FOSFOMYCIN SUSCEPTIBILITY IN MULTIDRUG-RESISTANT UROPATHOGENS: A RETROSPECTIVE STUDY IN THE ERA OF ANTIMICROBIAL RESISTANCE
DOI:
https://doi.org/10.22159/ajpcr.2024v17i11.51811Keywords:
Fosfomycin, Uropathogens,, Multidrug-resistance, Extended spectrum β lactamase’s, Metallo-betalactamase’s.Abstract
Objective: Urinary tract infection (UTI) is one of the most prevalent clinical entities affecting people worldwide. The accelerating rate of Antimicrobial resistance due to the unimpeded and rampant use of antimicrobials with over-the-counter availability of drugs has limited the therapeutic options for the treatment of UTIs. Fosfomycin, an old broad-spectrum antimicrobial with good pharmacokinetics has regained importance for the treatment of multidrug-resistant (MDR) isolates. The purpose of this study was to determine the in vitro Fosfomycin susceptibility of common uropathogens and to study the resistance pattern of these organisms against commonly prescribed antimicrobial agents.
Methods: A retrospective cross-sectional study was conducted in the Bacteriology section of the Microbiology laboratory at Adesh Institute of Medical Sciences and Research, Bathinda, Punjab for duration of 6 months from December 2022 to May 2023 from urine samples received from all clinically suspected cases of UTI. Samples were processed immediately as per standard microbiological techniques, followed by culture by a semi-quantitative method. Kass criteria was followed for interpretation of significant bacteriuria according to which significant growth was considered if the colony count was more than 105 colony forming units (CFU)/mL. Culture positives were analyzed by Gram staining and on the basis of colony characteristics, Gram staining, final identification, and Antimicrobial Susceptibility were done through Vitek 2 compact system.
Results: A total of 2292 urine samples received in the Microbiology laboratory were processed and cultured during the study period, which yielded 509 significant bacterial isolates i.e.509/2292 (22.2%) culture positivity. Among 509 culture-positive samples, Escherichia coli 235/509 (46.1%) was the most common uropathogens isolated followed by Klebsiella pneumoniae 107/509 (21.1%), Enterococcus species 40/509 (7.8%). Fosfomycin depicted good in vitro susceptibility of a minimum of 94% in both Gram-negative and Gram-positive uropathogens as compared to Nitrofurantoin, which showed sensitivity of 74% and 85%, respectively. Maximum resistance was observed toward Cephalosporins i.e., Ceftriaxone in E. coli (60%) and K. pneumoniae (64%), respectively, followed by 50% in Acinetobacter baumannii. Maximum resistance to Ciprofloxacin (62%) was seen in case of A. baumannii. 172/405(42.4%) isolates of Enterobacteriaceae family were extended-spectrum β-lactamase (ESBL) producers with an average Fosfomycin susceptibility of 95.9%. Among the total isolated uropathogens, 135/509 (26.5%) were MDR, out of which 116/135 (85.9%) depicted Fosfomycin susceptibility. Metallo-beta-lactamase (MBL) production was seen in 14.3% of the isolated Gram-negative uropathogens. 63/73(86.3%) of the MBL producers were found susceptible to Fosfomycin.
Conclusion: Fosfomycin has emerged as an effective alternative for the treatment of common uropathogens including the MDRs, ESBL producers, and the MBLs in the era of increasing antimicrobial resistance. It has the potential to act as a promising oral agent for the treatment of UTI in both community and healthcare setups.
Downloads
References
Sreenivasan S, Kali A, Pravin Charles MV, Kunigal S. Evaluation of in vitro susceptibility of fosfomycin among Enterobacteriaceae isolates from urine cultures: A study from Puducherry. J Lab Physicians. 2019;11:249-52. doi: 10.4103/JLP.JLP_27_19
Banerjee S, Sengupta M, Sarker TK. Fosfomycin susceptibility among multidrug-resistant, extended-spectrum beta-lactamase-producing, carbapenem-resistant uropathogens. Indian J Urol. 2017;33:149-54. doi: 10.4103/iju.IJU_285_16
Kothari A, Chaturvedi P, Bhumbla U. Fosfomycin susceptibility among multidrug-resistant extended-spectrum beta-lactamase and metallo-beta lactamase-producing uropathogens in a tertiary care hospital. Infect Dis Clin Pract. 2024;32:e1348. doi: 10.1097/IPC.0000000000001348
Procop GW, Church DL, Hall GS, Janda WM. Koneman’s Color
Atlas and Textbook of Diagnostic. Philadelphia, PA: Wolters Kluwer Health; 2017.
