Open Access
Vet. Res.
Volume 39, Number 6, November-December 2008
Number of page(s) 10
Published online 25 July 2008
How to cite this article Vet. Res. (2008) 39:56
References of  Vet. Res. (2008) 39:56
  1. Achaz G., Rocha E.P., Netter P., Coissac E., Origin and fate of repeats in bacteria, Nucleic Acids Res. (2002) 30:2987–2994 [CrossRef] [PubMed].
  2. Adair D.M., Worsham P.L., Hill K.K., Klevytska A.M., Jackson P.J., Friedlander A.M., Keim P., Diversity in a variable-number tandem repeat from Yersinia pestis, J. Clin. Microbiol. (2000) 38:1516–1519 [PubMed].
  3. Andersen A.A., Van Deusen R.A., Production and partial characterization of monoclonal antibodies to four Chlamydia psittaci isolates, Infect. Immun. (1988) 56:2075–2079 [PubMed].
  4. Bannantine J.P., Griffiths R.S., Viratyosin W., BrownW.J., Rockey D.D., A secondary structure motif predictive of protein localization to the chlamydial inclusion membrane, Cell. Microbiol. (2000) 2:35–47 [CrossRef] [PubMed].
  5. Bannantine J.P., Stamm W.E., Suchland R.J., Rockey D.D., Chlamydia trachomatis IncA is localized to the inclusion membrane and is recognized by antisera from infected humans and primates, Infect. Immun. (1998) 66:6017–6021 [PubMed].
  6. Bouakane A., Rekiki A., Rodolakis A., Protection of pregnant mice against placental and splenic infection by three strains of Chlamydophila abortus with a live 1B vaccine, Vet. Rec. (2005) 157:771–774 [PubMed].
  7. Boumedine K.S., Rodolakis A., AFLP allows the identification of genomic markers of ruminant Chlamydia psittaci strains useful for typing and epidemiological studies, Res. Microbiol. (1998) 149:735–744 [CrossRef] [PubMed].
  8. Caldwell H.D., Kromhout J., Schachter J., Purification and partial characterization of the major outer membrane protein of Chlamydia trachomatis, Infect. Immun. (1981) 31:1161–1176 [PubMed].
  9. Denamur E., Sayada C., Souriau A., Orfila J., Rodolakis A., Elion J., Restriction pattern of the major outer-membrane protein gene provides evidence for a homogeneous invasive group among ruminant isolates of Chlamydia psittaci, J. Gen. Microbiol. (1991) 137:2525–2530 [PubMed].
  10. Duan Y.J., Souriau A., Mahe A.M., Trap D., Andersen A.A., Rodolakis A., Serotyping of chlamydial clinical isolates from birds with monoclonal antibodies, Avian Dis. (1999) 43:22–28 [CrossRef] [PubMed].
  11. Everett K.D., Bush R.M., Andersen A.A., Emended description of the order Chlamydiales, proposal of Parachlamydiaceae fam. nov. and Simkaniaceae fam. nov., each containing one monotypic genus, revised taxonomy of the family Chlamydiaceae, including a new genus and five new species, and standards for the identification of organisms, Int. J. Syst. Bacteriol. (1999) 49:415–440 [PubMed].
  12. Faye P., Charton L., Mage C., Bernard C., Le Layec C., Propriétés hémagglutinantes du virus de l'avortement enzootique des petits ruminants (souches de Rakeia d'origine ovine et caprine), Bull. Acad. Vet. Fr. (1972) 45:169–173.
  13. Frothingham R., Meeker-O'Connell W.A., Genetic diversity in the Mycobacterium tuberculosis complex based on variable numbers of tandem DNA repeats, Microbiology (1998) 144:1189–1196 [PubMed].
  14. Geisler W.M., Suchland R.J., Rockey D.D., Stamm W.E., Epidemiology and clinical manifestations of unique Chlamydia trachomatis isolates that occupy nonfusogenic inclusions, J. Infect. Dis. (2001) 184:879–884 [CrossRef] [PubMed].
  15. Griffiths P.C., Plater J.M., Martin T.C., Hughes S.L., Hughes K.J., Hewinson R.G., Dawson M., Epizootic bovine abortion in a dairy herd: characterization of a Chlamydia psittaci isolate and antibody response, Br. Vet. J. (1995) 151:683–693 [CrossRef] [PubMed].
  16. Hackstadt T., Scidmore-Carlson M.A., Shaw E.I., Fischer E.R., The Chlamydia trachomatis IncA protein is required for homotypic vesicle fusion, Cell. Microbiol. (1999) 1:119–130 [CrossRef] [PubMed].
  17. Henderson I.R., Owen P., Nataro J.P., Molecular switches–the ON and OFF of bacterial phase variation, Mol. Microbiol. (1999) 33:919–932 [CrossRef] [PubMed].
