Open Access
Vet. Res.
Volume 38, Number 5, September-October 2007
Page(s) 729 - 739
Published online 10 July 2007
How to cite this article Vet. Res. (2007) 729-739
References of  Vet. Res. 38 (2007) 729-739
  1. Aguilera O., Quiros L.M., Fierro J.F., Transferrins selectively cause ion efflux through bacterial and artificial membranes, FEBS Lett. (2003) 548:5-10 [CrossRef] [PubMed].
  2. Andersen A.A., Vanrompay D., Avian chlamydiosis, Rev. Sci. Tech. (2000) 19:396-404 [PubMed].
  3. Appelmelk B.J., An Y.Q., Geerts M., Thijs B.G., de Boer H.A., MacLaren D.M., de Graaff J., Nuijens J.H., Lactoferrin is a lipid A-binding protein, Infect. Immun. (1994) 62:2628-2632 [PubMed].
  4. Arnold R.R., Cole M.F., McGhee J.R., A bactericidal effect for human lactoferrin, Science (1977) 197:263-265 [CrossRef].
  5. Ashida K., Sasaki H., Suzuki Y.A., Lonnerdal B., Cellular internalization of lactoferrin in intestinal epithelial cells, Biometals (2004) 17:311-315 [CrossRef] [PubMed].
  6. Beug H., von Kirchbach A., Doderlein G., Conscience J.F., Graf T., Chicken hematopoietic cells transformed by seven strains of defective avian leukemia viruses display three distinct phenotypes of differentiation, Cell (1979) 18:375-390 [CrossRef] [PubMed].
  7. Brandenburg K., Jurgens G., Muller M., Fukuoka S., Koch M.H., Biophysical characterization of lipopolysaccharide and lipid A inactivation by lactoferrin, Biol. Chem. (2001) 382:1215-1225 [PubMed].
  8. Carabeo R.A., Grieshaber S.S., Fischer E., Hackstadt T., Chlamydia trachomatis induces remodeling of the actin cytoskeleton during attachment and entry into HeLa cells, Infect. Immun. (2002) 70:3793-3803 [CrossRef] [PubMed].
  9. Carabeo R.A., Grieshaber S.S., Hasenkrug A., Dooley C., Hackstadt T., Requirement for the Rac GTPase in Chlamydia trachomatis invasion of non-phagocytic cells, Traffic (2004) 5:418-425 [PubMed].
  10. Clifton D.R., Fields K.A., Grieshaber S.S., Dooley C.A., Fischer E.R., Mead D.J., Carabeo R.A., Hackstadt T., A chlamydial type III translocated protein is tyrosine-phosphorylated at the site of entry and associated with recruitment of actin, Proc. Natl. Acad. Sci. USA (2004) 101:10166-10171 [CrossRef] [PubMed].
  11. Clifton D.R., Dooley C.A., Grieshaber S.S., Carabeo R.A., Fields K.A., Hackstadt T., Tyrosine phosphorylation of the chlamydial effector protein Tarp is species specific and not required for recruitment of actin, Infect. Immun. (2005) 73:3860-3868 [CrossRef] [PubMed].
  12. Ellison R.T. III, Giehl T.J., LaForce F.M., Damage of the outer membrane of enteric gram-negative bacteria by lactoferrin and transferrin, Infect. Immun. (1988) 56:2774-2781 [PubMed].
  13. Ellison R.T. III, LaForce F.M., Giehl T.J., Boose D.S., Dunn B.E., Lactoferrin and transferrin damage of the gram-negative outer membrane is modulated by Ca2+ and Mg2+, J. Gen. Microbiol. (1990) 136:1437-1446 [PubMed].
  14. Giansanti F., Rossi P., Massucci M.T., Botti D., Antonini G., Valenti P., Seganti L., Antiviral activity of ovotransferrin discloses an evolutionary strategy for the defensive activities of lactoferrin, Biochem. Cell Biol. (2002) 80:125-130 [CrossRef] [PubMed].
  15. Gomez H.F., Ochoa T.J., Carlin L.G., Cleary T.G., Human lactoferrin impairs virulence of Shigella flexneri, J. Infect. Dis. (2003) 187:87-95 [CrossRef] [PubMed].
  16. Hackstadt T., Cell Biology, in: Stephens R.S. (Ed.), Chlamydia: Intracellular Biology, Pathogenesis, and Immunity, ASM Press, Washington, DC, 1999, pp. 101-138.
  17. Ibrahim H.R., Iwamori E., Sugimoto Y., Aoki T., Identification of a distinct antibacterial domain within the N-lobe of ovotransferrin, Biochim. Biophys. Acta (1998) 1401:289-303 [PubMed].
  18. Ibrahim H.R., Sugimoto Y., Aoki T., Ovotransferrin antimicrobial peptide (OTAP-92) kills bacteria through a membrane damage mechanism, Biochim. Biophys. Acta (2000) 1523:196-205 [PubMed].
