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Emergence of Hemagglutinin Mutations During the Course of Influenza Infection.
Cushing, Anna; Kamali, Amanda; Winters, Mark; Hopmans, Erik S; Bell, John M; Grimes, Susan M; Xia, Li C; Zhang, Nancy R; Moss, Ronald B; Holodniy, Mark; Ji, Hanlee P.
Afiliação
  • Cushing A; Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States.
  • Kamali A; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, United States.
  • Winters M; VA Palo Alto Health Care System, Palo Alto, CA 94304, United States.
  • Hopmans ES; Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States.
  • Bell JM; Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States.
  • Grimes SM; Stanford Genome Technology Center, Stanford University, Palo Alto, CA, 94304, United States.
  • Xia LC; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, United States.
  • Zhang NR; Depart of Statistics, The Wharton School, University of Pennsylvania, Philadelphia, PA 19104 USA.
  • Moss RB; Ansun BioPharma, Inc., San Diego, CA, 92121, United States.
  • Holodniy M; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, United States.
  • Ji HP; VA Palo Alto Health Care System, Palo Alto, CA 94304, United States.
Sci Rep ; 5: 16178, 2015 Nov 05.
Article em En | MEDLINE | ID: mdl-26538451
ABSTRACT
Influenza remains a significant cause of disease mortality. The ongoing threat of influenza infection is partly attributable to the emergence of new mutations in the influenza genome. Among the influenza viral gene products, the hemagglutinin (HA) glycoprotein plays a critical role in influenza pathogenesis, is the target for vaccines and accumulates new mutations that may alter the efficacy of immunization. To study the emergence of HA mutations during the course of infection, we employed a deep-targeted sequencing method. We used samples from 17 patients with active H1N1 or H3N2 influenza infections. These patients were not treated with antivirals. In addition, we had samples from five patients who were analyzed longitudinally. Thus, we determined the quantitative changes in the fractional representation of HA mutations during the course of infection. Across individuals in the study, a series of novel HA mutations directly altered the HA coding sequence were identified. Serial viral sampling revealed HA mutations that either were stable, expanded or were reduced in representation during the course of the infection. Overall, we demonstrated the emergence of unique mutations specific to an infected individual and temporal genetic variation during infection.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glicoproteínas de Hemaglutininação de Vírus da Influenza / Influenza Humana / Vírus da Influenza A Subtipo H1N1 / Vírus da Influenza A Subtipo H3N2 / Mutação Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Glicoproteínas de Hemaglutininação de Vírus da Influenza / Influenza Humana / Vírus da Influenza A Subtipo H1N1 / Vírus da Influenza A Subtipo H3N2 / Mutação Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2015 Tipo de documento: Article