PLoS ONE (Jan 2015)

FC-TRIPLEX Chagas/Leish IgG1: a multiplexed flow cytometry method for differential serological diagnosis of chagas disease and leishmaniasis.

  • Andréa Teixeira-Carvalho,
  • Fernanda Magalhães Freire Campos,
  • Stefan Michael Geiger,
  • Roberta Dias Rodrigues Rocha,
  • Fernanda Fortes de Araújo,
  • Danielle Marquete Vitelli-Avelar,
  • Mariléia Chaves Andrade,
  • Márcio Sobreira Silva Araújo,
  • Elenice Moreira Lemos,
  • Anna Bárbara de Freitas Carneiro Proietti,
  • Ester Cerdeira Sabino,
  • Rafaella Gaiotti Caldas,
  • Carolina Renata Camargos Freitas,
  • Ana Carolina Campi-Azevedo,
  • Silvana Maria Elói-Santos,
  • Olindo Assis Martins-Filho

DOI
https://doi.org/10.1371/journal.pone.0122938
Journal volume & issue
Vol. 10, no. 4
p. e0122938

Abstract

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Differential serological diagnosis of Chagas disease and leishmaniasis is difficult owing to cross-reactivity resulting from the fact that the parasites that cause these pathologies share antigenic epitopes. Even with optimized serological assays that use parasite-specific recombinant antigens, inconclusive test results continue to be a problem. Therefore, new serological tests with high sensitivity and specificity are needed. In the present work, we developed and evaluated the performance of a new flow cytometric serological method, referred to as FC-TRIPLEX Chagas/Leish IgG1, for the all-in-one classification of inconclusive tests. The method uses antigens for the detection of visceral leishmaniasis, localized cutaneous leishmaniasis, and Chagas disease and is based on an inverted detuned algorithm for analysis of anti-Trypanosomatidae IgG1 reactivity. First, parasites were label with fluorescein isothiocyanate or Alexa Fluor 647 at various concentrations. Then serum samples were serially diluted, the dilutions were incubated with suspensions of mixed labeled parasites, and flow cytometric measurements were performed to determine percentages of positive fluorescent parasites. Using the new method, we obtained correct results for 76 of 80 analyzed serum samples (95% overall performance), underscoring the outstanding performance of the method. Moreover, we found that the fluorescently labeled parasite suspensions were stable during storage at room temperature, 4 °C, and -20 °C for 1 year. In addition, two different lots of parasite suspensions showed equivalent antigen recognition; that is, the two lots showed equivalent categorical segregation of anti-Trypanosomatidae IgG1 reactivity at selected serum dilutions. In conclusion, we have developed a sensitive and selective method for differential diagnosis of Chagas disease, visceral leishmaniasis, and localized cutaneous leishmaniasis.