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Journal of Clinical Microbiology, September 2007, p. 2985-2992, Vol. 45, No. 9
0095-1137/07/$08.00+0     doi:10.1128/JCM.00630-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

DNA Pyrosequencing-Based Bacterial Pathogen Identification in a Pediatric Hospital Setting{triangledown} ,{dagger}

Ruth Ann Luna,1,2 Lea R. Fasciano,1 Shaunte C. Jones,1 Bobby L. Boyanton Jr.,2 Trang T. Ton,1 and James Versalovic1,2*

Division of Molecular Pathology, Department of Pathology, Texas Children's Hospital, Houston, Texas,1 Department of Pathology, Baylor College of Medicine, Houston, Texas2

Received 21 March 2007/ Returned for modification 9 May 2007/ Accepted 18 July 2007

Sole reliance on biochemical methods can limit the clinical microbiology laboratory's ability to identify bacterial pathogens. This study describes the incorporation of DNA pyrosequencing-based identification for routine pathogen identification of atypical clinical isolates in a large children's hospital. The assay capitalized on the highly conserved nature of 16S rRNA genes by positioning amplification and sequencing primers in conserved target sequences flanking the variable V1 and V3 regions. A total of 414 isolates of 312 pediatric patients were tested by DNA pyrosequencing during the time period from December 2003 to July 2006. Seventy-eight different genera were specified by DNA pyrosequencing, and isolates were derived from diverse specimen types. By integrating DNA sequencing of bacterial pathogens with conventional microbiologic methods, isolates that lacked a definitive identification by biochemical testing yielded genus- or species-level identifications in approximately 90% of cases by pyrosequencing. Improvements incorporated into the assay process during the period of clinical testing included software enhancements, improvements in sequencing reagents, and refinements in database search strategies. Coupled with isolation by bacteriologic culture and biochemical testing, DNA pyrosequencing-based bacterial identification was a valuable tool that markedly improved bacterial pathogen identification in a pediatric hospital setting.

* Corresponding author. Mailing address: Department of Pathology, Texas Children's Hospital, 6621 Fannin MC 1-2261, Houston, TX 77030. Phone: (832) 824-2213. Fax: (832) 825-0164. E-mail: jamesv{at}bcm.edu

{triangledown} Published ahead of print on 25 July 2007.

{dagger} Supplemental material for this article may be found at http://jcm.asm.org/.

Journal of Clinical Microbiology, September 2007, p. 2985-2992, Vol. 45, No. 9
0095-1137/07/$08.00+0     doi:10.1128/JCM.00630-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Petrosino, J. F., Highlander, S., Luna, R. A., Gibbs, R. A., Versalovic, J. (2009). Metagenomic Pyrosequencing and Microbial Identification. Clin. Chem. 55: 856-866 [Abstract] [Full Text]  
  • Jordan, J. A., Jones-Laughner, J., Durso, M. B. (2009). Utility of Pyrosequencing in Identifying Bacteria Directly from Positive Blood Culture Bottles. J. Clin. Microbiol. 47: 368-372 [Abstract] [Full Text]  
  • Zhang, W. W., Versalovic, J. (2007). Expanding the Diagnostic Capabilities of Molecular Microbiology by Genomic Methods. J. Mol. Diagn. 9: 572-573 [Full Text]  


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