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Published on: March 1, 2019
Cell entry of the aphthovirus equine rhinitis A virus is dependent on endosome acidification
Elisabetta Groppelli1, Tobias J Tuthill, David J Rowlands
1Institute of Molecular and Cellular Biology and Astbury Centre for Structural Molecular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom.
Abstract:
Equine rhinitis A virus (ERAV) is genetically closely related to foot-and-mouth disease virus (FMDV), and both are now classified within the genus Aphthovirus of the family Picornaviridae. For disease security reasons, FMDV can be handled only in high-containment facilities, but these constraints do not apply to ERAV, making it an attractive alternative for the study of aphthovirus biology. Here, we show, using immunofluorescence, pharmacological agents, and dominant negative inhibitors, that ERAV entry occurs (as for FMDV) via clathrin-mediated endocytosis and acidification of early endosomes. This validates the use of ERAV as a model system to study the mechanism of cell entry by FMDV.
Insights
Equine rhinitis A virus (ERAV) offers a safer model for studying aphthovirus entry. ERAV utilizes clathrin-mediated endocytosis and early endosome acidification, similar to foot-and-mouth disease virus (FMDV).
Area of Science:
- Virology
- Cell Biology
- Molecular Biology
Background:
- Equine rhinitis A virus (ERAV) and foot-and-mouth disease virus (FMDV) are closely related aphthoviruses.
- FMDV research is restricted due to high-containment requirements, unlike ERAV.
Purpose of the Study:
- To investigate the cell entry mechanism of ERAV.
- To validate ERAV as a surrogate model for studying FMDV cell entry.
Main Methods:
- Immunofluorescence microscopy
- Pharmacological inhibitors
- Dominant-negative protein expression
Main Results:
- ERAV entry is dependent on clathrin-mediated endocytosis.
- Acidification of early endosomes is crucial for ERAV infection.
- ERAV employs a similar entry pathway to FMDV.
Conclusions:
- ERAV utilizes clathrin-mediated endocytosis and early endosome acidification for cell entry.
- ERAV serves as a suitable and safer model for studying aphthovirus cell entry mechanisms, including FMDV.
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