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Superinfection exclusion by P22 prophage and the replication complex.

O F Darlington, M Levine

    Journal of Virology
    |September 1, 1971
    PubMed
    Summary
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    Wild-type P22 prophage lysogens prevent superinfecting phage deoxyribonucleic acid (DNA) injection. In contrast, mutant lysogens allow superinfecting phage DNA to associate with the replication complex, revealing a key difference in phage exclusion mechanisms.

    Area of Science:

    • Bacteriology
    • Molecular Biology
    • Virology

    Background:

    • Bacteriophage P22 is a model system for studying lysogenic conversion and phage-host interactions.
    • Lysogenic conversion involves the modification of a host bacterium's properties by prophage genes.
    • Phage exclusion is a critical mechanism for maintaining lysogeny and preventing superinfection.

    Purpose of the Study:

    • To investigate the role of the sie gene in P22-mediated phage exclusion.
    • To determine the fate of superinfecting phage deoxyribonucleic acid (DNA) in wild-type versus mutant lysogens.
    • To elucidate the molecular mechanisms underlying P22-induced exclusion of superinfecting phage DNA.

    Main Methods:

    • Salmonella typhimurium strains lysogenized with wild-type (sie(+)) or mutant (sie(-)) P22 prophage were constructed.

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  • Superinfection experiments were performed using virulent P22 phage.
  • Association of superinfecting phage DNA with the bacterial replication complex was analyzed using biochemical methods.
  • Main Results:

    • Wild-type P22 lysogens effectively excluded deoxyribonucleic acid (DNA) from superinfecting phage.
    • In contrast, sie(-) P22 lysogens failed to exclude superinfecting phage DNA.
    • Superinfecting phage DNA associated with the replication complex in sie(-) lysogens but not in sie(+) lysogens.

    Conclusions:

    • The sie gene product of P22 prophage is essential for mediating exclusion of superinfecting phage DNA.
    • Sie-mediated exclusion likely involves preventing the association of superinfecting DNA with the host replication machinery.
    • This study clarifies a key aspect of P22 phage-host interactions and the maintenance of lysogeny.