Differential temporal release and lipoprotein loading in B. thetaiotaomicron bacterial extracellular vesicles.

BEV Bacteroides OMV bacterial extracellular vesicles outer membrane vesicles proteomics

Journal

Journal of extracellular vesicles
ISSN: 2001-3078
Titre abrégé: J Extracell Vesicles
Pays: United States
ID NLM: 101610479

Informations de publication

Date de publication:
Jan 2024
Historique:
revised: 24 11 2023
received: 05 07 2023
accepted: 01 01 2024
medline: 19 1 2024
pubmed: 19 1 2024
entrez: 19 1 2024
Statut: ppublish

Résumé

Bacterial extracellular vesicles (BEVs) contribute to stress responses, quorum sensing, biofilm formation and interspecies and interkingdom communication. However, the factors that regulate their release and heterogeneity are not well understood. We set out to investigate these factors in the common gut commensal Bacteroides thetaiotaomicron by studying BEV release throughout their growth cycle. Utilising a range of methods, we demonstrate that vesicles released at different stages of growth have significantly different composition, with early vesicles enriched in specifically released outer membrane vesicles (OMVs) containing a larger proportion of lipoproteins, while late phase BEVs primarily contain lytic vesicles with enrichment of cytoplasmic proteins. Furthermore, we demonstrate that lipoproteins containing a negatively charged signal peptide are preferentially incorporated in OMVs. We use this observation to predict all Bacteroides thetaiotaomicron OMV enriched lipoproteins and analyse their function. Overall, our findings highlight the need to understand media composition and BEV release dynamics prior to functional characterisation and define the theoretical functional capacity of Bacteroides thetaiotaomicron OMVs.

Identifiants

pubmed: 38240185
doi: 10.1002/jev2.12406
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e12406

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
Pays : United Kingdom

Informations de copyright

© 2024 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles.

