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Brazilian Journal of Medical and Biological Research

Print version ISSN 0100-879XOn-line version ISSN 1414-431X

Braz J Med Biol Res vol.38 no.12 Ribeirão Preto Dec. 2005 

Braz J Med Biol Res, December 2005, Volume 38(12) 1825-1834

Protein 3-nitrotyrosine formation during Trypanosoma cruzi infection in mice

M. Naviliat1,2, G. Gualco3, A. Cayota4 and R. Radi1

1Departamento de Bioquimica and Center for Free Radical and Biomedical Research, 2Departamento de Reumatología, 3Departamento de Anatomía Patológica, Hospital de Clínicas, 4Departamento de Medicina, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay

Material and Methods
Correspondence and Footnotes


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 NG-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.

Key words: Peroxynitrite, Nitric oxide, Nitrotyrosine, Free radicals, Trypanosoma cruzi, Chagas' disease


Chagas' disease is a parasitic condition caused by Trypanosoma cruzi that affects 16 to 18 million people in Central and South America and that can lead to impairment of heart function. During the acute phase of the disease the parasite actively replicates principally in macrophages and myocardial cells and a high parasitemia is observed. However, in immunologically competent individuals, an inflammatory and immune response develops controlling the parasite replication. Macrophages play a central role in the anti-parasitic defense, mainly due to the production of nitric oxide (·NO) (1).

·NO is a diffusible messenger produced by the reaction of L-arginine with different isoforms of nitric oxide synthases (NOS). ·NO has been implicated in different physiological functions, including vasodilation, inhibition of platelet aggregation, neurotransmission, and immune regulation (2), among others. In inflammatory conditions, large amounts of ·NO can be produced after the induction of inducible NOS (iNOS) in different cell types, notably macrophages. During T. cruzi infection, ·NO production, measured by its end products nitrite (NO2-) plus nitrate (NO3-) (NOx-) in serum or NO2- in splenocyte culture supernatants, rises early after the infection and remains high throughout the acute phase (3,4). Most of the current data indicate the necessity for ·NO to control the infection. The production of ·NO correlates with the resistance to T. cruzi infection in C57BL/6 mice (3), and the use of different iNOS inhibitors dramatically increases parasitemia and mortality (5). Indeed, interferon-g (INF-g) receptor or iNOS knock-out mice are extremely susceptible to T. cruzi infection (6-8). However, in contrast, a recent publication by Cummings and Tarleton (9) showed that iNOS knock-out mice are not more susceptible than wild type to T. cruzi infection.

Macrophage infection with T. cruzi may also induce the generation of reactive oxygen species (ROS) (10,11), particularly superoxide (O2·-) from the NADPH oxidase-dependent respiratory burst (12). ROS have been implicated early in T. cruzi killing. The J774 macrophage cell clone C3C, unable to produce O2·- and hydrogen peroxide (H2O2), cannot control parasite growth when infected with T. cruzi (13).

Tyrosine nitration is a post-translational modification resulting from the addition of a nitro (-NO2) group to the ortho-position of tyrosine residues. Two principal reaction pathways lead to 3-nitrotyrosine formation, both centered on the formation of nitrogen dioxide (·NO2) (14), a strong nitrating agent, namely, the peroxynitrite- and hemeperoxidase-dependent mechanisms. The formation of 3-nitrotyrosine is regarded as a marker of nitro-oxidative stress and is observed in inflammatory processes under excess production of ·NO and oxidants. 3-Nitrotyrosine-containing proteins have been described in different human and animal diseases, particularly in various forms of myocarditis (for a review, see Ref. 15).

Peroxynitrite, myeloperoxidase and eosinophil peroxidase are cytotoxic for T. cruzi. Previous work from our laboratory has shown that macrophage-derived peroxynitrite is able to kill T. cruzi epimastigotes and to impair their replication and motility as well as their energetic, calcium and trypanothione metabolism (16,17). In addition, peroxynitrite causes the nitration of T. cruzi proteins (18). Neutrophils are able to kill intracellular amastigotes by a mechanism mediated by myeloperoxidase and H2O2 (19). Also, eosinophil peroxidase-coated T. cruzi trypomastigotes became sensitized to macrophage destruction in the presence of H2O2 (20).

