Hirendra nath Banerjee, Monique Gramby and Zack Hawkins
Aim: Rapid detection of H. pylori strains by PCR-Sequencing.
Methods: 16S rDNA amplification by PCR from template genomic DNA,confirmation of amplicon size by agarose gel electrophoresis ,sequencing of amplicons by automated sequencer,analysis of sequences by NCBI -BLAST software.
Results: The PCR -Sequencing and analysis of the sequence data by BLAST resulted in detection of the strain to be of H. pylori strain#26695.
Conclusion: The pathogenicity of H. pylori depends on the strain of the bacteria, PCR-Sequencing and analysis of the sequence data by BLAST can be a very quick and useful diagnostic method of the pathogen.
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