Viability study of a multiplex diagnostic platform for Chagas disease

被引:14
|
作者
Foti, Leonardo [1 ]
Fonseca e Fonseca, Bruna de Paula [2 ]
Nascimento, Lilian Dias [2 ]
Silva Marques, Christiane de Fatima [2 ]
da Silva, Edmilson Domingos [2 ]
Barros Duarte, Cesar Augusto [1 ]
Probst, Christian M. [1 ]
Goldenberg, Samuel [1 ]
Pinto, Antonio Gomes [2 ]
Krieger, Marco Aurelio [1 ]
机构
[1] Fiocruz MS, Inst Carlos Chagas, BR-81350010 Curitiba, Parana, Brazil
[2] Fiocruz MS, Lab Tecnol Diagnost, BR-21045900 Rio De Janeiro, Brazil
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2009年 / 104卷
关键词
Chagas disease; diagnostic; multiplex; bead-based assay; Trypanosoma cruzi; TRYPANOSOMA-CRUZI; INFECTIOUS-DISEASES; ASSAY; IMMUNOASSAYS; ANTIBODIES; ANTIGENS;
D O I
10.1590/S0074-02762009000900019
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
A new multiplex assay platform was evaluated to detect Trypanosoma cruzi infection using the recombinant antigens CRA, FRA, CRAFRA fusion and parasite lysate. The antigens presented different sensitivity and specificity in a singleplex test when compared to a serial dilution of two pools comprising 10 positive serum samples and one pool of 10 negative samples. The recombinant protein CRA presented lower sensitivity (55%) in contrast to the 100% specificity and sensitivity of FRA, CRAFRA and T. cruzi lysate. These antigens also showed good results in a duplex test and the duplex test with CRAFRA/T. cruzi lysate showed better performance with 100% specificity and sensitivity, as well as a lower cut-off value in comparison to the other duplex test, FRA/T. cruzi lysate. Hence, when the antigens were used in duplex format, both tests showed decreased cut-off values and no interference between different bead sets, resulting in increasing sensitivity and specificity. The results of these multiplex tests show that they could be an alternative to singleplex detection for Chagas disease, and also indicate the necessity of using multiplex diagnostic tools to increase the sensitivity and specificity for diagnostic tests. Emerging data from the T. cruzi genome and from its ORFeome project will also allow the identification of new antigens for this disease detection application.
引用
收藏
页码:136 / 141
页数:6
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