Plasmodium infection and oxidative status in breeding great tits, Parus major
© The Author(s) 2016
Received: 24 May 2016
Accepted: 28 October 2016
Published: 4 November 2016
Plasmodium parasites may affect the oxidative status of their hosts, defined as the balance of pro-oxidant compounds and antioxidant defences in an organism. An increased energy requirement, the activation of immune functions or the parasite itself may lead to a higher production of pro-oxidants and/or an antioxidant depletion resulting in a higher oxidative stress and associated damage in infected individuals. Relatively little is known about the mechanisms underlying oxidative processes at play during host-Plasmodium interaction in the wild.
The effect of Plasmodium infection on host oxidative status was investigated in wild populations of breeding great tits, Parus major, naturally infected by Plasmodium spp. When chicks were 14 days old, the parents were blood-sampled to measure four complementary oxidative status markers: pro-oxidant production as mitochondrial superoxide production in red blood cells (RBC), antioxidant defences as plasma antioxidant capacity and oxidative damage as reactive oxygen metabolites in the plasma and RBC membrane resistance to oxidative attack.
Plasmodium-infected individuals produced more pro-oxidants compared to uninfected ones and pro-oxidant production positively correlated to infection intensity. There was also a conditional effect of reproductive effort on oxidative damage depending on Plasmodium infection status. There was no direct effect of infection on oxidative damage and no effect on antioxidant defences.
The results suggest that Plasmodium parasites may impose a cost in terms of increased oxidative stress possibly mediated via a higher energy requirement in infected hosts. This further suggests that Plasmodium parasites may modify host life history traits via an induction of oxidative stress. This study highlights that measuring several complementary oxidative status markers may enable to capture oxidative processes at play during host-Plasmodium interactions.
Plasmodium parasites, which cause malaria, are ubiquitous parasites infecting a wide range of vertebrate species  on which they impose fitness costs ranging from decreased survival [2–4], decreased fecundity  to lower levels of disease severity [6, 7]. Regardless of the direct fitness cost of parasite infection, malaria induces physiological changes in hosts, which may subsequently affect a host’s oxidative status. An organism’s oxidative status is the relative amount of pro-oxidant compounds and antioxidant defences. Pro-oxidants are generated as by-products of metabolism  or during particular physiological processes such as cell signalling [9, 10] or defence against parasites [11, 12]. They are highly reactive compounds that when not sufficiently balanced by antioxidant defences can react with other biomolecules generating oxidative damage to lipids, proteins and DNA . This imbalance, known as oxidative stress, is harmful and results in dysfunctions at the molecular, cellular and organ level . For instance, it has been linked with male infertility , cancer , chronic diseases , neurodegenerative diseases  and most notably the ageing process [17, 18]. Therefore, through their effect on host physiology, Plasmodium parasites may have a large impact on host life history traits.
The effect of Plasmodium infection on host oxidative status can also depend on other factors, such as reproduction (R pathway, Fig. 1). For example, it has recently been shown that infected individuals experienced increased susceptibility to oxidative stress during reproduction, but only during the phase of young provisioning, which requires a high energy investment . Reproduction can also affect oxidative status. High energy investment during reproduction has been linked with a decreased resistance to oxidative stress , decreased antioxidant defences [38, 39] and an increased oxidative stress [40, 41]. There can also be resource allocation trade-offs in reproductively active individuals  leading to a lower immunocompetence (i.e. the ability to mount an immune response) and/or higher parasitism rates [43–46]. Oxidative stress is therefore influenced by a range of factors, yet at the moment, little is known about how infection and reproduction interact to affect different aspects of the oxidative process.
Avian malaria is a popular biological system to study host-Plasmodium interactions in the wild and has been used as a model to study broad biological phenomena such as fitness consequences of parasite infection or host-parasite coevolution . The great tit, Parus major, the focus of the current study, can be infected by several Plasmodium lineages [48–50] among which one of the most common avian malaria lineage: Plasmodium relictum SGS1 . To date, there is no consensus on the effect of age or sex on the prevalence of infection [34, 43, 51, 52] but the infection has been shown to be highly persistent (i.e. chronic infection) across years . Infection does not appear to affect body mass or condition [34, 37, 52]. In studies where reproductive effort has been manipulated the prevalence of infection as well as the parasite intensity have been shown to increase in males but not in females [37, 43]. Infection has also been associated with a reduced probability of breeding in two consecutive years in males  but not in females . These sex differences in the susceptibility to Plasmodium could suggest a role for host physiology during the host-Plasmodium interaction.
