PREVALENCE OF AMPC Î’-LACTAMASES IN CLINICAL ISOLATES OF E. COLI FROM A TERTIARY CARE RURAL HOSPITAL

Authors

  • Dardi Charan Kaur Maharashtra Institute of Medical Education & Research (MIMER),Talegaon Dabhade, Pune. Approved by MCI 34 (41) /2003-Med/27286 Dt - 24/12/03 Affiliated to Maharashtra University of Health Sciences (MUHS) , Nashik.
  • Jaishreee S Puri MIMER Medical College
  • Sandhya S Kulkarni MIMER Medical College
  • Anjali Jayawant MIMER Medical College

Keywords:

Cefoxitin resistance, Escherichia coli, AmpC b lactamases, Combined disc diffusion test and Disk approximation test

Abstract

Objective: Organisms over expressing AmpC (Ambler Class C) β-lactamases are of clinical concern because they restrict therapeutic options causing treatment failures and are increasing in occurrence worldwide. So the present study was to undertaken with the aim to know the prevalence of plasmid mediated AmpC and inducible AmpC β-lactamases in clinical isolates of E. coli in our tertiary care rural hospital.

Methods: 74 cefoxitin resistant E. coli isolates were tested for AmpC production by combined disc diffusion test and disk approximation test.

Results: Out of 74 cefoxitin resistance E. coli isolated from various clinical specimen 25(33.78%) showed AmpC β-lactamases production. PMABL was seen in 22(29.73%) and inducible AmpC in 3(4.05%). Among 25 AmpC producing E. coli, 8(32%) were from urine, 5(20%) from miscellaneous, 4(16%) from sputum and 12% respectively from stool and Pus and in Blood 2(8%). Age-wise higher distribution of AmpC β-lactamase was in an age group below 1yr (44.44%) and in age group of 20-39yrs (40%). The higher distribution of AmpC b lactamases producer from Medicine, Obgy, ICU(20% respectively) paediatric 16%,surgery 8%, TB 12% and lower from OPD(4%). In our study, multidrug resistance has been observed among the PMABL producing strains. Higher resistance was seen in gentamicin 22(88%), ciprofloxacin 23(92%), ceptazidime 25(100%), cefaclor 25(100%). Whereas PMABL isolates was susceptible to tigecycline (100%), meropenem (92%), amikacin(60%).

Conclusion: The overall prevalence of 10.50% AmpC β-lactamase in E. coli and Multidrug resistance is a matter of concern. So identification of AmpC may help in formulating the hospital infection control committee decreasing the selective antibiotic pressure.

 

Downloads

Download data is not yet available.

Author Biographies

Dardi Charan Kaur, Maharashtra Institute of Medical Education & Research (MIMER),Talegaon Dabhade, Pune. Approved by MCI 34 (41) /2003-Med/27286 Dt - 24/12/03 Affiliated to Maharashtra University of Health Sciences (MUHS) , Nashik.

Assistant Professor,Dept of Microbiology

Jaishreee S Puri, MIMER Medical College

Associate professor

Sandhya S Kulkarni, MIMER Medical College

professor

Anjali Jayawant, MIMER Medical College

assistat professor

References

Philippon A, Arlet G, Jacoby GA. Plasmid-determined AmpC-type beta-lactamases. Antimicrob Agents Chemother 2002;46:1-11.

Jacoby GA. AmpC β-Lactamases. Clin Microbiol Rev 2009;22:161-82.

Coudron PE, Moland ES, Thomson KS. Occurrence and detection of AmpC beta-lactamases among Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis isolates at a veterans medical center. J Clin Microbiol 2000;38:1791-6.

Thomson KS. Controversies about extended-spectrum and AmpC beta-lactamases. Emerging Infect Dis 2001;7:333-6.

Tan TY, Ng SY, Teo L, Koh Y, Teok CH. Detection of plasmid mediated AmpC in Escherichia coli, Klebsiella pneumoniae and Proteus mirabilis. J Clin Pathol 2008;61:642-4.

Ding H, Y ang Y, Lu Q, Wang Y, Chen Y, Deng L, et al. The prevalence of plasmid-mediated AmpC β-lactamases among clinical isolates of Escherichia coli and Klebsiella pneumoniae from five children’s hospitals in China. Eur J Clin Microbiol Infect Dis 2008;27:915-21.

Alvarez M, Tran JH, Chow N, Jacoby GA. Epidemiology of conjugative plasmid mediated AmpC β-lactamases in the United States. Antimicrob Agents Chemother 2004;48:533-7.

Woodford N, S Reddy, EJ Fagan, RL Hill, KL Hopkins, ME Kaufmann, et al. Wide geographic spread of diverse acquired AmpC beta-lactamases among Escherichia coli and Klebsiella spp. in the UK and Ireland. J Antimicrob Chemother 2007;59:102–5.

Subha A, Renuka Devi V, Ananthan S. AmpC β-lactamases producing multidrug resistant strains of Klebsiella spp. & Escherichia coli isolated from children under five in Chennai. India. Indian J Med Res 2003;117:13-8.

Ratna AK, Menon I, Kapur I, Kulkarni R. Occurrence & detection of AmpC β-lactamases at a referral hospital in Karnataka. Indian J Med Res 2003;118:29-32.

Hernandez-Alles S, M Conejo, A Pascual, JM Tomas, VJ Benedi, et al. Relationship between outer membrane alterations and susceptibility to antimicrobial agents in isogenic strains of Klebsiella pneumoniae. J Antimicrob Chemother 2000;46:273–7.

