| Autor: |
Maryam Atif Salaheldin Ali, Abeer Babiker Idris, Hadeel Gassim Hassan, Amin Mohamed Abass, Leena Babiker Idris, Sulafa Mohamed Eltaher, Mohamed Hassan, M.M. Ibrahim, Hisham N. Altayb, El-Amin Mohamed Ibrahim |
| Rok vydání: |
2019 |
| Předmět: |
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| DOI: |
10.1101/2019.12.25.888396 |
| Popis: |
BackgroundH. pyloriis ubiquitous among humans, and one of the best studied examples of an intimate association between bacteria and humans. Under several diverse socio-demographic factors in Sudan, a continuous increase in the prevalence rate ofH. pyloriinfection has been noticed which represents a major public health challenge. In this study, we analyzed the molecular evolution ofH. pyloriStrains detected from different ethnic and regions of Sudan using16S rRNAgene and phylogenetic approach.Materials and methodsA total of 75 gastric biopsies taken from patients who had been referred for endoscopy from different regions of Sudan. The DNA extraction was done by using the guanidine chloride method. Two sets of primers (universal and specific for H. pylori) were used to amplify the16S ribosomalgene. Sanger sequencing was performed; then Blast these sequences with those available in the NCBI nucleotide database. The evolutionary aspects were analyzed using a MEGA7 software.ResultMolecular detection ofH. pylorihas shown that 28 (37.33%) of patients were positive forH. pylori. Bivariate analysis has found no significant differences exhibited across sociodemographic, endoscopy series andH. pyloriinfection. Nucleotide variations were found at five nucleotide positions (positions 219, 305, 578, 741 and 763-764) and one insertion mutation (750_InsC_751) was present in sixty-seven percent (7/12) of our strains. The phylogenetic tree diverged into two lineages.ConclusionThe phylogenetic analysis of16S rRNAsequences identified two lineages ofH. pyloristrains detected from different regions in Sudan. Sex mutations were detected in regions of the16S rRNAnot closely associated with either tetracycline or tRNA binding sites. 66.67% of them were located in the central domain of16S rRNA. Studying the effect of these mutations on the functions of16S rRNAmolecules in protein synthesis and antibiotic resistance is of great importance. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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