In this study, the link between natural Plasmodium infection and individual oxidative status was investigated in wild populations of breeding great tits. Plasmodium parasite development occurs in host red blood cells (RBC) , a key phase for Plasmodium parasites to complete their life cycle and for the host to mount an immune response . Oxidative status was therefore measured in the blood using four complementary oxidative status markers at the cellular and plasmatic levels (Fig. 1). Four markers were used to capture different aspects of the oxidative process: RBC superoxide production, reactive oxygen metabolites (ROMs) in the plasma, RBC membrane resistance to attack and plasma antioxidant capacity. Superoxides are the first pro-oxidant molecules released by the mitochondrial electron transport chain (ETC) during mitochondrial respiration . In contrast to mammals, avian RBCs have functional mitochondria in their cytoplasm  and so, superoxide production may reflect individual energy consumption. Superoxides can also generate further pro-oxidant compounds through the oxidative reaction chain . ROMs are oxidized molecules which may reflect oxidative processes occurring in the plasmatic compartment such as oxidation caused by immune effectors during the immune response. They also act as pro-oxidant compounds. Membrane resistance to oxidative attack reflects the amount of past oxidative attacks that have not been counteracted (i.e. oxidative damage) and the current resistance to oxidation (i.e. antioxidant defence, see [57, 58]). Infected red blood cells are characterised by rigid membranes , a phenomenon which could be associated with increased oxidative damage and a decreased resistance to oxidative attack. Finally, plasma contains antioxidant defences which can oppose the oxidative process of biomolecules. These circulating defences protect the free molecules and the membranes of (host and parasitic) cells present in the plasma. The bird reproductive season can be divided into two time points that are particularly energetically costly and could have an effect on oxidative status: egg laying and chick rearing reflecting an early and a later cost. Both phases were considered to investigate the interplay between infection and reproductive effort on oxidative status. Pro-oxidant production and oxidative damage were expected to be higher in infected individuals and to increase with reproductive effort. Plasma antioxidant defences were expected to be either depleted because of the oxidative processes associated with infection and reproduction or increased as a protective response against oxidative stress. In focusing on these four markers, the aim was to gain a comprehensive overview of the oxidative processes at play and to highlight which pathway leads to oxidative stress enhancement during host-Plasmodium interactions.
Great tit sampling
Three populations of great tits were monitored during the 2012 breeding season (from March to June) at three sites in Switzerland: the forests of Dorigny (46°31′N; 6°34′E; alt. 380 m), Monods (46°34′N; 6°24′E; alt. 668 m), and La Praz (46°40′N; 6°20′E; alt. 1000 m). The great tit is a species with a large geographical distribution that readily nests in artificial nest-boxes allowing a rigorous monitoring of natural populations. Nest boxes were visited periodically to estimate the date at which the first egg was laid, the clutch size (i.e. the number of incubated eggs) and the hatching date. Brood size was defined as the number of chicks surviving to 14 days. At that stage, parents were caught using door traps or mist nets. Once caught, parents were aged (<2 years old: sub-adult and ≥2 years old: adult), weighed (to the nearest 0.1 g) and blood-sampled by brachial venipuncture with sterile needles (Neolus 100, Terumo Europe) and blood was collected in lithium-heparinized microvettes (Sarstedt®, Germany).
Oxidative status markers
Directly after blood sampling, 16 µl of blood were transferred into 584 µl of KRL buffer (Kirial international, Laboratoires Spiral S.A., Dijon, France), a physiological buffer adjusted to bird cell osmolarity. These diluted blood samples were stored in the dark and on ice until laboratory analyses. The blood remaining in the microvette was centrifuged for 10 min at 15,000 rcf and 4 °C. Red blood cells and plasma were split and stored separately at −20 °C. There was no effect of time elapsed between field sampling and laboratory analyses on oxidative status measurements (mean time elapsed in hours ± standard deviation: 8.94 ± 2.87; Pearson’s correlations between each measurement and time elapsed: superoxides: r = −0.01, t = −0.07, p = 0.94; ROMs: r = −0.11, t = −1.30, p = 0.19; membrane resistance: r = 0.16, t = 1.88, p = 0.06; plasma antioxidants: r = −0.05, t = −0.43, p = 0.69).
Once in the laboratory, blood cells were washed by centrifuging the diluted samples for 5 min at 500 rcf at 4 °C, and cell pellets were resuspended in a volume of 700 µl of KRL buffer. Glucose was added in excess (30 mM final concentration) as a mitochondrial respiration substrate to control for possible inter-individual variation in cell substrate availability. This stock sample solution was then used as a starting solution for the flow cytometric measurements of superoxide production and mitochondria quantity and for spectrometric measurements of RBC membrane resistance to oxidative attack.
RBC superoxide production corrected for mitochondria quantity
Superoxide production was quantified per live RBC using the specific fluoroprobe MitoSOX Red (Molecular Probes, Invitrogen, ). In order to standardize superoxide production, the amount of mitochondria per RBC was also quantified using the fluorescent probe nonyl acridine orange (NAO, Molecular Probes, Invitrogen) which binds cardiolipins, phospholipids specific to the mitochondria inner membrane .
250 µl of stock sample solution of diluted blood was incubated for 30 min at 40 °C (i.e. ~avian body temperature) with MitoSOX Red fluorescent dye (12 µM final concentration once dye added to the sample, diluted in dimethyl sulfoxyde, DMSO). Another 250 µl of stock sample solution was incubated for 7 min at 40 °C with NAO (10 µM final concentration). At the end of the incubation period, cells were washed by centrifuging samples for 5 min at 500 rcf at 4 °C. Cells were then resuspended in 300 µl of KRL buffer and stored in the dark and on ice until flow cytometer measurement on a FACS Calibur (Becton–Dickinson) using the FL2 channel and excitation at 582 nm for superoxide production, and using the FL1 channel and excitation at 200 nm for mitochondria quantity. 50,000 events per sample were acquired and the median fluorescence value (i.e. arbitrary unit) was computed for each sample using the BD CellQuest Pro software (Becton–Dickinson, coefficient of intra-individual variation: superoxide production: CV = 2.51%; mitochondria quantity: CV = 2.14%, four individuals ran eight times).
