Haloarchaea May Contribute to the Colour of Avian Plumage in Marine Ecosystems

Some seabirds or coastal birds such as flamingos or pelicans display elegant pink or reddish colours. These colours are due to pigments that birds cannot synthesize de novo. Thus, this coloration is mainly originated from carotenoids ingested trough carotenoid rich food sources like microalgae ( Dunaliella ) or small shrimps ( Artemia ), which are microorganisms inhabiting the salty environments where the mentioned birds live. New advances in this field of knowledge have revealed that extreme microorganisms belonging to the haloarchaea group (Archaea Domain) may contribute significantly to the characteristic pink- red colour of flamingos’ feathers for instance. Alive haloarchaea cells have been found on the surface of the feathers. Besides, the major carotenoid produced by haloarchaea (bacterioruberin) has also been identify within the feathers structure. This work summarizes the main contributions recently reported about this topic as well as general aspects regarding bacterioruberin as a powerful colour carotenoid. Discussions about potential role of these microorganisms in the life of seaside birds are also included. Molecular


Introduction
Coloration is one of the most conspicuous traits that varies among organisms. In the case of animals, colour is mainly due to: (i) the presence of pigments (carotenoids, melanin, turacoverdin, biliverdin, protoporphyrin, etc); (ii) light phenomena such as reflection/emission from animal structures (skin, feathers, etc.); (iii) the presence of microscopic structure in scales, bristles, or feathers, which give them brilliant iridescent colours (commonly named "structural colours") [1]; and (iv) general aspects related to genetics [2]. Due to these reasons, animals show different colours, which can slightly vary even between individuals belonging to the same species. Animal colorations are strongly linked to different biological roles: camouflage, sexual, social, and interspecific signalling, physical protection (against UV radiation for instance), and sexual dimorphism [3][4][5][6].
In the case of the birds, feathers play a key role in general coloration. Those that are red orange show these colours thanks to the presence of different carotenoids within their structures. Carotenoids are natural pigments widely spread in nature: chloroplasts and chromoplasts of plants, bacteria, archaea, microalgae,

The colour of bird feathers
Bird feathers have been the aim of several works during the last two centuries. Thus, the first reports on bird plumage listed in databases like PUBMED, Web of Science or Scopus analysed aspects focused on the muscles in charge of the feathers movement [17] or their growth [18]. Other aspects of bird feathers related to biological roles like sexual selection, colonization strategies or signalling have also been extensively explored [19][20][21][22][23]. These aspects are intricately connected to the coloration of avian plumage.
The first detailed studies about the colour of bird feathers were published in indexed scientific journals in the middle fifties last century. Since then, around 500 manuscripts have been reported on this subject (Figure 1). It is worthy to note that the number of studies about the colouration of plumage significantly increased at the beginning of XXI century (Figure 1). However, the number of publications focused on the presence of carotenoids in bird feathers is lower compared to those related to other issues affecting the phenotype of birds (Figure 1). Bird coloration (mainly in feathers) is one of the most studied topics to elucidate the role of natural and sexual selection in the evolution of phenotypic diversity. Thus, the variety of vibrant plumage colours has evolved as a direct result of social and environmental pressures. The colour of plumage and other structures in animals and plants is due to the presence of pigments (pigment-based coloration) or the presence of microscopically structured surfaces fine enough to interfere with visible light (structural coloration) [24]. Iridescence for instance, is one of the better-known examples of it [25]. In some cases, feather colours are the result of a combination of both [26,27]. Table 1 summarizes the most representative pigments already identified as part of the colour of bird plumage. The most abundant are melanin and

Porphyrins
Turacoverdin Green [39] Coproporphyrin III Red Brown [40] Turacin Red [41]  carotenoids [28,42]. On the one hand, melanin-based coloration switches from brown to black due to the presence of phaeomelanin or eumelanin, respectively, or the number and distribution of the melanosomes [29,30]. On the other hand, carotenoids-based colorations vary from yellow to red as previously mentioned. The genetics of coloration in birds remains poorly described. However, it is extensively accepted that its expression is phenotypically plastic with a high sensitivity to variation in environmental conditions. Therefore, the melanin-based colour should be considered the key system to understand the molecular basis of phenotypic variations [43]. Some other pigments are only present in some species. This is the case of psittacofulvins, which are found just in a few species of parrots (Psittacidae) or penguins (Spheniscidae) [44][45][46] or turacoverdins, responsible for the bright green coloration of several birds of the family Musophagidae, most notably the turaco (Turaco sp.; Musophagidae). It is chemically related to turacin, a red pigment also found almost exclusively in turacos [39].

