C, Tenover FC, Issah A: Outbreak of vancomycin-, ampicillin-, and aminoglycoside-resistant Enterococcus faecium bacteremia in an adult oncology unit. Antimicrob Agents Chemother 1994, 38:1363-1367.
- [10]Chow JW, Kuritza A, Shlaes DM, Green M, Sahm DF, Zervos MJ: Clonal spread of vancomycin-resistant Enterococcus faecium between patients in three hospitals in two states. J Clin Microbiol 1993, 31:609-611.
- [11]Boyce JM, Opal SM, Chow JW, Zervos MJ, Potter-Bynoe G, Sherman CB, Romulo RL, Fortna S, Medeiros AA: Outbreak of multi-drug-resistant Enterococcus faecium with transferable vanB class vancomycin resistance. J Clin Microbiol 1994, 32:1148-1153.
- [12]Slaughter S, Hayden M, Nathan C, Hu TC, Rice T, Van Voorhis J, Matushek M, Franklin C, Weinstein RA: A comparison of the effect of universal use of gloves and gowns with that of glove use alone on acquisition of vancomycin-resistant enterococci in a medical intensive care unit. Ann Intern Med 1996, 125:448-456.
- [13]Clinical and Laboratory Standards Institute: Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically (M7-A8). Wayne, Pennsylvania: Clinical and Laboratory Standard Institute; 2009.
- [14]Clinical and Laboratory Standards Institute: Performance Standards for Antimicrobial Susceptibility Testing: Nineteenth Informational Supplement (M100-S19). Wayne, PA: Clinical and Laboratory Standard Institute; 2009.
- [15]Murray BE, Singh KV, Heath JD, Sharma BR, Weinstock GM: Comparison of genomic DNAs of different enterococcal isolates using restriction endonucleases with infrequent recognition sites. J Clin Microbiol 1990, 28:2059-2063.
- [16]Goering RV: Molecular epidemiology of nosocomial infection: analysis of chromosomal restriction patterns by pulsed-field gel electrophoresis. Infect Control Hosp Epidemiol 1993, 14:595-600.
- [17]Enright MC, Day NPJ, Davies CE, Peacock SJ, Spratt BG: Multilocus sequence typing for characterization of methicillin-resistant and methicillin-susceptible clones of Staphylococcus aureus. J Clin Microbiol 2000, 38:1008-1015.
- [18]Evers S, Sahm DF, Courvalin P: The vanB gene of vancomycin resistant Enterococcus faecalis V583 is structurally related to genes encoding D-Ala:D-Ala ligases and glycopeptide resistance proteins vanA and vanC. Gene 1993, 24:143-144.
- [19]Brisson-Noël A, Dutka-Malen S, Molinas C, Leclerq R, Courvalin P: Cloning and heterospecific expression of the resistance determinant vanA encoding high-level resistance to glycopeptides in Enterococcus faecium BM4147. Antimicrob Agents Chemother 1990, 34:924-927.
- [20]Smith TL, Iwen PC, Olson SB, Rupp ME: Environmental contamination with vancomycin-resistant enterococci in an outpatient setting. Infect Control Hosp Epidemiol 1998, 19:515-518.
- [21]Edmond MB, Ober JF, Weinbaum DL: Vancomycin-resistant Enterococcus faecium bacteremia: risk factors for infection. Clin Infect Dis 1995, 20:1126-1133.
- [22]Cho HH, Sung JY, Kwon KC, Lim JS, Koo SH: Antimicrobial resistance and multilocus sequence typing of vancomycin-resistant Enterococcus faecium isolated from the Chungcheong area. Korean J Clin Microbiol 2011, 14:60-66.
- [23]Lu CL, Chuang YC, Chang HC, Chen YC, Wang JT, Chang SC: Microbiological and clinical characteristics of vancomycin-resistant Enterococcus faecium bacteraemia in Taiwan: implication of sequence type for prognosis. J Antimicrob Chemother 2012, 67:2243-2249.