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Published on: April 11, 2020
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
Abstract:
Tailed dsDNA bacteriophage virions bind to susceptible cells with the tips of their tails and then deliver their DNA through the tail into the cells to initiate infection. This chapter discusses what is known about this process in the short-tailed phages (Podoviridae). Their short tails require that many of these virions adsorb to the outer layers of the cell and work their way down to the outer membrane surface before releasing their DNA. Interestingly, the receptor-binding protein of many short-tailed phages (and some with long tails) has an enzymatic activity that cleaves their polysaccharide receptors. Reversible adsorption and irreversible adsorption to primary and secondary receptors are discussed, including how sequence divergence in tail fiber and tailspike proteins leads to different host specificities. Upon reaching the outer membrane of Gram-negative cells, some podoviral tail machines release virion proteins into the cell that help the DNA efficiently traverse the outer layers of the cell and/or prepare the cell cytoplasm for phage genome arrival. Podoviruses utilize several rather different variations on this theme. The virion DNA is then released into the cell; the energetics of this process is discussed. Phages like T7 and N4 deliver their DNA relatively slowly, using enzymes to pull the genome into the cell. At least in part this mechanism ensures that genes in late-entering DNA are not expressed at early times. On the other hand, phages like P22 probably deliver their DNA more rapidly so that it can be circularized before the cascade of gene expression begins.
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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