|Year : 2016 | Volume
| Issue : 3 | Page : 346-349
Reduced susceptibility to chlorhexidine disinfectant among New Delhi metallo-beta-lactamase-1 positive Enterobacteriaceae and other multidrug-resistant organisms: Report from a tertiary care hospital in Karachi, Pakistan
PB Mal1, J Farooqi1, S Irfan1, MA Hughes2, E Khan1
1 Department of Pathology and Laboratory Medicine, Section of Clinical Microbiology, Aga Khan University, Karachi - 74800, Pakistan
2 Department of Medicine, Division of Infectious Diseases, University of Virginia 22908, USA
|Date of Submission||06-Dec-2015|
|Date of Acceptance||18-May-2016|
|Date of Web Publication||12-Aug-2016|
Department of Pathology and Laboratory Medicine, Section of Clinical Microbiology, Aga Khan University, Karachi - 74800
Source of Support: None, Conflict of Interest: None
We analysed susceptibility of multidrug-resistant organisms (MDROs) including New Delhi metallo-beta-lactamase-1 positive Enterobacteriaceae to chlorhexidine and compared results to their susceptible counterparts. Susceptibilities of chlorhexidine digluconate in a standard (CHX-S) preparation and two commercial disinfectants containing different CHX concentrations (2% w/v and 4% w/w) were performed. MDROs had narrower range of higher CHX-S minimum inhibitory concentrations (MICs) as compared to pan-sensitive organisms. The MIC values for commercial disinfectants products for MDROs were many folds higher (20-600 times), than CHX-S for in vitro use. Increasing antibiotic resistance among bacterial isolates can be an indirect marker of reduced susceptibility to chlorhexidine in hospital setting.
Keywords: Chlorhexidine digluconate, minimum inhibitory concentration, multidrug-resistant organism
|How to cite this article:|
Mal P B, Farooqi J, Irfan S, Hughes M A, Khan E. Reduced susceptibility to chlorhexidine disinfectant among New Delhi metallo-beta-lactamase-1 positive Enterobacteriaceae and other multidrug-resistant organisms: Report from a tertiary care hospital in Karachi, Pakistan. Indian J Med Microbiol 2016;34:346-9
|How to cite this URL:|
Mal P B, Farooqi J, Irfan S, Hughes M A, Khan E. Reduced susceptibility to chlorhexidine disinfectant among New Delhi metallo-beta-lactamase-1 positive Enterobacteriaceae and other multidrug-resistant organisms: Report from a tertiary care hospital in Karachi, Pakistan. Indian J Med Microbiol [serial online] 2016 [cited 2020 Oct 1];34:346-9. Available from: http://www.ijmm.org/text.asp?2016/34/3/346/188338
| ~ Introduction|| |
With the emergence of multidrug-resistant organisms (MDROs), there is increasing concern about the possible association of resistance to commonly used disinfectants.  Pathogens have the capability to survive on dry surfaces for several days; hence, they are continuous source of transmission if effective infection control strategies are not utilised.  Chlorhexidine has a broad spectrum of antimicrobial activity and is used extensively in hospitals for various applications.  Despite its widely accepted use and efficacy, studies investigating the emergence of chlorhexidine resistance among micro-organisms are limited.  In particular, impact of New Delhi metallo-beta-lactamase-1 (NDM-1) gene in Gram-negative organisms susceptibility to it remains largely unknown.
In this study, we performed a comparative analysis of chlorhexidine susceptibility of MDROs including Enterobacteriaceae, methicillin-resistant Staphylococcus aureus (MRSA), vancomycin resistant Enterococcus (VRE) and Acinetobacter spp. (AC), and corresponding susceptible strains.
| ~ Methods|| |
Chlorhexidine susceptibility testing was performed on two sets of organisms: (a) Pan-sensitive (PAN) group (124) that included methicillin-sensitive S. aureus (MSSA = 45), vancomycin sensitive Enterococcus (VSE = 14), PAN-AC (2), PAN-Escherichia coli (PAN-EC = 37) and PAN-Klebsiella pneumoniae (PAN-KP = 26); (b) MDRO (161), NDM-1 positive KP (37) and NDM-1 positive EC (25), MRSA (50), VRE (18), multidrug-resistant AC (28), and extremely drug-resistant AC (XDR-AC = 3).
Antimicrobial susceptibility testing and minimum inhibitory concentration (MIC) were performed using Vitek2 (bioMérieux France) and interpreted according to the Clinical and Laboratory Standards Institute breakpoints. 
Standard chlorhexidine digluconate susceptibility
The MICs of chlorhexidine digluconate susceptibility (CHX-S) (Sigma, St. Louis, MO, USA) were determined using agar dilution, with a concentration range of 0.25-256 μg/mL. KP ATCC 13883 and EC ATCC 25922 (chlorhexidine MIC 16 and 2 μg/mL, respectively) were included as controls. 
Clinical in-use chlorhexidine digluconate preparation susceptibility testing
The MICs of in use CHX (CHX-IU) preparations were determined using broth dilution method containing a series of 2-fold dilutions, ranging in concentration from 19.5 to 10,000 μg/mL.
The 90 th percentiles of MICs (MIC 90) of various drugs for resistant organism groups, namely, MRSA, MDR-AC and NDM-positive Enterobacteriaceae, were calculated. Frequencies of isolates with different CHX MICs were determined. The mean difference in MICs of CHX-S between different groups of organisms and their 95% confidence intervals were computed and a Student's t-test was run to determine the statistical significance of this difference.
| ~ Results and Discussion|| |
A total of 285 clinical bacterial isolates from different clinical sources was selected for this study.
