Establishment and characterization of transformed goat primary cells by expression of simian virus 40 large T antigen for orf virus propagations
Due to the limited host range of orf virus (ORFV), primary cells derived from its natural hosts, such as goats and sheep, are recommended for isolation and propagation of wild type ORFV. This situation limits the option for the study of virus-host interaction during ORFV infection since primary cell...
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Published in | PloS one Vol. 14; no. 12; p. e0226105 |
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Main Authors | , , , , |
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Language | English |
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05.12.2019
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Abstract | Due to the limited host range of orf virus (ORFV), primary cells derived from its natural hosts, such as goats and sheep, are recommended for isolation and propagation of wild type ORFV. This situation limits the option for the study of virus-host interaction during ORFV infection since primary cells only support a few numbers of passages. SV40 T antigen is a viral oncoprotein that can abrogate replicative senescence, leading to an extended life span of cells. In this study, the transformation of two goat primary cells, fibroblast (FB) and testis (GT) cells, were achieved by stably expressing SV40 T antigen using the lentiviral technique. The presence of the gene encoding SV40 T antigen was validated by polymerase chain reaction (PCR) and western blot analyses. As evidenced by immunofluorescent microscopy, the two types of cells expressing SV40 T antigen (namely, FBT and GTT) were purified to homogeneity. Moreover, faster growth kinetics and a lower serum dependency were noticed in FBT and GTT, as compared with their counterpart parental cells. FBT and GTT remain permissive and can form plaque of ORFV, despite with different profiles; generally speaking, with SV40 T expression, ORFV forms plaques with smaller size and distinct margin. Most importantly, the prolonged life span of goat FBT and GTT serves as an ideal cell culture resource for ORFV isolation from the field, studies of ORFV pathogenesis and efficient vaccine development. |
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AbstractList | Due to the limited host range of orf virus (ORFV), primary cells derived from its natural hosts, such as goats and sheep, are recommended for isolation and propagation of wild type ORFV. This situation limits the option for the study of virus-host interaction during ORFV infection since primary cells only support a few numbers of passages. SV40 T antigen is a viral oncoprotein that can abrogate replicative senescence, leading to an extended life span of cells. In this study, the transformation of two goat primary cells, fibroblast (FB) and testis (GT) cells, were achieved by stably expressing SV40 T antigen using the lentiviral technique. The presence of the gene encoding SV40 T antigen was validated by polymerase chain reaction (PCR) and western blot analyses. As evidenced by immunofluorescent microscopy, the two types of cells expressing SV40 T antigen (namely, FBT and GTT) were purified to homogeneity. Moreover, faster growth kinetics and a lower serum dependency were noticed in FBT and GTT, as compared with their counterpart parental cells. FBT and GTT remain permissive and can form plaque of ORFV, despite with different profiles; generally speaking, with SV40 T expression, ORFV forms plaques with smaller size and distinct margin. Most importantly, the prolonged life span of goat FBT and GTT serves as an ideal cell culture resource for ORFV isolation from the field, studies of ORFV pathogenesis and efficient vaccine development. Due to the limited host range of orf virus (ORFV), primary cells derived from its natural hosts, such as goats and sheep, are recommended for isolation and propagation of wild type ORFV. This situation limits the option for the study of virus-host interaction during ORFV infection since primary cells only support a few numbers of passages. SV40 T antigen is a viral oncoprotein that can abrogate replicative senescence, leading to an extended life span of cells. In this study, the transformation of two goat primary cells, fibroblast (FB) and testis (GT) cells, were achieved by stably expressing SV40 T antigen using the lentiviral technique. The presence of the gene encoding SV40 T antigen was validated by polymerase chain reaction (PCR) and western blot analyses. As evidenced by immunofluorescent microscopy, the two types of cells expressing SV40 T antigen (namely, FBT and GTT) were purified to homogeneity. Moreover, faster growth kinetics and a lower serum dependency were noticed in FBT and GTT, as compared with their