On the basis of this evidence, we hypothesize that nitrating molecules are formed during T. cruzi infection as part of the antiparasitic mechanisms, and also contribute to collateral host tissue damage. To test this hypothesis we estimated inflammatory cell-derived ·NO and nitrotyrosine production in the plasma of two strains of mice with different susceptibility to T. cruzi infection (11) and pharmacologically modulated its production during the acute phase of the disease. We also searched for protein 3-nitrotyrosine in the hearts of infected animals.

Material and Methods


All chemicals were purchased from Sigma (St. Louis, MO, USA), excepted otherwise indicated.


Eight- to 12-week-old BALB/c and C3H mice were obtained from the animal house of Instituto de Higiene (Facultad de Medicina, Universidad de la República, Montevideo, Uruguay) and breed and maintained as recommended (21).

Parasites and experimental infections

The Tulahuen-2 strain of T. cruzi was used in all studies. The animals were infected intraperitoneally with sublethal doses of blood-derived trypomastigote forms, i.e., 500 and 100 live parasites for BALB/c and C3H mice, respectively. Parasitemia was measured in 8 µL of blood obtained from the tail vein as described (22).

Pharmacological intervention

To modulate ·NO production we used the NOS inhibitors NG-nitro-L-arginine methyl ester (L-NAME) and guanido-ethyl disulfide (GED) as well as mercaptoethylguanidine (MEG), an iNOS inhibitor and peroxynitrite scavenger (23) that also reduces neutrophil infiltration (24). Mice received a daily intraperitoneal dose of 50 mg/kg L-NAME, 10 mg/kg MEG or 7 mg/kg GED diluted in PBS or vehicle from the day of infection and throughout the experimental period. Similar L-NAME doses have been shown to inhibit ·NO production during T. cruzi infection in mice (3,5). Also, 10 mg/kg MEG inhibited ·NO formation and nitrotyrosine immunoreactivity in a rat model of lung inflammation (24). GED (7 mg/kg) represents the quantity that provides the same molar amount of guanidine residues as 10 mg/kg MEG. Clinically healthy non-infected mice receiving L-NAME, MEG or GED were used as controls. MEG and GED were kindly provided by Dr. Csaba Szabó (Inoteck Pharmaceuticals Corporation, Beverly, MA, USA).

Blood collection

Blood was collected on day 17 post-infection (pi) from L-NAME-treated mice and on day 25 pi from MEG- and GED-treated mice, when parasitemia started to decline. The hearts were removed, washed in PBS and fixed in 10% formalin (v/v) in PBS. Blood leaking from the heart was collected into heparinized tubes and centrifuged and then submitted to five cycles of freezing and thawing in order to eliminate parasites. Finally, plasma samples were maintained at -20ºC until use.

Measurement of ·NO

The production of ·NO was estimated by measuring NOx- in plasma by the Griess method (25) adapted to work with small volumes of sample. Briefly, 10 µL of the sample or standard dilutions of NO3- were incubated on an ELISA plate (NUNC, Roskilde, Denmark) in the presence of 0.1 U/mL Aspergillus sp nitrate reductase, 5 µM flavin adenine dinucleotide (and 30 µM NADPH for 15 min at 37ºC in a final volume of 100 µL. Next, excess NADPH was oxidized with 100 U/mL lactate dehydrogenase and 0.3 mM sodium pyruvate for 5 min at 37ºC and then for 15 min at 4ºC, in a final volume of 200 µL. Diazotization was performed using 10 mM sulfanilamide and 0.6 M HCl. In order to eliminate the precipitated proteins, the samples were centrifuged at 3000 g for 15 min at 4ºC. The supernatant was then transferred to a new ELISA plate, 10 mM N-(1-naphthyl)-ethylenediamine was added, and absorbance was measured at 548 nm in a microplate reader (Labsystems Multiskan MS, Vantaa, Finland).

