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BioMed Research International
Volume 2015, Article ID 351289, 10 pages
http://dx.doi.org/10.1155/2015/351289
Review Article

Oxidative Stress Control by Apicomplexan Parasites

1Unit for Drug Discovery, Department of Parasitology, Institute of Biomedical Sciences, University of São Paulo, Avenida Professor Lineu Prestes 1374, 05508-000 São Paulo, SP, Brazil
2Department of Molecular Physiology, Westfälische Wilhelms-University Münster, Schlossplatz 8, 48143 Münster, Germany

Received 3 August 2014; Accepted 27 October 2014

Academic Editor: Kevin Tyler

Copyright © 2015 Soraya S. Bosch et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Apicomplexan parasites cause infectious diseases that are either a severe public health problem or an economic burden. In this paper we will shed light on how oxidative stress can influence the host-pathogen relationship by focusing on three major diseases: babesiosis, coccidiosis, and toxoplasmosis.

1. Apicomplexan Parasites Are Subject to Oxidative Stress from Their Host Cells

Apicomplexan parasites are the causative agents of several different diseases: malaria (Plasmodium spp.), toxoplasmosis (Toxoplasma spp.), cryptosporidiosis (Cryptosporidium spp.), and babesiosis (Babesia spp.). Apicomplexa form a large group of complex unicellular eukaryotes and belong to the higher group of the Alveolata along with Chromerida, dinoflagellates, and ciliates. Within the Apicomplexa phylum, all parasites have an infective stage, the sporozoite. The sporozoites enter the host via typical invasion machinery consisting of the apical complex, which is composed of distinct organelles such as rhoptries, micronemes, and dense granules [1]. This process is actin-myosin dependent and subsequently a new host-derived membrane, the parasitophorous vacuole, surrounds the parasite. The life cycles of these parasites are complex, containing asexual and sexual reproduction. However, all these parasites invade cells and have to adapt to the intracellular environment of their hosts. In particular, the apicomplexan parasites have to deal with the oxidative level inside their host cells. Reactive oxygen species (ROS) and oxidative stress are the result of an aerobic metabolism that generates highly reactive metabolites of molecular oxygen (O2) in the cytosol or in organelles such as the mitochondria or the peroxisomes [2]. These oxygen metabolites comprise superoxide anions and hydrogen peroxides (H2O2) or the highly reactive hydroxyl radical that is formed in the presence of metal ions via the Fenton and/or Haber-Weiss reactions [3]. Severe discrepancies in the ROS level can induce oxidative modifications in the indispensable cellular macromolecules such as DNA, proteins, and lipids [4], ultimately leading to cell death.

In order to tackle this challenge, parasites have developed a variety of different antioxidant systems such as the thioredoxin- and glutaredoxin-systems. These systems act as thiol/disulfide pairs and are thereby involved in controlling the redox state of the cell. Glutathione/glutathione disulfide (GSH/GSSG) is one of the major redox pairs that control the antioxidative capacity of the cell, while thioredoxins form an additional redox system that interacts with a different subset of proteins [5]. Trx plays an important role in different biological processes including the reduction of ribonucleotides, transcription control, and hydrogen peroxide detoxification [6, 7]. In addition to these thiol/disulfide pairs, enzymatic antioxidants are also present, which can be classified into primary or secondary antioxidants. Whereas the latter are involved in the regeneration of low molecular weight antioxidant species [8] the primary antioxidants react directly with prooxidants. The enzymes catalase (CAT) and superoxide dismutase (SOD) belong to this class. The CAT catalyses the reaction of 2H2O2 → 2H2O + O2 and thereby diminishes the cellular level of hydrogen peroxide. SODs are metallo- (M-) proteins that catalyse the dismutation of superoxide anions to form molecular oxygen and hydrogen peroxide as indicated below (Mox the oxidized and Mred the reduced state of the metalloproteins): Several common forms of SODs exist that are classified according to their metal cofactors such as Cu/Zn, Fe, or Mn. Different SODs can be present in a single cell; for example, the mammalian cells contain cytosolic Cu/ZnSODs and MnSODs in their mitochondria [9].

Antioxidants also include peroxiredoxins (Prx) which are involved in the conversion of peroxides and alkyl hydroperoxides to water or the respective alcohol and have two characteristic catalytic cysteine residues [10]. Furthermore, glutaredoxins utilize the reducing power of glutathione to catalyze disulfide reductions in the presence of NADPH and glutathione reductase (the glutaredoxin system).

Due to the fact that the redox systems play such a fundamental role for parasites [3] this paper highlights the importance of oxidative stress for host-pathogen interactions in apicomplexa; however, due to the recent article by Nepveu and Turrini [11] we would like to focus on different apicomplexan parasites other than Plasmodium.

2. Babesia: Infection and Host Response

Parasites of the genus Babesia are classified as apicomplexan and belong to the suborder Piroplasmida within the family Babesiidae. This classification is based on their capacity for invading erythrocytes, multiplication via budding rather than schizogony, and the lack of hemozoin [12]. Babesia gibsoni is a pathogen occurring in Indian dogs. The first species was described by Patton in 1910, and since then the disease has been widely reported all over the world [1315].

Babesia spp. are naturally transmitted by the bite of infected ticks, from the species I. ricinus. Other occasionally occurring mechanisms of transmission are via transplacental and perinatal routes and from contaminated blood products [15]. Among the known species, B. microti, B. divergens, and B. venatorum cause human babesiosis in Europe [12, 1618].

Similar to other members of this group, Babesia undergoes a complex life cycle involving arthropods and other mammalian hosts [19]. The cycle starts with ticks taking a blood meal thereby infecting the mammalian host with sporozoites [20], which then invade erythrocytes and reproduce through asynchronous binary fission. This results in two or sometimes four merozoites. Once present in a reservoir host, Babesia will develop into male and female gametes [18, 21].

The zoonotic Babesia reservoirs are quite diverse species including the white-footed mouse, cattle, wild ruminants, canids, shrews, and possibly cottontail rabbits. Several reservoirs are unknown for some human Babesia pathogens [18]. The cycle is completed when an ixodid tick feeds on a competent reservoir and the gametes fuse to form the zygote. Finally the pathogen undergoes a sporogonic cycle, forming the infectious sporozoites [20, 22].

The members of Babesia sensu stricto spp. group have a characteristic feature in common; they can infect ovary cells and thus be transmitted transovarially by eggs [12]. Despite this information, there are several species of Babesia, such as B. duncani, which are almost not characterised [16].

Like many aerobic parasites, Babesia lives in an oxygen-rich environment within its mammalian host (mainly during the erythrocytic stage). As a result, the pathogen is exposed to the toxic effects of ROS, which can cause damage to membrane lipids, nucleic acids, and proteins [23, 24]. Babesia is an example of the importance of the parasite’s antioxidant system for proliferation within erythrocytes [2527].

According to Regner et al., the biochemical properties of proteins of the Trx system from the bovine parasite B. bovis, the BboTrx(R) system, share several features with their counterparts in P. falciparum, such as kinetics and physical properties and the capacity for reducing S-nitrosoglutathione (GSNO) and GSSG [26] (Table 1).

Table 1: Predicted antioxidant enzymes according to the genome databases of Babesia and Cryptosporidium.

This latter competency is highly relevant, since GSH is the most abundant intracellular nonprotein thiol that represents a key-molecule within redox homeostasis. To date, three genomes of the genus Babesia were sequenced: B. bovis, B. microti, and B. equi. After sequence analysis of the B. bovis genome database, no homology to a specific glutathione reductase was identified, suggesting that B. bovis might lack this enzyme. Further, the 2-Cys peroxiredoxin present in the cytoplasm of the merozoite was characterized to be an important component of the Trx network in B. bovis and B. gibsoni, which is able to reduce ROS [23, 28].

