Veterinary Parasitology
| Autor: | Solcà, Manuela da Silva, Guedes, Carlos Eduardo Sampaio, Nascimento, Eliane Gomes, Oliveira, Geraldo Gileno de Sá, Santos, Washington Luis Conrado dos, Fraga, Deborah Bittencourt Mothé, Veras, Patrícia Sampaio Tavares |
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| Jazyk: | angličtina |
| Rok vydání: | 2012 |
| Předmět: | |
| Zdroj: | Repositório Institucional da UFBA Universidade Federal da Bahia (UFBA) instacron:UFBA |
| DOI: | 10.1016/j.vetpar.2011.08.026 |
| Popis: | Texto completo: acesso restrito. p. 133–140 Submitted by Edileide Reis (leyde-landy@hotmail.com) on 2014-08-19T11:46:25Z No. of bitstreams: 1 Manuela da Silva Solcà.pdf: 368652 bytes, checksum: bb70de492c7851bbfe4f5d24a419bae5 (MD5) Approved for entry into archive by Patricia Barroso (pbarroso@ufba.br) on 2014-08-22T21:37:31Z (GMT) No. of bitstreams: 1 Manuela da Silva Solcà.pdf: 368652 bytes, checksum: bb70de492c7851bbfe4f5d24a419bae5 (MD5) Made available in DSpace on 2014-08-22T21:37:31Z (GMT). No. of bitstreams: 1 Manuela da Silva Solcà.pdf: 368652 bytes, checksum: bb70de492c7851bbfe4f5d24a419bae5 (MD5) Previous issue date: 2012 Because infected dogs are widely considered to be the main domestic reservoir for Leishmania infantum (syn Leishmania chagasi) parasites in Brazil, the diagnosis of canine visceral leishmaniasis (CVL) must be made both accurately and promptly. The present study attempted to standardize a conventional polymerase chain reaction (cPCR) protocol for the detection of L. infantum DNA in canine spleen samples. Quantitative PCR (qPCR) technique was used to confirm the presence of Leishmania DNA in the canine spleen fragments. A comparison was made between the efficacies of these molecular diagnostic techniques and conventional parasitological and serological methods. cPCR protocols for spleen samples were standardized using primers that amplify a 145 bp fragment, located at the parasite kinetoplast minicircle. The genus specificity of the cPCR protocol was assessed by its inability to amplify the DNA of other common canine pathogens, such as Ehrlichia canis, Babesia canis, Toxoplasma gondii and Trypanosoma cruzi. cPCR protocol sensitivity was tested by assessing the reaction detection limit, determined to be 10 fg of L. infantum reference strain DNA, which corresponds to a range of 0.03–0.1 parasites per fragment. Standardized cPCR protocol was used to detect the presence of Leishmania in 45 dog spleen samples. Our results showed that 40% of the spleen fragment cultures were positive for Leishmania parasites, 58% of the dog serum samples tested positive using ELISA, and parasite DNA was detected in 44% using qPCR, while 47% of the spleen samples using cPCR. Diagnostic methods performance was assessed and revealed a better degree of ascertainment for cPCR when compared to other diagnostic methods. The sensitivity of ELISA was 83.3%, qPCR was 83.3%, and cPCR was 88.9%; PPV for ELISA was 57.7%, qPCR was 75% and cPCR was 76.2%; the Kappa coefficients were found to be 0.40 (fair) for ELISA, 0.64 (substantial) for qPCR and 0.68 (substantial) for cPCR. In both oligosymptomatic and polysymptomatic dogs, cPCR revealed the better performance analysis when compared to other diagnostic methods. The findings presented herein establish cPCR as the most indicated test to detect Leishmania when compared to the other two diagnostic methods evaluated. Despite the fact that the qPCR protocol provides a highly accurate quantification of parasites when targeting the SSU rRNA gene, this technique does not significantly improve the diagnosis of CVL when compared with the performance of the cPCR protocol, which focused on the kinetoplast minicircle. |
| Databáze: | OpenAIRE |
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