Analysis of Mixed Sequencing Chromatograms and Its Application in Direct 16S rRNA Gene Sequencing of Polymicrobial Samples

ABSTRACT Investigation of clinical samples by direct 16S rRNA gene sequencing provides the possibility to detect nonviable bacteria and bacteria with special growth requirements. This approach has been particularly valuable for the diagnosis of patients who have received antibiotics prior to sample collection. In specimens containing more than one bacterium, direct sequencing gives mixed chromatograms that complicate further interpretation. We designed an algorithm able to analyze these ambiguous chromatograms and implemented it as a Web-based service. The algorithm contains both a new base-calling procedure and a new database search procedure. 16S rRNA gene sequencing was performed on polybacterial suspensions prepared in the laboratory. The computer program identified all bacteria correctly to the species level in 23 out of 23 samples containing two different bacteria. For samples containing three different bacteria, correct identification to the species level was achieved for three out of five and to the genus level for five out of five.

[1]  O. Ruuskanen,et al.  Direct Amplification of rRNA Genes in Diagnosis of Bacterial Infections , 2000, Journal of Clinical Microbiology.

[2]  J. Møller,et al.  Broad-range real time PCR and DNA sequencing for the diagnosis of bacterial meningitis , 2006, Scandinavian journal of infectious diseases.

[3]  K. Harris,et al.  Development of broad-range 16S rDNA PCR for use in the routine diagnostic clinical microbiology service. , 2003, Journal of medical microbiology.

[4]  A. Kooistra-Smid,et al.  Prospective Study of Use of PCR Amplification and Sequencing of 16S Ribosomal DNA from Cerebrospinal Fluid for Diagnosis of Bacterial Meningitis in a Clinical Setting , 2004, Journal of Clinical Microbiology.

[5]  Cathy A Petti,et al.  Medical Microbiology: Detection and Identification of Microorganisms by Gene Amplification and Sequencing , 2007 .

[6]  D. Cowan,et al.  Review and re-analysis of domain-specific 16S primers. , 2003, Journal of microbiological methods.

[7]  P. Trieu-Cuot,et al.  Rapid and Accurate Species-Level Identification of Coagulase-Negative Staphylococci by Using the sodA Gene as a Target , 2001, Journal of Clinical Microbiology.

[8]  T Ezaki,et al.  Genetic approaches to the identification of the mitis group within the genus Streptococcus. , 1999, Microbiology.

[9]  R. Borrow,et al.  Contamination and Sensitivity Issues with a Real-Time Universal 16S rRNA PCR , 2000, Journal of Clinical Microbiology.

[10]  Tom Coenye,et al.  Intragenomic heterogeneity between multiple 16S ribosomal RNA operons in sequenced bacterial genomes. , 2003, FEMS microbiology letters.

[11]  J. Clarridge,et al.  Impact of 16S rRNA Gene Sequence Analysis for Identification of Bacteria on Clinical Microbiology and Infectious Diseases , 2004, Clinical Microbiology Reviews.

[12]  S. Vermeire,et al.  Coamplification of Eukaryotic DNA with 16S rRNA Gene-Based PCR Primers: Possible Consequences for Population Fingerprinting of Complex Microbial Communities , 2008, Current Microbiology.