Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus

Two Vero cell lines persistently infected with XJCl3 and Cl67 strains of Junin virus and named V3 and V7, respectively, have been characterized with respect to the presence and expression of the nucleoprotein (N) and the glycoprotein precursor (GPC) viral genes. After the acute phase of infection, w...

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Autores principales: Ellenberg, P., Edreira, M., Lozano, M., Scolaro, L.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03048608_v147_n8_p1543_Ellenberg
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spelling todo:paper_03048608_v147_n8_p1543_Ellenberg2023-10-03T15:20:58Z Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus Ellenberg, P. Edreira, M. Lozano, M. Scolaro, L. Animalia DNA viruses Junin virus nucleocapsid protein virus antigen virus envelope protein virus RNA animal article biosynthesis Cercopithecus genetics immunology Junin virus Vero cell Animals Antigens, Viral Cercopithecus aethiops Junin virus Nucleocapsid Proteins RNA, Viral Vero Cells Viral Envelope Proteins Two Vero cell lines persistently infected with XJCl3 and Cl67 strains of Junin virus and named V3 and V7, respectively, have been characterized with respect to the presence and expression of the nucleoprotein (N) and the glycoprotein precursor (GPC) viral genes. After the acute phase of infection, where a marked CPE and high titers of virus were obtained, JV persistently infected cells became morphologically undistinguishable from Vero cells and virus production dropped to undetectable levels. V3 and V7 were resistant to the superinfection with antigenically related viruses. This fact could not be attributed to the presence of defective interfering particles or non-infectious virus in the supernatant. Expression of N was consistently detected in both cultures and accumulation of two degradation products of N was evident during the late passages. Although no G1 (main surface glycoprotein) expression was observed, a marked fusogenic capacity was detected in both cultures indicating at least, the synthesis of a GPC derived fusogenic glycoprotein. Cell lysates from V3 and V7 subjected to RT-PCR, using specific primers for N gene, or to a nested RT-PCR using specific primers for GPC (G1 region) confirmed the presence of both viral genes. No viral DNA sequences could be detected in JV persistently infected cells. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03048608_v147_n8_p1543_Ellenberg
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Animalia
DNA viruses
Junin virus
nucleocapsid protein
virus antigen
virus envelope protein
virus RNA
animal
article
biosynthesis
Cercopithecus
genetics
immunology
Junin virus
Vero cell
Animals
Antigens, Viral
Cercopithecus aethiops
Junin virus
Nucleocapsid Proteins
RNA, Viral
Vero Cells
Viral Envelope Proteins
spellingShingle Animalia
DNA viruses
Junin virus
nucleocapsid protein
virus antigen
virus envelope protein
virus RNA
animal
article
biosynthesis
Cercopithecus
genetics
immunology
Junin virus
Vero cell
Animals
Antigens, Viral
Cercopithecus aethiops
Junin virus
Nucleocapsid Proteins
RNA, Viral
Vero Cells
Viral Envelope Proteins
Ellenberg, P.
Edreira, M.
Lozano, M.
Scolaro, L.
Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus
topic_facet Animalia
DNA viruses
Junin virus
nucleocapsid protein
virus antigen
virus envelope protein
virus RNA
animal
article
biosynthesis
Cercopithecus
genetics
immunology
Junin virus
Vero cell
Animals
Antigens, Viral
Cercopithecus aethiops
Junin virus
Nucleocapsid Proteins
RNA, Viral
Vero Cells
Viral Envelope Proteins
description Two Vero cell lines persistently infected with XJCl3 and Cl67 strains of Junin virus and named V3 and V7, respectively, have been characterized with respect to the presence and expression of the nucleoprotein (N) and the glycoprotein precursor (GPC) viral genes. After the acute phase of infection, where a marked CPE and high titers of virus were obtained, JV persistently infected cells became morphologically undistinguishable from Vero cells and virus production dropped to undetectable levels. V3 and V7 were resistant to the superinfection with antigenically related viruses. This fact could not be attributed to the presence of defective interfering particles or non-infectious virus in the supernatant. Expression of N was consistently detected in both cultures and accumulation of two degradation products of N was evident during the late passages. Although no G1 (main surface glycoprotein) expression was observed, a marked fusogenic capacity was detected in both cultures indicating at least, the synthesis of a GPC derived fusogenic glycoprotein. Cell lysates from V3 and V7 subjected to RT-PCR, using specific primers for N gene, or to a nested RT-PCR using specific primers for GPC (G1 region) confirmed the presence of both viral genes. No viral DNA sequences could be detected in JV persistently infected cells.
format JOUR
author Ellenberg, P.
Edreira, M.
Lozano, M.
Scolaro, L.
author_facet Ellenberg, P.
Edreira, M.
Lozano, M.
Scolaro, L.
author_sort Ellenberg, P.
title Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus
title_short Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus
title_full Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus
title_fullStr Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus
title_full_unstemmed Synthesis and expression of viral antigens in Vero cells persistently infected with Junin virus
title_sort synthesis and expression of viral antigens in vero cells persistently infected with junin virus
url http://hdl.handle.net/20.500.12110/paper_03048608_v147_n8_p1543_Ellenberg
work_keys_str_mv AT ellenbergp synthesisandexpressionofviralantigensinverocellspersistentlyinfectedwithjuninvirus
AT edreiram synthesisandexpressionofviralantigensinverocellspersistentlyinfectedwithjuninvirus
AT lozanom synthesisandexpressionofviralantigensinverocellspersistentlyinfectedwithjuninvirus
AT scolarol synthesisandexpressionofviralantigensinverocellspersistentlyinfectedwithjuninvirus
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