Anticytomegaloviral activity of esterified milk proteins and L-polylysines

Jean-Marc Chobert1, Mahmoud Sitohy, Sylviane Billaudel

  • 1UR 1268 Biopolymères Interactions Assemblages, INRA, Equipe Fonctions et Interactions des Protéines Laitières, Nantes, France. chobert@nantes.inra.fr

Insights

Methylated alpha-lactalbumin (Met-ALA) and methylated beta-lactoglobulin (Met-BLG) reduced human cytomegalovirus (HCMV) infection in fibroblasts. These basic proteins and polypeptides show potential against drug-resistant HCMV strains.

Area of Science:

  • Virology
  • Biochemistry
  • Drug Discovery

Background:

  • Human cytomegalovirus (HCMV) is a common pathogen causing significant morbidity, especially in immunocompromised individuals.
  • Emerging drug resistance and viral persistence pose challenges for effective HCMV treatment.
  • Novel antiviral agents are needed to combat HCMV infections.

Purpose of the Study:

  • To evaluate the antiviral activity of methylated alpha-lactalbumin (Met-ALA) and methylated beta-lactoglobulin (Met-BLG) against HCMV.
  • To assess the efficacy of peptic hydrolysates of Met-ALA and Met-BLG.
  • To compare the antiviral potential of these compounds with L-polylysines.

Main Methods:

  • MRC-5 fibroblasts were infected with HCMV (AD 169 strain).
  • Cells were treated with varying concentrations of Met-ALA, Met-BLG, their peptic hydrolysates, and L-polylysines.
  • Antiviral activity was quantified by comparing infected cell counts in treated versus untreated groups.

Main Results:

  • Both Met-ALA and Met-BLG, along with their peptic hydrolysates, demonstrated a reduction in HCMV infectious activity in fibroblast cells.
  • L-polylysines exhibited the highest antiviral activity among the tested substances.
  • The basic proteins and polypeptides, despite lower activity than L-polylysines, showed promising antiviral effects.

Conclusions:

  • Met-ALA and Met-BLG possess significant antiviral properties against HCMV.
  • These compounds, including their hydrolysates and other basic polypeptides, represent potential therapeutic candidates for HCMV infections.
  • Their utility may be particularly relevant in addressing drug-resistant and persistent HCMV strains.

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