Article | Open | Published:

Melanization in response to wounding is ancestral in arthropods and conserved in albino cave species

Scientific Reportsvolume 7, Article number: 17148 (2017) | Download Citation


Many species adapted to aphotic subterranean habitats have lost all body pigmentation. Yet, melanization is an important component of wound healing in arthropods. We amputated appendages in a variety of cave-adapted and surface-dwelling arthropods. A dark clot formed at the site of injury in most species tested, including even albino cave-adapted species. The dark coloration of the clots was due to melanin deposition. The speed of wound melanization was uncorrelated with a difference in metabolic rate between surface and cave populations of an amphipod. The chelicerate Limulus polyphemus, all isopod crustaceans tested, and the cave shrimp Troglocaris anophthalmus did not melanize wounds. The loss of wound melanization in T. anophthalmus was an apomorphy associated with adaptation to subterranean habitats, but in isopods it appeared to be a symplesiomorphy unrelated to colonization of subterranean habitats. We conclude that wound melanization i) is an important part of innate immunity because it was present in all major arthropod lineages, ii) is retained in most albino cave species, and iii) has been lost several times during arthropod evolution, indicating melanization is not an indispensable component of wound healing in arthropods.


The loss of body and eye pigmentation, or albinism, is a convergent feature found in a majority of species adapted to aphotic subterranean habitats, such as caves1. However, the evolutionary causes of albinism in cave organisms have not been fully explored, with only a few studies investigating molecular mechanisms underlying loss of pigmentation2,3,4. A longstanding idea is that relaxed selection for pigmented traits in darkness allows for accumulation of mutations that eventually eliminate pigment production. Indeed, functions of pigments, such as protection from harmful UV radiation, camouflage or aposematic coloration for escaping predation, attracting potential mates, etc., are unnecessary in aphotic environments. However, pigments or pigment synthesis pathways can have pleiotropic roles in different metabolic and physiological processes, such as scavenging of reactive oxygen species, physical protection, temperature regulation and innate immunity5,6,7,8. For example, blocking melanin synthesis may enable precursor molecules to be used in other metabolic pathways. In the fish Astyanax mexicanus, silencing of the oca2 gene in the surface form caused a loss of pigmentation and an increase of both the melanin precursor L-tyrosine as well as the catecholaminergic neurotransmitter dopamine9. Furthermore, the levels of catecholamines (CAT) are higher in Astyanax cavefish compared to the surface form9. CATs are involved in numerous physiological functions and behaviors. A suite of traits related to the CAT system were changed as cavefish evolved from surface-dwelling ancestors, including feeding behavior, stress response, and sleeping patterns, among others10,11,12. Therefore, the loss of melanin pigmentation might be adaptive in light depleted environments, but does it come with a cost?

The innate immune system is the only means of immunity in invertebrates, although there is some controversy surrounding the recent discovery of innate priming or innate memory as a type of adaptive immunity in invertebrates13. In arthropods, innate immunity consists of cellular and humoral defenses such as phagocytosis, nodulation and encapsulation, synthesis of antimicrobial peptides, production of reactive intermediates of oxygen and nitrogen, release of stress associated proteins and substances that function in opsonization and iron sequestration, and complex proteolytic cascades that culminate with coagulation, clotting and melanin formation7,14. Melanization has multiple roles in the immune response, including encapsulation of pathogens and parasites, wound healing, clot formation and production of cytotoxic intermediates that kill invading microorganisms15,16. Melanin also adds to the stiffness of clots, preventing the loss of hemolymph and invasion of pathogens into the hemocoel17.

Part of the melanin synthesis pathway is catalyzed by the enzyme phenoloxidase (PO). Normally phenoloxidase exists as the proenzyme prophenoloxidase (PPO) that is proteolytically activated by a cascade of serine proteases. Activation of PO must be tightly controlled temporally and spatially because intermediate products of its action are severely cytotoxic. PO catalyzes hydroxylation of phenolic substrates into o-diphenols and their subsequent oxidation into quinones, which polymerize into melanin. PPO is stored in cytoplasmic granules of hemocytes and is released into the hemolymph following the activation of pattern recognition proteins upon detection of bacterial or fungal antigens or both14,17,18. PO is extremely important in arthropods. PO functions in both exoskeleton formation as well as in effective immune system responses, and simultaneous appearance of these two processes is thought to have fostered the remarkable radiation of arthropods19.

In this study, we attempted to determine if cave arthropods lacking body pigmentation have also lost the melanization part of the innate immune response. This is not a trivial question because although the ability to immediately respond to an immune challenge is critical for survival, maintenance of parts of the innate immunity is costly in terms of resources7,20. Tyrosine is a critical component of the PO mediated melanin synthesis pathway, and it is derived from phenylalanine, which is obtainable only from ingested food21, while melanin is itself a nitrogen rich compound and requires significant input of protein rich resources for its synthesis22. Subterranean environments are relatively resource poor compared to surface environments primarily because of the lack of photosynthesis, and are generally nitrogen rather than carbon limited1; thus, it is conceivable that adaptations to such resource limited environments may require a compromise in resource intensive physiological systems. Subterranean environments are hypothesized to harbor lower abundance and diversity of parasites and pathogens than surface environments (e.g.23), and cave organisms may experience relaxed selection to maintain the highly resource demanding portion of the innate immune system such as the melanin synthesis pathway. We found that most albino cave arthropods retain the ability to melanize wounds, and that PO is involved in this response. We also found that the wound melanization response is highly conserved across arthropod taxa, but has been lost in isopods, the chelicerate Limulus polyphemus and the cave shrimp Troglocaris anophthalmus.