  18. Kato H., Takeuchi H., Oishi Y., Senpuku H., Shimura N., Hanada N., Nisizawa T., The immunogenicity of various peptide antigens inducing cross-reacting antibodies to a cell surface protein antigen of Streptococcus mutans, Oral Microbiol. Immunol. (1999) 14:213–219 [CrossRef] [PubMed].
  19. Keim P., Price L.B., Klevytska A.M., Smith K.L., Schupp J.M., Okinaka R., et al., Multiple-locus variable-number tandem repeat analysis reveals genetic relationships within Bacillus anthracis, J. Bacteriol. (2000) 182:2928–2936 [CrossRef] [PubMed].
  20. Ladefoged S.A., Molecular dissection of Mycoplasma hominis, APMIS Suppl. (2000) 97:1–45 [PubMed].
  21. Lasa I., David V., Gouin E., Marchand J.B., Cossart P., The amino-terminal part of ActA is critical for the actin-based motility of Listeria monocytogenes; the central proline-rich region acts as a stimulator, Mol. Microbiol. (1995) 18:425–436.
  22. Le Flèche P., Hauck Y., Onteniente L., Prieur A., Denoeud F., Ramisse V., et al., A tandem repeats database for bacterial genomes: application to the genotyping of Yersinia pestis and Bacillus anthracis, BMC Microbiol. (2001) 1:2 [CrossRef] [PubMed].
  23. Lee C.K., Moulder J.W., Persistent infection of mouse fibroblasts (McCoy cells) with a trachoma strain of Chlamydia trachomatis, Infect. Immun. (1981) 32:822–829 [PubMed].
  24. Longbottom D., Coulter L.J., Animal chlamydioses and zoonotic implications, J. Comp. Pathol. (2003) 128:217–244 [CrossRef] [PubMed].
  25. McClenaghan M., Herring A.J., Aitken I.D., Comparison of Chlamydia psittaci isolates by DNA restriction endonuclease analysis, Infect. Immun. (1984) 45:384–389 [PubMed].
  26. McColl K.A., Martin R.W., Gleeson L.J., Handasyde K.A., Lee A.K., Chlamydia infection and infertility in the female koala (Phascolarctos cinereus), Vet. Rec. (1984) 115:655 [PubMed].
  27. McNutt S.H., Waller E.F., Sporadic bovine encephalomyelitis (Buss disease), Cornell Vet. (1940) 30:437–448.
  28. Moulder J.W., Interaction of chlamydiae and host cells in vitro, Microbiol. Rev. (1991) 55:143–190 [PubMed].
  29. Moulder J.W., Levy N.J., Zeichner S.L., Lee C.K., Attachment defect in mouse fibroblasts (L cells) persistently infected with Chlamydia psittaci, Infect. Immun. (1981) 34:285–291 [PubMed].
  30. Norton W.L., Storz J., Observations on sheep with polyarthritis produced by an agent of the psittacosis-lymphogranuloma venereum-trachoma group, Arthritis Rheum. (1967) 10:1–12 [CrossRef] [PubMed].
  31. Peters J., Wilson D.P., Myers G., Timms P., Bavoil P.M., Type III secretion à la Chlamydia, Trends Microbiol. (2007) 15:241–251 [CrossRef] [PubMed].
  32. Rekiki A., Bouakane A., Hammami S., El Idrissi A.H., Bernard F., Rodolakis A., Efficacy of live Chlamydophila abortus vaccine 1B in protecting mice placentas and foetuses against strains of Chlamydophila pecorum isolated from cases of abortion, Vet. Microbiol. (2004) 99:295–299 [CrossRef] [PubMed].
  33. Rockey D.D., Heinzen R.A., Hackstadt T., Cloning and characterization of a Chlamydia psittaci gene coding for a protein localized in the inclusion membrane of infected cells, Mol. Microbiol. (1995) 15:617–626 [CrossRef] [PubMed].
  34. Rockey D.D., Rosquist J.L., Protein antigens of Chlamydia psittaci present in infected cells but not detected in the infectious elementary body, Infect. Immun. (1994) 62:106–112 [PubMed].
  35. Rodolakis A., Abortive infection of mice inoculated intraperitoneally with Chlamydia ovis, Ann. Rech. Vet. (1976) 7:195–205 [PubMed].
  36. Rodolakis A., Bernard F., Lantier F., Mouse models for evaluation of virulence of Chlamydia psittaci isolated from ruminants, Res. Vet. Sci. (1989) 46:34–39 [PubMed].
  37. Rodolakis A., Bernard F., Souriau A., Layachi K., Buzoni-Gatel D., Relationship between virulence of Chlamydia psittaci strains and establishment of persistent infection of McCoy cells, Vet. Microbiol. (1989) 19:65–73 [CrossRef] [PubMed].