Measurement of nitrated plasma proteins

Nitrated plasma proteins were measured by ELISA (26). A standard solution of 1 mg/mL bovine serum albumin (BSA) prepared in 100 mM phosphate buffer, pH 7.4, was nitrated with 1 mM peroxynitrite added as a single bolus. The nitrotyrosine content of the nitrated BSA was calculated spectrophotometrically as the difference of the absorbance at pH 6 and 11, at 420 nm (e = 4400 M-1 cm-1) (27). ELISA plates (NUNC) were coated with dilutions of nitrated BSA or plasma samples diluted 1/100 in carbonate buffer (50 mM, pH 9) overnight at 4ºC and then blocked with 1% gelatin diluted in PBS for 1 h at 37ºC. After washing, an anti-nitrotyrosine polyclonal antibody (Ab) generated in our laboratory (28) diluted to 250 ng/mL in PBS-0.05% Tween 20 was incubated for 1 h at 37ºC and detected using a goat anti-rabbit peroxidase-conjugated immunoglobulin polyclonal antibody (Amersham-Pharmacia, Arlington Height, IL, USA). The plates were then developed using o-phenylenediamine and absorbance was read at 452 nm using a microplate reader. The results are reported as pmol/mg plasma proteins.


Hearts were probed with anti-nitrotyrosine and anti-myeloperoxidase polyclonal Ab. After fixing, the specimens were cut into 5-µm sections on silanized microscope slides. The anti-nitrotyrosine polyclonal Ab (5 ng/mL) was diluted in Tris-saline (50 mM Tris, 150 mM NaCl, pH 7.4), incubated overnight, and then developed with a secondary antibody coupled to biotin using a streptavidin-peroxidase kit and diaminobenzidine as chromogen. Histological sections were counterstained with hemalum. Diaminobenzidine tetrahydrochloride staining was enhanced by adding 0.03% NiCl2 (w/v) to the solution. Controls were performed with a pre-immune rabbit serum as the first antibody. The technical control was omission of the primary Ab. The specificity of immunostaining was always assessed by competition with soluble 5 mM 3-nitrotyrosine. For anti-myeloperoxidase staining we used a rabbit anti-human myeloperoxidase polyclonal Ab (RDI Research Diagnosis Inc., Flanders, NY, USA) diluted in Tris-saline containing goat serum, 1/8 (v/v). A preliminary study on mouse bone marrow performed in order to confirm the cross-reaction was positive.

Statistical analysis

Five to eight animals were included in each experimental group. All experiments were repeated three times. The results were compared by the Mann-Whitney-Wilcoxon test and a P value £0.05 was considered to be significant.


Parasitemia and mortality

Previous studies have shown that, when infected with T. cruzi, BALB/c and C3H mice display different degrees of macrophage activation as indicated by different amounts of ROS and TNF-a production (11,29). Thus, since in the present study we evaluated the formation of ·NO and nitrotyrosine as a marker of nitro-oxidative stress during T. cruzi infection, we chose to work with the C3H and BALB/c strains. The animals were infected with a sublethal dose of parasites and treated with the NOS inhibitors L-NAME or GED or with MEG, the latter an iNOS inhibitor and peroxynitrite scavenger (23). L-NAME is a general NOS inhibitor which has already been used to inhibit ·NO production during T. cruzi infection (3,4,30). In turn, MEG and GED are guanidino compounds which are more specific for the inhibition of iNOS (31). In addition, due to its free thiol moiety, MEG reacts with peroxynitrite and its decomposition products, carbonate (CO3·-) and ·NO2 radicals, and inhibits the nitration and oxidation reactions of peroxynitrite (23). MEG also displays different anti-inflammatory effects, including the inhibition of neutrophil migration and thus can inhibit the two main pathways of 3-nitrotyrosine formation (24, 32).

The parasitemias of control and L-NAME-, MEG- or GED-treated BALB/c and C3H mice are shown in Figure 1A and B, respectively. Untreated C3H mice developed a parasitemia about one order of magnitude higher than untreated BALB/c animals. L-NAME-treated BALB/c mice had a significantly higher parasitemia (P < 0.05) throughout the infection than control animals. Unexpectedly, MEG-treated BALB/c and C3H mice developed a significantly lower parasitemia (P < 0.05, from day 15 to 25 pi, i.e., 4- and 10-fold less for MEG than control at day 20 for BALB/c and C3H, respectively) than non-treated animals. GED-treated BALB/c mice also showed a trend towards a decreased parasitemia which, however, was not statistically significant (P = 0.07). While L-NAME-treated BALB/c mice showed 100% mortality at day 19 pi, all the MEG- and GED-treated animals were alive at the end of the acute phase of the infection (Figure 2). Similarly, mortality of MEG-treated C3H mice was null at 25 days pi (data not shown). A direct lethal effect of MEG and GED on the parasite was ruled out because none of these compounds at a concentration up to 3 mM affected the growth of T. cruzi epimastigotes in culture (data not shown).

