APOBEC3-mediated restriction of RNA virus replication

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作者
Aleksandra Milewska
Eveline Kindler
Philip Vkovski
Slawomir Zeglen
Marek Ochman
Volker Thiel
Zenon Rajfur
Krzysztof Pyrc
机构
[1] Jagiellonian University,Microbiology Department, Faculty of Biochemistry, Biophysics and Biotechnology
[2] Gronostajowa 7,Virogenetics Laboratory of Virology, Malopolska Centre of Biotechnology
[3] Jagiellonian University,Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty
[4] Gronostajowa 7a,Graduate School for Cellular and Biomedical Sciences
[5] Institute for Virology and Immunology,Department of Cardiac Surgery and Transplantology
[6] Bern and Mittelhäusern,Head of Histology Department
[7] University of Bern,Department of Pharmacology, School of Medicine with the Division of Dentistry in Zabrze
[8] Länggassstrasse 122,Institute of Physics, Faculty of Physics, Astronomy and Applied Computer Sciences
[9] University of Bern,undefined
[10] Silesian Center for Heart Diseases,undefined
[11] Marii Curie-Skłodowskiej 9,undefined
[12] Medical Department,undefined
[13] University of Opole,undefined
[14] Medical University of Silesia in Katowice,undefined
[15] Jagiellonian University,undefined
[16] Lojasiewicza 11,undefined
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摘要
APOBEC3 family members are cytidine deaminases with roles in intrinsic responses to infection by retroviruses and retrotransposons, and in the control of other DNA viruses, such as herpesviruses, parvoviruses and hepatitis B virus. Although effects of APOBEC3 members on viral DNA have been demonstrated, it is not known whether they edit RNA genomes through cytidine deamination. Here, we investigated APOBEC3-mediated restriction of Coronaviridae. In experiments in vitro, three human APOBEC3 proteins (A3C, A3F and A3H) inhibited HCoV-NL63 infection and limited production of progeny virus, but did not cause hypermutation of the coronaviral genome. APOBEC3-mediated restriction was partially dependent on enzyme activity, and was reduced by the use of enzymatically inactive APOBEC3. Moreover, APOBEC3 proteins bound to the coronaviral nucleoprotein, and this interaction also affected viral replication. Although the precise molecular mechanism of deaminase-dependent inhibition of coronavirus replication remains elusive, our results further our understanding of APOBEC-mediated restriction of RNA virus infections.
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