- Open Access
Sarcoptes scabiei: genomics to proteomics to biology
© The Author(s). 2016
- Received: 4 May 2016
- Accepted: 22 June 2016
- Published: 1 July 2016
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.
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.
This analysis helps understand the biology of Sarcoptes scabiei var. canis and adds to the data already available in NCBI and VectorBase.
- Sarcoptes scabiei
- Scabies mite
- Genome sequence
- Biological processes
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 . Likewise, the genome has been sequenced for this strain of S. scabiei . 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.
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 . 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  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  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.
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 [4–15], and inhibit the complement pathway of the host . 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 . 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 . 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 . 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 . 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.
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
Tetraspanin-like protein 1
Tetraspanin-like protein 2
Tetraspanin-like protein 3
Tetraspanin-like protein 4
Tetraspanin-like protein 5
Tetraspanin-like protein 6
Tetraspanin-like protein 7
Tetraspanin-like protein 8
CD151 antigen-like protein
CD63 antigen-like protein
CD81 antigen-like protein
Hypothetical protein QR98_0011670
Hypothetical protein QR98_0030280
Hypothetical protein QR98_0032560
Hypothetical protein QR98_0065550, partial
Hypothetical protein QR98_0076100
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 . Interestingly, the scabies mite genome contains a homolog for the gene “scribbled” which in Drosophila promotes the development of both tracheae and salivary glands . 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 . In comparison, the closely related astigmatid house dust mite, Dermatophagoides farinae, is of similar size and utilizes 0.009 μl O2/h for females . 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)  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.
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
Cuticle protein-like protein 1
Cuticle protein-like protein 2
Cuticle protein-like protein 3
Cuticle protein-like protein 4
Cuticle protein-like protein 5
Cuticle protein-like protein 6
Cuticle protein-like protein 7
Cuticular protein-like protein 9
Cuticular protein-like protein 8
Cuticular protein-like protein 10
Cuticular protein-like protein 11, partial
Cuticle protein 57A-like protein 1
Cuticle protein 57A-like protein 2
Cuticle protein 92A-like protein
Cuticle protein viking-like protein
Structural constituent of cuticle-like protein
Drosophila melanogaster genes involved in ecdysteroidogenesis and their predicted Sarcoptes scabiei var. canis gene and protein homologs. Adapted from 
D. melanogaster gene
S. scabiei gene homolog
Name assigned to S. scabiei predicted protein
Rieske domain-containing protein
11-cis retinol dehydrogenase-like protein
cytochrome P450-like protein 16
cytochrome P450-like protein 20
cytochrome P450-like protein 26
cytochrome P450-like protein 10
cytochrome P450-like protein 15
cytochrome P450-like protein 9
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.
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 [32–34]. 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 . The presence of actin, myosin and tropomyosin in whole body extracts of scabies mites has already been confirmed by mass spectrometry . 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 . 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.
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
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
10 kDa Heat shock protein, mitochondrial-like protein
Heat shock protein 20-like protein 1
Heat shock protein 20-like protein 2
Heat Shock Protein 20-like protein 3
Heat Shock Protein 20-like protein 4
60 kDa Heat shock protein, mitochondrial-like protein
Sar s 28 (heat shock protein 70-like protein 1)
Sar s 28 (heat shock protein 70-like protein 2)
Sar s 28 (heat shock protein 70-like protein 3)
Sar s 28 (heat shock protein 70-like protein 4), partial
Sar s 28 (heat shock protein 70-like protein 5)
Sar s 28 (heat shock protein 70-like protein 6)
Sar s 28 (heat shock protein 70-like protein 7)
Sar s 28 (heat shock protein 70-like protein 8)
Heat shock protein 90-like protein 1
Heat shock protein 90-like protein 2
Heat shock protein 90-like protein 3
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 . 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 . 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 . Allatostatins are thought to inhibit juvenile hormone synthesis in the honeybee brain. However, the presence of juvenile hormones in mites and ticks remains controversial . Honeybee allatostatin  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.
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 . 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 . 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).
A classic host-seeking study has clearly shown that mites respond to host odor and are attracted to its source . 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 . 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 . 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 . Ticks secrete nitrogenous wastes and phenolic compounds that act in a pheromone like-manner to promote assembly and other behavior . 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 . 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.
