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Genomic variability correlates with biofilm phenotypes in multidrug resistant clinical isolates of Pseudomonas aeruginosa.
Islam, Ovinu Kibria; Islam, Israt; Saha, Otun; Rahaman, Md Mizanur; Sultana, Munawar; Bockmühl, Dirk P; Hossain, M Anwar.
Affiliation
  • Islam OK; Department of Microbiology, University of Dhaka, Dhaka, Bangladesh.
  • Islam I; Department of Microbiology, Jashore University of Science & Technology, Jashore, Bangladesh.
  • Saha O; Department of Microbiology, University of Dhaka, Dhaka, Bangladesh.
  • Rahaman MM; Department of Microbiology, Noakhali University of Science & Technology, Noakhali, Bangladesh.
  • Sultana M; Department of Microbiology, University of Dhaka, Dhaka, Bangladesh.
  • Bockmühl DP; Department of Microbiology, Noakhali University of Science & Technology, Noakhali, Bangladesh.
  • Hossain MA; Department of Microbiology, University of Dhaka, Dhaka, Bangladesh.
Sci Rep ; 13(1): 7867, 2023 05 15.
Article de En | MEDLINE | ID: mdl-37188866
ABSTRACT
The multifactorial nature of Pseudomonas aeruginosa biofilm development and genomic variabilities implicates its resistance to conventional antimicrobials and virulence. Therefore, genetic determinants need to be extensively studied to block the early steps of biofilm or already formed biofilms. In this study, a total of 20 multidrug resistant (MDR) clinical P. aeruginosa isolates were evaluated for their biofilm forming abilities and related genes. Of the isolates tested, all of them showed surface attachment tendencies in nutrient limiting conditions, and classified as strong (SBF = 45%), moderate (MBF = 30%) and weak (WBF = 25%) biofilm formers. Complete genome sequencing of representative strong (DMC-27b), moderate (DMC-20c) and weak biofilm former (DMC-30b) isolates was performed. Analysis of biofilm related genes in the sequenced genomes revealed that, 80 of the 88 biofilm related genes possess 98-100% sequence identity to the reference PAO1 strain. Complete and partial sequence data of LecB proteins from tested isolates indicate that isolates containing PA14-like LecB sequences produced strong biofilms. All of the 7 pel operon protein coding genes in weak biofilm former isolate 30b showed significant nucleotide sequence variation with other tested isolates, and their corresponding proteins are 99% identical with the pel operon proteins of PA7. Bioinformatics analyses identified divergent sequence and structural features that separate PA7 like pel operon proteins from reference PAO1-like pel operon. Congo red and pellicle forming assays revealed that the sequence and structure variations may have interfered with the Pel production pathway and resulted in impaired Pel production in isolate 30b that has a PA7 like pel operon. Expression analysis also showed that both pelB and lecB genes were about 5 to 6 folds upregulated after 24 h in SBF 27b in comparison with WBF 30b. Our findings indicate significant genomic divergence in biofilm related genes of P. aeruginosa strains that affect their biofilm phenotypes.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Pseudomonas aeruginosa / Protéines bactériennes Type d'étude: Prognostic_studies Langue: En Journal: Sci Rep Année: 2023 Type de document: Article Pays d'affiliation: Bangladesh

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Pseudomonas aeruginosa / Protéines bactériennes Type d'étude: Prognostic_studies Langue: En Journal: Sci Rep Année: 2023 Type de document: Article Pays d'affiliation: Bangladesh