Genetic Characterization of Carbapenem Resistant Acinetobacter baumannii in Tertiary care settings of Lahore, Pakistan
Abstract
Background: Acinetobacter baumannii is major cause of ventilator associated pneumoniae (VAP) as it is an opportunistic nosocomial organism. The current study was to find out the antibiotic resistance pattern of Acinetobacter baumannii, its phenotype and the genetic characterization of Metallo-β-Lactamase (MBL) genes that are responsible for carbapenem resistance.
Methods: One hundred and fifty Carbapenem resistant Acinetobacter baumannii (CRAB) specimens were isolated and PCR amplification of organism specific bla-OXA-51gene was performed and antibiotic susceptibility was checked. Phenotypic susceptibility analysis was performed by Modified Hodge Test (MHT) and Imipenem-EDTA Double Disc Synergy Test (IMP-EDTA DDST). The carbapenemases and MBL producing genes were amplified by PCR.
Results: CRAB showed high resistance against piperacillin/tazobactam (99.3%), cefepime and ceftazidime (99.3% each), amikacin (91.3%), ciprofloxacin (96.7%) and levofloxacin (96.7%). Only one isolate showed resistance to colistin. The isolates positive for both MHT and DDST (n=70) were further characterized to detect metallo-β-lactamase genes. Molecular characterization revealed the presence of bla-OXA-51 gene in all tested isolates (100%) followed by bla-VIM 89%, bla-OXA-23 64%, respectively and so on. Few genes coexisted with each other including bla VIM, bla OXA 23, bla OXA 51 and bla NDM-1. None of the isolate was found positive for bla-IMP gene.
Conclusion: It is concluded that CRAB isolates exhibited a high rate of resistance towards antimicrobials because of the presence of drug hydrolyzing enzymes, carbapenemases and MBLs. This is among the rare study reported recently indicating CRAB isolates co-harboring many resistant genes are very difficult to treat. There is a dire need to develop novel antibiotics against resistant A. baumannii to minimize its prevalence. Moreover, it is recommended that colistin treatment in the clinical settings should be continuously monitored in order to prevent the development of resistance.
Full Text:
PDFReferences
Doughari HJ, Ndakidemi PA, Human IS, Benade S. Virulence factors and antibiotic susceptibility among verotoxic non O157: H7 Escherichia coli isolates obtained from water and wastewater samples in Cape Town, South Africa. African Journal of Biotechnology. 2011;10(64):14160-14168.
Lin M-F, Lan C-Y. Antimicrobial resistance in Acinetobacter baumannii: From bench to bedside. World Journal of Clinical Cases: WJCC. 2014;2(12):787.
Yu Y-S, Yang Q, Xu X-W, Kong H-S, Xu G-Y, Zhong B-Y. Typing and characterization of carbapenem-resistant Acinetobacter calcoaceticus–baumannii complex in a Chinese hospital. Journal of medical microbiology. 2004;53(7):653-656.
Alfandari S, Gois J, Delannoy P-Y, Georges H, Boussekey N, Chiche A, et al. Management and control of a carbapenem-resistant Acinetobacter baumannii outbreak in an intensive care unit. Medecine et maladies infectieuses. 2014;44(5):229-231.
Szabó S, Feier B, Capatina D, Tertis M, Cristea C, Popa A. An overview of healthcare associated infections and their detection methods caused by pathogen bacteria in Romania and Europe. Journal of Clinical Medicine. 2022;11(11):3204.
Fishbain J, Peleg AY. Treatment of Acinetobacter infections. Clinical infectious diseases. 2010;51(1):79-84.
Towner K. Clinical importance and antibiotic resistance of Acinetobacter spp.: Proceedings of a symposium held on 4-5 November 1996 at Eilat, Israel. Journal of medical microbiology. 1997;46(9):721-746.
Gonzalez-Villoria AM, Valverde-Garduno VJJop. Antibiotic-resistant Acinetobacter baumannii increasing success remains a challenge as a nosocomial pathogen. 2016;2016.
Andrade SS, Jones RN, Gales AC, Sader HS. Increasing prevalence of antimicrobial resistance among Pseudomonas aeruginosa isolates in Latin American medical centres: 5 year report of the SENTRY Antimicrobial Surveillance Program (1997–2001). Journal of antimicrobial chemotherapy. 2003;52(1):140-141.
Lott H. Molecular mechanisms underpinning intraspecies co-infections with multiple Acinetobacter baumannii strains: Macquarie University; 2023.
