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CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans

Type 1 interferons (IFN) are critical for host control of HIV and simian immunodeficiency virus. However, it is unknown which of the hundreds of interferon-stimulated genes (ISGs) restrict HIV in vivo. We sequenced RNA from cells that support HIV replication (activated CD4(+) T cells) in 19 HIV-infe...

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Autores principales: El-Diwany, Ramy, Soliman, Mary, Sugawara, Sho, Breitwieser, Florian, Skaist, Alyza, Coggiano, Candelaria, Sangal, Neel, Chattergoon, Michael, Bailey, Justin R., Siliciano, Robert F., Blankson, Joel N., Ray, Stuart C., Wheelan, Sarah J., Thomas, David L., Balagopal, Ashwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070316/
https://www.ncbi.nlm.nih.gov/pubmed/30083606
http://dx.doi.org/10.1126/sciadv.aat0843
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author El-Diwany, Ramy
Soliman, Mary
Sugawara, Sho
Breitwieser, Florian
Skaist, Alyza
Coggiano, Candelaria
Sangal, Neel
Chattergoon, Michael
Bailey, Justin R.
Siliciano, Robert F.
Blankson, Joel N.
Ray, Stuart C.
Wheelan, Sarah J.
Thomas, David L.
Balagopal, Ashwin
author_facet El-Diwany, Ramy
Soliman, Mary
Sugawara, Sho
Breitwieser, Florian
Skaist, Alyza
Coggiano, Candelaria
Sangal, Neel
Chattergoon, Michael
Bailey, Justin R.
Siliciano, Robert F.
Blankson, Joel N.
Ray, Stuart C.
Wheelan, Sarah J.
Thomas, David L.
Balagopal, Ashwin
author_sort El-Diwany, Ramy
collection PubMed
description Type 1 interferons (IFN) are critical for host control of HIV and simian immunodeficiency virus. However, it is unknown which of the hundreds of interferon-stimulated genes (ISGs) restrict HIV in vivo. We sequenced RNA from cells that support HIV replication (activated CD4(+) T cells) in 19 HIV-infected people before and after interferon-α2b (IFN-α2b) injection. IFN-α2b administration reduced plasma HIV RNA and induced mRNA expression in activated CD4(+) T cells: The IFN-α2b–induced change of each mRNA was compared to the change in plasma HIV RNA. Of 99 ISGs, 13 were associated in magnitude with plasma HIV RNA decline. In addition to well-known restriction factors among the 13 ISGs, two novel genes, CMPK2 and BCL-G, were identified and confirmed for their ability to restrict HIV in vitro: The effect of IFN on HIV restriction in culture was attenuated with RNA interference to CMPK2, and overexpression of BCL-G diminished HIV replication. These studies reveal novel antiviral molecules that are linked with IFN-mediated restriction of HIV in humans.
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spelling pubmed-60703162018-08-06 CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans El-Diwany, Ramy Soliman, Mary Sugawara, Sho Breitwieser, Florian Skaist, Alyza Coggiano, Candelaria Sangal, Neel Chattergoon, Michael Bailey, Justin R. Siliciano, Robert F. Blankson, Joel N. Ray, Stuart C. Wheelan, Sarah J. Thomas, David L. Balagopal, Ashwin Sci Adv Research Articles Type 1 interferons (IFN) are critical for host control of HIV and simian immunodeficiency virus. However, it is unknown which of the hundreds of interferon-stimulated genes (ISGs) restrict HIV in vivo. We sequenced RNA from cells that support HIV replication (activated CD4(+) T cells) in 19 HIV-infected people before and after interferon-α2b (IFN-α2b) injection. IFN-α2b administration reduced plasma HIV RNA and induced mRNA expression in activated CD4(+) T cells: The IFN-α2b–induced change of each mRNA was compared to the change in plasma HIV RNA. Of 99 ISGs, 13 were associated in magnitude with plasma HIV RNA decline. In addition to well-known restriction factors among the 13 ISGs, two novel genes, CMPK2 and BCL-G, were identified and confirmed for their ability to restrict HIV in vitro: The effect of IFN on HIV restriction in culture was attenuated with RNA interference to CMPK2, and overexpression of BCL-G diminished HIV replication. These studies reveal novel antiviral molecules that are linked with IFN-mediated restriction of HIV in humans. American Association for the Advancement of Science 2018-08-01 /pmc/articles/PMC6070316/ /pubmed/30083606 http://dx.doi.org/10.1126/sciadv.aat0843 Text en Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
El-Diwany, Ramy
Soliman, Mary
Sugawara, Sho
Breitwieser, Florian
Skaist, Alyza
Coggiano, Candelaria
Sangal, Neel
Chattergoon, Michael
Bailey, Justin R.
Siliciano, Robert F.
Blankson, Joel N.
Ray, Stuart C.
Wheelan, Sarah J.
Thomas, David L.
Balagopal, Ashwin
CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans
title CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans
title_full CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans
title_fullStr CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans
title_full_unstemmed CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans
title_short CMPK2 and BCL-G are associated with type 1 interferon–induced HIV restriction in humans
title_sort cmpk2 and bcl-g are associated with type 1 interferon–induced hiv restriction in humans
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070316/
https://www.ncbi.nlm.nih.gov/pubmed/30083606
http://dx.doi.org/10.1126/sciadv.aat0843
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