High-content screening of diterpenoids from Isodon species as autophagy modulators and the functional study of their antiviral activities

• Published in: Cell biology and toxicology Vol. 37; no. 5; pp. 695 - 713
• Main Authors: Huang, Lihong, Fu, Qiang, Dai, Jia-Meng, Yan, Bing-Chao, Wang, Dawei, Puno, Pema-Tenzin, Yue, Jianbo
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.10.2021; Springer Nature B.V
• Subjects: Antiviral Agents - pharmacology; Antiviral drugs; Autophagy; Biochemistry; Biological activity; Biomedical and Life Sciences; Cell Biology; Dengue fever; Dimers; Diterpenes; Diterpenes - pharmacology; Encephalitis; Enteroviruses; Fluorescence; HeLa Cells; Humans; Infections; Isodon; Life cycles; Life Sciences; Lysosomes; Modulators; Neurodegeneration; Neuromodulation; Original Article; Phagocytosis; Phagosomes; Pharmacology/Toxicology; Vector-borne diseases; Viruses; Zika Virus; Zika Virus Infection; Dengue virus (DENV); Enterovirus-A71 (EV-A71); Lysosome; Zika virus (ZIKV); Japanese encephalitis virus (JEV); Diterpenoids; Autophagosome; Autophagy; Enanderinanin J
• ISSN: 0742-2091; 1573-6822
• DOI: 10.1007/s10565-021-09580-6

Autophagy is a conserved lysosomal degradation process, and abnormal autophagy has been associated with various pathological processes, e.g., neurodegeneration, cancer, and pathogen infection. Small chemical modulators of autophagy show the potential to treat autophagy-associated diseases. Diterpenoids, nature products found in various plants, exhibit a wide range of bioactivity, and we have recently isolated and characterized over 150 diterpenoids from Isodon species distributed in China. Here, we applied a high-content fluorescence imaging-based assay to assess these diterpenoids’ ability to affect autophagic flux in HeLa cells. We found that enanderinanin J, an ent -kauranoid dimer, is an autophagy inhibitor, manifested by its ability to increase lysosomal pH and inhibit the fusion between autophagosomes and lysosomes. Autophagy has been shown to be either positively or negatively involved in the life cycle of Zika virus (ZIKV), Japanese encephalitis virus (JEV), Dengue virus (DENV), and enterovirus-A71 (EV-A71). We found that enanderinanin J significantly inhibited the infection of ZIKV, DENV, JEV, or EV-A71. Interestingly, although ATG5 knockdown inhibited ZIKV or JEV infection, enanderinanin J further inhibited the infection of ZIKV or JEV in ATG5-knockdown cells. Taken together, our data indicate that enanderinanin J inhibits autophagosome-lysosome fusion and is a potential antiviral agent. Graphical abstract