Variations in the Peritrophic Matrix Composition of Heparan Sulphate from the Tsetse Fly, Glossina morsitans morsitans

Tsetse flies are the principal insect vectors of African trypanosomes—sleeping sickness in humans and Nagana in cattle. One of the tsetse fly species, Glossina morsitans morsitans, is host to the parasite, Trypanosoma brucei, a major cause of African trypanosomiasis. Precise details of the life cycle have yet to be established, but the parasite life cycle involves crossing the insect peritrophic matrix (PM). The PM consists of the polysaccharide chitin, several hundred proteins, and both glycosamino- and galactosaminoglycan (GAG) polysaccharides. Owing to the technical challenges of detecting small amounts of GAG polysaccharides, their conclusive identification and composition have not been possible until now. Following removal of PMs from the insects and the application of heparinases (bacterial lyase enzymes that are specific for heparan sulphate (HS) GAG polysaccharides), dot blots with a HS-specific antibody showed heparan sulphate proteoglycans (HSPGs) to be present, consistent with Glossina morsitans morsitans genome analysis, as well as the likely expression of the HSPGs syndecan and perlecan. Exhaustive HS digestion with heparinases, fluorescent labeling of the resulting disaccharides with BODIPY fluorophore, and separation by strong anion exchange chromatography then demonstrated the presence of HS for the first time and provided the disaccharide composition. There were no significant differences in the type of disaccharide species present between genders or between ages (24 vs. 48 h post emergence), although the HS from female flies was more heavily sulphated overall. Significant differences, which may relate to differences in infection between genders or ages, were evident, however, in overall levels of 2-O-sulphation between sexes and, for females, between 24 and 48 h post-emergence, implying a change in expression or activity for the 2-O-sulphotransferase enzyme. The presence of significant quantities of disaccharides containing the monosaccharide GlcNAc6S contrasts with previous findings in Drosophila melanogaster and suggests subtle differences in HS fine structure between species of the Diptera.

[1]  Yi-neng Wu,et al.  Mammalian African trypanosome VSG coat enhances tsetse’s vector competence , 2016, Proceedings of the National Academy of Sciences.

[2]  Sandra Gesing,et al.  VectorBase: an updated bioinformatics resource for invertebrate vectors and other organisms related with human diseases , 2014, Nucleic Acids Res..

[3]  Yi-neng Wu,et al.  The Peritrophic Matrix Mediates Differential Infection Outcomes in the Tsetse Fly Gut following Challenge with Commensal, Pathogenic, and Parasitic Microbes , 2014, The Journal of Immunology.

[4]  Geoffrey H. Siwo,et al.  Genome Sequence of the Tsetse Fly (Glossina morsitans): Vector of African Trypanosomiasis , 2014, Science.

[5]  J. Wastling,et al.  An Investigation into the Protein Composition of the Teneral Glossina morsitans morsitans Peritrophic Matrix , 2014, PLoS neglected tropical diseases.

[6]  Yi-neng Wu,et al.  Trypanosome Infection Establishment in the Tsetse Fly Gut Is Influenced by Microbiome-Regulated Host Immune Barriers , 2013, PLoS pathogens.

[7]  N. Perrimon,et al.  Drosophila Heparan Sulfate, a Novel Design* , 2012, The Journal of Biological Chemistry.

[8]  H. Nakato,et al.  In vivo manipulation of heparan sulfate structure and its effect on Drosophila development. , 2011, Glycobiology.

[9]  M. Carrington,et al.  Identification of the meiotic life cycle stage of Trypanosoma brucei in the tsetse fly , 2011, Proceedings of the National Academy of Sciences.

[10]  T. Pearson,et al.  Tsetse EP Protein Protects the Fly Midgut from Trypanosome Establishment , 2010, PLoS pathogens.

[11]  A. Ghosh,et al.  Plasmodium falciparum ookinetes require mosquito midgut chondroitin sulfate proteoglycans for cell invasion , 2007, Proceedings of the National Academy of Sciences.

[12]  J. Turnbull,et al.  High sensitivity separation and detection of heparan sulfate disaccharides. , 2006, Journal of chromatography. A.

[13]  Wallace D Bulimo,et al.  Molecular characterization of a tsetse fly midgut proteolytic lectin that mediates differentiation of African trypanosomes. , 2006, Insect biochemistry and molecular biology.

[14]  J. Turnbull,et al.  Interactions of heparin/heparan sulfate with proteins: appraisal of structural factors and experimental approaches. , 2004, Glycobiology.

[15]  C. M. Calvet,et al.  Heparan Sulfate Proteoglycans Mediate the Invasion of Cardiomyocytes by Trypanosoma cruzi , 2003, The Journal of eukaryotic microbiology.

[16]  W. Gibson,et al.  Tsetse immune responses and trypanosome transmission: Implications for the development of tsetse-based strategies to reduce trypanosomiasis , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[17]  N. Perrimon,et al.  Specificities of heparan sulphate proteoglycans in developmental processes , 2000, Nature.

[18]  Changben Li,et al.  Phytogeny of genusGlossina (Diptera:Glossinidae) according to ITS2 sequences , 1999, Science in China Series C: Life Sciences.

[19]  J. Esko,et al.  Turnover of Heparan Sulfate Depends on 2-O-Sulfation of Uronic Acids* , 1997, The Journal of Biological Chemistry.

[20]  J. Esko,et al.  Microbial adherence to and invasion through proteoglycans , 1997, Infection and immunity.

[21]  M. Lehane,et al.  Composition of the peritrophic matrix of the tsetse fly, Glossina morsitans morsitans , 1996, Cell and Tissue Research.

[22]  X. Bai,et al.  Differential expression of multiple cell-surface heparan sulfate proteoglycans during embryonic tooth development. , 1994, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[23]  U. R. Desai,et al.  Specificity studies on the heparin lyases from Flavobacterium heparinum. , 1993, Biochemistry.

[24]  M. Lehane,et al.  Ionic environment and the permeability properties of the peritrophic membrane of Glossina morsitans morsitans , 1993 .

[25]  X. Bai,et al.  Developmental changes in heparan sulfate expression: in situ detection with mAbs , 1992, The Journal of cell biology.

[26]  I. Maudlin,et al.  Sodalis gen. nov. and Sodalis glossinidius sp. nov., a microaerophilic secondary endosymbiont of the tsetse fly Glossina morsitans morsitans. , 1999, International journal of systematic bacteriology.

[27]  Gapped BLAST and PSI-BLAST: A new , 1997 .