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Related Concept Videos

DNA Bacteriophages01:26

DNA Bacteriophages

Bacteriophages, or phages, are viruses that specifically infect bacteria, utilizing their genetic material to hijack host cellular machinery for replication. DNA bacteriophages employ single-stranded DNA (ssDNA) or double-stranded DNA (dsDNA) genomes. These phages exhibit diverse replication strategies and host interactions, influencing their ecological roles and applications in biotechnology and medicine.ssDNA BacteriophagesssDNA phages, with their small genomes, utilize unique strategies to...
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...
Lytic Cycle of Bacteriophages01:30

Lytic Cycle of Bacteriophages

Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the lytic replication...
Lysogenic Cycle of Bacteriophages00:43

Lysogenic Cycle of Bacteriophages

In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
Viral Replication: Lysogenic Cycle01:16

Viral Replication: Lysogenic Cycle

The lysogenic cycle is a crucial viral replication strategy that allows bacteriophages to persist within host cells without immediately destroying them. This process is primarily observed in temperate phages, such as bacteriophage lambda (λ), which infects Escherichia coli. The cycle allows the viral genome to persist across bacterial generations while keeping host cells viable.Integration of the Viral GenomeUpon infection, bacteriophage lambda attaches to the bacterial surface and injects its...

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Updated: May 9, 2026

An Adapted Optical Density-Based Microplate Assay for Characterizing Actinobacteriophage Infection
03:33

An Adapted Optical Density-Based Microplate Assay for Characterizing Actinobacteriophage Infection

Published on: June 30, 2023

Bacteriophage PRD1 batch experiments to study attachment, detachment and inactivation processes.

Gholamreza Sadeghi1, Jack F Schijven, Thilo Behrends

  • 1Department of Environmental Health Engineering, Zanjan University of Medical Sciences, Zanjan, Iran.

Journal of Contaminant Hydrology
|July 9, 2013
PubMed
Summary

Kinetic batch experiments for virus removal in subsurface environments are as laborious as column experiments. Mixing conditions significantly impact attachment rates, questioning the advantage of batch over column studies for upscaling virus transport data.

Keywords:
Bacteriophage PRD1Batch experimentColloids

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

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Following Cell-fate in E. coli After Infection by Phage Lambda
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Following Cell-fate in E. coli After Infection by Phage Lambda

Published on: October 14, 2011

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Last Updated: May 9, 2026

An Adapted Optical Density-Based Microplate Assay for Characterizing Actinobacteriophage Infection
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An Adapted Optical Density-Based Microplate Assay for Characterizing Actinobacteriophage Infection

Published on: June 30, 2023

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

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Following Cell-fate in E. coli After Infection by Phage Lambda
06:10

Following Cell-fate in E. coli After Infection by Phage Lambda

Published on: October 14, 2011

Area of Science:

  • Environmental science
  • Microbiology
  • Water resource management

Background:

  • Virus contamination of water resources poses significant risks.
  • Subsurface environments are crucial for water purification.
  • Accurate assessment of virus removal is vital for protection measures.

Purpose of the Study:

  • To evaluate the utility of kinetic batch experiments for virus removal studies.
  • To investigate how batch experiment designs affect attachment, detachment, and inactivation rate coefficients.
  • To compare findings from batch experiments with column experiments for virus transport modeling.

Main Methods:

  • Conducted kinetic batch experiments using quartz sand, bacteriophage PRD1, and controlled water chemistry.
  • Varied container size, sand-water ratio, and mixing methods (rolling vs. tumbling).
  • Fitted analytical solutions of kinetic model equations to experimental data to derive rate coefficients.

Main Results:

  • Attachment rate coefficients were higher under tumbling (better mixing) than rolling conditions.
  • Increased sand-water ratio led to higher attachment rates.
  • Detachment rate coefficients increased linearly with the solid-water ratio under tumbling.
  • Collision efficiencies differed between batch and column experiments, influenced by mixing.

Conclusions:

  • Kinetic batch experiments are as labor-intensive as column experiments.
  • Upscaling virus attachment rates from batch to column requires understanding mixing dynamics.
  • The direct advantage of kinetic batch experiments over column experiments for virus transport studies is questionable.