Hanson DN. AmpC β-lactamases: what do we need to know for the future? J Antimicrob Chemother 2003;52:2-4.

Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing. 17th ed. CLSI document M100-S17. Wayne, Pa: Clinical and Laboratory Standards Institute; 2007.

Koneman EW, Allen SD, Janda WM, Schreckenberger PC, Winn WC Jr. The Enterobacteriaceae. In: Color atlas and textbook of diagnostic microbiology. editor 4th ed. Philadelphia: J. B. Lippincott Co; 1992. p. 105-84.

Pe´rez-Pe´rez FJ, Hanson ND. Detection of plasmid mediated 4. AmpC β-lactamase genes in clinical isolates by using multiplex PCR. J Clin Microbiol 2002;40:2153-62.

Black JA, Moland ES, Thomson KS. 3. AmpC disk test for detection of plasmid-mediated AmpC β-lactamases in Enterobacteriaceae lacking chromosomal AmpC β-lactamases. J Clin Microbiol 2005;43:3110-3.

Singhal S, Mathur T, Khan S, Upadhyay DJ, Chugh S, Gaind R, et al. Evaluation of methods for AmpC betalactamase in gram negative clinical isolates from tertiary care hospitals. Indian J Med Microbiol 2005;23:120-4.

Smitha O Bagali, BV Peerapur. Detection of AmpC Beta-lactamases among Escherichia coli isolates at a tertiary care hospital in Karnataka. Al Am J Med Sci 2013;6(1):85-7.

Anand Manoharan, Madhan Sugumar, Anil Kumar, Hepzibah Jose, Dilip Mathai, ICMR-ESBL study group. Phenotypic & molecular characterization of AmpC β-lactamases among Escherichia coli, Klebsiella spp. & Enterobacter spp. from five Indian Medical Centers. Indian J Med Res 2012;135:359-64.

Parveen R Mohamudha, BN Harish, SC Parija. Molecular description of plasmid-mediated AmpC β-lactamases among nosocomial isolates of Escherichia coli & Klebsiella pneumoniae from six different hospitals in India. Indian J Med Res 2012;135:114-9.

Shoorashetty RM, Nagarathnamma T, Prathibha J. Comparison of the boronic acid disk potentiation test and cefepime-clavulanic acid method for the detection of ESBL among AmpC-producing Enterobacteriaceae. Indian J Med Microbiol 2011;29:297-301.

Ananthan S, Subha A. Cefoxitin resistance mediated by loss of a porin in clinical strains of Klebsiella pneumoniae and Escherichia coli. Indian J Med Microbiol 2005;23:20-3.

Tondi D, Calò S, Shoichet BK, Costi MP. Structural study of phenyl boronic acid derivatives as AmpC β-lactamase inhibitors. Bioorg Med Chem Lett 2010;20:3416-9.

Qin X, SJ Weissman, MF Chesnut, B Zhang, L Shen. Kirby-Bauer disc approximation to detect inducible third-generation cephalosporin resistance in Enterobacteriaceae. Ann Clin Microbiol Antimicrob 2004;3:13.

Taneja N, Rao P, Arora J, Dogra A. Occurrence of ESBL and Amp-C beta-lactamases and susceptibility to newer antimicrobial agents in complicated UTI. Indian J Med Res 2008;127:85-8.

Pitout JD, Le PG, Moore KL, Church DL, Gregson DB. Detection of AmpC beta-lactamases in Escherichia coli, Klebsiella spp, Salmonella spp and Proteus mirabilis in a regional clinical microbiology laboratory. Clin Microbiol Infect 2010;16:165-70.

Song W, Jeong SH, Kim JS, Kim HS, Shin DH, Roh KH, et al. Use of boronic acid disk methods to detect the combined expression of plasmid-mediated AmpC β-lactamases and extended-spectrum β-lactamases in clinical isolates of Klebsiella spp., Salmonella spp., and Proteus mirabilis. Diagn Microbiol Infect Dis 2007;57:315-8.

Adler H, Fenner L, Walter P, Hohler D, Schultheiss E, Oezcan S, et al. Plasmid-mediated AmpC β-lactamases in Enterobacteriaceae lacking inducible chromosomal ampC genes: prevalence at a Swiss university hospital and occurrence of the different molecular types in Switzerland. J Antimicrob Chemother 2008;61:457-8.

Yong D, Choi YS, Park DY, Kim S, Lee H, Y um JH, et al. editors. Prevalence and characteristics of plasmid-mediated AmpC beta-lactamase in Escherichia coli and Klebsiella pneumoniae isolates in a Korean hospital. Proceedings of the 15th European Congress of Clinical Microbiology and Infectious Diseases Conference; 2005 April 2-5: Copenhagen, Denmark: Oxford; 2005.

Arora S, Bal M. AmpC β-lactamase producing bacterial isolates from Kolkata hospital. Indian J Med Res 2005;122:224-33.

Published

01-06-2015

How to Cite

Kaur, D. C., J. S. Puri, S. S. Kulkarni, and A. Jayawant. “PREVALENCE OF AMPC Î’-LACTAMASES IN CLINICAL ISOLATES OF E. COLI FROM A TERTIARY CARE RURAL HOSPITAL”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 6, June 2015, pp. 165-8, https://journals.innovareacademics.in/index.php/ijpps/article/view/4542.

Issue

Section

Original Article(s)