volume 34 pages 85-96

Citral, a monoterpenoid aldehyde interacts synergistically with norfloxacin against methicillin resistant Staphylococcus aureus

Publication typeJournal Article
Publication date2017-10-01
scimago Q1
wos Q1
SJR1.694
CiteScore11.6
Impact factor8.3
ISSN09447113, 1618095X
Drug Discovery
Pharmacology
Pharmaceutical Science
Molecular Medicine
Complementary and alternative medicine
Abstract
Staphylococcus aureus (SA), is a major human pathogen causing wide range of clinical infections, which has been further complicated by drug resistance like methicillin resistant S. aureus (MRSA), vancomycin intermediate S. aureus (VISA)/vancomycin resistant S. aureus (VRSA), etc. The present study was aimed at determining anti-staphylococcal potential of citral against drug resistant clinical isolates alone and in combination with antibiotics.To assess the potential of citral in combination with norfloxacin in treating drug resistant infections of SA.In the present study, synergistic interaction of citral and norfloxacin against drug resistant SA strains was evaluated. Further the efficacy and possible mechanism of action of the combination was also evaluated using in vitro and in vivo assays.The anti-staphylococcal activity of each of the monoterpene and the antibiotic was determined in terms of MIC and the effective concentration of both compounds in combination was obtained by checkerboard assay. In vivo efficacy and oral acute toxicity was evaluated in Swiss albino mice model. To understand the mechanism of action, time-kill curve, bacteriolysis, leakage, membrane depolarization, salt tolerance and ethidium bromide efflux assays were performed.Citral was found effective against clinical isolates of SA with MIC values ranging from 75 to 150 µg ml-1 exhibiting bacteriostatic activity. Citral interacted synergistically, reducing MIC of norfloxacin up to 32-folds with FICI ≤ 0.50. Citral did not affect cell wall, but could damage cell membrane, inhibit efflux pump and affect the membrane potential. Citral could reduce the staphylococcal load of spleen and liver tissues in a dose-dependent manner which was further reduced when used in combination with norfloxacin. Citral did not exhibit any mortality or morbidity up to 500 mg kg-1 body weight and found to prolong the post-antibiotic effect of norfloxacin.Based on these observations, citral could be a lead candidate phytomolecule for further developing it into an anti-staphylococcal agent. The observations of combination study will help in reducing the burden of antibiotics leading to delayed resistance development.
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GOST Copy
Gupta P. et al. Citral, a monoterpenoid aldehyde interacts synergistically with norfloxacin against methicillin resistant Staphylococcus aureus // Phytomedicine. 2017. Vol. 34. pp. 85-96.
GOST all authors (up to 50) Copy
Gupta P., Patel D. K., Gupta V. K., Pal A., Tandon S., Darokar M. P. Citral, a monoterpenoid aldehyde interacts synergistically with norfloxacin against methicillin resistant Staphylococcus aureus // Phytomedicine. 2017. Vol. 34. pp. 85-96.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.phymed.2017.08.016
UR - https://doi.org/10.1016/j.phymed.2017.08.016
TI - Citral, a monoterpenoid aldehyde interacts synergistically with norfloxacin against methicillin resistant Staphylococcus aureus
T2 - Phytomedicine
AU - Gupta, Priyanka
AU - Patel, Dinesh Kumar
AU - Gupta, Vivek Kumar
AU - Pal, Anirban
AU - Tandon, Sudeep
AU - Darokar, M P
PY - 2017
DA - 2017/10/01
PB - Elsevier
SP - 85-96
VL - 34
PMID - 28899514
SN - 0944-7113
SN - 1618-095X
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2017_Gupta,
author = {Priyanka Gupta and Dinesh Kumar Patel and Vivek Kumar Gupta and Anirban Pal and Sudeep Tandon and M P Darokar},
title = {Citral, a monoterpenoid aldehyde interacts synergistically with norfloxacin against methicillin resistant Staphylococcus aureus},
journal = {Phytomedicine},
year = {2017},
volume = {34},
publisher = {Elsevier},
month = {oct},
url = {https://doi.org/10.1016/j.phymed.2017.08.016},
pages = {85--96},
doi = {10.1016/j.phymed.2017.08.016}
}