Valeria Marasco1*
David Costantini1,2*- 1Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, UK
- 2Department of Biology, University of Antwerp, Antwerp, Belgium
The capacity to communicate effectively with other individuals plays a critical role in the daily life of an individual and can have important fitness consequences. Animals rely on a number of visual and non-visual signals, whose production brings costs to the individual. The theory of honest signaling states that these costs are higher for low than for high-quality individuals, which prevents cheating and makes signals, such as skin and plumage coloration, indicators of individual's quality or condition. The condition-dependent nature of signals makes them ideally suited as indicators of environmental quality, implying that signal production might be affected by contaminants. In this mini-review article, we have made the point that oxidative stress (OS) is one overlooked mechanism linking exposure to contaminants to signaling because (i) many contaminants can influence the individual's oxidative balance, and (ii) generation of both visual and non-visual signals is sensitive to OS. To this end, we have provided the first comprehensive review on the way both non-organic (heavy metals, especially mercury) and organic [persistent organic pollutants (POPs)] contaminants may influence either OS or sexual signaling. We have also paid special attention to emerging classes of pollutants like brominated flame-retardants (BFRs) and perfluoroalkoxy alkanes (PFAs) in order to stimulate research in this area. We have finally provided suggestions and warnings for future work on the links among OS, sexual signaling, and contaminant exposure.
Introduction
Work on honest signaling has been a major area of research in animal behavior and evolutionary ecology in recent decades. Honest signals reflect the individual quality, which depends on various interacting factors, such as foraging capability, functionality of the hormonal and immune systems, or oxidative balance (Hill, 2011). In 1999, Von Schantz et al. proposed that the association between oxidative stress (OS) and health might be a primary mechanism linking the expression of sexual ornaments to genetic variation in fitness-related traits, promoting the evolution of female's mate choice and male's sexual ornamentation (von Schantz et al., 1999). OS is a biochemical condition of cells, which occurs when there is an increase in oxidative molecular damage and oxidation of non-protein and protein thiols that regulate the cell oxidative balance. It is now increasingly recognized that OS may have an impact on the whole organism, for example as a modulator of some key life-history trade-offs (Costantini, 2014).
It is sometimes forgotten in ecological studies that some among individuals or species variation in life histories or physiological condition may simply be the by-product of contaminant exposure (Carere et al., 2010). In this context, the role of contaminants in influencing the production of honest signals and, consequently, sexual selection might be relevant. Pioneering work from Møller (1993), Manning and Chamberlain (1994), or Hill (1995) suggested that the condition-dependent nature of ornaments and armaments makes them suited indicators of environmental quality. The majority of the work in this area has been focused on the expression of colorations in birds. Both non-organic and organic contaminants may alter various, often inter-linked, physiological processes, causing changes in endocrine and neuroendocrine pathways (Frye et al., 2011), and oxidative balance (Metodiewa and Dunford, 1990; Whysner and Wang, 2001; Isaksson, 2010). Contaminants might either exacerbate costs of or constrain on physiological pathways underlying the production of honest signals.
In this review we have made the point that OS is an additional but overlooked mechanism linking contaminant accumulation in the body to the expression of sexual signals. OS has been extensively studied in ecotoxicology and this background knowledge can be used as a strong basis to establish mechanisms of action for signaling. We have provided the first comprehensive review of potential pathways through which both non-organic and organic contaminants would influence signaling through the induction of OS. We have also relied on studies of emerging pollutants of global concern for wildlife in order to stimulate research in this area. Although most of the work has been on birds, the implications of the examples provided are not taxon-specific.
Non-organic Contaminants
Non-organic contaminants can disrupt body colorations (Figure 1A) and induce OS through various mechanisms. For example, metal ions can induce cleavage of peroxides and organic hydroperoxides through the Fenton reaction, leading to the generation of new free radicals that can fuel OS. Metals can also bind to thiol groups, such as the endogenous antioxidant glutathione (Chan et al., 1992; Bridges and Zalups, 2006), inducing oxidation of the thiol without the generation of free radicals. These metals include, for example, cadmium, mercury, lead, and arsenic. For example, mercury has a strong propensity to react with cysteine and reduced glutathione (Stricks and Kolthoff, 1953; Mah and Jalilehvand, 2010) and animals have evolved adaptive mechanisms, in some species confined during specific stages of the life cycle, to actively eliminate such damaging contaminant from the body. For example, in birds, mercury is excreted through its deposition in the feathers during the molt (Monteiro and Furness, 1995). In this pathway, mercury is bound to keratin sulfhydryl groups during synthesis of feathers. Seabirds with slow molt cycles may have, however, a limited capacity for mercury detoxification (Thompson and Furness, 1989). Mercury may also be excreted from the body through the glutathione-pathway. Mercury binds to the thiol group of glutathione, forming a complex that is excreted in the feces (Ballatori and Clarkson, 1985). Sulfhydryl groups like thiols are important molecules that regulate the oxidative balance and any depletion leads to disruption of redox signaling and control, and increase in OS (Jones, 2006). Thus, high contamination with mercury might lead to a high depletion of thiols regardless of the pathway of excretion, which may compromise defenses against oxidation. Depletion of glutathione due to mercury may, for example, compromise the activity of the enzyme glutathione peroxidase (Hoffman and Heinz, 1998), which uses glutathione as a cofactor to detoxify the organism from peroxides and organic hydroperoxides, which is an important pathway through which organisms protect themselves against OS. The activity of selenium-dependent glutathione peroxidase may be further compromised by depletion of selenium that is being used to biosynthesize mineral granules containing mercury and selenium (Nigro and Leonzio, 1996).
