α-N-acetylglucosamine-linked O-glycans of sialoglycoproteins (Tc-mucins) from Trypanosoma cruzi Colombiana strain

Trypanosoma cruzi sialoglycoproteins (Tc-mucins) are mucin-like molecules linked to a parasite membrane via a glycosylphosphatidylinositol anchor. We previously determined the structures of Tc-mucin O-glycan domains from several T. cruzi strains and observed significant differences among them. We now report the amino acid content and structure of Tc-mucin O-glycan chains from T. cruzi Colombiana, a strain resistant to common trypanocidal drugs. Amino acid analysis demonstrated the predominance of threonine residues (42%) and helped to identify the O-glycans as belonging to a Tc-mucin family that contain a ²-galactofuranose (²-Galf) residue attached to an α-N-acetylglucosamine (α-GlcNAc) O-4, with the most complex glycan, a pentasaccharide-GlcNAc-ol with a branched trigalactopyranose chain, on the GlcNAc O-6. The presence of ²-Galf on O-glycans from T. cruzi Colombiana mucins supports the use of glycosylation as a phylogenetic marker for the classification of Colombiana in the T. cruzi I group.

The anticancer drug tamoxifen is active against Trypanosoma cruzi in vitro but ineffective in the treatment of the acute phase of Chagas disease in mice

The activity of the antineoplastic drug tamoxifen was evaluated against Trypanosoma cruzi. In vitro activity was determined against epimastigote, trypomastigote and amastigote forms of CL14, Y and Y benznidazole resistant T. cruzi strains. Regardless of the strain used, the drug was active against all life-cycle stages of the parasite with a half maximal effective concentration ranging from 0.7-17.9 µM. Two experimental models of acute Chagas disease were used to evaluate the in vivo efficacy of treatment with tamoxifen. No differences in parasitemia and mortality were observed between control mock-treated and tamoxifen-treated mice.

The level of ascorbate peroxidase is enhanced in benznidazole-resistant populations of Trypanosoma cruzi and its expression is modulated by stress generated by hydrogen peroxide

Ascorbate peroxidases (APX) are class I heme-containing enzymes that convert hydrogen peroxide into water molecules. The gene encoding APX has been characterized in 11 strains of Trypanosoma cruzi that are sensitive or resistant to benznidazole (BZ). Bioinformatic analysis revealed the presence of two complete copies of the T. cruzi APX (TcAPX) gene in the genome of the parasite, while karyotype analysis showed that the gene was present in the 2.000-kb chromosome of all of the strains analyzed. The sequence of TcAPX exhibited greater levels of similarity to those of orthologous enzymes from Leishmania spp than to APXs from the higher plant Arabidopsis thaliana. Northern blot and real-time reverse transcriptase polymerase chain reaction (RT-PCR) analyses revealed no significant differences in TcAPX mRNA levels between the T. cruzi strains analyzed. On the other hand, Western blots showed that the expression levels of TcAPX protein were, respectively, two and three-fold higher in T. cruzi populations with in vitro induced (17 LER) and in vivo selected (BZR) resistance to BZ, in comparison with their corresponding susceptible counterparts. Moreover, the two BZ-resistant populations exhibited higher tolerances to exogenous hydrogen peroxide than their susceptible counterparts and showed TcAPX levels that increased in a dose-dependent manner following exposure to 100 and 200 µM hydrogen peroxide.

The identification of two Trypanosoma cruzi I genotypes from domestic and sylvatic transmission cycles in Colombia based on a single polymerase chain reaction amplification of the spliced-leader intergenic region

A single polymerase chain reaction (PCR) reaction targeting the spliced-leader intergenic region of Trypanosoma cruzi I was standardised by amplifying a 231 bp fragment in domestic (TcIDOM) strains or clones and 450 and 550 bp fragments in sylvatic strains or clones. This reaction was validated using 44 blind coded samples and 184 non-coded T. cruzi I clones isolated from sylvatic triatomines and the correspondence between the amplified fragments and their domestic or sylvatic origin was determined. Six of the nine strains isolated from acute cases suspected of oral infection had the sylvatic T. cruzi I profile. These results confirmed that the sylvatic T. cruzi I genotype is linked to cases of oral Chagas disease in Colombia. We therefore propose the use of this novel PCR reaction in strains or clones previously characterised as T. cruziI to distinguish TcIDOMfrom sylvatic genotypes in studies of transmission dynamics, including the verification of population selection within hosts or detection of the frequency of mixed infections by both T. cruzi I genotypes in Colombia.

