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A systems approach to understanding human rhinovirus and influenza virus infection.
Kim, Taek-Kyun; Bheda-Malge, Anjali; Lin, Yakang; Sreekrishna, Koti; Adams, Rachel; Robinson, Michael K; Bascom, Charles C; Tiesman, Jay P; Isfort, Robert J; Gelinas, Richard.
Afiliação
  • Kim TK; The Institute for Systems Biology, Seattle, WA 98109, USA. Electronic address: taek-kyun.kim@systemsbiology.org.
  • Bheda-Malge A; The Institute for Systems Biology, Seattle, WA 98109, USA. Electronic address: Anjalee.Malge@systemsbiology.org.
  • Lin Y; The Procter & Gamble Company, Cincinnati, OH 45202, USA. Electronic address: Lin.y.2@pg.com.
  • Sreekrishna K; The Procter & Gamble Company, Cincinnati, OH 45202, USA. Electronic address: Sreekrishna.k@pg.com.
  • Adams R; The Procter & Gamble Company, Cincinnati, OH 45202, USA. Electronic address: adams.r.7@pg.com.
  • Robinson MK; The Procter & Gamble Company, Cincinnati, OH 45202, USA. Electronic address: Robinson.mk@pg.com.
  • Bascom CC; The Procter & Gamble Company, Cincinnati, OH 45202, USA. Electronic address: bascom.cc@pg.com.
  • Tiesman JP; The Procter & Gamble Company, Cincinnati, OH 45202, USA. Electronic address: tiesman.jp@pg.com.
  • Isfort RJ; The Procter & Gamble Company, Cincinnati, OH 45202, USA. Electronic address: isfort.rj@pg.com.
  • Gelinas R; The Institute for Systems Biology, Seattle, WA 98109, USA. Electronic address: rgelinas@systemsbiology.org.
Virology ; 486: 146-57, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26437235
ABSTRACT
Human rhinovirus and influenza virus infections of the upper airway lead to colds and the flu and can trigger exacerbations of lower airway diseases including asthma and chronic obstructive pulmonary disease. Novel diagnostic and therapeutic targets are still needed to differentiate between the cold and the flu, since the clinical course of influenza can be severe while that of rhinovirus is usually more mild. In our investigation of influenza and rhinovirus infection of human respiratory epithelial cells, we used a systems approach to identify the temporally changing patterns of host gene expression from these viruses. After infection of human bronchial epithelial cells (BEAS-2B) with rhinovirus, influenza virus or co-infection with both viruses, we studied the time-course of host gene expression changes over three days. We modeled host responses to these viral infections with time and documented the qualitative and quantitative differences in innate immune activation and regulation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rhinovirus / Infecções por Picornaviridae / Influenza Humana / Vírus da Influenza A Subtipo H1N1 Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rhinovirus / Infecções por Picornaviridae / Influenza Humana / Vírus da Influenza A Subtipo H1N1 Idioma: En Ano de publicação: 2015 Tipo de documento: Article