Publication:
Comprehensive proteomic analysis of white blood cells from chikungunya fever patients of different severities

dc.contributor.authorNitwara Wikanen_US
dc.contributor.authorSarawut Khongwichiten_US
dc.contributor.authorWeerawat Phukliaen_US
dc.contributor.authorSukathida Ubolen_US
dc.contributor.authorTipparat Thonsakulpraserten_US
dc.contributor.authorMontri Thannagithen_US
dc.contributor.authorDuangrudee Tanramluken_US
dc.contributor.authorAtchara Paemaneeen_US
dc.contributor.authorSuthathip Kittisenachaien_US
dc.contributor.authorSittiruk Roytrakulen_US
dc.contributor.authorSmith, Duncan Ren_US
dc.contributor.otherMahidol University. Institute of Molecular Biosciencesen_US
dc.contributor.otherMahidol University. Center for Emerging and Neglected Infectious Diseasesen_US
dc.date.accessioned2015-04-08T10:57:37Z
dc.date.accessioned2017-04-25T03:40:56Z
dc.date.available2015-04-08T10:57:37Z
dc.date.available2017-04-25T03:40:56Z
dc.date.created2015-04-08
dc.date.issued2014
dc.description.abstractBackground: Chikungunya fever (CHIKF) is a recently re-emerged mosquito transmitted viral disease caused by the chikungunya virus (CHIKV), an Alphavirus belonging to the family Togaviridae. Infection of humans with CHIKV can result in CHIKF of variable severity, although the factors mediating disease severity remain poorly defined. Methods: White blood cells were isolated from blood samples collected during the 2009-2010 CHIKF outbreak in Thailand. Clinical presentation and viral load data were used to classify samples into three groups, namely non chikungunya fever (non-CHIKF), mild CHIKF, and severe CHIKF. Five samples from each group were analyzed for protein expression by GeLC-MS/MS. Results: CHIKV proteins (structural and non-structural) were found only in CHIKF samples. A total of 3505 human proteins were identified, with 68 proteins only present in non-CHIKF samples. A total of 240 proteins were found only in CHIKF samples, of which 65 and 46 were found only in mild and severe CHIKF samples respectively. Proteins with altered expression mapped predominantly to cellular signaling pathways (including toll-like receptor and PI3K-Akt signaling) although many other processes showed altered expression as a result of CHIKV infection. Expression of proteins consistent with the activation of the inflammasome was detected, and quantitation of (pro)-caspase 1 at the protein and RNA levels showed an association with disease severity. Conclusions: This study confirms the infection of at least a component of white blood cells by CHIKV, and shows that CHIKV infection results in activation of the inflammasome in a manner that is associated with disease severity.en_US
dc.identifier.citationJournal of Translational Medicine. Vol. 12, No.96 (2014), 1-8en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/1813
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.subjectChikungunyaen_US
dc.subjectProteomeen_US
dc.subjectInflammasomeen_US
dc.subjectCaspase 1en_US
dc.subjectOpen Access articleen_US
dc.titleComprehensive proteomic analysis of white blood cells from chikungunya fever patients of different severitiesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mods.location.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022080/pdf/1479-5876-12-96.pdf

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