Haloarchaea
Archaea, one of the three Domains of life, make up a significant fraction of the microbial biomass on Earth [47]. It was thought that Archaea microbes were restricted to extreme environments, such as those with elevated temperatures, low or high pH, high salinity, or strict anoxia [48]. However, environmental sampling analysis based on rRNA sequences has revealed that archaea are widespread in "normal" ecosystems, including soils, oceans, marshlands, human colon, human oral cavity and even in human skin. They are particularly numerous in the oceans; thus, archaea in plankton may constitute one of the most abundant groups of organisms on the planet. From a metabolic point of view, they have evolved a variety of energy metabolisms using organic and/or inorganic electron donors and acceptors, playing important roles in the Earth's global geochemical cycles [49].
Halophilic archaea, also called Haloarchaea, are extreme or moderated halophilic species inhabiting neutral saline environments such as salt lakes, marine salterns, marshes, saltern crystallizer ponds or genuine environments like the Dead Sea [51,52]. In those natural ecosystems, salt concentrations are around 1.5-4 M, which corresponds to 9-30% of salts (w/v). NaCl is the predominant salt and ionic proportions are like those dissolved salts in seawater.
These halophilic ecosystems harbour a large diversity of microorganisms of all three domains: small eukaryotes such the shrimp Artemia salina, primary producers as the green algae Dunaliella [14] (Figure 2A and B), aerobic heterotrophic bacteria (mainly belonging to the family Halomonadaceae), anaerobic fermentative bacteria (families Halanaerobiaceae and Halobacteroidaceae) and archaeal microorganisms of the families Halobacteriaceae and Haloferacaceae (commonly named "Haloarchaea"). They are mainly characterised by their red-orange-pink colour, which is due to the pigments they produce to be protected against the high sun radiation (Figure 3). Salted ponds for salt crystallisation or other salty ecosystems like de Dead Sea become completely red, mainly in summer, due to microbial blooms, in which haloarchaea of the genera Haloarcula, Haloferax, Haloquadratum or bacterial species like Salinibacter ruber constitute de major populations (Figures 2C and 3).

Haloarchaea and their relation to avian plumage colour: the case of marine birds
Studies in the early nineties of the last century demonstrated that the carotenoids of the feathers were derived from the diet and deposited within tissues selectively [53] being the liver one of the most important organs involved in the conversion of carotenoids uptaken [54]. Some years before, other studies focused on seaside birds as flamingos stated that the major carotenoids in blood and feathers were canthaxanthin and a rare β-carotene derivative (4-keto-α-carotene) [55,56]. Limitations on chemical and analytical techniques have contribute to the poor knowledge about carotenoids in birds up to nowadays. Fortunately, new advances in spectrometry and HPLC have made possible a significant improvement in this field of knowledge [41,57]. Thus, during the last 15 years, several research groups worldwide have characterised the nature (and even the concentrations) of carotenoids in blood and feathers, mainly in finches [58,59] and parrots [44,60]. All the reported results show that the most important carotenoids contributing to the red-orange-pink colours in feathers are: canthaxanthin, astaxanthin, zeaxanthin and carotene (including its derivatives). In the case of seaside birds, it has been stated that the main rich carotenoids sources are the small shrimps and algae co-inhabiting the salty environments (Artemia and Dunaliella species, for instance) (Figure 2). Consequently, it is extensively assumed that the major pigments in marine bird's feathers would be those predominating in shrimps and algae (astaxanthin, canthaxanthin and carotene). However, some other studies indicate that in hypersaline habitats the birds do not feed extensively on brine shrimps Artemia to avoid salt stress [61]. Therefore, other carotenoid rich sources must be considered as part of the diet of marine birds to explain their pigmentation.

