This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Stothard, D. R.
Right arrow Articles by Jones, R. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stothard, D. R.
Right arrow Articles by Jones, R. B.

 Previous Article  |  Next Article 

Infect Immun, August 1998, p. 3618-3625, Vol. 66, No. 8
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Phylogenetic Analysis of the Chlamydia trachomatis Major Outer Membrane Protein and Examination of Potential Pathogenic Determinants

Diane R. Stothard,* George Boguslawski,dagger and Robert B. Jones

Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202

Received 21 November 1997/Returned for modification 24 March 1998/Accepted 26 May 1998

Phylogenetic analysis was utilized to investigate biological relationships (tissue tropism, disease presentation, and epidemiologic success), as evidenced by coevolution, among human strains of Chlamydia trachomatis. Nucleotide sequences of omp1, the gene encoding the major outer membrane protein (MOMP) of C. trachomatis, were determined for 40 strains representing 11 serovars. These data were combined with available omp1 sequences from GenBank for an analysis encompassing a total of 69 strains representing 17 serovars infecting humans. Phylogenetic analysis of the nucleotide and inferred amino acid sequences showed no evolutionary relationships among serovars that corresponded to biological or pathological phenotypes (tissue tropism, disease presentation, and epidemiologic success). In addition, no specific residues that may have evolved to play a role in determining biologically relevant characteristics of chlamydia, such as tissue specificity, disease presentation, and epidemiologic success, were apparent in the MOMP. These results suggest that variation in MOMP may have arisen from a need to be diverse in the presence of immune pressure rather than as a function of pathogenicity. Therefore, the role of MOMP in disease pathogenesis and infection may be passive, and it may not be the major ligand responsible for directing infection of various human cell types.


* Corresponding author. Mailing address: Department of Medicine, Infectious Diseases, Indiana University School of Medicine, 435 Emerson Hall, 545 Barnhill Dr., Indianapolis, IN 46202. Phone: (317) 278-1791. Fax: (317) 274-1587. E-mail: dstothar{at}iupui.edu.

dagger Present address: Department of Biochemistry, Indiana University School of Medicine, Indianapolis, IN 46202.