Materials and Methods

Animals used

Arthropods of diverse taxa belonging to multiple higher taxonomic groups were collected periodically between 2013 and 2017 from cave and surface habitats in Bosnia and Herzegovina, Croatia, and the United States, with special focus on albino subterranean species and their surface-dwelling relatives, including multiple geographically separated populations or genetically distinct clades of some of the species (see Tables 1 and 2). Most of the species belonged to the crustacean orders Amphipoda, Decapoda and Isopoda, but a variety of other higher taxonomic groups were included. After collection, the live animals were brought to laboratories or field facilities and maintained in conditions that closely resembled those of their natural habitats, including similar temperatures, high humidity for terrestrial organisms and native water for aquatic species. Experiments were performed after the animals had acclimated to the captive conditions from several hours up to three days.

Table 1 Higher taxonomic groupings and results of wound melanization assay for each species.
Table 2 Habitats and origins of species included in this study.

Wound melanization assays

To determine whether the targeted arthropods could synthesize melanin after an immune challenge, we induced wounds by amputating one or more of the body appendages, usually walking legs or antennae or both. For small organisms with short appendages such as springtails and mites, we pierced the cuticle with a fine-pointed needle. Prior to the procedure, the animals were sedated by being placed in a freezer for two to three minutes for terrestrial species or with chemical anesthetics such as tricane or menthol crystals for aquatic species. After the operation animals were left to recover and periodically inspected for the appearance of a dark plug at the site of injury over the next several days. The dark cuticle of some species, such as Pycnogonida and the surface-dwelling isopod Asellus aquaticus, rendered it difficult to ascertain whether melanization of the wound had occurred even under the microscope. Amputated limbs of such species were treated for several hours with formic acid, which removed body pigments but does not dissolve melanin, and then inspected for presence of a dark plug at the wound site.

Some animals were treated with phenylthiourea (PTU), an inhibitor of phenoloxidase24, the enzyme catalyzing critical steps in the melanin synthesis pathway of invertebrates. The PTU treatment was terminated when black plugs appeared in the wound sites of specimens not treated with PTU, usually within 24 to 48 hours. If PTU prevented darkening of the wound sites, then the dark coloration of wound sites observed in specimens not treated with PTU was interpreted as resulting from melanin pigment synthesis and deposition. Aquatic species were treated with 0.1% PTU in native water, except albino crangonyctid amphipods (see Table 1) were treated with 0.05% PTU. Initial trials with concentrations higher than 0.05% and 0.1% resulted in mortality of some of the albino crangonyctid amphipods and in the other species, respectively. Terrestrial species were placed in small, covered containers with absorbent paper moistened with 0.1% PTU, except 0.25% PTU was used for diplopods (see Table 1), and sufficient amount of the paper was used to ensure contact between the tips of the amputated legs and the PTU infused paper when the animals moved. The higher PTU concentration was used for diplopods because they had numerous walking legs (>40) and thus we expected less frequent contact between the two to three amputated legs and the PTU infused paper compared to the one amputated leg among only six or eight legs possessed by the other terrestrial species treated; however, whether this resulted in delivery of similar dosage of PTU to the wound sites between these two sets of terrestrial species was unknown. Because the wound melanization response was inhibited in all specimens treated with PTU regardless of concentration and habitat, we deemed our usage of different concentrations did not bias our results.

A reduction in metabolic rate in cave-adapted taxa compared to related surface-dwelling taxa is considered an adaptation to the relatively food poor subterranean environment1. We therefore compared the speed of the wound melanization process among two surface and two cave populations of the amphipod Gammarus minus because: 1) the wound melanization assays on this species were performed in the laboratory rather than under field conditions, 2) this species exists as multiple morphologically distinct populations inhabiting the surface and cave habitats, and 3) different cave populations had independently evolved the cave phenotype25.

Data availability statement

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.


Albino cave invertebrates retain the ability to synthesize melanin in response to wounding

All albino subterranean invertebrate species we tested, except for isopods and the atyid shrimp Troglocaris anophthalmus (discussed further below), showed melanization of experimentally induced wound sites (Table 1. See Fig. 1 for results from a subset of the arthropods tested). These included the following: all 14 species and clades of amphipods (e.g., Fig. 1C) belonging to five genera in three families occupying a variety of subterranean habitats such as the hypotelminorheic, epikarst, cave streams and phreatic aquifers; the palaemonid decapod shrimp Palaemon antrorum; three millipede species in two orders, the cleidogonid Pseudotremia fulgida in the Chordeumatida and two polydesmid Brachydesmus species (Fig. 1B) in the Polydesmida; and an insect, the cixiid planthopper Oliarus polyphemus (Fig. 1A). Furthermore, the wound melanization process was inhibited in all 14 of the albino species in addition to all seven non-albino species that were treated with PTU (Table 1, see also Fig. 1D–F). These results demonstrated for the first time that a diverse group of albino cave-adapted arthropod species from a variety of subterranean habitats, all showing no cuticular body pigment, retained the ability to synthesize melanin during wound healing, and that phenoloxidase played an important role in this reaction in both albino and non-albino species.

