Literature DB >> 33010587

Sapindus mukorossi Gaertn. and its bioactive metabolite oleic acid impedes methicillin-resistant Staphylococcus aureus biofilm formation by down regulating adhesion genes expression.

Anthonymuthu Selvaraj1, Alaguvel Valliammai1, Muruganatham Premika1, Arumugam Priya1, James Prabhanand Bhaskar2, Venkateswaran Krishnan2, Shunmugiah Karutha Pandian3.   

Abstract

Plants are boon to the mankind due to plenty of metabolites with medicinal values. Though plants have traditionally been used to treat various diseases, their biological values are not completely explored yet. Sapindus mukorossi is one such ethnobotanical plant identified for various biological activities. As biofilm formation and biofilm mediated drug resistance of methicillin-resistant Staphylococcus aureus (MRSA) have raised as serious global issue, search for antibiofilm agents has gained greater importance. Notably, antibiofilm potential of S. mukorossi is still unexplored. The aim of the study is to explore the effect of S. mukorossi methanolic extract (SMME) on MRSA biofilm formation and adhesive molecules production. Significantly, SMME exhibited 82 % of biofilm inhibition at 250 μg/mL without affecting the growth and microscopic analyses evidenced the concentration dependent antibiofilm activity of SMME. In vitro assays exhibited the reduction in slime, cell surface hydrophobicity, autoaggregation, extracellular polysaccharides substance and extracellular DNA synthesis upon SMME treatment. Further, qPCR analysis confirmed the ability of SMME to interfere with the expression of adhesion genes associated with biofilm formation such as icaA, icaD, fnbA, fnbB, clfA, cna, and altA. GC-MS analysis and molecular docking study revealed that oleic acid is responsible for the antibiofilm activity. FT-IR analysis validated the presence of oleic acid in SMME. These results suggest that SMME can be used as a promising therapeutic agent against MRSA biofilm-associated infections.
Copyright © 2020 Elsevier GmbH. All rights reserved.

Entities:  

Keywords:  Biofilm; GC–MS; Methicillin-resistant Staphylococcus aureus; Oleic acid; Sapindus mukorossi; qPCR

Mesh:

Substances:

Year:  2020        PMID: 33010587     DOI: 10.1016/j.micres.2020.126601

Source DB:  PubMed          Journal:  Microbiol Res        ISSN: 0944-5013            Impact factor:   5.415


  5 in total

1.  Comparative study on inhibitory effects of ferulic acid and p-coumaric acid on Salmonella Enteritidis biofilm formation.

Authors:  Jing-Guo Xu; Hui-Xue Hu; Jing-Yu Chen; Yan-Song Xue; Bekhzod Kodirkhonov; Bei-Zhong Han
Journal:  World J Microbiol Biotechnol       Date:  2022-06-14       Impact factor: 3.312

2.  7,8-Dihydroxyflavone attenuates the virulence of Staphylococcus aureus by inhibiting alpha-hemolysin.

Authors:  Nan Bian; Xiangqian Chen; Xinran Ren; Zishu Yu; Mengli Jin; Xiaoyu Chen; Chang Liu; Yanhe Luan; Lin Wei; Ying Chen; Wu Song; Yicheng Zhao; Bingmei Wang; Tao Jiang; Chi Zhang; Zunhua Shu; Xin Su; Li Wang
Journal:  World J Microbiol Biotechnol       Date:  2022-08-23       Impact factor: 4.253

Review 3.  Microbial silver resistance mechanisms: recent developments.

Authors:  Ergi Terzioğlu; Mevlüt Arslan; Berrak Gülçin Balaban; Zeynep Petek Çakar
Journal:  World J Microbiol Biotechnol       Date:  2022-07-12       Impact factor: 4.253

4.  Carvacrol Targets SarA and CrtM of Methicillin-Resistant Staphylococcus aureus to Mitigate Biofilm Formation and Staphyloxanthin Synthesis: An In Vitro and In Vivo Approach.

Authors:  Anthonymuthu Selvaraj; Alaguvel Valliammai; Pandiyan Muthuramalingam; Arumugam Priya; Manokaran Suba; Manikandan Ramesh; Shunmugiah Karutha Pandian
Journal:  ACS Omega       Date:  2020-11-24

5.  Polyphenols as Inhibitors of Antibiotic Resistant Bacteria-Mechanisms Underlying Rutin Interference with Bacterial Virulence.

Authors:  Marija Ivanov; Katarina Novović; Milka Malešević; Miroslav Dinić; Dejan Stojković; Branko Jovčić; Marina Soković
Journal:  Pharmaceuticals (Basel)       Date:  2022-03-21
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.