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Killing of Serratia marcescens biofilms with chloramphenicol
Serratia marcescens is a Gram-negative bacterium with proven resistance to multiple antibiotics and causative of catheter-associated infections. Bacterial colonization of catheters mainly involves the formation of biofilm. The objectives of this study were to explore the susceptibility of S. marcesc...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370475/ https://www.ncbi.nlm.nih.gov/pubmed/28356113 http://dx.doi.org/10.1186/s12941-017-0192-2 |
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author | Ray, Christopher Shenoy, Anukul T. Orihuela, Carlos J. González-Juarbe, Norberto |
author_facet | Ray, Christopher Shenoy, Anukul T. Orihuela, Carlos J. González-Juarbe, Norberto |
author_sort | Ray, Christopher |
collection | PubMed |
description | Serratia marcescens is a Gram-negative bacterium with proven resistance to multiple antibiotics and causative of catheter-associated infections. Bacterial colonization of catheters mainly involves the formation of biofilm. The objectives of this study were to explore the susceptibility of S. marcescens biofilms to high doses of common antibiotics and non-antimicrobial agents. Biofilms formed by a clinical isolate of S. marcescens were treated with ceftriaxone, kanamycin, gentamicin, and chloramphenicol at doses corresponding to 10, 100 and 1000 times their planktonic minimum inhibitory concentration. In addition, biofilms were also treated with chemical compounds such as polysorbate-80 and ursolic acid. S. marcescens demonstrated susceptibility to ceftriaxone, kanamycin, gentamicin, and chloramphenicol in its planktonic form, however, only chloramphenicol reduced both biofilm biomass and biofilm viability. Polysorbate-80 and ursolic acid had minimal to no effect on either planktonic and biofilm grown S. marcescens. Our results suggest that supratherapeutic doses of chloramphenicol can be used effectively against established S. marcescens biofilms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12941-017-0192-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5370475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53704752017-03-30 Killing of Serratia marcescens biofilms with chloramphenicol Ray, Christopher Shenoy, Anukul T. Orihuela, Carlos J. González-Juarbe, Norberto Ann Clin Microbiol Antimicrob Short Report Serratia marcescens is a Gram-negative bacterium with proven resistance to multiple antibiotics and causative of catheter-associated infections. Bacterial colonization of catheters mainly involves the formation of biofilm. The objectives of this study were to explore the susceptibility of S. marcescens biofilms to high doses of common antibiotics and non-antimicrobial agents. Biofilms formed by a clinical isolate of S. marcescens were treated with ceftriaxone, kanamycin, gentamicin, and chloramphenicol at doses corresponding to 10, 100 and 1000 times their planktonic minimum inhibitory concentration. In addition, biofilms were also treated with chemical compounds such as polysorbate-80 and ursolic acid. S. marcescens demonstrated susceptibility to ceftriaxone, kanamycin, gentamicin, and chloramphenicol in its planktonic form, however, only chloramphenicol reduced both biofilm biomass and biofilm viability. Polysorbate-80 and ursolic acid had minimal to no effect on either planktonic and biofilm grown S. marcescens. Our results suggest that supratherapeutic doses of chloramphenicol can be used effectively against established S. marcescens biofilms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12941-017-0192-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-29 /pmc/articles/PMC5370475/ /pubmed/28356113 http://dx.doi.org/10.1186/s12941-017-0192-2 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Ray, Christopher Shenoy, Anukul T. Orihuela, Carlos J. González-Juarbe, Norberto Killing of Serratia marcescens biofilms with chloramphenicol |
title | Killing of Serratia marcescens biofilms with chloramphenicol |
title_full | Killing of Serratia marcescens biofilms with chloramphenicol |
title_fullStr | Killing of Serratia marcescens biofilms with chloramphenicol |
title_full_unstemmed | Killing of Serratia marcescens biofilms with chloramphenicol |
title_short | Killing of Serratia marcescens biofilms with chloramphenicol |
title_sort | killing of serratia marcescens biofilms with chloramphenicol |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370475/ https://www.ncbi.nlm.nih.gov/pubmed/28356113 http://dx.doi.org/10.1186/s12941-017-0192-2 |
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