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dc.creatorFourati, S
dc.creatorTalla, A
dc.creatorMahmoudian, M
dc.creatorBurkhart, JG
dc.creatorKlén, R
dc.creatorHenao, R
dc.creatorYu, T
dc.creatorAydın, Z
dc.creatorYeung, KY
dc.creatorAhsen, ME
dc.creatorAlmugbel, R
dc.creatorJahandideh, S
dc.creatorLiang, X
dc.creatorNordling, TEM
dc.creatorShiga, M
dc.creatorStanescu, A
dc.creatorVogel, R
dc.creatorAbdallah, EB
dc.creatorAghababazadeh, FA
dc.creatorAmadoz, A
dc.creatorBhalla, S
dc.creatorBleakley, K
dc.creatorBongen, E
dc.creatorBorzacchielo, D
dc.creatorBucher, P
dc.creatorCarbonell-Caballero, J
dc.creatorChaudhary, K
dc.creatorChinesta, F
dc.creatorChodavarapu, P
dc.creatorChow, RD
dc.creatorCokelaer, T
dc.creatorCubuk, C
dc.creatorDhanda, SK
dc.creatorDopazo, J
dc.creatorFaux, T
dc.creatorFeng, Y
dc.creatorFlinta, C
dc.creatorGuziolowski, C
dc.creatorHe, D
dc.creatorHidalgo, MR
dc.creatorHou, J
dc.creatorInoue, K
dc.creatorJaakkola, MK
dc.creatorJi, J
dc.creatorKumar, R
dc.creatorKumar, S
dc.creatorKursa, MB
dc.creatorLi, Q
dc.creatorŁopuszyński, M
dc.creatorLu, P
dc.creatorMagnin, M
dc.creatorMao, W
dc.creatorMiannay, B
dc.creatorNikolayeva, I
dc.creatorObradovic, Z
dc.creatorPak, C
dc.creatorRahman, MM
dc.creatorRazzaq, M
dc.creatorRibeiro, T
dc.creatorRoux, O
dc.creatorSaghapour, E
dc.creatorSaini, H
dc.creatorSarhadi, S
dc.creatorSato, H
dc.creatorSchwikowski, B
dc.creatorSharma, A
dc.creatorSharma, R
dc.creatorSingla, D
dc.creatorStojkovic, I
dc.creatorSuomi, T
dc.creatorSuprun, M
dc.creatorTian, C
dc.creatorTomalin, LE
dc.creatorXie, L
dc.creatorYu, X
dc.creatorPandey, G
dc.creatorChiu, C
dc.creatorMcClain, MT
dc.creatorWoods, CW
dc.creatorGinsburg, GS
dc.creatorElo, LL
dc.creatorTsalik, EL
dc.creatorMangravite, LM
dc.creatorSieberts, SK
dc.identifier.other30356117 (pubmed)
dc.description.abstract© 2018, The Author(s). The response to respiratory viruses varies substantially between individuals, and there are currently no known molecular predictors from the early stages of infection. Here we conduct a community-based analysis to determine whether pre- or early post-exposure molecular factors could predict physiologic responses to viral exposure. Using peripheral blood gene expression profiles collected from healthy subjects prior to exposure to one of four respiratory viruses (H1N1, H3N2, Rhinovirus, and RSV), as well as up to 24 h following exposure, we find that it is possible to construct models predictive of symptomatic response using profiles even prior to viral exposure. Analysis of predictive gene features reveal little overlap among models; however, in aggregate, these genes are enriched for common pathways. Heme metabolism, the most significantly enriched pathway, is associated with a higher risk of developing symptoms following viral exposure. This study demonstrates that pre-exposure molecular predictors can be identified and improves our understanding of the mechanisms of response to respiratory viruses.
dc.relation.haspartNature Communications
dc.relation.isreferencedbySpringer Science and Business Media LLC
dc.rightsCC BY
dc.subjectGene Expression
dc.subjectHealthy Volunteers
dc.subjectInfluenza A Virus, H1N2 Subtype
dc.subjectInfluenza A Virus, H3N2 Subtype
dc.subjectRespiratory Syncytial Viruses
dc.titleA crowdsourced analysis to identify ab initio molecular signatures predictive of susceptibility to viral infection
dc.type.genreJournal Article
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