Girija SA, Priyadharsini JV, Paramasivam A. Prevalence of carbapenem-hydrolyzing OXA-type β-lactamases among Acinetobacter baumannii in patients with severe urinary tract infection. Acta Microbiologica et Immunologica Hungarica. 2020;67(1):49-55.
Bratu S, Mooty M, Nichani S, Landman D, Gullans C, Pettinato B, et al. Emergence of KPC-possessing Klebsiella pneumoniae in Brooklyn, New York: epidemiology and recommendations for detection. Antimicrobial agents and chemotherapy. 2005;49(7):3018-3020.
Cornaglia G, Riccio M, Mazzariol A, Lauretti L, Fontana R, Rossolini G. Appearance of IMP-1 metallo-β-lactamase in Europe. The Lancet. 1999;353(9156):899-900.
Héritier C, Poirel L, Lambert T, Nordmann P. Contribution of acquired carbapenem-hydrolyzing oxacillinases to carbapenem resistance in Acinetobacter baumannii. Antimicrobial agents and chemotherapy. 2005;49(8):3198-3202.
Quale J, Bratu S, Landman D, Heddurshetti R. Molecular epidemiology and mechanisms of carbapenem resistance in Acinetobacter baumannii endemic in New York City. Clinical infectious diseases. 2003;37(2):214-220.
Thomson JM, Bonomo RA. The threat of antibiotic resistance in Gram-negative pathogenic bacteria: β-lactams in peril! Current opinion in microbiology. 2005;8(5):518-524.
Amudhan MS, Sekar U, Kamalanathan A, Balaraman S. blaIMP and blaVIM mediated carbapenem resistance in Pseudomonas and Acinetobacter species in India. The Journal of Infection in Developing Countries. 2012;6(11):757-762.
Cicek AC, Saral A, Iraz M, Ceylan A, Duzgun A, Peleg A, et al. OXA-and GES-type β-lactamases predominate in extensively drug-resistant Acinetobacter baumannii isolates from a Turkish University Hospital. Clinical Microbiology and Infection. 2014;20(5):410-415.
Kusradze I, Diene SM, Goderdzishvili M, Rolain J-M. Molecular detection of OXA carbapenemase genes in multidrug-resistant Acinetobacter baumannii isolates from Iraq and Georgia. International journal of antimicrobial agents. 2011;38(2):164-168.
Ayukekbong JA, Ntemgwa M, Atabe ANJAR, Control I. The threat of antimicrobial resistance in developing countries: causes and control strategies. 2017;6(1):1-8.
O'neill JJRAR. Antimicrobial resistance: tackling a crisis for the health and wealth of nations. 2014.
Tripathi N, Sapra A. Gram staining. 2020.
Chauhan A, Jindal T, Chauhan A, Jindal TJMMfE, Food, Analysis P. Biochemical and molecular methods for bacterial identification. 2020:425-468.
Whitman WB. Bergey's manual of systematics of Archaea and Bacteria: Wiley Online Library; 2015.
Clinical, Institute LS. Performance standards for antimicrobial susceptibility testing. Clinical and Laboratory Standards Institute Wayne, PA; 2017.
CLSI C. M100-S25: Performance Standards for Antimicrobial Susceptibility Testing. Twenty-Fifth Informational Supplement. 2012.
Amjad A, Mirza I, Abbasi S, Farwa U, Malik N, Zia F. Modified Hodge test: A simple and effective test for detection of carbapenemase production. Iranian journal of microbiology. 2011;3(4):189.
Yong D, Lee K, Yum JH, Shin HB, Rossolini GM, Chong Y. Imipenem-EDTA disk method for differentiation of metallo-β-lactamase-producing clinical isolates of Pseudomonas spp. and Acinetobacter spp. Journal of Clinical Microbiology. 2002;40(10):3798-3801.
Woodford N, Ellington MJ, Coelho JM, Turton JF, Ward ME, Brown S, et al. Multiplex PCR for genes encoding prevalent OXA carbapenemases in Acinetobacter spp. International journal of antimicrobial agents. 2006;27(4):351-353.
Ellington MJ, Kistler J, Livermore DM, Woodford N. Multiplex PCR for rapid detection of genes encoding acquired metallo-β-lactamases. Journal of Antimicrobial Chemotherapy. 2007;59(2):321-322.