Figure 1. (A) Wild male mallards (Anas platyrhynchos) exposed to high concentrations of lead (Pb) had paler carotenoid-based colorations in both legs and beak. Reprinted from Vallverdú-Coll et al. (2016) with permission from John Wiley and Sons; (B) Wild female black-legged kittiwakes (Rissa tridactyla) with higher blood concentrations of persistent organic pollutants (POPs) had paler carotenoid-based colorations in the gapes. Modified from Blévin et al. (2014). Photographs were courteously provided by Frédéric Angelier.
The interaction between mercury and glutathione offers a potential way through which mercury might influence melanin-based colorations (Figures 2A,B). Melanins are pigments that animals synthesize from the aromatic amino acids phenylalanine and tyrosine (Hearing, 1993). Melanins occur in two chemically distinct forms: eumelanin is a brown-black polymer of dihydroxyindole carboxylic acids and their reduced forms; pheomelanin is a cysteine-containing red-brown polymer of benzothiazine units. Melanocyte-stimulating hormones and the adrenocorticotropic hormone regulate the activity of the enzyme tyrosinase, which favors eumelanogenesis to pheomelanogenesis when its activity is high (Ozeki et al., 1997; Benathan et al., 1999). Melanogenesis is also regulated by the availability of thiol groups, such as free cysteine and cysteine-containing peptides (Ozeki et al., 1997; Benathan et al., 1999). Dopaquinone (produced from hydroxylation of the amino acid tyrosine) can react with thiol groups to synthesize pheomelanin or, in the absence of thiol groups, undergo a cyclisation that leads to the synthesis of eumelanin (García-Borrón and Olivares Sαnchez, 2011). Given that thiol compounds like glutathione play an important role in the regulation of cell redox status and protection against oxidative damage, melanin-based ornaments might signal the individual OS level (Galván and Alonso-Alvarez, 2008; Galván and Solano, 2009; Grunst et al., 2014). The property of melanic traits to signal individual OS would be favored by the differentiation in color between eumelanic (black and gray) and pheomelanic (yellowish, reddish, chestnut, and brown) traits (Galván and Alonso-Alvarez, 2008; Galván and Solano, 2009). Production of pheomelanin requires cysteine, which is also needed for the synthesis of glutathione (Galván and Solano, 2009). Thus, there should be a trade-off between the use of cysteine for glutathione and for pheomelanin synthesis. Cysteine-containing peptides like glutathione can also be used in melanogenesis. Thus, when the synthesis of glutathione is not constrained, the organism can maintain high glutathione concentration, while using it for the production of pheomelanins. Using glutathione in melanogensis might indicate that the individual has sufficient alternative antioxidant resources to counteract the decrease in glutathione itself or is not exposed to pro-oxidants (Galván and Alonso-Alvarez, 2008; Galván and Solano, 2009). On the other hand, a decrease in glutathione and, consequently, in cysteine availability would result in increased production of eumelanins. If mercury decreases glutathione availability, we should expect an increase in eumelanin coloration, but this has never been tested experimentally in free-living nor captive animals.
