Host-pathogen interactions in specific pathogen-free chickens following aerogenous infection with Chlamydia psittaci and Chlamydia abortus

Veterinary Immunology and Immunopathology

Volumn 164, Issue 1-2, 2015, Pages 30-39

  Kalmar, Isabelle ^a   Berndt, Angela ^b   Yin, Lizi ^a   Chiers, Koen ^a   Sachse, Konrad ^b   Vanrompay, Daisy ^a  

^a GHENT UNIVERSITY   (Belgium)

^b FEDERAL RESEARCH INSTITUTE FOR ANIMAL HEALTH   (Germany)

Author keywords

Avian chlamydiosis; Chlamydia abortus; Chlamydia psittaci; Experimental infection; Host immune response; Pathogenesis

Indexed keywords

GAMMA INTERFERON; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 17; INTERLEUKIN 1BETA; INTERLEUKIN 22; INTERLEUKIN 6; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BACTERIAL GENE; CHLAMYDIA; CHLAMYDIA ABORTUS; CHLAMYDIA PSITTACI; CONJUNCTIVITIS; CONTROLLED STUDY; CPAF GENE; DYSPNEA; EPITHELIUM HYPERPLASIA; EROSION; EXPERIMENTAL INFECTION; FTSW GENE; GERMFREE CHICKEN; GROEL GENE; HEPATOMEGALY; HISTOPATHOLOGY; HOST PATHOGEN INTERACTION; HYPERPLASIA; IMMUNE RESPONSE; IMMUNOCOMPETENT CELL; INFLAMMATORY INFILTRATE; LIVER CONGESTION; LUNG CONGESTION; LYMPHOCYTE PROLIFERATION; LYMPHOCYTIC INFILTRATION; NONHUMAN; ORNITHOSIS; PERICARDITIS; PETECHIA; PROTEIN EXPRESSION; RHINITIS; SPLEEN CELL; ANIMAL; BIRD DISEASE; CHICKEN; CHLAMYDIASIS; GENE EXPRESSION REGULATION; GENETICS; GERMFREE ANIMAL; IMMUNOLOGY; LYMPHOCYTE ACTIVATION; MICROBIOLOGY; NEWBORN; PATHOGENICITY; PATHOLOGY; RESPIRATORY SYSTEM; VETERINARY;

ANIMALIA; AVES; CHLAMYDIA ABORTUS; CHLAMYDOPHILA PSITTACI; GALLUS GALLUS;

ANIMALS; ANIMALS, NEWBORN; CHICKENS; CHLAMYDIA; CHLAMYDIA INFECTIONS; CHLAMYDOPHILA PSITTACI; GENE EXPRESSION REGULATION, BACTERIAL; GENES, BACTERIAL; HOST-PATHOGEN INTERACTIONS; LYMPHOCYTE ACTIVATION; POULTRY DISEASES; PSITTACOSIS; RESPIRATORY SYSTEM; SPECIFIC PATHOGEN-FREE ORGANISMS;

EID: 84923525464     PISSN: 01652427     EISSN: 18732534     Source Type: Journal    
DOI: 10.1016/j.vetimm.2014.12.014     Document Type: Article

References (31)

