The N-terminal domain of Chlamydia psittaci Pmp19G modulates macrophage autophagy by targeting the NOD1 receptor and the ATG16L1–RAB7 signaling pathway

Our findings indicate that Pmp19G regulates macrophage autophagy through distinct mechanisms in early and late phases: activation of the NOD1-ATG16L1 signaling pathway initiates early autophagy, while enhanced RAB7 recruitment inhibits autophagosome-lysosome fusion during late autophagy. Collectively, Pmp19G-involved manipulation of the autophagic process represents a critical strategy employed by <i>C. psittaci</i> to evade host immune defenses, leading bacterial survival and spread.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-09-10
DOI
https://doi.org/10.3389/fimmu.2025.1645250
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
0.00
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article

The N-terminal domain of Chlamydia psittaci Pmp19G modulates macrophage autophagy by targeting the NOD1 receptor and the ATG16L1–RAB7 signaling pathway

Zongyang Huang, Qiang Li, Rongze He, Ying Cui et al.
Frontiers in Immunology
Autophagy in Disease and Therapy
article

The N-terminal domain of Chlamydia psittaci Pmp19G modulates macrophage autophagy by targeting the NOD1 receptor and the ATG16L1–RAB7 signaling pathway

Zongyang Huang, Qiang Li, Rongze He, Ying Cui, Cheng He, Huimin Wang, Xuedi Zhang
article en

Abstract

Our findings indicate that Pmp19G regulates macrophage autophagy through distinct mechanisms in early and late phases: activation of the NOD1-ATG16L1 signaling pathway initiates early autophagy, while enhanced RAB7 recruitment inhibits autophagosome-lysosome fusion during late autophagy. Collectively, Pmp19G-involved manipulation of the autophagic process represents a critical strategy employed by <i>C. psittaci</i> to evade host immune defenses, leading bacterial survival and spread.

Frontiers in ImmunologyVol. 16
China Agricultural University (CN)
Openalex Percentile: Top 67%
Autophagy in Disease and Therapy
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