The TcI and TcII Trypanosoma cruzi experimental infections induce distinct immune responses and cardiac fibrosis in dogs

Trypanosoma cruzi infection may be caused by different strains with distinct discrete typing units (DTUs) that can result in variable clinical forms of chronic Chagas disease. The present study evaluates the immune response and cardiac lesions in dogs experimentally infected with different T. cruzi strains with distinct DTUs, namely, the Colombian (Col) and Y strains of TcI and TcII DTU, respectively. During infection with the Col strain, increased levels of alanine aminotransferase, erythrocytes, haematocrit and haemoglobin were observed. In addition, CD8+ T-lymphocytes isolated from the peripheral blood produced higher levels of interleukin (IL)-4. The latter suggests that during the acute phase, infection with the Col strain may remain unnoticed by circulating mononuclear cells. In the chronic phase, a significant increase in the number of inflammatory cells was detected in the right atrium. Conversely, infection with the Y strain led to leucopoenia, thrombopoenia, inversion of the ratio of CD4+/CD8+ T-lymphocytes and alterations in monocyte number. The Y strain stimulated the production of interferon-γ by CD4+ and CD8+ T-lymphocytes and IL-4 by CD8+ T-cells. In the chronic phase, significant heart inflammation and fibrosis were observed, demonstrating that strains of different DTUs interact differently with the host.

Clearance-inducing antibodies are responsible for protection against the acute phase of Trypanosoma cruzi infection in mice

A study was conducted on mice infected with strains Y and CL of Trypanosoma cruzi. The ability of anti-Y and anti-CL sera to induce complement-mediated lysis, immune clearance and protection against the acute phase of the infection was studied using homologous anti-Y or anti-CL serum tested with the Y or CL strain, or heterologous anti-Y serum tested with the CL strain or anti-CL serum tested with the Y strain. Complement-mediated lysis was induced by both homologous and heterologous antisera but protection was afforded only by homologous antisera. Immune clearance was induced by homologous but not by heterologous antisera. Antisera with high clearance ability were able to confer protection whereas antisera with high lytic ability were not. These results show a high correlation between the antibody ability to induce clearance and to confer protection and suggest that clearance rather than lysis is responsible for protection against the acute phase of the infection. The mechanism of antibody protection against the acute phase of the infection is discussed.

Trypanosoma cruzi: amastigote polymorphism defined by monoclonal antibodies

We have raised monoclonal antibodies (mAbs) directed towards amastigote forms of Trypanosoma cruzi, and shown that mAbs 1D9 and 4B9 are carbohydrate while mAb 4B5 activity is resistant to periodate oxidation of the antigen. Here we used an ELISA to quantitate and compare the expression of surface epitopes on fixed parasites among different parasite isolates. The expression of markers varied among T. cruzi amastigotes isolated from infected cells or after extracellular differentiation of trypomastigotes. Moreover, we also observed an extensive polymorphic expression of these epitopes among amastigotes derived from different strains and clones. For instance, mAb 2C2 strongly and evenly reacted with 9 strains and clones (G, Y, CL, Tulahuen, MD, and F, and clones Sylvio X-10/4, D11, and CL.B), with absorbance at 492 nm (A492 nm) from 0.6 to 0.8. By contrast, mAb 4B5 had a higher expression in Tulahuen amastigotes (around 0.9 at 492 nm) whereas its reactivity with amastigotes from clones CL.B, Sylvio X-10/4 and D11 was much lower (around 0.4). mAb 1D9 displayed an interesting pattern of reactivity with amastigotes of the different strains and clones (A492 nm of G>D11³Sylvio X-10/4 = MD>Tulahuen = F = Y>CL>CL.B). Finally, we observed that mAb 4B9 had the lowest reaction with the parasites studied, with higher values of A492 nm with Y strain (around 0.6) and lower values with Tulahuen, F and CL.B strains (around 0.2). Immunoblotting analysis also showed extensive variations among amastigotes of the various parasite isolates and mAbs 4B9, 1D9 and 4B5 revealed significant differences in expression between clones and parental strains. These data describe a previously uncharacterized polymorphism of T. cruzi amastigote surface components.

