COMPARATIVE STUDY OF GELATINASE ACTIVITY AND PELLICLE FORMATION AMONG EXTENDED-SPECTRUM BETA-LACTAMASE AND NON-EXTENDED-SPECTRUM BETA-LACTAMASE PRODUCING ACINETOBACTER BAUMANNII FROM DIABETIC FOOT ULCER INFECTIONS
DOI:
https://doi.org/10.22159/ajpcr.2018.v11i9.28336Keywords:
Acinetobacter baumannii, Diabetic foot ulcer, Gelatinase, Multidrug resistance, PellicleAbstract
Objective: The aim of the study was to assess and compare the gelatinase activity and pellicle formation in extended-spectrum beta-lactamase (ESBL) and non-ESBL producing Acinetobacter baumannii isolates from diabetic foot ulcer infection (DFI).
Methods: A total of 42 isolates of A. baumannii recovered from patients of DFI from September 2016 to February 2018. Isolates were identified by the standard microbiological method and confirmed by the BD Phoenix 100 system. The antimicrobial susceptibility test was performed by the Kirby–Bauer disk diffusion method and ESBL was detected by double disk diffusion synergy test method. Gelatinase production was determined by the Luria Bertani agar supplemented with 30 g/L gelatin, and pellicle formation was determined by the Mueller-Hinton broth which is incubated at two different temperatures.
Results: A total of 42 A. baumannii isolates were multidrug resistant. Among 21 isolates, each was ESBL and non-ESBL producers. Pellicle formation at 25°C in ESBL and non-ESBL producer isolates was 47.61% (10/21) and 28.57% (06/21). Pellicle formation at 37°C in ESBL and non-ESBL producer isolates was 57.14% (12/21) and 42.85% (09/21), respectively. Gelatinase production was present in 38.09% ESBL and 28.57% in non-ESBL producers. ESBL strains were more virulent compared to non-ESBL producers among patients of DFIs.
Conclusion: This study showed that pellicle formation at 37°C was highly virulent due to ESBL producers. Gelatinase production was elevated in ESBL compared to non-ESBL producer isolates. This attribute of the isolates could render ESBL positive more pathogenic. Colistin and polymyxin B are the only choices of treatment for multidrug-resistant Acinetobacter baumannii infections.
Downloads
References
Bergogne-Bérézin E, Towner KJ. Acinetobacter spp. As nosocomial pathogens: Microbiological, clinical, and epidemiological features. Clin Microbiol Rev 1996;9:148-65.
Lahiri KK, Mani NS, Purai SS. Acinetobacter spp as nosocomial pathogen: Clinical significance and antimicrobial sensitivity. Med J Armed Forces India 2004;60:7-10.
Murali TS, Kavitha S, Spoorthi J, Bhat DV, Prasad AS, Upton Z, et al. Characteristics of microbial drug resistance and its correlates in chronic diabetic foot ulcer infections. J Med Microbiol 2014;63:1377-85.
Vatan A, Saltoglu N, Yemisen M, Balkan II, Surme S, Demiray T, et al. Association between biofilm and multi/extensive drug resistance in diabetic foot infection. Int J Clin Pract 2018:e13060.
Franco G, Costa DM, Cristina M, Tognim B, Cardoso CL, Carrara-Marrone FE, et al. Preliminary evaluation of adherence on abiotic and cellular surfaces of Acinetobacter baumannii strains isolated from catheter tips. Braz J Infect Dis 2006;10:346-51.
Nait Chabane Y, Marti S, Rihouey C, Alexandre S, Hardouin J, Lesouhaitier O, et al. Characterisation of pellicles formed by Acinetobacter baumannii at the air-liquid interface. PLoS One 2014;9:e111660.
Martà S, RodrÃguez-Bão J, Catel-Ferreira M, Jouenne T, Vila J, Seifert H, et al. Biofilm formation at the solid-liquid and air-liquid interfaces by Acinetobacter species. BMC Res Notes 2011;4:2-5.
Peleg AY, Seifert H, Paterson DL. Acinetobacter baumannii: Emergence of a successful pathogen. Clin Microbiol Rev 2008;21:538-82.
McConnell MJ, Actis L, Pachón J. Acinetobacter baumannii: Human infections, factors contributing to pathogenesis and animal models. FEMS Microbiol Rev 2013;37:130-55.
Endimiani A, Luzzaro F, Tamborini A, Lombardi G, Elia V, Belloni R, et al. Identification and antimicrobial susceptibility testing of clinical isolates of nonfermenting gram-negative bacteria by the phoenix automated microbiology system. New Microbiol 2002;25:323-9.
Clinical and Laboratory Standards Institute (CLSI). Performance Standards for Antimicrobial Susceptibility Testing. 26th ed Wayne PA: CLSI Supplements M100S; 2016.
Kumar SL, Ashutosh SR, Gokulshankar S, Ranjith MS, Mohanty BK, Lim MY. Is bacteriology a contributing factor in unsalvageable nature of diabetic foot infections? A study in a district hospital in Malaysia. Int J Pharm Pharm Sci 2015;8:262-5.
Kateel R, Augustine AJ, Prabhu S, Ullal S, Pai M, Adhikari P. Clinical and microbiological profile of diabetic foot ulcer patients in a tertiary care hospital. Diabetes Metab Syndr Clin Res Rev 2018;12:27-30.
Cevahir N, Demir M, Kaleli I, Gurbuz M, Tikvesli S. Evaluation of biofilm production, gelatinase activity, and mannose-resistant hemagglutination in Acinetobacter baumannii strains. J Microbiol Immunol Infect 2008;41:513-8.
Rasha JM, Al-Warid AL, Al-Thahab IJ. Isolation and identification of Acinetobacter baumannii in Hilla city. Int J Adv Biol Res 2014;4:4-8.
Giles SK, Stroeher UH, Eijkelkamp BA, Brown MH. Identification of genes essential for pellicle formation in Acinetobacter baumannii. BMC Microbiol 2015;15:116.
Zafar S, Naqvi SB, Abbas T, Qazi1 F. Synergistic combinations of broad-spectrum antibiotics against Acinetobacter spp. Int J Pharm Pharm Sci 2015;7:214-7.
Published
How to Cite
Issue
Section
The publication is licensed under CC By and is open access. Copyright is with author and allowed to retain publishing rights without restrictions.