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A novel combination of TaqMan RT-PCR and a suspension microarray assay for the detection and species identification of pestiviruses
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper, Klinisk virologi.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper, Klinisk virologi.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för medicinska vetenskaper, Klinisk virologi.
Vise andre og tillknytning
2010 (engelsk)Inngår i: Veterinary Microbiology, ISSN 0378-1135, E-ISSN 1873-2542, Vol. 142, nr 1-2, 81-86 s.Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The genus pestivirus contains four recognized species: classical swine fever virus, border disease virus, bovine viral diarrhoea virus types 1 and 2. All are economically important and globally distributed but classical swine fever is the most serious, concerning losses and control measures. It affects both domestic pigs and wild boars. Outbreaks of this disease in domestic pigs call for the most serious measures of disease control, including a stamping out policy in Europe. Since all the members of the pestivirus genus can infect swine, differential diagnosis using traditional methods poses some problems. Antibody tests may lack specificity due to cross-reactions, antigen capture ELISAs may have low sensitivity, and virus isolation may take several days or even longer time to complete. PCR-based tests overcome these problems for the most part, but in general lack the multiplexing capability to detect and differentiate all the pestiviruses simultaneously. The assay platform described here addresses all of these issues by combining the advantages of real-time PCR with the multiplexing capability of microarray technology. The platform includes a TaqMan real-time PCR designed for the universal detection of pestiviruses and a microarray assay that can use the amplicons produced in the real-time PCR to identify the specific pestivirus.

sted, utgiver, år, opplag, sider
2010. Vol. 142, nr 1-2, 81-86 s.
Emneord [en]
Pestivirus, CSFV, BDV, BVDV1, BVDV2, TaqMan real-time PCR, Suspension microarray
HSV kategori
Identifikatorer
URN: urn:nbn:se:uu:diva-147189DOI: 10.1016/j.vetmic.2009.09.046ISI: 000276800800012OAI: oai:DiVA.org:uu-147189DiVA: diva2:400058
Tilgjengelig fra: 2011-02-24 Laget: 2011-02-24 Sist oppdatert: 2018-01-12bibliografisk kontrollert

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