In general, Babesia spp. parasites, as well as species of Theileria and Plasmodium, invade erythrocytes and cause anaemia of the host [18, 29, 30]. Anaemia is considered as a severe complication of babesiosis, being the major cause of mortality in infected animals. However, its pathogenesis still remains uncertain [18]. Despite the correlation between parasitism and anaemia, the severity of anaemia is not always proportional to the parasitaemia [31, 32]. This phenomenon suggests that nonparasitized erythrocytes may also be damaged by an unknown mechanism of action [32].

The parasite does not always need to control elevated ROS levels present in the host. Studies in dogs naturally infected with B. gibsoni demonstrated the presence of a host response via an increased expression level of the SOD and CAT enzymes implying the generation of ROS by the pathogen. Additionally, an elevated level of lipid peroxides within the erythrocyte was detected. Moreover, in this study it was suggested that the low level of iron, zinc, and copper in the blood seems to have an additional role in the genesis of anaemia and oxidative stress [32].

In parasites that are proliferating in erythrocytes, the liver plays an essential role in clearing infected red blood cells [30]. It has been shown by flow cytometry analysis that B. divergens induces hepatic tissue damage via oxidative stress, leading to an alteration in the cell metabolism. Further, it has been demonstrated that ROS damage hepatocytes, thereby affecting the function of the liver [33]. This study also observed a significant decrease in the total antioxidant capacity during B. divergens infections. This was shown by decreased GSH and CAT levels as well as a significant increase in the concentration of malondialdehyde (MDA). The increased level of MDA strongly suggests lipid peroxidation and alteration of the nitrite/nitrate levels [34]. Increased levels of MDA have also been reported in B. gibsoni infections [32] and in double infections of Ehrlichia canis and B. gibsoni [34, 35].

Currently there are several drugs used for the treatment of human babesiosis. Atovaquone, azithromycin, clindamycin, and quinine are drugs that show activity in Babesia animal models [12]. Due to spreading drug resistance, there are currently only two major antimicrobial treatments present, which consist of a combination therapy of antimalarial drugs and antibiotics such as quinine and clindamycin or atovaquone and azithromycin [12, 36, 37]. The use of antibiotics is considered to target the apicoplast, an organelle which is also present in the apicomplexan parasites Toxoplasma and Plasmodium [38].

3. Cryptosporidium: A Resistant Pathogen

The protozoan pathogen Cryptosporidium was described first by Tyzzer, which is a worldwide occurring coccidian parasite causing gastroenteritis in mammals. The main pathway of infection is the uptake of oocysts via food consumption [39, 40].

Cryptosporidium spp., in contrast to other apicomplexan parasites, have a monoxenous life cycle that takes place in the gastrointestinal tract of the host. During the excystation, four infective sporozoites, which are released from the oocyst, glide over the intestinal cells until they invade the cell using the apical complex. After infection the parasite develops at the apical surface in the host cell; thus the parasite is in an intracellular but extracytoplasmic state. Inside the parasitophorous vacuole, Cryptosporidium spp. are protected from the gut environment and use nutrients via an Apicomplexa-unique feeder organelle. Uniquely amongst other apicomplexan parasites, Cryptosporidium spp. lack an apicoplast and also have lost the mitochondrial genome and most of its functions [41, 42].

The first report of cryptosporidiosis was in the early 20th century while the first case in humans was reported in 1976 [4345]. Today Cryptosporidium spp. are known as the major waterborne parasite worldwide with an important economic impact and a source of diarrhea in calves and lambs [46]. Although Cryptosporidium spp. are also pathogenic for humans, clinical symptoms such as diarrhea are restricted to immune-deficient people. However, immune-compromised patients (e.g., HIV/AIDS patients) are at higher risk and cryptosporidiosis can lead to dehydration, wasting, and even death [4754].

While various Cryptosporidium spp. were detected in humans, over 90% belong to the most common species C. hominis and C. parvum [55, 56]. Little is known about their pathogenic factors due to difficulties in in vitro culturing and only oocysts have been biochemically analyzed so far [5759]. To date, the genome sequencing project of C. hominis and C. parvum has discovered about 25 putative virulence factors [58].

One of these factors is an acid phosphatase in C. parvum [60]. Aguirre-García and Okhuysen have shown the activity of the membrane-bound enzyme in the oocyst [60]. They suggest that the acid phosphatase similar to those in Leishmania spp. Coxiella burnetii, Legionella micdadei, and Francisella tularensis has an important role for the survival of the intracellular pathogens [6164]. Acid phosphatases are known to inhibit the respiratory burst of human neutrophils and macrophages [6567].

Only limited information is present of the antioxidant enzymes in Cryptosporidium spp. While the enzymes glutathione transferase, glutathione reductase, and glutathione peroxidase seem to be absent in C. parvum (Table 1), some SOD activity has been detected [68]. Further, it has been shown that the parasite contains and synthesizes GSH and possesses a thioredoxin peroxidase that could be important for detoxification and thereby protection against ROS [6972] (Table 1). Previous studies suggested that the antioxidant enzymes might have a protective effect against ROS that occurs via inflammation or phagocytosis by macrophages [68].

To enhance the negative effect of oxidative stress on C. parvum, the use of selenium (Se) seems promising [73, 74]. Selenium compounds are able to react with thiols such as GSH which lead to elevated levels of superoxide and hydrogen peroxide [75]. Interestingly, Se-supplemented C. parvum-infected mice show a decreased number of oocysts in feces and a longer survival time than the respective control [73]. On the other hand Se-deficiency results in a heavy oocyst shedding, a higher susceptibility of the host to C. parvum, and a decreased immune response [73, 74].

A major problem is the high resistance of the parasite to common disinfectants such as chlorine [48, 76, 77]. The disinfecting effect of chlorine is based on free radicals, which seem to react with the plasma membrane [78]. As a response C. parvum initiates the expression of the chaperone Hsp70 [79]. Bajszár and Dekonenko suggest that this chaperone protects membrane proteins against protein denaturation caused by oxidative stress, as already known for the bacterial Hsp33 [79, 80].

4. Eimeria: Effect of Diet Supplementation upon Oxidative Balance

Eimeria spp. are etiologic agents of coccidiosis [81]. Although some organisms such as reptiles, mammals, and fish can be infected with coccidia, the majority of the studies were focussed on species infecting poultry, such as E. tenella, E. brunetti, E. praecox, E. mitis, E. acervulina, E. necatrix, and E. maxima. Due to the huge economic significance, there is an urgent need for strategies to control the parasite [82, 83]. Eimeria ssp. usually differ in pathogenesis and tissue tropism. The transmission of coccidiosis is facilitated by a faecal-oral-mechanism of contaminated water or food which initiates the comprehensive life cycle [83].

The current strategy for coccidiosis control relies on (i) the parasite’s cofactor metabolism (synthetic drugs), such as ethopabate, sulphonamides, pyrimethamine, and amprolium [84], (ii) the mitochondrial metabolism, employing drugs such as quinolone which blocks electron transport [85] and the triazinetrione compound toltrazuril, which reduces the activity of certain enzymes in the respiratory chain [86]; and (iii) the balance of ions, using drugs like polyether antibiotics or ionophores which induce osmotic damage [87]. Furthermore, some drug combinations of currently unknown mode of action have shown promising effects [88]. However, as already known from other drug based therapies, the indiscriminate use of anticoccidian compounds leads to the development of resistant strains [89].

Eimeria infections can harm the host, among other classically described mechanisms [22], due to an imbalance of the antioxidant defence system [90, 91]. In order to control the oxidative environment of the host, E. tenella increases the level of antioxidative enzymes such as CAT during infection [90].

As outlined above, interfering with the redox homeostasis makes the cell vulnerable to ROS and can cause cell damage. Classical biological markers such as MDA and lipid peroxidation (LPO) have elevated concentrations in E. tenella- and E. acervulina-infected birds [9294].

