Differential antibiotic resistance in biofilm forming Pseudomonas aeruginosa strains

Authors

  • Amol Jadhav
  • Bandu Pawar
  • Bhagvat Lad

DOI:

https://doi.org/10.63001/tbs.2026.v21.i02.S.I(2).pp1168-1176

Keywords:

Ps. aeruginosa,, micro-titer plate assay,, biofilm formation,, antibiotic resistance

Abstract

The Pseudomonas aeruginosa strains have ability to form biofilm a complex community, the differential antibiotic resistance is mainly due to unique biofilm composition and its extent of biofilm formation. In this study, five isolates of Ps. aeruginosa have been isolated from clinical environment of Government Medical College & Hospital, Nanded on cetrimide agar plate. The identification of Ps. aeruginosa strains were carried out on basis of morphological features and 16S rRNA gene sequencing. The biofilm formation ability of Ps. aeruginosa strains were evaluated by using congo-red agar plate and micro-titer plate assay. The resistance of biofilm forming Ps. aeruginosa strains to 20 antibiotics from diverse class had determined. The identified Ps. aeruginosa strains using 16S rRNA gene sequencing showed 98-100% nucleotide homology with biofilm forming and multi drug resistance Ps. aeruginosa strains on NCBI nucleotide database. The Ps. aeruginosa strains isolated in present investigation showed strong, moderate and weak biofilm formation ability. The strong biofilm forming strain PA5 showed resistance to 13 antibiotics, moderate biofilm forming Ps. aeruginosa strains PA2 and PA3 showed resistance to 10 antibiotics and week biofilm forming Ps. aeruginosa strains PA6 and PA7 showed resistance to 7 antibiotics. The biofilm, forming Ps. aeruginosa strains have differential resistance to diverse class of antibiotics due to extent of biofilm formation   

Downloads

Published

2026-05-26

How to Cite

Amol Jadhav, Bandu Pawar, & Bhagvat Lad. (2026). Differential antibiotic resistance in biofilm forming Pseudomonas aeruginosa strains. The Bioscan, 21(2), 1168–1176. https://doi.org/10.63001/tbs.2026.v21.i02.S.I(2).pp1168-1176