E-ISSN 2146-9369 | ISSN 2146-3158
 

Research Article 


In vitro efficacy of fosfomycin against clinical strains

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu.


Cited By:9

Abstract
Objectives: Fosfomycin is an alternative drug for treatment of uncomplicated urinary tract infections. This study aimed to investigate in vitro activity of fosfomycin against methicillin-resistant Staphylococcus aureus (MRSA), methicillin-resistant coagulase negative staphylococci (MRCoNS), vancomycin-resistant Enterococcus faecium (VR E. faecium), Escherichia coli, Klebsiella pneumoniae, and Enterobacter isolates.
Methods: Clinical isolates of MRSA, MRCoNS, E. coli, K. pneumoniae and Enterobacter spp. and VRE isolates which were isolated from rectal swaps were identified with Vitek 2 Compact (Biomeriux, France) and BD Phoenix (BD USA) automated systems. The Kirby-Bauer disc diffusion method was used to determine the susceptibility to fosfomycin.
Results: All the MRSA (n=40), MRCoNS (n=40), and VR E. faecium (n=62) isolates were susceptible to fosfomycin. The fosfomycin susceptibility rates for E. coli, K. pneumoniae, and Enterobacter spp. were 97.5% (39 of 40), 97.3% (36 of 37), and 86.9% (20 of 23), respectively. One (2.7%) isolate of K. pneumoniae and three (13.1%) isolates of Enterobacter spp. showed intermediate susceptibility to fosfomycin. Resistance to fosfomycin was detected in only one (2.5%) isolate of E. coli.
Conclusion: Based on the results of our study, fosfomycin is highly active against a collection of several gram-positive and gram-negative bacteria, including multidrug resistant isolates, and is an alternative drug in the treatment option. J Microbiol Infect Dis 2014;4(2): 55-58 doi: 10.5799/ahinjs.02.2014.02.0127

Key words: Fosfomycin, gram-positive bacteria, gram-negative bacteria, antimicrobial agent


 
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How to Cite this Article
Pubmed Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu. In vitro efficacy of fosfomycin against clinical strains. J Microbiol Infect Dis. 2014; 4(2): 55-58 . doi:10.5799/jmid0127


Web Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu. In vitro efficacy of fosfomycin against clinical strains. https://www.jmidonline.org/?mno=302656953 [Access: November 24, 2024]. doi:10.5799/jmid0127


AMA (American Medical Association) Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu. In vitro efficacy of fosfomycin against clinical strains. J Microbiol Infect Dis. 2014; 4(2): 55-58 . doi:10.5799/jmid0127



Vancouver/ICMJE Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu. In vitro efficacy of fosfomycin against clinical strains. J Microbiol Infect Dis. (2014), [cited November 24, 2024]; 4(2): 55-58 . doi:10.5799/jmid0127



Harvard Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu (2014) In vitro efficacy of fosfomycin against clinical strains. J Microbiol Infect Dis, 4 (2), 55-58 . doi:10.5799/jmid0127



Turabian Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu. 2014. In vitro efficacy of fosfomycin against clinical strains. Journal of Microbiology and Infectious Diseases, 4 (2), 55-58 . doi:10.5799/jmid0127



Chicago Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu. "In vitro efficacy of fosfomycin against clinical strains." Journal of Microbiology and Infectious Diseases 4 (2014), 55-58 . doi:10.5799/jmid0127



MLA (The Modern Language Association) Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu. "In vitro efficacy of fosfomycin against clinical strains." Journal of Microbiology and Infectious Diseases 4.2 (2014), 55-58 . Print. doi:10.5799/jmid0127



APA (American Psychological Association) Style

Adil Karadag, Yeliz Tanriverdi Caycı, Kemal Bilgin, Murat Gunaydin, Cafer Eroglu (2014) In vitro efficacy of fosfomycin against clinical strains. Journal of Microbiology and Infectious Diseases, 4 (2), 55-58 . doi:10.5799/jmid0127