Références

Adams, R. W., Holroyd, C. M., Aguilar, J. A., Nilsson, M., & Morris, G. A. (2013). “Perfecting” WATERGATE: Clean proton NMR spectra from aqueous solution. Chemical Communications, 49, 358-360.
Brenes, A., Hukelmann, J., Bensaddek, D., & Lamond, A. I. (2019). Multibatch TMT reveals false positives, batch effects and missing values. Molecular & Cellular Proteomics, 18, 1967-1980.
Briliūtė, J., Urbanowicz, P. A., Luis, A. S., Baslé, A., Paterson, N., Rebello, O., Hendel, J., Ndeh, D. A., Lowe, E. C., Martens, E. C., Spencer, D. I. R., Bolam, D. N., & Crouch, L. I. (2019). Complex N-glycan breakdown by gut Bacteroides involves an extensive enzymatic apparatus encoded by multiple co-regulated genetic loci. Nature Microbiology, 4, 1571-1581.
Ducret, A., Quardokus, E. M., & Brun, Y. V. (2016). MicrobeJ, a tool for high throughput bacterial cell detection and quantitative analysis. Nature Microbiology, 1, 1-7.
Durant, L., Stentz, R., Noble, A., Brooks, J., Gicheva, N., Reddi, D., O'Connor, M. J., Hoyles, L., McCartney, A. L., Man, R., Pring, E. T., Dilke, S., Hendy, P., Segal, J. P., Lim, D. N. F., Misra, R., Hart, A. L., Arebi, N., Carding, S. R., & Knight, S. C. (2020). Bacteroides thetaiotaomicron-derived outer membrane vesicles promote regulatory dendritic cell responses in health but not in inflammatory bowel disease. Microbiome, 8, 1-16.
Hirayama, S., & Nakao, R. (2020). Glycine significantly enhances bacterial membrane vesicle production: A powerful approach for isolation of LPS-reduced membrane vesicles of probiotic Escherichia coli. Microbial Biotechnology, 13, 1162-1178.
Jiang, M., Wang, Z., Xia, F., Wen, Z., Chen, R., Zhu, D., Wang, M., Zhuge, X., & Dai, J. (2022). Reductions in bacterial viability stimulate the production of extra-intestinal pathogenic Escherichia coli (ExPEC) cytoplasm-carrying extracellular vesicles (EVs). PLOS Pathogens, 18, e1010908.
Jones, E. J., Booth, C., Fonseca, S., Parker, A., Cross, K., Miquel-Clopés, A., Hautefort, I., Mayer, U., Wileman, T., Stentz, R., & Carding, S. R. (2020). The uptake, trafficking, and biodistribution of Bacteroides thetaiotaomicron generated outer membrane vesicles. Frontiers in Microbiology, 11, 1-14.
Juodeikis, R., & Carding, S. R. (2022). Outer membrane vesicles: Biogenesis, functions, and issues. Microbiology and Molecular Biology Reviews, 86(4), e0003222.
Juodeikis, R., Jones, E., Deery, E., Beal, D. M., Stentz, R., Kräutler, B., Carding, S. R., & Warren, M. J. (2022). Nutrient smuggling: Commensal gut bacteria-derived extracellular vesicles scavenge vitamin B12 and related cobamides for microbe and host acquisition. Journal of Extracellular Biology, 1(10), e61.
Kozlowski, L. P. (2016). IPC-Isoelectric point calculator. Biology Direct, 11, 1-16.
Lapébie, P., Lombard, V., Drula, E., Terrapon, N., & Henrissat, B. (2019). Bacteroidetes use thousands of enzyme combinations to break down glycans. Nature Communications, 10, 2043.
Lauber, F., Cornelis, G. R., & Renzi, F. (2016). Identification of a new lipoprotein export signal in Gram-negative bacteria. MBio, 7, e01232-16.
Le, L. H. M., Steele, J. R., Ying, L., Schittenhelm, R. B., & Ferrero, R. L. (2023). A new isolation method for bacterial extracellular vesicles providing greater purity and improved proteomic detection of vesicle proteins. Journal of Extracellular Biology, 2, e84.
Lee, J., Kim, O. Y., & Gho, Y. S. (2016). Proteomic profiling of Gram-negative bacterial outer membrane vesicles: Current perspectives. Proteomics. Clinical Applications, 10, 897-909.
Ley, R. E., Hamady, M., Lozupone, C., Turnbaugh, P. J., Ramey, R. R., Bircher, J. S., Schlegel, M. L., Tucker, T. A., Schrenzel, M. D., Knight, R., & Gordon, J. I. (2008). Evolution of mammals and their gut microbes. Science, 320, 1647-1651.
Lim, B., Zimmermann, M., Barry, N. A., & Goodman, A. L. (2017). Engineered regulatory systems modulate gene expression of human commensals in the gut. Cell, 169, 547-558.e15.
McMillan, H. M., & Kuehn, M. J. (2021). The extracellular vesicle generation paradox: A bacterial point of view. EMBO Journal, 40, 1-23.
Nickerson, J. L., & Doucette, A. A. (2020). Rapid and quantitative protein precipitation for proteome analysis by mass spectrometry. Journal of Proteome Research, 19, 2035-2042.
Orench-Rivera, N., & Kuehn, M. J. (2016). Environmentally controlled bacterial vesicle-mediated export. Cellular Microbiology, 18, 1525-1536.
Orench-Rivera, N., & Kuehn, M. J. (2021). Differential packaging into outer membrane vesicles upon oxidative stress reveals a general mechanism for cargo selectivity. Frontiers in Microbiology, 12, 1-14.
Perez-Riverol, Y., Bai, J., Bandla, C., García-Seisdedos, D., Hewapathirana, S., Kamatchinathan, S., Kundu, D. J., Prakash, A., Frericks-Zipper, A., Eisenacher, M., Walzer, M., Wang, S., Brazma, A., & Vizcaíno, J. A. (2022). The PRIDE database resources in 2022: A hub for mass spectrometry-based proteomics evidences. Nucleic Acids Research, 50, D543-D552.
Porter, N. T., Canales, P., Peterson, D. A., & Martens, E. C. (2017). A subset of polysaccharide capsules in the human symbiont Bacteroides thetaiotaomicron promote increased competitive fitness in the mouse gut. Cell Host & Microbe, 22, 494-506.e8.
Sartorio, M. G., Pardue, E. J., Feldman, M. F., & Haurat, M. F. (2021). Bacterial outer membrane vesicles: From discovery to applications. Annual Review of Microbiology, 75, 609-630.
Sartorio, M. G., Pardue, E. J., Scott, N. E., & Feldman, M. F. (2023). Human gut bacteria tailor extracellular vesicle cargo for the breakdown of diet- and host-derived glycans. Proceedings of the National Academy of Sciences of the United States of America, 120, e2306314120.
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., Tinevez, J. Y., White, D. J., Hartenstein, V., Eliceiri, K., Tomancak, P., & Cardona, A. (2012). Fiji: An open-source platform for biological-image analysis. Nature Methods, 9, 676-682.
Stentz, R., Jones, E., Juodeikis, R., Wegmann, U., Guirro, M., Goldson, A. J., Brion, A., Booth, C., Sudhakar, P., Brown, I. R., Korcsmáros, T., & Carding, S. R. (2022). The proteome of extracellular vesicles produced by the human gut bacteria Bacteroides thetaiotaomicron in vivo is influenced by environmental and host-derived factors. Applied and Environmental Microbiology, 88, e0053322.
Teufel, F., Almagro Armenteros, J. J., Johansen, A. R., Gíslason, M. H., Pihl, S. I., Tsirigos, K. D., Winther, O., Brunak, S., von Heijne, G., & Nielsen, H. (2022). SignalP 6.0 predicts all five types of signal peptides using protein language models. Nature Biotechnology, 40, 1023-1025.
Toyofuku, M., Nomura, N., & Eberl, L. (2019). Types and origins of bacterial membrane vesicles. Nature Reviews Microbiology, 17, 13-24.
Toyofuku, M., Schild, S., Kaparakis-Liaskos, M., & Eberl, L. (2023). Composition and functions of bacterial membrane vesicles. Nature Reviews Microbiology, 21, 415-430.
Turnbull, L., Toyofuku, M., Hynen, A. L., Kurosawa, M., Pessi, G., Petty, N. K., Osvath, S. R., Cárcamo-Oyarce, G., Gloag, E. S., Shimoni, R., Omasits, U., Ito, S., Yap, X., Monahan, L. G., Cavaliere, R., Ahrens, C. H., Charles, I. G., Nomura, N., Eberl, L., & Whitchurch, C. B. (2016). Explosive cell lysis as a mechanism for the biogenesis of bacterial membrane vesicles and biofilms. Nature Communications, 7, 11220.
Valguarnera, E., Scott, N. E., Azimzadeh, P., & Feldman, M. F. (2018). Surface exposure and packing of lipoproteins into outer membrane vesicles are coupled processes in Bacteroides. mSphere, 3, 1-14.
Vignoli, A., Ghini, V., Meoni, G., Licari, C., Takis, P. G., Tenori, L., Turano, P., & Luchinat, C. (2019). High-throughput metabolomics by 1D NMR. Angewandte Chemie International Edition, 58, 968-994.
Wexler, A. G., & Goodman, A. L. (2017). An insider's perspective: Bacteroides as a window into the microbiome. Nature microbiology, 2, 17026.
Wexler, H. M. (2007). Bacteroides: The good, the bad, and the nitty-gritty. Clinical Microbiology Reviews, 20, 593-621.
Whitaker, W. R., Shepherd, E. S., & Sonnenburg, J. L. (2017). Tunable expression tools enable single-cell strain distinction in the gut microbiome. Cell, 169, 538-546.e12.