Figure 2. (A) Simplistic diagram of the hypothetical links among heavy metals, oxidative stress, and coloration via the glutathione pathway; (B) Schema of the catalytic cycle for the depletion of the cellular glutathione pool by mercury, proposed on the basis of mass spectrometric behavior, and biochemical evidence (reprinted from (Rubino et al., 2006) with permission from Elsevier); GSH, glutathione; GS-Hg+, mono-S-glutathionyl-mercury(II); Hg, mercury; CSCyGlyOH, oxidized cysteinyl-glycine; Hg+-SCyGlyOH, mercury(II)-cysteinyl-glycine conjugate; Pyr, pyroglutamic acid; RSH, thiols; (C) Simplistic diagram of the hypothetical links among persistent organic pollutants (POPs), oxidative stress, and coloration. Different classes of POPs can generate oxidative stress via binding with specific cellular receptors, including the aryl hydrocarbon receptor (AhR), and proliferator-activated receptor-alpha (PPAR-α); (D) Schema of the effects of dioxin-like pollutants (e.g., co-planar PCBs, PBDEs) via induction of the cytochrome P450 pathway (adapted from Regoli and Giuliani, 2014) which induces uncoupling of the catalytic cycle of the cytochrome P450 1A subfamily allowing the heme iron within the active site of this enzyme complex to undergo cycles of oxidation and reduction, and act as a Fenton catalyst generating free radicals—AhR, aryl hydrocarbon receptor; Ah, aryl hydrocarbon genes (e.g., CYP1A, CYP1B); HSP 90, heat shock protein 90; ARNT, aryl hydrocarbon receptor nuclear translocator; DRE, dioxin responsive element. Different classes of pollutants can act on the same cellular targets altering the cell oxidative machinery, see Regoli and Giuliani (2014) for a full review on these aspects.
Persistent Organic Pollutants
Polychlorinated Biphenyls
Persistent organic pollutants (POPs) are a large variety of compounds, including polychlorinated biphenyls (PCBs), organochlorine pesticides, or dioxins. Although industrial production of some POPs is now banned in most countries, they still represent a major health hazard due to their high persistence in the environment and their lipophilic properties that facilitate bio-accumulation and bio-magnification via the food chain (Beyer and Biziuk, 2009). Exposure to PCBs has been associated with dramatic adverse effects in many species (e.g., eggshell thinning in birds of prey; Wiemeyer and Porter, 1970; Ross, 2004; Frye et al., 2011). Several studies have shown that increased OS may be an additional mechanism underlying the negative effects of PCBs on the organism (e.g., Oakley et al., 1996; Zhu et al., 2009).
One important mechanism of action of PCBs is the binding capacity of some “dioxin-like” congers, such as PCBs 77 and 126, with the aryl hydrocarbon receptor (AhR), activating the enzyme cytochrome P450 1A subfamily (Hennig et al., 1999, 2002; Figures 2C,D). These interactions can uncouple the catalytic cycle of the enzyme CYP1A, allowing the heme iron within the active site of this enzyme complex to undergo cycles of oxidation and reduction, and act as a Fenton catalyst, generating free radicals (Schlezinger et al., 1999). Therefore exposure to PCBs might increase production of pro-oxidants that, if not counteracted by antioxidants, may cause OS. PCBs might also cause OS through the de-regulation of specific antioxidants. Administration of PCB 77 to rats suppressed both transcription and enzymatic activity of selenium-dependent glutathione peroxidases and total selenium in liver (Twaroski et al., 2001), which are important components of the antioxidant machinery. Although this review specifically focuses on OS, we note that several PCBs are also known to influence hormonal systems that regulate signaling (Ottinger et al., 2002).
Exposure to PCBs can also disrupt body coloration in birds, and, therefore, potentially influence sexual communication (Figure 1B). Pioneering work by Bortolotti et al. (2003) demonstrated that oral exposure to environmentally relevant dose of a PCB mixture (i.e., 1:1:1 Aroclor 1254, 1248, and 1260) in American kestrels (Falco sparverius) affected both plasma carotenoids and carotenoid-dependent coloration in a complex sex- and season-dependent manner. Differences in coloration were also found in the juveniles produced by the PCB-exposed parents, a presumed long-term effect of exposure to PCBs in ovo (Bortolotti et al., 2003). The effects of PCBs on the adult colorations might have been the consequence of changes in the oxidative balance. PCB-exposed individuals may have diverted carotenoids from colorations to protection against PCB-induced OS (Bortolotti et al., 2003); this would imply a trade-off for allocation of carotenoids between sexual signaling and self-maintenance (Pérez-Rodriguez et al., 2010). Indeed, during the courtship period, PCB-exposed males were duller than control males, while PCB-exposed females maintained their plumage coloration conversely to the expected loss in color observed in control females when carotenoids are diverted towards the developing ovaries (Surai, 2002). Moreover, the same PCB-treated females as in Bortolotti et al. (2003) delayed egg laying (Fernie et al., 2001). Although the antioxidant role of carotenoids appears to be minor in birds (Costantini and Møller, 2008), carotenoids might be more important when individuals are exposed to environmental (and oxidative) challenges. It might also be that depletion of other antioxidants would cause increased passive oxidation of carotenoids (Hartley and Kennedy, 2004; “protection hypothesis” in Pérez et al., 2008). Therefore, depletion of carotenoids might still confer honesty to the signal as long as it conveys other individual quality- and fitness-dependent functions.
