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New functions of pirin proteins and a 2-ketoglutarate: Ferredoxin oxidoreductase ortholog in Bacteroides fragilis metabolism and their impact on antimicrobial susceptibility to metronidazole and amixicile.
Gough, Andrea M; Parker, Anita C; O'Bryan, Patricia J; Whitehead, Terence R; Roy, Sourav; Garcia, Brandon L; Hoffman, Paul S; Jeffrey Smith, C; Rocha, Edson R.
Affiliation
  • Gough AM; Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, North Carolina, USA.
  • Parker AC; Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, North Carolina, USA.
  • O'Bryan PJ; USDA Agricultural Research Service, Peoria, Illinois, USA.
  • Whitehead TR; USDA Agricultural Research Service, Peoria, Illinois, USA.
  • Roy S; Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, North Carolina, USA.
  • Garcia BL; Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, North Carolina, USA.
  • Hoffman PS; Department of Medicine, Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
  • Jeffrey Smith C; Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, North Carolina, USA.
  • Rocha ER; Department of Microbiology and Immunology, Brody School of Medicine at East Carolina University, Greenville, North Carolina, USA.
Microbiologyopen ; 13(4): e1429, 2024 Aug.
Article in En | MEDLINE | ID: mdl-39109824
ABSTRACT
The understanding of how central metabolism and fermentation pathways regulate antimicrobial susceptibility in the anaerobic pathogen Bacteroides fragilis is still incomplete. Our study reveals that B. fragilis encodes two iron-dependent, redox-sensitive regulatory pirin protein genes, pir1 and pir2. The mRNA expression of these genes increases when exposed to oxygen and during growth in iron-limiting conditions. These proteins, Pir1 and Pir2, influence the production of short-chain fatty acids and modify the susceptibility to metronidazole and amixicile, a new inhibitor of pyruvate ferredoxin oxidoreductase in anaerobes. We have demonstrated that Pir1 and Pir2 interact directly with this oxidoreductase, as confirmed by two-hybrid system assays. Furthermore, structural analysis using AlphaFold2 predicts that Pir1 and Pir2 interact stably with several central metabolism enzymes, including the 2-ketoglutarateferredoxin oxidoreductases Kor1AB and Kor2CDAEBG. We used a series of metabolic mutants and electron transport chain inhibitors to demonstrate the extensive impact of bacterial metabolism on metronidazole and amixicile susceptibility. We also show that amixicile is an effective antimicrobial against B. fragilis in an experimental model of intra-abdominal infection. Our investigation led to the discovery that the kor2AEBG genes are essential for growth and have dual functions, including the formation of 2-ketoglutarate via the reverse TCA cycle. However, the metabolic activity that bypasses the function of Kor2AEBG following the addition of phospholipids or fatty acids remains undefined. Overall, our study provides new insights into the central metabolism of B. fragilis and its regulation by pirin proteins, which could be exploited for the development of new narrow-spectrum antimicrobials in the future.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteroides fragilis / Metronidazole / Anti-Bacterial Agents Language: En Journal: Microbiologyopen Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteroides fragilis / Metronidazole / Anti-Bacterial Agents Language: En Journal: Microbiologyopen Year: 2024 Document type: Article Affiliation country: