•NO is considered to be a key macrophage-derived cytotoxic effector during Trypanosoma cruzi infection. On the other hand, the microbicidal properties of reactive oxygen species (ROS) are well recognized, but little importance has been attributed to them during in vivo infection with T. cruzi. In order to investigate the role of ROS in T. cruzi infection, mice deficient in NADPH phagocyte oxidase (gp91phox−/− or phox KO) were infected with Y strain of T. cruzi and the course of infection was followed. phox KO mice had similar parasitemia, similar tissue parasitism and similar levels of IFN-γ and TNF in serum and spleen cell culture supernatants, when compared to wild-type controls. However, all phox KO mice succumbed to infection between day 15 and 21 after inoculation with the parasite, while 60% of wild-type mice were alive 50 days after infection. Further investigation demonstrated increased serum levels of nitrite and nitrate (NOx) at day 15 of infection in phox KO animals, associated with a drop in blood pressure. Treatment with a NOS2 inhibitor corrected the blood pressure, implicating NOS2 in this phenomenon. We postulate that superoxide reacts with •NO in vivo, preventing blood pressure drops in wild type mice. Hence, whilst superoxide from phagocytes did not play a critical role in parasite control in the phox KO animals, its production would have an important protective effect against blood pressure decline during infection with T. cruzi.
When pathogens enter their hosts, they are fought by several resistance strategies, including capture by phagocytes and the production of pathogen-toxic molecules. Nitric oxide, a free radical, has been extensively studied as one of these toxic molecules that successfully mediates intracellular parasite killing, including Trypanosoma cruzi, the protozoan parasite that causes Chagas' disease. On the other hand, reactive oxygen species also mediate resistance to several pathogens, mainly bacterial. In this study, we addressed the role of reactive oxygen species in the resistance to T. cruzi using gene-deficient mice, a species which phagocytes lack the ability to produce (phox−/− mice). We found that phagocyte-derived reactive oxygen species are not critical to mediate resistance to parasite in the knock-out animals. However, phox−/− mice presented higher mortality and lower blood pressure due to infection with T. cruzi than non-deficient mice. The blood pressure was restored to normal by an inhibitor of nitric oxide synthesis by phagocytes. We hypothesize that superoxide (one of the oxygen reactive species) controls blood pressure during infection with T. cruzi, by reacting with nitric oxide and preventing its action on blood vessels.
Citation: Santiago HC, Gonzalez Lombana CZ, Macedo JP, Utsch L, Tafuri WL, et al. (2012) NADPH Phagocyte Oxidase Knockout Mice Control Trypanosoma cruzi Proliferation, but Develop Circulatory Collapse and Succumb to Infection. PLoS Negl Trop Dis 6(2): e1492. doi:10.1371/journal.pntd.0001492
Editor: Diane McMahon-Pratt, Yale School of Public Health, United States of America
Received: December 13, 2010; Accepted: December 9, 2011; Published: February 14, 2012
Copyright: © 2012 Santiago et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: FUNDEP was crucial for logistic suport. This work was supported by grants from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq473597/2006-3 and 304776/2009-2), CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) and INCT de Processos Redox em Biomedicina-Redoxoma (CNPq/FAPESP/CAPES573530/2008-4). HCS, CZGL, JPM, LU, WLT, MJCS, AJR, FQC, MMT and LQV are CNPq fellows. RR was supported by grants from the National Institutes of Health (1R01AI095173-01), Howard Hughes Medical Institute and Comisión Sectorial de Investigación Científica (CSIC)/Universidad de la República, Uruguay. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
For a long time, reactive oxygen species (ROS) were considered the main anti-microbial radical produced by the immune system, playing a role against bacterial, fungal and protozoa infections. After the discovery of nitric oxide (•NO), •NO found to play a major role in host defense, especially against protozoan parasites. A role against Toxoplasma , , Plasmodium  and Leishmania ,  infections was still attributed to ROS, albeit in some cases this role remains a matter of debate , , , .
Since •NO was found to be one of the most important IFN-γ-induced anti-parasitic mechanisms, the studies about its role in different diseases was intensified. The advent of gene knockout (KO) technology allowed the dissection of the real extent of •NO involvement in parasitic diseases. •NO was found to be crucially important in a variety of infections , , however, NOS2-deficient animals are less susceptible than ifn-γ KO to most microorganisms studied , , , , . So, the search for other mechanisms of host resistance induced by IFN-γ started, and the interest in ROS warmed up again.
Trypanosoma cruzi is an intracellular parasite associated with high morbidity during both acute and chronic phases of infection. Resistance to this parasite is mostly driven by IFN-γ. This cytokine mediates the control of parasite proliferation in tissues and blood in a NOS2-dependent way. However, •NO may not be necessary for host resistance to T. cruzi infection when less virulent strains are used . In addition, previously published data suggest that NOS2 deficient mice exhibit delayed mortality when compared to ifn-γ KO mice , , denoting an additional effector mechanism involved in T. cruzi immune resistance. Further studies suggested IFN-γ-induced p47GTPase LRG-47 as one major factor of resistance to T. cruzi infection along with •NO , . Although there is convincing evidence for the effects of ROS-induced damage to T. cruzi in vitro , , the role of these reactive species in vivo has not yet been addressed.
