Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 May 9;10(5):337.
doi: 10.3390/vetsci10050337.

Fosfomycin Resistance in Bacteria Isolated from Companion Animals (Dogs and Cats)

Affiliations
Review

Fosfomycin Resistance in Bacteria Isolated from Companion Animals (Dogs and Cats)

Marios Lysitsas et al. Vet Sci. .

Abstract

Fosfomycin is an old antibacterial agent, which is currently used mainly in human medicine, in uncomplicated Urinary Tract Infections (UTIs). The purpose of this review is to investigate the presence and the characteristics of Fosfomycin resistance in bacteria isolated from canine or feline samples, estimate the possible causes of the dissemination of associated strains in pets, and underline the requirements of prospective relevant studies. Preferred Reporting Items for Systematic Reviews (PRISMA) guidelines were used for the search of current literature in two databases. A total of 33 articles were finally included in the review. Relevant data were tracked down, assembled, and compared. Referring to the geographical distribution, Northeast Asia was the main area of origin of the studies. E. coli was the predominant species detected, followed by other Enterobacteriaceae, Staphylococci, and Pseudomonas spp. FosA and fosA3 were the more frequently encountered Antimicrobial Resistance Genes (ARGs) in the related Gram-negative isolates, while fosB was regularly encountered in Gram-positive ones. The majority of the strains were multidrug-resistant (MDR) and co-carried resistance genes against several classes of antibiotics and especially β-Lactams, such as blaCTX-M and mecA. These results demonstrate the fact that the cause of the spreading of Fosfomycin-resistant bacteria among pets could be the extended use of other antibacterial agents, that promote the prevalence of MDR, epidemic strains among an animal population. Through the circulation of these strains into a community, a public health issue could arise. Further research is essential though, for the comprehensive consideration of the issue, as the current data are limited.

Keywords: ARGs; Fosfomycin resistance; PRISMA guidelines; cat; companion animals; dog; pets.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Identification of studies regarding Fosfomycin resistance in companion animals via databases using PRISMA guidelines [47].
Figure 2
Figure 2
Distribution of the studies (countries in green) included in this review throughout the world. Numbers indicate the number of studies that investigated isolates from the corresponding country. (https://www.mapchart.net/world.html, accessed on 9 February 2023).

References

    1. Hendlin D., Stapley E.O., Jackson M., Wallick H., Miller A.K., Wolf F.J., Miller T.W., Chaiet L., Kahan F.M., Foltz E.L., et al. Phosphonomycin, a New Antibiotic Produced by Strains of Streptomyces. Science. 1969;166:122–123. doi: 10.1126/science.166.3901.122. - DOI - PubMed
    1. Zhanel G.G., Walkty A.J., Karlowsky J.A. Fosfomycin: A First-Line Oral Therapy for Acute Uncomplicated Cystitis. Can. J. Infect. Dis. Med. Microbiol. 2016;2016:2082693. doi: 10.1155/2016/2082693. - DOI - PMC - PubMed
    1. Falagas M.E., Vouloumanou E.K., Samonis G., Vardakas K.Z. Fosfomycin. Clin. Microbiol. Rev. 2016;29:321–347. doi: 10.1128/CMR.00068-15. - DOI - PMC - PubMed
    1. Díez-Aguilar M., Cantón R. New microbiological aspects of fosfomycin. Rev. Esp. Quimioter. 2019;32((Suppl. S1)):8–18. - PMC - PubMed
    1. Silver L.L. Fosfomycin: Mechanism and Resistance. Cold Spring Harb. Perspect. Med. 2017;7:a025262. doi: 10.1101/cshperspect.a025262. - DOI - PMC - PubMed

LinkOut - more resources