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Structural basis for hijacking of the host ACBD3 protein by bovine and porcine enteroviruses and kobuviruses
- Source :
- Archives of virology. 165(2)
- Publication Year :
- 2019
-
Abstract
- Picornaviruses infect a wide range of mammals including livestock such as cattle and swine. As with other picornavirus genera such as Aphthovirus, there is emerging evidence of a significant economic impact of livestock infections caused by members of the genera Enterovirus and Kobuvirus. While the human-infecting enteroviruses and kobuviruses have been intensively studied during the past decades in great detail, research on livestock-infecting viruses has been mostly limited to the genomic characterization of the viral strains identified worldwide. Here, we extend our previous studies of the structure and function of the complexes composed of the non-structural 3A proteins of human-infecting enteroviruses and kobuviruses and the host ACBD3 protein and present a structural and functional characterization of the complexes of the following livestock-infecting picornaviruses: bovine enteroviruses EV-E and EV-F, porcine enterovirus EV-G, and porcine kobuvirus AiV-C. We present a series of crystal structures of these complexes and demonstrate the role of these complexes in facilitation of viral replication.
- Subjects :
- Kobuvirus
Picornavirus
Viral protein
Swine
animal diseases
viruses
medicine.disease_cause
Virus Replication
Cell Line
03 medical and health sciences
Viral Proteins
Virology
medicine
Enterovirus Infections
Animals
Humans
Gene
030304 developmental biology
Adaptor Proteins, Signal Transducing
0303 health sciences
Aphthovirus
Picornaviridae Infections
biology
030306 microbiology
Host (biology)
virus diseases
Membrane Proteins
General Medicine
biology.organism_classification
HEK293 Cells
Viral replication
Enteroviruses, Porcine
Enterovirus
Cattle
Enterovirus, Bovine
Subjects
Details
- ISSN :
- 14328798
- Volume :
- 165
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Archives of virology
- Accession number :
- edsair.doi.dedup.....85d691d82bf01e0414e8f733686109ad