Open-access Diagnosis of Trypanosoma cruzi infection in Mexican populations: current conventional serology lacks adequate sensitivity and specificity

Abstract

BACKGROUND  The performance of serological tests for Trypanosoma cruzi diagnosis in Mexico has not included discordant control sera nor has it evaluated the role of immune response specificities, patient infection history or clinical status.

OBJECTIVES  The performance of commercial serological and molecular diagnostic tests and diagnostic algorithms was analysed in Mixtecan and Zapotecan ethnic populations having recent and long-term infection history.

METHODS  An amplified global gold standard for T. cruzi infection included serological (≥ 2 conventional tests positive) and molecular (sequence identity of any of five genes using end point polymerase chain reaction (epPCR) or any positive using quantitative polymerase chain reaction (qPCR) diagnostic test results.

FINDINGS  Only 81% of previously diagnosed untreated infections were reconfirmed using serology, while an additional 14% only using PCR. Serological diagnosis sensitivity (≥ 2 tests positive) in the primary diagnosis cohort was 8%, while specificity was 16%. Diagnosis sensitivity was similar using epPCR and qPCR only in primary diagnoses and all identified using the satellite (SAT) gene. The 18S ribosomal DNA identified T. cruzi and T. dionisii co-infections from Pacific coast sites.

MAIN CONCLUSIONS   The current study provides evidence for inadequate diagnostic performance of conventional serological tests and the need to develop appropriate antigenic tools and use molecular testing of seronegatives to ascertain absence of infection.

Key words:
Chagas disease; Trypanosoma cruzi ; serological diagnosis; performance; molecular diagnosis


location_on
Instituto Oswaldo Cruz, Ministério da Saúde Av. Brasil, 4365 - Pavilhão Mourisco, Manguinhos, 21040-900 Rio de Janeiro RJ Brazil, Tel.: (55 21) 2562-1222, Fax: (55 21) 2562 1220 - Rio de Janeiro - RJ - Brazil
E-mail: memorias@fiocruz.br
rss_feed Acompanhe os números deste periódico no seu leitor de RSS
Ir para o topo Reportar erro