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 Jado, I.
Right arrow Articles by Pérez, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jado, I.
Right arrow Articles by Pérez, A.

 Previous Article  |  Next Article 

Clinical and Diagnostic Laboratory Immunology, September 2001, p. 895-898, Vol. 8, No. 5
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.5.895-898.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Identification of the psaA Gene, Coding for Pneumococcal Surface Adhesin A, in Viridans Group Streptococci other than Streptococcus pneumoniae

Isabel Jado, Asunción Fenoll, Julio Casal,* and Amalia Pérez

Laboratorio de Referencia de Neumococos, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda E-28220, Madrid, Spain

Received 1 November 2000/Returned for modification 19 March 2001/Accepted 14 May 2001

The gene encoding the pneumococcal surface adhesin A (PsaA) protein has been identified in three different viridans group streptococcal species. Comparative studies of the psaA gene identified in different pneumococcal isolates by sequencing PCR products showed a high degree of conservation among these strains. PsaA is encoded by an open reading frame of 930 bp. The analysis of this fragment in Streptococcus mitis, Streptococcus oralis, and Streptococcus anginosus strains revealed a sequence identity of 95, 94, and 90%, respectively, to the corresponding open reading frame of the previously reported Streptococcus pneumoniae serotype 6B strain. Our results confirm that psaA is present and detectable in heterologous bacterial species. The possible implications of these results for the suitability and potential use of PsaA in the identification and diagnosis of pneumococcal diseases are discussed.


* Corresponding author. Mailing address: Laboratorio de Referencia de Neumococos, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda E-28220, Madrid, Spain. Phone: 34 915 097975. Fax: 34 915 097966. E-mail: jcasal{at}isciii.es.


Clinical and Diagnostic Laboratory Immunology, September 2001, p. 895-898, Vol. 8, No. 5
1071-412X/01/$04.00+0   DOI: 10.1128/CDLI.8.5.895-898.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Sa-Leao, R., Simoes, A. S., Nunes, S., Sousa, N. G., Frazao, N., de Lencastre, H. (2006). Identification, prevalence and population structure of non-typable Streptococcus pneumoniae in carriage samples isolated from preschoolers attending day-care centres. Microbiology 152: 367-376 [Abstract] [Full Text]  
  • Verhelst, R., Kaijalainen, T., De Baere, T., Verschraegen, G., Claeys, G., Van Simaey, L., De Ganck, C., Vaneechoutte, M. (2003). Comparison of Five Genotypic Techniques for Identification of Optochin-Resistant Pneumococcus-Like Isolates. J. Clin. Microbiol. 41: 3521-3525 [Abstract] [Full Text]  
  • Scott, J. A. G., Marston, E. L., Hall, A. J., Marsh, K. (2003). Diagnosis of Pneumococcal Pneumonia by psaA PCR Analysis of Lung Aspirates from Adult Patients in Kenya. J. Clin. Microbiol. 41: 2554-2559 [Abstract] [Full Text]