Immunomics analysis of excretory-secretory antigens from 3rd stage larva gnathostoma spinigerum for development of immunodiagnosis

dc.contributor.authorSupaporn Nuamtanongen_US
dc.contributor.authorสุภาพร น่วมทะนงen_US
dc.contributor.authorParon Dekumyoyen_US
dc.contributor.authorพารณ ดีคำย้อยen_US
dc.contributor.authorOnrapak Reamtongen_US
dc.contributor.authorอรภัค เลี่ยมทองen_US
dc.contributor.authorPoom Adisakwattanaen_US
dc.contributor.authorภูมิ อดิศักดิ์วัฒนาen_US
dc.contributor.authorMahidol University. Faculty of Tropical Medicine. Department of Molecular Tropical Medicine and Geneticsen_US
dc.contributor.otherMahidol University. Faculty of Tropical Medicine. Department of Helminthologyen_US
dc.date.accessioned2015-07-06T06:40:08Z
dc.date.accessioned2021-08-17T06:52:44Z
dc.date.available2015-07-06T06:40:08Z
dc.date.available2021-08-17T06:52:44Z
dc.date.created2015-07-06
dc.date.issued2014
dc.descriptionJoint International Tropical Medicine Meeting 2014: 3D perspectives on tropical medicine: drivers, diversity and determination the 8th seminar on food-and water-borne parasitic zoonoses: 2-4 December 2014: Centara Grand Bangkok Convention Center at Central World, Bangkok, Thailand. Bangkok: Faculty of Tropical Medicine, Mahidol University; 2014. p. 247.en
dc.description.abstractThe parasite Gnathostoma spinigerum is a causative agent of gnathostomiasis and can be found in several countries. Infection leads to permanent organ damage or death, therefore rapid and reliable diagnosis is necessary and a major priority for effective treatment. In our investigation we determined novel target proteins from excretory-secretory (ES) antigens of 3rd stage G. spinigerum larva using immunomics and mass spectrometry approaches. We prepared ES antigen of G. spinigerum for protein profiling analysis by 2D-gel electrophoresis and subsequently transferred it onto PVDF membrane. The membranes were reacted with G. spinigerum infected or other helminthic infected sera. Results show that approximately seven spots at the molecular size of 12, 20, and 50 kDa represented G. spinigerum infection. Next, these protein spots are going to be analyzed by mass spectrometry and available databases will be searched for annotation. Identifying the type of protein and/or tryptic peptide sequences will be useful for the development of future immunodiagnosis for gnathostomiasis.en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/63164
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.subjectGnathostoma spinigerumen_US
dc.subjectExcretory-secretory antigensen_US
dc.subjectImmunomicsen_US
dc.subjectImmunodiagnosisen_US
dc.titleImmunomics analysis of excretory-secretory antigens from 3rd stage larva gnathostoma spinigerum for development of immunodiagnosisen_US
dc.typeProceeding Posteren_US

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