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Related Concept Videos

Viral Replication: Lytic Cycle01:20

Viral Replication: Lytic Cycle

Bacteriophages, or phages, are viruses that specifically infect bacteria. Among them, T-even bacteriophages, such as T4, exhibit a well-characterized lytic replication cycle in Escherichia coli (E. coli). This process ensures the rapid proliferation of the virus while ultimately leading to the destruction of the bacterial host.Attachment and DNA InjectionThe infection process begins with the recognition and binding of the T4 phage to the E. coli cell surface. Tail fibers of the phage...
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Cryo-electron Microscopy01:28

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Lysogenic Cycle of Bacteriophages00:43

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Related Experiment Video

Updated: Jul 6, 2026

T4 Bacteriophage and E. coli Interaction in the Murine Intestine: A Prototypical Model for Studying Host-Bacteriophage Dynamics In Vivo
08:46

T4 Bacteriophage and E. coli Interaction in the Murine Intestine: A Prototypical Model for Studying Host-Bacteriophage Dynamics In Vivo

Published on: January 26, 2024

Cryo-EM structures of phage T4 infection intermediate.

Qianqian Shao1, Junhua Dong2, Aohan Wang1

  • 1School of Public Health (Shenzhen), Sun Yat-sen University, Shenzhen, Guangdong, China.

Journal of Molecular Biology
|July 4, 2026
PubMed
Summary

We revealed the structure of a key intermediate in myophage T4 infection, uncovering how its tail machinery delivers viral DNA into host cells. This provides new insights into bacteriophage genome delivery mechanisms.

Keywords:
Bacteriophage T4cryo-EMgenome deliverytape-measure proteinvirus-host interaction

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Area of Science:

  • Structural biology
  • Molecular biology
  • Virology

Background:

  • Bacteriophages, like myophage T4, possess complex contractile tails for host infection.
  • Mechanisms of host recognition, signal transduction, and genome delivery by myophages are not fully understood.

Purpose of the Study:

  • To elucidate the structural mechanisms underlying myophage T4 genome delivery.
  • To characterize a pre-genome-release intermediate of myophage T4.

Main Methods:

  • Cryo-electron microscopy (cryo-EM) was used to determine the structure of the myophage T4 intermediate.
  • Comparative structural analysis was performed between different T4 virion states.

Main Results:

  • The structure of a tail-contracted, pre-genome-release intermediate was determined.
  • Structural transitions in the tail, tape-measure protein (TMP), baseplate, and long tail fibers were identified.
  • Tail sheath contraction was found to be coupled with repositioning of the viral DNA-TMP complex, facilitating genome translocation.

Conclusions:

  • The study reveals key structural dynamics driving myophage T4 genome delivery.
  • Expelled TMP may form a transmembrane complex to aid genome translocation into the host cytosol.
  • Findings advance understanding of bacteriophage infection machinery and DNA delivery processes.