Skip to main content
Log in

Long-term Study of Chlamydophilosis in Slovenia

  • Published:
Veterinary Research Communications Aims and scope Submit manuscript

Abstract

Immune reactivity for Chlamydophila (C.) psittaci in Slovenia was monitored in parrots, canaries, finches and nine species of recently captured free-living birds (house sparrows, Eurasian goldfinches, tree sparrows, chaffinches, European greenfinches, European serines, Eurasian siskins, Eurasian linnets and Eurasian bullfinches) in the period from 1991 to 2001. In subsequent years, specific IgG antibodies were found using immunofluorescence in parrots (0.7– 53.6%), canaries (0.0–3.5%), finches (0.0–5.7%) and in captured free-living birds (33.3% of Eurasian goldfinches in 1994). An experimental infection with C. psittaci was performed in order to study clinical signs and pathological changes in canaries and finches. The C. psittaci strain used for experimental infection was isolated from a cockatiel (Nymphicus hollandicus). Chlamydial DNA was extracted from clinical material followed by RFLP-PCR analysis. Infection of canaries and finches was confirmed in organ smears by direct immunofluorescence and a modified Gimenez staining method. In addition, serological tests of indirect immunofluorescence and complement fixation were applied. However, in spite of positive immunological reaction there were no clinical signs three weeks after infection. The present study includes results of a serological survey of persons belonging to the most important risk groups (breeders, pet shopkeepers and veterinarians). The results of microimmunofluorescence to identify the presence of specific antibodies and correlation between appearance of infection in birds and important risk groups are presented. Out of 143 persons belonging to the high-risk group we found 10 (7%) persons who were immunologically positive. Testing of two successive samples was used to demonstrate an increase in IgG and IgA titres in human sera. However, IgM, which is indicative of acute infection, could not be detected.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  • Anderson, I., Baxter, S.I. I., Dunbar, S., Rae, A.G., Philips, H.L., Clarkson, M.J. and Herring A.J., 1996. Analyses of the genomes of chlamydial isolates from ruminants and pigs support the adoption of the new species Chlamydia pecorum. International Journal of Systematic Bacteriology, 46, 24–51

    Google Scholar 

  • Chahota, R., Katoch, R.C. and Joshi, V.B., 1997. Seroprevalence of Chlamydia psittaci in domestic poultry and wild birds. The Indian Journal of Poultry Science, 32, 67–71

    Google Scholar 

  • Deutz A.F.K., Hinterdorfer, F. and Schuller, W., 1996. Serologische Untersuchung von Tierärzten auf Zoonosen. 1. Mitteilung: Grunddaten und Seropravalenzen gegenüber bakteriellen Zoonosen. Wiener Tierä rztliche Monatsschrift, 83, 283–288

    Google Scholar 

  • Dorrestein, G.M., 1989. Chlamydiosis: a new approach in diagnosis and therapy. In: Proceedings of the Association of Avian Veterinarians, Munich; 1989:29–34

  • Dovč, A., 1998. Chlamydia psittaci infection in domestic and wild birds in Slovenia. Veterinarske novice, 24, 419–422

    Google Scholar 

  • Duan, Y.J., Souriau, A., Mahe, A.M., Trap, D., Andersen, A.A. and Rodolakis, A., 1999. Serotyping of chlamydial clinical isolates from birds with monoclonal antibodies. Avian Diseases, 43, 22–28

    Google Scholar 

  • Eugster, A.K., 1980. Handbook Series in Zoonoses. Section A, (CRC Press, Boca Raton)

    Google Scholar 

  • Everett, K.D., Bush, R.M. and Andersen, A.A., 1999. 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. International Journal of Systematic Bacteriology, 49, 415–440

    Google Scholar 

  • Gaydos, C.A., Palmer, L., Quinn, T.C., Falkow, S. and Eiden, J.J., 1993. Phylogenetic relationship of Chlamydia pneumoniae to Chlamydia psittaci and Chlamydia trachomatis as determined by analysis of 16S ribosomal DNA sequences. International Journal of Systematic Bacteriology, 43, 610–612

    Google Scholar 

  • Gosbell, I.B., Ross, A.D. and Turner, I.B., 1999. Chlamydia psittaci infection and reinfection in a veterinarian. Australian Veterinary Journal, 77, 511–513

    Google Scholar 

  • Hinton, D.G., Shipley, A., Galvin, J.W., Harkin, J.T. and Brunton, R.A., 1993. Chlamydiosis in workers at a duck farm and processing plant. Australian Veterinary Journal, 70, 174–176

    Google Scholar 

  • Huminer, D., Pitlik, S., Kitayin, D., Weissman, Y. and Samra, Z., 1992. Prevalence of Chlamydia psittaci infection among persons who work with birds. Israel Journal of Medical Sciences, 28, 739–741

    Google Scholar 

  • Huminer, D., Samra, Z., Weisman, Y. and Pitlik, S., 1988. Family outbreaks of psittacosis in Israel. The Lancet, 2, 615–618

