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Quantitative Analyses of all Influenza Type A Viral Hemagglutinins and Neuraminidases using Universal Antibodies in Simple Slot Blot Assays
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Quantitative Analyses of all Influenza Type A Viral Hemagglutinins and Neuraminidases using Universal Antibodies in Simple Slot Blot Assays

Published on: April 4, 2011

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Classification of Influenza Hemagglutinin Protein Sequences using Convolutional Neural Networks

Charalambos Chrysostomou, Floris Alexandrou, Mihalis A Nicolaou

    Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference
    |December 11, 2021
    PubMed

    Abstract:

    The Influenza virus can be considered as one of the most severe viruses that can infect multiple species with often fatal consequences to the hosts. The Hemagglutinin (HA) gene of the virus can be a target for antiviral drug development realised through accurate identification of its sub-types and possible the targeted hosts. This paper focuses on accurately predicting if an Influenza type A virus can infect specific hosts, and more specifically, Human, Avian and Swine hosts, using only the protein sequence of the HA gene. In more detail, we propose encoding the protein sequences into numerical signals using the Hydrophobicity Index and subsequently utilising a Convolutional Neural Network-based predictive model. The Influenza HA protein sequences used in the proposed work are obtained from the Influenza Research Database (IRD). Specifically, complete and unique HA protein sequences were used for avian, human and swine hosts. The data obtained for this work was 17999 human-host proteins, 17667 avian-host proteins and 9278 swine-host proteins. Given this set of collected proteins, the proposed method yields as much as 10% higher accuracy for an individual class (namely, Avian) and 5% higher overall accuracy than in an earlier study. It is also observed that the accuracy for each class in this work is more balanced than what was presented in this earlier study. As the results show, the proposed model can distinguish HA protein sequences with high accuracy whenever the virus under investigation can infect Human, Avian or Swine hosts.

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