Sepp and colleagues showed that greenfinches fed on an excess of carotenoids as an antioxidant were able to manage chronic Eimeria infection [95]. Based on this it has been suggested to use food supplements such as 2Gly·ZnCl2·2H2O [92], vitamin A, vitamin E, vitamin C, and low-molecular endogenic antioxidants for controlling E. tenella infections [82, 96, 97].

5. Toxoplasma: Oxidative Stress, a Source of Drug Targets

Infection with the parasite Toxoplasma gondii has a worldwide distribution [22]. The parasite is transmitted by warm-blooded animals, from the mother to fetus (congenital) and also by food-borne transmission [22]. In many cases the immune system can prevent the symptoms; however, T. gondii infections can be lethal for immune deficient people such as HIV patients [98]. Moreover, during pregnancy the fetus is at particular risk since the disease can affect the nervous system, eyes, and other organs [99].

The life cycle of T. gondii begins with the ingestion of tissue cysts by cats, the definitive host. Once inside the (human) intestine, the oocyst excysts and subsequently the tachyzoites invade cells using a characteristic active invasion mechanism. Within the tissues T. gondii is infective for various cell types. Like the malaria parasite T. gondii forms a parasitophorous vacuole during the invasion process [100].

In the parasitophorous vacuole the parasite already induces the production of IL-10 (interleukin 10) and TGF-β (transforming growth factor β). In this manner, T. gondii is able to modulate the innate and adaptative host immune system in order to reduce the immune response rather than its complete inhibition [101]. The stress deriving from the host’s immune system can induce differentiation from the highly replicative and invasive form (tachyzoite) towards the persisting bradyzoite stage [102].

In the early phases of invasion, macrophages and natural-killer cells are primarily responsible for defeating the parasite [103]. Classically, these cells use ROS against pathogens; therefore the antioxidant defence system of T. gondii became attractive for drug discovery.

Regardless of the CAT’s importance in detoxifying H2O2, this enzyme is lacking in most pathogenic protozoans [8]. Unusually, the T. gondii genome encodes for a catalase [104]. Based on similarity analysis with respective homologues, the enzyme requires NADPH and a haem group as cofactors [105]. Much had been discussed about the localisation and role of the catalase in the parasite. Initially a classical peroxisomal localisation was suggested, whereupon the parasite would use the catalase for detoxifying by-products within peroxisomes [10]. However, the cytosolic localisation has been recently confirmed by microscopy and corroborated by the absence of peroxisome biogenesis factor (PEX) proteins in T. gondii (Figure 1) [106]. A cytosolic catalase can act on the detoxification of the majority of host born peroxides due to its high substrate turnover [104, 105].

Figure 1: Toxoplasma gondii peroxidases: the cytosolic superoxide dismutase (SODB1) is involved in the conversion of superoxide anion into hydrogen peroxide (H2O2) followed by either the conversion to water by the peroxiredoxins (Prx1 and Prx3) or the conversion to water and molecular oxygen (O2) by the enzyme catalase (CAT). Within the mitochondrion, the superoxide anion can be converted to hydrogen peroxide via two different superoxide dismutases (SOD2 and SOD3), which can be converted to water when coupled with the 1-cys peroxiredoxin. Prx2 is also involved in the detoxification of organic peroxides (for instance, the nC-OOH) towards the respective alcohol [102, 104, 107, 109, 121].

Additionally, catalase seems to have an important role in invasion and replication inside the parasitophorous vacuoles according to knock-out studies [107]. Here, the knock-out cell line was more susceptible to peroxide exposure and was also less virulent to mice [107]. This is consistent with studies demonstrating that reduced catalase expression could diminish the infection efficacy in mice [108].

Peroxiredoxins can support the catalase in its detoxification of reactive oxygen species. Currently, three peroxiredoxins have been found in T. gondii. They have different catalytic mechanisms, subcellular localisations, and roles in the parasite metabolism.

The peroxiredoxin 2 (Prx2, Figure 1) belongs to the 1-cys group which, unlike the other peroxiredoxin groups, possesses just one catalytic cysteine residue. Despite this dissimilarity, Prx2 is still able to detoxify H2O2 in the presence of dithiothreitol [107, 109]. It is worth mentioning that up to date no endogenous reducing partner has been identified, despite the fact that glutathione, lipoic acid, thioredoxin, and glutaredoxin have all been tested as electron donors for the regeneration of the protein [109]. Prx2-overexpressing parasites showed an increased resistance against H2O2 stress, which allowed the pathogen to survive after applying oxidative stress [107]. Additionally, further experiments suggest another role for Prx2. The 1-cys peroxiredoxins are bifunctional enzymes with phospholipase activity and its overexpression is related to membrane protection against oxidative stress [110, 111].

Furthermore, T. gondii possesses two other peroxiredoxins, Prx1 and Prx3, which belong to the typical 2-cys peroxiredoxins habouring two cysteine residues for forming intermolecular disulphide bonds [10, 112]. Normally peroxiredoxins are considered as proteins with a slow conversion rate [10]. The TgPrx1 is a cytosolic enzyme with constitutive expression which, differentially from Prx2 and Prx3, has an unusually high efficiency in dealing with peroxides (Figure 1, Table 2) [109].

Table 2: Antioxidant enzymes in T. gondii.

Prx3 is localised in the mitochondrion and there likely to be involved in the detoxification of its own metabolism-derived ROS and their respective by-products [107, 113, 114]. The function of Prx3 might be assisted by another set of enzymes; two SODs are also present in the parasite’s mitochondrion (Table 2) [107].

SOD2 and SOD3 have been localised in the parasite’s mitochondrion. They have conserved residues to bind iron and although very similar in the primary sequence to SODs from P. falciparum, their configuration is more characteristic to prokaryotes [107]. There is a third cytosolic superoxide dismutase, SODB1, previously characterized as Fe-binding enzymes, which is different to the Mn-binding enzyme in humans. Studies have demonstrated that this gene is essential, as SODB1 knock-outs are lethal [115]. SODs are present in almost all developmental stages of T. gondii and in all organelles, pointing out the importance of a rapid detoxification of superoxide anions in order to protect the parasite.

The classical antioxidant systems such as Trx and GSH are also suggested to occur in Toxoplasma, which is corroborated by the presence of trx genes in the transcriptome as reviewed previously [116]. The glutathione biosynthetic enzymes are present in the genome of T. gondii (Table 2). However, no experimental data are available about these enzymes.

Currently, the treatment of toxoplasmosis relies on inhibitors such as pyrimethamine and atovaquone, in a similar way to the treatment of malaria [117]. In malaria artemisinin has been proposed to interfere with the parasite’s oxidative homeostasis, today being one of the most effective drugs for malaria treatment. Artemisinin has also been experimentally used against T. gondii, however, with only moderate effect in comparison to malaria [118, 119]. This, besides other factors, might underline the importance of the antioxidant systems for the parasite [120].

Regardless of the variety of antioxidant systems presented in this review, T. gondii is still highly susceptible to oxidative stress as demonstrated by the use of stress inductors, such as juglone, phenazine methylsulfate and t-BuOOH, affecting the tachyzoites stage even at the nanomolar range, without harming the host [109]. The antioxidant systems in T. gondii are essential and therefore good candidates for the discovery of novel drugs.

6. Conclusion

This review highlights the importance of the antioxidant systems of apicomplexan parasites, which are essential for tackling oxidative stress and consequently indispensable for the survival of the pathogens in their hosts. Parasites such as T. gondii and Babesia have developed a complex antioxidant defence system for surviving inside the host cell. Oxidative stress not only is a problem for intracellular survival but also occurs during infection when the parasite is exposed to the host’s immune system, which uses ROS to fight the infection. In summary all apicomplexa are highly susceptible to oxidative stress and therefore selective interference with the redox homeostasis of these pathogens presents excellent drug target qualities.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors’ Contribution

Soraya S. Bosch, Thales Kronenberger, Kamila A. Meissner, and Flávia M. Zimbres contributed equally to this work.