Protein 3-nitrotyrosine formation during Trypanosoma cruzi infection in mice

Nitric oxide (·NO) is a diffusible messenger implicated in Trypanosoma cruzi resistance. Excess production of ·NO and oxidants leads to the generation of nitrogen dioxide (·NO2), a strong nitrating agent. Tyrosine nitration is a post-translational modification resulting from the addition of a nitro (-NO2) group to the ortho-position of tyrosine residues. Detection of protein 3-nitrotyrosine is regarded as a marker of nitro-oxidative stress and is observed in inflammatory processes. The formation and role of nitrating species in the control and myocardiopathy of T. cruzi infection remain to be studied. We investigated the levels of ·NO and protein 3-nitrotyrosine in the plasma of C3H and BALB/c mice and pharmacologically modulated their production during the acute phase of T. cruzi infection. We also looked for protein 3-nitrotyrosine in the hearts of infected animals. Our results demonstrated that C3H animals produced higher amounts of ·NO than BALB/c mice, but their generation of peroxynitrite was not proportionally enhanced and they had higher parasitemias. While N G-nitro-arginine methyl ester treatment abolished ·NO production and drastically augmented the parasitism, mercaptoethylguanidine and guanido-ethyl disulfide, at doses that moderately reduced the ·NO and 3-nitrotyrosine levels, paradoxically diminished the parasitemia in both strains. Nitrated proteins were also demonstrated in myocardial cells of infected mice. These data suggest that the control of T. cruzi infection depends not only on the capacity to produce ·NO, but also on its metabolic fate, including the generation of nitrating species that may constitute an important element in parasite resistance and collateral myocardial damage.

Experiências sôbre a transmissão do Trypanosoma cruzi por sanguessugas e de tripanosomas de vertebrados de sangue frio por triatomíneos

Observou-se que o Trypanosoma cruzi não se multiplica na sanguessuga (Haementeria lutzi Pinto); os tripanosomas sugados degeneram após algum tempo; outros permanecem aparentemente normais, porém 48 horas após a ingestão infectante acabam morrendo. Observou-se ainda que os tripanosomas parasitas da rã (T. rotatorium e T. leptodactyli) bem como o T. hogei, parasita da serpente Rachidelus brazili, não se multiplicam no intestino dos triatomíneos. O mais resistente (o T. leptodactyli), permanece vivo até 72 horas após a ingestão infectante, porém as outras duas espécies (T. rotatorium e T. hogei) não resistem mais de 24 horas após serem sugadas pelos triatomíneos.

Esterilidad individual en Rhodnius prolixus Stal. tratados con metepa (oxido de tris (1-(2 metil) aziridinil) fosfuro), y accion del mismo sobre Trypanosoma cruzi

Se analizan los factores que interfieren en la esterilidad inducida químicamente en R. Prolixus mediante aplicaciones tópicas en distintas dosis de metepa. Se sugiere profundizar el estudio de la susceptibilidad individual para conocer la composición de la población frente al quimioesterilizante y la probable aparición de resistencia. Se investiga además la acción del metepa sobre T. cruzi en triatominos infectados experimentalmente, obteniéndose resultados negativos.

Nota sobre a infecção natural de Calomys expulsus, Lund, 1841 (Cricetidae-Rodentia) pelo Trypanosoma cruzi

Foi isolada uma amostra de T. cruzi do roedor silvestre, Calomys expulsus, Lund, 1841, capturado no norte do município de Formosa, Goiás, através de inoculações em animais de laboratório, e subseqüente xenodiagnósticos com R. neglectus, T. infestans e P. megistus. A amostra de T. cruzi apresentou patogenicidade muito baixa para os animais inoculados, mas conferiu resistência a reinjecções a cêpa Y de origem humana. As jornias sanguícolas tiveram um comprimento total médio de 21.8 µ e o índice nuclear foi 1.15.

Prevalência da infecção por Trypanosoma cruzi, em 1975, em dois bancos de sangue de Londrina, Paraná, Brasil

