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dc.contributor.authorChutatip Siripanthen_US
dc.contributor.authorจุฑาทิพ ศิริพันธุ์en_US
dc.contributor.authorBenjanee Punpoowongen_US
dc.contributor.authorเบญจนี พันธ์ภูวงศ์en_US
dc.contributor.authorPornsawan Ammarapalen_US
dc.contributor.authorพรสวรรค์ อัมระปาลen_US
dc.contributor.authorNiramol Thimaen_US
dc.contributor.otherMahidol University. Faculty of Tropical Medicine. Department of Protozoologyen_US
dc.contributor.otherMahidol University. Faculty of Tropical Medicine. Department of Tropical Pathologyen_US
dc.contributor.otherMahidol University. Faculty of Tropical Medicine. Department of Microbiology and Immunologyen_US
dc.date.accessioned2016-04-04T07:44:52Z
dc.date.accessioned2021-09-02T05:58:25Z-
dc.date.available2016-04-04T07:44:52Z
dc.date.available2021-09-02T05:58:25Z-
dc.date.created2016-04-04
dc.date.issued2004
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/63429-
dc.descriptionJoint International Tropical Medicine Meeting 2004: Ambassador Hotel, Thailand 29 November-1 December 2004: abstract. Bangkok: Faculty of Tropical Medicine, Mahidol University; 2004. p.224.en
dc.description.abstractIsospora belli, Cryptosporidium parvum sporozoites and Microsporidial spores were infected into culture cells. The developmental stages of these intracellular protozoa were described after the fresh observation and staining of infected cells on cover glasses. Paraffin tissue section was performed and compared to cover glass staining. Fresh observation was more advantages for the observation of the movement of I. belli merozoites but the development of merogony of Cryptosporidium could not be notified by fresh observation. The merogony stages of I. belli from paraffin tissue sections were not clear, compared to cover glass staining but the trophozoites of Cryptosporidium were clearly demonstrated by paraffin tissue sections. The typical characters of belt-like stripes of Microsporidial spores from culture were clearly observed from cover glass staining. In conclusion, cover glass staining could be used for an alternative method for the detection of intracellular protozoa from cultures. However, the properstaining methodsshould be selected for each protozoan parasite.en_US
dc.language.isoenen_US
dc.rightsMahidol Universityen_US
dc.subjectParasiteen_US
dc.titleObservation of intracellular protozoan development by tissue culture on cover glasses and detection by fresh observation and staining methodsen_US
dc.typeProceeding Posteren_US
Appears in Collections:TM-Proceeding Document

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