Superoxide production (log transformed to achieve normality) and mitochondria quantity (square root transformed to achieve normality) per RBC were positively correlated (Pearson’s correlation: r = 0.52, t = 7.15, df = 140, p < 0.001, Additional file 1). In order to obtain a corrected measurement of superoxide production per mitochondria, the ratio of RBC superoxide production on RBC mitochondria quantity was calculated for each sample. In the following text, “superoxide production” refers to this corrected measurement, unless otherwise specified.
Reactive oxygen metabolites in the plasma
ROMs were quantified in the plasma using the d-ROMs test (Diacron international, Grosseto, Italy), according to the manufacturer’s protocol (although see  for limitations associated with this test). In the presence of iron, reactive oxygen metabolites produce peroxyl and alkoxyl radicals (Fenton’s reaction). These radicals react directly with a chromogenic substrate. After 75 min of incubation at 40 °C, optical density was measured at 540 nm and plasma sample values were compared to values obtained from a calibrator (coefficient of intra-assay variation: CV = 2.25%; coefficient of inter-assay variation: CV = 3.00%, one control ran twice on each plate). Reactive oxygen metabolites were then expressed as the equivalent of hydroperoxide quantity in the plasma (mg H2O2 l−1) and was square root transformed to achieve normality.
RBC membrane resistance to oxidative attack
Membrane resistance was measured as the time needed to haemolyse half of the RBCs as described in . Cell haemolysis was quantified using a microplate reader by following the decrease of optical density at the wavelength of 540 nm and using the Kirial International processing analysis software (coefficient of intra-individual variation: CV = 2.83%, 133 individuals ran in duplicates).
Plasma antioxidant capacity
Plasma antioxidant capacity was assessed by measuring the power of the plasmatic barrier to oppose hypochlorite (HClO) induced oxidation using the Oxy-Adsorbent test (Diacron international, Grosseto, Italy), according to the manufacturer’s protocol. After 10 min of incubation at 40 °C, HClO excess was determined with a chromogenic substrate by optical density measurement at 540 nm and plasma sample values were compared to values obtained from a calibrator (coefficient of intra-assay variation: CV = 3.82%; coefficient of inter-assay variation: CV = 5.12%, one control ran twice on each plate). The final HClO concentration was expressed in µmol ml−1 and was used as a proxy of plasma antioxidant capacity. Plasma antioxidant capacity was log transformed to achieve normality.
Plasmodium detection and quantification
DNA was extracted from blood using the DNeasy blood and tissue extraction kit (Qiagen®, Valencia, CA, USA) according to the manufacturer’s protocol for the BioSprint 96. A nested PCR was performed to detect the infection status of individuals. Following a primary reaction with the primers HaemNF1 and HaemNR3, a secondary reaction with the primers HaemF and HaemR2 to amplify Plasmodium and Haemoproteus was conducted  and 5 μl of PCR product was run on a 2% agarose gel to assess infection status. PCRs were performed in duplicate, with one positive control for every 30 samples and one negative for every 15 (alternately water or an uninfected bird). To confirm the infection, the positive products were purified (Promega) and sent for sequencing in both directions using HaemF and HaemR2 primers (GATC- Biotech, Germany). Sequences were analysed with BioEdit and identified with a local BLAST search against the MalAvi database , unless there were multiple-lineage infections, identified as double-base callings on the chromatogram. Haemoproteus infected individuals (1.6% of infected individuals) were discarded from the analyses to focus on Plasmodium infection.
For Plasmodium positive samples, parasite quantification was performed by quantitative PCR as described in . Briefly, two separate qPCR reactions using a parasite cyt b TaqMan probe (CY3-CYTb-BHQ2) and a host 18 s rRNA probe (FAM-18S-BHQ1) were performed. For both parasite and host, DNA concentration was calculated from a standard curve and the parasitaemia was given by the ratio of the parasite DNA concentration on the host DNA concentration. Parasitaemia was log transformed to achieve normality.
The aim was to investigate the effect of Plasmodium infection on oxidative status, measured using four complementary markers, and to further explore the interaction between infection and reproductive effort. All statistical analyses were performed using R (version 3.1, ). The following oxidative status markers were analysed as response variables in linear mixed-effects models (lme function in nlme package): (1) RBC superoxide production (corrected for mitochondria quantity) (2) reactive oxygen metabolites in the plasma, (3) RBC membrane resistance to oxidative attack, and (4) plasma antioxidant capacity. A term was included for Plasmodium infection status (uninfected or infected). As clutch and brood sizes were correlated (Pearson’s correlation: r = 0.43, t = 4.58, df = 90, p < 0.001), they were not included simultaneously in a model, but the same models were alternatively tested with reproductive effort as brood size or as clutch size. The two-way interaction between infection status and reproductive effort was included. Terms for body mass, age (sub-adults or adults) and sex, which are known to influence oxidative stress [66–69], as well as hatching date which may account for seasonal variation were also included. To explore potential interactions with infection, the interaction terms between infection and age and between infection and sex were also fitted. Nest box nested in site was included as a random factor. To determine the explanatory power of each fitted parameter, likelihood ratio tests were conducted following a standard backward procedure by sequential elimination from the full model. Non-significant terms (p > 0.05) were dropped out from the full model to reach the minimal adequate one . Significant p values in the text come from minimal adequate models, and non-significant p values come from the likelihood ratio test before the term was dropped out. To look at the effect of each significant term individually, contrast analyses were performed .
