A domino-like chlamydial attachment process: Concurrent Parachlamydia acanthamoebae attachment to amoebae is required for several amoebal released molecules and serine protease activity

Microbiology (United Kingdom)

Volumn 158, Issue 6, 2012, Pages 1607-1614

  Hayashi, Yasuhiro ^a   Yimin, ^b   Matsuo, Junji ^a   Nakamura, Shinji ^c   Kunichika, Miyuki ^c   Yoshida, Mitsutaka ^c   Takahashi, Kaori ^c   Yamaguchi, Hiroyuki ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c JUNTENDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,10 PHENANTHROLINE; MONOCLONAL ANTIBODY; MONOCLONAL ANTIBODY 300; MONOCLONAL ANTIBODY 311; MONOCLONAL ANTIBODY 38; MONOCLONAL ANTIBODY 562; SERINE PROTEINASE; SERINE PROTEINASE INHIBITOR; UNCLASSIFIED DRUG;

ACANTHAMOEBA; AMOEBA MOLECULE; ARTICLE; BACTERIUM ADHERENCE; CHLAMYDIA; ENZYME ACTIVITY; HOST PARASITE INTERACTION; HYBRIDOMA; MOLECULE; NONHUMAN; PARACHLAMYDIA ACANTHAMOEBA; PRIORITY JOURNAL;

ACANTHAMOEBA; BACTERIAL ADHESION; CHLAMYDIALES; HOST-PARASITE INTERACTIONS; PROTOZOAN PROTEINS; SERINE PROTEASES;

ACANTHAMOEBA; BACTERIA (MICROORGANISMS); PARACHLAMYDIA ACANTHAMOEBAE;

EID: 84861895095     PISSN: 13500872     EISSN: None     Source Type: Journal    
DOI: 10.1099/mic.0.057190-0     Document Type: Article

References (30)