Figure 1
Figure 1

Albino cave invertebrates retain the ability to synthesize melanin in response to wounding. The site of cuticular injury turned dark in the cixiid Oliarus polyphemus (A), the diplopod Brachydesmus inferus (B), and the amphipod Stygobromus emarginatus (C). PTU treated specimens showed no black plug formation (DF), suggesting phenoloxidase is involved in the melanization pathway. Inset in A is a magnified image of another O. polyphemus amputated leg. Red arrows point out the wound site. Photographs by the authors.

The speed of wound melanization is similar between cave-adapted compared to surface-dwelling populations of the amphipod Gammarus minus

We compared the speed of formation of the melanized plug at tips of amputated appendages among two surface-dwelling and two cave-adapted Gammarus minus populations as well as G. cohabitus, the Gammarus species with the most cave-adapted morphology26. The wound healing process proceeded as follows. About 6 hours post amputation (hpa), a whitish plug had formed but it was only loosely bound to the wound site because the entire plug could be dislodged by gently swirling the water surrounding the animal. Darkening of the plug was observed at about 12 hpa although the plug was still easily dislodged. A dark-black plug was observed about 24 hpa and this plug was difficult but possible to dislodge by vigorous swirling of the water surrounding the animal. At 48 hpa the black plug was impossible to dislodge by swirling. The timing of these events was identical in all four G. minus populations as well as in G. cohabitus.

Cave shrimp Troglocaris anophthalmus lost the ability to synthesize melanin at the wound site

The albino atyid shrimp Troglocaris anophthalmus formed white plugs at wound sites but the plugs did not melanize even after four days (Fig. 2A and B). This was observed in all Troglocaris we collected from various geographic regions of Croatia (see Tables 1 and 2), and they belonged to phylogenetically distinct clades27. We further confirmed this observation by examining Troglocaris specimens in the collections of the Croatian Biospeleological Society in Zagreb (as of 6 July 2017). Research collections of albino cave-adapted crustaceans such as amphipods often contain specimens with dark spots at ends of broken appendages, presumably formed as part of the wound melanization reaction. We inspected 54 specimens from 17 caves spanning from northern Croatia to southern Herzegovina and found no dark coloration in any of the specimens with broken appendages. Therefore, we have high confidence that T. anophthalmus does not melanize its wounds. This loss of wound melanization in Troglocaris appears to be an apomorphy, because a closely related surface species, Atyaephyra desmarestii, also collected in Croatia, showed wound melanization (Fig. 2E). In addition, a surface marine shrimp in the genus Crangon in the family Crangonidae collected in Massachusetts, as well as both the surface-dwelling freshwater shrimp Palaemon paludosus and the cave-adapted albino shrimp P. antrorum from Texas also showed wound melanization (Fig. 2C and D). To our knowledge, this is the first documentation and, so far, the only example of loss of wound melanization as a derived condition associated with colonization of the subterranean environment.

Figure 2
Figure 2

Albino cave shrimp Troglocaris anophthalmus lost the ability to synthesize melanin at the wound site (A and B, indicated by red arrow). Surface shrimp show melanized clot at the wound site (C). The albinoTexas cave shrimp Palaemon antrorum melanizes wound sites (D). An Atyaephyra desmarestii specimen (surface shrimp) shows a melanized wound (E). Insets in C and E are magnified images of injured limb. Photographs by the authors.

Wound melanization is present in all major arthropod lineages and is the ancestral state in Arthropods but has been convergently lost at least three times

Wound melanization was present in the major arthropod lineages we tested, including Pycnogonida, Chelicerata, Myriapoda, and Pancrustacea, but it was absent in Merostomata and Isopoda (Table 1 and Fig. 3). The presence of the melanization response in the Pycnogonida, and in most of the lineages tested, suggests that wound melanization is an ancestral state in arthropods. This points to three independent losses of wound melanization among the groups we tested: in the atyid shrimp T. anophthalmus, in the merostome Limulus polyphemus, and in isopods. The situation with isopods is different from that of T. anophthalmus discussed above. All 15 species and clades, belonging to nine genera in four families, from both subterranean and especially surface environments, whether albino or not, lacked the response (Table 1). Thus, the loss of wound melanization appears plesiomorphic in isopods, and is likely to have occurred prior to colonization of the subterranean habitats and therefore not part of adaptation to the aphotic environment. Because no other merostome was investigated, no inferences can be made about whether lack of wound melanization was apomorphic for L. polyphemus or was lost earlier in the lineage.

Figure 3
Figure 3

Wound melanization is present in most major arthropod lineages. Light blue lines indicate a loss of wound melanization in that lineage; dotted light blue indicates both phenotypes are present in that lineage. Arthropod relationships based on Legg et al.62. Photographs by the authors.


The phenoloxidase reaction is one of the most effective immune mechanisms of invertebrates and it is present in many groups in addition to arthropods, including mollusks, annelids, echinoderms, tunicates and cephalocordates14. Melanin related enzymes and machinery can play a role in immunity in vertebrates as well. In zebrafish28 and Astyanax mexicanus (Bilandžija et al., in preparation) melanocytes migrate to the wound site in certain cases. There is evidence that melanin, melanosomes and melanocytes function as part of the innate immune system in humans as well29,30. Therefore, the role of melanin in immunity appears ancient and is present in different forms and to different extents throughout the animal kingdom. In arthropods melanin synthesis is a central mechanism of innate immunity and a major response to a variety of immune challenges14,16,18,31.

