Open Access

Sarcoptes scabiei: genomics to proteomics to biology

  • Larry G. Arlian1Email author,
  • Marjorie S. Morgan1 and
  • S. Dean RiderJr1
Parasites & Vectors20169:380

https://doi.org/10.1186/s13071-016-1663-6

Received: 4 May 2016

Accepted: 22 June 2016

Published: 1 July 2016

Abstract

Background

The common scabies mite, Sarcoptes scabiei is a cosmopolitan parasite of humans and other mammals. An annotated genome of Sarcoptes scabiei var. canis has been deposited in the National Center for Biotechnology Information (NCBI) and VectorBase and a proteomic analysis of proteins in extracts of mite bodies and eggs from this strain has been reported. Here we mined the data to identify predicted proteins that are known to be involved in specific biological processes in other animals.

Results

We identified predicted proteins that are associated with immunomodulation of the host defense system, and biological processes of the mite including oxygen procurement and aerobic respiration, oxidative metabolism, sensory reception and locating a host, neuronal transmission, stressors (heat shock proteins), molting, movement, nutrient procurement and digestion, and excretion and water balance. We used these data to speculate that certain biological processes may occur in scabies mites.

Conclusion

This analysis helps understand the biology of Sarcoptes scabiei var. canis and adds to the data already available in NCBI and VectorBase.

Keywords

Sarcoptes scabiei Scabies miteGenome sequenceBiological processes

Background

The scabies mite, Sarcoptes scabiei, is a permanent obligate ectoparasite that lives and reproduces in the epidermis of skin of humans and many other mammalian hosts. Scabies is an important, neglected disease afflicting populations worldwide causing significant human and animal morbidity and mortality. Although there has been much progress in understanding the mite biology and interaction with its host, much is yet unknown.

A recent proteomic analysis of S. scabiei var. canis provided a listing of some of the proteins found in an aqueous extract of mite bodies, an extract of insoluble pellet of mite bodies, and an aqueous extract made from scabies mite eggs [1]. Likewise, the genome has been sequenced for this strain of S. scabiei [2]. The genomic and proteomic data are available at the National Center for Biotechnology Information (NCBI) and VectorBase. The genomic and proteomic data for specific aspects of the biology of this mite species provides a greater understanding of its physiology and the biochemical pathways associated with specific functions. Also, it may provide the basis for further research of this parasite. In the present research, we focused on questions about the biology of scabies mites and then searched for proteins likely associated with these biological processes. With these data it is now possible to identify groups of predicted proteins and to postulate certain biological processes and mechanisms used by these mites to live on and interact with their hosts.

Methods

We have previously reported the sequencing of DNA from the scabies mite, Sarcoptes scabiei var. canis, and the assembly of a draft genome for this organism [2]. All data for this project were deposited into the National Center for Biotechnology Information (NCBI) under BioProject PRJNA268368. Data are also available through VectorBase at www.vectorbase.org. Along with the draft genome, the sequences of 10,470 predicted Sarcoptes scabiei var. canis proteins were also deposited with accession numbers KPL93347 to KPM12096. The production of > 150 of these predicted proteins was previously confirmed by mass spectrometry [1] and an additional 50 proteins have since been identified using identical methods.

Most of the data tables presented in this manuscript were constructed using keyword searches of the NCBI S. scabiei protein database which includes the 10,470 S. scabiei var. canis sequences described above as well as ~270 additional sequences for proteins from scabies mites collected from other hosts (mostly humans and pigs). These searches returned hits when the keyword was part of the name assigned to the protein as well as when the keyword was found in the annotated record for a protein. For example, a search for “heme” returned both Heme peroxidase-like protein (where “heme” is in the name) and globin-like protein 1 (since the protein record indicates that a “heme-binding site” is part of the predicted structure). Proteins whose production was confirmed by mass spectrometry (MS) are noted in the supplementary tables (Additional file 1: Tables S1–S13).

BLAST2GO version 3.2 [3] was used to identify GO terms from interpro domains identified in all S. scabiei var. canis proteins that were not designated as “hypothetical” proteins in the proteome. These data are available in Additional file 2. GO terms grouped by biological process, cellular location, and molecular function were exported and used in keyword searches to help identify proteins of interest.

Molecular phylogenies generated for groups of related proteins utilized alignments generated by ClustalOmega (available at http://www.ebi.ac.uk/Tools/msa/clustalo/), followed by reconstructions of Neighbor Joining trees using ClustalW2 Phylogeny. Fig Tree v1.4.2 was used to render the phylogenetic tree images.

Results and discussion

Immunomodulation

Molecules in extracts made from scabies mites have been shown to modulate the secretion or expression of cytokines, chemokines and cell adhesion molecules by cells of the epidermis and dermis of the skin and circulating blood lymphocytes [415], and inhibit the complement pathway of the host [16]. These data suggested that some aspects of this modulation delay the innate and adaptive immune responses to these mites and are responsible for the lack of clinical signs in the host for 4–8 weeks before skin symptoms are visible and patients seek diagnosis and treatment. Specifically, human peripheral blood mononuclear cells (PBMCs) stimulated with a whole body extract of scabies mites were shown to produce interleukin-10 (IL-10) but not IL-2 and IL-4 [9]. This cytokine profile suggested that the stimulated cell population consisted of T-regulatory (Treg) cells and not T-helper-1 (Th-1), Th-2, and Th-17 phenotypes. Studies have shown that cystatin, a 14 kDa protein in extracts of the parasitic round worm, Ascaris lumbricoides, up-regulated expression of IL-10 and transforming growth factor-β (TGFβ) from splenocytes from mice [17]. The genome for scabies mites contains two genes (QR98_0079060 and QR98_0079070) coding for cystatin-like proteins (KPM09372 and KPM09373) so it can be predicted that scabies mites may produce cystatin-like proteins and these proteins may be responsible for the up-regulated secretion of IL-10 observed from the Treg cells stimulated with a scabies mite extract. IL-10 is anti-inflammatory and immune-suppressive and among other things, down-regulates a T-cell mediated immune response by depressing the expression of MHC II on the surface of antigen-presenting cells (APCs) and thus the interaction of the MHC II/antigen complex on the APCs with the T-cell receptor needed to stimulate T-helper cells.

Interestingly, several tick species including Ixodes scapularis, Dermacentor variabilis, Rhipicephalus microplus, Haemaphysalis longicornis and Ornithodoros moubata (soft tick) have predicted cystatin-like proteins with some homology (< 31 % identity) to the scabies mite molecules (DELTA-BLAST search of KPM09372 and KPM09373 vs non-redundant protein sequences restricted to Acari, 16 Mar 2016). The two predicted scabies mite cystatin-like proteins also show limited (31 %) identity to each other. The gene for one of the predicted scabies mite proteins has a secretion signal (QR98_0079060).

Likewise, macrophage migration inhibitory factor (MIF) genes have been identified in both ticks and scabies mites [2, 18]. MIF is a chemokine that regulates macrophage and other leukocyte migration [19]. A MIF gene from scabies mites has high nucleotide sequence homology with a MIF gene from the ticks D. variabilis, Amyblomma americanum and H. longicornis [18]. Although the gene nucleotide sequences differed slightly, the putative amino acid sequences for the scabies mite and the tick D. variabilis MIF proteins are identical.

Many genes for homologs of salivary gland proteins from ticks and other blood-sucking arthropods are present in the scabies mite genome [2]. These include ferritins, cathepsins, glutathione-S-transferases and thioredoxins. Genes for multiple tetraspanins that are involved in cell adhesion, cell migration and proliferation [20] are also present. Scabies mites have ten tetraspanin-like proteins and eight others with tetraspanin domains (Table 1). Scabies mites also have several genes that code for production of calmodulin-like proteins [2], which are calcium-binding proteins found in tick saliva [21]. The presence of many of these putative sialoproteins, including camodulins and calreticulin, in scabies mite body extracts was also verified by mass spectrometry [1].
Table 1

Sarcoptes scabiei var. canis proteins containing tetraspanin domains. Proteins were identified by NBCI protein database search of “Sarcoptes scabiei [and] tetraspanin” on 28 Mar 16

Name assigned to S. scabiei predicted protein

# aa

Accession #

Tetraspanin-like protein 1

271

KPM03168

Tetraspanin-like protein 2

209

KPM03650

Tetraspanin-like protein 3

201

KPM04223

Tetraspanin-like protein 4

240

KPM04224

Tetraspanin-like protein 5

228

KPM06000

Tetraspanin-like protein 6

382

KPM08766

Tetraspanin-like protein 7

249

KPM08935

Tetraspanin-like protein 8

88

KPM11003

Tetraspanin-5-like protein

338

KPM02620

Tetraspanin-11-like protein

248

KPM04544

CD151 antigen-like protein

148

KPM06528

CD63 antigen-like protein

236

KPM04484

CD81 antigen-like protein

288

KPM04961

Hypothetical protein QR98_0011670

152

KPM02748

Hypothetical protein QR98_0030280

252

KPM04578

Hypothetical protein QR98_0032560

272

KPM04802

Hypothetical protein QR98_0065550, partial

302

KPM08042

Hypothetical protein QR98_0076100

176

KPM09080

Oxygen requirements

Scabies mites represent an unusual taxon of arthropods and metazoan animals that require oxygen (aerobic) but lack an organized respiratory system for obtaining it. They belong to the Astigmata group of Acari since no specialized surface or organ involved in oxygen uptake has yet been described or proposed. Scabies mites do not seem to have homologs for genes related to the known development of trachea that have been identified in Drosophila [22]. Interestingly, the scabies mite genome contains a homolog for the gene “scribbled” which in Drosophila promotes the development of both tracheae and salivary glands [22]. Apparently, the downstream genes representing the tracheal arm of this pathway are absent in scabies mites while the salivary gland pathway genes are present. In contrast, despite lacking the trachea-promoting genes identified in Drosophila, ticks and some other mites have tracheae [23, 24] so in some Acari there may be an alternative pathway for developing tracheae.

The oxygen requirements for scabies mites are low and were reported to be 0.002 and 0.0008 μl O2/h for female and male mites, respectively [25]. In comparison, the closely related astigmatid house dust mite, Dermatophagoides farinae, is of similar size and utilizes 0.009 μl O2/h for females [26]. Neither the source nor the mechanism for obtaining oxygen is known for any of these astigmatid mites. In the case of house dust and storage mites that are terrestrial, the source of oxygen is most likely ambient air. It is not clear what the source of oxygen is for scabies mites while they are burrowing in the epidermis but presumably when they wander on the surface of the skin, they obtain oxygen from the ambient air. How much O2 is available in the burrow in the skin is unknown. If the mites ingest serum as they burrow, dissolved oxygen in this fluid could provide the oxygen they need along with nutrients. In humans, the partial pressure of oxygen in the arterial blood and serum in the surrounding tissues that bathes cells is about 100 mmHg (0.003 μl O2/μl fluid) and drops to 40 mmHg (0.0012 μl O2/μl fluid) in venule blood. Could this be enough to meet their needs? These mites are too small to perform many physiological studies that would provide clues to how they obtain oxygen. Histology (electron microscopy) of both scabies and house dust mites provides no clues. However, genomic and proteomic data and associated genes and protein homologs that are associated with the process of obtaining oxygen and eliminating carbon dioxide in other organisms may provide some hints for these processes in scabies mites.

