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The Effect of Mice Adaptation Process on the Pathogenicity of Influenza A/South Africa/3626/2013 (H1N1)pdm09 Model Strain.
Al Farroukh, Mohammad; Kiseleva, Irina; Stepanova, Ekaterina; Bazhenova, Ekaterina; Krutikova, Elena; Tkachev, Artem; Chistyakova, Anna; Rekstin, Andrey; Puchkova, Ludmila; Rudenko, Larisa.
Afiliação
  • Al Farroukh M; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
  • Kiseleva I; Institute of Biomedical Systems and Biotechnology, Peter the Great St. Petersburg Polytechnic University, St. Petersburg 194021, Russia.
  • Stepanova E; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
  • Bazhenova E; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
  • Krutikova E; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
  • Tkachev A; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
  • Chistyakova A; Institute of Biomedical Systems and Biotechnology, Peter the Great St. Petersburg Polytechnic University, St. Petersburg 194021, Russia.
  • Rekstin A; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
  • Puchkova L; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
  • Rudenko L; Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
Int J Mol Sci ; 24(24)2023 Dec 12.
Article em En | MEDLINE | ID: mdl-38139214
ABSTRACT
Influenza virus strain A/South Africa/3626/2013 (H1N1)pdm09 (SA-WT) is a non-mouse-adapted model strain that has naturally high pathogenic properties in mice. It has been suggested that the high pathogenicity of this strain for mice could be due to the three strain-specific substitutions in the polymerase complex (Q687R in PB1, N102T in PB2, and E358E/K heterogeneity in PB2). To evaluate the role of these replacements, SA-WT was passaged five times in mouse lungs, and the genome of the mouse-adapted version of the SA-WT strain (SA-M5) was sequenced. SA-M5 lost E358E/K heterogeneity and retained E358, which is the prevalent amino acid at this position among H1N1pdm09 strains. In addition, in the hemagglutinin of SA-M5, two heterogeneous substitutions (G155G/E and S190S/R) were identified. Both viruses, SA-M5 and SA-WT, were compared for their toxicity, ability to replicate, pathogenicity, and immunogenicity in mice. In mice infected with SA-M5 or SA-WT strains, toxicity, virus titer in pulmonary homogenates, and mouse survival did not differ significantly. In contrast, an increase in the immunogenicity of SA-M5 compared to SA-WT was observed. This increase could be due to the substitutions G155G/E and S190S/R in the HA of SA-M5. The prospects for using SA-M5 in studying the immunogenicity mechanisms were also discussed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Influenza Humana / Vírus da Influenza A Subtipo H1N1 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Influenza Humana / Vírus da Influenza A Subtipo H1N1 Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article