  38. Rodolakis A., Souriau A., Response of ewes to temperature-sensitive mutants of Chlamydia psittaci (var ovis) obtained by NTG mutagenesis, Ann. Rech. Vet. (1983) 14:155–161 [PubMed].
  39. Rodolakis A., Souriau A., Restriction endonuclease analysis of DNA from ruminant Chlamydia psittaci and its relation to mouse virulence, Vet. Microbiol. (1992) 31:263–271 [CrossRef] [PubMed].
  40. Salinas J., Souriau A., De Sa C., Andersen A.A., Rodolakis A., Serotype 2-specific antigens from ruminant strains of Chlamydia pecorum detected by monoclonal antibodies, Comp. Immunol. Microbiol. Infect. Dis. (1996) 19:155–161 [CrossRef] [PubMed].
  41. Schorey J.S., Holsti M.A., Ratliff T.L., Allen P.M., Brown E.J., Characterization of the fibronectinattachment protein of Mycobacterium avium reveals a fibronectin-binding motif conserved among mycobacteria, Mol. Microbiol. (1996) 21:321–329 [CrossRef] [PubMed].
  42. Scidmore M.A., Rockey D.D., Fischer E.R., Heinzen R.A., Hackstadt T., Vesicular interactions of the Chlamydia trachomatis inclusion are determined by chlamydial early protein synthesis rather than route of entry, Infect. Immun. (1996) 64:5366–5372 [PubMed].
  43. Scidmore-Carlson M.A., Shaw E.I., Dooley C.A., Fischer E.R., Hackstadt T., Identification and characterization of a Chlamydia trachomatis early operon encoding four novel inclusion membrane proteins, Mol. Microbiol. (1999) 33:753–765 [CrossRef] [PubMed].
  44. Senyk G., Kerlan R., Stites D.P., Schanzlin D.J., Ostler H.B., Hanna L., et al., Cell-mediated and humoral immune responses to chlamydial antigens in guinea pigs infected ocularly with the agent of guinea pig inclusion conjunctivitis, Infect. Immun. (1981) 32:304–310 [PubMed].
  45. Siarkou V., Lambropoulos A.F., Chrisafi S., Kotsis A., Papadopoulos O., Subspecies variation in Greek strains of Chlamydophila abortus, Vet. Microbiol. (2002) 85:145–157 [CrossRef] [PubMed].
  46. Storz J., Superinfection of pregnant ewes latently infected with a psittacosis-lymphogranuloma agent, Cornell Vet. (1963) 53:469–480 [PubMed].
  47. Suchland R.J., Rockey D.D., Bannantine J.P., Stamm W.E., Isolates of Chlamydia trachomatis that occupy nonfusogenic inclusions lack IncA, a protein localized to the inclusion membrane, Infect. Immun. (2000) 68:360–367 [PubMed].
  48. Suchland R.J., Rockey D.D., Weeks S.K., Alzhanov D.T., Stamm W.E., Development of secondary inclusions in cells infected by Chlamydia trachomatis, Infect. Immun. (2005) 73:3954–3962 [CrossRef] [PubMed].
  49. van Belkum A., Scherer S., van Leeuwen W., Willemse D., van Alphen L., Verbrugh H., Variable number of tandem repeats in clinical strains of Haemophilus influenzae, Infect. Immun. (1997) 65:5017–5027 [PubMed].
  50. van Ham S.M., van Alphen L., Mooi F.R., van Putten J.P., Phase variation of H. influenzae fimbriae: transcriptional control of two divergent genes through a variable combined promoter region, Cell (1993) 73:1187–1196 [CrossRef] [PubMed].
  51. Weiser J.N., Love J.M., Moxon E.R., The molecular mechanism of phase variation of H. influenzae lipopolysaccharide, Cell (1989) 59:657–665 [CrossRef] [PubMed].
  52. Williamson M.P., The structure and function of proline-rich regions in proteins, Biochem. J. (1994) 297:249–260 [PubMed].
  53. Wilton J.L., Scarman A.L., Walker M.J., Djordjevic S.P., Reiterated repeat region variability in the ciliary adhesin gene of Mycoplasma hyopneumoniae, Microbiology (1998) 144:1931–1943 [PubMed].
  54. Zhang N., Harrex A.L., Holland B.R., Fenton L.E., Cannon R.D., Schmid J., Sixty alleles of the ALS7 open reading frame in Candida albicans: ALS7 is a hypermutable contingency locus, Genome Res. (2003) 13:2005–2017 [CrossRef] [PubMed].
  55. Zhao X., Pujol C., Soll D.R., Hoyer L.L., Allelic variation in the contiguous loci encoding Candida albicans ALS5, ALS1 and ALS9, Microbiology (2003) 149:2947–2960 [CrossRef] [PubMed].