» Articles » PMID: 30559222

The Obligate Intracellular Bacterium Targets NLRC5 To Modulate the Major Histocompatibility Complex Class I Pathway

Overview
Journal Infect Immun
Date 2018 Dec 19
PMID 30559222
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

is an obligate intracellular bacterium that infects mononuclear and endothelial cells to cause the emerging global health threat scrub typhus. The ability of to survive in monocytes facilitates bacterial dissemination to endothelial cells, which can subsequently lead to several potentially fatal sequelae. As a strict intracellular pathogen that lives in the cytoplasm of host cells, has evolved to counter adaptive immunity. How the pathogen does so and the outcome of this strategy in monocytes versus endothelial cells are poorly understood. This report demonstrates that reduces cellular levels of NOD-, LRR-, and CARD-containing 5 (NLRC5), a recently identified specific transactivator of major histocompatibility complex class I (MHC-I) component gene expression, to inhibit MHC-I biosynthesis. Importantly, the efficacy of this approach varies with the host cell type infected. In nonprofessional antigen-presenting HeLa and primary human aortic endothelial cells, the -mediated reduction of NLRC5 results in lowered MHC-I component transcription and, consequently, lower total and/or surface MHC-I levels throughout 72 h of infection. However, in infected THP-1 monocytes, which are professional antigen-presenting cells, the reductions in NLRC5 and MHC-I observed during the first 24 h reverse thereafter. is the first example of a microbe that targets NLRC5 to modulate the MHC-I pathway. The differential ability of to modulate this pathway in nonprofessional versus professional antigen-presenting cells could influence morbidity and mortality from scrub typhus.

Citing Articles

alters the intranuclear balance of cullin-1 and c-MYC to inhibit apoptosis.

Allen P, Adcox H, Siff T, Gupta S, Hunt J, Carlyon J Infect Immun. 2025; 93(3):e0055924.

PMID: 39976440 PMC: 11895443. DOI: 10.1128/iai.00559-24.


infection reduces host gluconeogenic but not glycolytic substrates.

Sanchez S, Chiarelli T, Park M, Carlyon J Infect Immun. 2024; 92(11):e0028424.

PMID: 39324805 PMC: 11556148. DOI: 10.1128/iai.00284-24.


Infection Stimulates Syk-Dependent Responses and Innate Cytosolic Defenses in Macrophages.

Fisher J, Gonzales C, Chroust Z, Liang Y, Soong L Pathogens. 2023; 12(1).

PMID: 36678402 PMC: 9861896. DOI: 10.3390/pathogens12010053.


Subversion of host cell signaling: The arsenal of Rickettsial species.

Huang D, Luo J, OuYang X, Song L Front Cell Infect Microbiol. 2022; 12:995933.

PMID: 36389139 PMC: 9659576. DOI: 10.3389/fcimb.2022.995933.


Orientia tsutsugamushi OtDUB Is Expressed and Interacts with Adaptor Protein Complexes during Infection.

Adcox H, Berk J, Hochstrasser M, Carlyon J Infect Immun. 2022; 90(12):e0046922.

PMID: 36374099 PMC: 9753657. DOI: 10.1128/iai.00469-22.


References
1.
Benko S, Magalhaes J, Philpott D, Girardin S . NLRC5 limits the activation of inflammatory pathways. J Immunol. 2010; 185(3):1681-91. DOI: 10.4049/jimmunol.0903900. View

2.
Vitiello A, POTTER T, Sherman L . The role of beta 2-microglobulin in peptide binding by class I molecules. Science. 1990; 250(4986):1423-6. DOI: 10.1126/science.2124002. View

3.
Xu G, Mendell N, Liang Y, Shelite T, Goez-Rivillas Y, Soong L . CD8+ T cells provide immune protection against murine disseminated endotheliotropic Orientia tsutsugamushi infection. PLoS Negl Trop Dis. 2017; 11(7):e0005763. PMC: 5536391. DOI: 10.1371/journal.pntd.0005763. View

4.
Diaz F, Abarca K, Kalergis A . An Update on Host-Pathogen Interplay and Modulation of Immune Responses during Orientia tsutsugamushi Infection. Clin Microbiol Rev. 2018; 31(2). PMC: 5967693. DOI: 10.1128/CMR.00076-17. View

5.
Taylor A, Paris D, Newton P . A Systematic Review of Mortality from Untreated Scrub Typhus (Orientia tsutsugamushi). PLoS Negl Trop Dis. 2015; 9(8):e0003971. PMC: 4537241. DOI: 10.1371/journal.pntd.0003971. View