Transfer of maternal haptoglobin to suckling piglets

Veterinary Immunology and Immunopathology

Volumn 144, Issue 1-2, 2011, Pages 104-110

  Hiss Pesch, Stephanie ^a   Daniel, Frauke ^a   Dunkelberg Denk, Sandra ^a   Mielenz, Manfred ^a   Sauerwein, Helga ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

Colostrum; Growth performance; Haptoglobin; Passive transfer; Pig

Indexed keywords

ACUTE PHASE PROTEIN; HAPTOGLOBIN;

ANIMAL EXPERIMENT; ARTICLE; ARTIFICIAL MILK; COLOSTRUM; CONTROLLED STUDY; IMMUNOHISTOCHEMISTRY; IMMUNOMODULATION; INNATE IMMUNITY; JEJUNUM; NEWBORN; NONHUMAN; PASSIVE IMMUNIZATION; PIGLET; PROGENY; PROTEIN DEGRADATION; PROTEIN SYNTHESIS; PROTEIN TRANSPORT; SOW (SWINE); SUCKLING; SWINE; WEANING; WEIGHT GAIN;

ADAPTIVE IMMUNITY; ANIMALS; ANIMALS, SUCKLING; COLOSTRUM; FEMALE; HAPTOGLOBINS; JEJUNUM; REAL-TIME POLYMERASE CHAIN REACTION; SWINE;

SUIDAE;

EID: 82555167028     PISSN: 01652427     EISSN: 18732534     Source Type: Journal    
DOI: 10.1016/j.vetimm.2011.07.015     Document Type: Article

References (32)

