Structural basis for hijacking of the host ACBD3 protein by bovine and porcine enteroviruses and kobuviruses
Jazyk angličtina Země Rakousko Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
17-07058Y
Grantová Agentura České Republiky
RVO: 61388963
Akademie Věd České Republiky
CZ.02.1.01/0.0/0.0/16_019/0000729
European Regional Development Fund
PubMed
31845156
DOI
10.1007/s00705-019-04490-9
PII: 10.1007/s00705-019-04490-9
Knihovny.cz E-zdroje
- MeSH
- adaptorové proteiny signální transdukční metabolismus MeSH
- bovinní enterovirus patogenita MeSH
- buněčné linie MeSH
- enterovirové infekce metabolismus veterinární virologie MeSH
- enteroviry prasat genetika patogenita MeSH
- HEK293 buňky MeSH
- Kobuvirus genetika patogenita MeSH
- lidé MeSH
- membránové proteiny metabolismus MeSH
- pikornavirové infekce metabolismus veterinární virologie MeSH
- prasata MeSH
- replikace viru genetika MeSH
- skot MeSH
- virové proteiny genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- skot MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- ACBD3 protein, human MeSH Prohlížeč
- adaptorové proteiny signální transdukční MeSH
- membránové proteiny MeSH
- virové proteiny MeSH
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.
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