In vitro, T. cruzi is readily phagocyted by macrophages and triggers respiratory burst , . However, production of ROS alone is not sufficient to kill parasites inside these cells , , and activation by IFN-γ, induction of NOS2 and production of •NO are required , , . In the infected macrophage, •NO reacts with superoxide yielding peroxynitrite , which is a powerful oxidant and seems to be the main effector molecule against T. cruzi . Peroxynitrite is more efficient to kill T. cruzi epimastigotes in vitro than superoxide or •NO alone . Moreover, evidence of peroxynitrite production during in vitro and in vivo infection with T. cruzi is available, as nitrated proteins are found both in macrophages and in mouse and human tissues , . Indeed, it has just been reported that internalized trypomastigotes in activated macrophages are killed by peroxynitrite-dependent mechanisms . The importance of nitro-oxidative mechanisms is underscored by the finding that virulent T. cruzi strains, which naturally have high peroxiredoxin levels , and strains overexpressing peroxiredoxins ,  are protected from peroxynitrite and macrophage-dependent nitro-oxidative killing (peroxiredoxins readily decompose peroxynitrite). Albeit nitration of proteins in vivo may be achieved independently of peroxynitrite, it is still dependent on the production of superoxide and •NO , ,  Hence, parasite damage is dependent not only on ·NO, but on both superoxide and nitric oxide.
In order to investigate the contribution of ROS in resistance to T. cruzi infection, mice deficient in the gp91phox (phox KO) subunit of NADPH oxidase, a model for chronic granulomatous disease , were used. These animals fail to produce ROS in endothelial cells, causing a defect in endothelium-derived relaxation of arteries , , and in phagocytic cells, leading to deficient resolution of bacterial and fungal infections . Although these animals were found somewhat more susceptible to Leishmania donovani , their susceptibility to L. major is still a matter of debate , . In the present study, phox KO mice were found to succumb to infection with T. cruzi, despite adequate control of parasite replication. The immunological and physiological functions of ROS in such model were investigated.
The procedures used in this study were approved by the Animal Ethics comittee at the Universidade Federal de Minas Gerais, protocol number 031/09. All care was taken to minimize animal suferring.
Inbred C57BL/6 (WT) mice (males and females, 4–6 week old) were used as controls (CEBIO, Instituto de Ciências Biológicas, UFMG, Belo Horizonte, MG, Brazil). Animals were kept in a conventional animal facility at controlled temperature, light/dark cycles and environmental barriers. The gp91phox-deficient (phox KO)  and IFN-γ- deficient (inf-γ KO)  mice, both in C57BL/6 background, were purchased from The Jackson Laboratories (Bar Harbor, ME, USA) and bred under specific pathogen free conditions at the Gnotobiology Laboratory, Departmento de Bioquímica e Imunologia, ICB, UFMG.
Parasite, infection, cytokines and serum NOx measurements
T. cruzi (Y strain) was maintained by weekly passage in Swiss mice. For in vivo experimental infections, mice were inoculated i.p. with 1000 blood-stage trypomastigotes. The parasitemia was evaluated by counting parasites in 5 µL of blood drawn from the tail vein . Mortality of infected mice was monitored daily. Spleen cell cultures were performed as previously described . Briefly, splenocytes from infected mice were obtained on day 10 after infection, and cultured at 5×106 cells/ml, in 24-well plates, with RPMI 1640 supplemented with 10% FCS, 2 mM l-glutamine, 0.05 mM 2-mercapto-ethanol, 100 U/ml penicillin, and 100 µg/ml streptomycin. Cultures were maintained at 37°C in 5% CO2 atmosphere. Supernatants were harvested 72 hours later for TNF and IFN-γ measurements. Mice were bled on days 0, 10 and 15 after infection and the level of serum cytokines was evaluated. IFN-γ and TNF were measured as described previously using specific ELISA kits (R&D Systems, Minneapolis, MN, USA) following the manufacturer's protocol. Nitrate was reduced to nitrite in lipid-free serum with nitrate reductase and measured by the Griess colorimetric reaction . ELISA and immunohistochemistry for 3-nitrotyrosine (or nitrated proteins) was performed as previously described .
Quantification of parasite tissue loads and nos2 mRNA expression by real-time PCR or real-time RT-PCR
Real-time PCR for parasite quantification was performed as described previously  with minor modifications. Briefly, on different days after infection, heart, spleen, and liver were digested with proteinase K, followed by a phenol-chloroform-isoamyl alcohol affinity extraction. Real-time PCR using 50 ng of total DNA was performed on an ABI PRISM 7900 sequence detection system (Applied Biosystems) using SYBR Green PCR Master Mix, according to the manufacturer's recommendations. The equivalence of host DNA in the samples was confirmed by measurement of genomic IL-12p40 PCR product levels in the same samples. Purified T. cruzi DNA (American Type Culture Collection) was sequentially diluted for curve generation in aqueous solution containing equivalent amounts of DNA from uninfected mouse tissues. The following primers were used for T. cruzi genomic DNA, TCZ, GCTCTTGCCCACACGGGTGC (forward), and CCAAGCAGCGGATAGTTCAGG (reverse); and for genomic il-12p40, GTAGAGGTGGACTGGACTCC (forward) and CAGATGTGAGTGGCTCAGAG (reverse).
Total RNA was isolated from spleens of WT and phox KO infected or non-infected mice and real-time RT-PCR was performed on an ABI PRISM 7900 sequence detection system (Applied Biosystems) using SYBR Green PCR Master Mix (Applied Biosystems) after RT of 1 µg RNA using SuperScript II reverse transcriptase (Invitrogen Life Technologies). The relative level of gene expression was determined by the comparative threshold cycle method as described by the manufacturer, whereby data for each sample were normalized to hypoxanthine phosphoribosyl transferase and expressed as a fold change compared with uninfected controls. The following primer pairs were used: for hypoxanthine phosphoribosyl transferase, GTTGGTTACAGGCCAGACTTTGTTG (forward) and GAGGGTAGGCTGGCCTATAGGCT (reverse); nos2, CAGCTGGGCTGTACAAACCTT (forward) and CATTGGAAGTGAAGCGTTTCG (reverse).
