Publication: Suppression of µ1 subunit of the adaptor protein complex 2 reduces dengue virus release
Issued Date
2020-02-01
Resource Type
ISSN
1572994X
09208569
09208569
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2-s2.0-85074972107
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Mahidol University
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SCOPUS
Bibliographic Citation
Virus Genes. Vol.56, No.1 (2020), 27-36
Suggested Citation
Nopprarat Tongmuang, Umpa Yasamut, Sansanee Noisakran, Gopinathan Pillai Sreekanth, Pa thai Yenchitsomanus, Thawornchai Limjindaporn Suppression of µ1 subunit of the adaptor protein complex 2 reduces dengue virus release. Virus Genes. Vol.56, No.1 (2020), 27-36. doi:10.1007/s11262-019-01710-x Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/49538
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Title
Suppression of µ1 subunit of the adaptor protein complex 2 reduces dengue virus release
Abstract
© 2019, Springer Science+Business Media, LLC, part of Springer Nature. Dengue virus (DENV) requires clathrin-mediated endocytosis for its entry into the cells where the adaptor protein complex (AP) is vital for the clathrin-coated vesicle formation. The role of AP-2 was previously examined in the early stages of DENV infection; however, the role of AP-2 in the late stage of DENV infection was not determined. The µ1 subunit of AP-2 (AP2M1) is one of the most important cytoplasmic carrier domains in clathrin-mediated endocytosis and the phosphorylation of this subunit by the kinase enzyme, AP-2 associated protein kinase 1 (AAK1), stimulates clathrin and supports the cell surface receptor incorporation. In the present study, we primarily aimed to investigate the role of AP2M1 by gene silencing approach as well as using naked DENV RNA transfection into AP2M1 knockdown cells. Secondarily, an inhibitor of AAK1, sunitinib was used to investigate whether AAK1 could influence the virus production in DENV-infected Huh7 cells. The knockdown of AP2M1 in the DENV-infected Huh7 cells displayed a reduction in the viral titer at 24 h post-infection. Furthermore, experiments were conducted to bypass the DENV internalization using a naked DENV RNA transfection into the AP2M1 knockdown cells. Higher intracellular DENV RNA, DENV E protein, and intracellular virion were observed, whereas the extracellular virion production was comparably less than that of control. Treatment with sunitinib in DENV-infected Huh7 cells was able to reduce extracellular virion production and was consistent with all four serotypes of DENV. Therefore, our findings demonstrate the role of AP2M1 in the exocytosis step of DENV replication leading to infectious DENV production and the efficacy of sunitinib in suppressing virus production during the infection with different serotypes of DENV.