Free Access
Vet. Res.
Volume 40, Number 5, September-October 2009
Number of page(s) 12
Published online 21 May 2009
How to cite this article Vet. Res. (2009) 40:47
References of  Vet. Res. (2009) 40:47
  1. Aitken I.D., Longbottom D., Chlamydial abortion, in: Aitken I.D. (Ed.), Diseases of sheep, Blackwell Publishing, Oxford, UK, 2007, pp. 105–111.
  2. Azuma Y., Hirakawa H., Yamashita A., Cai Y., Rahman M.A., Suzuki H., et al., Genome sequence of the cat pathogen, Chlamydophila felis, DNA Res. (2006) 13:15–23 [CrossRef] [PubMed].
  3. Crane D.D., Carlson J.H., Fischer E.R., Bavoil P., Hsia R.C., Tan C., et al., Chlamydia trachomatis polymorphic membrane protein D is a speciescommon pan-neutralizing antigen, Proc. Natl. Acad. Sci. USA (2006) 103:1894–1899 [CrossRef] [PubMed].
  4. Ehricht R., Slickers P., Goellner S., Hotzel H., Sachse K., Optimized DNA microarray assay allows detection and genotyping of single PCR-amplifiable target copies, Mol. Cell. Probes (2006) 20:60–63 [CrossRef] [PubMed].
  5. Entrican G., Immune regulation during pregnancy and host-pathogen interactions in infectious abortion, J. Comp. Pathol. (2002) 126:79–94 [CrossRef] [PubMed].
  6. Giannikopoulou P., Bini L., Simitsek P.D., Pallini V., Vretou E., Two-dimensional electrophoretic analysis of the protein family at 90 kDa of abortifacient Chlamydia psittaci, Electrophoresis (1997) 18:2104–2108 [CrossRef] [PubMed].
  7. Gomes J.P., Nunes A., Bruno W.J., Borrego M.J., Florindo C., Dean D., Polymorphisms in the nine polymorphic membrane proteins of Chlamydia trachomatis across all serovars: evidence for serovar Da recombination and correlation with tissue tropism, J. Bacteriol. (2006) 188:275–286 [CrossRef] [PubMed].
  8. Goodall J.C., Yeo G., Huang M.L., Raggiaschi R., Gaston J.S.H., Identification of Chlamydia trachomatis antigens recognized by human CD4(+) T lymphocytes by screening an expression library, Eur. J. Immunol. (2001) 31:1513–1522 [CrossRef] [PubMed].
  9. Graham S.P., Jones G.E., MacLean M., Livingstone M., Entrican G., Recombinant ovine interferon gamma inhibits the multiplication of Chlamydia psittaci in ovine cells, J. Comp. Pathol. (1995) 112:185–195 [CrossRef] [PubMed].
  10. Henderson I.R., Lam A.C., Polymorphic proteins of Chlamydia spp. – autotransporters beyond the Proteobacteria, Trends Microbiol. (2001) 9:573–578 [CrossRef] [PubMed].
  11. Henderson I.R., Navarro-Garcia F., Desvaux M., Fernandez R.C., Ala'Aldeen D., Type V protein secretion pathway: the autotransporter story, Microbiol. Mol. Biol. Rev. (2004) 68:692–744 [CrossRef] [PubMed].
  12. Livingstone M., Entrican G., Wattegedera S., Buxton D., McKendrick I.J., Longbottom D., Antibody responses to recombinant protein fragments of the major outer membrane protein and polymorphic outer membrane protein POMP90 in Chlamydophila abortus-infected pregnant sheep, Clin. Diagn. Lab. Immunol. (2005) 12:770–777 [PubMed].
  13. Livingstone M., Wheelhouse N., Maley S.W., Longbottom D., Molecular detection of Chlamydophila abortus in post-abortion sheep at oestrus and subsequent lambing, Vet. Microbiol. (2009) 135:134–141 [CrossRef] [PubMed].
  14. Longbottom D., Russell M., Jones G.E., Lainson F.A., Herring A.J., Identification of a multigene family coding for the 90 kda proteins of the ovine abortion subtype of Chlamydia psittaci, FEMS Microbiol. Lett. (1996) 142:277–281 [CrossRef] [PubMed].
  15. Longbottom D., Russell M., Dunbar S.M., Jones G.E., Herring A.J., Molecular cloning and characterization of the genes coding for the highly immunogenic cluster of 90-kilodalton envelope proteins from the Chlamydia psittaci subtype that causes abortion in sheep, Infect. Immun. (1998) 66:1317–1324 [PubMed].
  16. Longbottom D., Coulter L.J., Animal chlamydioses and zoonotic implications, J. Comp. Pathol. (2003) 128:217–244 [CrossRef] [PubMed].