Most cave-adapted arthropods have lost body and eye pigmentation in the light depleted cave environment, and we wondered whether they have also lost the ability to synthesize melanin pigment as a part of the immune response. If coloration and other important functions of pigment are not essential for the survival of cave-adapted species, then we would expect the complete inactivation of pigment production pathways in cave-adapted arthropods. Alternatively, selection could either maintain a pigment synthesis pathway only in specific tissues or cell types, or maintain the parts of the pathway involved in defense processes but not in body pigmentation. Only a few studies aimed at understanding the mechanism of albinism in cave organisms at the molecular level have been conducted, and none have examined the relationship between loss of body pigmentation and wound melanization. In the Mexican cavefish Astyanax mexicanus, albinism was a result of loss of function deletions in the oca2 gene that functions in the first step of melanin synthesis4. Similarly, in the cixiid planthoppers Oliarus polyphemus from Hawaii and Trirhacus helenae from Croatia, the loss of melanin was also due to disruption of the first step of melanin synthesis2.

We tested for cuticular wound melanization in multiple arthropod species spanning all known subphyla that have albino cave-adapted representatives. In addition to the cuticle, melanization occurs during wound healing of internal tissues in Drosophila, such as barrier epithelia of the epidermis, the trachael system and the gastrointestinal tract, and involvement of a host of different molecules, such as serpins and especially antimicrobial proteins have been demonstrated31,32,33,34,35. Therefore, results from this study are applicable only to wound melanization in the cuticle. Our data demonstrate for the first time that most albino cave-adapted arthropod species retain the ability to synthesize melanin during cuticular wound healing. This suggests that even if there is selection for albinism in cave animals (to conserve energy or to use precursors for alternative pathways), it does not affect the enzymatic machinery necessary for melanin synthesis needed in the immune response. Therefore, the melanin synthesis pathway is modular: some aspects of the pathway can be modified or inactivated while others remain intact. In the case of the cixiid planthopper, melanin synthesis pathway in the epidermis and cuticle is inactive2 and is activated after an immune challenge. On the contrary, in isopods melanin is synthesized for pigmentation of individual body parts but is not in response to wounding (see below). Decoupling of melanin synthesis between immune and body pigmentation contexts may be achieved by using different enzymes or different branches of the melanin synthesis pathway in different contexts. Alternatively, the same enzymes can be involved but specific functions are enabled by differential regulation, different activation pathways, or by their spatial localization.

The melanin synthesis pathway in arthropods is well categorized in insects6, and starts with hydroxylation of tyrosine into DOPA, catalyzed by tyrosine hydroxylase (TH) or phenoloxidase (PO) or both. The next step is a branch point where DOPA may be carboxylated to dopamine by dopadecarboxylase (DDC) or oxidized to dopaquinone by PO. Further downstream dopamine and dopaquinone are oxidized into dopamine melanin and dopamelanin, respectively17,36. There is evidence for using both different and the same enzymatic pathways for different functions of melanin. Many insect species possess multiple homologues of the PO genes (e.g. three PO genes in Drosophila, nine in Anopheles gambiae, 10 in Aedes aegypti 37,38). Subfunctionalization between different paralogues of PO has been demonstrated7,39. For example, in Armigeres subalbatus PO I is involved in melanization of microfilariae and PO II in hardening of egg chorion7. In Tribolium castaneum only laccase2 is involved in cuticle tanning40. In A. gambiae laccases function in cuticle tanning and not in immunity41 but in Anopheles sinensis laccase2 is involved in both cuticle tanning and immune response42. On the other hand, enzymes involved in cuticle darkening and sclerotization, such as phenylalanine hydroxylase, tyrosine hydroxylase, DOPA decarboxylase, and dopachrome conversion enzyme, separately or in various combinations, have been shown to be immune responsive42,43,44,45. Also, TH, DDC and laccase2 are expressed in epidermal and cuticular tissues as well as in immune tissues such as fat body and hemocytes42,45,46. Therefore, melanization processes involved in cuticular wound healing, in barrier epithelial wound healing, and in body pigmentation may be independently controlled or encompass different enzymatic machinery.

The only cave-adapted animal we investigated that has lost the ability to melanize cuticular wounds is the cave shrimp Troglocaris anophthalmus. The loss of cuticular wound melanization is likely related to cave adaptation since all surface shrimp species we tested, including the close surface relative Atyaephyra desmaresti synthesizes melanin as a response to wounding. The cave-adapted albino shrimp, Palaemon antrorum, is also still able to melanize their wounds. Therefore, loss of cuticular wound melanization does not necessarily accompany cave adaptation in decapod shrimp, but is lineage specific for T. anophthalmus. Troglocaris shrimp formed non-melanized plugs at the wound sites and survived the amputations, suggesting they have developed alternative mechanisms for wound healing. Similarly, successful defense from some pathogens does not require PO activity in Drosophila and Anopheles gambiae 18, suggesting that melanization is not an indispensable defense strategy.

