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EVALUATION OF 18S RDNA PCR ASSAY USING SKIN FRAGMENTS AS A DIAGNOSTIC TEST FOR TRYPANOSOMA CANINUM
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Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Vigilância em Leishmanioses. Programa de pós-graduação em Pesquisa Clínica em Doenças Infecciosas. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Laboratório de Diagnóstico Molecular e Hematologia. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em Dermatozoonoses de Animais Domésticos. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Vigilância em Leishmanioses. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Laboratório de Diagnóstico Molecular e Hematologia. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em Dermatozoonoses de Animais Domésticos. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Vigilância em Leishmanioses. Rio de Janeiro, RJ, Brasil.
Abstract
Trypanosoma caninum is a new species that has been recently identified in Brazil and infects
domestic dogs. To date, no accurate diagnostic assays for this parasite have been established;
thus, our aim was to evaluate more than one type of PCR for the diagnosis and
molecular screening of T. caninum in 229 dogs living in Rio de Janeiro state. The tests were
based on the amplification and sequencing of the 18S ribosomal DNA (rDNA) gene using
healthy skin fragments. Additionally, PCR amplification of the kDNA minicircles region specific
to the Leishmania genus was performed. The PCR results were compared with those
of culture-based analysis performed with the same specimen. Using cultures, T. caninum
and Leishmania chagasi were isolated from 11 and 12 dogs, respectively, whereas the 18S
rDNA PCR assay detected parasitic infection in 35 dogs. Among these, 25 dogs showed an
amplification pattern similar to T. caninum and 10 showed a pattern similar to L. chagasi;
these results were confirmed by sequencing analysis. The kDNA PCR analysis showed that
14 dogs were positive for Leishmania infection. Of these, 2 dogs showed negative culture
results and 12 were positive for L. chagasi, including 4 with negative 18S rDNA PCR results.
Thus far, culture-based testing has been the only tool used successfully for T. caninum diagnosis.
Our results demonstrate that 18S rDNA PCR-based test should be a useful diagnostic
tool, particularly for distinguishing between T. caninum and L. chagasi infections in areas
where these 2 parasites co-exist.
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