Palzkill T. Metallo-β-lactamase structure and function. Ann N Y Acad Sci. 2013;1277:91-104. doi: 10.1111/j.1749-6632.2012.06796.x
Karageorgopoulos DE, Wang R, Yu XH, Falagas ME. Fosfomycin: Evaluation of the published evidence on the emergence of antimicrobial resistance in gram-negative pathogens. J Antimicrob Chemother. 2012;67(2):255-68. doi: 10.1093/jac/dkr466
Mothibi LM, Bosman NN, Nana T. Fosfomycin susceptibility of uropathogens at Charlotte Maxeke Johannesburg Academic Hospital. S Afr J Infect Dis. 2020;35(1):a173. doi: 10.4102/sajid.v35i1.173
CLSI. Performance Standards for Antimicrobial Susceptibility Testing. 32nd ed. CLSI Supplement M100. United States: Clinical and Laboratory Standards Institute; 2022
Sharmin S, Mostofa Kamal SM, Reza MA, Ashik Elahi KM, Mostofa Elma SM, Habib B. Fosfomycin-a promising oral antibiotic for the treatment of Urinary Tract Infection (UTI). Open J Urol. 2022;12:257-70. doi: 10.4236/oju.2022.125026
Singh MM, Devi R, Garg S, Mehra M. Effectiveness of syndromic approach in management of reproductive tract infections in Women. Indian J Med Sci. 2001;55:209-14.
Sood S, Gupta R. Antibiotic resistance pattern of community acquired uropathogens at a tertiary care hospital in Jaipur, Rajasthan. Indian J Community Med. 2012;37:39-44. doi: 10.4103/0970-0218.94023
Sharlee R, Sumangala B. Fosfomycin susceptibility on uropathogens in a tertiary care hospital, Mandya institute of medical sciences, Mandya. Indian J Microbiol Res. 2019;6(1):15-17. doi: 10.18231/2394- 5478.2019.0004
Gopichand P, Agarwal G, Natarajan M, Mandal J, Deepanjali S, Parameswaran S, et al. In vitro effect of fosfomycin on multi-drug resistant gram-negative bacteria causing urinary tract infections. Infect Drug Resist. 2019;12:2005-13. doi: 10.2147/IDR.S207569
Bakshi R, Sehgal VK, Kansal P, Kaur S. Detection of extended-spectrum beta lactamases and AmpC beta lactamases producing uropathogenic Escherichia coli in a tertiary care hospital. Int J Med Dent Sci. 2019;8:1783-92. doi: 10.18311/ijmds/2019/23503
Anand M, Sahu C, Negi P, Singh A. In vitro assessment of fosfomycin: A beacon of hope in drug resistant organisms causing urinary tract infections. J Adv Med Med Res. 2019;30:1-9. doi: 10.9734/jammr/2019/ v30i230169
Das B, Mittal N, Goswami R, Adhana D, Rathore N. Prevalence of Multidrug Resistance (MDR) and Extended Spectrum Beta-lactamases (ESBLs) among uropathogenic Escherichia coli isolates from female patients in a tertiary care hospital in North India. Int J Reprod Contracept Obstet Gynecol. 2018;7:5031-6. doi: 10.18203/2320-1770. ijrcog20184961
Asha Pai KB, Rajagopalan B. Susceptibility of urinary Escherichia coli to fosfomycin and nitrofurantoin-re-exploration of old and forgotten oral antibiotics. J Evol Med Dent Sci. 2020;9:928-31. doi: 10.14260/ jemds/2020/200
Jain R, Pal N, Hooja S. Fosfomycin susceptibility among multidrug resistant and extended spectrum β-lactamase producing uropathogenic Escherichia coli isolates at a tertiary care hospital of Western India. CHRISMED J Health Res. 2022;9:125-9. doi: 10.4103/cjhr.cjhr_21_21
Dalai S, Modak M, Lahiri K. Fosfomycin susceptibility among uropathogenic E. coli and K. pneumoniae. Int J Sci Res. 2019;8:282-4.
Tellis RC, Moosabba MS, Roche RA. Correlation between biofilm formation and antibiotic resistance in uropathogenic Pseudomonas aeruginosa Causing catheter associated urinary tract infections. Eur J Pharm Med Res. 2017;4:248-52.
Kaur DC. Prevalence of metallo-β-lactamase in gram negative uropathogens from a tertiary care rural hospital. Dent Hist. 2015; 17(67):11-5.
Sundaramurthy R, Tiruvanamalai R, Sivaraman ST, Arunagiri R, Charles J. Study on clinico microbiological profile and antibiotic susceptibility pattern of urinary tract pathogens with special reference to susceptibility of Escherichia coli to fosfomycin. Indian J Microbiol Res. 2018;5:258-66. doi: 10.18231/2394-5478.2018.0054
Sahni RD, Balaji V, Varghese R, John J, Tansarli GS, Falagas ME. Evaluation of fosfomycin activity against uropathogens in a fosfomycin-naive population in South India: A prospective study. Future Microbiol. 2013;8:675-80. doi: 10.2217/fmb.13.31
Published
How to Cite
Issue
Section
Copyright (c) 2024 Upasana Bhumbla, Jasleen Kaur
This work is licensed under a Creative Commons Attribution 4.0 International License.
The publication is licensed under CC By and is open access. Copyright is with author and allowed to retain publishing rights without restrictions.