For the pro-oxidant production, supplementary models, similar to the ones described above, but considering superoxide production (not corrected for mitochondria quantity) as a response variable and including mitochondria quantity as an explanatory variable were run.
The correlations between the different oxidative status markers were explored. The relationships between each marker and parasitaemia were also investigated in infected individuals only.
Plasmodium infection prevalence
The following results provided in the text refer to the models considering reproductive effort as brood size and models considering reproductive effort as clutch size are provided in Additional file 2.
RBC superoxide production
Minimal adequate models of oxidative status markers
Infection: brood size
Infection: brood size
Infection: brood size
Infection: brood size
Reactive oxygen metabolites in the plasma
RBC membrane resistance to oxidative attack
Neither Plasmodium infection status nor its interaction with reproductive effort, age or sex had any effect on RBC membrane resistance (Table 2). Membrane resistance, however, decreased with brood size and with hatching date (Table 2) and was lower in females compared to males (mean ± standard error in females: 70.8753 ± 0.7655, in males: 74.0023 ± 0.7704; Table 2). When considering reproductive effort as clutch size, the same minimal adequate model was obtained (Additional file 2). There was no correlation between membrane resistance and parasitaemia (Pearson’s correlation: r = 0.00, t = −0.03, df = 45, p = 0.980).
Plasma antioxidant capacity
None of the fitted parameters explained variation in plasma antioxidant capacity and no minimal adequate model was reached after model selection when considering reproductive effort measured as brood or clutch size (Table 2, Additional file 2). Plasma antioxidant capacity was not correlated to parasitaemia (Pearson’s correlation: r = −0.14, t = −0.68, df = 22, p = 0.502).
Correlations among the different oxidative status markers
Pearson’s correlations between oxidative status markers
Membrane resistance–antioxidant capacity
In this study, the link between natural Plasmodium infection and oxidative status in wild breeding great tits was explored measuring four complementary oxidative status markers. The presence and the intensity of infection were associated with an elevated production of pro-oxidants. There was a link between reproductive effort and oxidative damage that was affected by infection status. There was however no effect of Plasmodium infection on antioxidant defences. These results illustrate the effect of Plasmodium infection on bird oxidative status and the importance of considering multiple physiological markers in oxidative stress research.
Infection and oxidative status
Plasmodium-infected individuals produced more RBC superoxides compared to uninfected ones. This is the first time an RBC superoxide production increase is reported in wild Plasmodium-infected animals and this result is in line with results from in vitro studies that have shown that there is an increase in pro-oxidant levels in Plasmodium-infected RBCs . RBC superoxide production increased with RBC mitochondria quantity, supporting that the superoxides were released by the host mitochondria. The allometry found for RBC superoxide further suggests that RBC superoxide production reflects individual energy consumption: the bigger the individual, the more energy consumed and the higher the superoxide production. These results suggest that the higher superoxide production could be due to an increased energy requirement in infected individuals (P pathway, Fig. 1). This could result from the activation of immune functions which can be energetically costly  or from energy diversion by the parasite for its own development. Both processes could also explain the positive correlation between infection burden and superoxide production observed in infected individuals. Superoxide produced in RBCs can further generate pro-oxidant compounds from the oxidative reaction chain  and lead to oxidative damage. This is supported by the positive correlation between RBC superoxide and plasma ROM levels that was found, by the negative trend observed between superoxide production and RBC membrane resistance as well as between ROM quantity and membrane resistance.
There was no direct effect of infection on host antioxidant defences or oxidative damage. The fact the Plasmodium infection differentially affected the four oxidative status markers may be explained by the ability of organisms to regulate their oxidative stress. Pro-oxidant production at the mitochondrial level is constrained by metabolic activity at the cellular level and its regulation is complex . In contrast, circulating antioxidants are partly obtained from food and can be made available when needed from storage sources, such as organs [72, 73]. Membrane resistance is partly explained by its composition in phospholipids . These are also partly obtained from food and can be selectively incorporated into the biomembranes . Compared to other tissues, red blood cells have a relatively high turn-over which may allow the maintenance of a resistant pool of cells. Therefore, these two traits, plasma antioxidant capacity and membrane resistance, might be more easily maintained stable under oxidative stress conditions which might explain why they were not affected by infection status. However, investing in the maintenance of the antioxidant barrier and in the repair of oxidative damage might have a cost too. Combined, these results highlight an effect of Plasmodium infection on host oxidative status in line with recent work . They further suggest that Plasmodium parasites may enhance host oxidative stress through a higher energy requirement in infected individuals.
