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Alterations of growth, biofilm-forming, and gene expression of Bordetella pertussis by antibiotics at sub-minimum inhibitory concentrations

  • Eda Delik
  • , Berfin Eroğlu
  • , Çiğdem Yılmaz Çolak
  • , Aysun Türkanoğlu Özçelik
  • , Burcu Emine Tefon Öztürk*
  • *Bu çalışma için yazışmadan sorumlu yazar
  • Akdeniz University
  • Scientific and Technological Research Council of Turkey

Araştırma sonucu: Dergiye katkıMakalebilirkişi

9 Atıf (Scopus)

Özet

Bordetella pertussis is the primary agent of the acute respiratory disease pertussis. It has been reported that the disease has recently become more common, especially in adults and adolescents, and adaptation of the pathogen is thought to have an important influence on the recurrence of the disease. This study aims to determine the effect of erythromycin, azithromycin, and trimethoprim-sulfamethoxazole used in the treatment of pertussis on the virulence gene expressions (prn, ptxS1, fhaB), biofilm-forming and growth of B. pertussis. In this study, the minimum inhibitory concentration (MIC) values of azithromycin and erythromycin in B. pertussis local strain Saadet were determined to be 0.09 μg/mL and 0.3 μg/mL, respectively. However, the Tohama-I and Saadet strains were resistant to trimethoprim-sulfamethoxazole (MIC>32 μg/mL). The biofilm-forming of the Saadet strain decreased with the increase in antibiotic doses. It was observed that 1/32MIC erythromycin and 1/32MIC azithromycin upregulated the expression of fhaB in Tohama-I, whereas the expression of ptxS1 and prn significantly decreased in sub-MICs of erythromycin. In the Saadet strain, only ptxS1 was highly expressed at 1/16MIC azithromycin and erythromycin (p > 0.05). This is the first study to investigate the effect of sub-MIC antibiotics on the expression of virulence genes and biofilm-forming of B. pertussis.

Orijinal dilİngilizce
Makale numarası104058
DergiResearch in Microbiology
Hacim174
Basın numarası5
DOI'lar
Yayın durumuYayınlandı - Haz 2023
Harici olarak yayınlandıEvet

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© 2023 Institut Pasteur

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