Changes in coloration in response to elevated PCBs have also been found in ornaments independent from carotenoids and other pigments. McCarty and Secord (2000) examined plumage color in sub-adult female tree swallows (Tachycineta bicolor) breeding in an area highly contaminated by PCBs in the Hudson River. Females from contaminated areas had significantly more adult-like structurally colored blue-green feathers than females from control areas. This result was interpreted as an effect of PCBs on plumage through endocrine disruption, however, mechanisms were not directly investigated.
Emerging Persistent Organic Pollutants
Emerging POPs can be broadly defined as contaminants that are suspect of negative effects for the environment and wildlife, either not yet or recently regulated. These can include compounds that have been recently discovered (“true” or “new” emerging contaminants), or contaminants that have been in the environment since decades but for which concerns have been raised more recently (Sauvé and Desrosiers, 2014).
Brominated Flame-Retardants
Brominated flame-retardants (BFRs) include various compounds, such as emerging BFRs [e.g., 2,3-dibromopropyl phosphate (TDBPP)], polybrominated diphenyl ethers (PBDEs), tetrabromibishenol-A (TBBPA), hexabromocyclodecane (HBCD), and polybrominated biphenyls (PBBs), present in plastics, textiles, and commonly used in electronic equipment from catching fire. Several BFRs have raised environmental health concerns since they are highly persistent in the environment and can bio-accumulate in the food chains (de Wit, 2002). Most work has mainly focused on PBDEs, which are structurally similar to PCBs, and are now recognized as global pollutants (de Wit, 2002). The adverse effects of PBDEs may involve neurotoxic action during brain development or disruption of the thyroid endocrine system (Dingemans et al., 2011). Both these two mechanisms are likely to be associated with perturbation of homeostasis and generation of OS. In mammals, commercially available mixtures of PBDEs can enhance production of free radicals among different tissues, including the brain (e.g., Cheng et al., 2009; Bellés et al., 2010), liver (Fernie et al., 2005), and kidney (Albina et al., 2010).
Although free-living organisms are exposed to PBDEs since the start of life (Sellström et al., 1992), only a handful of studies have examined the consequences of PBDEs exposure for the organism. In captive nestling American kestrels (F. sparverius), exposure to environmentally relevant doses of a commercial mixture of PBDEs led to alterations in the thyroid system as well as hepatic OS, with marginal increases in oxidative damage (lipid peroxidation), and increased oxidized glutathione and retinol (Fernie et al., 2005). Exposure to environmentally relevant doses of DE-71 (a commercially available PBDE congener) caused changes in reproductive performance during the pre-nesting period, reducing copulatory activities and altering frequency and timing of pair-bonding behaviors (Fernie et al., 2008). Given that PBDEs are structurally similar to PCBs and appear to induce similar effects on the individuals' oxidative balance, and given that they can alter social and sexual signaling, it is likely that PBDEs might affect signaling through OS. We need experimental work that aims to elucidating such potential functional links among PBDEs, OS, and honest signals.
Perfluoroalkoxy Alkanes
Perfluoroalkylated substances (PFAs) have been widely used since 1950s for industrial applications, such as impregnating agents for carpets and textiles, fire-fighting foam (Jensen and Leffers, 2008). Perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) have been the most widely used PFAs. Both PFOS and PFOA are highly persistent in the environment and have been detected globally in wildlife and humans (Lau et al., 2007). Vertebrates do not seem to be able to metabolize and excrete PFAs (Muir and de Wit, 2010). Thus, PFAs bio-accumulate via the food chain (Tittlemier et al., 2007) and high levels of PFOS have been recorded in Arctic top predators, such as polar bears (Bossi et al., 2005).
A suspected mechanism involved in the toxic effects of PFAs is the peroxisome proliferator-activated receptor-alpha (PPAR-alpha; Figure 2C). Both PFOS and PFOA are weak activators of this receptor (Abbott, 2009). The PPAR is considered an important POP-related pathway involved in cell differentiation and hormone homeostasis (Kennedy et al., 2004). In rodents, activation of the PPAR-α increases production of hydrogen peroxide, which may lead to generation of hydroxyl radicals, which can boost OS (Klaunig et al., 2003). Experimental evidence shows that PFAs may trigger OS through the stimulation of ROS production (Eriksen et al., 2010), increased oxidative damage to DNA (Yao and Zhong, 2005), and cell apoptosis (Panaretakis et al., 2001).