Reproductive effort and oxidative status
Several studies have found that reproduction is associated with antioxidant depletion and increased oxidative damage [37, 38, 68, 76], suggesting that oxidative stress is a physiological cost for breeding individuals. Consistent with these studies, we showed that reproductive effort positively correlated to pro-oxidant production and to oxidative damage measured as RBC membrane resistance, suggesting a higher oxidative stress in individuals investing more in their reproduction (R pathway, Fig. 1). There were also sex differences in oxidative status with females producing more pro-oxidants and accumulating more damage (both ROMs and membrane resistance) than males, consistent with previous study that have shown a higher oxidative stress in females than in males during reproduction . The sex difference in susceptibility to oxidative stress has been suggested to stem from physiological (e.g. hormones) and activity (e.g. parental tasks) differences between sexes during reproduction . Finally, there was a conditional effect of reproductive effort (measured as brood size) on oxidative damage (measured as ROMs) depending on the infection status, but no effect of either reproductive effort or infection status when considering reproductive effort as clutch size. A previous study on the Seychelles warblers, Acrocephalus sechellensis,  already reported increased oxidative damage in Plasmodium-infected individuals during the energetically costly phase of chick provisioning. In the present study, the results suggest that oxidative damage increased with reproductive effort in uninfected individuals only. However, the a posteriori contrast analysis did not allow to conclude whether ROMs increased with reproductive effort in uninfected individuals, ROMs decreased with reproductive effort in infected individuals or both. Nevertheless, the interaction suggests that the effect of infection and reproductive effort on oxidative status are not independent or simply additive. For instance, infected individuals could have a higher investment in antioxidant defences (other than those measured in this study) as a response to infection, which would confer them a greater protection from reproduction-induced oxidative stress. It is clear that the oxidative stress phenomenon and the interplay between Plasmodium infection and reproductive effort on host oxidative status are complex.
Age and oxidative status
It is well known that older individuals may experience a higher oxidative stress compared to younger ones [66, 67]. This has been partly attributed to accumulated damage to somatic cells, telomere degradation and progressive dysfunctions of metabolic pathways involved in oxidative stress regulation [17, 18]. Consistent with this result, in this study, adult birds had higher pro-oxidant production and oxidative damage (ROMs). Furthermore, a recent study in the great reed warbler, Acrocephalus arundinaceus, showed that chronic malaria infection was linked to faster telomere degradation  and subsequently faster ageing in Plasmodium-infected individuals. The increased RBC superoxide production in infected individuals could therefore be a mechanism explaining telomere reduction previously observed in blood samples of Plasmodium-infected individuals .
The present study illustrates how Plasmodium infection may affect host oxidative status in wild breeding individuals. The higher pro-oxidant release by mitochondria in infected individuals suggests that Plasmodium parasites impose a cost on their host in terms of an enhanced energy requirement resulting in increased oxidative stress. This may have further important consequences in terms of oxidative damage leading to telomere shortening in red blood cells  but also in other tissues  potentially triggering a faster ageing associated with malaria disease.
PC originally formulated the idea. JD developed the methods and conducted laboratory analyses. JD and TJ conducted fieldwork and performed statistical analyses. JD, TJ, PC wrote the manuscript.
The authors declare that they have no competing interests.
This study was conducted under licence according to Swiss animal legislation (authorization number VD1730.1). All applicable institutional and/or national guidelines for the care and use of animals were followed.
The project was funded by the Swiss National Science Foundation Grant (31003A-138187 and 31003A-159600).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Valkiunas G. Avian malaria parasites and other haemosporidia. Boca Ratón: CRC Press; 2005.Google Scholar
- Asghar M, Hasselquist D, Hansson B, Zehtindjiev P, Westerdahl H, Bensch S. Hidden costs of infection: chronic malaria accelerates telomere degradation and senescence in wild birds. Science. 2015;347:436–8.View ArticlePubMedGoogle Scholar
