Killing of Serratia marcescens biofilms with chloramphenicol

Abstract 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...

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Main Authors: Christopher Ray, Anukul T. Shenoy, Carlos J. Orihuela, Norberto González-Juarbe
Format: Article
Language:English
Published: BMC 2017-03-01
Series:Annals of Clinical Microbiology and Antimicrobials
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12941-017-0192-2
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spelling doaj-b357c9a3e9294500ba26b0b52cf620052020-11-24T22:20:15ZengBMCAnnals of Clinical Microbiology and Antimicrobials1476-07112017-03-011611610.1186/s12941-017-0192-2Killing of Serratia marcescens biofilms with chloramphenicolChristopher Ray0Anukul T. Shenoy1Carlos J. Orihuela2Norberto González-Juarbe3Department of Microbiology, The University of Alabama at BirminghamDepartment of Microbiology, The University of Alabama at BirminghamDepartment of Microbiology, The University of Alabama at BirminghamDepartment of Microbiology, The University of Alabama at BirminghamAbstract 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.http://link.springer.com/article/10.1186/s12941-017-0192-2Serratia marcescensBiofilmAntibioticsChloramphenicol
collection DOAJ
language English
format Article
sources DOAJ
author Christopher Ray
Anukul T. Shenoy
Carlos J. Orihuela
Norberto González-Juarbe
spellingShingle Christopher Ray
Anukul T. Shenoy
Carlos J. Orihuela
Norberto González-Juarbe
Killing of Serratia marcescens biofilms with chloramphenicol
Annals of Clinical Microbiology and Antimicrobials
Serratia marcescens
Biofilm
Antibiotics
Chloramphenicol
author_facet Christopher Ray
Anukul T. Shenoy
Carlos J. Orihuela
Norberto González-Juarbe
author_sort Christopher Ray
title Killing of Serratia marcescens biofilms with chloramphenicol
title_short 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_sort killing of serratia marcescens biofilms with chloramphenicol
publisher BMC
series Annals of Clinical Microbiology and Antimicrobials
issn 1476-0711
publishDate 2017-03-01
description Abstract 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.
topic Serratia marcescens
Biofilm
Antibiotics
Chloramphenicol
url http://link.springer.com/article/10.1186/s12941-017-0192-2
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AT carlosjorihuela killingofserratiamarcescensbiofilmswithchloramphenicol
AT norbertogonzalezjuarbe killingofserratiamarcescensbiofilmswithchloramphenicol
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