Figure 1. Parasitemia of Trypanosoma cruzi-infected BALB/c (A) and C3H/c mice (B). Mice were infected with sublethal doses of Tulahuen-2 trypomastigotes and treated with mercaptoethylguanidine (filled squares), guanido-ethyl disulfide (circles) or NG-nitro-L-arginine methyl ester (triangles), or not treated (open squares). Data are reported as means ± SEM for 5 to 8 mice per group.

[View larger version of this image (37 K JPG file)]

Figure 2. Mortality of BALB/c mice infected with sublethal doses of Tulahuen-2 trypomastigotes and treated with different iNOS inhibitors or a peroxynitrite scavenger or not treated (open squares). Mercaptoethylguanidine (filled squares), guanido-ethyl disulfide (circles), NG-nitro-L-arginine methyl ester (triangles). Five to 8 mice were used in each group.

[View larger version of this image (31 K JPG file)]

Production of ·NO

·NO production during the immune response was evaluated by measuring the NOx- levels in plasma of control and infected, treated and untreated animals, at day 25 pi. T. cruzi infection led to an elevation of NOx-in both strains of mice (Table 1). However, the infected C3H mice produced higher levels of ·NO (similar to published data, 33) than infected BALB/c animals. In turn, while L-NAME produced a profound inhibition of ·NO synthesis, MEG and GED induced only a partial inhibition. Thus, there was no direct correlation between ·NO levels (Table 1) and parasitemia (Figure 1), indicating that ·NO is not the only molecule implicated in the control of the parasite growth, and that some ·NO-derived intermediate may participate in T. cruzi clearance.

Table 1. NOx- levels in plasma of Trypanosoma cruzi-infected and treated mice and controls.

[View larger version of this table (88 K JPG file)]

Detection of nitrated plasma proteins

We measured the levels of nitrated plasma proteins in MEG- and GED-treated mice by ELISA as an index of the systemic formation of nitrating species. Table 2 shows that infected BALB/c mice had significantly higher levels of nitrated plasma proteins than uninfected mice (>7-fold), while MEG or GED treatment of infected animals significantly decreased the amount of protein 3-nitrotyrosine in plasma. Uninfected C3H mice had significantly higher basal levels of nitrated serum proteins than BALB/c mice and, when infected with T. cruzi, showed a moderate increase (~1.6-fold) in nitrated proteins compared to controls. Thus, in spite of the capacity of C3H mice to produce much higher amounts of ·NO than BALB/c mice (Table 1), in infected animals the levels of nitrated proteins were ~2-fold lower than those of BALB/c animals. In BALB/c mice, a significant decrease of nitrated serum proteins was observed when the animals were treated with MEG.

Table 2. Nitrotyrosine in plasma proteins of Trypanosoma cruzi-infected and treated mice and controls.

[View larger version of this table (87 K JPG file)]

Protein 3-nitrotyrosine in chagasic myocardiopathy

3-Nitrotyrosine in heart proteins was evaluated by immunohistochemistry. Protein 3-nitrotyrosine residues were not detected in hearts of infected animals until day 25 pi (data not shown). At this time, hemalum-eosin staining of the hearts indicated scarce inflammatory infiltrate and fibrosis. No polymorphonuclear cells were observed. Immunohistochemistry with a polyclonal anti-nitrotyrosine Ab showed diffuse myocardial immunoreactivity in infected animals (Figure 3D). The immunochemical labeling was stronger in the inflammatory areas. Intense labeling was observed in myocardial cells, with a membranous and granular cytoplasmic pattern (Figure 4). This study could not be performed in L-NAME-treated mice since all the animals died before protein 3-nitrotyrosine was detectable in the hearts. In MEG- and GED-treated mice, a trend towards less intense immunostaining was observed (data not shown), although the technique was not sensitive enough for quantitative purposes. In non-infected animals, no immunoreactivity against nitrotyrosine was observed (Figure 3A). Controls were performed to substantiate the specificity of the immunostaining, including specimens incubated with pre-immune serum (Figure 3B) and the co-incubation of the first Ab with 5 mM nitrotyrosine, which completely blocked the reactivity (Figure 3C). Anti-myeloperoxidase immunostaining showed no reactivity, consistent with the lack of neutrophil infiltration in this model.