Hepatic and pancreatic function
Serum AST and serum Amylase were measured in sera of infected and control animals using commercially available kits and following manufactures instructions (KATAL, Belo Horizonte, MG, Brazil).
Determination of blood pressure by tail-cuff
After exposed for 5 minutes to a white lamp, WT and phox KO mice were placed in a plastic restrainer. Tail blood pressure (TBP) from the animals was measured using a pneumatic cuff placed in the base of the tail with a distally attached pulse sensor. Mice were allowed to adjust to this procedure three times a week for two weeks before experiments were performed. TBP values were recorded on a tail-cuff plethysmography Model MK-2000 using Windaq software to analyze the data. At least 10 good measurements for each animal were obtained per time point and the average of selected 5 bests readings were used as TPB for an animal (n = 6 animals per group).
Determination of blood pressures by carotid catheterization
Mean arterial pressure (MAP) was recorded continuously in anesthetized animals by Biopac System (model MP150 A-CE, Biopac Systems, CA, USA) like described previously. In brief, mice were anesthetized by using urethane (1.2 g/kpv) administered by intraperitoneal injection at different points after infection with T. cruzi. The adequacy of anesthesia was verified by the absence of a withdrawal response to nociceptive stimulation of a hindpaw. The left common carotid artery was exposed through a 1.0- to 1.5-cm midline incision in the ventral neck region. A catheter from polyethylene tubing (PE 5 Intramedic, Clay Adams, Becton Dickinson, Franklin Lakes, NJ, USA) was inserted approximately 0.25 cm into the common carotid artery and connected to pressure transducers. Supplemental doses of urethane (0.1 g/kg IV) were administered if necessary. The data were converted from digital to numeric form using acquisition software. Data were processed by calculation of 10-min means of MAP variable. Results are expressed as means ± SE. (measured in millimeters of mercury) of 2–6 animals per time point pooled from 3 independent experiments.
Treatment with iNOS inhibitors
Animals were treated with 1400SW, a NOS2 inhibitor (15 mg/Kg), i.p. on days 15 and 16 after infection with T. cruzi. On day 16, 1400W was administered 1 h before measuring MAP. During survival experiments, 1400W (20 mg/Kg) was administered i.p. daily divided in two doses or once a day beginning on day 13 after infection (a time found to not affect parasite control with NOS2 inhibition  and before MAP starts declining) for 10 days. Mice treated with vehicle were used as controls. Alternatively, animals were treated with aminoguanidine (1% w/v) in drinking water from day 13 after infection.
The significance of differences between sample means was determined by Student's t test to compare WT to phox KO group or one-way ANOVA if inf KO animals were being compared as well. A mortality difference was tested using Mantel-Cox test and groups compared using one-way ANOVA. A value of p<0.05 was considered significant.
Mice deficient in functional NADPH oxidase control T. cruzi proliferation, but do not survive infection. T. cruzi infection is known to induce a strong oxidative stress in the host with high production of ROS and NO leading to nitration of serum and target organs proteins . Results from our lab have shown that not only the ROS production is deficient in gp91phox NADPH oxidase (phox KO) genetically deficient mice as described before , but the level of nitration of serum proteins induced by T. cruzi infection in phox KO mice is only 25% of that observed in WT controls (data not shown). To better investigate the role of ROS in T. cruzi infection in vivo, phox KO animals were inoculated with the Y strain of T. cruzi. Because this is a reticulotropic strain, it is more appropriate to evaluate the effects of ROS deficiency in phagocytes in vivo. WT and phox KO mice displayed similar parasitemia, which peaked around 9 days post-infection (Fig. 1A) and was subsequently controlled. In contrast, ifn-γ KO mice presented uncontrolled parasite counts throughout the infection. WT mice presented 60–70% of survival after day 50 of infection and all IFN-γ-deficient mice died by day 15 of infection. Surprisingly, phox KO animals exhibited high mortality when compared to WT controls, starting at day 15 and reaching 100% mortality by 21 days of infection (Fig. 1B). This unexpected result led us to investigate a possible parasite proliferation in tissues. Coherently with the parasitemia data, tissue parasitism was controlled by phox KO and WT groups at 15 days post-infection in spleens, livers, and heart; ifn-γ KO animals exhibited high parasite proliferation in these organs (Fig. 2).
WT, phox KO and inf-γ KO mice were infected with 1000 blood-born trypomastigotes of Y strain of T. cruzi. Parasitemia (A) and mortality (B) were accessed daily. (A) Points represent mean ± SE of 5 animals per group of one from three different experiments performed with similar results. Asterisks represent P<0.05 by Student's t test. (B) Mortality curve is pooled from three different experiments and P<0.05 among all groups in the graph.
WT, phox KO and inf-γ KO mice infected with T. cruzi were sacrificed on days 10 and 15 post-infection and tissue parasitism in spleen, heart and liver evaluated by real-time PCR as described in material and methods. Bars represent mean ± SE of four animals per group. Arrows indicate P<0.05 between WT and phox KO animals. The parasitism of ifn-γ KO group is statistically different from WT and phox groups in all organs and times analyzed, except for the heart at day 10 post-infection.
phox KO and WT mice presented similar immune responses and pathology
The immune response from both WT and phox KO groups was analyzed. Both mouse strains displayed similar levels of TNF and IFN-γ in sera at 9 and 15 days post-infection (Fig. 3A). In addition, splenocytes from both groups produced expressive and equivalent levels of IFN-γ and TNF after 9 days of infection (Fig. 3B). Importantly, tissues from both animals exhibited similar quantitative and qualitative cellular infiltration in spleens, livers and hearts (not shown). Hepatic and pancreatic proofs were slightly increased after infection, but similar in both groups (Table 1).
