T7
T7 simulates intracellular infection kinetics of bacteriophage T7 to model how genetic variation and environmental resource availability affect growth rates, fitness, and robustness.
Key Features:
- In Silico Mutant Generation: Generates over 150,000 in silico mutants of bacteriophage T7 to explore genetic variation effects on intracellular growth kinetics.
- Environmental Simulation: Evaluates growth rates and growth efficiencies across two host resource regimes: a realistic finite-resource environment and a hypothetical infinite-resource environment.
- Robustness Analysis: Assesses robustness to parameter perturbations and to changes in genetic element ordering, finding general robustness to parameter changes and fragility when genetic element order is altered.
- Fitness Evaluation: Identifies that wild-type T7 exhibits near-optimal fitness in finite-resource environments, consistent with minimizing resource wastage.
- Correlation Analysis: Quantifies a strong correlation between fitness and growth efficiency in finite-resource environments.
Scientific Applications:
- Evolutionary Biology Research: Simulation of evolutionary pressures on phage T7 to study robustness and adaptive strategies under resource constraints.
- Genetic Engineering and Synthetic Biology: Analysis of the impact of genetic element ordering on phage growth to inform engineering of viral vectors or synthetic organisms.
- Pharmaceutical Development: Informing phage therapy design by optimizing phage growth and fitness under resource-limited conditions.
Methodology:
Computational modeling to simulate and analyze growth kinetics of T7 mutants and compare simulations across finite and infinite resource environments.
Topics
Details
- Tool Type:
- library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Java, C++
- Added:
- 8/3/2017
- Last Updated:
- 11/25/2024
Operations
Publications
You L, Yin J. Evolutionary design on a budget: robustness and optimality of bacteriophage T7. IEE Proceedings - Systems Biology. 2006;153(2):46. doi:10.1049/ip-syb:20050026. PMID:16986252.
PMID: 16986252