Literature DB >> 36258071

Antibiotic Resistance in Pseudomonas.

Pablo Laborda1, Sara Hernando-Amado1, José Luis Martínez2, Fernando Sanz-García1.   

Abstract

Pseudomonas is a bacterial genus, with a bona fide environmental habitat that comprises different species, some of them causing diseases in humans and plants, as well as some strains with biotechnological potential. Amongst them, Pseudomonas aeruginosa is currently one of the most important nosocomial pathogens. In addition, this microorganism is a prevalent cause of chronic infections in cystic fibrosis patients and in people suffering from chronic obstructive pulmonary disease. The success of P. aeruginosa in colonising different habitats largely relies on its metabolic versatility and robustness. Besides, this bacterial pathogen harbours in its core genome a large set of virulence determinants that allows it to colonise/infect a variety of hosts, from unicellular organisms to humans. Nevertheless, these are not just the only conditions needed for infecting patients at hospitals. Taking into consideration that infected patients are regularly under antibiotic treatment, the ability to avoid antibiotics' action is also needed. In this sense, P. aeruginosa displays a characteristic low susceptibility to several antibiotics currently used in therapy. This is due to the reduced permeability of its cellular envelopes and the presence in its genome of an arrangement of genes encoding multidrug efflux pumps and antibiotic-inactivating enzymes that contribute to its resilience to antibiotics. Besides intrinsic resistance, P. aeruginosa is able to evolve towards antibiotic resistance through mutations (particularly relevant in the case of chronic infections) and via acquisition of antibiotic resistance genes. It is worth mentioning that acquired resistance is not the only venue that P. aeruginosa has for avoiding the action of antibiotics. Transient resistance can also confer this phenotype. Indeed, the induction of the expression of intrinsic resistance genes by conditions or compounds that P. aeruginosa could face during infection can compromise the effectiveness of antibiotics for treating such infections. In addition, tolerant cells able to survive during the exposure to bactericidal antibiotics without an increase in their antibiotic resistance phenotype are found as well in these patients, and they are the prelude of the evolution towards antibiotic resistance. Finally, P. aeruginosa biofilms, frequently encountered in the lungs of cystic fibrosis patients, in prostheses, or in catheters, present low antibiotic susceptibility and are associated with recalcitrance and disease worsening.
© 2022. The Author(s), under exclusive license to Springer Nature Switzerland AG.

Entities:  

Keywords:  Antibiotic resistance; Bactericidal antibiotics; Biofilms; Chronic infections; ESKAPE; Multidrug efflux pumps

Mesh:

Substances:

Year:  2022        PMID: 36258071     DOI: 10.1007/978-3-031-08491-1_5

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   3.650


  217 in total

1.  The impaired quorum sensing response of Pseudomonas aeruginosa MexAB-OprM efflux pump overexpressing mutants is not due to non-physiological efflux of 3-oxo-C12-HSL.

Authors:  Manuel Alcalde-Rico; Jorge Olivares-Pacheco; Nigel Halliday; Miguel Cámara; José Luis Martínez
Journal:  Environ Microbiol       Date:  2020-09-06       Impact factor: 5.491

Review 2.  The intrinsic resistome of Pseudomonas aeruginosa to β-lactams.

Authors:  Carolina Alvarez-Ortega; Irith Wiegand; Jorge Olivares; Robert E W Hancock; José Luis Martínez
Journal:  Virulence       Date:  2011-03-01       Impact factor: 5.882

Review 3.  The role of multidrug efflux pumps in the antibiotic resistance of Pseudomonas aeruginosa and other gram-negative bacteria. Insights from the Society of Infectious Diseases Pharmacists.

Authors:  Jeffrey R Aeschlimann
Journal:  Pharmacotherapy       Date:  2003-07       Impact factor: 4.705

4.  Role of efflux pumps: MexAB-OprM and MexXY(-OprA), AmpC cephalosporinase and OprD porin in non-metallo-β-lactamase producing Pseudomonas aeruginosa isolated from cystic fibrosis and burn patients.

Authors:  Mohammad Aghazadeh; Zoya Hojabri; Reza Mahdian; Mohammad Reza Nahaei; Marveh Rahmati; Tina Hojabri; Tahereh Pirzadeh; Omid Pajand
Journal:  Infect Genet Evol       Date:  2014-03-30       Impact factor: 3.342

5.  Dissemination of aminoglycoside-modifying enzymes and 16S rRNA methylases among acinetobacter baumannii and Pseudomonas aeruginosa isolates.

Authors:  Mohammad Aghazadeh; Mohammad Ahangarzadeh Rezaee; Mohammad Reza Nahaei; Reza Mahdian; Omid Pajand; Fereshteh Saffari; Maryam Hassan; Zoya Hojabri
Journal:  Microb Drug Resist       Date:  2013-04-11       Impact factor: 3.431

Review 6.  Pseudomonas aeruginosa biofilms: mechanisms of immune evasion.

Authors:  Maria Alhede; Thomas Bjarnsholt; Michael Givskov; Morten Alhede
Journal:  Adv Appl Microbiol       Date:  2014       Impact factor: 5.086

Review 7.  Mechanisms and clinical relevance of bacterial heteroresistance.

Authors:  Dan I Andersson; Hervé Nicoloff; Karin Hjort
Journal:  Nat Rev Microbiol       Date:  2019-06-24       Impact factor: 60.633

8.  The MexGHI-OpmD multidrug efflux pump controls growth, antibiotic susceptibility and virulence in Pseudomonas aeruginosa via 4-quinolone-dependent cell-to-cell communication.

Authors:  Séverine Aendekerk; Stephen P Diggle; Zhijun Song; Niels Høiby; Pierre Cornelis; Paul Williams; Miguel Cámara
Journal:  Microbiology (Reading)       Date:  2005-04       Impact factor: 2.777

9.  Role of the Multidrug Resistance Efflux Pump MexCD-OprJ in the Pseudomonas aeruginosa Quorum Sensing Response.

Authors:  Manuel Alcalde-Rico; Jorge Olivares-Pacheco; Carolina Alvarez-Ortega; Miguel Cámara; José Luis Martínez
Journal:  Front Microbiol       Date:  2018-11-23       Impact factor: 5.640

Review 10.  Definitions and guidelines for research on antibiotic persistence.

Authors:  Nathalie Q Balaban; Sophie Helaine; Kim Lewis; Martin Ackermann; Bree Aldridge; Dan I Andersson; Mark P Brynildsen; Dirk Bumann; Andrew Camilli; James J Collins; Christoph Dehio; Sarah Fortune; Jean-Marc Ghigo; Wolf-Dietrich Hardt; Alexander Harms; Matthias Heinemann; Deborah T Hung; Urs Jenal; Bruce R Levin; Jan Michiels; Gisela Storz; Man-Wah Tan; Tanel Tenson; Laurence Van Melderen; Annelies Zinkernagel
Journal:  Nat Rev Microbiol       Date:  2019-07       Impact factor: 60.633

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