Regardless of how oxygen enters the mite body, scabies mites possess a wide variety of proteins typically involved in oxygen transport and utilization in other animals. Our analysis has predicted many proteins that may have an oxygen binding/transporting function in S. scabiei (Additional file 1: Table S1). Among these are more than 150 predicted proteins that contain heme, an oxygen-binding prosthetic group. Four genes code for globin proteins (QR98_0021760 = KPM03742 = globin-like protein 1; QR98_0035350 = KPM05076 = globin-like protein 2; QR98_0086180 = KPM10070 = cytoglobin-1-like protein; and QR98_0042210 = KPM05052 = neuroglobin-like protein) that could be involved in the transport of oxygen. The predicted proteome also contains a complete set of oxidative respiration (tricarboxylic acid cycle) enzymes (several of which were previously identified by MS) [1] as well as > 130 enzymes involved in oxidative/reduction processes (Additional file 1: Table S2).

Thus, scabies mites require oxygen and they have many genes and predicted protein products associated with this requirement but the anatomy and biochemistry of getting O2 into the body and to the cells are unknown.

Post-embryonic development/molting

The life-cycle of scabies mites includes the egg, larva, protonymph, tritonymph and adult male or female [27]. Larvae hatch from eggs, feed, grow, undergo metamorphosis and molt to protonymphs. The process is repeated for protonymphs that give rise to tritonymphs and tritomymphs that give rise to adults. The molting process is well detailed for insects where it is regulated by ecdysteroids, and presumably, it is similar in mites. It involves digestion and reabsorption of some of the old cuticle (procuticle and endocuticle if both are present) and development of a new cuticle (procuticle) and varied degrees of sclerotization to harden the new procuticle. Hardening involves cross-linking of linear proteins and chitin molecules, the major components of the cuticle [28, 29]. Chitin is a polymer of N-acetyl-D-glucosamine molecules that are linked by β-1,4 covalent bonds. Chitin can be hydrolyzed by chitinase and exochitinase (or β-N-acetylglucosaminidase) [30]. Chitin synthase promotes polymerization of the linear chitin molecule. Proteases hydrolyze the protein filaments. Many enzymes and biochemical pathways and several hormones are involved in the synthesis, translocation and degradation of the chitin and protein in the cuticle during the molting process. The scabies mite proteome contains 16 proteins that are predicted to serve as structural constituents of the cuticle (Table 2). This proteome also contains two chitin synthase-like proteins and four chitin deacetylase-like proteins (the latter catalyzes cleavage of acetate from the glucosamine molecule). In addition, there are 12 chitinase-like proteins, two (Sar s 15 and 18) that are homologs of house dust mite allergens (Additional file 1: Table S3). The scabies mite proteome also contains several glucosidases but it is unknown if they may play a role in degrading the cuticle. The genome also contains homologs of all of the enzymes known to be involved in ecdysteroidogenesis [31], indictating ecdysteroids are likely to regulate development in this mite (Table 3).
Table 2

Structural constituents of Sarcoptes scabiei var. canis cuticle. Proteins were identified by NBCI protein database search of “Sarcoptes scabiei [and] cuticle” on 11 Feb 16

Name assigned to S. scabiei predicted protein

# aa

Accession #

Cuticle protein-like protein 1

104

KPL98302

Cuticle protein-like protein 2

663

KPM03015

Cuticle protein-like protein 3

168

KPM06751

Cuticle protein-like protein 4

404

KPM08892

Cuticle protein-like protein 5

225

KPM10980

Cuticle protein-like protein 6

341

KPM10998

Cuticle protein-like protein 7

314

KPM11880

Cuticular protein-like protein 9

160

KPM09762

Cuticular protein-like protein 8

360

KPM02447

Cuticular protein-like protein 10

189

KPM09771

Cuticular protein-like protein 11, partial

245

KPM10754

Cuticle protein 57A-like protein 1

107

KPM08966

Cuticle protein 57A-like protein 2

189

KPM08973

Cuticle protein 92A-like protein

121

KPM08994

Cuticle protein viking-like protein

584

KPM06292

Structural constituent of cuticle-like protein

214

KPM09986

Table 3

Drosophila melanogaster genes involved in ecdysteroidogenesis and their predicted Sarcoptes scabiei var. canis gene and protein homologs. Adapted from [31]

D. melanogaster gene

S. scabiei gene homolog

Name assigned to S. scabiei predicted protein

Accession #

neverland

QR98_0055560

Rieske domain-containing protein

KPM07074

shroud

QR98_0023390

11-cis retinol dehydrogenase-like protein

KPM03900

spook/spookier

QR98_0048390

cytochrome P450-like protein 16

KPM06364

phantom

QR98_0078290

cytochrome P450-like protein 20

KPM09295

disembodied

QR98_0104600

cytochrome P450-like protein 26

KPM11882

shadow

QR98_0023200

cytochrome P450-like protein 10

KPM03882

shadow

QR98_0044620

cytochrome P450-like protein 15

KPM05989

shade

QR98_0022240

cytochrome P450-like protein 9

KPM03790

Compounds that target and interfere with specific steps in the formation of the cuticle and the molting process have been developed for use as insecticides to control some insect species. As more is learned about these processes in mites and in particular scabies mites, specific aspects of these processes may be targets for developing new methods for controlling these mites on their hosts.

