Cargando…

Defective interfering particles of mouse hepatitis virus

After six to eight serial undiluted passages of mouse hepatitis virus (JHM strain) in DBT cell culture, a decrease in the yield of infectious virus occurred, and with further passages fluctuating yields of infectious virus were observed. The serially passaged virus interfered with the multiplication...

Descripción completa

Detalles Bibliográficos
Autores principales: Makino, Shinji, Taguchi, Fumihiro, Fujiwara, Kosaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131828/
https://www.ncbi.nlm.nih.gov/pubmed/6322437
http://dx.doi.org/10.1016/0042-6822(84)90420-3
_version_ 1783517327941173248
author Makino, Shinji
Taguchi, Fumihiro
Fujiwara, Kosaku
author_facet Makino, Shinji
Taguchi, Fumihiro
Fujiwara, Kosaku
author_sort Makino, Shinji
collection PubMed
description After six to eight serial undiluted passages of mouse hepatitis virus (JHM strain) in DBT cell culture, a decrease in the yield of infectious virus occurred, and with further passages fluctuating yields of infectious virus were observed. The serially passaged virus interfered with the multiplication of the standard JHM virus, but not with vesicular stomatitis virus. After sucrose equilibrium centrifugation of high passage virus, a single peak contained both infectious virus and interfering activity. This virus population resembled the original JHM virus in its structural proteins, but it contained an increased proportion of a protein with a molecular weight of 65 × 10(3). Genomic RNA from standard JHM virus contained a single species of RNA with a molecular weight of 5.4 × 10(6). After five undiluted passages, however, the virion population contained two RNA species with molecular weights of 5.4 × 10(6) and 5.2 × 10(6). RNase T(1) resistant oligonucleotide finger-printing of these RNAs showed that the lower molecular weight RNA had lost several oligonucleotide spots that were present in the genomic RNA of the standard JHM virus. After several serial diluted passages of passage 10 virus, a single virus population was obtained which again had only standard virus RNA with a molecular weight of 5.4 × 10(6) and lacked interfering activity. These results indicated that defective interfering particles were generated by serial undiluted passages of JHM virus.
format Online
Article
Text
id pubmed-7131828
institution National Center for Biotechnology Information
language English
publishDate 1984
publisher Published by Elsevier Inc.
record_format MEDLINE/PubMed
spelling pubmed-71318282020-04-08 Defective interfering particles of mouse hepatitis virus Makino, Shinji Taguchi, Fumihiro Fujiwara, Kosaku Virology Article After six to eight serial undiluted passages of mouse hepatitis virus (JHM strain) in DBT cell culture, a decrease in the yield of infectious virus occurred, and with further passages fluctuating yields of infectious virus were observed. The serially passaged virus interfered with the multiplication of the standard JHM virus, but not with vesicular stomatitis virus. After sucrose equilibrium centrifugation of high passage virus, a single peak contained both infectious virus and interfering activity. This virus population resembled the original JHM virus in its structural proteins, but it contained an increased proportion of a protein with a molecular weight of 65 × 10(3). Genomic RNA from standard JHM virus contained a single species of RNA with a molecular weight of 5.4 × 10(6). After five undiluted passages, however, the virion population contained two RNA species with molecular weights of 5.4 × 10(6) and 5.2 × 10(6). RNase T(1) resistant oligonucleotide finger-printing of these RNAs showed that the lower molecular weight RNA had lost several oligonucleotide spots that were present in the genomic RNA of the standard JHM virus. After several serial diluted passages of passage 10 virus, a single virus population was obtained which again had only standard virus RNA with a molecular weight of 5.4 × 10(6) and lacked interfering activity. These results indicated that defective interfering particles were generated by serial undiluted passages of JHM virus. Published by Elsevier Inc. 1984-02 2004-06-09 /pmc/articles/PMC7131828/ /pubmed/6322437 http://dx.doi.org/10.1016/0042-6822(84)90420-3 Text en Copyright © 1984 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Makino, Shinji
Taguchi, Fumihiro
Fujiwara, Kosaku
Defective interfering particles of mouse hepatitis virus
title Defective interfering particles of mouse hepatitis virus
title_full Defective interfering particles of mouse hepatitis virus
title_fullStr Defective interfering particles of mouse hepatitis virus
title_full_unstemmed Defective interfering particles of mouse hepatitis virus
title_short Defective interfering particles of mouse hepatitis virus
title_sort defective interfering particles of mouse hepatitis virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131828/
https://www.ncbi.nlm.nih.gov/pubmed/6322437
http://dx.doi.org/10.1016/0042-6822(84)90420-3
work_keys_str_mv AT makinoshinji defectiveinterferingparticlesofmousehepatitisvirus
AT taguchifumihiro defectiveinterferingparticlesofmousehepatitisvirus
AT fujiwarakosaku defectiveinterferingparticlesofmousehepatitisvirus