Acknowledgments

The authors would like to thank Dr. Matthew R. Groves, University of Groningen, for critical reading of the paper and helpful comments. This work was financially supported by Grant nos. 2009/54325-2, 2010/20647-0, 2011/13706-3, 2011/19703-6, 2012/12807-3, 2013/17577-9, and 2013/10288-1 from the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (Grant no. 445391/2014-6). The authors would also like to acknowledge the CAPES/DAAD support within the UNIBRAL programme entitled “INFECTBIO-USP-WWU” (081/14) between the Universities of Münster (WWU) and São Paulo (USP).

References

  1. H. Mehlhorn, Encyclopedia of Parasitology, Springer, 3rd edition, 2008.
  2. A. Y. Andreyev, Y. E. Kushnareva, and A. A. Starkov, “Mitochondrial metabolism of reactive oxygen species,” Biochemistry, vol. 70, no. 2, pp. 200–214, 2005. View at Publisher · View at Google Scholar · View at Scopus
  3. K. M. Massimine, M. T. McIntosh, L. T. Doan et al., “Eosin B as a novel antimalarial agent for drug-resistant Plasmodium falciparum,” Antimicrobial Agents and Chemotherapy, vol. 50, no. 9, pp. 3132–3141, 2006. View at Publisher · View at Google Scholar · View at Scopus
  4. D. Trachootham, W. Lu, M. A. Ogasawara, N. R.-D. Valle, and P. Huang, “Redox regulation of cell survival,” Antioxidants and Redox Signaling, vol. 10, no. 8, pp. 1343–1374, 2008. View at Publisher · View at Google Scholar · View at Scopus
  5. D. P. Jones and Y.-M. Go, “Redox compartmentalization and cellular stress,” Diabetes, Obesity and Metabolism, vol. 12, supplement 2, pp. 116–125, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. E. S. J. Arnér and A. Holmgren, “Physiological functions of thioredoxin and thioredoxin reductase,” European Journal of Biochemistry, vol. 267, no. 20, pp. 6102–6109, 2000. View at Publisher · View at Google Scholar · View at Scopus
  7. J. Nordberg and E. S. J. Arnér, “Reactive oxygen species, antioxidants, and the mammalian thioredoxin system,” Free Radical Biology and Medicine, vol. 31, no. 11, pp. 1287–1312, 2001. View at Publisher · View at Google Scholar · View at Scopus
  8. B. Halliwell, “Antioxidant defence mechanisms: from the beginning to the end (of the beginning),” Free Radical Research, vol. 31, no. 4, pp. 261–272, 1999. View at Publisher · View at Google Scholar · View at Scopus
  9. I. Fridovich, “Superoxide radical and superoxide dismutases,” Annual Review of Biochemistry, vol. 64, pp. 97–112, 1995. View at Publisher · View at Google Scholar · View at Scopus
  10. B. Hofmann, H. J. Hecht, and L. Flohe, “Peroxiredoxins,” The Journal of Biological Chemistry, vol. 383, pp. 347–364, 2002. View at Google Scholar
  11. F. Nepveu and F. Turrini, “Targeting the redox metabolism of Plasmodium falciparum,” Future Medicinal Chemistry, vol. 5, no. 16, pp. 1993–2006, 2013. View at Publisher · View at Google Scholar · View at Scopus
  12. A. Hildebrandt, J. S. Gray, and K.-P. Hunfeld, “Human Babesiosis in Europe: what clinicians need to know,” Infection, vol. 41, no. 6, pp. 1057–1072, 2013. View at Publisher · View at Google Scholar · View at Scopus
  13. C. J. Muhlnickel, R. Jefferies, U. M. Morgan-Ryan, and P. J. Irwin, “Babesia gibsoni infection in three dogs in Victoria,” Australian Veterinary Journal, vol. 80, no. 10, pp. 606–610, 2002. View at Publisher · View at Google Scholar · View at Scopus
  14. A. M. Kjemtrup, A. A. Kocan, L. Whitworth et al., “There are at least three genetically distinct small piroplasms from dogs,” International Journal for Parasitology, vol. 30, no. 14, pp. 1501–1505, 2000. View at Publisher · View at Google Scholar · View at Scopus
  15. W. S. Patton, “Preliminary report on a new piroplasm (Piroplasma gibsoni sp. nov.) found in the blood of the hounds of the Madras Hunt and subsequently discovered in the blood of the jackal Canis aureus,” Bulletin de la Société de Pathologie Exotique, vol. 3, pp. 274–280, 1910. View at Google Scholar
  16. D. A. Leiby, “Transfusion-transmitted Babesia spp.: Bull's-eye on Babesia microti,” Clinical Microbiology Reviews, vol. 24, no. 1, pp. 14–28, 2011. View at Publisher · View at Google Scholar · View at Scopus
  17. E. Vannier and P. J. Krause, “Human babesiosis,” The New England Journal of Medicine, vol. 366, no. 25, pp. 2397–2407, 2012. View at Publisher · View at Google Scholar · View at Scopus
  18. J. Gray, A. Zintl, A. Hildebrandt, K.-P. Hunfeld, and L. Weiss, “Zoonotic babesiosis: overview of the disease and novel aspects of pathogen identity,” Ticks and Tick-borne Diseases, vol. 1, no. 1, pp. 3–10, 2010. View at Publisher · View at Google Scholar · View at Scopus
  19. M. T. E. P. Allsopp, T. Cavalier-Smith, D. T. de Waal, and B. A. Allsopp, “Phylogeny and evolution of the piroplasms,” Parasitology, vol. 108, part 2, pp. 147–152, 1994. View at Publisher · View at Google Scholar · View at Scopus
  20. G. Uilenberg, “Babesia—a historical overview,” Veterinary Parasitology, vol. 138, no. 1-2, pp. 3–10, 2006. View at Publisher · View at Google Scholar · View at Scopus
  21. S. Gohil, L. M. Kats, A. Sturm, and B. M. Cooke, “Recent insights into alteration of red blood cells by Babesia bovis: moovin' forward,” Trends in Parasitology, vol. 26, no. 12, pp. 591–599, 2010. View at Publisher · View at Google Scholar · View at Scopus
  22. K. J. Esch and C. A. Petersen, “Transmission and epidemiology of zoonotic protozoal diseases of companion animals,” Clinical Microbiology Reviews, vol. 26, no. 1, pp. 58–85, 2013. View at Publisher · View at Google Scholar · View at Scopus
  23. T. Masatani, M. Asada, M. Ichikawa-Seki et al., “Cloning and characterization of a 2-Cys peroxiredoxin from Babesia gibsoni,” Journal of Veterinary Medical Science, vol. 76, no. 1, pp. 139–143, 2014. View at Publisher · View at Google Scholar · View at Scopus
  24. M. W. Robinson, A. T. Hutchinson, J. P. Dalton, and S. Donnelly, “Peroxiredoxin: a central player in immune modulation,” Parasite Immunology, vol. 32, no. 5, pp. 305–313, 2010. View at Publisher · View at Google Scholar · View at Scopus
  25. K. Becker, S. Gromer, R. Heiner Schirmer, and S. Müller, “Thioredoxin reductase as a pathophysiological factor and drug target,” European Journal of Biochemistry, vol. 267, no. 20, pp. 6118–6125, 2000. View at Publisher · View at Google Scholar · View at Scopus
  26. E. L. Regner, C. S. Thompson, A. A. Iglesias, S. A. Guerrero, and D. G. Arias, “Biochemical characterization of thioredoxin reductase from Babesia bovis,” Biochimie, vol. 99, no. 1, pp. 44–53, 2014. View at Publisher · View at Google Scholar · View at Scopus
