Publication:
Development of a method for concentrating and detecting rotavirus in oysters

dc.contributor.authorLeera Kittigulen_US
dc.contributor.authorKannika Pombubpaen_US
dc.contributor.authorTippawan Rattanathamen_US
dc.contributor.authorPornphan Diraphaten_US
dc.contributor.authorFuangfa Utrarachkijen_US
dc.contributor.authorSupornvit Pungchittonen_US
dc.contributor.authorPattara Khamrinen_US
dc.contributor.authorHiroshi Ushijimaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherInstitute of International Healthen_US
dc.date.accessioned2018-07-12T02:15:06Z
dc.date.available2018-07-12T02:15:06Z
dc.date.issued2008-02-29en_US
dc.description.abstractIdentification of enteric viruses in outbreak-implicated bivalve shellfish is difficult because of low levels of contamination and natural inhibitors present in shellfish tissue. In this study, the acid adsorption-alkaline elution method developed in our laboratory was proposed for the detection of rotavirus from oyster samples. The acid adsorption-alkaline elution process included the following steps: acid adsorption at pH 4.8, elution with 2.9% tryptose phosphate broth containing 6% glycine, pH 9.0, two polyethylene glycol precipitations, chloroform extraction and reconcentration using speedVac centrifugation. Oyster concentrates were extracted for RNA and examined for rotavirus using reverse transcription-nested polymerase chain reaction (RT-nested PCR). A comparison of SuperScript™ One-Step RT-PCR system and RT followed by PCR before the nested PCR reaction showed the former detecting four-fold lower concentration of rotavirus (78.12 plaque forming units [PFU]/ml or 0.26 PFU/assay) than the latter (3.12 × 102 PFU/ml or 1.04 PFU/assay). In the seeding experiment, the developed acid adsorption-alkaline elution gave high sensitivity of rotavirus detection (125 PFU/g of oyster). From August 2005 to February 2006, 120 oyster samples (Crassostrea belcheri) were collected from local markets and oyster farms, concentrated, and tested for naturally occurring rotaviruses. Four oyster samples were group A rotavirus-positive. Based on phylogenetic analysis of rotavirus DNA sequences in those positive samples, the oyster samples contained the sequences associated with human rotavirus G9 (two samples), G3 (one sample), and G1 (one sample). The present study demonstrates the successful application of developed virus concentration method and RT-nested PCR for the detection of rotaviruses in naturally contaminated oyster samples. The method might be used as a tool for evaluating the presence of enteric viruses in shellfish for monitoring and control of public health. © 2007 Elsevier B.V. All rights reserved.en_US
dc.identifier.citationInternational Journal of Food Microbiology. Vol.122, No.1-2 (2008), 204-210en_US
dc.identifier.doi10.1016/j.ijfoodmicro.2007.11.071en_US
dc.identifier.issn01681605en_US
dc.identifier.other2-s2.0-39149128266en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/18756
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=39149128266&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectEngineeringen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleDevelopment of a method for concentrating and detecting rotavirus in oystersen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=39149128266&origin=inwarden_US

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