Figure 2. (A) Artemia salina and (B) Dunaliella salina. They constitute the major microbial populations in salted waters in coastal environments, salted lagoons, salty ponds from where NaCl is isolated from human consumption, etc. (C) Aerial overview of the saltern ponds located in Santa Pola city (Southeast of Spain) (http://paisajesturisticosvalencianos.com/paisajes/las-salinas-de-santa-pola-torrevieja/). This kind of ecosystems are warm places frequently inhabited by seaside birds like flamingos (D). The colour of the ponds is due to microbial blooms, which occur mainly in summer.
Recent contributions in this field have revealed that there are other important factors contributing to the red-orange-pink colour of the feathers. Between them, it is important to highlight the following: (i) genetics [2]; (ii) variation in carotenoidprotein interactions in bird feathers structures, which produces novel plumage coloration [62] and (iii) the presence of alive red-orange microorganisms on the surface of the feathers [63]. This last factor has recently been reported from flamingos growing up in captivity: viable, red-coloured archaeal strains belonging to the genera Halococcus and Halogeometricum were isolated from the surface of the plumage [63]. Apart from these viable cells, metagenomics approaches showed that cells belonging to other genera such as Haloquadratum, Haloferax, Haloarcula, Halorubrum and Natronomonas are also present on the surface of the flamingos' feathers. This kind of haloarchaea can produce significant amounts of bacterioruberin, a carotenoid mainly synthesised by them giving the microbial cells red-orange colours [8,64,65]. Besides, the analysis of the flamingo plumage pigments shows that bacterioruberin is not only in the alive microbial cells on the feathers' surface, but also found inside the flamingo feathers structure. This result directly suggests that haloarchaea are also part of the diet of flamingos. Bacterioruberin is responsible for the colour of these extremophilic microorganisms (Figures 3 and 4) [8,65]. It has a primary conjugated isoprenoid chain length of 13 C=C units with no subsidiary conjugation arising from terminal groups, which contain four -OH group functionalities only (Figure 4).
This carotenoid is involved in several biological roles in haloarchaea: it protects the cells against the damage produced by high intensities of sun radiation, it provides aid in photoreactivation [66] and it promotes membranes stability [8,65]. Characterisation of pure bacterioruberin samples revealed that it is more powerful than carotene as antioxidant compound [67,68]. Due to these facts, bacterioruberin could be used in biotechnology and biomedicine for different purposes [8,69]. Chemical structure of bacterioruberin. This compound has promising potential uses as antioxidant, antitumoral and immunomodulatory molecule for pharmaceutical and cosmetical formulations [64,65]. DOI: http://dx.doi.org /10.5772/intechopen.96414 Consequently, haloarchaea in general and their pigments in particular, may contribute to the orange-red colour of the feathers in two ways: (i) pink-red haloarchaea cells on the surface contribute to the pink-red phenotype in flamingos' feathers and (ii) haloarchaeal cells are part of the marine birds' diet (at least flamingos), consequently their carotenoids (mainly bacterioruberin) are ingested, metabolised and further assimilated.

Conclusions
New advances in the knowledge of animal pigmentation state that not only the pigments (carotenoids, melanin, etc.), but also the microstructure of the feathers as well as external factors, contribute to the final phenotype in terms of coloration. Related to birds, and particularly to seaside birds, it was thought that microalgae and small shrimps were the major sources of carotenoids so far. Nevertheless, recent results revealed that other small microbes such as haloarchaea could contribute significantly to the red-orange colours showed by birds like flamingos. In that sense, bacterioruberin becomes a new pigment to be considered to explain animal colours in marine environments. The potential influence of haloarchaea as an environmental factor determining avian plumage coloration or even protecting the microstructures of feathers against UV radiation must be investigated in further studies. Although bacterioruberin has been very well described, only few studies about its biological implications are available at the time of writing this review. Thus, more efforts must be done to explain basic aspects related to bacterioruberin metabolism and its effects on animal health and animal phenotypes. On the other hand, associations between different haloarchaeal-bird species as well as changes in these associations promoted by environmental conditions or anthropogenic actions are worthy to be analysed into detail. Hypothesis based on potential symbiotic relationship between haloarchaea and seaside birds remains unexplored.