Navegando por Autor "Laurenti, Marcia Dalastra"
Agora exibindo 1 - 2 de 2
Resultados por página
Opções de Ordenação
Item Canine visceral leishmaniasis : performance of a rapid diagnostic test (Kalazar Detect TM ) in dogs with and without signs of the disease.(2008) Lemos, Elenice Moreira; Laurenti, Marcia Dalastra; Moreira, Márcio Antônio Batistela; Reis, Alexandre Barbosa; Giunchetti, Rodolfo Cordeiro; Raychaudhuri, Syamal; Dietze, ReynaldoCurrent visceral leishmaniasis (VL) control programs in Brazil include the infected dog elimination but, despite this strategy, the incidence of human VL is still increasing. One of the reasons is the long delay between sample collection, analysis, control implementation and the low sensitivity of diagnostic tests. Due to the high prevalence of asymptomatic dogs, the diagnosis of these animals is important considering their vector infection capacity. Hence, a rapid and accurate diagnosis of canine visceral leishmaniasis is essential for an efficient surveillance program. In this study we evaluated the performance of rK39 antigen in an immunochromatographic format to detect symptomatic and asymptomatic Leishmania chagasi infection in dogs and compared the results with those using a crude antigen ELISA. The sensitivity of rK39 dipstick and ELISA were 83% vs. 95%, respectively, while the specificity was both 100%. Our results also demonstrated that the dipstick test was able to detect infected dogs presenting different clinical forms.Item Leishmania amazonensis from distinct clinical forms/hosts has polymorphisms in Lipophosphoglycans, displays variations in immunomodulatory properties and, susceptibility to antileishmanial drugs.(2022) Rêgo, Felipe Dutra; Cardoso, Camila Almeida; Moreira, Paulo Otávio Lourenço; Nogueira, Paula Monalisa; Araújo, Márcio Sobreira Silva; Borges, Valéria Matos; Laurenti, Marcia Dalastra; Bartholomeu, Daniella Castanheira; Reis, Alexandre Barbosa; Monte Neto, Rubens Lima do; Soares, Rodrigo Pedro PintoLipophosphoglycan (LPG), the major Leishmania glycoconjugate, induces pro‐ inflammatory/immunosuppressive innate immune responses. Here, we evaluated functional/biochemical LPG properties from six Leishmania amazonensis strains from different hosts/clinical forms. LPGs from three strains (GV02, BA276, and LV79) had higher pro‐inflammatory profiles for most of the mediators, including tumor necrosis factor alpha and interleukin 6. For this reason, glycoconjugates from all strains were biochemically characterized and had polymorphisms in their repeat units. They consisted of three types: type I, repeat units devoid of side chains; type II, containing galactosylated side chains; and type III, containing glucosylated side chains. No relationship was observed between LPG type and the pro‐inflammatory properties. Finally, to evaluate the susceptibility against antileishmanial agents, two strains with high (GV02, BA276) and one with low (BA336) pro‐inflammatory activity were selected for chemotherapeutic tests in THP‐1 cells. All analyzed strains were susceptible to amphotericin B (AmB) but displayed various responses against miltefosine (MIL) and glucantime (GLU). The GV02 strain (canine visceral leishmaniasis) had the highest IC50 for MIL (3.34 μM), whereas diffuse leishmaniasis strains (BA276 and BA336) had a higher IC50 for GLU (6.87–12.19 mM). The highest IC50 against MIL shown by the GV02 strain has an impact on clinical management. Miltefosine is the only drug approved for dog treatment in Brazil. Further studies into drug susceptibility of L. amazonensis strains are warranted, especially in areas where dog infection by this species overlaps with those caused by Leishmania infantum.