Full text
| |
| Author(s): |
Iara Silveira
Total Authors: 1
|
| Document type: | Master's Dissertation |
| Press: | São Paulo. |
| Institution: | Universidade de São Paulo (USP). Faculdade de Medicina Veterinária e Zootecnia (FMVZ/SBD) |
| Defense date: | 2006-09-14 |
| Examining board members: |
Marcelo Bahia Labruna;
Paulo Eduardo Brandão;
Matias Pablo Juan Szabo
|
| Advisor: | Marcelo Bahia Labruna |
| Abstract | |
In January 2005, 31 adult free-living ticks of the species Amblyomma triste were collected in the CESP rural farm located in the city of Paulicéia, state of São Paulo, Brazil. In the laboratory, 3 of these ticks were positive by the hemolymph test, showing structures compatible with Rickettsia within the hemocytes. Attempts to isolate Rickettsia were performed in two hemolymph-positive ticks by the Shell-vial technique. One isolate was successful obtained, being established in Vero cell culture, with several passages performed. DNA extracted from infected cells was submitted to PCR targeting fragments of four Rickettsia genes: gltA, htrA, ompA and ompB. DNA sequences obtained from PCR products of these four genes showed 99.8 to 100% of similarity with corresponding sequences of Rickettsia parkeri in the Genbank. DNA was extracted from all 31 ticks and processed by PCR targeting a fragment of the rickettsial gltA gene and a fragment of ompA gene. Three (9.7%) ticks were positive for both genes, being the same ticks previously positive by the hemolymph test. PCR products of these ticks were sequenced, being 100% identical to the corresponding sequence of Rickettsia parkeri in GenBanK. This study perfoms the first report of R. parkeri in Brazil, confirmed by the isolation of the agent in cell culture (AU) | |