Journals / Turkish Journal of Medical Sciences / 2015 / Cilt: 45 - Sayı: 6

Molecular characteristics of extended spectrum β-lactamase and carbapenemase genes carried by carbapenem-resistant Enterobacter cloacae in a Chinese university hospital

Pages
1321–1328
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Effective measures should be taken to control the spreadof CREC.

📌 3 Key Takeaways

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Objective & Hypothesis:Background/aim: In recent years, the increase in the prevalence of carbapenem-resistant Enterobacter cloacae (CREC) has beensignificant and has become a global problem.
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Key Findings & Data:The aim of this study is to characterize CREC extended spectrum β-lactamases (ESBLs)and CREC carbapenemase genes and evaluate the risk factors for CREC infections in a university hospital in China.Materials and methods: The identification and assessment of the antimicrobial susceptibility of CREC isolates were performed usinga VITEK-2 compact system.
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Conclusion & Impact:Effective measures should be taken to control the spreadof CREC.
🔬Design:Research Article
📍Scope:2009 Verileri
⚙️Variables:Domain Parameters

Abstract

Background/aim: In recent years, the increase in the prevalence of carbapenem-resistant Enterobacter cloacae (CREC) has beensignificant and has become a global problem. The aim of this study is to characterize CREC extended spectrum β-lactamases (ESBLs)and CREC carbapenemase genes and evaluate the risk factors for CREC infections in a university hospital in China.Materials and methods: The identification and assessment of the antimicrobial susceptibility of CREC isolates were performed usinga VITEK-2 compact system. Clonal relatedness was investigated by pulsed-field gel electrophoresis (PFGE). β-Lactamase genes wereexamined using polymerase chain reaction and nucleotide sequencing.Results: A total of 64 CREC isolates were included in the study. The rate of CREC infections significantly increased between 2009 and2012. Among the CREC isolates, 39 (60.9%) isolates possessed ESBL genes, and 49 (76.6%) carried carbapenemase genes; blaSHV-12 andblaKPC-2 were the most common genes, respectively. PFGE showed that there were no obvious clonal associations between these CRECisolates, except for 3 isolates. A univariate analysis demonstrated that prior treatment with antibiotics, intravascular catheterization,urinary catheterization, mechanical ventilation, and parenteral nutrition were significant risk factors for CREC infections.Conclusion: The emergence and increase of CREC infections is worrisome. Effective measures should be taken to control the spreadof CREC.

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Cite This Article

CUI, L., ZHAO, J., LU, J. (2022). Molecular characteristics of extended spectrum β-lactamase and carbapenemase genes carried by carbapenem-resistant Enterobacter cloacae in a Chinese university hospital. Turkish Journal of Medical Sciences, Cilt: 45 - Sayı: 6, 1321–1328. https://ajindex.com/articles/610943

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References (12)

  1. Yang FC, Yan JJ, Hung KH, Wu JJ. Characterization of ertapenem–resistant Enterobacter cloacae in a Taiwanese university hospital. J Clin Microbiol 2012; 50: 223–226
  2. Patel G, Huprikar S, Factor SH, Jenkins SG, Calfee DP. Outcomes of carbapenem-resistant Klebsiella pneumoniae infection and the impact of antimicrobial and adjunctive therapies. Infect Control Hosp Epidemiol 2008; 29: 1099–1106
  3. Marchain D, Navon-Venezia S, Schwaber MJ, Carmeli Y. Isolation of imipenem-resistant Enterobacter species: emergence of KPC-2 carbapenemase, molecular characterization, epidemiology, and outcomes. Antimicrob Agents Chemother 2008; 52: 1413–1418
  4. Souli M, Galani I, Antoniadou A, Papadomichelakis E, Poulakou G, Panagea T, Vourli S, Zerva L, Armaganidis A, Kanellakopoulou K et al. An outbreak of infection due to beta- Lactamase Klebsiella pneumoniae carbapenemase 2-producing K. pneumoniae in a Greek university hospital: molecular characterization, epidemiology, and outcomes. Clin Infect Dis 2010; 50: 364–373
  5. Monteiro J, Santos AF, Asensi MD, Peirano G, Gales AC. First report of KPC-producing Klebsiella pneumoniae strains in Brazil. Antimicrob Agents Chemother 2009; 53: 333–334
  6. Peirano G, Seki LM, Val Passos VL, Pinto MCFG, Guerra LR, Asensi MD. Carbapenem-hydrolysing β-lactamase KPC-2 in Klebsiella pneumoniae isolated in Rio de Janeiro, Brazil. J Antimicrob Chemother 2009; 63: 265–268
  7. Iabadene H, Messai Y, Ammari H, Ramdani-Bouguessa N, Lounes S, Bakour R, Arlet G. Dissemination of ESBL and Qnr determinants in Enterobacter cloacae in Algeria. J Antimicrob Chemother 2008; 62: 133–136
  8. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing, 21st Informational Supplement 2011, M100-S21. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2011
  9. Xia Y, Liang Z, Su X, Xiong Y. Characterization of carbapenemase genes in Enterobacteriaceae species exhibiting decreased susceptibility to carbapenems in a University Hospital in Chongqing, China. Ann Lab Med 2012; 32: 270–275
  10. Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, Swaminathan B. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 1995; 33: 2233–2239
  11. Gupta N, Limbago BM, Patel JB, Kallen AJ. Carbapenem- resistant Enterobacteriaceae: epidemiology and prevention. Clin Infect Dis 2011; 53: 60–67
  12. Yang Q,