Centers for Disease Control and Prevention
 CDC Home Search Health Topics A-Z
peer-reviewed.gif (582 bytes)
eid_header.gif (2942 bytes)
second_navbar.gif (585 bytes)
Current Issue

Vol. 6, No. 4
Jul–Aug 2000
 

Download Article
PDF
Help
Feedback

Journal Information
About the Journal
Instructions to Authors
Suggested Citation

Other Journal Resources
Announcements
Translations
Image Library

Current Issue
Perspectives
Research
Dispatches
Commentary
Letters
News and Notes

Journal Quick Search

Enter Keywords:



Advanced search



Past Issues


Subscribe
To Subscribe to the EID Listserve to receive email notifications of Journal updates please click here.

For Subscriptions to hard copies...

More on Infectious Diseases
MMWR
Disease Information
Educational Materials

 


Letter

Phylogenetic Analysis of the Chinese Rickettsia Isolate BJ-90

To the Editor: Five species of tick-associated rickettsiae have been identified in China; of these, three are human pathogens and two are of unknown pathogenicity (1). In 1990, one isolate, BJ-90, was first obtained from a Dermacentor sinicus tick, a newly recognized vector collected in a Beijing suburb, an atypical location for Rickettsia sibirica (2). Several taxonomic studies of the phenotype, antigenicity, and genotype of BJ-90 have been performed, with inconsistent results (2-6). Recently, phylogenetic analysis based on several gene comparisons has enabled the phylogenetic classification of this rickettsial species (7-11). To confirm the phylogenetic relationships between the BJ-90 strain and other rickettsiae, the 16S rRNA, gltA, and OmpA encoding genes were amplified and sequenced. Phylogenetic relationships between the BJ-90 strain and other rickettsia in the GenBank database were inferred by the parsimony and neighbor-joining methods (9). Bootstrap analyses were used to assess the reliability of the phylogenetic analysis.

Both methods showed a high degree of similarity between BJ-90, R. sibirica and R. mongolotimonae, which were grouped in the same cluster in three inferred dendrograms. The data from the 16S rRNA and gltA sequences showed low statistical significance in the cluster (bootstrap values for the nodes 50% and 33%, respectively). However, data from the rompA gene sequence showed highly significant similarity in the cluster (bootstrap value 100%), confirming the reliability of the phylogenetic analysis. The results of this phylogenetic analysis are consistent with those of previous phenotypic, genotypic, and phylogenetic analyses (2,3,5-11), as well as taxonomy derived from direct antigenic comparison of the species (4). The sequences of 16S rRNA, gltA, and OmpA have been assigned the following GenBank accession numbers: AF178036 for 16S rRNA, AF178035 for gltA, AF179365 for the 611-bp sequence of ompA, and AF179367 for the 3174-bp sequence of ompA. According to previous genotypic and antigenic studies and our phylogenetic analysis, in which the BJ-90 strain is closer to R. sibirica than R. mongolotimonae in the dendrogram inferred from comparison of the ompA encoding gene sequences, the BJ-90 strain should be considered a variant of R. sibirica.

Jian Z. Zhang,*† Min Y. Fan,† Xue J. Yu,‡ and D. Raoult*
*Faculté de Médecine, Marseille, France; †Chinese Academy of Preventive Medicine, Beijing, P.R. China; University of Texas Medical Branch, Galveston, Texas, USA‡

References

  1. Fan MY, Zhang JZ, Chen M, Yu XJ. Spotted fever group rickettsioses in China. In: Rickettsiae and rickettsial diseases at the turn of the third millennium. Raoult D, Brouqui P, editors. Paris: Elsevier; 1999. p. 247-57.
  2. Yu XJ, Fan MY, Bi DZ. Primary identification of spotted fever group rickettsiae isolated from Dermacentor sinicus in the Beijing area. Chin J Microbiol Immunol 1991;11:305.
  3. Yu XJ, Jin Y, Fan MY, Xu GM, Liu QH, Raoult D. Genotypic and antigenic identification of two new strains of spotted fever group rickettsiae isolated from China. J Clin Microbiol 1993;31:83-9.
  4. Xu WB, Raoult D. Taxonomic relationships among spotted fever group Rickettsiae as revealed by antigenic analysis with monoclonal antibodies. J Clin Microbiol 1997;36:887-96.
  5. Chen M, Fan MY, Bi DZ, Zhang JZ. Sequence analysis of PCR products amplified from five strains of spotted fever group rickettsiae with Rr with Rr 190. 70p and Rr 190. 602n primers. Acta Virologica 1998;42:91-3.
  6. Zhang JZ, Fan MY, Bi DZ. Isolation and identification of spotted fever group rickettsiae BJ-93 strain. Chin J Microbiol Immunol 1997;1:28-33.
  7. Fournier PE, Roux V, Raoult D. Phylogenetic analysis of spotted fever group rickettsiae by study of the outer surface protein OmpA. Int J Syst Bacteriol 1998;48:839-49.
  8. Roux V, Raoult D. Phylogenetic analysis of the genus Rickettsia by 16S rDNA sequencing. Res Microbiol 1995;146:385-96.
  9. Roux V, Rydkina E, Eremeeva M, Raoult D. Citrate synthase gene comparison, a new tool for phylogenetic analysis, and its application for the rickettsiae. Int J Syst Bacteriol 1997;47:252-61.
  10. Stothard DR, Fuerst PA. Evolution analysis of the spotted fever and typhus group of Rickettsia using 16S rRNA gene sequences. Syst Appl Microbiol 1995;18:52-61.
  11. Weisburg WG, Dobson ME, Samuel JE, Dasch GA, Mallavia LP, Baca O, et al. Phylogenetic diversity of the rickettsiae. J Bacteriol 1989;171:4202-6.

Comments to the EID Editors
Please use this form to submit comments to the EID Editors.

Email (optional)


 

Home | Top of Page | Current Issue | Expedited | Upcoming Issue | Past Issue | EID Search | Contact Us

CDC Home | Search | Health Topics A-Z

This page last reviewed June 20, 2000

Emerging Infectious Diseases Journal
National Center for Infectious Diseases
Centers for Disease Control and Prevention