4.7 Article

Antrodia cinnamomea Suppress Dengue Virus Infection through Enhancing the Secretion of Interferon-Alpha

Journal

PLANTS-BASEL
Volume 11, Issue 19, Pages -

Publisher

MDPI
DOI: 10.3390/plants11192631

Keywords

dengue virus; Antrodia cinnamomea; megakaryocytes; interferon-alpha; inflammatory cytokines

Categories

Funding

  1. Ministry of Science and Technology (MOST), Taiwan, Republic of China [MOST 107-2314-B-006-063-MY3]

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Dengue, a mosquito-borne disease caused by dengue virus, currently lacks effective and safe therapeutics. This study found that extracts from Antrodia cinnamomea, a precious medical mushroom in Taiwan, exhibited anti-DENV effects by suppressing viral infection and reducing inflammatory cytokine levels. The extracts also increased the levels of the antiviral cytokine interferon-alpha. These findings provide insights into the potential use of A. cinnamomea extracts as therapeutic agents against DENV infection, but further investigation into the underlying mechanisms is needed.
Dengue caused by dengue virus (DENV) is a mosquito-borne disease. Dengue exhibits a wide range of symptoms, ranging from asymptomatic to flu-like illness, and a few symptomatic cases may develop into severe dengue, leading to death. However, there are no effective and safe therapeutics for DENV infections. We have previously reported that cytokine expression, especially inflammatory cytokines, was altered in patients with different severities of dengue. Antrodia cinnamomea (A. cinnamomea) is a precious and endemic medical mushroom in Taiwan. It contains unique chemical components and exhibits biological activities, including suppressing effects on inflammation and viral infection-related diseases. According to previous studies, megakaryocytes can support DENV infection, and the number of megakaryocytes is positively correlated with the viral load in the serum of acute dengue patients. In the study, we investigated the anti-DENV effects of two ethanolic extracts (ACEs 1-2) and three isolated compounds (ACEs 3-5) from A. cinnamomea on DENV infection in Meg-01 cells. Our results not only demonstrated that ACE-3 and ACE-4 significantly suppressed DENV infection, but also reduced interleukin (IL)-6 and IL-8 levels. Moreover, the level of the antiviral cytokine interferon (IFN)-alpha was also increased by ACE-3 and ACE-4 in Meg-01 cells after DENV infection. Here, we provide new insights into the potential use of A. cinnamomea extracts as therapeutic agents against DENV infection. However, the detailed mechanisms underlying these processes require further investigation.

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