Modulatory Effect of Linoleic Acid During Brucella abortus 544 Infection in Murine Macrophage RAW264.7 Cells and Murine Model BALB/c Mice

In this study, we investigated the effects of linoleic acid (LA) treatment on Brucella abortus infection in professional phagocyte RAW264.7 cells, particularly during the pathogen’s invasion and intracellular growth in these cells, as well as in murine model BALB/c mice focusing on bacterial splenic...

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Published inJournal of microbiology and biotechnology Vol. 30; no. 5; pp. 642 - 648
Main Authors Reyes, Alisha Wehdnesday Bernardo, Vu, Son Hai, Huy, Tran Xuan Ngoc, Min, Wongi, Lee, Hu Jang, Chang, Hong Hee, Lee, John Hwa, Kim, Suk
Format Journal Article
LanguageKorean
Published 한국미생물생명공학회 31.05.2020
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Summary:In this study, we investigated the effects of linoleic acid (LA) treatment on Brucella abortus infection in professional phagocyte RAW264.7 cells, particularly during the pathogen’s invasion and intracellular growth in these cells, as well as in murine model BALB/c mice focusing on bacterial splenic proliferation and immunoregulatory activities. LA inhibited the growth of Brucella in a doseand time-dependent manner. The ability of the pathogen to enter the phagocytes was inhibited as was its survival within these cells. This was accompanied by increased nitrite accumulation in these cells at 24 h post-infection. The concentration of LA used in the present study did not affect the total body weight or liver function of the mice. During Brucella infection, the total splenic weight of these animals was not changed; rather, resistance to bacterial proliferation was enhanced in the spleen. Furthermore, mice treated with LA displayed elevated levels of IL-12 and IFN-γ but reduced levels of IL-10 during infection. The findings in this study showed the regulatory role of LA against B. abortus infection suggesting its potential use in designing intervention strategy for brucellosis.
Bibliography:The Korean Society for Applied Microbiology
KISTI1.1003/JNL.JAKO202015762903253
ISSN:1017-7825
1738-8872