Microbiota-Derived Extracellular Vesicles Detected in Human Blood from Healthy Donors

被引:31
作者
Schaack, Beatrice [1 ,2 ]
Hindre, Thomas [1 ]
Quansah, Nyamekye [1 ]
Hannani, Dalil [1 ]
Mercier, Corinne [1 ]
Laurin, David [3 ,4 ,5 ]
机构
[1] Univ Grenoble Alpes, TIMC, Grenoble INP, VetAgro Sup,UMR 5525,CNRS, F-38000 Grenoble, France
[2] Univ Grenoble Alpes, IBS, CNRS, CEA, F-38044 Grenoble, France
[3] Dept Sci Auvergne Rhone Alpes, Etab Francais Sang, F-38000 Grenoble, France
[4] Univ Grenoble Alpes, Inst Adv Biosci, INSERM, U1209, F-38000 Grenoble, France
[5] Univ Grenoble Alpes, Inst Adv Biosci, CNRS, UMR 5309, F-38000 Grenoble, France
关键词
extracellular vesicles (EVs); outer membrane vesicles (OMVs); membrane fusion; red blood cell concentrates; lipopolysaccharide (LPS); OmpA; gut microbiota; OUTER-MEMBRANE VESICLES; LIPOPOLYSACCHARIDE; AGGREGATION;
D O I
10.3390/ijms232213787
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The microbiota constitutes an important part of the holobiont in which extracellular vesicles (EVs) are key players in health, especially regarding inter- and intra-kingdom communications. Analysis of EVs from the red blood cell concentrates of healthy donors revealed variable amounts of OmpA and LPS in 12 of the 14 analyzed samples, providing indirect experimental evidence of the presence of microbiota EVs in human circulating blood in the absence of barrier disruption. To investigate the role of these microbiota EVs, we tracked the fusion of fluorescent Escherichia coli EVs with blood mononuclear cells and showed that, in the circulating blood, these EVs interacted almost exclusively with monocytes. This study demonstrates that bacterial EVs constitute critical elements of the host-microbiota cellular communication. The analysis of bacterial EVs should thus be systematically included in any characterization of human EVs.
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页数:12
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共 30 条
[1]   Outer Membrane Vesicles and Soluble Factors Released by Probiotic Escherichia coil Nissle 1917 and Commensal ECOR63 Enhance Barrier Function by Regulating Expression of Tight Junction Proteins in Intestinal Epithelial Cells [J].
Alvarez, Carina-Shianya ;
Badia, Josefa ;
Bosch, Manel ;
Gimenez, Rosa ;
Baldoma, Laura .
FRONTIERS IN MICROBIOLOGY, 2016, 7
[2]   Caspase-4 disaggregates lipopolysaccharide micelles via LPS-CARD interaction [J].
An, Jinsu ;
Kim, Seong Ho ;
Hwang, Dohyeon ;
Lee, Kyung Eun ;
Kim, Min Jung ;
Yang, Eun Gyeong ;
Kim, So Yeon ;
Chung, Hak Suk .
SCIENTIFIC REPORTS, 2019, 9 (1)
[3]   Critical aggregation concentrations of gram-negative bacterial lipopolysaccharides (LPS) [J].
Aurell, CA ;
Wistrom, AO .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 253 (01) :119-123
[4]   Outer Membrane Vesicles of Gram-Negative Bacteria: An Outlook on Biogenesis [J].
Avila-Calderon, Eric Daniel ;
del Socorro Ruiz-Palma, Maria ;
Aguilera-Arreola, Ma. Guadalupe ;
Velazquez-Guadarrama, Norma ;
Ruiz, Enrico A. ;
Gomez-Lunar, Zulema ;
Witonsky, Sharon ;
Contreras-Rodriguez, Araceli .
FRONTIERS IN MICROBIOLOGY, 2021, 12
[5]   Microbiota-Derived Extracellular Vesicles as New Systemic Regulators [J].
Badi, Sara Ahmadi ;
Moshiri, Arfa ;
Fateh, Abolfazl ;
Jamnani, Fatemeh Rahimi ;
Sarshar, Meysam ;
Vaziri, Farzam ;
Siadat, Seyed Davar .
FRONTIERS IN MICROBIOLOGY, 2017, 8
[6]   Protein selection and export via outer membrane vesicles [J].
Bonnington, K. E. ;
Kuehn, M. J. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2014, 1843 (08) :1612-1619
[7]   Emerging role of bacterial extracellular vesicles in cancer [J].
Chronopoulos, Antonios ;
Kalluri, Raghu .
ONCOGENE, 2020, 39 (46) :6951-6960
[8]   Naturally Produced Outer Membrane Vesicles from Pseudomonas aeruginosa Elicit a Potent Innate Immune Response via Combined Sensing of Both Lipopolysaccharide and Protein Components [J].
Ellis, Terri N. ;
Leiman, Sara A. ;
Kuehn, Meta J. .
INFECTION AND IMMUNITY, 2010, 78 (09) :3822-3831
[9]   Role of Vγ9vδ2 T lymphocytes in infectious diseases [J].
Gay, Laetitia ;
Mezouar, Soraya ;
Cano, Carla ;
Frohna, Paul ;
Madakamutil, Loui ;
Mege, Jean-Louis ;
Olive, Daniel .
FRONTIERS IN IMMUNOLOGY, 2022, 13
[10]   Potent Bidirectional Cross-Talk Between Plasmacytoid Dendritic Cells and γδT Cells Through BTN3A, Type I/II IFNs and Immune Checkpoints [J].
Girard, Pauline ;
Ponsard, Benedicte ;
Charles, Julie ;
Chaperot, Laurence ;
Aspord, Caroline .
FRONTIERS IN IMMUNOLOGY, 2020, 11