(A) WT and phox KO animals infected with T. cruzi were bled at days 10 and 15 post-infection for cytokine measurements. (B) Infected mice were sacrificed at 10 days post-infection and spleen cells isolated and cultured for 72 hours, when supernatants were harvested. IFN-γ and TNF were measured by ELISA as described in material and methods. Bars represent mean ± SE of at least 4 animals per group. Experiment was repeated once with similar results.
NOx levels were exacerbated in phox KO mice with possible involvement in hemodynamic disturbances
Nitrate and nitrite (NOx) levels were evaluated in serum of infected mice. Phox KO mice exhibited about two fold higher levels when compared to WT-infected controls (Fig. 4A). Of note, NOx levels were increased in the phox KO group at the same time that mice began to die, about 15 days post-infection. The expression of nos2 gene in the liver was measured by real-time RT-PCR and both WT and phox KO mice displayed similar levels of mRNA (Fig. 4B). Because NOx levels closely relate with pressoric regulation, the blood pressure was evaluated in the tail (TBP) using the non-invasive tail-cuff method and in the carotid artery by catheterization, at different time points (Fig. 5). When we evaluated the blood pressure in the tail, we observed that WT mice presented a good control of pressure variation as infection progressed, but phox KO mice exhibited dramatic oscillations of TBP after peak parasitemia (Fig. 5A). In order to have a more accurate picture of this phenomenon, we investigated the mean arterial pressure (MAP) in a central vessel, the carotid artery. As can be observed in figure 5B, the MAP of phox KO mice dropped from levels between 80–90 mmHg before infection to 70–60 mmHg by the time the NOx levels starts to increase in the serum, at day 8 post-infection, and further down as infection progressed. WT group displayed a good control of MAP till day 12 post-infection, but a drop in the blood pressure at day 14 to a level similar to that observed in the phox KO group occurred. While WT mice restored blood pressure to normal levels, phox KO counterparts were unable to restore physiological MAP (Fig. 5B).
(A) T. cruzi-infected mice were bled at 10 and 15 days post-infection and levels of nitrate and nitrite evaluated. Bars represent mean ± SE of 4 animals per group. Asterisks indicate P<0.05 by Student's t test. (B) Spleens from infected animals were harvested at 10 and 15 days post-infection and used for RNA extraction and real-time RT-PCR as described in material and methods. NOS2 expression was evaluated after normalization with HPRT constitutive gene.
WT and phox KO animals were infected with T. cruzi and blood pressure evaluated in the tail (TBP) (A) or in the carotid artery (MAP) (B). Values represent mean ± SE of 6 mice of one from two performed (A) or 2–6 mice per time point pooled from 3 independent experiments (B). Asterisks represent P<0.05. (C) Drop in blood pressure is reverted by iNOS-specific inhibitor 1400SW. phox KO animals were infected with T. cruzi and blood pressure evaluated in the carotid artery (MAP) 16 days post-infection. Mice treated with 1400W received 15 mg/kg 24 and 1 hour before measurements. Values represent mean ± SE of 4 mice of one from two performed. Asterisks represent P<0.05. (D) 1400W did not revert mortality in phox KO mice. Mice were treated with 20 mg/kg of 1400W ip daily in single dose or divided in 2 doses starting on day 13 post-infection for 14 days. Mortality was accessed daily. Points represent mean cumulative mortality of 18–20 animals per group. Pool from 3 experiments performed with similar results (two experiments using one dose per day regime and one using two doses per day regime).
In order to verify the role of •NO produced by NOS2 in the drop of blood pressure and in mortality, phox KO mice were treated with 1400W, a selective inhibitor of NOS2. Injections with 1400W were able to inhibit •NO levels in the blood (data not shown) and to restore blood pressure levels (Fig. 5C). However, animals treated daily (not shown) or every 12 hours with 1400W displayed similar mortality rates to that of control mice (Fig. 5D). We treated the animals with a less selective NOS2 inhibitor (aminoguanidine) in the drinking water (1% w/v) from day 13 of infection and no effect was observed on the mortality of phox KO infected mice (data not shown). These treatments did not impact the control of parasite proliferation in either WT or phox KO animals, nor changed the outcome of the disease in WT mice (data not shown).
The involvement of ROS in host resistance against infectious diseases is well known , especially for bacterial and fungal infections. However, while some reports suggest the involvement of ROS in protozoa infections , , , , , others fail to find a major effect of these radicals in control of infections with L. major , T. gondii  and Plasmodium . Importantly, chronic granulomatous disease patients are known to suffer from severe bacterial and fungal infections , but rarely from severe protozoa infections . Interestingly, data from our laboratory suggests that infection with T. cruzi can induce a strong oxidative state in the host with production of •NO, ROS and superoxide causing nitration of proteins in serum and target tissue  (and data not shown). ROS is known to be produced by macrophages following in vitro T. cruzi infection and to be one of the major oxidative agents on T. cruzi, reducing its viability dramatically , , . In this study, we investigated the role of ROS on T. cruzi infection in vivo and surprisingly we found an important physiological effect of ROS, unrelated to the control of parasite.
