Short noncontractile tail machines: adsorption and DNA delivery by podoviruses

Sherwood R Casjens1, Ian J Molineux

  • 1Pathology Department, University of Utah School of Medicine, Salt Lake City, UT 84112, USA. sherwood.casjen@path.utah.edu

Insights

Short-tailed bacteriophages (Podoviridae) deliver DNA into bacterial cells using specialized tail machinery. Their adsorption, DNA injection, and host specificity are influenced by tail proteins and receptor interactions.

Area of Science:

  • Microbiology
  • Virology
  • Molecular Biology

Background:

  • Tailed double-stranded DNA (dsDNA) bacteriophages infect bacteria by injecting their genetic material.
  • Short-tailed phages (Podoviridae) possess unique tail structures influencing their infection mechanism.
  • Adsorption to host cells involves specific receptor-binding proteins, often with enzymatic activity.

Purpose of the Study:

  • To review the mechanisms of DNA delivery by short-tailed bacteriophages (Podoviridae).
  • To explore the roles of tail proteins, receptors, and adsorption processes in phage infection.
  • To discuss variations in DNA injection energetics and timing.

Main Methods:

  • Literature review of studies on Podoviridae infection dynamics.
  • Analysis of protein structure-function relationships in tail fibers and spikes.
  • Comparison of DNA injection strategies among different phage species.

Main Results:

  • Podoviridae utilize tail tips for initial cell binding and DNA delivery.
  • Enzymatic activity of receptor-binding proteins facilitates host cell entry.
  • Sequence variations in tail proteins determine host specificity.
  • Intracellular protein delivery aids DNA translocation and host preparation.
  • DNA injection can be slow (e.g., T7, N4) or rapid (e.g., P22), impacting gene expression timing.

Conclusions:

  • Short-tailed phages exhibit diverse strategies for DNA injection.
  • Tail protein evolution drives host range and infection efficiency.
  • The energetics and kinetics of DNA delivery are critical for successful phage replication.

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