  27. S. Müller, E. Liebau, R. D. Walter, and R. L. Krauth-Siegel, “Thiol-based redox metabolism of protozoan parasites,” Trends in Parasitology, vol. 19, no. 7, pp. 320–328, 2003. View at Publisher · View at Google Scholar · View at Scopus
  28. M. Tanaka, T. Sakurai, N. Yokoyama, N. Inoue, and S.-I. Kawazu, “Cloning and characterization of peroxiredoxin in Babesia bovis,” Parasitology Research, vol. 105, no. 5, pp. 1473–1477, 2009. View at Publisher · View at Google Scholar · View at Scopus
  29. L. L. Callow and P. M. Pepper, “Measurement of and correlations between fever, changes in the packed cell volume and parasitaemia in the evaluation of the susceptibility of cattle to infection with Babesia argentina,” Australian Veterinary Journal, vol. 50, no. 1, pp. 1–5, 1974. View at Publisher · View at Google Scholar · View at Scopus
  30. N. Ben Musa and H. A. Dawoud, “Immunity of Babesia divergens in the rat. Histology of the infected liver and its possible role in removing PRBC's,” Journal of the Egyptian Society of Parasitology, vol. 34, no. 3, pp. 791–806, 2004. View at Google Scholar · View at Scopus
  31. M. Kawamura, Y. Maede, and S. Namioka, “Mitogenic responsibilities of lymphocytes in canine babesiosis and the effects of splenectomy on it,” Japanese Journal of Veterinary Research, vol. 35, no. 1, pp. 1–10, 1987. View at Google Scholar · View at Scopus
  32. S. Chaudhuri, J. P. Varshney, and R. C. Patra, “Erythrocytic antioxidant defense, lipid peroxides level and blood iron, zinc and copper concentrations in dogs naturally infected with Babesia gibsoni,” Research in Veterinary Science, vol. 85, no. 1, pp. 120–124, 2008. View at Publisher · View at Google Scholar · View at Scopus
  33. L. Váli, G. Taba, K. Szentmihályi et al., “Reduced antioxidant level and increased oxidative damage in intact liver lobes during ischaemia-reperfusion,” World Journal of Gastroenterology, vol. 12, no. 7, pp. 1086–1091, 2006. View at Google Scholar · View at Scopus
  34. M. A. Dkhil, A. S. Abdel-Baki, S. Al-Quraishy, and A. E. Abdel-Moneim, “Hepatic oxidative stress in Mongolian gerbils experimentally infected with Babesia divergens,” Ticks and Tick-borne Diseases, vol. 4, no. 4, pp. 346–351, 2013. View at Publisher · View at Google Scholar · View at Scopus
  35. A. Kumar, J. P. Varshney, and R. C. Patra, “A comparative study on oxidative stress in dogs infected with Ehrlichia canis with or without concurrent infection with Babesia gibsoni,” Veterinary Research Communications, vol. 30, no. 8, pp. 917–920, 2006. View at Publisher · View at Google Scholar · View at Scopus
  36. K. P. Hunfeld, A. Hildebrandt, and J. S. Gray, “Babesiosis: Recent insights into an ancient disease,” International Journal for Parasitology, vol. 38, no. 11, pp. 1219–1237, 2008. View at Publisher · View at Google Scholar · View at Scopus
  37. G. P. Wormser, R. J. Dattwyler, E. D. Shapiro et al., “The clinical assessment, treatment, and prevention of lyme disease, human granulocytic anaplasmosis, and babesiosis: clinical practice guidelines by the Infectious Diseases Society of America,” Clinical Infectious Diseases, vol. 43, pp. 1089–1134, 2006. View at Publisher · View at Google Scholar
  38. G. Pradel and M. Schlitzer, “Antibiotics in malaria therapy and their effect on the parasite apicoplast,” Current Molecular Medicine, vol. 10, no. 3, pp. 335–349, 2010. View at Publisher · View at Google Scholar · View at Scopus
  39. E. E. Tyzzer, “An extracellular Coccidium, Cryptosporidium muris (Gen. Et Sp. Nov.), of the gastric glands of the common mouse,” The Journal of Medical Research, vol. 23, pp. 487–510, 1910. View at Google Scholar
  40. E. E. Tyzzer, “A sporozoon found in the peptic glands of the common mouse,” Proceedings of the Society for Experimental Biology and Medicine, vol. 5, pp. 12–13, 1907. View at Google Scholar
  41. J. S. Keithly, S. G. Langreth, K. F. Buttle, and C. A. Mannella, “Electron tomographic and ultrastructural analysis of the Cryptosporidium parvum relict mitochondrion, its associated membranes, and organelles,” Journal of Eukaryotic Microbiology, vol. 52, no. 2, pp. 132–140, 2005. View at Publisher · View at Google Scholar · View at Scopus
  42. G. Zhu, M. J. Marchewka, and J. S. Keithly, “Cryptosporidium parvum appears to lack a plastid genome,” Microbiology, vol. 146, part 2, pp. 315–321, 2000. View at Google Scholar · View at Scopus
  43. M. Bouzid, P. R. Hunter, R. M. Chalmers, and K. M. Tyler, “Cryptosporidium pathogenicity and virulence,” Clinical Microbiology Reviews, vol. 26, no. 1, pp. 115–134, 2013. View at Publisher · View at Google Scholar · View at Scopus
  44. J. L. Meisel, D. R. Perera, C. Meligro, and C. E. Rubin, “Overwhelming watery diarrhea associated with a cryptosporidium in an immunosuppressed patient,” Gastroenterology, vol. 70, no. 6, pp. 1156–1160, 1976. View at Google Scholar · View at Scopus
  45. F. A. Nime, J. D. Burek, D. L. Page, M. A. Holscher, and J. H. Yardley, “Acute enterocolitis in a human being infected with the protozoan Cryptosporidium,” Gastroenterology, vol. 70, no. 4, pp. 592–598, 1976. View at Google Scholar · View at Scopus
  46. C. Kourenti, P. Karanis, and H. Smith, “Waterborne transmission of protozoan parasites: a worldwide review of outbreaks and lessons learnt,” Journal of Water and Health, vol. 5, no. 1, pp. 1–38, 2007. View at Publisher · View at Google Scholar · View at Scopus
  47. P. J. O'Donoghue, “Cryptosporidium and cryptosporidiosis in man and animals,” International Journal for Parasitology, vol. 25, no. 2, pp. 139–195, 1995. View at Publisher · View at Google Scholar · View at Scopus
  48. W. L. Current, “Cryptosporidiosis,” Journal of the American Veterinary Medical Association, vol. 187, pp. 1334–1338, 1985. View at Google Scholar
  49. R. Fayer and B. L. P. Ungar, “Cryptosporidium spp. and cryptosporidiosis,” Microbiological Reviews, vol. 50, no. 4, pp. 458–483, 1986. View at Google Scholar · View at Scopus
  50. P. Forgacs, A. Tarshis, M. Federman, L. Mele, M. L. Silverman, and J. A. Shea, “Intestinal and bronchial cryptosporidiosis in an immunodeficient homosexual man,” Annals of Internal Medicine, vol. 99, no. 6, pp. 793–794, 1983. View at Publisher · View at Google Scholar · View at Scopus
  51. P. Ma and R. Soave, “Three-step stool examination for cryptosporidiosis in 10 homosexual men with protracted watery diarrhea,” Journal of Infectious Diseases, vol. 147, no. 5, pp. 824–828, 1983. View at Publisher · View at Google Scholar · View at Scopus
  52. R. Soave, R. L. Danner, C. L. Honig et al., “Cryptosporidiosis in homosexual men,” Annals of Internal Medicine, vol. 100, no. 4, pp. 504–511, 1984. View at Publisher · View at Google Scholar · View at Scopus
