Effects of weaning and infection with Teladorsagia circumcincta on mucin carbohydrate profiles of early weaned lambs

Veterinary Parasitology

Volumn 171, Issue 3-4, 2010, Pages 354-360

  Hoang, V C ^a   Williams, M A K ^a   Simpson, H V ^a  

^a MASSEY UNIVERSITY   (New Zealand)

Author keywords

Histochemistry; Lectins; Monosaccharide; Mucin; Teladorsagia (Ostertagia) circumcincta; Weaning

Indexed keywords

FUCOSE; GALACTOSE; MUCIN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CEREAL; CONTROLLED STUDY; DUODENUM; FUCOSYLATION; INFECTION SENSITIVITY; LAMB; MILK; NEMATODE; NEMATODIASIS; NEWBORN; NONHUMAN; PROTEIN GLYCOSYLATION; SIALYLATION; STOMACH ANTRUM; STOMACH FUNDUS; SULFATION; TELADORSAGIA CIRCUMCINCTA; WEANING;

AGING; ANIMALS; GASTRIC MUCINS; GASTROINTESTINAL DISEASES; OSTERTAGIA; OSTERTAGIASIS; SHEEP; SHEEP DISEASES; WEANING;

OVIS ARIES; TELADORSAGIA CIRCUMCINCTA;

EID: 77954622430     PISSN: 03044017     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetpar.2010.04.007     Document Type: Article

References (38)