1. Albera E., Kankofer M. Antioxidants in colostrum and milk of sows and cows. Reprod. Dom. Anim. 2009, 44:606-611.
2. Arredouani M., Matthijs P., Van Hoeyveld E., Karsan A., Baumann H., Ceuppens J.L., Stevens E. Haptoglobin directly affects T cells and suppresses T helper cell type 2 cytokine release. Immunology 2003, 108:144-151.
3. Baumann H., Gauldie J. The acute phase response. Immunol. Today 1994, 15:74-80.
4. Butler J.E., Weber P., Wertz N. Antibody repertoire development in fetal and neonatal pigs. XIII. Hybrid VH genes and the preimmune repertoire revisited. J. Immunol. 2006, 177:5459-5470.
5. Butler J.E. Isolator and other neonatal piglet models in developmental immunology and identification of virulence factors. Anim. Health Res. Rev. 2009, 10:35-52.
6. Eckersall P.D., Saini P.K., McComb C. The acute phase response of acid soluble glycoprotein, α-1-acid glycoprotein, ceruloplasmin, haptoglobin and C-reactive protein, in the pig. Vet. Immunol. Immunopathol. 1996, 51:377-385.
7. Eurell T.E., Bane D.P., Hall W.F., Schaeffer D.J. Serum haptoglobin concentration as an indicator of weight gain in pigs. Can. J. Vet. Res. 1992, 56:6-9.
8. Guiraudie-Capraz G., Slomianny M.-C., Pageat P., Malosse C., Cain A.-H., Orgeur P., Nagnan-Le Meillour P. Biochemical and chemical supports for a transnatal olfactory continuity through sow maternal fluids. Chem. Senses 2005, 30:241-251.
9. Hiss S., Knura-Deszczka S., Regula G., Hennies M., Gymnich S., Petersen B., Sauerwein H. Development of an enzyme immuno assay for the determination of porcine haptoglobin in various body fluids: testing the significance of meat juice measurements for quality monitoring programs. Vet. Immunol. Immunopathol. 2003, 96:73-82.
10. Hiss S., Weinkauf C., Hachenberg S., Sauerwein H. Short communication: relationship between metabolic status and the milk concentrations of haptoglobin and lactoferrin in dairy cows during early lactation. J. Dairy Sci. 2009, 92:4439-4443.
11. Johnson R.M., Johnson T.M., Londraville R.L. Evidence for leptin expression in fishes. J. Exp. Zool. 2000, 286:718-724.
12. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970, 227:680-685.
13. Lemor A., Hosseini A., Sauerwein H., Mielenz M. Transition period-related changes in the abundance of the mRNAs of adiponectin and its receptors, of visfatin, and of fatty acid binding receptors in adipose tissue of high-yielding dairy cows. Dom. Anim. Endocrinol. 2009, 37:37-44.
14. Lin J., Richard Barb C., Kraeling R.R., Rampacek G.B. Developmental changes in the long form leptin receptor and related neuropeptide gene expression in the pig brain. Biol. Reprod. 2001, 64:1614-1618.
15. Llamas Moya S., Boyle L.A., Lynch P.B., Arkins S. Age-related changes in pro-inflammatory cytokines, acute phase proteins and cortisol concentrations in neonatal pigs. Neonatology 2007, 91:44-48.
16. Lockhart W.L., Chung W.P., Smith D.B. Studies on the dissociation of porcine haptoglobin. Can. J. Biochem. 1972, 50:775-781.
17. Maffei M., Funicello M., Vottari T., Gamucci O., Costa M., Lisi S., Viegi A., Ciampi O., Bardi G., Vitti P., Pinchera A., Santini F. The obesity and inflammatory marker haptoglobin attracts monocytes via interaction with chemokine (C-C motif) receptor 2 (CCR2). BMC Biol. 2009, 7:87.
18. Martin M., Tesouro M.A., Gonzalez-Ramon N., Pineiro A., Lampreave F. Major plasma proteins in pig serum during postnatal development. Reprod. Fertil. Dev. 2005, 17:439-445.
19. Morein B., Abusugra I., Blomqvist G. Immunity in neonates. Vet. Immunol. Immunopathol. 2002, 87:207-213.
20. Nguyen T.V., Yuan L., Azevedo M.S., Jeong K.-I., Gonzalez A.-M., Saif L.J. Transfer of maternal cytokines to suckling piglets: in vivo and in vitro models with implications for immunomodulation of neonatal immunity. Vet. Immunol. Immunopathol. 2007, 117:236-248.
21. Pineiro C., Pineiro M., Morales J., Andres M., Lorenzo E., Pozo M.-D., Alava M.-A., Lampreave F. Pig-MAP and haptoglobin concentration reference values in swine from commercial farms. Vet. J. 2009, 179:78-84.
22. Quaye I.K. Haptoglobin, inflammation and disease. Trans. R. Soc. Trop. Med. Hyg. 2008, 102:735-742.
23. Reeds P.J., Fjeld C.R., Jahoor F. Do the differences between the amino acid compositions of acute-phase and muscle proteins have a bearing on nitrogen loss in traumatic states. J. Nutr. 1994, 124:906-910.
24. Richter H. Haptoglobin bei haussäugetieren. 1. Mitteilung: untersuchung über die qualitativen eigenschaften tierischer haptoglobine. Arch. Exp. Vet. Med. 1973, 27:89-114.
25. Sauerwein H., Schmitz S., Hiss S. The acute phase protein haptoglobin and its relation to oxidative status in piglets undergoing weaning-induced stress. Redox Rep. 2005, 10:295-302.
26. Stone R.T. Isolation and characterization of recombinant cDNA clones corresponding to developmentally regulated genes in pig liver. J. Anim. Sci. 1989, 67:1082-1089.
27. Verheyen A.J.M., Maes D.G.D., Mateusen B., Deprez P., Janssens G.P.J., de Lange L., Counotte G. Serum biochemical reference values for gestating and lactating sows. Vet. J. 2007, 174:92-98.
28. Wagstrom E.A., Yoon K.J., Zimmerman J.J. Immune components in porcine mammary secretions. Viral Immunol. 2000, 13:383-397.
29. Weström B.R., Ohlsson B.G., Svendsen J., Tagesson C., Karlsson B.W. Intestinal transmission of macromolecules (BSA and FITC-Dextran) in the neonatal pig: enhancing effects of colostrum, proteins and proteinase inhibitors. Neonatology 1985, 47:359-366.
30. Williams P.P. Immunomodulating effects of intestinal absorbed maternal colostral leukocytes by neonatal pigs. Can. J. Vet. Res. 1993, 57:1-8.
31. Xu R.J., Wang F., Zhang S.H. Postnatal adaptation of the gastrointestinal tract in neonatal pigs: a possible role of milk-borne growth factors. Livest. Sci. 2000, 66:95-107.
32. Zhu Y., Österlundh I., Hulten F., Magnusson U. Tumor necrosis factor-α, interleukin-6, serum amyloid A, haptoglobin, and cortisol concentrations in sows following intramammary inoculation of Escherichia coli. Am. J. Vet. Res. 2004, 65:1434-1439.