Identifying virus-cell fusion in two-channel fluorescence microscopy image sequences based on a layered probabilistic approach

IEEE Trans Med Imaging. 2012 Sep;31(9):1786-808. doi: 10.1109/TMI.2012.2203142. Epub 2012 Jun 6.

Abstract

The entry process of virus particles into cells is decisive for infection. In this work, we investigate fusion of virus particles with the cell membrane via time-lapse fluorescence microscopy. To automatically identify fusion for single particles based on their intensity over time, we have developed a layered probabilistic approach. The approach decomposes the action of a single particle into three abstractions: the intensity over time, the underlying temporal intensity model, as well as a high level behavior. Each abstraction corresponds to a layer and these layers are represented via stochastic hybrid systems and hidden Markov models. We use a maxbelief strategy to efficiently combine both representations. To compute estimates for the abstractions we use a hybrid particle filter and the Viterbi algorithm. Based on synthetic image sequences, we characterize the performance of the approach as a function of the image noise. We also characterize the performance as a function of the tracking error. We have also successfully applied the approach to real image sequences displaying pseudotyped HIV-1 particles in contact with host cells and compared the experimental results with ground truth obtained by manual analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Bayes Theorem
  • Cell Fusion
  • Cell Tracking
  • HIV-1 / physiology
  • HIV-1 / ultrastructure
  • HeLa Cells
  • Host-Pathogen Interactions / physiology*
  • Humans
  • Markov Chains
  • Microscopy, Fluorescence / methods*
  • Models, Biological*
  • Stochastic Processes
  • Virion / physiology*
  • Virion / ultrastructure
  • Virus Attachment*
  • Virus Internalization