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Use of ProteinChip technology for identifying biomarkers of parasitic diseases: the example of porcine cysticercosis (Taenia solium)
Authors:Deckers N  Dorny P  Kanobana K  Vercruysse J  Gonzalez A E  Ward B  Ndao M
Affiliation:aDepartment of Animal Health, Institute of Tropical Medicine, Nationalestraat 155, B-2000, Antwerp, Belgium;bLaboratory of Veterinary Parasitology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium;cSchool of Veterinary Medicine, Universidad Nacional Mayor de San Marcos, Av. Circunvalación Cdra. 28 s/n, San Borja, Lima, Peru;dNational Reference Centre for Parasitology, McGill University Centre for Tropical Diseases, Montreal General Hospital, 1650 Cedar Avenue, Montreal, Que., Canada H3G 1A4
Abstract:Taenia solium cysticercosis is a significant public health problem in endemic countries. The current serodiagnostic techniques are not able to differentiate between infections with viable cysts and infections with degenerated cysts. The objectives of this study were to identify specific novel biomarkers of these different disease stages in the serum of experimentally infected pigs using ProteinChip technology (Bio-Rad) and to validate these biomarkers by analyzing serum samples from naturally infected pigs. In the experimental sample set 30 discriminating biomarkers (p < 0.05) were found, 13 specific for the viable phenotype, 9 specific for the degenerated phenotype and 8 specific for the infected phenotype (either viable or degenerated cysts). Only 3 of these biomarkers were also significant in the field samples; however, the peak profiles were not consistent among the two sample sets. Five biomarkers discovered in the sera from experimentally infected pigs were identified as clusterin, lecithin-cholesterol acyltransferase, vitronectin, haptoglobin and apolipoprotein A-I.
Keywords:Pig   Taenia solium   Cysticercosis   Cestode   Biological markers   Surface Enhanced Laser Desorption&ndash  Ionization Time of Flight (SELDI-TOF)   Apo A-I, apolipoprotein A-I   Apo A-IV, apolipoprotein A-IV   CHAPS, 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate   CV, coefficient of variation   DTT, dithiothreitol   EDM, expression difference mapping   HDL, high density lipoprotein   IEF, isoelectric focusing   IgG, immunoglobulin G   IMAC, immobilized metal affinity capture   m/z, mass to charge ratio   LCAT, lecithin-cholesterol acyltransferase   MW, molecular weight   QC, quality control   S/N, signal to noise ratio   SDS, sodium dodecyl sulfate   SELDI-TOF MS, surface enhanced laser desorption&ndash  ionization time-of-flight mass spectrometry   WCX, weak cation exchange
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