Reactivity of purified and axenic amastigotes as a source of antigens to be used in serodiagnosis of canine visceral leishmaniasis

• Published in: Parasitology international Vol. 79; p. 102177
• Main Authors: da Silva, Thais Bruna Ferreira, Silveira, Fernando Tobias, Tomokane, Thaise Yumie, Batista, Luis Fábio da Silva, Nunes, Juliana Barbosa, da Matta, Vânia Lúcia Ribeiro, Passero, Luiz Felipe Domingues, Laurenti, Márcia Dalastra
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.12.2020
• Subjects: Amastigotes; Animals; Antigens, Protozoan - blood; Canine visceral leishmaniasis; Dog Diseases - diagnosis; Dog Diseases - parasitology; Dogs; Enzyme linked ImunoSorbent assay; Enzyme-Linked Immunosorbent Assay - veterinary; Leishmania (L.) infantum chagasi; Leishmania infantum - isolation & purification; Leishmaniasis, Visceral - diagnosis; Leishmaniasis, Visceral - parasitology; Leishmaniasis, Visceral - veterinary; Serologic Tests - veterinary; Serological diagnosis; Enzyme linked ImunoSorbent assay; Serological diagnosis; Amastigotes; Leishmania (L.) infantum chagasi; Canine visceral leishmaniasis
• ISSN: 1383-5769; 1873-0329
• DOI: 10.1016/j.parint.2020.102177

Although there is a great diversity of techniques and antigens used in the serodiagnosis of canine visceral leishmaniasis (CVL), total sensitivity and specificity have not yet been found. Since the use of amastigote forms in the indirect immunofluorescence assay has shown an improvement in the specificity of the test for the diagnosis of CVL, the performance of amastigotes forms of L. (L.) infantum chagasi as antigen source were evaluated in automatized ELISA test using crude antigen of axenic amastigote and purified amastigote from spleen of hamster chronically infected comparing with ELISA using total antigen produced with promastigote forms of L. (L.) infantum chagasi. One hundred and fifteen sera from dogs with positive parasitological diagnosis by PCR were used. The animals were classified into 2 groups: symptomatic (n = 67) and asymptomatic (n = 48) animals, in accordance with the clinical signs and laboratory tests were. As control, ninety-four sera from dogs with negative parasitological diagnosis were included. No significant difference was found in sensitivity, specificity, predictive values and accuracy between ELISA using whole antigens produced with both axenic and purified amastigotes in comparison with promastigotes forms. Correlation and concordance between the three total antigens tested in ELISA was observed. According to the similar performance among antigens, data pointed out to use antigen from promastigote forms for diagnosing canine leishmaniasis, especially due the easily in the production, lower cost and the abundance of correlative literature.