Literature DB >> 26238982

Detection of parasite-specific IgG and IgA in paired serum and saliva samples for diagnosis of human strongyloidiasis in northern Paraná state, Brazil.

Larissa R Bosqui1, Ana Lúcia R Gonçalves2, Maria do Rosário F Gonçalves-Pires2, Luiz Antonio Custodio3, Maria Cláudia N D de Menezes1, Valter A Murad3, Fabiana M de Paula4, Wander R Pavanelli1, Ivete Conchon-Costa1, Julia Maria Costa-Cruz2, Idessania N Costa5.   

Abstract

Human strongyloidiasis is an infection caused by the helminth Strongyloides stercoralis that can be fatal, especially in immunosuppressed patients. The aim of this study is to evaluate parasite-specific IgG and IgA levels using S. venezuelensis third-stage (L3) infective larvae alkaline extract as a heterologous antigen by ELISA in paired serum and saliva samples with improved sensitivity and specificity. Individuals from northern Paraná state, Brazil were divided into three groups: 30 patients copropositive for S. stercoralis (Group I); 30 clinically healthy individuals (Group II); and 30 patients copropositive for other parasites (Group III). The area under ROC curve (AUC), an overall index of diagnostic accuracy, and Kappa index were calculated. Data were analyzed using analysis of variance (ANOVA) followed by a Kruskal-Wallis test. Probability (p) values of <0.05 were regarded as significant. In Group I, IgG was detected in 96.7% serum and in 6.7% saliva samples. IgG was not detected in Group II. In Group III, cross-reactivity was observed for serum IgG in 26.7% and in 6.7% for saliva samples. In Group I, IgA was detected in 76.7% serum and 56.7% saliva samples. In Group II, 3.3% were positive for IgA in serum, whereas IgA was not detected in any saliva samples. Group III showed 6.7% serum and 26.7% saliva-positive samples. The sensitivity values for detection of IgG and IgA in serum samples were 96.7% and 76.7%, respectively. In saliva samples, the sensitivity values for detection of IgG and IgA were 6.7% and 56.7%, respectively. The specificity value was 100% for the detection of IgG in serum and for detection of IgG and IgA in saliva, and 96.7% for detection of IgA in serum samples. The proper choice of immunological diagnosis to supplement parasitological methods is essential to estimate the true prevalence of the parasite, and will permit analysis of population immune response profiles, particularly in northern Paraná state, where there are no previous reports.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Brazil; Immunodiagnostic; Paraná state; Saliva; Strongyloidiasis

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Year:  2015        PMID: 26238982     DOI: 10.1016/j.actatropica.2015.07.026

Source DB:  PubMed          Journal:  Acta Trop        ISSN: 0001-706X            Impact factor:   3.112


  4 in total

1.  Molecular and Immnune Diagnosis: Further Testing for Human Strongyloidiasis.

Authors:  Larissa R Bosqui; Priscilla D Marques; Gessica B de Melo; Maria do Rosário F Gonçalves-Pires; Fernanda M Malta; Wander R Pavanelli; Ivete Conchon-Costa; Julia M Costa-Cruz; Fabiana M Paula; Idessania N Costa
Journal:  Mol Diagn Ther       Date:  2018-08       Impact factor: 4.074

Review 2.  Strongyloidiasis Current Status with Emphasis in Diagnosis and Drug Research.

Authors:  Tiago Mendes; Karen Minori; Marlene Ueta; Danilo Ciccone Miguel; Silmara Marques Allegretti
Journal:  J Parasitol Res       Date:  2017-01-22

3.  Diagnostic Potential of an IgE-ELISA in Detecting Strongyloidiasis.

Authors:  Hussain Ahmad; Dinesh Balachandra; Norsyahida Arifin; Thomas J Nolan; James B Lok; Amjad Hayat Khan; Muhammad Hafiznur Yunus; Rahmah Noordin
Journal:  Am J Trop Med Hyg       Date:  2020-09-24       Impact factor: 3.707

4.  Strongyloides-Specific IgE Phage cDNA Clones and Development of a Novel ELISA for Strongyloidiasis.

Authors:  Hussain Ahmad; Norsyahida Arifin; Thomas J Nolan; James B Lok; Nor Suhada Anuar; Rahmah Noordin
Journal:  Diagnostics (Basel)       Date:  2021-05-28
  4 in total

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