In agreement with mammalian studies (e.g., Lau et al., 2006), Yanai et al. (2008) reported that exposure to PFOA in ovo in chicken reduced hatching success. Intriguingly, the latter study also showed that the surviving individuals exposed to the higher doses of PFOA were partially or completely missing their typical yellow pigmentation post-hatching (Yanai et al., 2008). Although neither antioxidant nor oxidative damage markers were measured, the results provided by Yanai et al. (2008) suggest that pre-natal exposure to PFOA might have interfered with the metabolism of carotenoids (Surai, 1998). The latter work offers preliminary evidence that PFAs can alter carotenoid-dependent colorations, similarly as the exposure to PCBs.
Contaminant Dose and Signaling
An important point that is often forgotten in research on the impacts of contaminants on wildlife is that low dose exposure may stimulate organism's defense mechanisms. This phenomenon, called “hormesis,” is increasingly recognized to be strongly associated with exposure to contaminants (Calabrese and Blain, 2005) and OS (Costantini, 2014). For example, sublethal lead exposure may increase male coloration (Vallverdú-Coll et al., 2015). Male starlings exposed to environmentally relevant levels of synthetic and natural estrogen mimics developed longer and more complex songs, and had larger brain areas controlling song complexity than controls (Markman et al., 2008). Moreover, females preferred the song of males which had higher pollutant exposure, despite experimentally dosed males showed reduced immune function (Markman et al., 2008). The low dose stimulation of traits involved in signaling may therefore have serious implications at the population level whether contaminants paradoxically enhance a signal of male quality biasing female choice towards contaminated males.
Conclusive Remarks and Future Perspectives
Many contaminants can affect either oxidative balance or expression of signals. We now need experimental work that seeks to assess the extent to which contamination-induced OS impacts on sexual signaling. We also need more studies to fully understand whether sexual signals could reliably be applied to monitor contaminant exposure in natural animal populations (Blévin et al., 2014; Giraudeau et al., 2015). Although in our mini-review we have not included literature on the impact of pesticides on OS and signaling, we highlight that our argumentations also apply to this important class of contaminants. Future work should pay special attention to the many factors that likely influence the impact of contaminant-induced OS on signaling. For instance, we might expect differences between males and females in those species where their investment into reproduction differs largely. We would also expect differences among age classes because both reproductive investment and resistance to OS vary with age (Costantini et al., 2014).
Most of the work about either OS or honest signals to date has focused on melanin and carotenoid-based colorations. Contaminants can also influence other components of signaling, such as vocalizations (DeLeon et al., 2013), or olfactory detection (Olsén, 2011). More research on these sexual communication components would be useful to deeper our understanding of the links among contaminants, OS, and individual's quality. We also stress that very little is known on the effects of emerging POPs such as BFRs and PFAs on honest signaling and OS in wild populations. Experimental work on these emerging POPs is a fruitful area for future research. We finally highlight that acknowledging the significance of hormesis will be fundamental for the interpretation of results.
Author Contributions
Design of review protocol: DC and VM; wrote the manuscript: DC and VM.
Funding
Preparation of this article was supported by a postdoctoral fellowship from FWO-Flanders (DC) and by the College of Medical, Veterinary and Life Sciences of the University of Glasgow (VM).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We thank the reviewers for the constructive and useful comments on previous drafts of the manuscript. DC thanks very much Jordi Figuerola for inviting him to organize the research topic “Oxidative stress and signal honesty.”
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Keywords: contaminants, POPs, oxidative stress, honest signals, heavy metals, hormesis
Citation: Marasco V and Costantini D (2016) Signaling in a Polluted World: Oxidative Stress as an Overlooked Mechanism Linking Contaminants to Animal Communication. Front. Ecol. Evol. 4:95. doi: 10.3389/fevo.2016.00095
Received: 21 January 2016; Accepted: 21 July 2016;
Published: 04 August 2016.
Edited by:
Carlos Alonso Alvarez, Spanish National Research Council, SpainReviewed by:
Rafael Mateo, Instituto de Investigación en Recursos Cinegéticos, Consejo Superior de Investigaciones Científicas (CSIC), la Universidad de Castilla–La Mancha (UCLM), SpainMichelle Lee Beck, Virginia Polytechnic Institute and State University, USA
Copyright © 2016 Marasco and Costantini. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Valeria Marasco, dmFsZXJpYS5tYXJhc2NvQGdsYXNnb3cuYWMudWs=
David Costantini, ZGF2aWQuY29zdGFudGluaUB1YW50d2VycGVuLmJl