1. Amerongen A.V.N., Bolscher J.G.M., Bloemena E., Veerman E.C.O. Sulfomucins in the human body. Biol. Chem. 1998, 379:1-18.
2. Brown P.J., Miller B.G., Stokes C.R., Blazquez N.B., Bourne F.J. Histochemistry of mucins of pig intestinal secretory epithelial cells before and after weaning. J. Comp. Pathol. 1988, 98:313-323.
3. Cebra J.J. Influences of microbiota on intestinal immune system development. Am. J. Clin. Nutr. 1999, 69:1046S-1051S.
4. Chance D.L., Mawhinney T.P. Carbohydrate sulfation effects on growth of Pseudomonas aeruginosa. Microbiology 2000, 146:1717-1725.
5. Dai D., Walker W.A. Protective nutrients and bacterial colonization in the immature human gut. Adv. Pediatr. 1999, 46:353-382.
6. Freitas M., Axelsson L.G., Cayuela C., Midtvedt T., Trugnan G. Microbial-host interactions specifically control the glycosylation pattern in intestinal mouse mucosa. Histochem. Cell. Biol. 2002, 118:149-161.
7. Gardiner C.H. Habitat and reproductive behavior of Trichinella spiralis. J. Parasitol. 1976, 62:865-870.
8. Hakansson A., Carlstedt I., Davies J., Mossberg A.K., Sabharwal H., Svanborg C. Aspects on the interaction of Streptococcus pneumoniae and Haemophilus influenzae with human respiratory tract mucosa. Am. J. Respir. Crit. Care Med. 1996, 154:S187-191.
9. Hoang, V.C., Williams, M.A.K., Simpson, H.V. Monosaccharide composition of fundic and duodenal mucins in sheep infected with Haemonchus contortus or Teladorsagia circumcincta. Vet. Parasitol. (in press).
10. Holmen J.M., Olson F.J., Karlsson H., Hansson G.C. Two glycosylation alterations of mouse intestinal mucins due to infection caused by the parasite Nippostrongylus brasiliensis. Glycoconj. J. 2002, 19:67-75.
11. Ishikawa N., Horii Y., Oinuma T., Suganuma T., Nawa Y. Goblet cell mucins as the selective barrier for the intestinal helminths: T-cell-independent alteration of goblet cell mucins by immunologically 'damaged' Nippostrongylus brasiliensis worms and its significance on the challenge infection with homologous and heterologous parasites. Immunology 1994, 81:480-486.
12. Karlsson N.G., Olson F.J., Jovall P.A., Andersch Y., Enerback L., Hansson G.C. Identification of transient glycosylation alterations of sialylated mucin oligosaccharides during infection by the rat intestinal parasite Nippostrongylus brasiliensis. Biochem. J. 2000, 350:805-814.
13. Maruyama H., Hirabayashi Y., el-Malky M., Okamura S., Aoki M., Itagaki T., Nakamura-Uchiyama F., Nawa Y., Shimada S., Ohta N. Strongyloides venezuelensis: longitudinal distribution of adult worms in the host intestine is influenced by mucosal sulfated carbohydrates. Exp. Parasitol. 2002, 100:179-185.
14. Matsuno K., Suzuki S. Simple fluorimetric method for quantification of sialic acids in glycoproteins. Anal. Biochem. 2008, 375:53-59.
15. Miller H.R., Jackson F., Newlands G., Appleyard W.T. Immune exclusion, a mechanism of protection against the ovine nematode Haemonchus contortus. Res. Vet. Sci. 1983, 35:357-363.
16. Newburg D.S. Oligosaccharides and glycoconjugates in human milk: their role in host defense. J. Mammary Gland Biol. Neoplasia 1996, 1:271-283.
17. Newlands G.F., Miller H.R., Jackson F. Immune exclusion of Haemonchus contortus larvae in the sheep: effects on gastric mucin of immunization, larval challenge and treatment with dexamethasone. J. Comp. Pathol. 1990, 102:433-442.
18. Ohwada S., Suzuki H. Lectin histochemistry on the Brunner's glands of domestic ruminants. Tohoku J. Agr. Res. 1992, 42:55-66.
19. Oinuma T., Abe T., Nawa Y., Kawano J., Suganuma T. Glycoconjugates in rat small intestinal mucosa during infection with the intestinal nematode Nippostrongylus brasiliensis. Adv. Exp. Med. Biol. 1995, 371B:975-978.
20. Pedini V., Scocco P., Gargiulo A.M., Ceccarelli P. Carbohydrate histochemistry of lamb duodenum. Acta. Histochem. 2001, 103:315-323.
21. Piotrowski J., Slomiany A., Murty V.L., Fekete Z., Slomiany B.L. Inhibition of Helicobacter pylori colonization by sulfated gastric mucin. Biochem. Int. 1991, 24:749-756.
22. Porter D. The effect of milk diet on the development of Haemonchus contortus in calves. J. Parasitol. Suppl. 1941, 27:18-19.
23. Rohrbacher G.H., Porter D.A., Herlich H. The effect of milk in the diet of calves and rabbits upon the development of trichostrongylid nematodes. Am. J. Vet. Res. 1958, 19:625-631.
24. Rowe A., Gondro C., Emery D., Sangster N. Sequential microarray to identify timing of molecular responses to Haemonchus contortus infection in sheep. Vet. Parasitol. 2009, 161:76-87.
25. Ruiz-Palacios G.M., Cervantes L.E., Ramos P., Chavez-Munguia B., Newburg D.S. Campylobacter jejuni binds intestinal H(O) antigen (Fuc alpha 1, 2Gal beta 1, 4GlcNAc), and fucosyloligosaccharides of human milk inhibit its binding and infection. J. Biol. Chem. 2003, 278:14112-14120.
26. Satrija F., Nansen P., Christensen C.M. Ostertagia ostertagi in neonatal calves: establishment of infection in ruminating and non-ruminating calves. Res. Vet. Sci. 1991, 51:344-346.
27. Shi B.B., Ishikawa N., Khan A.I., Tsuchiya K., Horii Y., Nawa Y. Strongyloides venezuelensis infection in Syrian golden hamster. Mesocricetus auratus, with reference to the phenotype of intestinal mucosal mast cells. Parasite Immunol. 1994, 16:545-551.
28. Shub M.D., Pang K.Y., Swann D.A., Walker W.A. Age-related changes in chemical composition and physical properties of mucus glycoproteins from rat small intestine. Biochem. J. 1983, 215:405-411.
29. Slomiany B.L., Murty V.L., Piotrowski J., Liau Y.H., Sundaram P., Slomiany A. Glycosulfatase activity of Helicobacter pylori toward gastric mucin. Biochem. Biophys. Res. Commun. 1992, 183:506-513.
30. Smith W.D., Jackson F., Jackson E., Williams J. Age immunity to Ostertagia circumcincta: comparison of the local immune responses of 4 1/2- and 10-month-old lambs. J. Comp. Pathol. 1985, 95:235-245.
31. Spicer S.S. Diamine methods for differentiating mucosubstances histochemically. J. Histochem. Cytochem. 1965, 13:211-234.
32. Theodoropoulos G., Hicks S.J., Corfield A.P., Miller B.G., Carrington S.D. The role of mucins in host-parasite interactions: Part II - Helminth parasites. Trends in Parasitol. 2001, 17:130-135.
33. Theodoropoulos G., Hicks S.J., Corfield A.P., Miller B.G., Kapel C.M.O., Trivizaki M., Balaskas C., Petrakos G., Carrington S.D. Trichinella spiralis: enteric mucin-related response to experimental infection in conventional and SPF pigs. Exp. Parasitol. 2005, 109:63-71.
34. Torres-Pinendo R., Mahmood A. Postnatal changes in biosynthesis of microvillus membrane glycans of rat small intestine. I. Evidence of a developmental shift from terminal sialylation to fucosylation. Biochem. Biophys. Res. Commun. 1984, 125:546-553.
35. Wadstrom T., Hirmo S., Boren T. Biochemical aspects of Helicobacter pylori colonization of the human gastric mucosa. Aliment. Pharmacol. Ther. 1996, 10(Suppl. 1):17-27.
36. Yamauchi J., Kawai Y., Yamada M., Uchikawa R., Tegoshi T., Arizono N. Altered expression of goblet cell- and mucin glycosylation-related genes in the intestinal epithelium during infection with the nematode Nippostrongylus brasiliensis in rat. Apmis 2006, 114:270-278.
37. Zeng S., Lawton D.E., Przemeck S.M., Simcock D.C., Simpson H.V. Reduced Ostertagia circumcincta burdens in milk-fed lambs. N. Z. Vet. J. 2001, 49:2-7.
38. Zeng S., Brown S., Przemeck S.M., Simpson H.V. Milk and milk components reduce the motility of Ostertagia circumcincta larvae in vitro. N. Z. Vet. J. 2003, 51:174-178.