  17. Longbottom D., Livingstone M., Vaccination against chlamydial infections of man and animals, Vet. J. (2006) 171:263–275 [CrossRef] [PubMed].
  18. Nicholson T.L., Olinger L., Chong K., Schoolnik G., Stephens R.S., Global stage-specific gene regulation during the developmental cycle of Chlamydia trachomatis, J. Bacteriol. (2003) 185:3179–3189 [CrossRef] [PubMed].
  19. Nicholson T.L., Chiu K., Stephens R.S., Chlamydia trachomatis lacks an adaptive response to changes in carbon source availability, Infect. Immun. (2004) 72:4286–4289 [CrossRef] [PubMed].
  20. Nunes A., Gomes J.P., Mead S., Florindo C., Correia H., Borrego M.J., Dean D., Comparative expression profiling of the Chlamydia trachomatis pmp gene family for clinical and reference strains, PLoS ONE (2007) 2:e878.
  21. Nunes A., Nogueira P.J., Borrego M.J., Gomes J.P., Chlamydia trachomatis diversity viewed as a tissue-specific coevolutionary arms race, Genome Biol. (2008) 9:R153 [CrossRef] [PubMed].
  22. Pedersen A.S., Christiansen G., Birkelund S., Differential expression of Pmp10 in cell culture infected with Chlamydia pneumoniae CWL029, FEMS Microbiol. Lett. (2001) 203:153–159 [CrossRef] [PubMed].
  23. Read T.D., Brunham R.C., Shen C., Gill S.R., Heidelberg J.F., White O., et al., Genome sequences of Chlamydia trachomatis MoPn and Chlamydia pneumoniae AR39, Nucleic Acids Res. (2000) 28:1397–1406 [CrossRef] [PubMed].
  24. Read T.D., Myers G.S., Brunham R.C., Nelson W.C., Paulsen I.T., Heidelberg J., et al., Genome sequence of Chlamydophila caviae (Chlamydia psittaci GPIC): examining the role of niche-specific genes in the evolution of the Chlamydiaceae, Nucleic Acids Res. (2003) 31:2134–2147 [CrossRef] [PubMed].
  25. Sachse K., Vretou E., Livingstone M., Borel N., Pospischil A., Longbottom D., Recent developments in the laboratory diagnosis of chlamydial infections, Vet. Microbiol. (2009) 135:2–21 [CrossRef] [PubMed].
  26. Saren A., Pascolo S., Stevanovic S., Dumrese T., Puolakkainen M., Sarvas M., et al., Identification of Chlamydia pneumoniae-derived mouse CD8 epitopes, Infect. Immun. (2002) 70:3336–3343 [CrossRef] [PubMed].
  27. Stephens R.S., Kalman S., Lammel C., Fan J., Marathe R., Aravind L., et al., Genome sequence of an obligate intracellular pathogen of humans: Chlamydia trachomatis, Science (1998) 282:754–759 [CrossRef] [PubMed].
  28. Stothard D.R., Toth G.A., Batteiger B.E., Polymorphic membrane protein H has evolved in parallel with the three disease-causing groups of Chlamydia trachomatis, Infect. Immun. (2003) 71:1200–1208 [CrossRef] [PubMed].
  29. Tanzer R.J., Hatch T.P., Characterization of outer membrane proteins in Chlamydia trachomatis LGV serovar L2, J. Bacteriol. (2001) 183:2686–2690 [CrossRef] [PubMed].
  30. Tanzer R.J., Longbottom D., Hatch T.P., Identification of polymorphic outer membrane proteins of Chlamydia psittaci 6BC, Infect. Immun. (2001) 69:428–2434.
  31. Thomson N.R., Yeats C., Bell K., Holden M.T., Bentley S.D., Livingstone M., et al., The Chlamydophila abortus genome sequence reveals an array of variable proteins that contribute to interspecies variation, Genome Res. (2005) 15:629–640 [CrossRef] [PubMed].
  32. Vandahl B.B., Pedersen A.S., Gevaert K., Holm A., Vandekerckhove J., Christiansen G., Birkelund S., The expression, processing and localization of polymorphic membrane proteins in Chlamydia pneumoniae strain CWL029, BMC Microbiol. (2002) 2:36 [CrossRef] [PubMed].
  33. Wehrl W., Brinkmann V., Jungblut P.R., Meyer T.F., Szczepek A.J., From the inside out - processing of the Chlamydial autotransporter PmpD and its role in bacterial adhesion and activation of human host cells, Mol. Microbiol. (2004) 51:319–334 [CrossRef] [PubMed].