Long-Read- and Short-Read-Based Whole-Genome Sequencing Reveals the Antibiotic Resistance Pattern of Helicobacter pylori
single nucleotide variation
antibiotic resistance
Nanopore sequencing
Helicobacter pylori
Nucleotides
Furazolidone
Drug Resistance, Microbial
Levofloxacin
Microbial Sensitivity Tests
Tetracycline
Microbiology
QR1-502
3. Good health
Helicobacter Infections
Anti-Bacterial Agents
RNA, Ribosomal, 23S
whole-genome sequencing
Clarithromycin
Metronidazole
Drug Resistance, Bacterial
Humans
Research Article
DOI:
10.1128/spectrum.04522-22
Publication Date:
2023-04-17T14:01:44Z
AUTHORS (8)
ABSTRACT
The rates of antibiotic resistance Helicobacter pylori are increasing, and the patterns region population specific. Here, we elucidated pattern H. in a single center China compared short-read- long-read-based whole-genome sequencing for identifying genotypes. Resistance 38.5%, 61.5%, 27.9%, 13.5% against clarithromycin, metronidazole, levofloxacin, amoxicillin were determined, respectively, while no strain was resistant to tetracycline or furazolidone. Single nucleotide variations (SNVs) 23S rRNA GyrA/B genes revealed by Illumina short-read showed good diagnostic abilities clarithromycin levofloxacin resistance, respectively. Nanopore long-read also efficiency elucidating SNVs gene and, thus, ability detect resistance. two technologies displayed consistency discovering shared 76% detected gene. Taking Sanger as gold standard, slightly higher accuracy than sequencing. There copies genome pylori, found that not same at least 26% strains tested, indicating their heterozygous status. Especially, three harboring 2143G/A status gene, which is most important site found. In conclusion, our results provide evidence an empirical first-line treatment eradication clinical settings. Moreover, show potential tool predicting
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