Loop-mediated isothermal amplification for the detection of goose circovirus

<p>Abstract</p> <p>Background</p> <p>Goose circovirus (GCV) presents an immunosuppressive problem in production of geese. The infection’s clinical symptoms include growth retardation or feathering disorders but the infection process may remain non-symptomatic what makes...

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Main Authors: Woźniakowski Grzegorz, Kozdruń Wojciech, Samorek-Salamonowicz Elżbieta
Format: Article
Language:English
Published: BMC 2012-06-01
Series:Virology Journal
Subjects:
Online Access:http://www.virologyj.com/content/9/1/110
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spelling doaj-7f2964893ed94c7e8fee526b6e702aa32020-11-24T22:38:51ZengBMCVirology Journal1743-422X2012-06-019111010.1186/1743-422X-9-110Loop-mediated isothermal amplification for the detection of goose circovirusWoźniakowski GrzegorzKozdruń WojciechSamorek-Salamonowicz Elżbieta<p>Abstract</p> <p>Background</p> <p>Goose circovirus (GCV) presents an immunosuppressive problem in production of geese. The infection’s clinical symptoms include growth retardation or feathering disorders but the infection process may remain non-symptomatic what makes the infected birds more susceptible for secondary viral, bacterial and fungal infections. Diagnosis of GCV infection is made by histopathological examination, dot blot hybridization, polymerase chain reaction (PCR) and real-time PCR. However these techniques require application of thermocyclers and qualified staff which may be cost-consuming for some diagnostic units. The aim of this study was to develop loop-mediated isothermal amplification assay (LAMP) as a simple method of GCV detection.</p> <p>Results</p> <p>The presented study has shown LAMP as a rapid tool of detecting DNA of goose circovirus (GCV) as soon in 30 min time. The method used three sets of primers: two outer primers (F3 and B3), two inner primers (FIP and BIP) and two loop primers (FL and BL) to accelerate the reaction. The optimum reaction temperature and the time were 61°C for 30 min, respectively. The results were analysed using SYBR Green dye and GelRedTM solutions. Thirty-eight isolates of GCV collected from geese flocks in Poland were examined. For comparison, real-time polymerase chain reaction with F3 and B3 primers and SYBR Green dye was conducted. The obtained results have shown GCV-LAMP as a sensitive, rapid and specific assay and alternative for PCR-based methods.</p> <p>Conclusions</p> <p>The developed technique due to its simplicity may be applied by any veterinary laboratory or even mobile diagnostics units for the routine detection of GCV.</p> http://www.virologyj.com/content/9/1/110Goose circovirusLoop-mediated isothermal amplificationSYBR GreenGelRedTM stain solution
collection DOAJ
language English
format Article
sources DOAJ
author Woźniakowski Grzegorz
Kozdruń Wojciech
Samorek-Salamonowicz Elżbieta
spellingShingle Woźniakowski Grzegorz
Kozdruń Wojciech
Samorek-Salamonowicz Elżbieta
Loop-mediated isothermal amplification for the detection of goose circovirus
Virology Journal
Goose circovirus
Loop-mediated isothermal amplification
SYBR Green
GelRedTM stain solution
author_facet Woźniakowski Grzegorz
Kozdruń Wojciech
Samorek-Salamonowicz Elżbieta
author_sort Woźniakowski Grzegorz
title Loop-mediated isothermal amplification for the detection of goose circovirus
title_short Loop-mediated isothermal amplification for the detection of goose circovirus
title_full Loop-mediated isothermal amplification for the detection of goose circovirus
title_fullStr Loop-mediated isothermal amplification for the detection of goose circovirus
title_full_unstemmed Loop-mediated isothermal amplification for the detection of goose circovirus
title_sort loop-mediated isothermal amplification for the detection of goose circovirus
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2012-06-01
description <p>Abstract</p> <p>Background</p> <p>Goose circovirus (GCV) presents an immunosuppressive problem in production of geese. The infection’s clinical symptoms include growth retardation or feathering disorders but the infection process may remain non-symptomatic what makes the infected birds more susceptible for secondary viral, bacterial and fungal infections. Diagnosis of GCV infection is made by histopathological examination, dot blot hybridization, polymerase chain reaction (PCR) and real-time PCR. However these techniques require application of thermocyclers and qualified staff which may be cost-consuming for some diagnostic units. The aim of this study was to develop loop-mediated isothermal amplification assay (LAMP) as a simple method of GCV detection.</p> <p>Results</p> <p>The presented study has shown LAMP as a rapid tool of detecting DNA of goose circovirus (GCV) as soon in 30 min time. The method used three sets of primers: two outer primers (F3 and B3), two inner primers (FIP and BIP) and two loop primers (FL and BL) to accelerate the reaction. The optimum reaction temperature and the time were 61°C for 30 min, respectively. The results were analysed using SYBR Green dye and GelRedTM solutions. Thirty-eight isolates of GCV collected from geese flocks in Poland were examined. For comparison, real-time polymerase chain reaction with F3 and B3 primers and SYBR Green dye was conducted. The obtained results have shown GCV-LAMP as a sensitive, rapid and specific assay and alternative for PCR-based methods.</p> <p>Conclusions</p> <p>The developed technique due to its simplicity may be applied by any veterinary laboratory or even mobile diagnostics units for the routine detection of GCV.</p>
topic Goose circovirus
Loop-mediated isothermal amplification
SYBR Green
GelRedTM stain solution
url http://www.virologyj.com/content/9/1/110
work_keys_str_mv AT wozniakowskigrzegorz loopmediatedisothermalamplificationforthedetectionofgoosecircovirus
AT kozdrunwojciech loopmediatedisothermalamplificationforthedetectionofgoosecircovirus
AT samoreksalamonowiczelzbieta loopmediatedisothermalamplificationforthedetectionofgoosecircovirus
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