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Yadegar, A.

Publications and source records attributed to Yadegar, A..

3 recordsLinked to original sources

Meat without vegetables: An ancient ecotype of Helicobacter pylori found in Indigenous populations and animal adapted lineages.

The colonization of our stomachs by Helicobacter pylori is believed to predate the oldest splits between extant human populations. We identify a "Hardy" ecospecies of H. pylori associated with indigenous groups, isolated from people in Siberia, Canada, USA and Chile. The ecospecies shares the ancestry of "Ubiquitous" H. pylori from the same geographical region in most of the genome but has nearly fixed SNP differences in 100 genes, many of which encode outer membrane proteins and host interaction factors. For these parts of the genome, the ecospecies has a separate, independently evolving gene pool with a distinct evolutionary history. H. acinonychis, found in big cats, and a newly identified primate-associated lineage both belong to the Hardy ecospecies and both represent human to animal host jumps. Most strains from the ecospecies encode an additional iron-dependent urease that is shared by Helicobacter from carnivorous hosts, as well as a tandem duplication of vacA, encoding the vacuolating toxin. We conclude that H. pylori split into two highly distinct ecospecies in Africa and that both dispersed around the globe with humans, but the Hardy ecospecies has gone extinct in most parts of the world. Our analysis also pushes back the likely length of the association between H. pylori and humans.

microbiology↗

Evolution of miR-155 and its probable targets: MST1R, Adam10, and CD9 genes expression levels in adults and children gastritis patients with H. pylori infection

IntroductionH. pylori accounts for the main factor of gastric cancer which contributes to an immune response with the promotion of inflammation. Recently, the effect of miRNAs on the prognosis of diseases is gaining the attraction of investigators. Herein, we studied the expression levels of miR-155 and its identified targets (MST1R, Adam10, and CD9) along with miR-155 expression correlation with virulence factors of H. pylori (vacA and cag genes), H. pylori colonization, and inflammation, in patients candidates for gastric endoscopy due to gastritis. Methodsin this study total of 50 and 26 biopsy samples were taken from adults and children respectively. Biochemical and molecular identification of samples was performed using culture and PCR of ureC, 16sRNA, along with amplification of vacA and cagA genes for pathogenicity of bacteria. The qRT-PCR was carried out using STEM-LOOP RT-PCR (dye-based) for the evaluation of miR-155 expression level and Adam10, CD9, and MST1R expression levels. All Real-Time PCR reactions were carried out in triplicate and data analysis was conducted using REST. ResultsA total of 30 out of 17 biopsy samples in adults and children were positive for H. pylori in both PCR and culture, respectively. The expression level of miR-155 is closely related to the H. pylori infection and the down-regulation of CD9, and MST1R genes in H. pylori (+) samples compared to H. pylori (-) in adults biopsy (p=0.0001). Although, there wasnt any relation between cagA and vacA genes with the expression of miR-155 in evaluated biopsy samples in both adults and children.i ConclusionThis study for the first time revealed that the expression of MST1R, CD9, and adam10 genes was relatively related to the expression of miR-155, and indicated that the miR-155 overexpression promoted the poor prognosis of H. pylori infection in adults.

microbiology↗

High prevalence of antibiotic resistance in Helicobacter pylori isolates from Iran: importance of functional and mutational analysis of resistance genes and virulence genotyping

The high prevalence of antibiotic resistance in Helicobacter pylori has become a great challenge in Iran. The genetic mutations that contribute to the resistance have yet to be precisely identified. This study aimed to investigate the prevalence of antibiotic resistance and virulence markers in Iranian H. pylori isolates and to analyze if there is any association between resistance and genotype. Antibiotic susceptibility patterns of 33 H. pylori isolates were investigated against metronidazole, clarithromycin, amoxicillin, rifampicin, ciprofloxacin, levofloxacin and tetracycline by the agar dilution method. The frxA, rdxA, gyrA, gyrB and 23S rRNA genes of the isolates were sequenced. The virulence genotypes were also determined using PCR. Metronidazole resistance was present in 81.8% of the isolates, followed by clarithromycin (36.4%), ciprofloxacin (36.4%), amoxicillin (30.3%), rifampicin (30.3%), levofloxacin (27.3%) and tetracycline (6.1%). Most of the metronidazole-resistant isolates carried frameshift mutations in both frxA and rdxA genes, and premature termination was occurred in positions Q5Stop and Q50Stop, respectively. Amino acid substitutions M191I, G208E, and V199A were predominantly found in gyrA gene of fluoroquinolone-resistant isolates. A2143G and C2195T mutations of 23S rRNA were found in four isolates. Interestingly, significant associations were demonstrated between intact cagPAI and resistance to rifampicin (P = 0.027), and between susceptibility to amoxicillin and cagPAI intactness (P = 0.016). The prevalence of H. pylori antibiotic resistance is high in our region, particularly that of metronidazole, clarithromycin, ciprofloxacin and multidrug resistance. Occurrence of mutations in resistance genes were involved in the development of resistance, especially in less virulent isolates.

microbiology↗