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The effect of varying acidity on helicobacter pylori growth and the bactericidal efficacy of ampicillin
- Publication Year :
- 2012
-
Abstract
- Summary Background Penicillins inhibit cell wall synthesis; therefore, Helicobacter pylori must be dividing for this class of antibiotics to be effective in eradication therapy. Identifying growth responses to varying medium pH may allow design of more effective treatment regimens. Aim To determine the effects of acidity on bacterial growth and the bactericidal efficacy of ampicillin. Methods H. pylori were incubated in dialysis chambers suspended in 1.5-L of media at various pHs with 5 mM urea, with or without ampicillin, for 4, 8 or 16 h, thus mimicking unbuffered gastric juice. Changes in gene expression, viability and survival were determined. Results At pH 3.0, but not at pH 4.5 or 7.4, there was decreased expression of ~400 genes, including many cell envelope biosynthesis, cell division and penicillin-binding protein genes. Ampicillin was bactericidal at pH 4.5 and 7.4, but not at pH 3.0. Conclusions Ampicillin is bactericidal at pH 4.5 and 7.4, but not at pH 3.0, due to decreased expression of cell envelope and division genes with loss of cell division at pH 3.0. Therefore, at pH 3.0, the likely pH at the gastric surface, the bacteria are nondividing and persist with ampicillin treatment. A more effective inhibitor of acid secretion that maintains gastric pH near neutrality for 24 h/day should enhance the efficacy of amoxicillin, improving triple therapy and likely even allowing dual amoxicillin-based therapy for H. pylori eradication.
- Subjects :
- Cell division
medicine.drug_class
Antibiotics
Bacterial growth
Polymerase Chain Reaction
Article
Microbiology
Ampicillin
medicine
Humans
Urea
Pharmacology (medical)
Secretion
Gastric Juice
Hepatology
biology
Helicobacter pylori
Gastroenterology
Amoxicillin
Hydrogen-Ion Concentration
biology.organism_classification
Anti-Bacterial Agents
Bacteria
medicine.drug
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....4a4588a9c44afc95e010bc6649bdfd3f