Muscle physiology

A general description of the mechanism for striated muscle activation and contraction can be found in many general physiology textbooks. Presumably scabies mites have striated muscles with morphology and contractile physiology similar to those of other arthropods and vertebrates. These would include actin and myosin protein fibers and the interaction sites involving dihydropyridine receptors, ryanodine receptors, calcium channels and pumps, tropomyosin, troponin subunits T, C, and I and calsequestrin. The fundamental mechanism based mostly on vertebrate studies, is that action potentials (depolarization), traveling into T-tubules mediated through dihydropyridine receptors and ryanodine receptors, cause opening of calcium channels in the sarcoplasmic reticulum (SR) membrane and the release of calcium from the SR into the myoplasm [3234]. Activation of the actin and myosin contraction complex that results in sliding of the filaments to shorten the sarcomere (thus muscle), is calcium mediated and involves a calcium flux from the SR lumen into the myoplasm around the actin and myosin filaments. Relaxation of the muscle results from lower calcium concentration in the myoplasm by sequestration of calcium back into the SR. Lower calcium concentration in the myoplasm is accomplished by transmembrane proteins that pump calcium from the myoplasm back into the SR lumen where it binds to calsequestrin [35]. The presence of actin, myosin and tropomyosin in whole body extracts of scabies mites has already been confirmed by mass spectrometry [1]. The predicted proteome of scabies mites includes multiple actins (many of which may be involved in cytoskeletal movement) and myosins, tropomyosin, troponin T-, C- and I-like proteins, ryanodine receptors, and numerous calcium pump proteins (Additional file 1: Table S4). Also, the scabies mite predicted proteome includes the calcium-binding proteins, calmodulin and calsequestrin-2-like proteins, as well. These proteins play a key role in sequestering calcium in the SR and in muscle contraction [35]. All this taken together is indirect evidence that muscle contraction and movement in scabies mites are accomplished by anatomy and contractile mechanisms that are similar to those used by insects, other arthropods and vertebrates.

Calcium-binding proteins

Approximately 143 calcium-binding proteins are predicted in the S. scabiei proteome and these are listed in Additional file 1: Table S5. Many such as calsequestrin and calmodulin, that are important in sequestration of calcium ions in the SR, are essential to muscle function and have already been mentioned. Another group appears to be low-density lipoprotein receptor-like proteins while many are hypothetical proteins of undetermined function.

Heat shock proteins and others involved in protein folding and conformation

Heat shock proteins (HSPs) are a large family of intracellular proteins that have multiple functions including acting as chaperones and maintaining the conformation and folding/unfolding of proteins, assembly of protein complexes, and transporting and sorting of proteins [3638]. Each protein is designated by its molecular weight in kilodaltons. They are ubiquitous in organisms and are generally expressed when organisms encounter stressful conditions. HSPs with molecular weights, including 22, 23, 26, 27, 40, 60, 68, 70, 75, 78, 83 and 90, have been reported in a variety of insect species [37]. We found a large number of heat shock proteins in the proteome of scabies mites (Table 4) and the production of many of them has been confirmed by MS analysis [1]. Eight heat shock protein 70-like proteins (Sar s 28) are homologs of house dust mite allergens. HSP 10, 20, 60 and 90 family members are also present in the scabies mite proteome. This proteome also contains many other chaperone-type proteins (Additional file 1: Table S6).
Table 4

Sarcoptes scabiei var. canis heat shock proteins. Proteins were identified by NBCI protein database search of “Sarcoptes scabiei [and] heat shock” on 11 Feb 16

Name assigned to S. scabiei predicted protein

# aa

Accession #

10 kDa Heat shock protein, mitochondrial-like protein

101

KPM11276

Heat shock protein 20-like protein 1

168

KPM02991

Heat shock protein 20-like protein 2

155

KPM04326

Heat Shock Protein 20-like protein 3

208

KPM04511

Heat Shock Protein 20-like protein 4

194

KPM09528

60 kDa Heat shock protein, mitochondrial-like protein

584

KPM06690

Sar s 28 (heat shock protein 70-like protein 1)

836

KPL97880

Sar s 28 (heat shock protein 70-like protein 2)

634

KPM03927

Sar s 28 (heat shock protein 70-like protein 3)

414

KPM07069

Sar s 28 (heat shock protein 70-like protein 4), partial

496

KPM07870

Sar s 28 (heat shock protein 70-like protein 5)

520

KPM08853

Sar s 28 (heat shock protein 70-like protein 6)

703

KPM10172

Sar s 28 (heat shock protein 70-like protein 7)

917

KPM10783

Sar s 28 (heat shock protein 70-like protein 8)

567

KPM11560

Heat shock protein 90-like protein 1

587

KPM03324

Heat shock protein 90-like protein 2

469

KPM07599

Heat shock protein 90-like protein 3

796

KPM09034

Neurotransmitters and receptors

Incoming signals (chemo-, mechano-, photo-) travel along neurons as action potentials (APs). A membrane potential is maintained by the regulated pumping of sodium and potassium ions. Many sodium and potassium ion channel proteins have been predicted in the scabies mite proteome (Additional file 1: Table S7). Upon reaching the pre-synaptic membrane, the AP causes calcium channels to open and extracellular calcium diffuses into the neuron, which in turn triggers fusion of the synaptic vessel with the presynaptic membrane and the release of neurotransmitter that docks with the appropriate receptor on the postsynaptic membrane. There are four known classes of neural transmitters in insects: acetylcholine, biogenic amines, amino acids and peptides [39]. A gene for the receptor for the biogenic amine dopamine is present in the scabies mite genome (QR98_0022910). This neurotransmitter and GABA (γ- amino butyric acid) may play a role in salivary gland secretion in ticks [40, 41]. Could it be involved in scabies mite salivary secretion as well? We have identified a number of specific receptors for various neurotransmitters in these classes in the predicted S. scabiei proteome (Additional file 1: Table S8). These neurotransmitter receptor proteins include those predicted to bind acetylcholine, nicotinic, dopamine, serotonin, GABA and neuropeptide Y. Because the scabies mite proteome includes these neural receptors, presumably, these mites utilize the corresponding neurotransmitters.

