dc.contributor.author |
Yarlagadda, Venkateswarlu
|
|
dc.contributor.author |
Samaddar, Sandip
|
|
dc.contributor.author |
Haldar, Jayanta
|
|
dc.date.accessioned |
2017-01-24T09:11:14Z |
|
dc.date.available |
2017-01-24T09:11:14Z |
|
dc.date.issued |
2016 |
|
dc.identifier.citation |
Yarlagadda, V.; Samaddar, S.; Haldar, J., Intracellular activity of a membrane-active glycopeptide antibiotic against meticillin-resistant Staphylococcus aureus infection. Journal of Global Antimicrobial Resistance 2016, 5, 71-74 http://dx.doi.org/10.1016/j.jgar.2015.12.007 |
en_US |
dc.identifier.citation |
Journal of Global Antimicrobial Resistance |
en_US |
dc.identifier.citation |
5 |
en_US |
dc.identifier.issn |
2213-7165 |
|
dc.identifier.uri |
https://libjncir.jncasr.ac.in/xmlui/10572/2306 |
|
dc.description |
Restricted Access |
en_US |
dc.description.abstract |
Staphylococcus aureus is a facultative intracellular pathogen and there are limited options for the treatment of severe intracellular bacterial infections. The membrane-active glycopeptide antibiotic Van-QC(8) is a permanent positively charged lipophilic vancomycin analogue that demonstrates high activity against clinically relevant drug-resistant Gram-positive bacteria both in vitro and in vivo. In this study, the intracellular activity of Van-QC(8) was evaluated against meticillin-resistant S. aureus (MRSA) infection in RAW macrophages. Furthermore, the mechanism of intracellular uptake of Van-QC(8) was investigated. Van-QC(8) showed time-and concentration-dependent bactericidal activity against intracellular MRSA. Van-QC(8) displayed significantly higher intracellular activity compared with vancomycin and linezolid. Cellular uptake of Van-QC(8) was found to be through clathrin-dependent and independent and caveolin-dependent and -independent endocytic pathways. The findings of this study suggest that Van-QC(8) could be translated clinically for the treatment of intracellular infections due to MRSA. (C) 2016 International Society for Chemotherapy of Infection and Cancer. Published by Elsevier Ltd. All rights reserved. |
en_US |
dc.description.uri |
2213-7173 |
en_US |
dc.description.uri |
http://dx.doi.org/10.1016/j.jgar.2015.12.007 |
en_US |
dc.language.iso |
English |
en_US |
dc.publisher |
Elsevier Sci Ltd |
en_US |
dc.rights |
@Elsevier Sci Ltd, 2016 |
en_US |
dc.subject |
Infectious Diseases |
en_US |
dc.subject |
Pharmacology & Pharmacy |
en_US |
dc.subject |
Glycopeptides |
en_US |
dc.subject |
Membrane-active antibiotic |
en_US |
dc.subject |
Intracellular activity |
en_US |
dc.subject |
Meticillin-resistant Staphylococcus aureus |
en_US |
dc.subject |
MRSA |
en_US |
dc.subject |
In-Vivo |
en_US |
dc.subject |
Pharmacological-Properties |
en_US |
dc.subject |
Vancomycin |
en_US |
dc.subject |
Telavancin |
en_US |
dc.subject |
Bacteremia |
en_US |
dc.title |
Intracellular activity of a membrane-active glycopeptide antibiotic against meticillin-resistant Staphylococcus aureus infection |
en_US |
dc.type |
Article |
en_US |