Related Experiment Video
Updated: Oct 8, 2025

Coincubation Assay for Quantifying Competitive Interactions between Vibrio fischeri Isolates
Published on: July 22, 2019
Interactions between the Prophage 919TP and Its Vibrio cholerae Host: Implications of gmd Mutation for Phage
Na Li1, Yigang Zeng2, Bijie Hu1
1Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Abstract:
Prophage 919TP is widely distributed among Vibrio cholera and is induced to produce free φ919TP phage particles. However, the interactions between prophage φ919TP, the induced phage particle, and its host remain unknown. In particular, phage resistance mechanisms and potential fitness trade-offs, resulting from phage resistance, are unresolved. In this study, we examined a prophage 919TP-deleted variant of V. cholerae and its interaction with a modified lytic variant of the induced prophage (φ919TP cI-). Specifically, the phage-resistant mutant was isolated by challenging a prophage-deleted variant with lytic phage φ919TP cI-. Further, the comparative genomic analysis of wild-type and φ919TP cI-resistant mutant predicted that phage φ919TP cI- selects for phage-resistant mutants harboring a mutation in key steps of lipopolysaccharide (LPS) O-antigen biosynthesis, causing a single-base-pair deletion in gene gmd. Our study showed that the gmd-mediated O-antigen defect can cause pleiotropic phenotypes, e.g., cell autoaggregation and reduced swarming motility, emphasizing the role of phage-driven diversification in V. cholerae. The developed approach assists in the identification of genetic determinants of host specificity and is used to explore the molecular mechanism underlying phage-host interactions. Our findings contribute to the understanding of prophage-facilitated horizontal gene transfer and emphasize the potential for developing new strategies to optimize the use of phages in bacterial pathogen control.
Insights
Vibrio cholerae develops phage resistance through mutations in lipopolysaccharide (LPS) O-antigen biosynthesis, specifically in the gmd gene. This resistance impacts bacterial traits like autoaggregation and motility, highlighting phage-driven evolution.
Area of Science:
- Microbiology
- Genetics
- Bacteriology
Background:
- Prophage 919TP is common in Vibrio cholerae, capable of producing infectious phage particles.
- The molecular mechanisms of phage-host interactions and resistance in Vibrio cholerae remain largely unexplored.
Purpose of the Study:
- To investigate phage resistance mechanisms in Vibrio cholerae against the induced prophage φ919TP cI-.
- To identify genetic changes and fitness trade-offs associated with phage resistance.
Main Methods:
- Isolation of phage-resistant mutants by challenging a prophage-deleted Vibrio cholerae strain with lytic phage φ919TP cI-.
- Comparative genomic analysis of wild-type and resistant strains.
- Phenotypic characterization of mutants, including motility and aggregation assays.
Main Results:
- Phage resistance is conferred by a mutation in the gmd gene, affecting lipopolysaccharide (LPS) O-antigen biosynthesis.
- The gmd mutation leads to pleiotropic effects, including cell autoaggregation and reduced swarming motility.
- Phage φ919TP cI- selects for specific phage-resistant mutants.
Conclusions:
- Phage-driven evolution significantly impacts Vibrio cholerae populations by selecting for specific resistance mutations.
- Understanding these phage-host interactions is crucial for developing novel phage-based control strategies against bacterial pathogens.
- The study provides insights into genetic determinants of host specificity and phage-host dynamics.
More Related Videos
12:13TransFLP — A Method to Genetically Modify Vibrio cholerae Based on Natural Transformation and FLP-recombination
Published on: October 8, 2012
07:58Laboratory Techniques Used to Maintain and Differentiate Biotypes of Vibrio cholerae Clinical and Environmental Isolates
Published on: May 30, 2017
Related Concept Videos
Viral Replication: Lysogenic Cycle
DNA Bacteriophages
Lysogenic Cycle of Bacteriophages
Viral Replication: Lytic Cycle
Transduction
Intracellular Movement of Viruses and Bacteria