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Anti-influenza A (H1N1) virus effect of gallic acid through inhibition of virulent protein production and association with autophagy.
Chang, Cheng-Chieh; You, Huey-Ling; Su, Huey-Jen; Hung, I-Ling; Kao, Chao-Wei; Huang, Sheng-Teng.
Afiliação
  • Chang CC; Department of Chinese Medicine Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung Taiwan.
  • You HL; Graduate Institute of Chinese Medicine China Medical University Taichung Taiwan.
  • Su HJ; Department of Laboratory Medicine Kaohsiung Chang Gung Memorial Hospital Kaohsiung Taiwan.
  • Hung IL; Department of Nursing Meiho University Neipu Shiang Taiwan.
  • Kao CW; Department of Chinese Medicine Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine Kaohsiung Taiwan.
  • Huang ST; Department of Chinese Medicine Jen-Ai Hospital Taichung Taiwan.
Food Sci Nutr ; 12(3): 1605-1615, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38455214
ABSTRACT
Influenza remains one of the most serious infectious diseases. Gallic acid is one of the most common and representative phenolic acids found in various plants. This is an interesting subject to explore how gallic acid could inhibit H1N1 influenza virus infection by reducing the production of virulent proteins and interrupting autophagy machinery for influenza virus replication on the host cell. Cellular viability was assessed by XTT assay. The inhibitory effects on the H1N1 influenza virus were assessed by hemagglutination assay, plaque assay, and qRT-PCR. Western blot analysis was used for detecting protein levels of M1, M2, NP, LC3B, and beclin-1. Autophagy activity was demonstrated by acridine orange staining assay. The result demonstrated that there was no cytotoxic effect of gallic acid on A549 cells, and gallic acid could restore the cellular viability of H1N1 influenza virus-infected A549 cells within the experimental concentration treatment. Moreover, gallic acid could effectively restrain viral activity of the H1N1 influenza virus. After the treatment of gallic acid, the production of virulent H1N1 influenza virus proteins, that is, M1, M2, and NP protein were reduced. As for autophagic mechanism, both of the LC3B II conversion and the level ratio of LC3B II to LC3B I were notably decreased. The acridine orange staining assay also revealed decreased accumulation of autophagosomes in H1N1 influenza virus-infected cells. In conclusion, gallic acid suppresses H1N1 influenza viral infectivity through restoration of autophagy pathway and inhibition of virulent M1, M2, and NP protein production.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article