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The role of methionine deficiency in poliovirus replication in tissue cultures
Abstract:
The role of methionine in poliovirus infection in HeLa and monkey kidney cells was investigated by using the methionine analogue l-ethionine. In the presence of 2.0 x 10(-3) and 4.0 x 10(-3) moles ethionine, the growth of HeLa and monkey kidney cells was significantly inhibited. Under the same experimental conditions, ethionine had no significant effect on the biosynthesis of two strains of poliovirus (Mahoney and Lansing) in HeLa cells, whereas in primary monkey kidney cells, it markedly inhibited the biosynthesis of the Lansing strain of poliovirus. HeLa cells partly depleted of their intracellular amino acids did not change the rate of viral biosynthesis. The inhibitory effect of ethionine on cell growth and viral biosynthesis was reversed by addition of an excess of l-methionine.
Insights
Methionine
Area of Science:
- Virology
- Cell Biology
- Biochemistry
Background:
- Methionine is an essential amino acid crucial for protein synthesis.
- Poliovirus relies on host cell machinery for replication.
- Understanding nutrient roles in viral infections is key to developing antivirals.
Purpose of the Study:
- To investigate the role of methionine in poliovirus replication.
- To determine the effects of a methionine analogue, ethionine, on host cell growth and viral biosynthesis.
- To explore the potential for reversing these effects with methionine.
Main Methods:
- Utilized HeLa and primary monkey kidney cells for experiments.
- Administered the methionine analogue l-ethionine at varying concentrations.
- Assessed cell growth inhibition and poliovirus (Mahoney and Lansing strains) biosynthesis.
- Investigated the impact of intracellular amino acid depletion.
- Evaluated the reversibility of ethionine's effects using excess l-methionine.
Main Results:
- Ethionine significantly inhibited the growth of both HeLa and monkey kidney cells.
- Ethionine did not significantly affect poliovirus biosynthesis in HeLa cells.
- Ethionine markedly inhibited the Lansing strain of poliovirus biosynthesis in monkey kidney cells.
- Partial depletion of intracellular amino acids in HeLa cells did not alter viral biosynthesis rates.
- The inhibitory effects of ethionine on cell growth and viral biosynthesis were reversed by adding excess l-methionine.
Conclusions:
- Methionine availability influences poliovirus replication differently across cell types.
- Ethionine's inhibitory effect on poliovirus biosynthesis in monkey kidney cells highlights cell-specific nutrient dependencies.
- Reversibility by methionine suggests a direct role in viral replication pathways, offering potential therapeutic targets.