Foi realizado inquérito sobre a positividade de reações sorológicas para o diagnóstico de tripanossomíase americana, em 4.500 candidatos a doadores não selecionados, atendidos em 1975, em dois bancos de sangue de Londrina, Paraná, Brasil. Observou-se resultado positivo da reação de fixação do complemento em 299 (7,9%) dos 3.774 candidatos a doadores atendidos no Banco de Sangue do Hospital Universitário (indivíduos residentes predominantemente na zona rural), tendo também sido positivos os resultados da reação de fixação do complemento e do teste de imunofluorescência indireta em 38 (5,2%) dos 726 candidatos a doadores atendidos no Instituto de Hematologia e Hemoterapia (indivíduos residentes predominantemente na zona urbana). Na casuística global a positividade observada foi de 7,4%. Dentre os 337 candidatos a doadores com reação sorológica positiva, 97 (28,7%) informaram ter doado sangue anteriormente, em outro local, 71 (21,0%) dos quais em período prévio menor que um ano, e 42 (12,4%) em período prévio menor que seis meses, em relação à data do nosso exame. Comparando os dados obtidos nesta avaliação com os de inquéritos semelhantes efetuados em 1958 em bancos de sangue deste município, concluiu-se que não houve, nesse período, alteração significativa nos índices de infecção por Trypanosoma cruzi em Londrina. Chamam a atenção para a discrepância entre o reduzido número de casos de doença de Chagas pós-transfusional relatados na literatura e os altos índices de positividade de reações sorológicas para o diagnóstico de tripanossomíase americana registrados em bancos de sangue de diversas regiões do Brasil. Foi ressaltada, a importância de exigir-se maior rigor e parcimônia nas indicações de transfusões de sangue, e dada ênfase às normas que devem ser respeitadas quando o uso desse recurso terapêutico tiver indicação formal.

Alguns aspectos do comportamento de cepas silvestres de Trypanosoma cruzi em camundongos e Calomys callosus (Rodentia)

Foram estudadas quatro cepas silvestres de T. cruzi: M226 isolada de Calomys callosus (Rodentia) e R52, R64 e R65 isoladas de Didelphis albiventris (Marsupialia). Estes animais foram coletados no município de Formosa, Goiás, Brasil. Os aspectos abordados, relacionados com o comportamento destas cepas em camundongos "swiss" 40 e C. callosus nascidos em laboratório, foram: parasitemia, prepatência, letalidade e histopatologia. Os resultados indicaram que as quatro cepas tinham baixa virulência para os animais testados. A parasitemia sempre se apresentou baixa e regular para os C. callosus. Nos camundongos, só raramente a parasitemia era patente. A prepatência nos C. callosus variou em média entre 9,2 a 10,2 dias, enquanto nos camundongos ficou entre 12-48 dias. A letalidade para C. callosus foi 7,7% e para camundongos 12,0%. Os estudos histopatológicos mostraram que somente 17,2% dos C. callosus apresentaram parasitismo tissular, enquanto em 25% dos camundongos foram encontrados pseudocistos íntegros ou rompidos. Houve um nítido miotropismo das quatro cepas tanto nos camundongos quanto nos C. callosus.

Crescimento e diferenciação "In vitro" de cepas de Trypanosoma cruzi, isoladas de animais silvestres

Foram estudadas três cepas de T. cruzi isoladas de Didelphis albiventris (R52, R64 e R65) e uma isolada de Calomys callosus (M226), quanto ao comportamento "In vitro" no meio LIT. A evolução da população dos tripanossomas com relação ao crescimento e morfogênese foi acompanhada por um período de 13 dias (312 horas), em intervalos regulares. As contagens diferenciais, separando-se formas amastigotas, epimastigotas e tripomastigotas, foram realizadas na câmara de Neubauer. Os resultados obtidos levaram à conclusão de que as 4 cepas estudadas têm comportamento distintos. O melhor crescimento obtido ocorreu para a cepa M226, seguindo-se por ordem decrescente a R65, R52 e R64. Os picos das populações ocorreram como segue: M226, entre 192-264 horas; R65 entre 168-240 horas; R52 às 240 horas e R64 entre 264-312 horas.

Infecção experimental de Calomys callosus (Rodentia Cricetidae) com Trypanosoma cruzi

São apresentados resultados sobre a infecção experimental de Calomys callosus (Rodentia) e duas cepas (Y e Berenice) de Trypanosoma cruzi, isoladas de casos humanos. O estudo da evolução foi feito comparado com Mus musculus albino cepa "Swiss", quanto a prepatência, parasitemia, patência e letalidade. Análise histopatológica foi também conduzida em C. callosus, com o objetivo de verificar o tropismo tissular e agressividade das cepas neste roedor. Os experimentos mostraram que a evolução da infecção em C. Callosus foi diferente para as duas cepas de T. cruzi. A cepa Y apresentou maior parasitemia do que a cepa Berenice. O período prepatente variou com as doses utilizadas tendo sido mais curto nos animais inoculados com a cepa Y (2, 2-5, 2 dias) do que naquelas com a cepa Berenice (3, 2-7 dias). Embora as duas cepas inoculadas nos C. callosus tenham-se mostrado miotrópicas, as alterações tissulares foram mais acentuadas com a Y. Os resultados obtidos abrem perspectivas quanto à possibilidade do uso de C. callosus como animal experimental para T. cruzi.