Auteurs

Rokas Juodeikis (R)

Food, Microbiome, and Health Research Programme, Quadram Institute Bioscience, Norwich, UK.

Carlo Martins (C)

Proteomics Facility, John Innes Centre, Norwich, UK.

Gerhard Saalbach (G)

Proteomics Facility, John Innes Centre, Norwich, UK.

Jake Richardson (J)

Proteomics Facility, John Innes Centre, Norwich, UK.

Trey Koev (T)

Food, Microbiome, and Health Research Programme, Quadram Institute Bioscience, Norwich, UK.
School of Pharmacy, University of East Anglia, Norwich, UK.

Dave J Baker (DJ)

Food, Microbiome, and Health Research Programme, Quadram Institute Bioscience, Norwich, UK.

Marianne Defernez (M)

Food, Microbiome, and Health Research Programme, Quadram Institute Bioscience, Norwich, UK.

Martin Warren (M)

Food, Microbiome, and Health Research Programme, Quadram Institute Bioscience, Norwich, UK.
School of Biosciences, University of Kent, Canterbury, UK.
School of Biological Sciences, University of East Anglia, Norwich, UK.

Simon R Carding (SR)

Food, Microbiome, and Health Research Programme, Quadram Institute Bioscience, Norwich, UK.
Norwich Medical School, University of East Anglia, Norwich, UK.

Classifications MeSH