In the present study, we found that animals deficient in gp91phox subunit of NADPH oxidase, a mouse model for chronic granulomatous disease , were able to efficiently control proliferation of Y strain of T. cruzi. Hence, parasitemia and parasite loads in spleen, liver and heart were similar in phox KO and WT mice. This result could suggest that ROS play a minor role in restriction of protozoal infection during in vivo infections. On the other hand, when carefully examined in vitro, the effects of ROS on parasite control can be appreciated, especially the effect of peroxynitrite. For example, macrophage-derived ROS and peroxynitrite were found to cause major oxidative burden on T. cruzi, reducing its viability dramatically , , . Indeed, the virulence of different parasite strains can be predicted by the expression of some enzymes involved in the parasite anti-oxidant network such as TcTS, TXN, TcMPX, TcAPX and FeSOD-A . The fact that macrophage-derived ROS were found to have little involvement in parasite control in phox KO mice may be related to other mechanisms of resistance operating in vivo such as compensatory •NO production, p47GTPases expression , , CD8 T cells involvement  and alternative cellular sources of superoxide and peroxynitrite. Regarding this last point, we should indicate that normally, in activated macrophages, phagocyte-derived superoxide reacts with •NO to yield peroxynitrite ; thus, in wild type animals superoxide from inflammatory cells plays a key role in •NO-dependent cytotoxicity towards T. cruzi . However, in the phox KO mice, the lack of macrophage-derived superoxide, increases the •NO levels diffusing into the parasite, which in turn, inhibit the parasite mitochondrial respiration and secondarily enhance mitochondrial superoxide formation . Overall, these processes lead to intramitochondrial formation of peroxynitrite and T. cruzi cytoxicity. Indeed, the exceeding available •NO in phox KO could be responsible for parasite control, including the formation of peroxynitrite in parasite mitochondria  or by NOX4, recently found in macrophages . Higher levels of •NO found in sera from phox KO mice could not be attributed to higher expression of NOS2. This could be explained simply by the fact that •NO is not reacting with superoxide to yield peroxinitrite in phox KO. Another possibility is raised by the fact that superoxide facilitates uncoupling of NOS and oxidation of tetrahidrobiopterin, therefore in its absence NOS would be more active and produce more •NO .
In addition to their anti-infection role, ROS are involved in enhancing TLR signaling. Recently, it was demonstrated that ROS production is activated by TLR signaling through MyD88 and via the p38 MAPKinase cascade . After their production is activated by TLR-dependent or independent pathways, ROS are able to enhance TLR4 expression on the cell surface  and to strength NF-κB activation . The resistance to infection with T. cruzi is known to depend on appropriate MyD88 signaling  after stimulation of TLR2 and TLR9 , and TLR4 . Although this function of ROS could result in improved immunity to T. cruzi, it seemed to have no critical role in our system. Our results show that phox KO mice exhibited no immune impairment, producing equivalent amounts of IFN-γ and TNF in response to infection and presenting similar histopathology (data not shown) to their WT partners.
Surprisingly, despite the ability of phox KO mice to restrict T. cruzi infection and mount an efficient immune response, they completely succumbed to infection by day 20 post-inoculation with T. cruzi. Further investigation showed that both WT and phox KO animals exhibited increased levels of NOx in sera from day 8 to 15 post-infection. However, the levels of nitrogen intermediates were higher in phox KO at day 15, coinciding with the initiation of mortality. •NO is produced by three different isoforms of nitric oxide synthase (NOS1 or neuronal NOS, NOS2 or inducible and NOS3 or endothelial) and is known to play a pleiotropic role in host physiology , , , . In addition to having potent anti-microbial properties, •NO is involved in neurotransmission, gene expression and blood pressure regulation. For example, hyper-production of •NO has severe consequences to the host, being the cause of hypotension during septic shock . During T. cruzi infection, uncontrolled immune response has been proven to be deleterious to the host, as is the case of infection in the absence of IL10 , . In phox KO animals excess •NO was associated with peripheral blood pressure variations, not observed in WT controls and, more importantly, with early and permanent drop in central MAP. An important drop in MAP of WT animals was also observed, but this hypotension happened later than in phox KO mice and was transitory, lasting for no longer than 3 days. Although WT mice showed death rate of 40% starting on day 20 post-infection, we do not think this mortality is associated with the levels of •NO since it starts after full recovery of blood pressure levels. From this study, we can conclude also that several factors might be involved in death associated with experimental T. cruzi infection. For example, the fact that treatment with 1400W prevented blood pressure drop in phox KO mice implicates NOS2. However, treatment was not able to prevent death. Inhibition of NOS using NOS inhibitors early in T. cruzi infection results in higher mortality due to infection , . In contrast, treatment of T. cruzi-infected mice with NOS inhibitors in the chronic phase of the infection (Tulahuen strain) was not detrimental to the host's ability to control parasitism . In addition, NOS2-deficient animals, in contrast to ifn-γ KO mice, can survive if treated with suboptimal doses of benzonidazole during peak of parasitemia even if the drug is withdrawn after parasite control . We followed parasitemia in animals treated with NOS2 inhibitors after parasitemia was controlled and we did not observe recrudescence of parasite proliferation. These data suggest that •NO may have an important role especially in the acute phase of the infection, in contrast to chronic phase when other IFN-γ-dependent mechanism controls the infection. The fact that NOS2 inhibition, although improving blood pressure, did not prevent mortality in our experiment could suggest that the cause of death may be multi-factorial possibly involving changes in hematological parameters (infection associated anemia and leucopenia)  or cardiac function ,  and demands further investigation. However, data from shock models show that restoring blood pressures to normal levels may not rescue animals from death. The reason for this failure would be that the iNOS inhibition enhances the accumulation of activated leukocytes into vital organs, thus increasing tissue lesions. Also, inhibition of iNOS reduces the perfusion of the organs , , , , .