Reduction of metabolic rate is a common adaptation in many cave animals1 and specifically in cave-adapted compared to surface-dwelling amphipods47. The less cave-adapted Gammarus troglophilus showed a two- to four-fold higher oxygen consumption rate compared to the closely related and highly cave-adapted G. acherondytes 47. Our preliminary data using an intermittent flow respirometer system (Fong, unpublished data, in preparation) indicate a lower oxygen consumption rate in the two cave-adapted compared to the two surface-dwelling populations of G. minus used in this study, and they showed identical speeds of wound melanization. Although there is no data on oxygen consumption rate of G. cohabitus, it is sympatric with and is closely related to surface-dwelling G. minus 26, and may show a parallel reduction in oxygen consumption rate similar to the situation of G. acherondytes and G. troglophilus. Indeed, the timing of events during the melanization of wounds was nearly identical in most amphipod species used in this study regardless of habitat and higher taxonomic grouping, and they were unlikely to have identical metabolic rates, which strongly suggests that the speed of wound melanization is unaffected by differences in metabolic rates. One hypothesis for a potential evolutionary advantage of colonizing caves proposes reduced pressure on the immune system because of lower occurrence of parasites and pathogens (e.g.23, but see48). Our data does not support this hypothesis, because albino cave arthropods (except for T. anophthalmus) retain the wound melanization response at equal speeds as their closely related surface counterparts as we demonstrate in cave and surface G. minus populations.

To understand how important and widespread the melanization reaction is in wound healing we inflicted injuries on a range of arthropod species spanning all major subphyla. Our results showed that arthropods from diverse groups melanize wounds, suggesting that wound melanization was most likely already present in the last common ancestor of all Arthropoda. However, we found that wound melanization was lost in at least three lineages - the order Isopoda, the chelicerate Limulus polyphemus, and the atyid shrimp T. anophthalmus.

We tested 15 albino and non-albino isopod species and clades belonging to nine genera in four families from terrestrial and aquatic habitats in surface and subterranean environments, and none showed wound melanization. However, isopods have darkened mouthparts and tips of walking appendages, presumably due to melanin49,50 which contributes to the hardness of these structures. Moreover, we have observed melanized mouthparts and tips of dactyls of walking legs even in the cave-adapted albino isopods, meaning their melanin synthesis pathway is functional at least during intermolt stages. Furthermore, isopods can melanize and encapsulate parasites51 or invading bacteria52, indicating that melanin synthesis in isopods is independently regulated in response to different immune challenges. Similarly, different regulatory modules direct wound melanization and pathogen encapsulation in Aedes aegypti 39. Also, different signals induce PPO activation in different species. For instance, inner membrane lipids and not bacterial elicitors lipopolysaccharide nor peptidoglycan induce melanization in Drosophila melanogaster, whereas the opposite is true in the moth Galleria mellonella 53. In the mosquito Armigeres subalbatus, Escherichia coli were predominantly phagocytosed and Micrococcus luteus were mostly melanized54. Therefore, although the cause is unknown, only the cuticular wound melanization reaction is lost in isopods, indicating melanin synthesis is context dependent, being active in certain body parts and in response to some immune stimuli, but is inactive in the immune response during cuticular wound healing.

Limulus polyphemus also did not melanize wounds, even a week after limb amputation. We also checked the entire collection of horseshoe crabs in the Woods Hole Marine Biology Lab aquarium facility and found more than 10 individuals that had injuries and none of them had any dark pigmentation in the scar. We therefore concluded that L. polyphemus does not use melanin in wound healing.

A common trait of both L. polyphemus and isopods is that they lack the PO gene and that hemocyanins perform an analogous function in the immune response55,56. However, isopods can melanize encapsulated parasites, indicating that their melanin synthesis is functional. It is known that hemocyanins can be functionally transformed into phenoloxidase and can perform melanin synthesis57,58, that hemocyanins are also present in the cuticle and involved in sclerotization59, and that transformation of hemocyanins into immune functioning enzymes can be achieved similarly like PPO activation56. It is possible that the lack of wound melanization in Limulus and in isopods is due to different modes of activation of hemocyanins compared to phenoloxidases.

All chelicerate groups we tested (scorpions, spiders and pseudoscorpions) melanized wounds except for L. polyphemus. There are differing reports as to whether Chelicerata, or various chelicerate lineages, have PO genes55,60,61. The fact that arachnids melanize wounds suggests that either phenoloxidases are present in Chelicerates, or their hemocyanins are capable of synthesizing melanin as part of the wound healing process.


We conclude that melanization is an important part of the cuticular wound healing process in arthropods. It is present in all major arthropod subphyla and was likely already present in the last common ancestor of all arthropods. Melanization of cuticular wounds is maintained even in aphotic subterranean environments where the loss of body and eye pigmentation is a convergent feature in diverse animal groups. Additionally, melanization reactions occur at similar rates in both cave and surface G. minus, despite cave populations having lower metabolic rates. To our knowledge, this is the first documentation of cuticular wound melanization in albino arthropods.

However, cuticular wound melanization has been lost in several arthropod lineages, including isopod crustaceans, the chelicerate Limulus polyphemus, and the cave shrimp Troglocaris anophthalmus. Therefore, melanization is not an indispensable process in cuticular wound healing. The loss of cuticular wound melanization in T. anophthalmus likely resulted from colonization of the subterranean environment because all other shrimp species we tested, including the most closely related surface relative, melanize wounds. This is the first documentation of loss of cuticular wound melanization as a derived condition associated with subterranean environments.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.


  1. 1.

    Culver, D. C. & Pipan, T. The biology of caves and other subterranean habitats. (Oxford University Press, 2009).