Sequencing of the scabies mite genome predicted the presence of a neuropeptide receptor in the somatostatin/allatostatin family. In mammals, somatostatin is a peptide produced by neuroendrocrine neurons that has multiple functions including effecting neurotransmission [42]. Generally, it has inhibitory functions. Genes for the closely related neuropeptide allatostatins and their receptors have been found in the genome of the honeybee and in D. melanogaster and these share high homologies to somatostatin [43]. Allatostatins are thought to inhibit juvenile hormone synthesis in the honeybee brain. However, the presence of juvenile hormones in mites and ticks remains controversial [44]. Honeybee allatostatin [45] shares ~36 % identity with a hypothetical scabies mite protein (KPM07409). Thus, an allatostatin-like peptide hormone regulatory network probably also functions in S. scabiei, although its basic function remains unknown.

Photoreception

Ability to detect environmental stimuli is important to survival of S. scabiei. Laboratory studies show that scabies mites respond positively to thermo-, chemo- and odor stimuli and will seek the source [46]. These mites respond to light even though they have no visible simple eyes on their body surface like some species of mites. However, simple light receptor cells could be located beneath the cuticle surface and stimulated when light passes through the clear cuticle. Opsin is a ubiquitous protein associated with light reception among most animals that respond to light. Opsin is coupled with the carotenoid light sensitive photopigment retinal to make the molecule rhodopsin [47]. Many predicted G-proteins, receptor-like proteins for rhodopsin and retinal, retinal degradation proteins, and molecules associated with the photochemistry of photoreception of electromagnetic radiation are present in the scabies mite proteome (Additional file 1: Table S9).

Chemoreception

A classic host-seeking study has clearly shown that mites respond to host odor and are attracted to its source [46]. Several previous studies have also shown that scabies mites are attracted to 17 lipids that are present in or on the epidermis of mammalian skin [48]. Likewise, scabies mites are attracted by the odor from a host independent of body heat or contact with the skin and its various chemical components and physical properties [46]. Presumably these attractions facilitate location of a host and/or guide mites to specific areas of the host body.

In addition, our previous study revealed that scabies mites are attracted to several nitrogenous wastes and phenolic compounds that act in a pheromone-like manner and induce aggregation of these mites [49]. Ticks secrete nitrogenous wastes and phenolic compounds that act in a pheromone like-manner to promote assembly and other behavior [50]. The test methods used for the scabies mite behavior studies were not designed to determine the purpose of this assembly, but it may play a key role in attraction of sexes for mating. Early and ordinary scabies infestations involve few mites on the host so mite produced nitrogen wastes such as guanine, purine, adenine, allantoin, hypoxanthine, xanthine, uric acid, ammonium chloride, ammonium nitrate and ammonium sulfate and pheromones, likely play key roles in the reproduction of scabies mites during this time. The fact that scabies mites respond to these compounds indicates that they have chemoreceptors that recognize the volatile and contact compounds.

Taken together, all of these studies have shown that S. scabiei var. canis must have chemoreceptors. Like insects, it is expected that mites have odorant (OR), gustatory (GR) and ionotropic (IR) chemoreceptors. In the insects, and probably the Acari, chemoreceptors are usually located in hollow pegs or setae known as sensilla that are located on the antenna, terminal segments of the legs (tarsus), proboscis/mouthparts, wing margins, ovipositor and possibly pedipalps [51, 52]. Typically, these sensilla are perforated along the sides or at the tip and this allows stimulant molecules from the air (odor/pheromones) or contact (gustatory) to enter hemolymph in the sensilla bathing the neuron and bind to an odorant/tastant-binding protein that transports the stimulating molecule to the sensory receptor on the neuron [51]. The odorant/transporting complex or the released stimulant molecule activates the sensory receptor. Mites have hollow sensilla on the terminal segments of the legs that presumably function in a similar manner. It is not known if the oral cavity has chemoreceptors beneath the cuticle lining or if there are chemoreceptors on the pretarsal stocked empodia, chelicera, pedipalps and other body areas of scabies and other mites.

A scabies mite protein database search identified 13 predicted proteins that may be involved in chemoreception (Table 5). These include various sweet-taste receptor-like proteins, and a gustatory receptor-like protein. Our analysis of S. scabiei predicts fewer chemoreceptors in scabies mites than are reported in the genomes of some blood-sucking insects but approximately the same as for the body louse Pediculus humanus corporis. For example, the bedbug, Cimex lectularius, has genes coding for 49 olfactory receptors, 36 gustatory receptors and 30 ionotropic receptors [53]. The tsetse fly, Glossina morsitans morsitans, has 46 and 14 annotated gene loci for ORs and GRs, respectively [54]. The mosquitoes, Anopheles gambiae and Aedes aegypti, have many more ORs and GRs than both the tsetse flies and scabies mites. The genome for the human body louse contains ten odorant receptor genes [55].
Table 5

Sarcoptes scabiei var. canis proteins predicted to be involved in chemoreception. Proteins were identified by NBCI protein database search of “Sarcoptes scabiei [and] taste [or] sensory” on 1 Mar 16

Name assigned to S. scabiei predicted protein

# aa

Accession #

7 transmembrane sweet-taste receptor-like protein 1

140

KPM05630

7 transmembrane sweet-taste receptor-like protein 2

321

KPM06440

7 transmembrane sweet-taste receptor-like protein 3, partial

385

KPM09849

Class C metabotropic glutamate-like protein G-protein coupled receptor-like protein

