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Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment

Multidrug resistance of bacteria has prompted intensive development work on new medicines, but also the search for effective options among the oldest antibiotics. Although intravenous fosfomycin (IVFOS) seems to be an interesting proposal, the recommended agar dilution method for susceptibility dete...

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Autores principales: Kowalska-Krochmal, Beata, Mączyńska, Beata, Rurańska-Smutnicka, Danuta, Secewicz, Anna, Krochmal, Grzegorz, Bartelak, Małgorzata, Górzyńska, Aleksandra, Laufer, Klaudyna, Woronowicz, Krystyna, Łubniewska, Joanna, Łappo, Jolanta, Czwartos, Magdalena, Dudek-Wicher, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786176/
https://www.ncbi.nlm.nih.gov/pubmed/36558775
http://dx.doi.org/10.3390/pathogens11121441
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author Kowalska-Krochmal, Beata
Mączyńska, Beata
Rurańska-Smutnicka, Danuta
Secewicz, Anna
Krochmal, Grzegorz
Bartelak, Małgorzata
Górzyńska, Aleksandra
Laufer, Klaudyna
Woronowicz, Krystyna
Łubniewska, Joanna
Łappo, Jolanta
Czwartos, Magdalena
Dudek-Wicher, Ruth
author_facet Kowalska-Krochmal, Beata
Mączyńska, Beata
Rurańska-Smutnicka, Danuta
Secewicz, Anna
Krochmal, Grzegorz
Bartelak, Małgorzata
Górzyńska, Aleksandra
Laufer, Klaudyna
Woronowicz, Krystyna
Łubniewska, Joanna
Łappo, Jolanta
Czwartos, Magdalena
Dudek-Wicher, Ruth
author_sort Kowalska-Krochmal, Beata
collection PubMed
description Multidrug resistance of bacteria has prompted intensive development work on new medicines, but also the search for effective options among the oldest antibiotics. Although intravenous fosfomycin (IVFOS) seems to be an interesting proposal, the recommended agar dilution method for susceptibility determination poses a major problem in routine diagnostic testing. As a consequence, there is a lack of comprehensive data on the frequency of isolation of susceptible or resistant strains. This fact triggered the disposition of EUCAST concerning the revision of IVFOS breakpoints (BPs), including withdrawal of BPs for Enterobacterales (excluding E. coli) and coagulase-negative staphylococci. Therefore, the aim of this study was to assess the activity of fosfomycin against numerous clinical strains using recommended methods. Materials and methods: A total of 997 bacterial strains were tested from the following genera: Enterobacterales, Pseudomonas spp., Staphylococcus spp., Acinetobacter spp., and Enterococcus spp., for which there are currently no BPs. The strains were isolated from various clinical materials from patients hospitalized in five hospitals. During the investigation, the recommended agar dilution method was used. Susceptibility to other antibiotics and resistance mechanisms were determined using an automatic method (Phoenix) the disk diffusion method, and E-tests. MIC values of fosfomycin were estimated for all strains and for susceptible and multidrug-resistant (MDR) strains individually. Results: Except for Acinetobacter and Enterococcus, 83% of the strains were susceptible to IVFOS, including the largest percentage of S. aureus and E. coli. Klebsiella spp. turned out to be the least susceptible strains (66%). The highest proportion of susceptibility to fosfomycin was found among strains that were sensitive to other antibiotics (80.9%), and the lowest was found among Gram-negative carbapenemase-producing bacteria (55.6%) and ESBL+ bacteria (61.6%). The MIC evaluation revealed the lowest MIC(50) and MIC(90) values for S. aureus (0.5 mg/L and 1 mg/L, respectively) and E. coli (4 mg/L and 32 mg/L, respectively). The highest values of MIC(50) were found for Acinetobacter spp. (256 mg/L), while the highest values of MIC(90) were found for Acinetobacter spp. and Klebsiella spp. (256 mg/L and 512 mg/L, respectively). Conclusions: IVFOS appears to be suitable for the treatment of many infections, including the empirical treatment of polymicrobial infections and those caused by MDR strains, since the sensitivity of the studied strains to this antibiotic in different groups ranged from 66% to as much as 99%. Sensitivity to fosfomycin was also demonstrated by 60% of carbapenem-resistant strains; therefore, IVFOS is one of the few therapeutic options that can be effective against the most resistant Gram-negative rods. In light of the general consultation posted by EUCAST, obtaining data such as IVFOS MIC value distributions may be vital for the decision of implementing fosfomycin into breakpoint tables.