  2. 2.

    Bilandžija, H., Ćetković, H. & Jeffery, W. R. Evolution of albinism in cave planthoppers by a convergent defect in the first step of melanin biosynthesis. Evol. Dev. 14 (2012).

  3. 3.

    Protas, M. E., Trontelj, P. & Patel, N. H. Genetic basis of eye and pigment loss in the cave crustacean. Asellus aquaticus. Proc. Natl. Acad. Sci. USA 108, 5702–5707 (2011).

  4. 4.

    Protas, M. E. et al. Genetic analysis of cavefish reveals molecular convergence in the evolution of albinism. Nat. Genet. 38, 107–111 (2006).

  5. 5.

    Ducrest, A.-L., Keller, L. & Roulin, A. Pleiotropy in the melanocortin system, coloration and behavioural syndromes. Trends Ecol. Evol. 23, 502–510 (2008).

  6. 6.

    True, J. R. Insect melanism: the molecules matter. Trends Ecol. Evol. 18, 640–647 (2003).

  7. 7.

    Christensen, B. M., Li, J., Chen, C.-C. C. & Nappi, A. J. Melanization immune responses in mosquito vectors. Trends Parasitol. 21, 192–199 (2005).

  8. 8.

    Sugumaran, M. & Barek, H. Critical analysis of the melanogenic pathway in insects and higher animals. Int. J. Mol. Sci. 17, 1–24 (2016).

  9. 9.

    Bilandžija, H., Ma, L., Parkhurst, A. & Jeffery, W. R. A potential benefit of albinism in Astyanax cavefish: Downregulation of the oca2 gene increases tyrosine and catecholamine levels as an alternative to melanin synthesis. PLoS ONE 8(11), e80823 (2013).

  10. 10.

    Kowalko, J. E. et al. Convergence in feeding posture occurs through different genetic loci in independently evolved cave populations of Astyanax mexicanus. Proc. Natl. Acad. Sci. USA 110, 16933–16938 (2013).

  11. 11.

    Gallo, N. D. & Jeffery, W. R. Evolution of space dependent growth in the teleost Astyanax mexicanus. PLoS ONE 7(8), e41443 (2012).

  12. 12.

    Duboué, E. R., Borowsky, R. L. & Keene, A. C. β-adrenergic signaling regulates evolutionarily derived sleep loss in the Mexican cavefish. Brain. Behav. Evol. 80, 233–243 (2012).

  13. 13.

    Milutinović, B. & Kurtz, J. Immune memory in invertebrates. Semin. Immunol. 28, 328–342 (2016).

  14. 14.

    Cerenius, L. & Söderhäll, K. The prophenoloxidase-activating system in invertebrates. Immunol. Rev. 198, 116–126 (2004).

  15. 15.

    Söderhäll, K. & Cerenius, L. Role of the prophenoloxidase-activating system in invertebrate immunity. Curr. Opin. Immunol. 10, 23–28 (1998).

  16. 16.

    Ashida, M. & Brey, P. T. Role of the integument in insect defense: pro-phenol oxidase cascade in the cuticular matrix. Proc. Natl. Acad. Sci. USA 92, 10698–10702 (1995).

  17. 17.

    Sugumaran, M. Comparative biochemistry of eumelanogenesis and the protective roles of phenoloxidase and melanin in insects. Pigment Cell Res. 15, 2–9 (2002).

  18. 18.

    Cerenius, L., Lee, B. L. & Söderhäll, K. The proPO-system: pros and cons for its role in invertebrate immunity. Trends Immunol. 29, 263–271 (2008).

  19. 19.

    Burmester, T. Origin and evolution of arthropod hemocyanins and related proteins. J. Comp. Physiol. B Biochem. Syst. Environ. Physiol. 172, 95–107 (2002).

  20. 20.

    González-Santoyo, I. & Córdoba-Aguilar, A. Phenoloxidase: A key component of the insect immune system. Entomol. Exp. Appl. 142, 1–16 (2012).

  21. 21.

    Chapman R. F. The insects: structure and function. (Cambridge University Press, 1998).

  22. 22.

    Lee, K. P., Simpson, S. J. & Wilson, K. Dietary protein-quality influences melanization and immune function in an insect. Funct. Ecol. 22, 1052–1061 (2008).

  23. 23.

    Tobler, M., Schlupp, I., García De León, F. J., Glaubrecht, M. & Plath, M. Extreme habitats as refuge from parasite infections? Evidence from an extremophile fish. Acta Oecol. 31, 270–275 (2007).

  24. 24.

    Ryazanova, A. D., Alekseev, A. A. & Slepneva, I. A. The phenylthiourea is a competitive inhibitor of the enzymatic oxidation of DOPA by phenoloxidase. J. Enzyme Inhib. Med. Chem. 27, 78–83 (2012).

  25. 25.

    Carlini, D. B., Manning, J., Sullivan, P. G. & Fong, D. W. Molecular genetic variation and population structure in morphologically differentiated cave and surface populations of the freshwater amphipod Gammarus minus. Mol. Ecol. 18, 1932–1945 (2009).

  26. 26.

    Holsinger, J. R., Shafer, J., Fong, D. W. & Culver, D. C. Gammarus cohabitus, a new species of subterranean amphipod crustacean (Gammaridae) from groundwater habitats in central Pennsylvania, USA. Subterr. Biol. 6, 31–41 (2003).