Standard chlorhexidine digluconate susceptibility
We found a narrower range of higher chlorhexidine MIC values for all MDROs as compared to pan-sensitive organisms as shown in [Table 1]. The current study showed Gram-negative bacteria to be more resistant to CHX-S (MIC range: 1-256 μg/ml) than Gram-positive bacteria (MIC range 0.5-32 μg/ml), as reported in previous studies. ,, Among Gram-positive bacteria VRE and Gram-negative bacteria colistin-resistant AC exhibited the highest chlorhexidine MICs as compared to other MDROs [Table 1]. This finding suggests that frequent use of colistin induces chlorhexidine resistance among Gram-negative bacteria. Both colistin and chlorhexidine act through outer cell membrane disruption with leakage of intracellular contents and bacterial death.  The mean difference in chlorhexidine MICs for MRSA versus MSSA, VRE versus VSE and NDM-1 positive-KP and NDM-1 positive-EC versus PAN-EC and PAN-KP was statistically significant (P < 0.0001) with a 95% confidence interval. Although the mean difference in chlorhexidine MIC values for MDR-AC versus PAN-AC was statistically significant (P = 0.013), the number of isolates was too few (n = 2). The MIC 90 values for all tested isolates are shown in [Table 1].
|Table 1: Comparison of standard chlorhexidine digluconate minimum inhibitory concentration values for multi - drug resistant and pan - sensitive organisms tested at the microbiology clinical laboratory at the Aga Khan University in Karachi, Pakistan |
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In-use chlorhexidine digluconate preparation susceptibility
The MICs of CHX-IU1 and CHX-IU2 for MDROs were many times higher than CHX-S. For NDM-1 positive-EC, NDM-1 positive-KP, XDR-AC, MRSA, MSSA and VRE, the MIC values of CHX-IU1 were 20-150-fold higher and MIC values of CHX-IU2 were 40,600-fold higher than those of CHX-S. Both CHX-IU were found to have inhibitory effects at the maximum concentration (undiluted form) only and failed to inhibit bacterial growth when diluted. In most hospitals throughout Pakistan, activities related to housekeeping services including choice of disinfectants, preparations of disinfectants and frequency of preparations (daily versus weekly) are done by personnel with little or no formal education. Label instructions are often ignored, and with limited resources, the tendency may be to dilute the disinfectant for longer use. EC ATCC 25922 and KP ATCC 13883 exhibited highest chlorhexidine MIC >10000 μg/ml when tested against the two commercial preparations. These results suggest that the effective concentration of chlorhexidine in these products was 2500-5000-fold less than CHX-S. This finding raises a concern about the quality of the product and preparation on site which is alarming and reflects poor quality control in commercial product manufacturing in the local market. Alternatively, the breakdown of chlorhexidine due to storage at improper temperatures for extended periods of time might be responsible for high MIC values observed with commercial products. Use of sub-standard (diluted) disinfectants in hospital environmental cleaning gives ineffective infection control practices. Strict implementation of hospital disinfectant policies and legislative regulations in production and import of disinfectants are required.
| ~ Conclusion|| |
In the absence of standardised methods for CHX-S, hospital antibiogram can be a useful predictor for CHX susceptibility among pathogens. Moreover, use of colistin might induce resistance to CHX in Gram-negative rods. Further studies are recommended to investigate this association. Proper implementations of hospital disinfectant policies coupled with strict manufacture regulations are strongly recommended.
We would like to thank Professor Afia Zafar, Department of Pathology and Laboratory Medicine at the Aga Khan University, for ATCC control isolates used in this study.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| ~ References|| |
Kõljalg S, Naaber P, Mikelsaar M. Antibiotic resistance as an indicator of bacterial chlorhexidine susceptibility. J Hosp Infect 2002;51:106-13.
Kramer A, Schwebke I, Kampf G. How long do nosocomial pathogens persist on inanimate surfaces? A systematic review. BMC Infect Dis 2006;6:130.
Jones CG. Chlorhexidine: Is it still the gold standard? Periodontol 2000 1997;15:55-62.
Fritz SA, Hogan PG, Camins BC, Ainsworth AJ, Patrick C, Martin MS, et al.
Mupirocin and chlorhexidine resistance in Staphylococcus aureus
in patients with community-onset skin and soft tissue infections. Antimicrob Agents Chemother 2013;57:559-68.
Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing - CLSI Document CLSI M100-S22. Twenty Second Informational Supplement. Wayne, Pennsylvania, USA: Clinical and Laboratory Standards Institute; 2012. p. 46-68.
Naparstek L, Carmeli Y, Chmelnitsky I, Banin E, Navon-Venezia S. Reduced susceptibility to chlorhexidine among extremely-drug-resistant strains of Klebsiella pneumoniae
. J Hosp Infect 2012;81:15-9.
Russell AD. Bacterial resistance to disinfectants: Present knowledge and future problems. J Hosp Infect 1999;43 Suppl 1:S57-68.
Fang CT, Chen HC, Chuang YP, Chang SC, Wang JT. Cloning of a cation efflux pump gene associated with chlorhexidine resistance in Klebsiella pneumoniae
. Antimicrob Agents Chemother 2002;46:2024-8.