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 Severina, E.
Right arrow Articles by Tomasz, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Severina, E.
Right arrow Articles by Tomasz, A.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, October 1999, p. 3308-3315, Vol. 37, No. 10
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Prophage Carriage as a Molecular Epidemiological Marker in Streptococcus pneumoniae

Elena Severina,1,dagger Mario Ramirez,1,2 and Alexander Tomasz1,*

The Rockefeller University, New York, New York,1 and ITQB/UNL, Oeiras, Portugal2

Received 26 May 1999/Returned for modification 2 July 1999/Accepted 16 July 1999

The great majority of clinical isolates of Streptococcus pneumoniae carry prophages that may be identified through their hybridization with a DNA probe specific for the pneumococcal lytA gene (M. Ramirez, E. Severina, and A. Tomasz, J. Bacteriol. 181:3618-3625, 1999). We now show that the lytA hybridization pattern of chromosomal SmaI digests is stable for a given strain during extensive serial culturing in the laboratory; the pattern is specific for the strain's clonal type, as defined by pulsed-field gel electrophoretis (PFGE) pattern, and variations in PFGE subtypes may be explained by changes in the number and chromosomal localization of this prophage(s). These observations indicate that the lytA hybridization pattern may be used as a molecular epidemiological marker that offers additional resolution of the genetic background of S. pneumoniae strains.


* Corresponding author. Mailing address: The Rockefeller University, 1230 York Ave., New York, NY 10021. Phone: (212) 327-8277. Fax: (212) 327-8688. E-mail: tomasz{at}rockvax.rockefeller.edu.

dagger Permanent address: Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Pushchino, Moscow Region, 142292 Russia.


Journal of Clinical Microbiology, October 1999, p. 3308-3315, Vol. 37, No. 10
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Frias, M. J., Melo-Cristino, J., Ramirez, M. (2009). The Autolysin LytA Contributes to Efficient Bacteriophage Progeny Release in Streptococcus pneumoniae. J. Bacteriol. 191: 5428-5440 [Abstract] [Full Text]  
  • Loeffler, J. M., Fischetti, V. A. (2006). Lysogeny of Streptococcus pneumoniae with MM1 Phage: Improved Adherence and Other Phenotypic Changes.. Infect. Immun. 74: 4486-4495 [Abstract] [Full Text]  
  • Canchaya, C., Proux, C., Fournous, G., Bruttin, A., Brussow, H. (2003). Prophage Genomics. Microbiol. Mol. Biol. Rev. 67: 238-276 [Abstract] [Full Text]  
  • Sa-Leao, R., Tomasz, A., Santos Sanches, I., de Lencastre, H. (2002). Pilot Study of the Genetic Diversity of the Pneumococcal Nasopharyngeal Flora among Children Attending Day Care Centers. J. Clin. Microbiol. 40: 3577-3585 [Abstract] [Full Text]  
  • Gindreau, E., López, R., García, P. (2000). MM1, a Temperate Bacteriophage of the Type 23F Spanish/USA Multiresistant Epidemic Clone of Streptococcus pneumoniae: Structural Analysis of the Site-Specific Integration System. J. Virol. 74: 7803-7813 [Abstract] [Full Text]