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Indian Journal of Medical Microbiology
Medknow Publications on behalf of Indian Association of Medical Microbiology
ISSN: 0255-0857 EISSN: 1998-3646
Vol. 29, Num. 2, 2011, pp. 198-199

Indian Journal of Medical Microbiology, Vol. 29, No. 2, April-June, 2011, pp. 198-199

Correspondence

VITEK 2 and PHOENIX fail to detect high-level gentamicin-resistant Enterococcus faecium isolates with aac-aph gene

1 Department of Clinical Microbiology, Selcuk University Selcuklu Faculty of Medicine, Konya, Turkey
2 Adnan Menderes Universitesi Tip Fakültesi, Tibbi Mikrobiyoloji AD and Adu Biltem Epidemiyoloji Birimi, Aydin, Turkey

Correspondence Address:B Bozdogan Adnan Menderes Universitesi Tip Fakültesi, Tibbi Mikrobiyoloji AD and Adu Biltem Epidemiyoloji Birimi, Aydin Turkey bbozdogan@adu.edu.tr

Date of Submission: 19-Jan-2011
Date of Acceptance: 09-Mar-2011

Code Number: mb11051

PMID: 21654126

DOI: 10.4103/0255-0857.81785

Dear Editor,

Detection of high-level gentamicin resistance is important to evaluate the use of β-lactam and aminoglycoside combination for treatment. The most common mechanism of high-level resistance to gentamicin is due to the presence of bifunctional inactivation enzyme AAC-APH. Twenty-seven vancomycin-resistant strains were tested for gentamicin susceptibility by using automated methods VITEK and PHOENIX systems as well as agar dilution MICs, E test, and disk diffusion using 120 μg disks. The presence of resistance genes was tested by PCR using specific primers. All isolates tested carried vanA and aac-aph genes. No inhibition zone was obtained with highly charged gentamicin disks as well as E test. Agar dilution MICs showed that 5, 3, and 19 strains had MIC 256, 512, and 1024 mg/L, respectively. Four of five isolates with gentamicin MICs 256 mg/L were susceptible by both VITEK and PHOENIX systems, and the remaining one was susceptible by PHOENIX and resistant by VITEK. Three isolates with MICs 520 mg/L were reported resistant by both systems. One isolate with MIC >1024 mg/L was reported susceptible by both automates which may be due to a growth problem. Gentamicin breakpoints for Enterococcus faecium of British, French, European, and American institutions have some differences [Table - 1]. EUCAST accepts that there is no synergy between β-lactams and aminoglycosides for strains with MICs >128 mg/L and this MIC level should be accepted as high level gentamicin resistance, which indicates acquisition of a resistance mechanism. BSAC also agrees with EUCAST recommendation. CA-SFM accepts ≤256 mg/L as susceptible, while for CLSI <512 mg/L is susceptible. [1],[2],[3],[4] MIC testing for gentamicin is useful only to evaluate the presence of β-lactam-aminoglycoside synergy. E. faecium isolates with MIC >128 mg/L, this synergy is broken. Our study showed that some of the strains with aac-aph gene reported as susceptible by VITEK and PHOENIX. We believe that the concentration used by automates to detect gentamicin-resistant enterococci should be re-evaluated.

Table 2

References

1.EUCAST Clinical breakpoints. Available from: http://www.eucast.org/clinical_breakpoints/ [Last Accessed on 2010 Dec 1].  Back to cited text no. 1    
2.Recommandations du CASFM. Available from: http://www.sfm.asso.fr/nouv/general.php?pa=2 [Last Accessed on 2010 Dec 1].  Back to cited text no. 2    
3.BSAC Methods for Antimicrobial Susceptibility Testing, Version 9.1. Available from: http://www.bsac.org.uk/Resources/BSAC/Version_9.1_March_2010_final.pdf. [March 2010].  Back to cited text no. 3    
4.Clinical and Laboratory Standards Institute Performance standards for antimicrobial susceptibility testing. 15 th informational supplement. Approved standard MS100-S16. Wayne, PA: CLSI; 2006.  Back to cited text no. 4    

Copyright 2011 - Indian Journal of Medical Microbiology


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