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Published on: November 6, 2019
Scabies mite peritrophins are potential targets of human host innate immunity
Angela Mika1, Priscilla Goh, Deborah C Holt
1Queensland Institute of Medical Research and Australian Centre for International and Tropical Health and Nutrition, University of Queensland, Brisbane, Queensland, Australia.
Background:
Pruritic scabies lesions caused by Sarcoptes scabiei burrowing in the stratum corneum of human skin facilitate opportunistic bacterial infections. Emerging resistance to current therapeutics emphasizes the need to identify novel targets for protective intervention. We have characterized several protein families located in the mite gut as crucial factors for host-parasite interactions. Among these multiple proteins inhibit human complement, presumably to avoid complement-mediated damage of gut epithelial cells. Peritrophins are major components of the peritrophic matrix often found in the gut of arthropods. We hypothesized that a peritrophin, if abundant in the scabies mite gut, could be an activator of complement.
Methodology/Principal Findings:
A novel full length scabies mite peritrophin (SsPTP1) was identified in a cDNA library from scabies mites. The amino acid sequence revealed four putative chitin binding domains (CBD). Recombinant expression of one CBD of the highly repetitive SsPTP1 sequence as TSP-hexaHis-fusion protein resulted in soluble protein, which demonstrated chitin binding activity in affinity chromatography assays. Antibodies against a recombinant SsPTP1 fragment were used to immunohistochemically localize native SsPTP1 in the mite gut and in fecal pellets within the upper epidermis, co-localizing with serum components such as host IgG and complement. Enzymatic deglycosylation confirmed strong N- and O-glycosylation of the native peritrophin. Serum incubation followed by immunoblotting with a monoclonal antibody against mannan binding lectin (MBL), the recognition molecule of the lectin pathway of human complement activation, indicated that MBL may specifically bind to glycosylated SsPTP1.
Conclusions/Significance:
This study adds a new aspect to the accumulating evidence that complement plays a major role in scabies mite biology. It identifies a novel peritrophin localized in the mite gut as a potential target of the lectin pathway of the complement cascade. These initial findings indicate a novel role of scabies mite peritrophins in triggering a host innate immune response within the mite gut.
Insights
Researchers identified a novel scabies mite peritrophin (SsPTP1) in the mite gut. This protein may activate the human complement system, offering a potential new target for scabies therapies.
Area of Science:
- Parasitology
- Immunology
- Molecular Biology
Background:
- Scabies lesions facilitate bacterial infections due to mite burrowing.
- Drug resistance necessitates novel therapeutic targets.
- Mite gut proteins are key to host-parasite interactions, with some inhibiting complement.
Purpose of the Study:
- To investigate scabies mite peritrophins as potential activators of the human complement system.
- To characterize a novel peritrophin from Sarcoptes scabiei.
Main Methods:
- Identified and sequenced a novel scabies mite peritrophin (SsPTP1).
- Expressed and purified a chitin-binding domain (CBD) of SsPTP1.
- Used antibodies for immunohistochemical localization of SsPTP1 in mite tissues and fecal pellets.
- Investigated binding of Mannan-Binding Lectin (MBL) to glycosylated SsPTP1.
Main Results:
- A novel peritrophin, SsPTP1, with four putative chitin-binding domains was identified.
- Recombinant SsPTP1 CBD showed chitin-binding activity.
- Native SsPTP1 localized to the mite gut and fecal pellets, co-localizing with host IgG and complement.
- SsPTP1 is heavily N- and O-glycosylated, and MBL may bind to it, suggesting lectin pathway activation.
Conclusions:
- SsPTP1 is a novel scabies mite peritrophin found in the mite gut.
- SsPTP1 is a potential target for the human lectin complement pathway.
- Scabies mite peritrophins may trigger host innate immune responses within the mite gut.
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