Another very interesting side of ROS actions started to be depicted recently. ROS have been shown to regulate vasoactive properties of •NO. Nitric oxide is known to react with the heme group of guanylate cyclase activating the production of cGMP that promotes vasodilation . Accordingly, some inhibitors of guanylate cyclase, such as methylene blue, induce ROS production. In addition, ROS derived from endothelial NAPDH oxidase containing gp91phox is a potent vasoconstrictor because it scavenges •NO before •NO activates guanilate cyclase , . Hence, one unifying hypothesis to explain an important part of our observations is that T. cruzi infection stimulates a strong production of •NO and phox KO animals cannot produce ROS in order to counteract the systemic effect of •NO. Coherently, despite elevated levels of NOx detected in sera of phox KO animals, they expressed similar levels of NOS2 by real-time RT-PCR in the spleen. This fact and the finding that IFN-γ and TNF are not increased in phox KO animals suggest that it is not likely that elevated NOx in serum is due to augmented production, but may be related to impaired ROS production and its role in scavenging •NO. We propose that the reaction of ROS and •NO to generate peroxynitrite, in addition to strengthening the killing effects of •NO by augmenting its oxidative properties , has an important role in regulating •NO signaling and its systemic effects during T. cruzi infection.
We are indebted to Antonio Mesquita Vaz for excellent animal care, to Dr. Tom Nuttman for providing 1400W, to Dr. Yara Quercia Vieira and Mr. Edgar Sleifer for reagents and to Dr. Fabiana Romão Machado for help in experiments and useful suggestions.
Conceived and designed the experiments: HCS CZGL FQC MMT RR LQV. Performed the experiments: HCS CZGL JPM LU WLT. Analyzed the data: HCS CZGL FQC MMT RR LQV. Contributed reagents/materials/analysis tools: MJCS ROA JCFAF AJR FQC MMT. Wrote the paper: HCS CZGL RR LQV.
- 1. Murray HW, Rubin BY, Carriero SM, Harris AM, Jaffee EA (1985) Human mononuclear phagocyte antiprotozoal mechanisms: oxygen-dependent vs oxygen-independent activity against intracellular Toxoplasma gondii. J Immunol 134: 1982–1988.
- 2. Shrestha SP, Tomita T, Weiss LM, Orlofsky A (2006) Proliferation of Toxoplasma gondii in inflammatory macrophages in vivo is associated with diminished oxygen radical production in the host cell. Int J Parasitol 36: 433–441.
- 3. Golenser J, Kamyl M, Tsafack A, Marva E, Cohen A, et al. (1992) Correlation between destruction of malarial parasites by polymorphonuclear leucocytes and oxidative stress. Free Radic Res Commun 17: 249–262.
- 4. Blos M, Schleicher U, Soares Rocha FJ, Meissner U, Rollinghoff M, et al. (2003) Organ-specific and stage-dependent control of Leishmania major infection by inducible nitric oxide synthase and phagocyte NADPH oxidase. Eur J Immunol 33: 1224–1234.
- 5. Murray HW, Nathan CF (1999) Macrophage microbicidal mechanisms in vivo: reactive nitrogen versus oxygen intermediates in the killing of intracellular visceral Leishmania donovani. J Exp Med 189: 741–746.
- 6. Assreuy J, Cunha FQ, Epperlein M, Noronha-Dutra A, O'Donnell CA, et al. (1994) Production of nitric oxide and superoxide by activated macrophages and killing of Leishmania major. Eur J Immunol 24: 672–676.
- 7. Ding M, Kwok LY, Schluter D, Clayton C, Soldati D (2004) The antioxidant systems in Toxoplasma gondii and the role of cytosolic catalase in defence against oxidative injury. Mol Microbiol 51: 47–61.
- 8. Plewes KA, Barr SD, Gedamu L (2003) Iron superoxide dismutases targeted to the glycosomes of Leishmania chagasi are important for survival. Infect Immun 71: 5910–5920.
- 9. Sobolewski P, Gramaglia I, Frangos JA, Intaglietta M, van der Heyde H (2005) Plasmodium berghei resists killing by reactive oxygen species. Infect Immun 73: 6704–6710.
- 10. Brunet LR (2001) Nitric oxide in parasitic infections. Int Immunopharmacol 1: 1457–1467.
- 11. Green SJ, Scheller LF, Marletta MA, Seguin MC, Klotz FW, et al. (1994) Nitric oxide: cytokine-regulation of nitric oxide in host resistance to intracellular pathogens. Immunol Lett 43: 87–94.
- 12. Adams LB, Dinauer MC, Morgenstern DE, Krahenbuhl JL (1997) Comparison of the roles of reactive oxygen and nitrogen intermediates in the host response to Mycobacterium tuberculosis using transgenic mice. Tuber Lung Dis 78: 237–246.
- 13. Cummings KL, Tarleton RL (2004) Inducible nitric oxide synthase is not essential for control of Trypanosoma cruzi infection in mice. Infect Immun 72: 4081–4089.
- 14. Michailowsky V, Silva NM, Rocha CD, Vieira LQ, Lannes-Vieira J, et al. (2001) Pivotal role of interleukin-12 and interferon-gamma axis in controlling tissue parasitism and inflammation in the heart and central nervous system during Trypanosoma cruzi infection. Am J Pathol 159: 1723–1733.
- 15. Scharton-Kersten TM, Yap G, Magram J, Sher A (1997) Inducible nitric oxide is essential for host control of persistent but not acute infection with the intracellular pathogen Toxoplasma gondii. J Exp Med 185: 1261–1273.
- 16. Huang H, Chan J, Wittner M, Jelicks LA, Morris SA, et al. (1999) Expression of cardiac cytokines and inducible form of nitric oxide synthase (NOS2) in Trypanosoma cruzi-infected mice. J Mol Cell Cardiol 31: 75–88.
