Dynamics of macrophage polarization support Salmonella persistence in a whole living organism

Author:

Leiba Jade1,Sipka Tamara1,Begon-Pescia Christina1,Bernardello Matteo2,Tairi Sofiane1,Bossi Lionello3,Gonzalez Anne-Alicia4,Mialhe Xavier4,Gualda Emilio J2,Loza-Alvarez Pablo2ORCID,Blanc-Potard Anne1,Lutfalla Georges1,Nguyen-Chi Mai E1ORCID

Affiliation:

1. LPHI, Université de Montpellier, CNRS, INSERM

2. ICFO - Institute of Photonic Sciences, The Barcelona Institute of Science and Technology

3. Institute for Integrative Biology of the Cell-I2BC, Université Paris-Saclay, CEA, CNRS

4. MGX-Montpellier GenomiX, Université de Montpellier, CNRS, INSERM

Abstract

Numerous intracellular bacterial pathogens interfere with macrophage function, including macrophage polarization, to establish a niche and persist. However, the spatiotemporal dynamics of macrophage polarization during infection within host remain to be investigated. Here, we implement a model of persistent Salmonella Typhimurium infection in zebrafish, which allows visualization of polarized macrophages and bacteria in real time at high resolution. While macrophages polarize toward M1-like phenotype to control early infection, during later stages, Salmonella persists inside non-inflammatory clustered macrophages. Transcriptomic profiling of macrophages showed a highly dynamic signature during infection characterized by a switch from pro-inflammatory to anti-inflammatory/pro-regenerative status and revealed a shift in adhesion program. In agreement with this specific adhesion signature, macrophage trajectory tracking identifies motionless macrophages as a permissive niche for persistent Salmonella. Our results demonstrate that zebrafish model provides a unique platform to explore, in a whole organism, the versatile nature of macrophage functional programs during bacterial acute and persistent infections.

Funder

Horizon 2020 Framework Programme

Agence Nationale de la Recherche

Region Occitanie

Spanish Ministerio de Economía y Competitividad

MINECO/FEDER

Fundació Privada Cellex

Fundación Mig-Puig

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3