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dc.contributor.authorVoltersvik, Pålen_US
dc.contributor.authorAqrawi, Lara Adnanen_US
dc.contributor.authorDudman, Susanne Gjeruldsenen_US
dc.contributor.authorHungnes, Olaven_US
dc.contributor.authorBostad, Leifen_US
dc.contributor.authorBrokstad, Karl Alberten_US
dc.contributor.authorCox, Rebecca Janeen_US
dc.date.accessioned2017-04-26T08:55:52Z
dc.date.available2017-04-26T08:55:52Z
dc.date.issued2016-11
dc.PublishedVoltersvik P, Aqrawi LA, Dudman SMR, Hungnes O, Bostad L, Brokstad KA, Cox RJ. Pulmonary changes in Norwegian fatal cases of pandemic influenza H1N1 (2009) infection: a morphologic and molecular genetic study. Influenza and Other Respiratory Viruses. 2016;10(6):525-531eng
dc.identifier.urihttps://hdl.handle.net/1956/15711
dc.description.abstractBackground: During the pandemic outbreak of the 2009 swine influenza (A(H1N1) pdm09), 32 fatal cases occurred in Norway and 19 of these were included in this study. Objectives: We characterised pulmonary changes in these fatal Norwegian cases. Patients and Methods: Upon hospitalisation, detailed clinical information and specimens from the upper and lower respiratory pathways were collected. At post-mortem, lung tissue was collected, formalin-fixed and paraffin-embedded. Immunohistochemical and light microscopic examination was performed to visualise the local expression of the A(H1N1) pdm09 virus. Reverse transcription-polymerase chain reaction (RT-PCR) and pyrosequencing of the non-fixed specimens allowed the identification of mutations in the influenza virus surface glycoprotein (haemagglutinin gene) particularly at position 222. Results and Conclusions: The overall course of illness lasted from 2 to 40 days (median 9 days). Diffused alveolar damage (DAD) was evident in 11 cases, 4 of which had no apparent underlying illness. Obesity was prominent in 12 cases, where three individuals were classified as otherwise healthy. The HA D222G mutation was detected in six cases, 3 of which had no underlying illness. Immunohistochemistry showed the A(H1N1)pdm09 virus to be prominent at the site of inflammation both in close proximity to and inside alveolar structures in the lung tissue. In addition to a possible role for the HA D222G mutation, our findings indicate that host factors and underlying conditions in the infected individuals are fundamental for disease outcome in many cases. This study increases our understanding of determinants for the clinical outcome of pandemic influenza, which could guide future treatment.en_US
dc.language.isoengeng
dc.publisherWileyeng
dc.relation.urihttp://onlinelibrary.wiley.com/doi/10.1111/irv.12410/epdf
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/eng
dc.subject2009 pandemiceng
dc.subjectHA pyrosequencingeng
dc.subjectimmunohistochemistryeng
dc.subjectinfluenzaeng
dc.subjectlungeng
dc.titlePulmonary changes in Norwegian fatal cases of pandemic influenza H1N1 (2009) infection: a morphologic and molecular genetic studyen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2017-02-16T12:03:19Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2016 The Author(s)
dc.identifier.doihttps://doi.org/10.1111/irv.12410
dc.identifier.cristin1402967
dc.source.journalInfluenza and Other Respiratory Viruses


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