187

KPM06441

Gamma-aminobutyric acid type B receptor subunit 1-like protein, partial

861

KPM06518

Glutamate receptor, metabotropic-like protein 2

164

KPM11384

Gustatory receptor-like protein

441

KPM04823

Metabotropic glutamate receptor 1-like protein 1, partial

429

KPM05105

Metabotropic glutamate receptor-like protein 3

526

KPM07738

Metabotropic glutamate receptor-like protein 4

476

KPM08699

Pheromone and odorant receptor-like protein

1650

KPM05712

Sensory neuron membrane protein 1-like protein

346

KPM11235

Sweet-taste receptor-like protein

429

KPM09147

Previous studies showed that scabies mites respond to host odor in the absence of carbon dioxide [46]. Whether or not CO2 by itself will arouse activity in scabies mites has not been determined. CO2 from a host is a stimulus for blood feeding mosquitoes and other insects [56, 57] and ticks [50]. Chemosensory neurons in Drosophila that are CO2-sensitive express the chemoreceptors Gr21a and Gr63a. The An. gambiae mosquito homologs are GPPRGR22 and GPRRGR24 [58]. The scabies mite predicted proteome does not have orthologs of the CO2 receptors from insects. Thus, if CO2 sensing occurs in scabies mites it utilizes an unknown pathway. However, scabies mites will seek a host in the absence of CO2. Genes for CO2 receptors have not been identified in the tick genome even though ticks do respond to CO2.

The family of ionotropic receptors can be located on post-synaptic membranes and form ion channels. These receptors have an extracellular domain that binds the neurotransmitter and other domains that cross the membrane and form the ion channel [59]. When activated by the neurotransmitter, the flow of ions through the pore is either increased or decreased. The scabies mite genome has 16 predicted “ionotropic receptor proteins” (Table 6). In contrast, bedbugs have 30 predicted ionotropic receptors [53], 24 of which have significant homology with 15 different S. scabiei var. canis proteins (Additional file 1: Table S10).
Table 6

Sarcoptes scabiei var. canis ionotropic receptors. Proteins were identified by NBCI protein database search of “Sarcoptes scabiei [and] ionotropic” on 24 Mar 16

Name assigned to S. scabiei predicted protein

# aa

Accession #

Glutamate receptor, ionotropic kainate 2 precursor-like protein 1

147

KPM04302

Glutamate receptor, ionotropic kainate 2 precursor-like protein 2

465

KPM04471

Glutamate receptor, ionotropic kainate 2-like protein 1

298

KPM02574

Glutamate receptor, ionotropic kainate 2-like protein 2

652

KPM04300

Glutamate receptor, ionotropic kainate 2-like protein 3

887

KPM05200

Glutamate receptor, ionotropic kainate 2-like protein 4

357

KPM05378

Glutamate receptor, ionotropic kainate 3-like protein 1

1102

KPL94547

Glutamate receptor, ionotropic kainate 3-like protein 2

883

KPM06129

Glutamate receptor, ionotropic kainate-like protein 1, partial

746

KPM03138

Glutamate receptor, ionotropic kainate-like protein 2

553

KPM05237

Glutamate receptor, ionotropic, kainate-like protein 3

180

KPM04472

Glutamate receptor, ionotropic, N-methyl D-aspartate-associated protein 1-like protein

223

KPM05160

Ionotropic kainate 2-like protein glutamate receptor-like protein

651

KPM04303

Kainate-selective ionotropic glutamate receptor-like protein 1, partial

461

KPL97052

Kainate-selective ionotropic glutamate receptor-like protein 2

234

KPM04473

Kainate-selective ionotropic glutamate receptor-like protein 3

1141

KPM09535

Proteases and other enzymes

In a previous study, we used a variety of assays to characterize some of the enzymatic activities present in aqueous extracts of nine species of astigmatid mites [60]. Of the mite species tested, S. scabiei had the most limited enzymatic repertoire. Phosphatase, phosphohydrolase, esterase, aminopeptidase and glycosidase activities were detected in the scabies mite extract and proteins predicted to carry out these catalytic activities are all present in the proteome (Additional file 1: Table S11). Esterase lipase (C8) activity was detected in the extract while lipase (C14) activity was not even though the proteome is predicted to contain at least 20 lipase-like proteins of varying specificity.

Our previous study also failed to detect either chymotrypsin or trypsin catalytic activity in the scabies mite extract, a finding that was consistent with previous reports for other ectoparasites [6163]. This is interesting since the S. scabiei var. canis proteome is predicted to contain one chymotrypsin-like protein and at least 13 trypsin-like serine proteases and ten serine protease-like proteins in addition to 18 serine protease-like proteins that are dust mite Group 3 allergen homologs (Sar s 3) (Additional file 1: Table S12).

