78
Views
0
CrossRef citations to date
0
Altmetric
Antimicrobial Original Research Paper

Macrolides impact the growth ability of clinical Pseudomonas aeruginosa through quorum-sensing systems

, , &
Pages 24-30 | Received 14 Sep 2023, Accepted 12 Dec 2023, Published online: 29 Dec 2023

References

  • Livermore DM. Current epidemiology and growing resistance of gram-negative pathogens. Korean J Intern Med. 2012;27(2):128–142. doi: 10.3904/kjim.2012.27.2.128.
  • WHO. Global Priority List of Antibiotic-Resistant Bacteria to Guide Research, Discovery, and Development of New Antibiotics. 2017. Available from: http://www.who.int/medicines/publications/global-prioritylistantibiotic-resistant-bacteria/en/.
  • Nicolle LE, AMMI Canada Guidelines Committee*. Complicated urinary tract infection in adults. Can J Infect Dis Med Microbiol. 2005;16(6):349–360. doi: 10.1155/2005/385768.
  • Zhang J, Xu LL, Gan D, et al. In vitro study of bacteriophage AB3 endolysin LysAB3 activity against Acinetobacter baumannii biofilm and biofilm-bound Acinetobacter baumannii. Clin Lab. 2018;64(06/2018):1021–1030. doi: 10.7754/Clin.Lab.2018.180342.
  • Greene C, Vadlamudi G, Newton D, et al. The influence of biofilm formation and multidrug resistance on environmental survival of clinical and environmental isolates of Acinetobacter baumannii. Am J Infect Control. 2016;44(5):e65–71. doi: 10.1016/j.ajic.2015.12.012.
  • Di Domenico EG, Farulla I, Prignano G, et al. Biofilm is a major virulence determinant in bacterial colonization of chronic skin ulcers independently from the multidrug resistant phenotype. Int J Mol Sci. 2017;18(5):1077. doi: 10.3390/ijms18051077.
  • Rao RS, Karthika RU, Singh SP, et al. Correlation between biofilm production and multiple drug resistance in imipenem resistant clinical isolates of Acinetobacter baumannii. Indian J Med Microbiol. 2008;26(4):333–337. doi: 10.4103/0255-0857.43566.
  • Davies DG, Parsek MR, Pearson JP, et al. The involvement of cell-to-cell signals in the development of a bacterial biofilm. Science. 1998;280(5361):295–298. doi: 10.1126/science.280.5361.295.
  • Passador L, Cook JM, Gambello MJ, et al. Expression of Pseudomonas aeruginosa virulence genes requires cell-to-cell communication. Science. 1993;260(5111):1127–1130. doi: 10.1126/science.8493556.
  • Lee J, Zhang L. The hierarchy quorum sensing network in Pseudomonas aeruginosa. Protein Cell. 2015;6(1):26–41. doi: 10.1007/s13238-014-0100-x.
  • Jack AA, Khan S, Powell LC, et al. Alginate oligosaccharide-induced modification of the lasI-lasR and rhlI-rhlR quorum-sensing systems in Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2018;62(5):e02318-17. doi: 10.1128/AAC.02318-17.
  • Tateda K, Standiford TJ, Pechere JC, et al. Regulatory effects of macrolides on bacterial virulence: potential role as quorum-sensing inhibitors. Curr Pharm Des. 2004;10(25):3055–3065. doi: 10.2174/1381612043383377.
  • Wayne PA. Clinical and laboratory standards institute. Performance standards for antimicrobial susceptibility testing; CLSI 2013, 23rd international supplement, CLSI document M100-S23. Wayne (PA): Clinical and Laboratory Standards Institute; 2013.
  • Papagiannitsis CC, Medvecky M, Chudejova K, et al. Molecular characterization of carbapenemase-producing Pseudomonas aeruginosa of czech origin and evidence for clonal spread of extensively resistant sequence type 357 expressing IMP-7 metallo-β-lactamase. Antimicrob Agents Chemother. 2017;61(12):e01811-17. Print 2017 Dec. doi: 10.1128/AAC.01811-17.
  • Curran B, Jonas D, Grundmann H, et al. Development of a multilocus sequence typing scheme for the opportunistic pathogen Pseudomonas aeruginosa. J Clin Microbiol. 2004;42(12):5644–5649. doi: 10.1128/JCM.42.12.5644-5649.2004.
  • Packiavathy IA, Priya S, Pandian SK, et al. Inhibition of biofilm development of uropathogens by curcumin – an anti-quorum sensing agent from curcuma longa. Food Chem. 2014;148:453–460. doi: 10.1016/j.foodchem.2012.08.002.
  • Banerjee M, Moulick S, Bhattacharya KK, et al. Attenuation of Pseudomonas aeruginosa quorum sensing, virulence and biofilm formation by extracts of andrographis paniculata. Microb Pathog. 2017;113:85–93. doi: 10.1016/j.micpath.2017.10.023.
  • Anju VT, Busi S, Ranganathan S, et al. Sesamin and sesamolin rescues Caenorhabditis elegans from Pseudomonas aeruginosa infection through the attenuation of quorum sensing regulated virulence factors. Microb Pathog. 2021;155:104912. doi: 10.1016/j.micpath.2021.104912.
  • Oliveira VC, Steixner S, Nascimento CD, et al. Expression of virulence factors by Pseudomonas aeruginosa biofilm after bacteriophage infection. Microb Pathog. 2021;154:104834. doi: 10.1016/j.micpath.2021.104834.
  • Lau GW, Hassett DJ, Ran H, et al. The role of pyocyanin in Pseudomonas aeruginosa infection. Trends Mol Med. 2004;10(12):599–606. doi: 10.1016/j.molmed.2004.10.002.
  • Stehling EG, Silveira WDd, Leite DdS Study of biological characteristics of Pseudomonas aeruginosa strains isolated from patients with cystic fibrosis and from patients with extra-pulmonary infections. Braz J Infect Dis. 2008;12(1):86–88. doi: 10.1590/s1413-86702008000100018.
  • Jurado-Martín I, Sainz-Mejías M, McClean S. Pseudomonas aeruginosa: an audacious pathogen with an adaptable arsenal of virulence factors. Int J Mol Sci. 2021;22(6):3128. doi: 10.3390/ijms22063128.
  • Singh VK, Mishra A, Jha B. Anti-quorum sensing and anti-biofilm activity of Delftia tsuruhatensis extract by attenuating the quorum sensing-controlled virulence factor production in Pseudomonas aeruginosa. Front Cell Infect Microbiol. 2017;7:337. doi: 10.3389/fcimb.2017.00337.
  • Hnamte S, Parasuraman P, Ranganathan S, et al. Mosloflavone attenuates the quorum sensing controlled virulence phenotypes and biofilm formation in Pseudomonas aeruginosa PAO1: in vitro, in vivo and in silico approach. Microb Pathog. 2019;131:128–134. doi: 10.1016/j.micpath.2019.04.005.
  • Rajkumari J, Borkotoky S, Murali A, et al. Attenuation of quorum sensing controlled virulence factors and biofilm formation in Pseudomonas aeruginosa by pentacyclic triterpenes, betulin and betulinic acid. Microb Pathog. 2018;118:48–60. doi: 10.1016/j.micpath.2018.03.012.
  • Henriksen K, Rørbo N, Rybtke ML, et al. Pseudomonas aeruginosa flow-cell biofilms are enhanced by repeated phage treatments but can be eradicated by phage-ciprofloxacin combination. Pathog Dis. 2019;77(2):ftz011. doi: 10.1093/femspd/ftz011.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.