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spelling pubmed-97861762022-12-24 Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment Kowalska-Krochmal, Beata Mączyńska, Beata Rurańska-Smutnicka, Danuta Secewicz, Anna Krochmal, Grzegorz Bartelak, Małgorzata Górzyńska, Aleksandra Laufer, Klaudyna Woronowicz, Krystyna Łubniewska, Joanna Łappo, Jolanta Czwartos, Magdalena Dudek-Wicher, Ruth Pathogens Article Multidrug resistance of bacteria has prompted intensive development work on new medicines, but also the search for effective options among the oldest antibiotics. Although intravenous fosfomycin (IVFOS) seems to be an interesting proposal, the recommended agar dilution method for susceptibility determination poses a major problem in routine diagnostic testing. As a consequence, there is a lack of comprehensive data on the frequency of isolation of susceptible or resistant strains. This fact triggered the disposition of EUCAST concerning the revision of IVFOS breakpoints (BPs), including withdrawal of BPs for Enterobacterales (excluding E. coli) and coagulase-negative staphylococci. Therefore, the aim of this study was to assess the activity of fosfomycin against numerous clinical strains using recommended methods. Materials and methods: A total of 997 bacterial strains were tested from the following genera: Enterobacterales, Pseudomonas spp., Staphylococcus spp., Acinetobacter spp., and Enterococcus spp., for which there are currently no BPs. The strains were isolated from various clinical materials from patients hospitalized in five hospitals. During the investigation, the recommended agar dilution method was used. Susceptibility to other antibiotics and resistance mechanisms were determined using an automatic method (Phoenix) the disk diffusion method, and E-tests. MIC values of fosfomycin were estimated for all strains and for susceptible and multidrug-resistant (MDR) strains individually. Results: Except for Acinetobacter and Enterococcus, 83% of the strains were susceptible to IVFOS, including the largest percentage of S. aureus and E. coli. Klebsiella spp. turned out to be the least susceptible strains (66%). The highest proportion of susceptibility to fosfomycin was found among strains that were sensitive to other antibiotics (80.9%), and the lowest was found among Gram-negative carbapenemase-producing bacteria (55.6%) and ESBL+ bacteria (61.6%). The MIC evaluation revealed the lowest MIC(50) and MIC(90) values for S. aureus (0.5 mg/L and 1 mg/L, respectively) and E. coli (4 mg/L and 32 mg/L, respectively). The highest values of MIC(50) were found for Acinetobacter spp. (256 mg/L), while the highest values of MIC(90) were found for Acinetobacter spp. and Klebsiella spp. (256 mg/L and 512 mg/L, respectively). Conclusions: IVFOS appears to be suitable for the treatment of many infections, including the empirical treatment of polymicrobial infections and those caused by MDR strains, since the sensitivity of the studied strains to this antibiotic in different groups ranged from 66% to as much as 99%. Sensitivity to fosfomycin was also demonstrated by 60% of carbapenem-resistant strains; therefore, IVFOS is one of the few therapeutic options that can be effective against the most resistant Gram-negative rods. In light of the general consultation posted by EUCAST, obtaining data such as IVFOS MIC value distributions may be vital for the decision of implementing fosfomycin into breakpoint tables. MDPI 2022-11-30 /pmc/articles/PMC9786176/ /pubmed/36558775 http://dx.doi.org/10.3390/pathogens11121441 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kowalska-Krochmal, Beata
Mączyńska, Beata
Rurańska-Smutnicka, Danuta
Secewicz, Anna
Krochmal, Grzegorz
Bartelak, Małgorzata
Górzyńska, Aleksandra
Laufer, Klaudyna
Woronowicz, Krystyna
Łubniewska, Joanna
Łappo, Jolanta
Czwartos, Magdalena
Dudek-Wicher, Ruth
Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment
title Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment
title_full Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment
title_fullStr Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment
title_full_unstemmed Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment
title_short Assessment of the Susceptibility of Clinical Gram-Negative and Gram-Positive Bacterial Strains to Fosfomycin and Significance of This Antibiotic in Infection Treatment
title_sort assessment of the susceptibility of clinical gram-negative and gram-positive bacterial strains to fosfomycin and significance of this antibiotic in infection treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786176/
https://www.ncbi.nlm.nih.gov/pubmed/36558775
http://dx.doi.org/10.3390/pathogens11121441
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