- 17. Koga R, Hamano S, Kuwata H, Atarashi K, Ogawa M, et al. (2006) TLR-dependent induction of IFN-beta mediates host defense against Trypanosoma cruzi. J Immunol 177: 7059–7066.
- 18. Santiago HC, Feng CG, Bafica A, Roffe E, Arantes RM, et al. (2005) Mice deficient in LRG-47 display enhanced susceptibility to Trypanosoma cruzi infection associated with defective hemopoiesis and intracellular control of parasite growth. J Immunol 175: 8165–8172.
- 19. Alvarez MN, Piacenza L, Irigoin F, Peluffo G, Radi R (2004) Macrophage-derived peroxynitrite diffusion and toxicity to Trypanosoma cruzi. Arch Biochem Biophys 432: 222–232.
- 20. Piacenza L, Alvarez MN, Peluffo G, Radi R (2009) Fighting the oxidative assault: the Trypanosoma cruzi journey to infection. Curr Opin Microbiol 12: 415–421.
- 21. Alvarez MN, Peluffo G, Piacenza L, Radi R (2010) Intraphagosomal peroxynitrite as a macrophage-derived cytotoxin against internalized Trypanosoma cruzi: Consequences for oxidative killing and role of microbial peroxiredoxins in infectivity. J Biol Chem 286: 6627–6640.
- 22. Gazzinelli RT, Oswald IP, Hieny S, James SL, Sher A (1992) The microbicidal activity of interferon-gamma-treated macrophages against Trypanosoma cruzi involves an L-arginine-dependent, nitrogen oxide-mediated mechanism inhibitable by interleukin-10 and transforming growth factor-beta. Eur J Immunol 22: 2501–2506.
- 23. Dhiman M, Estrada-Franco JG, Pando JM, Ramirez-Aguilar FJ, Spratt H, et al. (2009) Increased myeloperoxidase activity and protein nitration are indicators of inflammation in patients with Chagas' disease. Clin Vaccine Immunol 16: 660–666.
- 24. Naviliat M, Gualco G, Cayota A, Radi R (2005) Protein 3-nitrotyrosine formation during Trypanosoma cruzi infection in mice. Braz J Med Biol Res 38: 1825–1834.
- 25. Piacenza L, Zago MP, Peluffo G, Alvarez MN, Basombrio MA, et al. (2009) Enzymes of the antioxidant network as novel determiners of Trypanosoma cruzi virulence. Int J Parasitol 39: 1455–1464.
- 26. Piacenza L, Peluffo G, Alvarez MN, Kelly JM, Wilkinson SR, et al. (2008) Peroxiredoxins play a major role in protecting Trypanosoma cruzi against macrophage- and endogenously-derived peroxynitrite. Biochem J 410: 359–368.
- 27. Radi R (2004) Nitric oxide, oxidants, and protein tyrosine nitration. Proc Natl Acad Sci U S A 101: 4003–4008.
- 28. Pollock JD, Williams DA, Gifford MA, Li LL, Du X, et al. (1995) Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production. Nat Genet 9: 202–209.
- 29. Gorlach A, Brandes RP, Nguyen K, Amidi M, Dehghani F, et al. (2000) A gp91phox containing NADPH oxidase selectively expressed in endothelial cells is a major source of oxygen radical generation in the arterial wall. Circ Res 87: 26–32.
- 30. Jung O, Schreiber JG, Geiger H, Pedrazzini T, Busse R, et al. (2004) gp91phox-containing NADPH oxidase mediates endothelial dysfunction in renovascular hypertension. Circulation 109: 1795–1801.
- 31. Dalton DK, Pitts-Meek S, Keshav S, Figari IS, Bradley A, et al. (1993) Multiple defects of immune cell function in mice with disrupted interferon-gamma genes. Science 259: 1739–1742.
- 32. Campos MA, Closel M, Valente EP, Cardoso JE, Akira S, et al. (2004) Impaired production of proinflammatory cytokines and host resistance to acute infection with Trypanosoma cruzi in mice lacking functional myeloid differentiation factor 88. J Immunol 172: 1711–1718.
- 33. Ding AH, Nathan CF, Stuehr DJ (1988) Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production. J Immunol 141: 2407–2412.
- 34. Cummings KL, Tarleton RL (2003) Rapid quantitation of Trypanosoma cruzi in host tissue by real-time PCR. Mol Biochem Parasitol 129: 53–59.
- 35. Saeftel M, Fleischer B, Hoerauf A (2001) Stage-dependent role of nitric oxide in control of Trypanosoma cruzi infection. Infect Immun 69: 2252–2259.
- 36. Nathan C, Shiloh MU (2000) Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens. Proc Natl Acad Sci U S A 97: 8841–8848.
- 37. Alexander J, Scharton-Kersten TM, Yap G, Roberts CW, Liew FY, et al. (1997) Mechanisms of innate resistance to Toxoplasma gondii infection. Philos Trans R Soc Lond B Biol Sci 352: 1355–1359.
- 38. Heyworth PG, Cross AR, Curnutte JT (2003) Chronic granulomatous disease. Curr Opin Immunol 15: 578–584.
- 39. Asensi V, Tricas L, Meana A, Roos D, Carton JA, et al. (2000) Visceral leishmaniasis and other severe infections in an adult patient with p47-phox-deficient chronic granulomatous disease. Infection 28: 171–174.
- 40. Piacenza L, Irigoin F, Alvarez MN, Peluffo G, Taylor MC, et al. (2007) Mitochondrial superoxide radicals mediate programmed cell death in Trypanosoma cruzi: cytoprotective action of mitochondrial iron superoxide dismutase overexpression. Biochem J 403: 323–334.
