Multiplex real-time RT-PCR assay for bovine viral diarrhea virus type 1, type 2 and HoBi-like pestivirus
•A multiplex TaqMan assay for differentiation of bovine pestiviruses was developed.•The assay was proven to be specific allowing to discriminate among pestiviruses.•The emerging HoBi-like strains were correctly typed by the new assay. HoBi-like pestiviruses are emerging pestiviruses that infect catt...
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Veröffentlicht in: | Journal of virological methods 2016-03, Vol.229, p.1-7 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •A multiplex TaqMan assay for differentiation of bovine pestiviruses was developed.•The assay was proven to be specific allowing to discriminate among pestiviruses.•The emerging HoBi-like strains were correctly typed by the new assay.
HoBi-like pestiviruses are emerging pestiviruses that infect cattle causing clinical forms overlapping to those induced by bovine viral diarrhea virus (BVDV) 1 and 2. As a consequence of their widespread distribution reported in recent years, molecular tools for rapid discrimination among pestiviruses infecting cattle are needed. The aim of the present study was to develop a multiplex real-time RT-PCR assay, based on the TaqMan technology, for the rapid and unambiguous characterisation of all bovine pestiviruses, including the emerging HoBi-like strains. The assay was found to be sensitive, specific and repeatable, ensuring detection of as few as 100–101 viral RNA copies. No cross-reactions between different pestiviral species were observed even in samples artificially contaminated with more than one pestivirus. Analysis of field samples tested positive for BVDV-1, BVDV-2 or HoBi-like virus by a nested PCR protocol revealed that the developed TaqMan assay had equal or higher sensitivity and was able to discriminate correctly the viral species in all tested samples, whereas a real-time RT-PCR assay previously developed for HoBi-like pestivirus detection showed cross-reactivity with few high-titre BVDV-2 samples. |
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ISSN: | 0166-0934 1879-0984 |
DOI: | 10.1016/j.jviromet.2015.12.003 |