Perry JD, Naqvi SH, Mirza IA, Alizai SA, Hussain A, Ghirardi S, et al. Prevalence of faecal carriage of Enterobacteriaceae with NDM-1 carbapenemase at military hospitals in Pakistan, and evaluation of two chromogenic media. Journal of Antimicrobial Chemotherapy.
;66(10):2288-2294.
Kiat Y, Vortman Y, Sapir N. Feather moult and bird appearance are correlated with global warming over the last 200 years. Nature Communications. 2019;10(1):1-7.
Kaleem F, Usman J, Hassan A, Khan A. Frequency and susceptibility pattern of metallo-beta-lactamase producers in a hospital in Pakistan. The Journal of infection in developing countries. 2010;4(12):810-813.
Evans BA, Hamouda A, Abbasi SA, Khan FA, Amyes SG. High prevalence of unrelated multidrug-resistant Acinetobacter baumannii isolates in Pakistani military hospitals. International journal of antimicrobial agents (Print). 2011;37(6):580-581.
Vijayakumar S, Mathur P, Kapil A, Das BK, Ray P, Gautam V, et al. Molecular characterization & epidemiology of carbapenem-resistant Acinetobacter baumannii collected across India. The Indian journal of medical research. 2019;149(2):240.
Nowak J, Zander E, Stefanik D, Higgins PG, Roca I, Vila J, et al. High incidence of pandrug-resistant Acinetobacter baumannii isolates collected from patients with ventilator-associated pneumonia in Greece, Italy and Spain as part of the MagicBullet clinical trial. Journal of Antimicrobial Chemotherapy. 2017;72(12):3277-3282.
Benmahmod AB, Said HS, Ibrahim RH. Prevalence and mechanisms of carbapenem resistance among Acinetobacter baumannii clinical isolates in Egypt. Microbial Drug Resistance. 2019;25(4):480-488.
Anwar M, Ejaz H, Zafar A, Hamid H. Phenotypic detection of metallo-beta-lactamases in carbapenem resistant Acinetobacter baumannii isolated from pediatric patients in Pakistan. Journal of pathogens. 2016;2016.
Fallah F, Noori M, Hashemi A, Goudarzi H, Karimi A, Erfanimanesh S, et al. Prevalence of blaNDM, blaPER, blaVEB, blaIMP, and blaVIM genes among Acinetobacter baumannii isolated from two hospitals of Tehran, Iran. Scientifica. 2014;2014.
Huang Z-Y, Li J, Shui J, Wang H-C, Hu Y-M, Zou M-X. Co-existence of bla OXA-23 and bla VIM in carbapenem-resistant Acinetobacter baumannii isolates belonging to global complex 2 in a Chinese teaching hospital. Chinese medical journal. 2019;132(10):1166-1172.
Ruiz M, Marti S, Fernandez-Cuenca F, Pascual A, Vila J. High prevalence of carbapenem-hydrolysing oxacillinases in epidemiologically related and unrelated Acinetobacter baumannii clinical isolates in Spain. Clinical microbiology and infection. 2007;13(12):1192-1198.
Sharma S, Banerjee T, Yadav G, Kumar AJFiC, Microbiology I. Susceptibility profile of blaOXA-23 and metallo-β-lactamases co-harbouring isolates of carbapenem resistant Acinetobacter baumannii (CRAB) against standard drugs and combinations. 2023;12:1068840.
Zhao F, Liu H, Yao Y, Zhang L, Zhou Z, Leptihn S, et al. Description of a Rare Pyomelanin-Producing Carbapenem-Resistant Acinetobacter baumannii Strain Coharboring Chromosomal OXA-23 and NDM-1. 2022;10(4):e02144-02122.
Anane YA, Apalata T, Vasaikar S, Okuthe GE, Songca SJIjom. Molecular detection of carbapenemase-encoding genes in multidrug-resistant Acinetobacter baumannii clinical isolates in South Africa. 2020;2020.
Sen B, Joshi SJJoam. Studies on Acinetobacter baumannii involving multiple mechanisms of carbapenem resistance. 2016;120(3):619-629.
Kallel H, Bahloul M, Hergafi L, Akrout M, Ketata W, Chelly H, et al. Colistin as a salvage therapy for nosocomial infections caused by multidrug-resistant bacteria in the ICU. International journal of antimicrobial agents. 2006;28(4):366-369.
DOI: http://dx.doi.org/10.62940/als.v10i3.1628
Refbacks
- There are currently no refbacks.