  53. D. D. Juranek, “Cryptosporidiosis: sources of infection and guidelines for prevention,” Clinical Infectious Diseases, vol. 21, supplement 1, pp. S57–S61, 1995. View at Publisher · View at Google Scholar · View at Scopus
  54. Y. C. Manabe, D. P. Clark, R. D. Moore et al., “Cryptosporidiosis in patients with AIDS: correlates of disease and survival,” Clinical Infectious Diseases, vol. 27, no. 3, pp. 536–542, 1998. View at Publisher · View at Google Scholar · View at Scopus
  55. S. M. Cacciò, “Molecular epidemiology of human cryptosporidiosis,” Parassitologia, vol. 47, no. 2, pp. 185–192, 2005. View at Google Scholar · View at Scopus
  56. M. Bouzid, K. M. Tyler, R. Christen, R. M. Chalmers, K. Elwin, and P. R. Hunter, “Multi-locus analysis of human infective Cryptosporidium species and subtypes using ten novel genetic loci,” BMC Microbiology, vol. 10, article 213, 2010. View at Publisher · View at Google Scholar · View at Scopus
  57. R. M. Chalmers, R. Smith, K. Elwin, F. A. Clifton-Hadley, and M. Giles, “Epidemiology of anthroponotic and zoonotic human cryptosporidiosis in England and Wales, 2004–2006,” Epidemiology and Infection, vol. 139, no. 5, pp. 700–712, 2011. View at Publisher · View at Google Scholar · View at Scopus
  58. M. S. Abrahamsen, T. J. Templeton, S. Enomoto et al., “Complete genome sequence of the apicomplexan, Cryptosporidium parvum,” Science, vol. 304, no. 5669, pp. 441–445, 2004. View at Publisher · View at Google Scholar · View at Scopus
  59. P. L. Meinhardt, D. P. Casemore, and K. B. Miller, “Epidemiologic aspects of human cryptosporidiosis and the role of waterborne transmission,” Epidemiologic Reviews, vol. 18, no. 2, pp. 118–136, 1996. View at Publisher · View at Google Scholar · View at Scopus
  60. M. M. Aguirre-Garcia and P. C. Okhuysen, “Cryptosporidium parvum: identification and characterization of an acid phosphatase,” Parasitology Research, vol. 101, no. 1, pp. 85–89, 2007. View at Publisher · View at Google Scholar · View at Scopus
  61. A. T. Remaley, D. B. Kuhns, R. E. Basford, R. H. Glew, and S. S. Kaplan, “Leishmanial phosphatase blocks neutrophil O-2 production,” The Journal of Biological Chemistry, vol. 259, pp. 11173–11175, 1984. View at Google Scholar · View at Scopus
  62. A. K. Saha, J. N. Dowling, K. L. LaMarco et al., “Properties of an acid phosphatase from Legionella micdadei which blocks superoxide anion production by human neutrophils,” Archives of Biochemistry and Biophysics, vol. 243, no. 1, pp. 150–160, 1985. View at Publisher · View at Google Scholar · View at Scopus
  63. O. G. Baca, M. J. Roman, R. H. Glew, R. F. Christner, J. E. Buhler, and A. S. Aragon, “Acid phosphatase activity in Coxiella burnetii: a possible virulence factor,” Infection and Immunity, vol. 61, no. 10, pp. 4232–4239, 1993. View at Google Scholar · View at Scopus
  64. T. J. Reilly, G. S. Baron, F. E. Nano, and M. S. Kuhlenschmidt, “Characterization and sequencing of a respiratory burst-inhibiting acid phosphatase from Francisella tularensis,” The Journal of Biological Chemistry, vol. 271, no. 18, pp. 10973–10983, 1996. View at Publisher · View at Google Scholar · View at Scopus
  65. Y. P. Li, G. Curley, M. Lopez et al., “Protein-tyrosine phosphatase activity of Coxiella burnetii that inhibits human neutrophils,” Acta Virologica, vol. 40, no. 5-6, pp. 263–272, 1996. View at Google Scholar · View at Scopus
  66. J. B. Bliska and D. S. Black, “Inhibition of the Fc receptor-mediated oxidative burst in macrophages by the Yersinia pseudotuberculosis tyrosine phosphatase,” Infection and Immunity, vol. 63, no. 2, pp. 681–685, 1995. View at Google Scholar · View at Scopus
  67. S. P. Green, E. L. Hartland, R. M. Robins-Browne, and W. A. Phillips, “Role of YopH in the suppression of tyrosine phosphorylation and respiratory burst activity in murine macrophages infected with Yersinia enterocolitica,” Journal of Leukocyte Biology, vol. 57, no. 6, pp. 972–977, 1995. View at Google Scholar · View at Scopus
  68. E. Entrala, C. Mascaro, and J. Barrett, “Anti-oxidant enzymes in Cryptosporidium parvum oocysts,” Parasitology, vol. 114, no. 1, pp. 13–17, 1997. View at Publisher · View at Google Scholar · View at Scopus
  69. S. Yoon, W.-Y. Park, and J.-R. Yu, “Recombinant thioredoxin peroxidase from Cryptosporidium parvum has more powerful antioxidant activity than that from Cryptosporidium muris,” Experimental Parasitology, vol. 131, no. 3, pp. 333–338, 2012. View at Publisher · View at Google Scholar · View at Scopus
  70. B. H. Al-Adhami, R. A. B. Nichols, J. R. Kusel, J. O'Grady, and H. V. Smith, “Cryptosporidium parvum sporozoites contain glutathione,” Parasitology, vol. 133, no. 5, pp. 555–563, 2006. View at Publisher · View at Google Scholar · View at Scopus
  71. V. Adler, Z. Yin, K. D. Tew, and Z. Ronai, “Role of redox potential and reactive oxygen species in stress signaling,” Oncogene, vol. 18, no. 45, pp. 6104–6111, 1999. View at Publisher · View at Google Scholar · View at Scopus
  72. M. Joung, S. Yoon, K. Choi, J.-Y. Kim, W.-Y. Park, and J.-R. Yu, “Characterization of the thioredoxin peroxidase from Cryptosporidium parvum,” Experimental Parasitology, vol. 129, no. 4, pp. 331–336, 2011. View at Publisher · View at Google Scholar · View at Scopus
  73. K. Huang and S. Yang, “Inhibitory effect of selenium on Cryptosporidium parvum infection in vitro and in vivo,” Biological Trace Element Research, vol. 90, no. 1–3, pp. 261–272, 2002. View at Publisher · View at Google Scholar · View at Scopus
  74. C. Wang, Y. Wu, J. Qin, H. Sun, and H. He, “Induced susceptibility of host is associated with an impaired antioxidant system following infection with Cryptosporidium parvum in se-deficient mice,” PLoS ONE, vol. 4, no. 2, Article ID e4628, 2009. View at Publisher · View at Google Scholar
  75. G. Spyrou, M. Björnstedt, S. Skog, and A. Holmgren, “Selenite and selenate inhibit human lymphocyte growth via different mechanisms,” Cancer Research, vol. 56, no. 19, pp. 4407–4412, 1996. View at Google Scholar · View at Scopus
  76. A. R. Keegan, S. Fanok, P. T. Monis, and C. P. Saint, “Cell culture-Taqman PCR assay for evaluation of Cryptosporidium parvum disinfection,” Applied and Environmental Microbiology, vol. 69, no. 5, pp. 2505–2511, 2003. View at Publisher · View at Google Scholar · View at Scopus
  77. D. G. Korich, J. R. Mead, M. S. Madore, N. A. Sinclair, and C. R. Sterling, “Effects of ozone, chlorine dioxide, chlorine, and monochloramine on Cryptosporidium parvum oocyst viability,” Applied and Environmental Microbiology, vol. 56, no. 5, pp. 1423–1428, 1990. View at Google Scholar · View at Scopus
