Publication:
Proteomic analysis of monkey kidney LLC-MK2 cells infected with a Thai strain Zika virus

dc.contributor.authorThamonwan Diteepengen_US
dc.contributor.authorSarawut Khongwichiten_US
dc.contributor.authorAtchara Paemaneeen_US
dc.contributor.authorSittiruk Roytrakulen_US
dc.contributor.authorDuncan R. Smithen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.date.accessioned2020-01-27T09:00:20Z
dc.date.available2020-01-27T09:00:20Z
dc.date.issued2019-03-01en_US
dc.description.abstract© 2019, Springer-Verlag GmbH Austria, part of Springer Nature. Zika virus (ZIKV) has been endemic in Southeast Asian countries for several years, but the presence of the virus has not been associated with significant outbreaks of infection unlike other countries around the world where the Asian lineage ZIKV was introduced recently. However, few studies have been undertaken using the endemic virus. The Thai isolate was shown to have a similar tissue tropism to an African isolate of ZIKV, albeit that the Thai isolate infected cells at a lower level as compared to the African isolate. To further understand the pathogenesis of the Thai isolate, a 2D-gel proteomic analysis was undertaken of ZIKV infected LLC-MK2 cells. Seven proteins (superoxide dismutase [Mn], peroxiredoxin 2, ATP synthase subunit alpha, annexin A5 and annexin A1, carnitine o-palmitoyltransferase 2 and cytoskeleton-associated protein 2) were identified as differentially regulated. Of four proteins selected for validation, three (superoxide dismutase [Mn], peroxiredoxin 2, ATP synthase subunit alpha, and annexin A1) were shown to be differentially regulated at both the transcriptional and translational levels. The proteins identified were primarily involved in energy production both directly, and indirectly through mediation of autophagy, as well as in the response to oxidative stress, possibly occurring as a consequence of increased energy production. This study provides further new information on the pathogenesis of ZIKV.en_US
dc.identifier.citationArchives of Virology. Vol.164, No.3 (2019), 725-737en_US
dc.identifier.doi10.1007/s00705-018-04137-1en_US
dc.identifier.issn03048608en_US
dc.identifier.other2-s2.0-85059593682en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/51094
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059593682&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titleProteomic analysis of monkey kidney LLC-MK2 cells infected with a Thai strain Zika virusen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059593682&origin=inwarden_US

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