Detection of Trypanosoma vivax using PCR and LAMP during aparasitemic periods
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 |