  78. R. Virto, P. Mañas, I. Álvarez, S. Condon, and J. Raso, “Membrane damage and microbial inactivation by chlorine in the absence and presence of a chlorine-demanding substrate,” Applied and Environmental Microbiology, vol. 71, no. 9, pp. 5022–5028, 2005. View at Publisher · View at Google Scholar · View at Scopus
  79. G. Bajszár and A. Dekonenko, “Stress-induced Hsp70 gene expression and inactivation of Cryptosporidium parvum oocysts by chlorine-based oxidants,” Applied and Environmental Microbiology, vol. 76, no. 6, pp. 1732–1739, 2010. View at Publisher · View at Google Scholar · View at Scopus
  80. J. Winter, M. Ilbert, P. C. F. Graf, D. Özcelik, and U. Jakob, “Bleach activates a redox-regulated chaperone by oxidative protein unfolding,” Cell, vol. 135, no. 4, pp. 691–701, 2008. View at Publisher · View at Google Scholar · View at Scopus
  81. P. M. S. Katja Becker, Apicomplexan Parasites, Wiley-Blackwell, 2011.
  82. P. C. Allen, H. D. Danforth, and P. C. Augustine, “Dietary modulation of avian coccidiosis,” International Journal for Parasitology, vol. 28, no. 7, pp. 1131–1140, 1998. View at Publisher · View at Google Scholar · View at Scopus
  83. R. A. Walker, D. J. P. Ferguson, C. M. D. Miller, and N. C. Smith, “Sex and Eimeria: a molecular perspective,” Parasitology, vol. 140, no. 14, pp. 1701–1717, 2013. View at Publisher · View at Google Scholar · View at Scopus
  84. G. Greif, A. Harder, and A. Haberkorn, “Chemotherapeutic approaches to protozoa: coccidiae—current level of knowledge and outlook,” Parasitology Research, vol. 87, no. 11, pp. 973–975, 2001. View at Google Scholar · View at Scopus
  85. C. C. Wang, “Studies of the mitochondria from Eimeria tenella and inhibition of the electron transport by quinolone coccidiostats,” Biochimica et Biophysica Acta, vol. 396, no. 2, pp. 210–219, 1975. View at Publisher · View at Google Scholar · View at Scopus
  86. A. Harder and A. Haberkorn, “Possible mode of action of toltrazuril: Studies on two Eimeria species and mammalian and Ascaris suum enzymes,” Parasitology Research, vol. 76, no. 1, pp. 8–12, 1989. View at Publisher · View at Google Scholar · View at Scopus
  87. R. F. Shumard and M. E. Callender, “Anticoccidial drugs: screening methods,” Experimental Parasitology, vol. 28, no. 1, pp. 13–24, 1970. View at Publisher · View at Google Scholar · View at Scopus
  88. H. D. Chapman, “Biochemical, genetic and applied aspects of drug resistance in Eimeria parasites of the fowl,” Avian Pathology, vol. 26, no. 2, pp. 221–244, 1997. View at Publisher · View at Google Scholar · View at Scopus
  89. A. C. Cuckler and C. M. Malanga, “Studies on drug resistance in Coccidia,” The Journal of parasitology, vol. 41, no. 3, pp. 302–311, 1955. View at Publisher · View at Google Scholar · View at Scopus
  90. G. Eraslan, Y. Cam, M. Eren, and B. C. Liman, “Changes in malondialdehyde level and catalase activity and effect of toltrazuril on these parameters in chicks infected with Eimeria tenella,” Bulletin of the Veterinary Institute in Pulawy, vol. 48, no. 3, pp. 251–254, 2004. View at Google Scholar · View at Scopus
  91. T. Sepp, U. Karu, J. D. Blount, E. Sild, M. Männiste, and P. Hõrak, “Coccidian infection causes oxidative damage in greenfinches,” PLoS ONE, vol. 7, no. 5, Article ID e36495, 2012. View at Publisher · View at Google Scholar · View at Scopus
  92. V. Koinarski, M. Gabrashanska, N. Georgiva, and P. Petkov, “Antioxidant parameters in Eimeria acervulina infected chicks after treatment with a new zinc compound,” Bulletin of the Veterinary Institute in Pulawy, vol. 50, no. 1, pp. 55–61, 2006. View at Google Scholar · View at Scopus
  93. N. V. Georgieva, V. Koinarski, and V. Gadjeva, “Antioxidant status during the course of Eimeria tenella infection in broiler chickens,” The Veterinary Journal, vol. 172, no. 3, pp. 488–492, 2006. View at Publisher · View at Google Scholar · View at Scopus
  94. S. D. Bun, Y. M. Guo, F. C. Guo, F. J. Ji, and H. Cao, “Influence of organic zinc supplementation on the antioxidant status and immune responses of broilers challenged with Eimeria tenella,” Poultry Science, vol. 90, no. 6, pp. 1220–1226, 2011. View at Publisher · View at Google Scholar · View at Scopus
  95. T. Sepp, U. Karu, E. Sild, M. Männiste, and P. Hõrak, “Effects of carotenoids, immune activation and immune suppression on the intensity of chronic coccidiosis in greenfinches,” Experimental Parasitology, vol. 127, no. 3, pp. 651–657, 2011. View at Publisher · View at Google Scholar · View at Scopus
  96. P. C. Allen, H. Danforth, and O. A. Levander, “Interaction of dietary flaxseed with coccidia infections in chickens,” Poultry Science, vol. 76, no. 6, pp. 822–827, 1997. View at Publisher · View at Google Scholar · View at Scopus
  97. P. C. Allen, “Production of free radical species during Eimeria maxima infections in chickens,” Poultry Science, vol. 76, no. 6, pp. 814–821, 1997. View at Publisher · View at Google Scholar · View at Scopus
  98. B. J. Luft and J. S. Remington, “Toxoplasmic encephalitis in AIDS,” Clinical Infectious Diseases, vol. 15, no. 2, pp. 211–222, 1992. View at Publisher · View at Google Scholar · View at Scopus
  99. G. Desmonts and J. Couvreur, “Congenital toxoplasmosis. A prospective study of 378 pregnancies,” The New England Journal of Medicine, vol. 290, no. 20, pp. 1110–1116, 1974. View at Publisher · View at Google Scholar · View at Scopus
  100. V. Carruthers and J. C. Boothroyd, “Pulling together: an integrated model of Toxoplasma cell invasion,” Current Opinion in Microbiology, vol. 10, no. 1, pp. 83–89, 2007. View at Publisher · View at Google Scholar · View at Scopus
  101. C. Lang, U. Groß, and C. G. K. Lüder, “Subversion of innate and adaptive immune responses by Toxoplasma Gondii,” Parasitology Research, vol. 100, no. 2, pp. 191–203, 2007. View at Publisher · View at Google Scholar · View at Scopus
  102. W. Bohne, M. Holpert, and U. Gross, “Stage differentiation of the protozoan parasite Toxoplasma gondii,” Immunobiology, vol. 201, no. 2, pp. 248–254, 1999. View at Publisher · View at Google Scholar · View at Scopus
  103. E. Y. Denkers, L. Kim, and B. A. Butcher, “In the belly of the beast: Subversion of macrophage proinflammatory signalling cascades during Toxoplasma gondii infection,” Cellular Microbiology, vol. 5, no. 2, pp. 75–83, 2003. View at Publisher · View at Google Scholar · View at Scopus
  104. M. Ding, C. Clayton, and D. Soldati, “Toxoplasma gondii catalase: are there peroxisomes in Toxoplasma,” Journal of Cell Science, vol. 113, part 13, pp. 2409–2419, 2000. View at Google Scholar · View at Scopus