Figure 3. Immunohistochemical staining for protein nitrotyrosine residues in heart of BALB/c mice. The immunostaining was carried out as described in Material and Methods. A, Non-infected animal; B, C and D, infected animals. B, Control with pre-immune serum; C, the anti-nitrotyrosine Ab binding was blocked with 5 mM nitrotyrosine; D, slide incubated with anti-nitrotyrosine Ab. A diffuse immunostaining (brown color) is observed in infected mice (D), but not in non-infected mice (A), neither in control (B, C). Magnification 2X.

[View larger version of this image (53 K JPG file)]

Figure 4. Immunohistochemical staining for protein nitrotyrosine residues in heart of an infected BALB/c mice. Diffuse immunostaining is observed in the myocardium (brown color), with stronger labeling in inflammatory areas, particularly around inflammatory cells (asterisk). Exceptionally, an amastigote nest was found in this slide (thin arrow), (magnification 10X). Hemalum stain nuclei in dark violet. Insert: NiCl2-intensified immunostaining. A strong immunostaining is observed in a myocardial cell membrane (thick arrow) and in the cytoplasm, where the immunostaining shows a clear granular pattern (arrowhead). Magnification, 40X.

[View larger version of this image (62 K JPG file)]


Over the last few years, abundant evidence has been obtained for a role of ·NO in the host defense against T. cruzi infection as well as in other infectious and inflammatory diseases. It is now thought that many of the toxic effects of ·NO are due to its conversion to secondary ·NO-derived oxidants including peroxynitrite (14).

In the present study, we investigated the production of 3-nitrotyrosine as an index of nitro-oxidative stress in order to determine if there is a link between 3-nitrotyrosine formation and host defense and/or pathology. Our results demonstrate that in C3H animals, despite a higher ·NO synthesis than in BALB/c mice, the generation of 3-nitrotyrosine was not proportionally enhanced and the infection was poorly controlled. L-NAME treatment effectively reduced ·NO synthesis, inducing high parasitism and mortality. As expected, MEG- and GED-treated mice produced lower levels of ·NO and 3-nitrotyrosine than untreated animals, but surprisingly a lower extent of parasitism was observed. Thus, in untreated animals, the anti-parasitic mechanisms seem to depend not only on the individual capacity to produce ·NO, but also on the way its metabolism is directed, i.e., the ability to generate ·NO-derived oxidants constitutes an important element in parasite resistance. In agreement with this idea, the results of Cardoni et al. (11) demonstrated that, when infected with T. cruzi, BALB/c mice produced higher levels of ROS (O2·-, H2O2) than C3H mice. These results could not be reproduced with MEG and GED treatments since the inhibition of ·NO and 3-nitrotyrosine formation occurred with a decreased parasitemia. In addition to its capacity to scavenge peroxynitrite, MEG has been shown to reduce IL-1ß and TNF- a and to prevent Ik-B degradation (32). On the basis of these data, we reasoned that the results obtained with pharmacological intervention of NOS should be interpreted with caution since a drug (i.e., MEG) can modulate other processes in addition to the inflammatory response. There are no data on the effects of L-NAME and GED on the inflammatory response.

Except for the work of Cummings and Tarleton (9), the current consensus is that there is a need for ·NO to control T. cruzi infection. It has been proved that mice treated with the ·NO inhibitors L-NAME (5) or NG-monomethyl-arginine (NMMA) (3,4) and iNOS knock-out mice (6) are very susceptible to the infection. However, it is important to note that ·NO induces immunosuppression by impairing T cell function. Early works have suggested its participation in the immunosuppression developed during infectious diseases characterized by strong macrophage activation, including T. brucei (34) and Salmonella typhimurium (35). During T. cruzi infection, it has been shown that the inhibition of the proliferative response of T lymphocytes of infected mice could be restored by the addition of L-NMMA (30). In addition, spleen cells from T. cruzi-infected INF-g knockout mice, that are unable to produce ·NO, have a normal proliferative response (7). Thus, ·NO cannot be regarded as a simple parasitized molecule since it displays multiple functions in the homeostasis of immune response.

