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dc.contributor.authorOzkan, S.,
dc.contributor.authorCoutts, Robert
dc.date.accessioned2018-07-04T16:13:47Z
dc.date.available2018-07-04T16:13:47Z
dc.date.issued2018-05-08
dc.identifier.citationOzkan , S & Coutts , R 2018 , ' Multiplex Detection of Aspergillus fumigatus Mycoviruses. ' , Viruses , vol. 10 , no. 5 , 247 . https://doi.org/10.3390/v10050247
dc.identifier.issn1999-4915
dc.identifier.urihttp://hdl.handle.net/2299/20265
dc.description© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
dc.description.abstractMycoviruses are viruses that naturally infect and replicate in fungi. They are widespread in all major fungal groups including plant and animal pathogenic fungi. Several dsRNA mycoviruses have been reported in Aspergillus fumigatus. Multiplex polymerase chain reaction (PCR) amplification is a version of PCR that enables amplification of different targets simultaneously. This technique has been widely used for detection and differentiation of viruses especially plant viruses such as those which infect tobacco, potato and garlic. For rapid detection, multiplex RT-PCR was developed to screen new isolates for the presence of A. fumigatus mycoviruses. Aspergillus fumigatus chrysovirus (AfuCV), Aspergillus fumigatus partitivirus (AfuPV-1), and Aspergillus fumigatus tetramycovirus-1 (AfuTmV-1) dsRNAs were amplified in separate reactions using a mixture of multiplex primer pairs. It was demonstrated that in the presence of a single infection, primer pair mixtures only amplify the corresponding single virus infection. Mixed infections using dual or triple combinations of dsRNA viruses were also amplified simultaneously using multiplex RT-PCR. Up until now, methods for the rapid detection of Aspergillus mycoviruses have been restricted to small scale dsRNA extraction approaches which are laborious and for large numbers of samples not as sensitive as RT-PCR. The multiplex RT-PCR assay developed here will be useful for studies on determining the incidence of A. fumigatus mycoviruses. This is the first report on multiplex detection of A. fumigatus mycovirusesen
dc.format.extent3370437
dc.language.isoeng
dc.relation.ispartofViruses
dc.subjectAspergillus fumigatus chrysovirus
dc.subjectAspergillus fumigatus partitivirus-1
dc.subjectAspergillus fumigatus tetramycovirus-1
dc.subjectDsRNA mycoviruses
dc.subjectMultiplex PCR
dc.subjectInfectious Diseases
dc.subjectVirology
dc.titleMultiplex Detection of Aspergillus fumigatus Mycoviruses.en
dc.contributor.institutionDepartment of Biological and Environmental Sciences
dc.contributor.institutionGeography, Environment and Agriculture
dc.contributor.institutionAgriculture, Food and Veterinary Sciences
dc.contributor.institutionCrop Protection and Climate Change
dc.contributor.institutionSchool of Life and Medical Sciences
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85047111990&partnerID=8YFLogxK
rioxxterms.versionofrecord10.3390/v10050247
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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