  27. 27.

    Jugovic, J., Jalžić, B., Prevorčnik, S. & Sket, B. Cave shrimps Troglocaris s. str. (Dormitzer, 1853), taxonomic revision and description of new taxa after phylogenetic and morphometric studies. Zootaxa 3421, 1–31 (2012).

  28. 28.

    Lévesque, M., Feng, Y., Jones, R. A. & Martin, P. Inflammation drives wound hyperpigmentation in zebrafish by recruiting pigment cells to sites of tissue damage. Dis. Model. Mech. 6, 508–515 (2013).

  29. 29.

    Mackintosh, J. A. The antimicrobial properties of melanocytes, melanosomes and melanin and the evolution of black skin. J. Theor. Biol. 211, 101–113 (2001).

  30. 30.

    Nappi, A. J. & Christensen, B. M. Melanogenesis and associated cytotoxic reactions: Applications to insect innate immunity. Insect Biochem. Mol. Biol. 35, 443–459 (2005).

  31. 31.

    Tang, H., Kambris, Z., Lemaitre, B. & Hashimoto, C. A serpin that regulates immune melanization in the respiratory system of Drosophila. Dev. Cell 15, 617–626 (2008).

  32. 32.

    Scherfer, C. et al. Drosophila Serpin-28D regulates hemolymph phenoloxidase activity and adult pigmentation. Dev. Biol. 323, 189–196 (2008).

  33. 33.

    Davis, M. M. & Engström, Y. Immune response in the barrier epithelia: Lessons from the fruit fly Drosophila melanogaster. J Innate Immun 4, 273–283 (2012).

  34. 34.

    Lee, W.-J. & Miura, M. Mechanisms of systemic wound response in Drosophila. in Current Topics in Developmental Biology (ed. Galliot, B.) 108, 153–183 (Academic Press, 2014).

  35. 35.

    Nakhleh, J., El Moussawi, L. & Osta, M. A. The melanization response in insect immunity. in Advances in Insect Physiology (ed. Ligoxygakis, P.) 52, 83–109 (Academic Press, 2017).

  36. 36.

    Arakane, Y., Noh, M. Y., Asano, T. & Kramer, K. J. Tyrosine metabolism for insect cuticle pigmentation and sclerotization. in Extracellular Composite Matrices in Arthropods (eds Cohen, E. & Moussian, B.) 165–220 (Springer International Publishing, 2016).

  37. 37.

    Zdobnov, E. M. et al. Comparative genome and proteome analysis of Anopheles gambiae and Drosophila melanogaster. Science 298, 149–159 (2002).

  38. 38.

    Chase, M. R. & Sugumaran, M. Genomic and cDNA sequence of prophenoloxidases from Drosophila melanogaster. in Phylogenetic Perspectives on the Vertebrate Immune System. Advances in Experimental Medicine and Biology (eds Beck, G., Sugumaran, M. & Cooper, E. L.) 349–362 (Springer, 2001).

  39. 39.

    Zou, Z., Shin, S. W., Alvarez, K. S., Kokoza, V. & Raikhel, A. S. Distinct melanization pathways in the mosquito Aedes aegypti. Immunity 32, 41–53 (2010).

  40. 40.

    Arakane, Y., Muthukrishnan, S., Beeman, R. W., Kanost, M. R. & Kramer, K. J. Laccase 2 is the phenoloxidase gene required for beetle cuticle tanning. Proc. Natl. Acad. Sci. USA 102, 11337–11342 (2005).

  41. 41.

    Dittmer, N. T. et al. Characterization of cDNAs encoding putative laccase-like multicopper oxidases and developmental expression in the tobacco hornworm, Manduca sexta, and the malaria mosquito, Anopheles gambiae. Insect Biochem. Mol. Biol. 34, 29–41 (2004).

  42. 42.

    Du, M.-H. et al. Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae). Parasit. Vectors 10, 171 (2017).

  43. 43.

    De Gregorio, E., Spellman, P. T., Rubin, G. M. & Lemaitre, B. Genome-wide analysis of the Drosophila immune response by using oligonucleotide microarrays. Proc. Natl. Acad. Sci. USA 98, 12590–12595 (2001).

  44. 44.

    Bartholomay, L. C. et al. Description of the transcriptomes of immune response-activated hemocytes from the mosquito vectors Aedes aegypti and Armigeres subalbatus. Infect. Immun. 72, 4114–4126 (2004).

  45. 45.

    Qiao, L. et al. Tyrosine hydroxylase is crucial for maintaining pupal tanning and immunity in Anopheles sinensis. Sci. Rep. 6, 29835 (2016).

  46. 46.

    Sideri, M., Tsakas, S., Markoutsa, E., Lampropoulou, M. & Marmaras, V. J. Innate immunity in insects: surface-associated dopa decarboxylase-dependent pathways regulate phagocytosis, nodulation and melanization in medfly haemocytes. Immunology 123, 528–537 (2008).

  47. 47.

    WIilhelm, F. M., Taylor, S. J. & Adams, G. L. Comparison of routine metabolic rates of the stygobite, Gammarus acherondytes (Amphipoda: Gammaridae) and the stygophile, Gammarus troglophilus. Freshw. Biol. 51, 1162–1174 (2006).

  48. 48.