We demonstrated anti-nitrotyrosine staining in hearts of infected mice. While the diffuse immunostaining suggests the formation of nitrotyrosine by myocardial cells, the concomitant induction of iNOS (36) and the presence of a stronger labeling in inflammatory areas indicate that these cells also participate in the generation of nitrating agents. A partial inhibition of iNOS and the scavenging of peroxynitrite resulted in a lower formation of 3-nitrotyrosine in chagasic myocardium. There is abundant evidence that peroxynitrite participates in different cardiac diseases, including autoimmune myocarditis, heart failure and cardiac allograft rejection (15) secondary to the nitration and inhibition of myofibrillar creatine kinase and the reduction of cell contractility. Thus, it can be postulated that peroxynitrite can mediate myocardial dysfunction during Chagas' disease. Another interesting point to investigate in chagasic myocardiopathy is the role of peroxynitrite in the loss of peripheral autonomic neurons. It has been demonstrated that T. cruzi-infected rats treated with NMMA have a decreased loss of peripheral autonomic neurons in heart and colon than untreated animals in spite of an increased parasitism in these tissues (37). A question that rises from these results is whether the neuronal damage is due directly to the inhibition of ·NO or to peroxynitrite production.

The nitrating species in our experimental model cannot be identified with certainty. However, we can speculate that peroxynitrite is responsible for most of the nitration observed. The anti-parasite response is developed mainly in lymphoid organs where the synthesis of peroxynitrite has been described (8) and in the myocardium where the anti-nitrotyrosine staining co-localizes with anti-iNOS labeling (36). In the present study, the reduced participation of polynuclear cells in the inflammatory infiltrate of the myocardium, even during the early stages of the infection, and the negativity of the immunostaining against myeloperoxidase (data not shown) allow us to suggest the idea that, in our experimental model, peroxynitrite is the main nitrating species.

The precise role of these nitrogen and ROS during T. cruzi infection in vivo remains to be elucidated. In the particular case of peroxynitrite we can speculate, in the light of published data, that it could have a direct toxic effect on the parasite and a role in the regulation of the immune response. Work from our group has demonstrated that peroxynitrite impairs the antioxidant defenses (18) as well as the energy and calcium metabolism of cultured epimastigotes and reduces their motility and replication rates (38). In agreement with this idea, Linares et al. (39) showed that peroxynitrite is the molecule responsible for the resistance of C57BL/6 mice to L. amazonensis infection. In addition, by affecting tyrosine phosphorylation pathways, peroxynitrite is able to modulate the activation and proliferation of T lymphocytes (28).

In the light of current data, we consider that the precise role of ·NO during T. cruzi infection needs to be reconsidered. In general, these data suggest that while ·NO is necessary for parasite clearance, when efficiently synergizing with other ROS (14), high ·NO levels can inhibit the anti-parasite response and produce tissue injury through the formation of peroxynitrite or other nitrating molecule. An efficient control of the infection requires ·NO levels high enough for a lytic effect, probably due to the generation of peroxynitrite or other nitrating molecule, but insufficient to promote the suppression of the immune response and tissue injury. Further work is necessary to understand the respective role of ·NO and peroxynitrite in the pathophysiology of Chagas' disease1.


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We thank Dr. Otto Pritsch for a critical reading of the manuscript.

Correspondence and Footnotes

Address for correspondence: R. Radi, Departamento de Bioquímica, Facultad de Medicina, Universidad de la República, Avda. General Flores, 2125, Montevideo 11800, Uruguay. E-mail:

Research supported by CSIC, Universidad de la República and the Howard Hughes Medical Institute. Received January 4, 2005. Accepted August 30, 2005.

1Moreover, the genetically modified NADPH oxidase knock-out mice (40) can help to define the role of macrophage-derived superoxide in infection control for which no good pharmacological strategies exist.

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