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Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients
Fluoroquinolones (FQs) and ciprofloxacin (Cp) are important antimicrobials that pollute the environment in trace amounts. Although Cp has been recommended as prophylaxis for patients undergoing leech therapy to prevent infections by the leech gut symbiont Aeromonas, a puzzling rise in Cp-resistant (...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058295/ https://www.ncbi.nlm.nih.gov/pubmed/30042201 http://dx.doi.org/10.1128/mBio.01328-18 |
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author | Beka, Lidia Fullmer, Matthew S. Colston, Sophie M. Nelson, Michael C. Talagrand-Reboul, Emilie Walker, Paul Ford, Bradley Whitaker, Iain S. Lamy, Brigitte Gogarten, Johann Peter Graf, Joerg |
author_facet | Beka, Lidia Fullmer, Matthew S. Colston, Sophie M. Nelson, Michael C. Talagrand-Reboul, Emilie Walker, Paul Ford, Bradley Whitaker, Iain S. Lamy, Brigitte Gogarten, Johann Peter Graf, Joerg |
author_sort | Beka, Lidia |
collection | PubMed |
description | Fluoroquinolones (FQs) and ciprofloxacin (Cp) are important antimicrobials that pollute the environment in trace amounts. Although Cp has been recommended as prophylaxis for patients undergoing leech therapy to prevent infections by the leech gut symbiont Aeromonas, a puzzling rise in Cp-resistant (Cp(r)) Aeromonas infections has been reported. We report on the effects of subtherapeutic FQ concentrations on bacteria in an environmental reservoir, the medicinal leech, and describe the presence of multiple antibiotic resistance mutations and a gain-of-function resistance gene. We link the rise of Cp(r) Aeromonas isolates to exposure of the leech microbiota to very low levels of Cp (0.01 to 0.04 µg/ml), <1/100 of the clinical resistance breakpoint for Aeromonas. Using competition experiments and comparative genomics of 37 strains, we determined the mechanisms of resistance in clinical and leech-derived Aeromonas isolates, traced their origin, and determined that the presence of merely 0.01 µg/ml Cp provides a strong competitive advantage for Cp(r) strains. Deep-sequencing the Cp(r)-conferring region of gyrA enabled tracing of the mutation-harboring Aeromonas population in archived gut samples, and an increase in the frequency of the Cp(r)-conferring mutation in 2011 coincides with the initial reports of Cp(r) Aeromonas infections in patients receiving leech therapy. |
format | Online Article Text |
id | pubmed-6058295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-60582952018-07-27 Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients Beka, Lidia Fullmer, Matthew S. Colston, Sophie M. Nelson, Michael C. Talagrand-Reboul, Emilie Walker, Paul Ford, Bradley Whitaker, Iain S. Lamy, Brigitte Gogarten, Johann Peter Graf, Joerg mBio Research Article Fluoroquinolones (FQs) and ciprofloxacin (Cp) are important antimicrobials that pollute the environment in trace amounts. Although Cp has been recommended as prophylaxis for patients undergoing leech therapy to prevent infections by the leech gut symbiont Aeromonas, a puzzling rise in Cp-resistant (Cp(r)) Aeromonas infections has been reported. We report on the effects of subtherapeutic FQ concentrations on bacteria in an environmental reservoir, the medicinal leech, and describe the presence of multiple antibiotic resistance mutations and a gain-of-function resistance gene. We link the rise of Cp(r) Aeromonas isolates to exposure of the leech microbiota to very low levels of Cp (0.01 to 0.04 µg/ml), <1/100 of the clinical resistance breakpoint for Aeromonas. Using competition experiments and comparative genomics of 37 strains, we determined the mechanisms of resistance in clinical and leech-derived Aeromonas isolates, traced their origin, and determined that the presence of merely 0.01 µg/ml Cp provides a strong competitive advantage for Cp(r) strains. Deep-sequencing the Cp(r)-conferring region of gyrA enabled tracing of the mutation-harboring Aeromonas population in archived gut samples, and an increase in the frequency of the Cp(r)-conferring mutation in 2011 coincides with the initial reports of Cp(r) Aeromonas infections in patients receiving leech therapy. American Society for Microbiology 2018-07-24 /pmc/articles/PMC6058295/ /pubmed/30042201 http://dx.doi.org/10.1128/mBio.01328-18 Text en Copyright © 2018 Beka et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Beka, Lidia Fullmer, Matthew S. Colston, Sophie M. Nelson, Michael C. Talagrand-Reboul, Emilie Walker, Paul Ford, Bradley Whitaker, Iain S. Lamy, Brigitte Gogarten, Johann Peter Graf, Joerg Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients |
title | Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients |
title_full | Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients |
title_fullStr | Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients |
title_full_unstemmed | Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients |
title_short | Low-Level Antimicrobials in the Medicinal Leech Select for Resistant Pathogens That Spread to Patients |
title_sort | low-level antimicrobials in the medicinal leech select for resistant pathogens that spread to patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058295/ https://www.ncbi.nlm.nih.gov/pubmed/30042201 http://dx.doi.org/10.1128/mBio.01328-18 |
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