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      Prolonged excretion of amantadine-resistant influenza a virus quasi species after cessation of antiviral therapy in an immunocompromised patient.

      Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
      Amantadine, pharmacology, therapeutic use, Antiviral Agents, Drug Resistance, Microbial, genetics, Genotype, Humans, Immunocompromised Host, Influenza A virus, drug effects, Male, Middle Aged, Mutation, Phenotype, Polymerase Chain Reaction

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          Abstract

          Phenotypic and molecular studies were conducted to characterize multiple influenza A isolates recovered from an immunocompromised patient who died of viral and fungal pneumonitis. The recovery of amantadine-resistant isolates was correlated with the detection of 2 drug-resistant M2 variants (codons 27 and 31) in combination with a wild-type virus. The mutant viruses persisted within the viral population in variable proportions >1 month after cessation of antiviral therapy. These results confirm animal studies reported elsewhere regarding the genetic stability of influenza M2 mutants and their potential for transmission in humans.

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