- 41. Padilla AM, Bustamante JM, Tarleton RL (2009) CD8+ T cells in Trypanosoma cruzi infection. Curr Opin Immunol 21: 385–390.
- 42. Lee CF, Qiao M, Schroder K, Zhao Q, Asmis R (2010) Nox4 is a novel inducible source of reactive oxygen species in monocytes and macrophages and mediates oxidized low density lipoprotein-induced macrophage death. Circ Res 106: 1489–1497.
- 43. Sun J, Druhan LJ, Zweier JL (2010) Reactive oxygen and nitrogen species regulate inducible nitric oxide synthase function shifting the balance of nitric oxide and superoxide production. Arch Biochem Biophys 494: 130–137.
- 44. Laroux FS, Romero X, Wetzler L, Engel P, Terhorst C (2005) Cutting edge: MyD88 controls phagocyte NADPH oxidase function and killing of gram-negative bacteria. J Immunol 175: 5596–5600.
- 45. Powers KA, Szaszi K, Khadaroo RG, Tawadros PS, Marshall JC, et al. (2006) Oxidative stress generated by hemorrhagic shock recruits Toll-like receptor 4 to the plasma membrane in macrophages. J Exp Med 203: 1951–1961.
- 46. Ryan KA, Smith MF Jr, Sanders MK, Ernst PB (2004) Reactive oxygen and nitrogen species differentially regulate Toll-like receptor 4-mediated activation of NF-kappa B and interleukin-8 expression. Infect Immun 72: 2123–2130.
- 47. Bafica A, Santiago HC, Goldszmid R, Ropert C, Gazzinelli RT, et al. (2006) Cutting edge: TLR9 and TLR2 signaling together account for MyD88-dependent control of parasitemia in Trypanosoma cruzi infection. J Immunol 177: 3515–3519.
- 48. Oliveira AC, Peixoto JR, de Arruda LB, Campos MA, Gazzinelli RT, et al. (2004) Expression of functional TLR4 confers proinflammatory responsiveness to Trypanosoma cruzi glycoinositolphospholipids and higher resistance to infection with T. cruzi. J Immunol 173: 5688–5696.
- 49. Assreuy J (2006) Nitric oxide and cardiovascular dysfunction in sepsis. Endocr Metab Immune Disord Drug Targets 6: 165–173.
- 50. Beck KF, Eberhardt W, Frank S, Huwiler A, Messmer UK, et al. (1999) Inducible NO synthase: role in cellular signalling. J Exp Biol 202: 645–653.
- 51. Bogdan C (2001) Nitric oxide and the immune response. Nat Immunol 2: 907–916.
- 52. MacMicking J, Xie QW, Nathan C (1997) Nitric oxide and macrophage function. Annu Rev Immunol 15: 323–350.
- 53. Holscher C, Mohrs M, Dai WJ, Kohler G, Ryffel B, et al. (2000) Tumor necrosis factor alpha-mediated toxic shock in Trypanosoma cruzi-infected interleukin 10-deficient mice. Infect Immun 68: 4075–4083.
- 54. Hunter CA, Ellis-Neyes LA, Slifer T, Kanaly S, Grunig G, et al. (1997) IL-10 is required to prevent immune hyperactivity during infection with Trypanosoma cruzi. J Immunol 158: 3311–3316.
- 55. Vespa GN, Cunha FQ, Silva JS (1994) Nitric oxide is involved in control of Trypanosoma cruzi-induced parasitemia and directly kills the parasite in vitro. Infect Immun 62: 5177–5182.
- 56. Malvezi AD, Cecchini R, de Souza F, Tadokoro CE, Rizzo LV, et al. (2004) Involvement of nitric oxide (NO) and TNF-alpha in the oxidative stress associated with anemia in experimental Trypanosoma cruzi infection. FEMS Immunol Med Microbiol 41: 69–77.
- 57. Durand JL, Mukherjee S, Commodari F, De Souza AP, Zhao D, et al. (2009) Role of NO synthase in the development of Trypanosoma cruzi-induced cardiomyopathy in mice. Am J Trop Med Hyg 80: 782–787.
- 58. Durand JL, Tang B, Gutstein DE, Petkova S, Teixeira MM, et al. (2006) Dyskinesis in Chagasic myocardium: centerline analysis of wall motion using cardiac-gated magnetic resonance images of mice. Magn Reson Imaging 24: 1051–1057.
- 59. Avontuur JA, Bruining HA, Ince C (1995) Inhibition of nitric oxide synthesis causes myocardial ischemia in endotoxemic rats. Circ Res 76: 418–425.
- 60. Henderson JL, Statman R, Cunningham JN, Cheng W, Damiani P, et al. (1994) The effects of nitric oxide inhibition on regional hemodynamics during hyperdynamic endotoxemia. Arch Surg 129: 1271–1274. discussion 1275.
- 61. Hickey MJ, Sharkey KA, Sihota EG, Reinhardt PH, Macmicking JD, et al. (1997) Inducible nitric oxide synthase-deficient mice have enhanced leukocyte-endothelium interactions in endotoxemia. FASEB J 11: 955–964.
- 62. Laubach VE, Shesely EG, Smithies O, Sherman PA (1995) Mice lacking inducible nitric oxide synthase are not resistant to lipopolysaccharide-induced death. Proc Natl Acad Sci U S A 92: 10688–10692.
- 63. MacMicking JD, Nathan C, Hom G, Chartrain N, Fletcher DS, et al. (1995) Altered responses to bacterial infection and endotoxic shock in mice lacking inducible nitric oxide synthase. Cell 81: 641–650.
- 64. Ignarro LJ (1990) Nitric oxide. A novel signal transduction mechanism for transcellular communication. Hypertension 16: 477–483.