Scabies mites collected from human patients have previously been reported to possess a single, active Sar s 3 homolog and 16 structurally similar proteins (designated as Scabies Mite Inactivated Protease Paralogs or SMIPP-S) in which the catalytic triad is mutated so as to make them inactive [64]. The active protease is reported to be a digestive enzyme that is able to partially digest filaggrin, a protein found in human skin [65], while some of the inactive paralogs can inhibit the human complement system, presumably playing a role in allowing the parasite to evade the host’s immune defense systems [16]. Examination of the structures predicted for the various serine proteases of S. scabiei var. canis revealed that only five of 13 trypsin-like serine proteases, five of 10 serine protease-like proteins and two of the 18 Sar s 3 serine protease-like proteins had intact catalytic triads while the other members of these three groups of proteins had mutations similar to those in the SMIPP-S proteins (Additional file 1: Table S13). Phylogenetic comparisons of the Sar s 3 homologs from both human and dog scabies mites indicated that the sequences in both lineages that contain an active catalytic triad are derived from a common ancestral gene (Fig. 1). The remaining inactive protease genes appear to have undergone duplications and acquired inactivating mutations both before and after the split between the two mite lineages. Additionally, most of the mutant S. scabiei var. canis proteins did have intact substrate-binding sites. In the case of the ten predicted Sar s 1 cysteine protease-like proteins, five (KPM05039 – KPM05043) had intact catalytic triads and were orthologs of previously-reported Sar s 1 proteins (AAS93667–AAS93671) [66], suggesting an ancient and essential function for these five proteins (Fig. 2). The other five Sar s 1 family members had mutations in the catalytic triad like those in the SMIPP-C protein group, but the relationships of the S. scabiei var. canis homologs to those found in human scabies mites suggest that both recent and ancient duplications have occurred in the two scabies mite lineages.
Fig. 1

Neighbor joining tree of select serine proteases. Asterisks indicate members containing active site residues that are intact. Accessions beginning with “A” are Sarcoptes scabiei var. hominis, and those with “K” are S. scabiei var. canis. All putatively active members cluster together

Fig. 2

Neighbor joining tree of cysteine protease homologs. Asterisks indicate those containing active site residues that are intact. Accessions beginning with “A” are Sarcoptes scabiei var. hominis, and those with “K” are S. scabiei var. canis. All putatively active members cluster together

The strain of scabies mites used to prepare the draft genome has been shown to be resistant to the acaricide permethrin [67, 68]. High levels of various detoxifying enzymes can be responsible for pesticide resistance in arthropods and we previously demonstrated that these mites had higher levels of esterase, cytochrome P450 monooxygenase and glutathione S-transferase (GST) activities than were present in permethrin-sensitive S. scabiei mites [68]. In addition to the esterases described above, these mites also are likely capable of producing 26 cytochrome P450-like proteins (Additional file 1: Table S2) and a variety of GSTs (Table 7).
Table 7

Sarcoptes scabiei var. canis glutathione S-transferases (GSTs). Proteins were identified by NBCI protein database search of “Sarcoptes scabiei [and] glutathione” on 22 Apr 16

Name assigned to S. scabiei predicted protein

# aa

Accession #

Glutathione S transferase-like protein 1

227

KPM02265

Glutathione S transferase-like protein 2

265

KPM02492

Glutathione S transferase-like protein 3

210

KPM03123

Glutathione S transferase-like protein 4

236

KPM03124

Glutathione S transferase-like protein 5

383

KPM11027

Glutathione S-transferase delta class 3

221

KPM09608

Glutathione S-transferase-like protein

227

KPM02264

Sar s 8 allergen (Glutathione S transferase mu-like protein 1)

262

KPM02280

Sar s 8 allergen (Glutathione S transferase mu-like protein 2)

200

KPM11584

Sar s 8 allergen (Glutathione S transferase mu-like protein 3)

219

KPM11585

Sar s 8 allergen (Glutathione S transferase mu-like protein 4)

219

KPM11586

Sar s 8 allergen (Glutathione S transferase mu-like protein 5)

219

KPM11587

In addition to the various enzymatic activities described above, scabies mites also appear to be able to synthesize the enzymes required to catalyze the vast spectrum of anabolic and catabolic reactions that are required by multicellular aerobic organisms (Additional file 2).

Peritrophic membrane in the midgut

The peritrophic membrane in the insect and mite midgut protects the mucosa and may play a role in digestion. It contains a chitin and peritrophin protein complex. This membrane is sloughed as undigested food passes out of the midgut and it forms a membrane around (encapsulates) the fecal pellets. The fecal pellets can be seen in skin scrapes from scabietic patients and are an important observation for the diagnosis of this disease. We found at least 30 peritrophin homologs including a variety of proteins that contain the chitin-binding peritrophin-A domain (Table 8). One protein containing this chitin-binding domain is a homolog of the Group 23 dust mite allergens (Sar s 23). These proteins seem to provide evidence that even though S. scabiei may consume primarily a liquid diet of serum and digested epidermal stratum corneum, the peritrophic membrane (along with many digestive enzymes) has an important function in nutrient procurement, digestion and defecation in these mites.
Table 8

Sarcoptes scabiei var. canis proteins containing a peritrophin domain. Proteins were identified by NBCI protein database search of “Sarcoptes scabiei [and] peritrophin” on 20 Apr 16

Name assigned to S. scabiei predicted protein

# aa

Accession #

Chitin binding Peritrophin-A domain containing protein 1

101

KPM02161

Chitin binding Peritrophin-A domain containing protein 2

387

KPM03068

Chitin binding Peritrophin-A domain containing protein 3, partial

1167

KPM03793

Chitin binding Peritrophin-A domain containing protein 4, partial

379

KPM06347

Chitin binding Peritrophin-A domain containing protein 5, partial

452

KPM07124

Chitin binding Peritrophin-A domain containing protein 6

346

KPM07304

Chitin binding Peritrophin-A domain containing protein 7

222

KPM07429

Chitin binding Peritrophin-A domain containing protein 8

174

KPM07489

Chitin binding Peritrophin-A domain containing protein 9

309

KPM08965

Chitin binding Peritrophin-A domain containing protein 10, partial

583

KPM09937

Chitin binding Peritrophin-A domain containing protein 11

93

KPM11506

Chitin binding peritrophin-A-like protein 2

149

KPM09480

Chitin deacetylase-like protein 3

514

KPM11442

Chitinase-like protein 1, partial

1236

KPM05982

Chitinase-like protein 4

259

KPM08718

Chitinase-like protein 10, partial

653

KPM11497

Hypothetical protein QR98_0026710

691

KPM04228

Hypothetical protein QR98_0028980

485

KPM04450

Hypothetical protein QR98_0029710

290

KPM04522

Hypothetical protein QR98_0036850

289

KPM05225

Hypothetical protein QR98_0037360

256

KPM05275

Hypothetical protein QR98_0041930

348

KPM05724

Hypothetical protein QR98_0049080, partial

700

KPM06433

Hypothetical protein QR98_0065480

368

KPM08035

Hypothetical protein QR98_0075900

185

KPM09060

Hypothetical protein QR98_0086540

318

KPM10104

Peritrophin

486

AEA34990

Peritrophin-like protein

186

KPM09194

Sar s 15 allergen (chitinase-like protein)

