Darta Pupola, Dita Gudra, Girts Skenders, Marcis Leja, and Davids Fridmanis
University of Latvia, Latvia
Posters & Accepted Abstracts: J Mol Genet Med
Introduction: H. pylori infections are present in 80% of Latvian population thus increasing the
susceptibility of numerous of the gastric tract diseases, including gastric adenocarcinoma.1 The 1st line
H. pylori eradication therapy includes treatment with clarithromycin in combination with amoxicillin or
metronidazole and a proton pump inhibitor. However, potential adverse events caused by such therapies
to microbiome are insufficiently studied. Therefore, the aim of this study was to evaluate the long-term
effects of H. pylori eradication on gastrointestinal (GIT) microbiome.
Methodology & Theoretical Orientation: The assessment of H. pylori eradication therapy on GIT
microbiome was performed on 120 faecal samples that were acquired from 60 adults: samples from each
individual were collected before starting the eradication therapy, and one year after the final treatment.
Samples were collected in OC-Sensor (Eiken Chemical Co., Tokyo, Japan) sample collection containers
and stored at -86â??. Total DNA was extracted using FastDNA Spin Kit for Soil (MP Biomedicals, USA) and
was followed by 16S rRNA V3 gene sequencing employing Ion Torrent Personal Genome Machine (Life
Technologies, USA). The obtained raw 16S reads were analyzed using QIIME v.1.9.0 and UPARSE v.7.0.1001.
Conclusion & Significance: Overall microbiome community composition remained stable between preand
post-eradication microbiome samples, however, shifts between predominant enterotypes as well
as positive correlation for certain bacteria between the two categories was found in relation to age,
individual, experience respiratory and/or allergic diseases and if the eradication therapy was used as
prescribed. Modest global differences at the community level exist between individuals before and after
the eradication therapy when considering the long-term impact; however, the microbiome structure is
more related with the patient-specific parameters, such as age or experienced diseases, rather than by
the eradication therapy itself.
Darta Pupola has finished University of Latvia as a biologist. She has experience in genomics, cell culturing and signaling pathway analysis in a field of oncology and GIT microbiome, where combining all knowledge from different kind of fields it becomes possible to look at disease and health conditions as a complex interaction network.
E-mail: pupoladarta@gmail.com
Molecular and Genetic Medicine received 3919 citations as per Google Scholar report