» Articles » PMID: 35008950

The PE_PGRS Protein Family Acts As an Immunological Decoy to Subvert Host Immune Response

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2022 Jan 11
PMID 35008950
Authors
Affiliations
Soon will be listed here.
Abstract

() is a successful pathogen that can reside within the alveolar macrophages of the host and can survive in a latent stage. The pathogen has evolved and developed multiple strategies to resist the host immune responses. escapes from host macrophage through evasion or subversion of immune effector functions. genome codes for PE/PPE/PE_PGRS proteins, which are intrinsically disordered, redundant and antigenic in nature. These proteins perform multiple functions that intensify the virulence competence of majorly by modulating immune responses, thereby affecting immune mediated clearance of the pathogen. The highly repetitive, redundant and antigenic nature of PE/PPE/PE_PGRS proteins provide a critical edge over other proteins in terms of imparting a higher level of virulence and also as a decoy molecule that masks the effect of effector molecules, thereby modulating immuno-surveillance. An understanding of how these proteins subvert the host immunological machinery may add to the current knowledge about virulence and pathogenesis. This can help in redirecting our strategies for tackling infections.

Citing Articles

Deciphering the functional roles of PE18 and PPE26 proteins in modulating pathogenesis and immune response.

Ehtram A, Shariq M, Quadir N, Jamal S, Pichipalli M, Zarin S Front Immunol. 2025; 16:1517822.

PMID: 39949767 PMC: 11821933. DOI: 10.3389/fimmu.2025.1517822.


A comparative study of antibiotic resistance patterns in Mycobacterium tuberculosis.

Serajian M, Testagrose C, Prosperi M, Boucher C Sci Rep. 2025; 15(1):5104.

PMID: 39934219 PMC: 11814411. DOI: 10.1038/s41598-025-89087-w.


Protease shaving of facilitates vaccine antigen discovery and delivery of novel cargoes to the Mtb surface.

Lepe B, Zheng C, Leddy O, Allsup B, Solomon S, Bryson B Microbiol Spectr. 2024; 13(2):e0227724.

PMID: 39688428 PMC: 11792546. DOI: 10.1128/spectrum.02277-24.


Universal Lineage-Independent Markers of Multidrug Resistance in .

Hlanze H, Mutshembele A, Reva O Microorganisms. 2024; 12(7).

PMID: 39065108 PMC: 11278869. DOI: 10.3390/microorganisms12071340.


Protease shaving of facilitates vaccine antigen discovery and delivery of novel cargoes to the Mtb surface.

Lepe B, Zheng C, Leddy O, Allsup B, Solomon S, Bryson B bioRxiv. 2024; .

PMID: 39005324 PMC: 11245043. DOI: 10.1101/2024.07.02.601718.


References
1.
Peng X, Luo T, Zhai X, Zhang C, Suo J, Ma P . PPE11 of Mycobacterium tuberculosis can alter host inflammatory response and trigger cell death. Microb Pathog. 2018; 126:45-55. DOI: 10.1016/j.micpath.2018.10.031. View

2.
Meena L . An overview to understand the role of PE_PGRS family proteins in Mycobacterium tuberculosis H37 Rv and their potential as new drug targets. Biotechnol Appl Biochem. 2014; 62(2):145-53. DOI: 10.1002/bab.1266. View

3.
Thi E, Lambertz U, Reiner N . Sleeping with the enemy: how intracellular pathogens cope with a macrophage lifestyle. PLoS Pathog. 2012; 8(3):e1002551. PMC: 3310772. DOI: 10.1371/journal.ppat.1002551. View

4.
Asaad M, Ali M, Abo-Kadoum M, Lambert N, Gong Z, Wang H . Mycobacterium tuberculosis PPE10 (Rv0442c) alters host cell apoptosis and cytokine profile via linear ubiquitin chain assembly complex HOIP-NF-κB signaling axis. Int Immunopharmacol. 2021; 94:107363. DOI: 10.1016/j.intimp.2020.107363. View

5.
Bettencourt P, Muller J, Nicastri A, Cantillon D, Madhavan M, Charles P . Identification of antigens presented by MHC for vaccines against tuberculosis. NPJ Vaccines. 2020; 5(1):2. PMC: 6941960. DOI: 10.1038/s41541-019-0148-y. View