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Published on: July 26, 2019
Immune response to seasonal influenza A virus infection: a proteomic approach
Luis M Teran1, Sabrina Rüggeberg, Julio Santiago
1Department of Immunogenetics and Allergy, National Institute of Respiratory Diseases, México, D.F., Mexico. lmteran@iner.gob.mx
Insights
Influenza virus infection alters nasal secretions in children. This study identified specific proteins upregulated during flu, offering new insights into how influenza causes respiratory illness.
Area of Science:
- Proteomics
- Virology
- Immunology
Background:
- Influenza viruses cause significant respiratory illness and economic burden.
- The precise mechanisms of influenza pathogenesis remain incompletely understood.
Purpose of the Study:
- To investigate the proteomic differences in nasal secretions of children infected with seasonal influenza A virus compared to healthy controls.
- To identify specific proteins associated with influenza infection in pediatric patients.
Main Methods:
- Nasal aspirates from 12 children with influenza A symptoms were analyzed using two-dimensional electrophoresis (2-DE).
- Control samples were collected from the same children when asymptomatic.
- Differentially expressed protein spots were identified using mass spectrometry.
Main Results:
- Eight protein spots showed differential expression between infected and healthy states.
- Ten proteins were upregulated in children with influenza A, including PLUNC, cystatins (S and SA), S100A9, lipocalin 1 fragments, and immunoglobulin fragments.
- Specific protein fragments from lactotransferrin and immunoglobulins (kappa and lambda) were also identified.
Conclusions:
- The proteomic composition of nasal secretions differs significantly between children with influenza A virus infection and healthy children.
- These findings enhance our understanding of the pathogenesis of seasonal influenza A virus respiratory infections.
Background And Aims:
Influenza viruses cause respiratory infection in humans and result in substantial illness, death, and economic burden. To date, however, the mechanisms by which these viruses cause disease are not fully understood.
Methods:
To investigate the proteomic profile of children infected with seasonal influenza A virus, nasal aspirates derived from children (n = 12) experiencing flu symptoms caused by seasonal influenza A virus were analyzed using two-dimensional electrophoresis (2-DE). Control nasal samples were taken from the same group of children 8-10 weeks later when they were symptom free.
Results:
Analysis of the 2-DE gels revealed eight spots differentially expressed, which were further analyzed using mass spectrometry. Ten proteins were found to be differentially upregulated in the infected children including PLUNC, cystatin S, cystatin SA, S100A9, lipocalin 1 fragments (n = 2), truncated lactotransferrin, two immunoglobulin (Ig) kappa fragments and one immunoglobulin (Ig) lambda fragment.
Conclusions:
Our findings reveal that the composition of nasal secretions in influenza virus respiratory infections is different from that when children are healthy and may provide further insights into the pathogenesis of respiratory infections caused by seasonal influenza A viruses.
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