A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on filter paper and analyzed by PCR. Fifty T infestans were fed on experimentally infected Balb/C mice with high T. cruzi parasitemia and divided into five groups of len triatomines, and 100 triatomines were infected with lower parasitemia and divided into five groups of 20 triatomines, One dry fecal spot was analyzed per group on days 1, 2, 3, 4 and 5 post feeding. Amplification targeted T. cruzi TCZ sequence and resulted positive from day 4 after bugs feeding in the two models (high and lower parasitemia). The rapid DNA isolation and PCR proposed are suitable for detection of T. cruzi DNA in in filter paper and should be considered in field res...
The polymerase chain reaction was used to amplify the highly variable region of the kinetoplast mini...
Abstract. For effective control programs, accurate assessment of Trypanosoma cruzi infection in vect...
Introduction The aim of the present study was to assess the polymerase chain reaction (PCR) as a met...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
We designed a PCR assay targeted on repeated elements of the ribosomal intergenic spacer which produ...
Abstract Background Chagas disease is a complex anthropozoonosis with distinct domestic and sylvatic...
We designed a PCR assay targeted on repeated elements of the ribosomal intergenic spacer which produ...
Triatomine vectors were collected on human dwellings in Michoac�n M�xico. Blood meal sources were id...
The polymerase chain reaction was used to amplify the highly variable region of the kinetoplast mini...
Abstract. For effective control programs, accurate assessment of Trypanosoma cruzi infection in vect...
Introduction The aim of the present study was to assess the polymerase chain reaction (PCR) as a met...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
A rapid DNA extraction was used for T. cruzi detection in triatomines dry fecal spots collected on f...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
Due to the overlapping distribution of Trypanosoma rangeli and T. cruzi in Central and South America...
We designed a PCR assay targeted on repeated elements of the ribosomal intergenic spacer which produ...
Abstract Background Chagas disease is a complex anthropozoonosis with distinct domestic and sylvatic...
We designed a PCR assay targeted on repeated elements of the ribosomal intergenic spacer which produ...
Triatomine vectors were collected on human dwellings in Michoac�n M�xico. Blood meal sources were id...
The polymerase chain reaction was used to amplify the highly variable region of the kinetoplast mini...
Abstract. For effective control programs, accurate assessment of Trypanosoma cruzi infection in vect...
Introduction The aim of the present study was to assess the polymerase chain reaction (PCR) as a met...