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Cytokine systems approach demonstrates differences in innate and pro-inflammatory host responses between genetically distinct MERS-CoV isolates.

Identifieur interne : 001668 ( Main/Exploration ); précédent : 001667; suivant : 001669

Cytokine systems approach demonstrates differences in innate and pro-inflammatory host responses between genetically distinct MERS-CoV isolates.

Auteurs : Christian Selinger [États-Unis] ; Jennifer Tisoncik-Go [États-Unis] ; Vineet D. Menachery [États-Unis] ; Sudhakar Agnihothram [États-Unis] ; G Lynn Law [États-Unis] ; Jean Chang [États-Unis] ; Sara M. Kelly [États-Unis] ; Pavel Sova [États-Unis] ; Ralph S. Baric [États-Unis] ; Michael G. Katze [États-Unis]

Source :

RBID : pubmed:25534508

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English descriptors

Abstract

The recent emergence of a novel coronavirus in the Middle East (designated MERS-CoV) is a reminder of the zoonotic and pathogenic potential of emerging coronaviruses in humans. Clinical features of Middle East respiratory syndrome (MERS) include atypical pneumonia and progressive respiratory failure that is highly reminiscent of severe acute respiratory syndrome (SARS) caused by SARS-CoV. The host response is a key component of highly pathogenic respiratory virus infection. Here, we computationally analyzed gene expression changes in a human airway epithelial cell line infected with two genetically distinct MERS-CoV strains obtained from human patients, MERS-CoV SA 1 and MERS-CoV Eng 1.

DOI: 10.1186/1471-2164-15-1161
PubMed: 25534508


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">The recent emergence of a novel coronavirus in the Middle East (designated MERS-CoV) is a reminder of the zoonotic and pathogenic potential of emerging coronaviruses in humans. Clinical features of Middle East respiratory syndrome (MERS) include atypical pneumonia and progressive respiratory failure that is highly reminiscent of severe acute respiratory syndrome (SARS) caused by SARS-CoV. The host response is a key component of highly pathogenic respiratory virus infection. Here, we computationally analyzed gene expression changes in a human airway epithelial cell line infected with two genetically distinct MERS-CoV strains obtained from human patients, MERS-CoV SA 1 and MERS-CoV Eng 1.</div>
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