Publication:
Colorimetric detection of scale drop disease virus in Asian sea bass using loop-mediated isothermal amplification with xylenol orange

dc.contributor.authorSirintip Dangtipen_US
dc.contributor.authorJantana Kampeeraen_US
dc.contributor.authorRapheephat Suvannakaden_US
dc.contributor.authorPakapreud Khumwanen_US
dc.contributor.authorWansadaj Jaroenramen_US
dc.contributor.authorMolruedee Sonthien_US
dc.contributor.authorSaengchan Senapinen_US
dc.contributor.authorWansika Kiatpathomchaien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherBurapha Universityen_US
dc.date.accessioned2020-01-27T07:22:32Z
dc.date.available2020-01-27T07:22:32Z
dc.date.issued2019-08-15en_US
dc.description.abstract© 2019 Elsevier B.V. Scale drop disease virus (SDDV) is an emerging pathogen that causes multiple outbreaks in farmed Asian sea bass across many regions in Southeast Asia and results in severe economic losses to the exports of fish. With no current standard vaccination protocol against this virus, routine testing that probes for SDDV in Asian sea bass culture can help farmers prevent a large-scale epidemic from occurring. Fish samples can be sent to accredited laboratories for SDDV test that is performed via polymerase chain reaction (PCR) and related methods, such as qPCR. Albeit its high sensitivity, PCR requires skilled labors and equipment only available in centralized laboratory settings, and therefore, not appropriate for the timely determination of SDDV. Herein, we report the development of a colorimetric assay based on loop-mediated isothermal amplification (LAMP) with a pH-sensitive xylenol orange (XO) reporter. With a rapid total DNA extraction method developed in this research, we were able to demonstrate that the sensitivity of the naked-eye detection was 100 picograms of total DNA extracted from the SDDV-infected Asian sea bass samples. In addition to its affordability, our LAMP-XO circumvents the technical challenges faced by PCR and allows the SDDV detection to be conveniently performed and analyzed at the potential site of an outbreak.en_US
dc.identifier.citationAquaculture. Vol.510, (2019), 386-391en_US
dc.identifier.doi10.1016/j.aquaculture.2019.05.071en_US
dc.identifier.issn00448486en_US
dc.identifier.other2-s2.0-85067244588en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/49742
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067244588&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleColorimetric detection of scale drop disease virus in Asian sea bass using loop-mediated isothermal amplification with xylenol orangeen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067244588&origin=inwarden_US

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