- Møller AP, Nielsen JT. Malaria and risk of predation: a comparative study of birds. Ecology. 2007;88:871–81.View ArticlePubMedGoogle Scholar
- Atkinson CT, Saili KS, Utzurrum RB, Jarvi SI. Experimental evidence for evolved tolerance to avian malaria in a wild population of low elevation Hawai’i’Amakihi (Hemignathus virens). EcoHealth. 2013;10:366–75.View ArticlePubMedGoogle Scholar
- Knowles SCL, Palinauskas V, Sheldon BC. Chronic malaria infections increase family inequalities and reduce parental fitness: experimental evidence from a wild bird population. J Evol Biol. 2010;23:557–69.View ArticlePubMedGoogle Scholar
- World Health Organization. Severe malaria. Trop Med Int Health. 2014;19:7–131.View ArticleGoogle Scholar
- Bartoloni A, Zammarchi L. Clinical aspects of uncomplicated and severe malaria. Mediterr J Hematol Infect Dis. 2012;4:e2012026.View ArticlePubMedPubMed CentralGoogle Scholar
- Halliwell B, Gutteridge J. Free Radicals in Biology and Medicine. 4th ed. Oxford: Oxford University Press; 2007.Google Scholar
- Apel K, Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol. 2004;55:373–99.View ArticlePubMedGoogle Scholar
- Finkel T. Signal transduction by reactive oxygen species. J Cell Biol. 2011;194:7–15.View ArticlePubMedPubMed CentralGoogle Scholar
- Wink DA, Hines HB, Cheng RYS, Switzer CH, Flores-Santana W, Vitek MP, et al. Nitric oxide and redox mechanisms in the immune response. J Leukoc Biol. 2011;89:873–91.View ArticlePubMedPubMed CentralGoogle Scholar
- Nathan C, Cunningham-Bussel A. Beyond oxidative stress: an immunologist’s guide to reactive oxygen species. Nat Rev Immunol. 2013;13:349–61.View ArticlePubMedPubMed CentralGoogle Scholar
- Tremellen K. Oxidative stress and male infertility—a clinical perspective. Hum Reprod Update. 2008;14:243–58.View ArticlePubMedGoogle Scholar
- Waris G, Ahsan H. Reactive oxygen species: role in the development of cancer and various chronic conditions. J Carcinog. 2006;5:14.View ArticlePubMedPubMed CentralGoogle Scholar
- Lambeth JD. Nox enzymes, ROS, and chronic disease: an example of antagonistic pleiotropy. Free Radic Biol Med. 2007;43:332–47.View ArticlePubMedPubMed CentralGoogle Scholar
- Federico A, Cardaioli E, Da Pozzo P, Formichi P, Gallus GN, Radi E. Mitochondria, oxidative stress and neurodegeneration. J Neurol Sci. 2012;322:254–62.View ArticlePubMedGoogle Scholar
- Perez-Campo R, López-Torres M, Cadenas S, Rojas C, Barja G. The rate of free radical production as a determinant of the rate of aging: evidence from the comparative approach. J Comp Physiol B, Biochem Syst Environ Physiol. 1998;168:149–58.View ArticlePubMedGoogle Scholar
- Finkel T, Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature. 2000;408:239–47.View ArticlePubMedGoogle Scholar
- Adelman JS, Martin LB. Vertebrate sickness behaviors: adaptive and integrated neuroendocrine immune responses. Integr Comp Biol. 2009;49:202–14.View ArticlePubMedGoogle Scholar
- Lochmiller RL, Deerenberg C. Trade-offs in evolutionary immunology: just what is the cost of immunity? Oikos. 2000;88:87–98.View ArticleGoogle Scholar
- Demas GE, Chefer V, Talan MI, Nelson RJ. Metabolic costs of mounting an antigen-stimulated immune response in adult and aged C57BL/6 J mice. Am J Physiol. 1997;273:R1631–7.PubMedGoogle Scholar
- Freitak D, Ots I, Vanatoa A, Hõrak P. Immune response is energetically costly in white cabbage butterfly pupae. Proc R Soc B Biol Sci. 2003;270:S220–2.View ArticleGoogle Scholar
- Martin LB II, Scheuerlein A, Wikelski M. Immune activity elevates energy expenditure of house sparrows: a link between direct and indirect costs? Proc R Soc B Biol Sci. 2003;270:153–8.View ArticleGoogle Scholar
- Hasselquist D, Nilsson J-Å. Physiological mechanisms mediating costs of immune responses: what can we learn from studies of birds? Anim Behav. 2012;83:1303–12.View ArticleGoogle Scholar
- Bertrand S, Criscuolo F, Faivre B, Sorci G. Immune activation increases susceptibility to oxidative tissue damage in Zebra Finches. Funct Ecol. 2006;20:1022–7.View ArticleGoogle Scholar
- Sorci G, Faivre B. Inflammation and oxidative stress in vertebrate host-parasite systems. Philos Trans R Soc Lond B Biol Sci. 2009;364:71–83.View ArticlePubMedGoogle Scholar
- Sadd BM, Siva-Jothy MT. Self-harm caused by an insect’s innate immunity. Proc R Soc B Biol Sci. 2006;273:2571–4.View ArticleGoogle Scholar
- Costantini D, Dell’Omo G. Effects of T-cell-mediated immune response on avian oxidative stress. Comp Biochem Physiol A Mol Integr Physiol. 2006;145:137–42.View ArticlePubMedGoogle Scholar
- Finney OC, Riley EM, Walther M. Regulatory T cells in malaria—friend or foe? Trends Immunol. 2010;31:63–70.View ArticlePubMedGoogle Scholar
- Hansen DS, Schofield L. Natural regulatory T cells in malaria: host or parasite allies? PLoS Pathog. 2010;6:e1000771.View ArticlePubMedPubMed CentralGoogle Scholar