  105. A. J. Kaasch and K. A. Joiner, “Targeting and subcellular localization of Toxoplasma gondii catalase. Identification of peroxisomes in an apicomplexan parasite,” Journal of Biological Chemistry, vol. 275, no. 2, pp. 1112–1118, 2000. View at Publisher · View at Google Scholar · View at Scopus
  106. S. Subramani, A. Koller, and W. B. Snyder, “Import of peroxisomal matrix and membrane proteins,” Annual Review of Biochemistry, vol. 69, pp. 399–418, 2000. View at Publisher · View at Google Scholar · View at Scopus
  107. L. Y. Kwok, D. Schlüter, C. Clayton, and D. Soldati, “The antioxidant systems in Toxoplasma gondii and the role of cytosolic catalase in defence against oxidative injury,” Molecular Microbiology, vol. 51, no. 1, pp. 47–61, 2004. View at Publisher · View at Google Scholar · View at Scopus
  108. N. Nischik, B. Schade, K. Dytnerska, H. Długońska, G. Reichmann, and H.-G. Fischer, “Attenuation of mouse-virulent Toxoplasma gondii parasites is associated with a decrease in interleukin-12-inducing tachyzoite activity and reduced expression of actin, catalase and excretory proteins,” Microbes and Infection, vol. 3, no. 9, pp. 689–699, 2001. View at Publisher · View at Google Scholar · View at Scopus
  109. S. E. Akerman and S. Müller, “Peroxiredoxin-linked detoxification of hydroperoxides in Toxoplasma gondii,” Journal of Biological Chemistry, vol. 280, no. 1, pp. 564–570, 2005. View at Publisher · View at Google Scholar · View at Scopus
  110. J. W. Chen, C. Dodia, S. I. Feinstein, M. K. Jain, and A. B. Fisher, “1-Cys peroxiredoxin, a bifunctional enzyme with glutathione peroxidase and phospholipase A2 activities,” Journal of Biological Chemistry, vol. 275, no. 37, pp. 28421–28427, 2000. View at Publisher · View at Google Scholar · View at Scopus
  111. Y. Manevich, T. Sweitzer, J. H. Pak, S. I. Feinstein, V. Muzykantov, and A. B. Fisher, “1-Cys peroxiredoxin overexpression protects cells against phospholipid peroxidation-mediated membrane damage,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, no. 18, pp. 11599–11604, 2002. View at Publisher · View at Google Scholar · View at Scopus
  112. S. W. Kang, I. C. Baines, and S. G. Rhee, “Characterization of a mammalian peroxiredoxin that contains one conserved cysteine,” Journal of Biological Chemistry, vol. 273, no. 11, pp. 6303–6311, 1998. View at Publisher · View at Google Scholar · View at Scopus
  113. A. E. Vercesi, C. O. Rodrigues, S. A. Uyemura, L. Zhong, and S. N. J. Moreno, “Respiration and oxidative phosphorylation in the apicomplexan parasite Toxoplasma gondii,” The Journal of Biological Chemistry, vol. 273, no. 47, pp. 31040–31047, 1998. View at Publisher · View at Google Scholar · View at Scopus
  114. E. J. L. Melo, M. Attias, and W. de Souza, “The single mitochondrion of tachyzoites of Toxoplasma gondii,” Journal of Structural Biology, vol. 130, no. 1, pp. 27–33, 2000. View at Publisher · View at Google Scholar · View at Scopus
  115. C. Ödberg-Ferragut, J. Philippe Renault, E. Viscogliosi et al., “Molecular cloning, expression analysis and iron metal cofactor characterisation of a superoxide dismutase from Toxoplasma gondii,” Molecular and Biochemical Parasitology, vol. 106, no. 1, pp. 121–129, 2000. View at Publisher · View at Google Scholar · View at Scopus
  116. S. Rahlfs, R. H. Schirmer, and K. Becker, “The thioredoxin system of Plasmodium falciparum and other parasites,” Cellular and Molecular Life Sciences, vol. 59, no. 6, pp. 1024–1041, 2002. View at Publisher · View at Google Scholar · View at Scopus
  117. C. P. Hencken, L. Jones-Brando, C. Bordón et al., “Thiazole, oxadiazole, and carboxamide derivatives of artemisinin are highly selective and potent inhibitors of Toxoplasma gondii,” Journal of Medicinal Chemistry, vol. 53, no. 9, pp. 3594–3601, 2010. View at Publisher · View at Google Scholar · View at Scopus
  118. E. Holfels, J. McAuley, D. Mack, W. K. Milhous, and R. McLeod, “In vitro effects of artemisinin ether, cycloguanil hydrochloride (alone and in combination with sulfadiazine), quinine sulfate, mefloquine, primaquine phosphate, trifluoperazine hydrochloride, and verapamil on Toxoplasma gondii,” Antimicrobial Agents and Chemotherapy, vol. 38, no. 6, pp. 1392–1396, 1994. View at Publisher · View at Google Scholar · View at Scopus
  119. M. E. Sarciron, C. Saccharin, A. F. Petavy, and F. Peyron, “Effects of artesunate, dihydroartemisinin, and an artesunate-dihydroartemisinin combination against Toxoplasma gondii,” The American Journal of Tropical Medicine and Hygiene, vol. 62, no. 1, pp. 73–76, 2000. View at Google Scholar · View at Scopus
  120. W. E. Ho, H. Y. Peh, T. K. Chan, and W. S. F. Wong, “Artemisinins: pharmacological actions beyond anti-malarial,” Pharmacology & Therapeutics, vol. 142, no. 1, pp. 126–139, 2014. View at Publisher · View at Google Scholar · View at Scopus
  121. L. D. Sibley, R. Lawson, and E. Weidner, “Superoxide dismutase and catalase in Toxoplasma gondii,” Molecular and Biochemical Parasitology, vol. 19, no. 1, pp. 83–87, 1986. View at Publisher · View at Google Scholar · View at Scopus
  122. K. A. Brayton, A. O. T. Lau, D. R. Herndon et al., “Genome sequence of Babesia bovis and comparative analysis of apicomplexan hemoprotozoa,” PLoS Pathogens, vol. 3, no. 10, pp. 1401–1413, 2007. View at Publisher · View at Google Scholar · View at Scopus
  123. L. S. Kappmeyer, M. Thiagarajan, D. R. Herndon et al., “Comparative genomic analysis and phylogenetic position of Theileria equi,” BMC Genomics, vol. 13, no. 1, article 603, 2012. View at Publisher · View at Google Scholar · View at Scopus
  124. J.-M. Kang, H.-I. Cheun, J. Kim et al., “Identification and characterization of a mitochondrial iron-superoxide dismutase of Cryptosporidium parvum,” Parasitology Research, vol. 103, no. 4, pp. 787–795, 2008. View at Publisher · View at Google Scholar · View at Scopus
  125. P. Becuwe, C. Slomianny, A. Valentin, J. Schrevel, D. Camus, and D. Dive, “Endogenous superoxide dismutase activity in two Babesia species,” Parasitology, vol. 105, no. 2, pp. 177–182, 1992. View at Publisher · View at Google Scholar · View at Scopus
  126. P. Xu, G. Widmer, Y. Wang et al., “The genome of Cryptosporidium hominis,” Nature, vol. 431, no. 7012, pp. 1107–1112, 2004. View at Publisher · View at Google Scholar
  127. E. S. Son, K. J. Song, J. C. Shin, and H. W. Nam, “Molecular cloning and characterization of peroxiredoxin from Toxoplasma gondii,” Korean Journal of Parasitology, vol. 39, no. 2, pp. 133–141, 2001. View at Publisher · View at Google Scholar · View at Scopus