571

KPM07813

Sar s 23 allergen (chitin binding domain containing protein)

92

KPM09573

Vesicle coat complex COPII, subunit SFB3-like protein

230

KPM03439

Aquaporins/water balance and transport

Aquaporins are a family of transmembrane proteins that form pores through which water can flow in and out of cells and they are found in many different tissues and are in most organisms [6973]. Aquaporins are essential components of the excretory system in Malpighian tubules of insects where they regulate water and solute concentrations [69, 73]. The scabies mite genome encodes two complete aquaporin genes, and fragments for three others were identified in the assembly. One of the complete genes encodes a traditional aquaporin (QR98_0011640 = KPM02745), while the second encodes an aquaglyceroporin (QR98_0057420 = KPM07253). It is likely that these proteins regulate both water balance and solute movement in this mite, concentrating nitrogenous waste in the Malpighian tubules and processing it for elimination.

Excretion of nitrogenous wastes

Nitrogenous waste products are produced from the metabolism of proteins and purines. The nitrogenous waste produced by an organism is generally related to its solubility and the availability of water. In terrestrial ticks and mites, nitrogenous waste is shunted through the purine metabolism pathway, where guanine and xanthine are major waste products [7476]. In S. scabiei var. canis, the gene for guanosine monophosphate synthase is present, which would allow the conversion of xanthosine monophosphate into guanosine monophosphate. Genes are also present for the multistep conversion of these monophosphates into their respective nucleobases through a purine nucleoside intermediate, or via the single step conversion to a nucleobase using phosphoribosyltransferases (Table 9). However, genes for guanine deaminase, which converts guanine to xanthine, were not found. Additionally, genes encoding xanthine dehydrogenase/oxidase were also not found. Thus, S. scabiei probably lacks the ability to produce urate. The pathway in Ixodes ticks (based on genomic information) is the same, thus the presence of guanine and xanthine in excrement likely results from the separate metabolism of the respective monophosphates, rather than the conversion of guanine to xanthine.
Table 9

Sarcoptes scabiei var. canis genes and proteins predicted to be involved in nitrogenous waste production

Gene locus

Predicted protein function

Accession #

QR98_0098200

GMP synthase

KPM11250

QR98_0088290

5′ nucleotidase

KPM10277

QR98_0037400

5′ nucleotidase

KPM05279

QR98_0082120

5′ nucleotidase

KPM09671

QR98_0000820

5′ nucleotidase

KPL94019

QR98_0039780

5′ nucleotidase

KPM05513

QR98_0057060

Purine nucleoside phosphorylase

KPM07218

QR98_0020510

Phosphoribosyltransferase

KPM03618

QR98_0100210

Hypoxanthine-guanine phosphoribosyltransferase

KPM11451

Conclusions

Most biological processes in the scabies mite are not understood. Here, we have mined the draft S. scabiei var. canis genome and associated proteome in an attempt to identify homologs of genes and proteins already recognized to have known functions in some physiological processes in other animals. We have restricted this search to those genes and predicted proteins that are associated with basic biological processes or requirements. We were particularly interested in genes that encode for proteins known to be associated with vital biological processes such as immune modulation, obtaining oxygen for aerobic respiration and oxidative metabolism, sensory reception and locating a host, neuronal transmission, stressors (heat shock proteins), molting, movement, excretion and water balance, nutrient procurement and digestion. We have not attempted to identify gene groups coding for enzymes and proteins associated with the many anabolic and catabolic processes and biochemical pathways such as 2nd messenger signaling, regulation of gene expression, transcription, translation, Golgi and mitochondrial function, energy metabolism, endocrine system function and hormone synthesis, secretion, etc.

This research is obviously limited by the data that are already available for other organisms in the public databases. At this time there are ~3350 S. scabiei var. canis genes without orthologs in other mite species and ~4100 predicted proteins in scabies mites identified as “hypothetical” since they have no matches in any database. This does not mean that all these genes and proteins are unique to scabies mites although some probably are. As more genomes for other animals and in particular arthropods are sequenced and the data made available, the list of unassigned genes and proteins will likely shrink. For now, we are able to use the available data to speculate on some biological processes for scabies mites that may help understand their biology.

Declarations

Acknowledgements

The authors wish to thank Dr. Joshua Benoit of the University of Cincinnati for providing the amino acid sequences used in the analysis presented in Additional file 1: Table S10.

Funding

Research reported in this publication was supported by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under Award Number R01AI017252. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Availability of data and materials

Data for this project were deposited into the National Center for Biotechnology Information (NCBI) under BioProject PRJNA268368 and are also available through VectorBase at www.vectorbase.org. All other pertinent data are included in the manuscript and accompanying Additional files 1 and 2.

Authors’ contributions

LGA conceived the study. SDR and MSM performed the computer searches and organized the data. LGA, MSM and SDR interpreted the data and prepared the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Not applicable.

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.

Authors’ Affiliations

(1)
Department of Biological Sciences, Wright State University

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