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Cited 6 time in webofscience Cited 6 time in scopus
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Emodin Successfully Inhibited Invasion of Brucella abortus Via Modulting Adherence, Microtubule Dynamics and ERK Signaling Pathway in RAW 264.7 Cellsopen access

Authors
Huy, Tran Xuan NgocReyes, Alisha Wehdnesday BernardoHop, Huynh TanArayan, Lauren TogononSon, Vu HaiMin, WongiLee, Hu JangKim, Suk
Issue Date
Oct-2018
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
Keywords
Brucella abortus; emodin; antibacterial; invasion
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.28, no.10, pp.1723 - 1729
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume
28
Number
10
Start Page
1723
End Page
1729
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/11233
DOI
10.4014/jmb.1804.04040
ISSN
1017-7825
Abstract
The aim of this work is to investigate the protective efficacy of emodin, an active, naturally-occurring anthraquinone derivative of several traditional Chinese herbs, against Brucella abortus infection in macrophages. Brucella were incubated with different concentrations of emodin and showed that bacterial survival rates were markedly reduced in a dose-dependent manner at increasing incubation time points. Through bacterial infection assay, the highest non-cytotoxic concentration of emodin demonstrated attenuated invasion of Brucella into macrophages, however it did not inhibit the growth of these pathogens within the host cells. On the other hand, emodin effectively decreased the number of bacteria that adhered to host cells, which indicated its potential as an anti-adhesin agent. Furthermore, using immunoblotting and FACS assay for detecting MAPK signaling proteins and F-actin polymerization, respectively, the results showed that the emodin-incubated cells displayed modest reduction in the phosphorylation levels of ERK1/2 and inhibition of F-actin polymerization as compared to control cells. These findings indicate the potential use of emodin as a naturally-occurring alternative method for the prevention of animal brucellosis although this requires confirmation of safe clinical doses.
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