Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15450
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dc.contributor.authorAreekit S.
dc.contributor.authorKhuchareontaworn S.
dc.contributor.authorKanjanavas P.
dc.contributor.authorSriyapai T.
dc.contributor.authorPakpitchareon A.
dc.contributor.authorKhawsak P.
dc.contributor.authorChansiri K.
dc.date.accessioned2021-04-05T04:34:13Z-
dc.date.available2021-04-05T04:34:13Z-
dc.date.issued2009
dc.identifier.issn1251562
dc.identifier.other2-s2.0-59149096508
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15450-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-59149096508&partnerID=40&md5=24252070eec891fb81e050971c319f5f
dc.description.abstractThis study described the diagnosis of a mixed infection of Brugia malayi and Brugia pahangi in a single domestic cat using the internal transcribed spacer 1 (ITS1) region. Following polymerase chain reaction amplification of the ITS1 region, the 580 bp amplicon was cloned, and 29 white colonies were randomly selected for DNA sequencing and phylogenetic tree construction. A DNA parsimony tree generated two groups of Brugia spp with one group containing 6 clones corresponding to B. pahangi and the other 23 clones corresponding to B. malayi. This indicated that mixed infection of the two Brugia spp, B. pahangi and B. malayi, had occurred in a single host.
dc.titleMolecular genetics analysis for Co-infection of Brugia Malayi and brugia pahangi in cat reservoirs based on internal transcribed spacer region 1
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationSoutheast Asian Journal of Tropical Medicine and Public Health. Vol 40, No.1 (2009), p.30-34
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