Infect Immun, August 1998, p. 3618-3625, Vol. 66, No. 8
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Nunes, A., Borrego, M. J., Nunes, B., Florindo, C., Gomes, J. P. (2009). Evolutionary Dynamics of ompA, the Gene Encoding the Chlamydia trachomatis Key Antigen. J. Bacteriol. 191: 7182-7192 [Abstract] [Full Text]  
  • Magbanua, J. P. V, Goh, B. T., Michel, C.-E., Aguirre-Andreasen, A., Alexander, S., Ushiro-Lumb, I., Ison, C., Lee, H. (2007). Chlamydia trachomatis variant not detected by plasmid based nucleic acid amplification tests: molecular characterisation and failure of single dose azithromycin. Sex. Transm. Infect. 83: 339-343 [Abstract] [Full Text]  
  • Klint, M., Lofdahl, M., Ek, C., Airell, A., Berglund, T., Herrmann, B. (2006). Lymphogranuloma Venereum Prevalence in Sweden among Men Who Have Sex with Men and Characterization of Chlamydia trachomatis ompA Genotypes. J. Clin. Microbiol. 44: 4066-4071 [Abstract] [Full Text]  
  • Hsu, M.-C., Tsai, P.-Y., Chen, K.-T., Li, L.-H., Chiang, C.-C., Tsai, J.-J., Ke, L.-Y., Chen, H.-Y., Li, S.-Y. (2006). Genotyping of Chlamydia trachomatis from clinical specimens in Taiwan.. J Med Microbiol 55: 301-308 [Abstract] [Full Text]  
  • Brunelle, B. W., Sensabaugh, G. F. (2006). The ompA Gene in Chlamydia trachomatis Differs in Phylogeny and Rate of Evolution from Other Regions of the Genome. Infect. Immun. 74: 578-585 [Abstract] [Full Text]  
  • Bastianel, C., Garnier-Semancik, M., Renaudin, J., Bove, J. M., Eveillard, S. (2005). Diversity of "Candidatus Liberibacter asiaticus," Based on the omp Gene Sequence. Appl. Environ. Microbiol. 71: 6473-6478 [Abstract] [Full Text]  
  • Solomon, A. W., Peeling, R. W., Foster, A., Mabey, D. C. W. (2004). Diagnosis and Assessment of Trachoma. Clin. Microbiol. Rev. 17: 982-1011 [Abstract] [Full Text]  
  • Eko, F. O., He, Q., Brown, T., McMillan, L., Ifere, G. O., Ananaba, G. A., Lyn, D., Lubitz, W., Kellar, K. L., Black, C. M., Igietseme, J. U. (2004). A Novel Recombinant Multisubunit Vaccine against Chlamydia. J. Immunol. 173: 3375-3382 [Abstract] [Full Text]  
  • Molano, M., Meijer, C. J. L. M., Morre, S. A., Pol, R., van den Brule, A. J. C. (2004). Combination of PCR Targeting the VD2 of omp1 and Reverse Line Blot Analysis for Typing of Urogenital Chlamydia trachomatis Serovars in Cervical Scrape Specimens. J. Clin. Microbiol. 42: 2935-2939 [Abstract] [Full Text]  
  • Stevens, M. P., Tabrizi, S. N., Muller, R., Krause, V., Garland, S. M. (2004). Characterization of Chlamydia trachomatis omp1 Genotypes Detected in Eye Swab Samples from Remote Australian Communities. J. Clin. Microbiol. 42: 2501-2507 [Abstract] [Full Text]  
  • Lister, N. A, Tabrizi, S. N., Fairley, C. K., Smith, A., Janssen, P. H., Garland, S. (2004). Variability of the Chlamydia trachomatis omp1 Gene Detected in Samples from Men Tested in Male-Only Saunas in Melbourne, Australia. J. Clin. Microbiol. 42: 2596-2601 [Abstract] [Full Text]  
  • Millman, K., Black, C. M., Johnson, R. E., Stamm, W. E., Jones, R. B., Hook, E. W., Martin, D. H., Bolan, G., Tavare, S., Dean, D. (2004). Population-Based Genetic and Evolutionary Analysis of Chlamydia trachomatis Urogenital Strain Variation in the United States. J. Bacteriol. 186: 2457-2465 [Abstract] [Full Text]  
  • Lysen, M., Osterlund, A., Rubin, C.-J., Persson, T., Persson, I., Herrmann, B. (2004). Characterization of ompA Genotypes by Sequence Analysis of DNA from All Detected Cases of Chlamydia trachomatis Infections during 1 Year of Contact Tracing in a Swedish County. J. Clin. Microbiol. 42: 1641-1647 [Abstract] [Full Text]  
  • Murillo, L. S., Land, J. A., Pleijster, J., Bruggeman, C. A., Pena, A. S., Morre, S. A. (2003). Interleukin-1B (IL-1B) and interleukin-1 receptor antagonist (IL-1RN) gene polymorphisms are not associated with tubal pathology and Chlamydia trachomatis-related tubal factor subfertility. Hum Reprod 18: 2309-2314 [Abstract] [Full Text]  