  19. Keung W.M., Azari P., Structure and function of ovotransferrin. II. Iron-transferring activity of iron-binding fragments of ovotransferrin with chicken embryo red cells, J. Biol. Chem. (1982) 257:1184-1188 [PubMed].
  20. Martin-Mateo M.C., Planas J., Conalbumin and serum iron transport in birds. I. Study in the chicken (Gallus domesticus), Rev. Esp. Fisiol. (1965) 21:1-7 [PubMed].
  21. Metz-Boutigue M.H., Jolles J., Mazurier J., Schoentgen F., Legrand D., Spik G., Montreuil J., Jolles P., Human lactotransferrin: amino acid sequence and structural comparisons with other transferrins, Eur. J. Biochem. (1984) 145:659-676 [PubMed].
  22. Mosmann T., Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays, J. Immunol. Methods (1983) 65:55-63 [CrossRef] [PubMed].
  23. Ochoa T.J., Noguera-Obenza M., Ebel F., Guzman C.A., Gomez H.F., Cleary T.G., Lactoferrin impairs type III secretory system function in enteropathogenic Escherichia coli, Infect. Immun. (2003) 71:5149-5155 [CrossRef] [PubMed].
  24. Ochoa T.J., Clearly T.G., Lactoferrin disruption of bacterial type III secretion systems, Biometals (2004) 17:257-260 [CrossRef] [PubMed].
  25. Rossi P., Giansanti F., Boffi A., Ajello M., Valenti P., Chiancone E., Antonini G., Ca2+ binding to bovine lactoferrin enhances protein stability and influences the release of bacterial lipopolysaccharide, Biochem. Cell Biol. (2002) 80:41-48 [CrossRef] [PubMed].
  26. Stephens R.S., Koshiyama K., Lewis E., Kubo A., Heparin-binding outer membrane protein of chlamydiae, Mol. Microbiol. (2001) 40:691-699 [PubMed].
  27. Stevens L., Egg white proteins, Comp. Biochem. Physiol. B (1991) 100:1-9 [PubMed].
  28. Su H., Raymond L., Rockey D.D., Fischer E., Hackstadt T., Caldwell H.D., A recombinant Chlamydia trachomatis major outer membrane protein binds to heparan sulfate receptors on epithelial cells, Proc. Natl. Acad. Sci. USA (1996) 93:11143-11148 [CrossRef] [PubMed].
  29. Subtil A., Wyplosz B., Balana M.E., Dautry-Varsat A., Analysis of Chlamydia caviae entry sites and involvement of Cdc42 and Rac activity, J. Cell Sci. (2004) 117:3923-3933 [CrossRef] [PubMed].
  30. Taraktchoglou M., Pacey A.A., Turnbull J.E., Eley A., Infectivity of Chlamydia trachomatis serovar LGV but not E is dependent on host cell heparan sulfate, Infect. Immun. (2001) 69:968-976 [CrossRef] [PubMed].
  31. Valenti P., Antonini G., Von Hunolstein C., Visca P., Orsi N., Antonini E., Studies of the antimicrobial activity of ovotransferrin, Int. J. Tissue React. (1983) 5:97-105 [PubMed].
  32. Valenti P., Antonini G., Lactoferrin: an important host defence against microbial and viral attack, Cell. Mol. Life Sci. (2005) 62:2576-2587 [CrossRef] [PubMed].
  33. Valnes K., Brandtzaeg P., Retardation of immunofluorescence fading during microscopy, J. Histochem. Cytochem. (1985) 33:755-761 [PubMed].
  34. Van Loock M., Loots K., Van Heerden M., Vanrompay D., Goddeeris B.M., Exacerbation of Chlamydophila psittaci pathogenicity in turkeys superinfected by Escherichia coli, Vet. Res. (2006) 37:745-755 [CrossRef] [PubMed] [EDP Sciences].
  35. Vanrompay D., Ducatelle R., Haesebrouck F., Diagnosis of avian chlamydiosis: specificity of the modified Gimenez staining on smears and comparison of the sensitivity of isolation in eggs and three different cell cultures, Zentralbl. Veterinarmed. B (1992) 39:105-112 [PubMed].
  36. Vanrompay D., Andersen A.A., Ducatelle R., Haesebrouck F., Serotyping of European isolates of Chlamydia psittaci from poultry and other birds, J. Clin. Microbiol. (1993) 31:134-137 [PubMed].
  37. Vanrompay D., Charlier G., Ducatelle R., Haesebrouck F., Ultrastructural changes in avian Chlamydia psittaci serovar A-, B-, and D-infected Buffalo Green Monkey cells, Infect. Immun. (1996) 64:1265-1271 [PubMed].
  38. Vorland L.H., Lactoferrin: a multifunctional glycoprotein, APMIS (1999) 107:971-981 [PubMed].