Target intelligence / Profile preview

Type 3 fimbrial protein MrpA (MrpA) (MrpA)

Target
MrpA
Molecular classification
Bacterial surface protein, Adhesin, Structural protein, Pilin subunit
01

Overview

Type 3 fimbriae are rigid, hair-like surface appendages primarily found in Gram-negative pathogens such as Klebsiella pneumoniae and Proteus mirabilis (UniProt, PubMed: 11274108). These structures are composed of a major subunit protein called MrpA and a specific tip-positioned adhesin, MrpD, which facilitates mannose-resistant attachment to both biotic surfaces and abiotic surfaces like urinary catheters (PubMed: 23681461). They are considered critical virulence factors due to their central role in the initiation and maturation of biofilms, which protect bacteria from host immune responses and conventional antibiotics (PubMed: 20023023). Therapeutic targeting of MrpA via experimental vaccines or small molecule inhibitors of the chaperone-usher assembly pathway aims to prevent bacterial colonization. Such anti-virulence strategies are particularly relevant for preventing catheter-associated urinary tract infections (CAUTI) and managing multi-drug resistant strains (PubMed: 26341258). By disrupting the initial adherence phase, these interventions offer a potential alternative or adjunct to traditional antibiotic therapy in hospital settings.

Other names
Mrp fimbriaeType 3 piliMannose-resistant Proteus-like fimbriaeType 3 fimbriaeKlebsiella pneumoniae type 3 fimbriaeMrpA major subunit
02

Mechanism of action

Inhibition of bacterial attachment to host tissues and medical device surfaces by targeting the structural assembly of fimbriae or blocking the interaction between the tip adhesin and the host receptor.

03

Biological functions

Bacterial adhesionBiofilm formationHost-pathogen interactionSurface colonizationMannose-resistant hemagglutination
04

Disease associations

InfectionUrinary tract infectionPneumoniaCatheter-associated urinary tract infection (CAUTI)Healthcare-associated infection
05

Safety considerations

Potential for bacterial redundancy (switching to other fimbriae types)High strain variability requiring broad-spectrum targetingRisk of limited efficacy against pre-established biofilmsNecessity for high specificity to avoid impacting commensal microbiota
06

Interacting drugs

Experimental MrpA-based vaccines

2 more in the full profile.

07

Biomarkers

mrpa gene expressionMannose-resistant hemagglutination (MR/K) activityBiofilm densitySurface expression of MrpA

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