Abstract

Neospora caninum is one of the main causes of abortion and natimortality in cattle. Host immune defense is capable to inhibit tachyzoite activity during acute infection, but there is no action against bradyzoites in tissue cysts. Activation and modulation of this response is controlled by cell mediators. The real-time RT-PCR technique was employed to detect some of those mediators during N. caninum infection. Holstein and Nelore calves intramuscularly infected with tachyzoites and uninfected controls were slaughtered at the sixth day post-infection and popliteal lymph node, liver and brain cortex samples were analyzed. Real-time RT-PCR detected gene expression in all tissues. No significant variation of GAPDH gene expression was detected among groups, its amplification efficiency was similar to the other genes tested and it was used as the endogenous control for the analysis. Comparisons between infected and uninfected groups allowed the relative gene expression quantification. IFN-gamma and TNF-alpha genes showed increased expression in some samples. iNOS and TGF-beta1 genes had some non-significant variations and IL-4 and IL-10 stayed practically unaltered.

Highlights

  • Neospora caninum is one of the main causes of abortion and natimortality in cattle

  • there is no action against bradyzoites in tissue cysts

  • Activation and modulation of this response is controlled by cell mediators

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Summary

Animais

Sete da raça Holandesa e sete da raça Nelore, sorologicamente negativos para N. caninum e com idade aproximada de seis meses. Todos os bezerros foram mantidos em instalações sem acesso a pasto, em grupos de três a quatro bezerros por baia, diariamente alimentados com feno e ração própria para bezerros e água ad libitum em conformidade com os princípios éticos de experimentação animal da Comissão de Bioética da FMVZ – USP (protocolo no 814/2005). Quatro bezerros Holandeses e quatro Nelores receberam uma suspensão contendo 108 taquizoítos de N. caninum obtidos de cultivos celulares (cepa NC-1) por via IM no membro posterior e três bezerros de cada raça foram mantidos como controle sem infecção e receberam uma suspensão de células Vero pela mesma via. As amostras de tecido permaneceram congeladas a –70 °C até o momento das extrações de RNA

Desenho de “primers” e sondas
Extração de RNA
Síntese de cDNA
PCR em tempo real
Eficiência de amplificação
Eletroforese em gel de agarose
Análise estatística
Full Text
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