Toxoplasma gondii: P30 peptides recognition pattern in human toxoplasmosis

In this study, human sera reactivity against nine peptides derived from the Toxoplasma gondii P30 protein was assessed by ELISA in patients with different clinical forms of toxoplasmosis. Same as has been reported in mice, sera from congenital, ocular and chronic asymptomatic toxoplasmosis patients...

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Autores:
Tipo de recurso:
Fecha de publicación:
2009
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/24038
Acceso en línea:
https://doi.org/10.1016/j.exppara.2009.06.017
https://repository.urosario.edu.co/handle/10336/24038
Palabra clave:
Immunoglobulin G antibody
Protein p30
Article
Carboxy terminal sequence
Chorioretinopathy
Clinical article
Congenital toxoplasmosis
Controlled study
Eye infection
Human
Humoral immunity
Infant
Molecular recognition
Nonhuman
Nucleotide sequence
Parasite immunity
Priority journal
Toxoplasma gondii
Toxoplasmosis
Amino Acid Sequence
Analysis of Variance
Animals
Chronic Disease
Enzyme-Linked Immunosorbent Assay
Humans
Immune Sera
Immunoglobulin G
Infant
Molecular Sequence Data
Peptides
Protozoan Proteins
Toxoplasma
Toxoplasmosis
Mus
Toxoplasma gondii
Human antibodies
Peptides
SAG1
Toxoplasma gondii
Surface
Protozoan
Ocular
Congenital
Antigens
Antigens
Toxoplasmosis
Toxoplasmosis
Rights
License
Abierto (Texto Completo)
Description
Summary:In this study, human sera reactivity against nine peptides derived from the Toxoplasma gondii P30 protein was assessed by ELISA in patients with different clinical forms of toxoplasmosis. Same as has been reported in mice, sera from congenital, ocular and chronic asymptomatic toxoplasmosis patients recognized more strongly peptides from the protein's carboxy-terminus, being peptide 2017 (amino acids 301-320) the one most strongly recognized by sera from patients with ocular toxoplasmosis. Serum samples collected from 13 patients without ocular infection, 13 with inactive chorioretinal scars, 6 with active ocular infection and 10 seronegative individuals were then screened for anti-2017 IgG. Peptide 2017 was recognized by all patients' samples but not by sera from T. gondii-seronegative individuals. No statistically significant differences were found between the absorbance levels of groups with and without lesions or with active or inactive ocular lesions, as determined by ANOVA. © 2009 Elsevier Inc. All rights reserved.