Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplification

<p>Abstract</p> <p>Background</p> <p>In this study we utilized padlock probes and rolling circle amplification as a mean to detect and study the replication of porcine circovirus type 2 (PCV2) in cultured cells and in infected tissue. Porcine circovirus type 2 is a sing...

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Main Authors: Berg Mikael, Fossum Caroline, Fuxler Lisbeth, Blomström Anne-Lie, Henriksson Sara, Nilsson Mats
Format: Article
Language:English
Published: BMC 2011-01-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/8/1/37
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spelling doaj-e68cbba076d448f7a3867476d66646302020-11-24T23:30:08ZengBMCVirology Journal1743-422X2011-01-01813710.1186/1743-422X-8-37Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplificationBerg MikaelFossum CarolineFuxler LisbethBlomström Anne-LieHenriksson SaraNilsson Mats<p>Abstract</p> <p>Background</p> <p>In this study we utilized padlock probes and rolling circle amplification as a mean to detect and study the replication of porcine circovirus type 2 (PCV2) in cultured cells and in infected tissue. Porcine circovirus type 2 is a single-stranded circular DNA virus associated with several severe diseases, porcine circovirus diseases (PCVD) in pigs, such as postweaning multisystemic wasting syndrome. The exact reason and mechanisms behind the trigger of PCV2 replication that is associated with these diseases is not well-known. The virus replicates with rolling circle replication and thus also exists as a double-stranded replicative form.</p> <p>Results</p> <p>By applying padlock probes and rolling circle amplification we could not only visualise the viral genome but also discriminate between the genomic and the replicative strand in situ. The genomic strand existed in higher numbers than the replicative strand. The virus accumulated in certain nuclei but also spread into the cytoplasm of cells in the surrounding tissue. In cultured cells the average number of signals increased with time after infection.</p> <p>Conclusions</p> <p>We have developed a method for detection of both strands of PCV2 in situ that can be useful for studies of replication and in situ detection of PCV2 as well as of DNA viruses in general.</p> http://www.virologyj.com/content/8/1/37
collection DOAJ
language English
format Article
sources DOAJ
author Berg Mikael
Fossum Caroline
Fuxler Lisbeth
Blomström Anne-Lie
Henriksson Sara
Nilsson Mats
spellingShingle Berg Mikael
Fossum Caroline
Fuxler Lisbeth
Blomström Anne-Lie
Henriksson Sara
Nilsson Mats
Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplification
Virology Journal
author_facet Berg Mikael
Fossum Caroline
Fuxler Lisbeth
Blomström Anne-Lie
Henriksson Sara
Nilsson Mats
author_sort Berg Mikael
title Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplification
title_short Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplification
title_full Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplification
title_fullStr Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplification
title_full_unstemmed Development of an in situ assay for simultaneous detection of the genomic and replicative form of PCV2 using padlock probes and rolling circle amplification
title_sort development of an in situ assay for simultaneous detection of the genomic and replicative form of pcv2 using padlock probes and rolling circle amplification
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2011-01-01
description <p>Abstract</p> <p>Background</p> <p>In this study we utilized padlock probes and rolling circle amplification as a mean to detect and study the replication of porcine circovirus type 2 (PCV2) in cultured cells and in infected tissue. Porcine circovirus type 2 is a single-stranded circular DNA virus associated with several severe diseases, porcine circovirus diseases (PCVD) in pigs, such as postweaning multisystemic wasting syndrome. The exact reason and mechanisms behind the trigger of PCV2 replication that is associated with these diseases is not well-known. The virus replicates with rolling circle replication and thus also exists as a double-stranded replicative form.</p> <p>Results</p> <p>By applying padlock probes and rolling circle amplification we could not only visualise the viral genome but also discriminate between the genomic and the replicative strand in situ. The genomic strand existed in higher numbers than the replicative strand. The virus accumulated in certain nuclei but also spread into the cytoplasm of cells in the surrounding tissue. In cultured cells the average number of signals increased with time after infection.</p> <p>Conclusions</p> <p>We have developed a method for detection of both strands of PCV2 in situ that can be useful for studies of replication and in situ detection of PCV2 as well as of DNA viruses in general.</p>
url http://www.virologyj.com/content/8/1/37
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