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

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...

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Hauptverfasser: Godinez, William J. (VerfasserIn) , Lampe, Marko (VerfasserIn) , Koch, Peter (VerfasserIn) , Eils, Roland (VerfasserIn) , Müller, Barbara (VerfasserIn) , Rohr, Karl (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 06 June 2012
In: IEEE transactions on medical imaging
Year: 2012, Jahrgang: 31, Heft: 9, Pages: 1786-1808
ISSN:1558-254X
DOI:10.1109/TMI.2012.2203142
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1109/TMI.2012.2203142
Verlag, Volltext: https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=6213119&tag=1
Volltext
Verfasserangaben:William J. Godinez* (student member, IEEE), Marko Lampe, Peter Koch, Roland Eils, Barbara Müller, and Karl Rohr, (member, IEEE)

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520 |a 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. 
650 4 |a Algorithms 
650 4 |a Approximation methods 
650 4 |a Bayes Theorem 
650 4 |a Behavior identification 
650 4 |a biomedical imaging 
650 4 |a biomedical optical imaging 
650 4 |a biomembranes 
650 4 |a Cell Fusion 
650 4 |a cell membrane 
650 4 |a Cell Tracking 
650 4 |a Cells (biology) 
650 4 |a cellular biophysics 
650 4 |a Computational modeling 
650 4 |a diseases 
650 4 |a fluorescence 
650 4 |a HeLa Cells 
650 4 |a hidden Markov models 
650 4 |a Hidden Markov models 
650 4 |a HIV-1 
650 4 |a Host-Pathogen Interactions 
650 4 |a Humans 
650 4 |a hybrid particle filter 
650 4 |a image denoising 
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650 4 |a image sequences 
650 4 |a infection 
650 4 |a layered probabilistic approach 
650 4 |a Markov Chains 
650 4 |a maxbelief strategy 
650 4 |a maximum likelihood estimation 
650 4 |a medical image processing 
650 4 |a microorganisms 
650 4 |a Microscopy 
650 4 |a microscopy images 
650 4 |a Microscopy, Fluorescence 
650 4 |a Models, Biological 
650 4 |a optical microscopy 
650 4 |a particle filtering (numerical methods) 
650 4 |a Predictive models 
650 4 |a probability 
650 4 |a pseudotyped HIV-1 particles 
650 4 |a stochastic hybrid systems 
650 4 |a Stochastic processes 
650 4 |a Stochastic Processes 
650 4 |a synthetic image sequences 
650 4 |a temporal intensity model 
650 4 |a time-lapse ίuorescence microscopy 
650 4 |a tracking 
650 4 |a tracking error function 
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