    Google Scholar 

  • Janeczek, F., 1989. Chlamydia psittaci — diagnostic procedures in Psittaciformes: comparative studies on antigen detection in the cell culture and in the ELISA as well as antibody detection in the complement fixation and in blocking ELISA, (PhD thesis, University of Munich)

  • Kaleta, E.F. and Taday, E.M.A., 2003. Avian host range of Chlamydophila spp. based on isolation, antigens detection and serology. Avian Pathology, 32, 435–462

    Google Scholar 

  • Kaltenboeck, B., Kousoulas, K.G. and Storz, J., 1991. Detection and strain differentiation of Chlamydia psittaci mediated by a two-step polymerase chain reaction. Journal of Clinical Microbiology, 29, 1969–1975

    Google Scholar 

  • Ketz, C.J. and Carpenter, J.W., 1999. What is your diagnosis? Journal of Avian Medicine and Surgery, 13, 218–222

    Google Scholar 

  • Kruszewicz, A.H. and Paszowska, K., 1992. Occurrence of Chlamydia psittaci in house sparrows (Passer domesticus). In: VIII. Tagung der Fachgruppe “Geflügelkrankheiten”, München; 1992: 124–129

  • Meijer, A., Morre, S.A., van den Brule, A.J., Savelkoul, P.H. and Ossewaarde, J.M., 1999. Genomic relatedness of Chlamydia isolates determined by amplified fragment length polymorphism analysis. Journal of Bacteriology, 181, 4469–4475

    Google Scholar 

  • OIE, 1996. Manual of standards for diagnostic test and vaccines for list A and B diseases of mammals, birds and bees, (Office International des Epizooties, Paris)

    Google Scholar 

  • Olsen, B., Persson, K. and Broholm, K.A., 1998. PCR detection of Chlamydia psittaci in faecal samples from passerine birds in Sweden. Epidemiology and Infection, 121, 481–483

    Google Scholar 

  • Pearson, J.E., Gustafson G.A., Senne D.A. and Peterson L.A., 1989. Isolation and identification of Chlamydia psittaci from pet birds. Journal of the American Veterinary Medical Association, 195, 1564–1566

    Google Scholar 

  • Pudjiatmoko, Fukushi, H., Ochiai, Y., Yamaguchi, T. and Hirai, K., 1997. Phylogenetic analysis of the genus Chlamydia based on 16S rRNA gene sequences. International Journal of Systematic Bacteriology, 47, 425–431

    Google Scholar 

  • Rasmussen, S. and Timms, P., 1991. Detection of Chlamydia psittaci using DNA probes and the polymerase chain reaction. FEMS Microbiology Letters, 61, 169–173

    Google Scholar 

  • Rodolakis, A. and Souriau, A., 1992. Restriction endonuclease analysis of DNA from ruminant Chlamydia psittaci and its relation to mouse virulence. Veterinary Microbiology, 31, 263–271

    Google Scholar 

  • Sayada, C., Andersen, A.A., Storey, C., Milon, A., Eb. F., Hashimoto, N., Hirai, K., Elion, J. and Denamur, E., 1995. Usefulness of omp1 restriction mapping for avian Chlamydia psittaci isolate differentiation. Research in Microbiology, 146, 155–165

    Google Scholar 

  • Simpson, V.R. and Bevan, R., 1989. Chlamydia psittaci infection in robins. The Veterinary Record, 21, 537

    Google Scholar 

  • Vanrompay, D., Butaye, P., Sayada, C., Ducatelle, R. and Haesebrouck, F., 1997. Characterization of avian Chlamydia psittaci strains using omp1 restriction mapping and serovar-specific monoclonal antibodies. Research in Microbiology, 148, 327–333

    Google Scholar 

  • Vanrompay, D., De Meurichy, W., Ducatelle, R. and Haesebrouck, F., 1994. Pneumonia in Moorish tortoises (Testudo graeca) associated with avian serovar A Chlamydia psittaci. The Veterinary Record, 135, 284–285

    Google Scholar 

  • Vlahović, K., Župančić, Z., Gregurić, J. and Pavlak M., 1998. Zur Zuverlässigkeit diagnostischer Verfahren beim Nachweis von Infektionen mit Chlamydia spp. bei Vögein — Reliability of diagnostic methods in proving infections of Chlamydia spp. in birds. Zeitschrift für Jagdwissenschaft, 44, 133–139

    Google Scholar 

  • Wilcke, B.W., Jr., Newcomer, C.E., Anver, M.R., Simmons, J.L. and Nace, G.W., 1983. Isolation of Chlamydia psittaci from naturally infected African clawed frogs (Xenopus laevis). Infection and Immunity, 41, 789–794

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. Dovc.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dovc, A., Dovc, P., Kese, D. et al. Long-term Study of Chlamydophilosis in Slovenia. Vet Res Commun 29 (Suppl 1), 23–36 (2005). https://doi.org/10.1007/s11259-005-0834-2

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11259-005-0834-2

Keywords

Navigation