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HIV-1 drug resistance profiling using amino acid sequence space cartography.
Pikalyova, Karina; Orlov, Alexey; Lin, Arkadii; Tarasova, Olga; Marcou, MarcouGilles; Horvath, Dragos; Poroikov, Vladimir; Varnek, Alexandre.
Afiliación
  • Pikalyova K; Laboratoire de Chémoinformatique, UMR 7140, Université de Strasbourg, Strasbourg 67000, France.
  • Orlov A; Laboratoire de Chémoinformatique, UMR 7140, Université de Strasbourg, Strasbourg 67000, France.
  • Lin A; Laboratoire de Chémoinformatique, UMR 7140, Université de Strasbourg, Strasbourg 67000, France.
  • Tarasova O; Institute of Biomedical Chemistry, Moscow 119121, Russia.
  • Marcou M; Laboratoire de Chémoinformatique, UMR 7140, Université de Strasbourg, Strasbourg 67000, France.
  • Horvath D; Laboratoire de Chémoinformatique, UMR 7140, Université de Strasbourg, Strasbourg 67000, France.
  • Poroikov V; Institute of Biomedical Chemistry, Moscow 119121, Russia.
  • Varnek A; Laboratoire de Chémoinformatique, UMR 7140, Université de Strasbourg, Strasbourg 67000, France.
Bioinformatics ; 38(8): 2307-2314, 2022 04 12.
Article en En | MEDLINE | ID: mdl-35157024
ABSTRACT
MOTIVATION Human immunodeficiency virus (HIV) drug resistance is a global healthcare issue. The emergence of drug resistance influenced the efficacy of treatment regimens, thus stressing the importance of treatment adaptation. Computational methods predicting the drug resistance profile from genomic data of HIV isolates are advantageous for monitoring drug resistance in patients. However, existing computational methods for drug resistance prediction are either not suitable for emerging HIV strains with complex mutational patterns or lack interpretability, which is of paramount importance in clinical practice. The approach reported here overcomes these limitations and combines high accuracy of predictions and interpretability of the models.

RESULTS:

In this work, a new methodology based on generative topographic mapping (GTM) for biological sequence space representation and quantitative genotype-phenotype relationships prediction purposes was introduced. The GTM-based resistance landscapes allowed us to predict the resistance of HIV strains based on sequencing and drug resistance data for three viral proteins [integrase (IN), protease (PR) and reverse transcriptase (RT)] from Stanford HIV drug resistance database. The average balanced accuracy for PR inhibitors was 0.89 ± 0.01, for IN inhibitors 0.85 ± 0.01, for non-nucleoside RT inhibitors 0.73 ± 0.01 and for nucleoside RT inhibitors 0.84 ± 0.01. We have demonstrated in several case studies that GTM-based resistance landscapes are useful for visualization and analysis of sequence space as well as for treatment optimization purposes. Here, GTMs were applied for the in-depth analysis of the relationships between mutation pattern and drug resistance using mutation landscapes. This allowed us to predict retrospectively the importance of the presence of particular mutations (e.g. V32I, L10F and L33F in HIV PR) for the resistance development. This study highlights some perspectives of GTM applications in clinical informatics and particularly in the field of sequence space exploration. AVAILABILITY AND IMPLEMENTATION https//github.com/karinapikalyova/ISIDASeq. SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Infecciones por VIH / VIH-1 Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Francia