dc.contributor.author |
Cosa, Sekelwa
|
|
dc.contributor.author |
Rakoma, Jostina R.
|
|
dc.contributor.author |
Yusuf, Abdullahi Ahmed
|
|
dc.contributor.author |
Tshikalange, Thilivhali Emmanuel
|
|
dc.date.accessioned |
2021-05-21T11:49:25Z |
|
dc.date.available |
2021-05-21T11:49:25Z |
|
dc.date.issued |
2020-05-13 |
|
dc.description.abstract |
Pseudomonas aeruginosa is the causative agent of several life-threatening human infections.
Like many other pathogens, P. aeruginosa exhibits quorum sensing (QS) controlled virulence factors
such as biofilm during disease progression, complicating treatment with conventional antibiotics.
Thus, impeding the pathogen’s QS circuit appears as a promising alternative strategy to overcome
pseudomonas infections. In the present study, Calpurnia aurea were evaluated for their antibacterial
(minimum inhibitory concentrations (MIC)), anti-quorumsensing/antivirulence (AQS), and antibiofilm
potential against P. aeruginosa. AQS and antivirulence (biofilm formation, swimming, and swarming
motility) activities of plant extracts were evaluated against Chromobacterium violaceum and P. aeruginosa,
respectively. The in vitro AQS potential of the individual compounds were validated using in
silico molecular docking. Acetone and ethanolic extracts of C. aurea showed MIC at 1.56 mg/mL.
The quantitative violacein inhibition (AQS) assay showed ethyl acetate extracts as the most potent at
a concentration of 1 mg/mL. GCMS analysis of C. aurea revealed 17 compounds; four (pentadecanol,
dimethyl terephthalate, terephthalic acid, and methyl mannose) showed potential AQS through
molecular docking against the CviR protein of C. violaceum. Biofilm of P. aeruginosa was significantly
inhibited by 60% using 1-mg/mL extract of C. aurea. Confocal laser scanning microscopy correlated
the findings of crystal violet assay with the extracts significantly altering the swimming motility.
C. aurea extracts reduced the virulence of pseudomonas, albeit in a strain- and extract-specific manner,
showing their suitability for the identification of lead compounds with QS inhibitory potential for the
control of P. aeruginosa infections. |
en_ZA |
dc.description.department |
Biochemistry |
en_ZA |
dc.description.department |
Genetics |
en_ZA |
dc.description.department |
Microbiology and Plant Pathology |
en_ZA |
dc.description.department |
Plant Science |
en_ZA |
dc.description.department |
Zoology and Entomology |
en_ZA |
dc.description.librarian |
am2021 |
en_ZA |
dc.description.sponsorship |
The South African National Research Foundation (NRF) Thuthuka Grant, South African Medical Research Council–Self Initiated Research (SAMRC-SIR), South African National Research Foundation’s (NRF) Incentive Funding for Rated Researchers and the DST/NRF SARChI in Mathematical Models and Methods in Bioengineering and Biosciences. |
en_ZA |
dc.description.uri |
http://www.mdpi.com/journal/molecules |
en_ZA |
dc.identifier.citation |
Cosa, S, RAkoma, JR & Yusuf, AA 2020, 'Calpurnia aurea (Aiton) benth extracts reduce quorum sensing controlled virulence factors in Pseudomonas aeruginosa', Molecules, vol. 25, no. 2283, pp. 1-21. |
en_ZA |
dc.identifier.issn |
1420-3049 (online) |
|
dc.identifier.other |
10.3390/molecules25102283 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/80001 |
|
dc.language.iso |
en |
en_ZA |
dc.publisher |
MDPI Publishing |
en_ZA |
dc.rights |
© 2020 by the authors.
This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY). |
en_ZA |
dc.subject |
Antipathogenic |
en_ZA |
dc.subject |
Biofilm formation |
en_ZA |
dc.subject |
Cell-to-cell communication |
en_ZA |
dc.subject |
Plant extract |
en_ZA |
dc.subject |
Molecular docking |
en_ZA |
dc.subject |
Pseudomonas aeruginosa |
en_ZA |
dc.subject |
Minimum inhibitory concentrations (MIC) |
en_ZA |
dc.subject |
Anti-quorumsensing/antivirulence (AQS) |
en_ZA |
dc.title |
Calpurnia aurea (Aiton) benth extracts reduce quorum sensing controlled virulence factors in Pseudomonas aeruginosa |
en_ZA |
dc.type |
Article |
en_ZA |