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Pseudomonas aeruginosa surface receptors

Molecular classification
Outer membrane protein [Galdiero et al., 2012, Current Protein & Peptide Science], Receptor [UniProt, 2023], Adhesin [Wagner et al., 2016, Molecules], Lectin [Wagner et al., 2016, Molecules], Porin [Galdiero et al., 2012, Current Protein & Peptide Science]
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Overview

Pseudomonas aeruginosa surface receptors represent a broad class of proteins and glycoconjugates situated on the outer membrane of the bacterium that facilitate interaction with the external environment. This category includes porins like OprD, which regulate antibiotic entry, siderophore receptors such as FpvA involved in iron acquisition, and adhesins like Type IV pili and lectins (LecA/LecB) that mediate attachment to host tissues [Wagner et al., 2016, Molecules; Galdiero et al., 2012, Current Protein & Peptide Science]. These receptors are fundamental to the pathogen's virulence, enabling the formation of biofilms and the evasion of the host immune system, particularly in chronic respiratory infections like those seen in cystic fibrosis [DiGiandomenico et al., 2014, Science Translational Medicine; UniProt, 2023]. Therapeutically, these surface structures are highly significant as they are accessible to large molecules; for instance, monoclonal antibodies like MedI3902 target surface polysaccharides and proteins to enhance bacterial clearance [DiGiandomenico et al., 2014, Science Translational Medicine]. Additionally, Trojan horse antibiotics like cefiderocol exploit siderophore receptors to bypass traditional resistance mechanisms, highlighting the dual role of these receptors as both virulence factors and gateways for drug delivery [Shizuma, 2022, Antibiotics].

Other names
P. aeruginosa outer membrane proteinsPseudomonas surface antigensP. aeruginosa adhesinsPseudomonas porins
02

Mechanism of action

Inhibition of bacterial adhesion, disruption of nutrient acquisition via siderophore mimicry, and neutralization of the type III secretion system machinery [Shizuma, 2022, Antibiotics; DiGiandomenico et al., 2014, Science Translational Medicine; Wagner et al., 2016, Molecules].

03

Biological functions

Cell adhesion [Wagner et al., 2016, Molecules]Nutrient transport [Shizuma, 2022, Antibiotics]Virulence [DiGiandomenico et al., 2014, Science Translational Medicine]Biofilm formation [Wagner et al., 2016, Molecules]Signal transduction [UniProt, 2023]
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Disease associations

Infection [Shizuma, 2022, Antibiotics; DiGiandomenico et al., 2014, Science Translational Medicine]
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Safety considerations

Rapid emergence of mutational resistance [Shizuma, 2022, Antibiotics]Target heterogeneity across clinical isolates [DiGiandomenico et al., 2014, Science Translational Medicine]Potential for narrow-spectrum activity requiring precise diagnostics [Galdiero et al., 2012, Current Protein & Peptide Science]
06

Interacting drugs

Cefiderocol

4 more in the full profile.

07

Biomarkers

OprD expression levels [Galdiero et al., 2012, Current Protein & Peptide Science]LPS O-antigen serotype [DiGiandomenico et al., 2014, Science Translational Medicine]PcrV expression levels [DiGiandomenico et al., 2014, Science Translational Medicine]

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