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How rotavirus infection accelerates autoimmune diabetes in a mouse model

Date:
March 27, 2014
Source:
PLOS
Summary:
A combination of genetic predisposition and environmental factors is believed to cause autoimmune (type 1) diabetes. A new study gets at the mechanisms by which rotavirus infection contributes to autoimmune diabetes in a mouse model of the disease.

This is a cartoon of rotavirus particles (gray) containing their genome (red) on a background of real rotavirus particles imaged by electron microscopy (green). The rotavirus genome is detected by the immune response. This leads to increased activity of immune cells that possess the potential to destroy pancreatic islets.
Credit: Barbara Coulson, et al., CC-BY Creative Commons Attribution license

A combination of genetic predisposition and environmental factors is believed to cause autoimmune (type 1) diabetes. A study published on March 27th in PLOS Pathogens gets at the mechanisms by which rotavirus infection contributes to autoimmune diabetes in a mouse model of the disease.

NOD (for non-obese diabetic) mice are prone to develop diabetes, and infection with rotavirus accelerates onset of the disease. Barbara Coulson and colleagues, from The University of Melbourne, Australia, tested the hypothesis that the virus does this by inducing "bystander activation."

Bystander activation assumes that a foreign intruder (in this case rotavirus) provokes a strong but non-specific activation of the immune system, and that this heightened state of activation "spills over" to a subset of specific immune cells that can recognize and attack not the viral intruder but some of the body's own cells, in this case the insulin-producing islet cells in the pancreas.

Indeed, the researchers found that when spleen cells from NOD mice encounter rotavirus, they activate two types of immune cells: antibody-producing B cells and so-called dendritic cells that are a key part of a coordinated immune response. They could show that this activation involves "unpacking" of the virus (thereby exposing its viral immune activators), as well as specific immune mediators of the host, including one called TLR7 and type 1 interferons.

Rotavirus activation of a specific dendritic cell type called plasmacytoid dendritic cells was necessary for activation of another type of immune cells called T cells. These T cells can recognize and destroy islet cells and are ultimately responsible for type 1 diabetes. When activated, plasmacytoid dendritic cells produce very high levels of type 1 interferons, suggesting it has a specific role in mediating the bystander effect that connects rotavirus infection to accelerated diabetes.

Taken together, the results suggest that viral infection is capable of accelerating type 1 diabetes through an immune bystander effect and points to a number of key players--immune cells and immune modulators like interferon--that are linked to disease acceleration in the mouse model and worth investigating in humans. The authors conclude that, in particular, "the role of type 1 interferon signaling in diabetes acceleration following rotavirus infection deserves further analysis."


Story Source:

The above story is based on materials provided by PLOS. Note: Materials may be edited for content and length.


Journal Reference:

  1. Jessica A. Pane, Nicole L. Webster, Barbara S. Coulson. Rotavirus Activates Lymphocytes from Non-Obese Diabetic Mice by Triggering Toll-Like Receptor 7 Signaling and Interferon Production in Plasmacytoid Dendritic Cells. PLoS Pathogens, 2014; 10 (3): e1003998 DOI: 10.1371/journal.ppat.1003998

Cite This Page:

PLOS. "How rotavirus infection accelerates autoimmune diabetes in a mouse model." ScienceDaily. ScienceDaily, 27 March 2014. <www.sciencedaily.com/releases/2014/03/140327222342.htm>.
PLOS. (2014, March 27). How rotavirus infection accelerates autoimmune diabetes in a mouse model. ScienceDaily. Retrieved July 29, 2014 from www.sciencedaily.com/releases/2014/03/140327222342.htm
PLOS. "How rotavirus infection accelerates autoimmune diabetes in a mouse model." ScienceDaily. www.sciencedaily.com/releases/2014/03/140327222342.htm (accessed July 29, 2014).

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