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.

Documentation

Links