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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...
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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...
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Updated: Jul 3, 2025

Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
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PB-LKS: a python package for predicting phage-bacteria interaction through local K-mer strategy.

Jingxuan Qiu1, Wanchun Nie1, Hao Ding2

  • 1School of Health Science and Engineering, University of Shanghai for Science and Technology, Shanghai, 200093, China.

Briefings in Bioinformatics
|February 12, 2024
PubMed
Summary
This summary is machine-generated.

A new computational model, PB-LKS, improves prediction of phage-bacteria interactions, advancing phage therapy development. This tool accurately predicts relationships across bacterial strain mutants, enhancing therapeutic design.

Keywords:
bioinformaticsgenome sequence analysislocal K-mer strategymachine learningphage–bacteria interaction

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Area of Science:

  • Microbiology
  • Bioinformatics
  • Computational Biology

Background:

  • Bacteriophages are promising for treating bacterial infections but require accurate in-silico models due to high genetic diversity.
  • Current prediction models are limited to species-level accuracy, failing to predict interactions with bacterial strain mutants, hindering phage therapy development.

Purpose of the Study:

  • To introduce PB-LKS, a novel computational approach utilizing a local k-mer strategy for enhanced prediction of phage-bacteria interactions.
  • To develop a model with wider applicability and higher performance than existing methods for predicting phage-bacteria relationships.

Main Methods:

  • The PB-LKS model employs a local k-mer strategy to analyze genetic similarities and predict interactions.
  • Model validation involved large-scale historical screening, a class-level case study, and in vitro simulations of bacterial antiphage resistance at the strain mutant level.

Main Results:

  • PB-LKS demonstrated superior performance compared to current state-of-the-art methods in predicting phage-bacteria interactions.
  • The model accurately predicted interactions across bacterial strain mutants, addressing limitations of previous species-level approaches.

Conclusions:

  • PB-LKS offers improved accuracy and broader applicability for predicting phage-bacteria interactions.
  • The PB-LKS approach shows significant potential for clinical utility in designing optimized phage therapy strategies.