Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15236
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dc.contributor.authorChansiri K.
dc.contributor.authorKhuchareontaworn S.
dc.contributor.authorNopporn S.
dc.date.accessioned2021-04-05T04:33:08Z-
dc.date.available2021-04-05T04:33:08Z-
dc.date.issued2002
dc.identifier.issn8908508
dc.identifier.other2-s2.0-0036599194
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15236-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0036599194&doi=10.1006%2fmcpr.2002.0412&partnerID=40&md5=16244021d9b25f79a513e1a66c9c4cb0
dc.description.abstractA highly sensitive and specific polymerase chain reaction (PCR) based assay for the detection of Trypanosoma evansi present in the blood of different animals and vector was developed. A simple lysis method was used to remove of the red blood cells to facilitate direct input of samples into the PCR reactions. The primer set was designed and synthesized to amplify a single band of 257 bp PCR product that was subsequently examined by enzyme-linked immunosorbent assay (ELISA). The sensitivity limit of PCR-ELISA was 0.01 pg that was corresponded to 1 parasite/ml of blood. No cross-reactivity of the assay was observed against Babesia boris, B. bigemina, Anaplasma marginale, Theileria sp. and host DNA. The PCR-ELISA was shown to detect 33 samples of T. evansi infected blood of animals and 10 mosquitoes from different geographical area in Thailand. The results were corresponded to those of the PCR and mouse inoculation. This implies that the technique of PCR-ELISA is not only beneficial for diagnosis of the parasite but also useful for epidemiological study and designing rational trypanosomiasis control program. © 2002 Elsevier Science Ltd. All rights reserved.
dc.subjectDNA
dc.subjectprotozoal DNA
dc.subjectanalytic method
dc.subjectAnaplasma
dc.subjectAnaplasma marginale
dc.subjectarticle
dc.subjectBabesia
dc.subjectBabesia bigemina
dc.subjectBabesia bovis
dc.subjectbuffalo
dc.subjectcattle
dc.subjectcontrolled study
dc.subjectcross reaction
dc.subjectdeer
dc.subjectdiagnostic accuracy
dc.subjectdiagnostic value
dc.subjectenzyme linked immunosorbent assay
dc.subjectmosquito
dc.subjectmouse
dc.subjectnonhuman
dc.subjectpolymerase chain reaction
dc.subjectpriority journal
dc.subjectsensitivity and specificity
dc.subjectswine
dc.subjectThailand
dc.subjectTheileria
dc.subjectTrypanosoma evansi
dc.subjectanimal
dc.subjectanimal disease
dc.subjectcomparative study
dc.subjectdisease carrier
dc.subjectenzyme linked immunosorbent assay
dc.subjectevaluation
dc.subjectgenetics
dc.subjectmethodology
dc.subjectparasitology
dc.subjectpolymerase chain reaction
dc.subjectstandard
dc.subjectTrypanosoma
dc.subjecttrypanosomiasis
dc.subjectAnaplasma
dc.subjectAnaplasma marginale
dc.subjectAnimalia
dc.subjectBabesia
dc.subjectTheileria
dc.subjectTheileria sp.
dc.subjectTrypanosoma
dc.subjectTrypanosoma evansi
dc.subjectAnimals
dc.subjectBuffaloes
dc.subjectCattle
dc.subjectCross Reactions
dc.subjectCulicidae
dc.subjectDeer
dc.subjectDNA, Protozoan
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectInsect Vectors
dc.subjectMice
dc.subjectPolymerase Chain Reaction
dc.subjectSensitivity and Specificity
dc.subjectTrypanosoma
dc.subjectTrypanosomiasis
dc.titlePCR-ELISA for diagnosis of Trypanosoma evansi in animals and vector
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationMolecular and Cellular Probes. Vol 16, No.3 (2002), p.173-177
dc.identifier.doi10.1006/mcpr.2002.0412
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