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dc.contributor.authorThunyamas Guntawangen_US
dc.contributor.authorTidaratt Sittisaken_US
dc.contributor.authorPallop Tankaewen_US
dc.contributor.authorChatchote Thitaramen_US
dc.contributor.authorVarangkana Langkapinen_US
dc.contributor.authorTaweepoke Angkawanishen_US
dc.contributor.authorTawatchai Singhlaen_US
dc.contributor.authorNattawooti Sthitmateeen_US
dc.contributor.authorWei Li Hsuen_US
dc.contributor.authorRoongroje Thanawongnuwechen_US
dc.contributor.authorKidsadagon Pringproaen_US
dc.date.accessioned2022-10-16T06:40:07Z-
dc.date.available2022-10-16T06:40:07Z-
dc.date.issued2022-07-01en_US
dc.identifier.issn20762615en_US
dc.identifier.other2-s2.0-85134704691en_US
dc.identifier.other10.3390/ani12141747en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85134704691&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/74333-
dc.description.abstractDisease caused by elephant endotheliotropic herpesvirus (EEHV) infection is the most highly fatal hemorrhagic disease in Asian elephant calves worldwide. To date, adult elephants that have been infected with EEHV have predominantly displayed mild clinical signs, while they are believed to serve as EEHV shedders to other elephants. Hence, the diagnostic tools employed for monitoring EEHV-active infection are considered vitally important. In this study, partial EEHV-DNA polymerase (DNApol) nonstructural proteins (NSPs) were used to detect anti-EEHV antibodies through the use of an inhouse indirect enzyme-linked immunosorbent assay (ELISA). The results were then compared to those obtained from a PCR test. In this study, a total of 175 serum samples were collected from Asian elephants living in elephant camps located in Chiang Mai and Lampang Provinces, Thailand. The elephants were aged between 2 and 80 years old. The overall percentages of positive samples by the PCR and EEHV-DNApol ELISA tests were 4% (21/175) and 12% (21/175), respectively. The ELISAs demonstrated values of 77.9% (95% posterior probability interval (PPI) = 52.5– 95%) sensitivity and 87.7% (PPI = 82.5–91.9%) specificity, respectively. Accordingly, the sera obtained from the elephants exhibiting no clinical signs of EEHV infection, and those who were negative according to PCR tests, revealed a value of 14% seropositivity for EEHV-DNApol. Our results indicate that these asymptomatic, active EEHV-infected elephants could likely serve as a source of EEHV shedding within elephant herds. Consequently, the developed EEHV-DNApol NSPs-based ELISA test employed in the present study may be of use for routine monitoring and identification of EEHV shedders in elephant herds, and could be an alternative diagnostic tool for EEHV detection in Asian elephants.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleDevelopment of Nonstructural Protein-Based Indirect ELISA to Identify Elephant Endotheliotropic Herpesvirus (EEHV) Infection in Asian Elephants (Elephas maximus)en_US
dc.typeJournalen_US
article.title.sourcetitleAnimalsen_US
article.volume12en_US
article.stream.affiliationsChulalongkorn Universityen_US
article.stream.affiliationsThailand Forest Industry Organizationen_US
article.stream.affiliationsNational Chung Hsing Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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