Characterization of polybacterial clinical samples using a set of group-specific broad-range primers targeting the 16S rRNA gene followed by DNA sequencing and RipSeq analysis
2011

Improving Detection of Bacteria in Clinical Samples

Sample size: 25 publication 10 minutes Evidence: high

Author Information

Author(s): Øyvind Kommedal, Katrine Lekang, Nina Langeland, Harald G. Wiker

Primary Institution: University of Bergen

Hypothesis

Can a set of group-specific broad-range PCRs increase the number of detectable bacterial species in polybacterial clinical samples compared to a single universal PCR?

Conclusion

The use of group-specific PCRs significantly increased the number of identified bacterial species from 51 to 95 in polybacterial clinical samples.

Supporting Evidence

  • The group-specific PCRs identified 44 additional bacterial species compared to standard sequencing.
  • All bacteria identified with the universal primer were also detected with the group-specific primers.
  • Only 32 out of the 95 bacteria identified by group-specific direct sequencing were cultivable.

Takeaway

This study shows that using special tests can help find more types of bacteria in samples from sick people, which is important for getting the right treatment.

Methodology

The study used three group-specific broad-range PCRs to analyze 25 polybacterial clinical samples and compared the results with those obtained from a single universal PCR.

Potential Biases

Potential bias from antibiotic treatment prior to sample collection affecting bacterial detection.

Limitations

The study may have false positives due to low-level DNA contamination and the complexity of some chromatograms.

Participant Demographics

The study involved clinical samples from patients with various types of abscesses.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1099/jmm.0.028373-0

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