- Postma NS, Mommers EC, Eling WMC, Zuidema J. Oxidative stress in malaria; implications for prevention and therapy. Pharm World Sci. 1996;18:121–9.View ArticlePubMedGoogle Scholar
- Schirmer RH, Schöllhammer T, Eisenbrand G, Krauth-Siegel RL. Oxidative stress as a defense mechanism against parasitic infections. Free Radic Res Commun. 1987;3:3–12.View ArticlePubMedGoogle Scholar
- Bichet C, Cornet S, Larcombe S, Sorci G. Experimental inhibition of nitric oxide increases Plasmodium relictum (lineage SGS1) parasitaemia. Exp Parasitol. 2012;132:417–23.View ArticlePubMedGoogle Scholar
- Isaksson C, Sepil I, Baramidze V, Sheldon BC. Explaining variance of avian malaria infection in the wild: the importance of host density, habitat, individual life-history and oxidative stress. BMC Ecol. 2013;13:15.View ArticlePubMedPubMed CentralGoogle Scholar
- Asghar M, Palinauskas V, Zaghdoubi-Allan N, Valkiunas G, Mukhin A, Platonova E, et al. Parallel telomere shortening in multiple body tissues owing to malaria infection. Proc R Soc B Biol Sci. 1836;2016(283):20161184.Google Scholar
- van de Crommenacker J, Richardson DS, Koltz AM, Hutchings K, Komdeur J. Parasitic infection and oxidative status are associated and vary with breeding activity in the Seychelles warbler. Proc R Soc B Biol Sci. 2012;279:1466–76.View ArticleGoogle Scholar
- Christe P, Glaizot O, Strepparava N, Devevey G, Fumagalli L. Twofold cost of reproduction: an increase in parental effort leads to higher malarial parasitaemia and to a decrease in resistance to oxidative stress. Proc R Soc B Biol Sci. 2012;279:1142–9.View ArticleGoogle Scholar
- Alonso-Alvarez C, Bertrand S, Devevey G, Prost J, Faivre B, Sorci G. Increased susceptibility to oxidative stress as a proximate cost of reproduction. Ecol Lett. 2004;7:363–8.View ArticleGoogle Scholar
- Wiersma P, Selman C, Speakman JR, Verhulst S. Birds sacrifice oxidative protection for reproduction. Proc R Soc B Biol Sci. 2004;271:S360–3.View ArticleGoogle Scholar
- Fletcher QE, Selman C, Boutin S, McAdam AG, Woods SB, Seo AY, et al. Oxidative damage increases with reproductive energy expenditure and is reduced by food-supplementation. Evolution. 2012;67:1527–36.PubMedPubMed CentralGoogle Scholar
- Guindre-Parker S, Baldo S, Gilchrist HG, Macdonald CA, Harris CM, Love OP. The oxidative costs of territory quality and offspring provisioning. J Evol Biol. 2013;26:2558–65.View ArticlePubMedGoogle Scholar
- Stearns SC. The evolution of life histories. Oxford: Oxford University Press; 1992.Google Scholar
- Richner H, Christe P, Oppliger A. Paternal investment affects prevalence of malaria. Proc Natl Acad Sci USA. 1995;92:1192–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Ilmonen P, Hasselquist D, Langefors A, Wiehn J. Stress, immunocompetence and leukocyte profiles of pied flycatchers in relation to brood size manipulation. Oecologia. 2003;136:148–54.View ArticlePubMedGoogle Scholar
- Tomás G, Merino S, Moreno J, Morales J, Martínez-De La Puente J. Impact of blood parasites on immunoglobulin level and parental effort: a medication field experiment on a wild passerine. Funct Ecol. 2007;21:125–33.View ArticleGoogle Scholar
- Knowles SCL, Nakagawa S, Sheldon BC. Elevated reproductive effort increases blood parasitaemia and decreases immune function in birds: a meta-regression approach. Funct Ecol. 2009;23:405–15.View ArticleGoogle Scholar
- Marzal A. Recent advances in studies on avian malaria parasites. In: Okwa OO, editor. malaria parasites. Rijeka: InTech; 2012. p. 135–58.Google Scholar
- Glaizot O, Fumagalli L, Iritano K, Lalubin F, Van Rooyen J, Christe P. High prevalence and lineage diversity of avian malaria in wild populations of great tits (Parus major) and mosquitoes (Culex pipiens). PLoS ONE. 2012;7:e34964.View ArticlePubMedPubMed CentralGoogle Scholar
- Mata VA, da Silva LP, Lopes RJ, Drovetski SV. The Strait of Gibraltar poses an effective barrier to host-specialised but not to host-generalised lineages of avian Haemosporidia. Int J Parasitol. 2015;45:711–9.View ArticlePubMedGoogle Scholar
- van Rooyen J, Lalubin F, Glaizot O, Christe P. Altitudinal variation in haemosporidian parasite distribution in great tit populations. Parasit Vectors. 2013;6:139.View ArticlePubMedPubMed CentralGoogle Scholar
- Oppliger A, Christe P, Richner H. Clutch size and malarial parasites in female great tits. Behav Ecol. 1997;8:148–52.View ArticleGoogle Scholar
- Jenkins T, Delhaye J, Christe P. Testing local adaptation in a natural great tit-malaria system: an experimental approach. PLoS ONE. 2015;10:e0141391.View ArticlePubMedPubMed CentralGoogle Scholar
- van Rooyen J, Lalubin F, Glaizot O, Christe P. Avian haemosporidian persistence and co-infection in great tits at the individual level. Malar J. 2013;12:40.View ArticlePubMedPubMed CentralGoogle Scholar