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
7 transmembrane sweet-taste receptor-like protein 1
7 transmembrane sweet-taste receptor-like protein 2
7 transmembrane sweet-taste receptor-like protein 3, partial
Class C metabotropic glutamate-like protein G-protein coupled receptor-like protein
Gamma-aminobutyric acid type B receptor subunit 1-like protein, partial
Glutamate receptor, metabotropic-like protein 2
Gustatory receptor-like protein
Metabotropic glutamate receptor 1-like protein 1, partial
Metabotropic glutamate receptor-like protein 3
Metabotropic glutamate receptor-like protein 4
Pheromone and odorant receptor-like protein
Sensory neuron membrane protein 1-like protein
Sweet-taste receptor-like protein
Previous studies showed that scabies mites respond to host odor in the absence of carbon dioxide . 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 . Chemosensory neurons in Drosophila that are CO2-sensitive express the chemoreceptors Gr21a and Gr63a. The An. gambiae mosquito homologs are GPPRGR22 and GPRRGR24 . 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.
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
Glutamate receptor, ionotropic kainate 2 precursor-like protein 1
Glutamate receptor, ionotropic kainate 2 precursor-like protein 2
Glutamate receptor, ionotropic kainate 2-like protein 1
Glutamate receptor, ionotropic kainate 2-like protein 2
Glutamate receptor, ionotropic kainate 2-like protein 3
Glutamate receptor, ionotropic kainate 2-like protein 4
Glutamate receptor, ionotropic kainate 3-like protein 1
Glutamate receptor, ionotropic kainate 3-like protein 2
Glutamate receptor, ionotropic kainate-like protein 1, partial
Glutamate receptor, ionotropic kainate-like protein 2
Glutamate receptor, ionotropic, kainate-like protein 3
Glutamate receptor, ionotropic, N-methyl D-aspartate-associated protein 1-like protein
Ionotropic kainate 2-like protein glutamate receptor-like protein
Kainate-selective ionotropic glutamate receptor-like protein 1, partial
Kainate-selective ionotropic glutamate receptor-like protein 2
Kainate-selective ionotropic glutamate receptor-like protein 3
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 . 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 [61–63]. 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).
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
Glutathione S transferase-like protein 1
Glutathione S transferase-like protein 2
Glutathione S transferase-like protein 3
Glutathione S transferase-like protein 4
Glutathione S transferase-like protein 5
Glutathione S-transferase delta class 3
Glutathione S-transferase-like protein
Sar s 8 allergen (Glutathione S transferase mu-like protein 1)
Sar s 8 allergen (Glutathione S transferase mu-like protein 2)
Sar s 8 allergen (Glutathione S transferase mu-like protein 3)
Sar s 8 allergen (Glutathione S transferase mu-like protein 4)
Sar s 8 allergen (Glutathione S transferase mu-like protein 5)
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
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
Chitin binding Peritrophin-A domain containing protein 1
Chitin binding Peritrophin-A domain containing protein 2
Chitin binding Peritrophin-A domain containing protein 3, partial
Chitin binding Peritrophin-A domain containing protein 4, partial
Chitin binding Peritrophin-A domain containing protein 5, partial
Chitin binding Peritrophin-A domain containing protein 6
Chitin binding Peritrophin-A domain containing protein 7
Chitin binding Peritrophin-A domain containing protein 8
Chitin binding Peritrophin-A domain containing protein 9
Chitin binding Peritrophin-A domain containing protein 10, partial
Chitin binding Peritrophin-A domain containing protein 11
Chitin binding peritrophin-A-like protein 2
Chitin deacetylase-like protein 3
Chitinase-like protein 1, partial
Chitinase-like protein 4
Chitinase-like protein 10, partial
Hypothetical protein QR98_0026710
Hypothetical protein QR98_0028980
Hypothetical protein QR98_0029710
Hypothetical protein QR98_0036850
Hypothetical protein QR98_0037360
Hypothetical protein QR98_0041930
Hypothetical protein QR98_0049080, partial
Hypothetical protein QR98_0065480
Hypothetical protein QR98_0075900
Hypothetical protein QR98_0086540
Sar s 15 allergen (chitinase-like protein)
Sar s 23 allergen (chitin binding domain containing protein)
Vesicle coat complex COPII, subunit SFB3-like protein
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 [69–73]. 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
Sarcoptes scabiei var. canis genes and proteins predicted to be involved in nitrogenous waste production
Predicted protein function
Purine nucleoside phosphorylase
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.
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.
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.
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.
The authors declare that they have no competing interests.
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