Detection of Trypanosoma vivax using PCR and LAMP during aparasitemic periods


Autoria(s): Cadioli, Fabiano Antonio; Fidelis Junior, Otavio Luiz; Sampaio, Paulo Henrique; Santos, Giuliana Nascimento dos; André, Marcos Rogério; Almeida Castilho, Kayo José Garcia de; Machado, Rosangela Zacarias
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

07/12/2015

07/12/2015

03/09/2015

Resumo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Processo FAPESP: 2011/15945-5

Processo FAPESP: 2012/02284-3

Processo FAPESP: 2014/04066-9

Processo FAPESP: 2014/11600-1

Trypanosoma vivax affects cattle herds in Africa and Americas and has been spreading rapidly in Brazil, through introduction of animals with subclinical infections and without apparent parasitemia, which makes its diagnosis challenging. PCR and LAMP are effective in detecting the presence of T. vivax DNA in situations of low parasitemia. LAMP is simpler and faster technique than PCR, and can be performed in the field, with limited resources. In this study, the capacities of conventional PCR and LAMP for detecting T. vivax in bovine blood samples classified as aparasitemic were evaluated. The capacity of conventional PCR (56.25%) for detecting positive samples was lower than that of LAMP (93.73%). This may influence the choice of screening tests for cattle herds infected with T. vivax.

Formato

1-4

Identificador

http://dx.doi.org/10.1016/j.vetpar.2015.09.001

Veterinary Parasitology, p. 1-4, 2015.

1873-2550

http://hdl.handle.net/11449/131557

10.1016/j.vetpar.2015.09.001

26414906

Idioma(s)

eng

Publicador

Elsevier B. V.

Relação

Veterinary Parasitology

Direitos

closedAccess

Palavras-Chave #Elisa #Loop-mediated isothermal amplification #Polymerase chain reaction #Trypanosomiasis
Tipo

info:eu-repo/semantics/article