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Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae

AIM: Multidrug-resistant enterobacteria are highly associated with invasive devices and intensive care units. Increasing resistance to carbapenems is leading to the use of older and neglected antibiotics such as nitrofurantoin (NFT). The genomics of NFT resistance was investigated. RESULTS & CON...

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Autor principal: Osei Sekyere, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961450/
https://www.ncbi.nlm.nih.gov/pubmed/29796297
http://dx.doi.org/10.4155/fsoa-2017-0156
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author Osei Sekyere, John
author_facet Osei Sekyere, John
author_sort Osei Sekyere, John
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description AIM: Multidrug-resistant enterobacteria are highly associated with invasive devices and intensive care units. Increasing resistance to carbapenems is leading to the use of older and neglected antibiotics such as nitrofurantoin (NFT). The genomics of NFT resistance was investigated. RESULTS & CONCLUSION: High-level resistance to NFT (minimum inhibitory concentration ≥128–512 mg/l) was recorded in 31/36 isolates (89.6%), many of which were from intensive care units (n = 20), urine (n = 17) or invasive procedures (n = 10). Efflux pump inhibitors had little effect on NFT's minimum inhibitory concentrations albeit oqxAB was prevalent in most isolates (n = 32). Various species- and clone-specific mutations mediating high-level NFT resistance were detected in nfsA, nfsB and ribE proteins through comparative genomics. Global phylogenomics showed local and independent emergence of NFT resistance in Enterobacteriaceae. NFT stewardship is advised.
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spelling pubmed-59614502018-05-24 Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae Osei Sekyere, John Future Sci OA Research Article AIM: Multidrug-resistant enterobacteria are highly associated with invasive devices and intensive care units. Increasing resistance to carbapenems is leading to the use of older and neglected antibiotics such as nitrofurantoin (NFT). The genomics of NFT resistance was investigated. RESULTS & CONCLUSION: High-level resistance to NFT (minimum inhibitory concentration ≥128–512 mg/l) was recorded in 31/36 isolates (89.6%), many of which were from intensive care units (n = 20), urine (n = 17) or invasive procedures (n = 10). Efflux pump inhibitors had little effect on NFT's minimum inhibitory concentrations albeit oqxAB was prevalent in most isolates (n = 32). Various species- and clone-specific mutations mediating high-level NFT resistance were detected in nfsA, nfsB and ribE proteins through comparative genomics. Global phylogenomics showed local and independent emergence of NFT resistance in Enterobacteriaceae. NFT stewardship is advised. Future Science Ltd 2018-02-27 /pmc/articles/PMC5961450/ /pubmed/29796297 http://dx.doi.org/10.4155/fsoa-2017-0156 Text en © 2018 John Osei Sekyere This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Research Article
Osei Sekyere, John
Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae
title Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae
title_full Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae
title_fullStr Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae
title_full_unstemmed Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae
title_short Genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical Enterobacteriaceae
title_sort genomic insights into nitrofurantoin resistance mechanisms and epidemiology in clinical enterobacteriaceae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961450/
https://www.ncbi.nlm.nih.gov/pubmed/29796297
http://dx.doi.org/10.4155/fsoa-2017-0156
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