  • Polley, S. D., Chokejindachai, W., Conway, D. J. (2003). Allele Frequency-Based Analyses Robustly Map Sequence Sites Under Balancing Selection in a Malaria Vaccine Candidate Antigen. Genetics 165: 555-561 [Abstract] [Full Text]  
  • Stothard, D. R., Toth, G. A., Batteiger, B. E. (2003). Polymorphic Membrane Protein H Has Evolved in Parallel with the Three Disease-Causing Groups of Chlamydia trachomatis. Infect. Immun. 71: 1200-1208 [Abstract] [Full Text]  
  • Rocha, E. P. C., Pradillon, O., Bui, H., Sayada, C., Denamur, E. (2002). A new family of highly variable proteins in the Chlamydophila pneumoniae genome. Nucleic Acids Res 30: 4351-4360 [Abstract] [Full Text]  
  • Yamamoto, Y. (2002). PCR in Diagnosis of Infection: Detection of Bacteria in Cerebrospinal Fluids. CVI 9: 508-514 [Full Text]  
  • Bandea, C I, Kubota, K, Brown, T M, Kilmarx, P H, Bhullar, V, Yanpaisarn, S, Chaisilwattana, P, Siriwasin, W, Black, C M (2001). Typing of Chlamydia trachomatis strains from urine samples by amplification and sequencing the major outer membrane protein gene (omp1). Sex. Transm. Infect. 77: 419-422 [Abstract] [Full Text]  
  • Jurstrand, M., Falk, L., Fredlund, H., Lindberg, M., Olcen, P., Andersson, S., Persson, K., Albert, J., Backman, A. (2001). Characterization of Chlamydia trachomatis omp1 Genotypes among Sexually Transmitted Disease Patients in Sweden. J. Clin. Microbiol. 39: 3915-3919 [Abstract] [Full Text]  
  • Millman, K. L., Tavare, S., Dean, D. (2001). Recombination in the ompA Gene but Not the omcB Gene of Chlamydia Contributes to Serovar-Specific Differences in Tissue Tropism, Immune Surveillance, and Persistence of the Organism. J. Bacteriol. 183: 5997-6008 [Abstract] [Full Text]  
  • Stothard, D. R. (2001). Use of a Reverse Dot Blot Procedure To Identify the Presence of Multiple Serovars in Chlamydia trachomatis Urogenital Infection. J. Clin. Microbiol. 39: 2655-2659 [Abstract] [Full Text]  
  • Pannekoek, Y., Westenberg, S. M., de Vries, J., Repping, S., Spanjaard, L., Eijk, P. P., van der Ende, A., Dankert, J. (2000). PCR Assessment of Chlamydia trachomatis Infection of Semen Specimens Processed for Artificial Insemination. J. Clin. Microbiol. 38: 3763-3767 [Abstract] [Full Text]  
  • Morré, S. A., Ossewaarde, J. M., Savelkoul, P. H. M., Stoof, J., Meijer, C. J. L. M., van den Brule, A. J. C. (2000). Analysis of Genetic Heterogeneity in Chlamydia trachomatis Clinical Isolates of Serovars D, E, and F by Amplified Fragment Length Polymorphism. J. Clin. Microbiol. 38: 3463-3466 [Abstract] [Full Text]  
  • Musser, J. M., Amin, A., Ramaswamy, S. (2000). Negligible Genetic Diversity of Mycobacterium tuberculosis Host Immune System Protein Targets: Evidence of Limited Selective Pressure. Genetics 155: 7-16 [Abstract] [Full Text]  
  • Sturm-Ramirez, K., Brumblay, H., Diop, K., Guèye-Ndiaye, A., Sankalé, J.-L., Thior, I., N'Doye, I., Hsieh, C.-C., Mboup, S., Kanki, P. J. (2000). Molecular Epidemiology of Genital Chlamydia trachomatis Infection in High-Risk Women in Senegal, West Africa. J. Clin. Microbiol. 38: 138-145 [Abstract] [Full Text]  
  • Meijer, A., Morré, S. A., Van Den Brule, A. J. C., Savelkoul, P. H. M., Ossewaarde, J. M. (1999). Genomic Relatedness of Chlamydia Isolates Determined by Amplified Fragment Length Polymorphism Analysis. J. Bacteriol. 181: 4469-4475 [Abstract] [Full Text]  
  • Dean, D., Millman;, K., Stothard, D. R., Jones, R. B. (1999). Phylogenetic Analysis of Chlamydia trachomatis. Infect. Immun. 67: 1009-1010 [Full Text]  
  • Stothard, D. R., Williams, J. A., Van Der Pol, B., Jones, R. B. (1998). Identification of a Chlamydia trachomatis Serovar E Urogenital Isolate Which Lacks the Cryptic Plasmid. Infect. Immun. 66: 6010-6013 [Abstract] [Full Text]  
  • Stothard, D. R., Van Der Pol, B., Smith, N. J., Jones, R. B. (1998). Effect of Serial Passage in Tissue Culture on Sequence of omp1 from Chlamydia trachomatis Clinical Isolates. J. Clin. Microbiol. 36: 3686-3688 [Abstract] [Full Text]