Still Searching for a Suitable Molecular Test to Detect Hidden Plasmodium Infection: A Proposal for Blood Donor Screening in Brazil

Autor(es)

Maciel de Castro Lima, Giselle Fernandes ^[1] ; Lucchi, Naomi W. ^[2] ; Silva-Flannery, Luciana ^{[2, 3]} ; Macedo-de-Oliveira, Alexandre ^[2] ; Hristov, Angelica D. ^[1] ; Inoue, Juliana ^[1] ; Costa-Nascimento, Maria de Jesus ^[4] ; Udhayakumar, Venkatachalam ^[2] ; Di Santi, Silvia M. ^{[1, 4]}

Afiliação do(s) autor(es)

^[1] Univ Sao Paulo, Fac Med, Dept Molestias Infecciosas & Parasitarias, Sao Paulo, SP - Brazil

^[2] Ctr Dis Control & Prevent, Malaria Branch, Div Parasit Dis & Malaria, 4770 Buford Highway, Mail Stop F-12, Atlanta, GA - USA

^[3] Atlanta Res & Educ Fdn, Atlanta, GA - USA

^[4] Univ Sao Paulo, Secretaria Estado Saude Sao Paulo, Nucleo Estudos Malaria Superintendencia Controle, Inst Med Trop Sao Paulo, Sao Paulo, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: PLoS One; v. 11, n. 3 MAR 9 2016.
• Citações Web of Science: 6

Resumo

Background Efforts have been made to establish sensitive diagnostic tools for malaria screening in blood banks in order to detect malaria asymptomatic carriers. Microscopy, the malaria reference test in Brazil, is time consuming and its sensitivity depends on microscopist experience. Although molecular tools are available, some aspects need to be considered for large-scale screening: accuracy and robustness for detecting low parasitemia, affordability for application to large number of samples and flexibility to perform on individual or pooled samples. Methodology In this retrospective study, we evaluated four molecular assays for detection of malaria parasites in a set of 56 samples previously evaluated by expert microscopy. In addition, we evaluated the effect of pooling samples on the sensitivity and specificity of the molecular assays. A well-characterized cultured sample with 1 parasite/mu L was included in all the tests evaluated. DNA was extracted with QIAamp DNA Blood Mini Kit and eluted in 50 mu L to concentrate the DNA. Pools were assembled with 10 samples each. Molecular protocols targeting 18S rRNA, included one qPCR genus specific (Lima-genus), one duplex qPCR genus/Pf (PET-genus, PET-Pf) and one duplex qPCR specie-specific (Rougemont: RougPf/Pv and Roug-Pm/Po). Additionally a nested PCR protocol specie-specific was used (Snou-Pf, Snou-Pv, Snou-Pm and Snou-Po). Results The limit of detection was 3.5 p/mu L and 0.35p/mu l for the PET-genus and Lima-genus assays, respectively. Considering the positive (n = 13) and negative (n = 39) unpooled individual samples according to microscopy, the sensitivity of the two genus qPCR assays was 76.9% (Lima-genus) and 72.7% (PET-genus). The Lima-genus and PET-genus showed both sensitivity of 86.7% in the pooled samples. The genus protocols yielded similar results (Kappa value of 1.000) in both individual and pooled samples. Conclusions Efforts should be made to improve performance of molecular tests to enable the detection of low-density parasitemia if these tests are to be utilized for blood transfusion screening. (AU)

• Processo FAPESP: 12/18014-5 - Plataforma para diagnóstico de malária aplicada em amostras de doadores de sangue de áreas endêmicas e não endêmicas brasileiras processadas em pool: determinação da frequência de positividade utilizando marcadores moleculares e sorológicos
• Beneficiário: Silvia Maria Fátima Di Santi
• Modalidade de apoio: Auxílio à Pesquisa - Regular