Identification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs

African swine fever virus (ASFV) has become widespread in Europe, Asia and elsewhere, thereby causing extensive economic losses. The viral genome includes nearly 200 genes, but their expression within infected pigs has not been well characterized previously. In this study, four pigs were infected wi...

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Autores principales: Ann Sofie Olesen, Miyako Kodama, Louise Lohse, Francesc Accensi, Thomas Bruun Rasmussen, Christina M. Lazov, Morten T. Limborg, M. Thomas P. Gilbert, Anette Bøtner, Graham J. Belsham
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/764a825623974a19a4c325897d4448f0
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spelling oai:doaj.org-article:764a825623974a19a4c325897d4448f02021-11-25T19:14:40ZIdentification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs10.3390/v131123331999-4915https://doaj.org/article/764a825623974a19a4c325897d4448f02021-11-01T00:00:00Zhttps://www.mdpi.com/1999-4915/13/11/2333https://doaj.org/toc/1999-4915African swine fever virus (ASFV) has become widespread in Europe, Asia and elsewhere, thereby causing extensive economic losses. The viral genome includes nearly 200 genes, but their expression within infected pigs has not been well characterized previously. In this study, four pigs were infected with a genotype II strain (ASFV POL/2015/Podlaskie); blood samples were collected before inoculation and at both 3 and 6 days later. During this period, a range of clinical signs of infection became apparent in the pigs. From the blood, peripheral blood mononuclear cells (PBMCs) were isolated. The transcription of the ASFV genes was determined using RNAseq on poly(A)+ mRNAs isolated from these cells. Only very low levels of virus transcription were detected in the PBMCs at 3 days post-inoculation (dpi) but, at 6 dpi, extensive transcription was apparent. This was co-incident with a large increase in the level of ASFV DNA within these cells. The pattern of the virus gene expression was very reproducible between the individual pigs. Many highly expressed genes have undefined roles. Surprisingly, some genes with key roles in virus replication were expressed at only low levels. As the functions of individual genes are identified, information about their expression becomes important for understanding their contribution to virus biology.Ann Sofie OlesenMiyako KodamaLouise LohseFrancesc AccensiThomas Bruun RasmussenChristina M. LazovMorten T. LimborgM. Thomas P. GilbertAnette BøtnerGraham J. BelshamMDPI AGarticleAfrican swine fever virustranscriptomicsgene expressionPBMCsRNAseqMicrobiologyQR1-502ENViruses, Vol 13, Iss 2333, p 2333 (2021)
institution DOAJ
collection DOAJ
language EN
topic African swine fever virus
transcriptomics
gene expression
PBMCs
RNAseq
Microbiology
QR1-502
spellingShingle African swine fever virus
transcriptomics
gene expression
PBMCs
RNAseq
Microbiology
QR1-502
Ann Sofie Olesen
Miyako Kodama
Louise Lohse
Francesc Accensi
Thomas Bruun Rasmussen
Christina M. Lazov
Morten T. Limborg
M. Thomas P. Gilbert
Anette Bøtner
Graham J. Belsham
Identification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs
description African swine fever virus (ASFV) has become widespread in Europe, Asia and elsewhere, thereby causing extensive economic losses. The viral genome includes nearly 200 genes, but their expression within infected pigs has not been well characterized previously. In this study, four pigs were infected with a genotype II strain (ASFV POL/2015/Podlaskie); blood samples were collected before inoculation and at both 3 and 6 days later. During this period, a range of clinical signs of infection became apparent in the pigs. From the blood, peripheral blood mononuclear cells (PBMCs) were isolated. The transcription of the ASFV genes was determined using RNAseq on poly(A)+ mRNAs isolated from these cells. Only very low levels of virus transcription were detected in the PBMCs at 3 days post-inoculation (dpi) but, at 6 dpi, extensive transcription was apparent. This was co-incident with a large increase in the level of ASFV DNA within these cells. The pattern of the virus gene expression was very reproducible between the individual pigs. Many highly expressed genes have undefined roles. Surprisingly, some genes with key roles in virus replication were expressed at only low levels. As the functions of individual genes are identified, information about their expression becomes important for understanding their contribution to virus biology.
format article
author Ann Sofie Olesen
Miyako Kodama
Louise Lohse
Francesc Accensi
Thomas Bruun Rasmussen
Christina M. Lazov
Morten T. Limborg
M. Thomas P. Gilbert
Anette Bøtner
Graham J. Belsham
author_facet Ann Sofie Olesen
Miyako Kodama
Louise Lohse
Francesc Accensi
Thomas Bruun Rasmussen
Christina M. Lazov
Morten T. Limborg
M. Thomas P. Gilbert
Anette Bøtner
Graham J. Belsham
author_sort Ann Sofie Olesen
title Identification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs
title_short Identification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs
title_full Identification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs
title_fullStr Identification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs
title_full_unstemmed Identification of African Swine Fever Virus Transcription within Peripheral Blood Mononuclear Cells of Acutely Infected Pigs
title_sort identification of african swine fever virus transcription within peripheral blood mononuclear cells of acutely infected pigs
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/764a825623974a19a4c325897d4448f0
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