Latently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV

Kaposi’s sarcoma-associated herpesvirus (KSHV) is a cancer-related virus which engages in two forms of infection: latent and lytic. Latent infection allows the virus to establish long-term persistent infection, whereas the lytic cycle is needed for the maintenance of the viral reservoir and for viru...

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Autores principales: Chen Gam ze Letova, Inna Kalt, Meir Shamay, Ronit Sarid
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:8377516422ee408097867aef96eee8982021-11-11T17:24:35ZLatently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV10.3390/ijms2221119941422-00671661-6596https://doaj.org/article/8377516422ee408097867aef96eee8982021-11-01T00:00:00Zhttps://www.mdpi.com/1422-0067/22/21/11994https://doaj.org/toc/1661-6596https://doaj.org/toc/1422-0067Kaposi’s sarcoma-associated herpesvirus (KSHV) is a cancer-related virus which engages in two forms of infection: latent and lytic. Latent infection allows the virus to establish long-term persistent infection, whereas the lytic cycle is needed for the maintenance of the viral reservoir and for virus spread. By using recombinant KSHV viruses encoding mNeonGreen and mCherry fluorescent proteins, we show that various cell types that are latently-infected with KSHV can be superinfected, and that the new incoming viruses establish latent infection. Moreover, we show that latency establishment is enhanced in superinfected cells compared to primary infected ones. Further analysis revealed that cells that ectopically express the major latency protein of KSHV, LANA-1, prior to and during infection exhibit enhanced establishment of latency, but not cells expressing LANA-1 fragments. This observation supports the notion that the expression level of LANA-1 following infection determines the efficiency of latency establishment and avoids loss of viral genomes. These findings imply that a host can be infected with more than a single viral genome and that superinfection may support the maintenance of long-term latency.Chen Gam ze LetovaInna KaltMeir ShamayRonit SaridMDPI AGarticleKaposi’s sarcoma-associated herpesvirus (KSHV)superinfectionprimary infectionlatency-associated nuclear antigen 1 (LANA-1)latent infectionBiology (General)QH301-705.5ChemistryQD1-999ENInternational Journal of Molecular Sciences, Vol 22, Iss 11994, p 11994 (2021)
institution DOAJ
collection DOAJ
language EN
topic Kaposi’s sarcoma-associated herpesvirus (KSHV)
superinfection
primary infection
latency-associated nuclear antigen 1 (LANA-1)
latent infection
Biology (General)
QH301-705.5
Chemistry
QD1-999
spellingShingle Kaposi’s sarcoma-associated herpesvirus (KSHV)
superinfection
primary infection
latency-associated nuclear antigen 1 (LANA-1)
latent infection
Biology (General)
QH301-705.5
Chemistry
QD1-999
Chen Gam ze Letova
Inna Kalt
Meir Shamay
Ronit Sarid
Latently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV
description Kaposi’s sarcoma-associated herpesvirus (KSHV) is a cancer-related virus which engages in two forms of infection: latent and lytic. Latent infection allows the virus to establish long-term persistent infection, whereas the lytic cycle is needed for the maintenance of the viral reservoir and for virus spread. By using recombinant KSHV viruses encoding mNeonGreen and mCherry fluorescent proteins, we show that various cell types that are latently-infected with KSHV can be superinfected, and that the new incoming viruses establish latent infection. Moreover, we show that latency establishment is enhanced in superinfected cells compared to primary infected ones. Further analysis revealed that cells that ectopically express the major latency protein of KSHV, LANA-1, prior to and during infection exhibit enhanced establishment of latency, but not cells expressing LANA-1 fragments. This observation supports the notion that the expression level of LANA-1 following infection determines the efficiency of latency establishment and avoids loss of viral genomes. These findings imply that a host can be infected with more than a single viral genome and that superinfection may support the maintenance of long-term latency.
format article
author Chen Gam ze Letova
Inna Kalt
Meir Shamay
Ronit Sarid
author_facet Chen Gam ze Letova
Inna Kalt
Meir Shamay
Ronit Sarid
author_sort Chen Gam ze Letova
title Latently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV
title_short Latently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV
title_full Latently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV
title_fullStr Latently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV
title_full_unstemmed Latently KSHV-Infected Cells Promote Further Establishment of Latency upon Superinfection with KSHV
title_sort latently kshv-infected cells promote further establishment of latency upon superinfection with kshv
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/8377516422ee408097867aef96eee898
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AT meirshamay latentlykshvinfectedcellspromotefurtherestablishmentoflatencyuponsuperinfectionwithkshv
AT ronitsarid latentlykshvinfectedcellspromotefurtherestablishmentoflatencyuponsuperinfectionwithkshv
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