    Day, J., Starkey, D. E. & Gerken, J. E. Prevalence of parasitism in the Grotto Sculpin (Cottus specus), a new species of cave-adapted fish from southeastern Missouri, USA. Subterr. Biol. 12, 3–14 (2014).

  49. 49.

    Brehme, K. S. The effect of adult body color mutations upon the larva of Drosophila melanogaster. Proc. Natl. Acad. Sci. USA 27, 254–61 (1941).

  50. 50.

    Gorman, M. J. & Arakane, Y. Tyrosine hydroxylase is required for cuticle sclerotization and pigmentation in Tribolium castaneum. Insect Biochem. Mol. Biol. 40, 267–273 (2010).

  51. 51.

    Koehler, A. V. & Poulin, R. Host partitioning by parasites in an intertidal crustacean community. J. Parasitol. 96, 862–868 (2010).

  52. 52.

    Chevalier, F. et al. The immune cellular effectors of terrestrial isopod Armadillidium vulgare: Meeting with their invaders, Wolbachia. PLoS ONE 6(4), e18531 (2011).

  53. 53.

    Bidla, G., Hauling, T., Dushay, M. S. & Theopold, U. Activation of insect phenoloxidase after injury: Endogenous versus foreign elicitors. J. Innate Immun. 1, 301–308 (2009).

  54. 54.

    Hillyer, J. F., Schmidt, S. L. & Christensen, B. M. Hemocyte-mediated phagocytosis and melanization in the mosquito Armigeres subalbatus following immune challenge by bacteria. Cell Tissue Res. 313, 117–127 (2003).

  55. 55.

    Jaenicke, E. et al. Is activated hemocyanin instead of phenoloxidase involved in immune response in woodlice? Dev. Comp. Immunol. 33, 1055–1063 (2009).

  56. 56.

    Coates, C. J. & Nairn, J. Diverse immune functions of hemocyanins. Dev. Comp. Immunol. 45, 43–55 (2014).

  57. 57.

    Decker, H. & Tuczek, F. Tyrosinase/catecholoxidase activity of hemocyanins: structural basis and molecular mechanism. Trends Biochem. Sci. 25, 392–397 (2000).

  58. 58.

    Adachi, K. et al. An oxygen transporter hemocyanin can act on the late pathway of melanin synthesis. Pigment Cell Res. 18, 214–219 (2005).

  59. 59.

    Kuballa, A. V. & Elizur, A. Differential expression profiling of components associated with exoskeletal hardening in crustaceans. BMC Genomics 9, 575 (2008).

  60. 60.

    Palmer, W. J. & Jiggins, F. M. Comparative genomics reveals the origins and diversity of arthropod immune systems. Mol. Biol. Evol. 32, 2111–2129 (2015).

  61. 61.

    Bechsgaard, J. et al. Comparative genomic study of arachnid immune systems indicates loss of beta-1,3-glucanase-related proteins and the immune deficiency pathway. J. Evol. Biol. 29, 277–91 (2016).

  62. 62.

    Legg, D. A., Sutton, M. D. & Edgecombe, G. D. Arthropod fossil data increase congruence of morphological and molecular phylogenies. Nat. Commun. 4, 2485 (2013).

Download references


We wish to thank cave biologists Branko Jalžić, Jana Bedek and Martina Pavlek for collecting cave arthropods and identifying crustacean, spider and coleopteran species as well as Petra Bregović, Tamara Čuković, Vedran Sudar, Anđela Čukušić, Alen Kirin and Luca Dorigo for their help with collecting cave arthropods in Croatia. We thank Ben Hutchins and Benjamin Schwartz for their hospitality and providing animals and lab space for our work in Texas, and Dave and Sandy Cowan for hosting us during our work in West Virginia. We also thank Wil Orndorff, Steve Taylor, Kirk Zigler and Mike Slay for providing various animals from US locales, Ben Friedel for performing some of the work on US amphipods and isopods, and Austen Barnett for work on the mites. We are grateful to William R. Jeffery for discussion and advice as well as providing lab space at MBL, Woods Hole. We are thankful to Helena Ćetković for providing lab space in Zagreb and some of the supplies for this project. Parts of this study were supported by funds from the Cave Conservancy of the Virginias to DWF. HB received funding support from the European Union Seventh Framework Programme (FP7 2007-2013) under grant agreement no. 291823 Marie Curie FP7-PEOPLE-2011-COFUND – NEWFELPRO as part of the project EACAA, grant agreement No. 50.

Author information


  1. Department of Molecular Biology, Ruđer Bošković Institute, Zagreb, 10000, Croatia

    • Helena Bilandžija
  2. Museum of Comparative Zoology, Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, 02138, USA

    • Mara Laslo
  3. Department of Biology, University of Hawai’i at Mānoa, Honolulu, HI, 96822, USA

    • Megan L. Porter
  4. Department of Biology, American University, Washington, DC, 20016, USA

    • Daniel W. Fong


  1. Search for Helena Bilandžija in:

  2. Search for Mara Laslo in:

  3. Search for Megan L. Porter in:

  4. Search for Daniel W. Fong in:


H.B., M.L., D.W.F. conceived the study. All authors performed the experiments. H.B. wrote the original manuscript draft. M.L. prepared the figures. All authors reviewed and edited the manuscript.

Competing Interests

The authors declare that they have no competing interests.

Corresponding author

Correspondence to Daniel W. Fong.

About this article

Publication history






By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.