1. Abromaitis, S. & Stephens, R. S. (2009). Attachment and entry of Chlamydia have distinct requirements for host protein disulfide isomerase. PLoS Pathog 5, e1000357.
2. Anger, C. & Lally, J. M. (2008). Acanthamoeba: a review of its potential to cause keratitis, current lens care solution disinfection standards and methodologies, and strategies to reduce patient risk. Eye Contact Lens 34, 247-253.
3. Bartlett, J. G. (2008). Is activity against "atypical" pathogens necessary in the treatment protocols for community-acquired pneumonia? Issues with combination therapy. Clin Infect Dis 47 (Suppl. 3), S232-S236.
4. Baud, D., Goy, G., Osterheld, M. C., Borel, N., Vial, Y., Pospischil, A. & Greub, G. (2011). Waddlia chondrophila: from bovine abortion to human miscarriage. Clin Infect Dis 52, 1469-1471.
5. Casson, N. & Greub, G. (2006). Resistance of different Chlamydia-like organisms to quinolones and mutations in the quinoline resistancedetermining region of the DNA gyrase A-and topoisomeraseencoding genes. Int J Antimicrob Agents 27, 541-544.
6. Chen, J. C. & Stephens, R. S. (1997). Chlamydia trachomatis glycosaminoglycan-dependent and independent attachment to eukaryotic cells. Microb Pathog 22, 23-30.
7. Christian, J. G., Heymann, J., Paschen, S. A., Vier, J., Schauenburg, L., Rupp, J., Meyer, T. F., Häcker, G. & Heuer, D. (2011). Targeting of a chlamydial protease impedes intracellular bacterial growth. PLoS Pathog 7, e1002283.
8. Corsaro, D., Venditti, D. & Valassina, M. (2002). New parachlamydial 16S rDNA phylotypes detected in human clinical samples. Res Microbiol 153, 563-567.
9. Dudley, R., Alsam, S. & Khan, N. A. (2008). The role of proteases in the differentiation of Acanthamoeba castellanii. FEMS Microbiol Lett 286, 9-15.
10. Fukumoto, T., Matsuo, J., Hayashi, M., Oguri, S., Nakamura, S., Mizutani, Y., Yao, T., Akizawa, K., Suzuki, H. & other authors (2010). Impact of free-living amoebae on presence of Parachlamydia acanthamoebae in the hospital environment and its survival in vitro without requirement for amoebae. J Clin Microbiol 48, 3360-3365.
11. Greub, G. (2009). Parachlamydia acanthamoebae, an emerging agent of pneumonia. Clin Microbiol Infect 15, 18-28.
12. Greub, G., Boyadjiev, I., La Scola, B., Raoult, D. & Martin, C. (2003). Serological hint suggesting that Parachlamydiaceae are agents of pneumonia in polytraumatized intensive care patients. Ann N Y Acad Sci 990, 311-319.
13. Hodinka, R. L. & Wyrick, P. B. (1986). Ultrastructural study of mode of entry of Chlamydia psittaci into L-929 cells. Infect Immun 54, 855-863.
14. Horn, M. (2008). Chlamydiae as symbionts in eukaryotes. Annu Rev Microbiol 62, 113-131.
15. Horn, M., Collingro, A., Schmitz-Esser, S., Beier, C. L., Purkhold, U., Fartmann, B., Brandt, P., Nyakatura, G. J., Droege, M. & other authors (2004). Illuminating the evolutionary history of chlamydiae. Science 304, 728-730.
16. Jordan, N. N., Lee, S. E., Nowak, G., Johns, N. M. & Gaydos, J. C. (2011). Chlamydia trachomatis reported among U.S. active duty service members, 2000-2008. Mil Med 176, 312-319.
17. Jorgensen, I., Bednar, M. M., Amin, V., Davis, B. K., Ting, J. P., McCafferty, D. G. & Valdivia, R. H. (2011). The Chlamydia protease CPAF regulates host and bacterial proteins to maintain pathogen vacuole integrity and promote virulence. Cell Host Microbe 10, 21-32.
18. Khan, N. A. (2006). Acanthamoeba: biology and increasing importance in human health. FEMS Microbiol Rev 30, 564-595.
19. Kim, J. H., Jiang, S., Elwell, C. A. & Engel, J. N. (2011). Chlamydia trachomatis co-opts the FGF2 signaling pathway to enhance infection. PLoS Pathog 7, e1002285.
20. Matsuo, J., Hayashi, Y., Nakamura, S., Sato, M., Mizutani, Y., Asaka, M. & Yamaguchi, H. (2008). Novel Parachlamydia acanthamoebae quantification method based on coculture with amoebae. Appl Environ Microbiol 74, 6397-6404.
21. Moon, E. K., Chung, D. I., Hong, Y. C. & Kong, H. H. (2008). Characterization of a serine proteinase mediating encystation of Acanthamoeba. Eukaryot Cell 7, 1513-1517.
22. Nascimento-Carvalho, C. M., Cardoso, M. R., Paldanius, M., Barral, A., Araújo-Neto, C. A., Saukkoriipi, A., Vainionpää, R., Leinonen, M. & Ruuskanen, O. (2009). Simkania negevensis infection among Brazilian children hospitalized with community-acquired pneumonia. J Infect 58, 250-253.
23. Rasmussen-Lathrop, S. J., Koshiyama, K., Phillips, N. & Stephens, R. S. (2000). Chlamydia-dependent biosynthesis of a heparan sulphate-like compound in eukaryotic cells. Cell Microbiol 2, 137-144.
24. Sutherland, E. R. & Martin, R. J. (2007). Asthma and atypical bacterial infection. Chest 132, 1962-1966.
25. Taraktchoglou, M., Pacey, A. A., Turnbull, J. E. & Eley, A. (2001). Infectivity of Chlamydia trachomatis serovar LGV but not E is dependent on host cell heparan sulfate. Infect Immun 69, 968-976.
26. Watson, C. & Alp, N. J. (2008). Role of Chlamydia pneumoniae in atherosclerosis. Clin Sci (Lond) 114, 509-531.
27. Weiss, E., Williams, J. C., Dasch, G. A. & Kang, Y. H. (1989). Energy metabolism of monocytic Ehrlichia. Proc Natl Acad Sci U S A 86, 1674-1678.
28. Wuppermann, F. N., Hegemann, J. H. & Jantos, C. A. (2001). Heparan sulfate-like glycosaminoglycan is a cellular receptor for Chlamydia pneumoniae. J Infect Dis 184, 181-187.
29. Zhang, J. P. & Stephens, R. S. (1992). Mechanism of C. trachomatis attachment to eukaryotic host cells. Cell 69, 861-869.
30. Zhong, G. (2011). Chlamydia trachomatis secretion of proteases for manipulating host signaling pathways. Front Microbiol 2, 14.