A biomechanical model of virus-to-cell and cell-to-cell fusion is presented. Virus and the cells are modelled as initially spherical membranes of nonlinear elastic material that undergo large deformations. The membranes are connected by a cytoplasmic bridge which expands, resulting in the formation of a larger single sphere. In virus-to-cell fusion, a smaller spherical membrane is connected to a much larger one. Fusion is completed when the smaller membrane is completely incorporated into the larger one. The numerical results predict the existence of a ring force in the so-called furrow plane. It is possible that the microfilaments of the cortical layer form the furrow band which may provide this ring force.

Download full-text PDF

Source
http://dx.doi.org/10.1016/0141-5425(84)90071-2DOI Listing

Publication Analysis

Top Keywords

virus-to-cell cell-to-cell
8
cell-to-cell fusion
8
ring force
8
biomechanics virus-to-cell
4
fusion
4
fusion biomechanical
4
biomechanical model
4
model virus-to-cell
4
fusion presented
4
presented virus
4

Similar Publications

Human immunodeficiency virus (HIV) can persist in infected individuals despite prolonged antiretroviral therapy and it may spread through two modes: virus-to-cell and cell-to-cell transmissions. Understanding viral infection dynamics is pivotal for elucidating HIV pathogenesis. In this study, we incorporate the loss term of virions, and both virus-to-cell and cell-to-cell infection modes into a within-host HIV model, which also takes into consideration the proliferation of healthy target cells stimulated by free viruses.

View Article and Find Full Text PDF
Article Synopsis
  • * A study using human bronchial epithelium cells (BEAS-2B) compared the cell entry and fusion capabilities of various Omicron subvariants (BA.1, BA.5, etc.) using specialized assays.
  • * Findings revealed that while Omicron variants entered BEAS-2B cells more effectively than older strains like D614G, they did not show significant advantages over the Delta variant, indicating that immune evasion, rather than improved entry or fusion, is the
View Article and Find Full Text PDF

In this article, a cytokine-enhanced viral infection model with cytotoxic T lymphocytes (CTLs) immune response and antibody immune response is proposed and analyzed. The model contains six compartments: uninfected CD4T cells, infected CD4T cells, inflammatory cytokines, viruses, CTLs and antibodies. Different from the previous works, this model not only considers virus-to-cell transmission and cell-to-cell transmission, but also includes a new infection mode, namely cytokine-enhanced viral infection.

View Article and Find Full Text PDF

Local and global stability of an HCV viral dynamics model with two routes of infection and adaptive immunity.

Comput Methods Biomech Biomed Engin

August 2024

Laboratory of Mathematics, Computer Science and Applications, Faculty of Sciences and Technologies, University Hassan II of Casablanca, PO Box 146, Mohammedia, Morocco.

The aim of this article is to formulate and study a mathematical model describing hepatitis C virus (HCV) infection dynamics. The model includes two essential modes of infection transmission, namely, virus-to-cell and cell-to-cell. The effect of therapy and adaptive immunity are incorporated in the suggested model.

View Article and Find Full Text PDF

In this work, we analyse the dynamics of a five-dimensional hepatitis C virus infection mathematical model including the spatial mobility of hepatitis C virus particles, the transmission of hepatitis C virus infection by mitosis process of infected hepatocytes with logistic growth, time delays, antibody response and cytotoxic T lymphocyte (CTL) immune response with general incidence functions for both modes of infection transmission, namely virus-to-cell as well as cell-to-cell. Firstly, we prove rigorously the existence, the uniqueness, the positivity and the boundedness of the solution of the initial value and boundary problem associated with the new constructed model. Secondly, we found that the basic reproductive number is the sum of the basic reproduction number determined by cell-free virus infection, determined by cell-to-cell infection and determined by proliferation of infected cells.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!