4.7 Article

Host Gene Expression in Nose and Blood for the Diagnosis of Viral Respiratory Infection

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 219, Issue 7, Pages 1151-1161

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiy608

Keywords

diagnosis; human gene expression; microarray; respiratory viruses; viral infection

Funding

  1. National Institute of Allergy and Infectious Diseases, Division of Microbiology and Infectious Diseases, NIH, Department of Health and Human Services [HHSN272201200005C]
  2. National Cancer Institute Cancer Center Support Grant [P30 CA91842]
  3. Institute of Clinical and Translational Sciences/ Clinical and Translational Sciences Award from the NCRR, a component of NIH [UL1TR002345]
  4. NIH Roadmap for Medical Research

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Background. Recently there has been a growing interest in the potential for host transcriptomic analysis to augment the diagnosis of infectious diseases. Methods. We compared nasal and blood samples for evaluation of the host transcriptomic response in children with acute respiratory syncytial virus (RSV) infection, symptomatic non-RSV respiratory virus infection, asymptomatic rhinovirus infection, and virus-negative asymptomatic controls. We used nested leave-one-pair-out cross-validation and supervised principal components analysis to define small sets of genes whose expression patterns accurately classified subjects. We validated gene classification scores using an external data set. Results. Despite lower quality of nasal RNA, the number of genes detected by microarray in each sample type was equivalent. Nasal gene expression signal derived mainly from epithelial cells but also included a variable leukocyte contribution. The number of genes with increased expression in virus-infected children was comparable in nasal and blood samples, while nasal samples also had decreased expression of many genes associated with ciliary function and assembly. Nasal gene expression signatures were as good or better for discriminating between symptomatic, asymptomatic, and uninfected children. Conclsusions. Our results support the use of nasal samples to augment pathogen-based tests to diagnose viral respiratory infection.

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