counterpart parental cells. FBT and GTT remain permissive and can form plaque of ORFV, despite with different profiles; generally speaking, with SV40 T expression, ORFV forms plaques with smaller size and distinct margin. Most importantly, the prolonged life span of goat FBT and GTT serves as an ideal cell culture resource for ORFV isolation from the field, studies of ORFV pathogenesis and efficient vaccine development.Due to the limited host range of orf virus (ORFV), primary cells derived from its natural hosts, such as goats and sheep, are recommended for isolation and propagation of wild type ORFV. This situation limits the option for the study of virus-host interaction during ORFV infection since primary cells only support a few numbers of passages. SV40 T antigen is a viral oncoprotein that can abrogate replicative senescence, leading to an extended life span of cells. In this study, the transformation of two goat primary cells, fibroblast (FB) and testis (GT) cells, were achieved by stably expressing SV40 T antigen using the lentiviral technique. The presence of the gene encoding SV40 T antigen was validated by polymerase chain reaction (PCR) and western blot analyses. As evidenced by immunofluorescent microscopy, the two types of cells expressing SV40 T antigen (namely, FBT and GTT) were purified to homogeneity. Moreover, faster growth kinetics and a lower serum dependency were noticed in FBT and GTT, as compared with their counterpart parental cells. FBT and GTT remain permissive and can form plaque of ORFV, despite with different profiles; generally speaking, with SV40 T expression, ORFV forms plaques with smaller size and distinct margin. Most importantly, the prolonged life span of goat FBT and GTT serves as an ideal cell culture resource for ORFV isolation from the field, studies of ORFV pathogenesis and efficient vaccine development. |
Author | Liao, Guan-Ru Yamada, Yumiko Tseng, Yeu-Yang Hsu, Wei-Li Tseng, Ching-Yu |
AuthorAffiliation | 1 Graduate Institute of Microbiology and Public Health, National Chung Hsing University, Taichung, Taiwan 2 Department of Immunology and Infectious Diseases, John Curtin School of Medical Research, Australian National University, Canberra, Australia Kansas State University, UNITED STATES |
AuthorAffiliation_xml | – name: 2 Department of Immunology and Infectious Diseases, John Curtin School of Medical Research, Australian National University, Canberra, Australia – name: 1 Graduate Institute of Microbiology and Public Health, National Chung Hsing University, Taichung, Taiwan – name: Kansas State University, UNITED STATES |
Author_xml | – sequence: 1 givenname: Yumiko orcidid: 0000-0002-8527-2376 surname: Yamada fullname: Yamada, Yumiko – sequence: 2 givenname: Guan-Ru surname: Liao fullname: Liao, Guan-Ru – sequence: 3 givenname: Ching-Yu surname: Tseng fullname: Tseng, Ching-Yu – sequence: 4 givenname: Yeu-Yang surname: Tseng fullname: Tseng, Yeu-Yang – sequence: 5 givenname: Wei-Li orcidid: 0000-0002-1392-163X surname: Hsu fullname: Hsu, Wei-Li |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31805146$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1093_biolre_ioab231 crossref_primary_10_1186_s12985_025_02672_3 crossref_primary_10_3390_ijms222111660 crossref_primary_10_3389_frfst_2023_1126455 crossref_primary_10_1002_1873_3468_14099 crossref_primary_10_1002_1873_3468_14231 crossref_primary_10_1007_s00253_023_12412_8 |
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Copyright | 2019 Yamada et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2019 Yamada et al 2019 Yamada et al |
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J Vet Sci doi: 10.4142/jvs.2013.14.2.227 |
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Snippet | Due to the limited host range of orf virus (ORFV), primary cells derived from its natural hosts, such as goats and sheep, are recommended for isolation and... |
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SubjectTerms | Animals Antigen T (large) Antigens Antigens, Viral, Tumor - genetics Biology and life sciences Cell culture Cell Line Cell Transformation, Viral - genetics Dermatitis Fibroblasts Gene Expression Goats Growth kinetics Homogeneity Host range Humans Infections Life span Medicine and Health Sciences Mortality Orf Orf virus - physiology Pathogenesis Physical Sciences Plaques Polymerase chain reaction Propagation Public health Reaction kinetics Research and Analysis Methods Senescence Sheep Simian virus 40 - immunology Smallpox Telomerase Vaccine development Vaccines Virus Replication - genetics Viruses |
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Title | Establishment and characterization of transformed goat primary cells by expression of simian virus 40 large T antigen for orf virus propagations |
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