1. Bai H., Cheng J., Gao X., Joyee A.G., Fan Y., Wang S., Jiao L., Yao Z., Yang X. IL-17/Th17 promotes type 1T cell immunity against pulmonary intracellular bacterial infection through modulating dendritic cell function. J. Immunol. 2009, 183:5886-5895.
2. Berndt A., Wilhelm A., Jugert C., Pieper J., Sachse K., Methner U. Chicken cecum immune response to Salmonella enterica serovars of different levels of invasiveness. Infect. Immun. 2007, 75:5993-6007.
3. Braukmann M., Sachse K., Jacobsen I.D., Westermann M., Menge C., Saluz H.P., Berndt A. Distinct intensity of host-pathogen interactions in Chlamydia psittaci- and Chlamydia abortus-infected chicken embryos. Infect. Immun. 2012, 80:2976-2988.
4. Dunon D., Schwager J., Dangy J.P., Cooper M.D., Imhof B.A. T cell migration during development: homing is not related to TCR V beta 1 repertoire selection. EMBO J. 1994, 13:808-815.
5. 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.
6. Gaede W., Reckling K.F., Dresenkamp B., Kenklies S., Schubert E., Noack U., Irmscher H.M., Ludwig C., Hotzel H., Sachse K. Chlamydophila psittaci infections in humans during an outbreak of psittacosis from poultry in Germany. Zoonoses Public Health 2008, 55:184-188.
7. Germolec D.R., Kashon M., Nyska A., Kuper C.F., Portier C., Kommineni C., Johnson K.A., Luster M.I. The accuracy of extended histopathology to detect immunotoxic chemicals. Toxicol. Sci. 2004, 82:504-514.
8. Goellner S., Schubert E., Liebler-Tenorio E., Hotzel H., Saluz H.P., Sachse K. Transcriptional response patterns of Chlamydophila psittaci in different in vitro models of persistent infection. Infect. Immun. 2006, 74:4801-4808.
9. Harkinezhad T., Geens T., Vanrompay D. Chlamydophila psittaci infections in birds: a review with emphasis on zoonotic consequences. Vet. Microbiol. 2009, 135:68-77.
10. Huang J., Wang M.D., Lenz S., Gao D.Y., Kaltenboeck B. IL-12 administered during Chlamydia psittaci lung infection in mice confers immediate and long-term protection and reduces macrophage inflammatory protein-2 level and neutrophil infiltration in lung tissue. J. Immunol. 1999, 162:2217-2226.
11. Jeurissen S.H., Janse E.M., Koch G., De Boer G.F. Postnatal development of mucosa-associated lymphoid tissues in chickens. Cell Tissue Res. 1989, 258:119-124.
12. Jeurissen S.H., Janse E.M., Kok G.L., De Boer G.F. Distribution and function of non-lymphoid cells positive for monoclonal antibody CVI-ChNL-68.2 in healthy chickens and those infected with Marek's disease virus. Vet. Immunol. Immunopathol. 1989, 22:123-133.
13. Jeurissen S.H., Vervelde L., Janse E.M. Structure and function of lymphoid tissues of the chicken. Poult. Sci. Rev. 1994, 5:183-207.
14. Kaspers B., Gutlich M., Witter K., Losch U., Goldberg M., Ziegler I. Coordinate induction of tetrahydrobiopterin synthesis and nitric oxide synthase activity in chicken macrophages: upregulation of GTP-cyclohydrolase I activity. Comparat. Biochem. Physiol. B: Biochem. Mol. Biol. 1997, 117:209-215.
15. Khader S.A., Gaffen S.L., Kolls J.K. Th17 cells at the crossroads of innate and adaptive immunity against infectious diseases at the mucosa. Mucosal Immunol. 2009, 2:403-411.
16. Khader S.A., Gopal R. IL-17 in protective immunity to intracellular pathogens. Virulence 2010, 1:423-427.
17. Mast J., Goddeeris B.M. Development of immunocompetence of broiler chickens. Vet. Immunol. Immunopathol. 1999, 70:245-256.
18. Mayr, A., Bachmann, P., Bibrack, B., Wittmann, G., 1974. Zellkulturen - Bebrütete Hühnereier - Versuchstiere. In: Virologische Arbeitsmethoden. Gustav-Fischer-Verlag Jena, p. 35.
19. McClenaghan M., Herring A.J., Aitken I.D. Comparison of Chlamydia psittaci isolates by DNA restriction endonuclease analysis. Infect. Immun. 1984, 45:384-389.
20. Novak M., Moldoveanu Z., Schafer D.P., Mestecky J., Compans R.W. Murine model for evaluation of protective immunity to influenza virus. Vaccine 1993, 11:55-60.
21. Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29:e45.
22. Read T.D., Joseph S.J., Didelot X., Liang B., Patel L., Dean D. Comparative analysis of Chlamydia psittaci genomes reveals the recent emergence of a pathogenic lineage with a broad host range. MBio 2013, 4.
23. Tan C., Spitznagel J.K., Shou H., Hsia R.C., Bavoil P.M. The polymorphic membrane protein gene family of the Chlamydiaceae. Chlamydia: Genomics and Pathogenesis 2006, 195-218. Horizon Bioscience, Norfolk, UK. P.M. Bavoil, P.B. Wyrick (Eds.).
24. Vanrompay D., Cox E., Volckaert G., Goddeeris B. Turkeys are protected from infection with Chlamydia psittaci by plasmid DNA vaccination against the major outer membrane protein. Clin. Exp. Immunol. 1999, 118:49-55.
25. 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.
26. Verminnen K., Van Loock M., Hafez H.M., Ducatelle R., Haesebrouck F., Vanrompay D. Evaluation of a recombinant enzyme-linked immunosorbent assay for detecting Chlamydophila psittaci antibodies in turkey sera. Vet. Res. 2006, 37:623-632.
27. Voigt A., Schöfl G., Saluz H.P. The Chlamydia psittaci genome: a comparative analysis of intracellular pathogens. PLoS One 2012, 7:e35097.
28. Wang Y., Kahane S., Cutcliffe L.T., Skilton R.J., Lambden P.R., Clarke I.N. Development of a transformation system for Chlamydia trachomatis: restoration of glycogen biosynthesis by acquisition of a plasmid shuttle vector. PLoS Pathog. 2011, 7:e1002258.
29. Wu Q., Martin R.J., Rino J.G., Breed R., Torres R.M., Chu H.W. IL-23-dependent IL-17 production is essential in neutrophil recruitment and activity in mouse lung defense against respiratory Mycoplasma pneumoniae infection. Microbes Infect. 2007, 9:78-86.
30. Yin L., Kalmar I.D., Lagae S., Vandendriessche S., Vanderhaeghen W., Butaye P., Cox E., Vanrompay D. Emerging Chlamydia psittaci infections in the chicken industry and pathology of Chlamydia psittaci genotype B and D strains in specific pathogen free chickens. Vet. Microbiol. 2013, 162:740-749.
31. Zhang X., Gao L., Lei L., Zhong Y., Dube P., Berton M.T., Arulanandam B., Zhang J., Zhong G. A MyD88-dependent early IL-17 production protects mice against airway infection with the obligate intracellular pathogen Chlamydia muridarum. J. Immunol. 2009, 183:1291-1300.