- Taylor-Robinson AW. Regulation of immunity to Plasmodium: implications from mouse models for blood stage malaria vaccine design. Exp Parasitol. 2010;126:406–14.View ArticlePubMedGoogle Scholar
- Brand MD, Affourtit C, Esteves TC, Green K, Lambert AJ, Miwa S, et al. Mitochondrial superoxide: production, biological effects, and activation of uncoupling proteins. Free Radic Biol Med. 2004;37:755–67.View ArticlePubMedGoogle Scholar
- Stier A, Bize P, Schull Q, Zoll J, Singh F, Geny B, Gros F, Royer C, Massemin S, Criscuolo F. Avian erythrocytes have functional mitochondria, opening novel perspectives for birds as animal models in the study of ageing. Front Zool. 2013;10:33.View ArticlePubMedPubMed CentralGoogle Scholar
- Alonso-Alvarez C, Bertrand S, Devevey G, Prost J, Faivre B, Chastel O, et al. An experimental manipulation of life-history trajectories and resistance to oxidative stress. Evolution. 2006;60:1913–24.View ArticlePubMedGoogle Scholar
- Bize P, Devevey G, Monaghan P, Doligez B, Christe P. Fecundity and survival in relation to resistance to oxidative stress in a free-living bird. Ecology. 2008;89:2584–93.View ArticlePubMedGoogle Scholar
- Paulitschke M, Nash G. Membrane rigidity of red blood cells parasitized by different strains of Plasmodium falciparum. J Lab Clin Med. 1993;122:581–9.PubMedGoogle Scholar
- Mukhopadhyay P, Rajesh M, Yoshihiro K, Haskó G, Pacher P. Simple quantitative detection of mitochondrial superoxide production in live cells. Biochem Biophys Res Commun. 2007;358:203–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Mileykovskaya E, Dowhan W. Cardiolipin membrane domains in prokaryotes and eukaryotes. Biochim Biophys Acta. 2009;1788:2084–91.View ArticlePubMedPubMed CentralGoogle Scholar
- Kilk K, Meitern R, Härmson O, Soomets U, Hõrak P. Assessment of oxidative stress in serum by d-ROMs test. Free Radic Res. 2014;48:883–9.View ArticlePubMedGoogle Scholar
- Hellgren O, Waldenström J, Bensch S. A new PCR assay for simultaneus studies of Leucocytozoon, Plasmodium, and Haemoproteus from avian blood. J Parasitol. 2004;90:797–802.View ArticlePubMedGoogle Scholar
- Bensch S, Hellgren O, Pérez-Tris J. MalAvi: a public database of malaria parasites and related haemosporidians in avian hosts based on mitochondrial cytochrome b lineages. Mol Ecol Resour. 2009;9:1353–8.View ArticlePubMedGoogle Scholar
- R Development Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. 2011. http://www.R-project.org/.
- Bize P, Cotting S, Devevey G, van Rooyen J, Lalubin F, Glaizot O, Christe P. Senescence in cell oxidative status in two bird species with contrasting life expectancy. Oecologia. 2014;174:1097–105.View ArticlePubMedGoogle Scholar
- Alonso-Alvarez C, Pérez-Rodríguez L, García JT, Viñuela J, Mateo R. Age and breeding effort as sources of individual variability in oxidative stress markers in a bird species. Physiol Biochem Zool. 2010;83:110–8.View ArticlePubMedGoogle Scholar
- Rubolini D, Colombo G, Ambrosini R, Caprioli M, Clerici M, Colombo R, et al. Sex-related effects of reproduction on biomarkers of oxidative damage in free-living barn swallows (Hirundo rustica). PLoS ONE. 2012;7:e48955.View ArticlePubMedPubMed CentralGoogle Scholar
- Marko G, Costantini D, Michl G, Torok J. Oxidative damage and plasma antioxidant capacity in relation to body size, age, male sexual traits and female reproductive performance in the collared flycatcher (Ficedula albicollis). J Comp Physiol B. 2011;181:73–81.View ArticlePubMedGoogle Scholar
- Crawley MJ. The R Book. Chichester: Wiley; 2007.View ArticleGoogle Scholar
- Rigoulet M, Yoboue ED, Devin A. Mitochondrial ROS generation and its regulation: mechanisms involved in H2O2 signaling. Antioxid Redox Signal. 2011;14:459–68.View ArticlePubMedGoogle Scholar
- Beaulieu M, Schaefer HM. Rethinking the role of dietary antioxidants through the lens of self-medication. Anim Behav. 2013;86:17–24.View ArticleGoogle Scholar
- Elsayed NM. Antioxidant mobilization in response to oxidative stress: a dynamic environmental-nutritional interaction. Nutrition. 2001;17:828–34.View ArticlePubMedGoogle Scholar
- Pamplona R, Barja G, Portero-Otín M. Membrane fatty acid unsaturation, protection against oxidative stress and maximum life span. A homeoviscous-longevity adaptation? Ann N Y Acad Sci. 2002;959:475–90.View ArticlePubMedGoogle Scholar
- Buttemer WA, Battam H, Hulbert AJ. Fowl play and the price of petrel: long-living Procellariiformes have peroxidation-resistant membrane composition compared with short-living Galliformes. Biol Lett. 2008;4:351–4.View ArticlePubMedPubMed CentralGoogle Scholar
- Costantini D, Bonisoli-Alquati A, Rubolini D, Caprioli M, Ambrosini R, Romano M, et al. Nestling rearing is antioxidant demanding in female barn swallows (Hirundo rustica). Naturwissenschaften. 2014;101:541–8.View ArticlePubMedGoogle Scholar