Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides

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Standard

Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides. / Garcia-Vello, Pilar; Tytgat, Hanne L P; Gray, Joe; Elzinga, Janneke; Lorenzo, Flaviana Di; Biboy, Jacob; Vollmer, Daniela; Castro, Cristina De; Vollmer, Waldemar; Vos, Willem M de; Molinaro, Antonio.

I: Glycobiology, Bind 32, Nr. 8, 2022, s. 712–719.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Garcia-Vello, P, Tytgat, HLP, Gray, J, Elzinga, J, Lorenzo, FD, Biboy, J, Vollmer, D, Castro, CD, Vollmer, W, Vos, WMD & Molinaro, A 2022, 'Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides', Glycobiology, bind 32, nr. 8, s. 712–719. https://doi.org/10.1093/glycob/cwac027

APA

Garcia-Vello, P., Tytgat, H. L. P., Gray, J., Elzinga, J., Lorenzo, F. D., Biboy, J., Vollmer, D., Castro, C. D., Vollmer, W., Vos, W. M. D., & Molinaro, A. (2022). Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides. Glycobiology, 32(8), 712–719. https://doi.org/10.1093/glycob/cwac027

Vancouver

Garcia-Vello P, Tytgat HLP, Gray J, Elzinga J, Lorenzo FD, Biboy J o.a. Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides. Glycobiology. 2022;32(8):712–719. https://doi.org/10.1093/glycob/cwac027

Author

Garcia-Vello, Pilar ; Tytgat, Hanne L P ; Gray, Joe ; Elzinga, Janneke ; Lorenzo, Flaviana Di ; Biboy, Jacob ; Vollmer, Daniela ; Castro, Cristina De ; Vollmer, Waldemar ; Vos, Willem M de ; Molinaro, Antonio. / Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides. I: Glycobiology. 2022 ; Bind 32, Nr. 8. s. 712–719.

Bibtex

@article{de6f2f024e004cc9855cbb3930d1fe3e,
title = "Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides",
abstract = "Akkermansia muciniphila is an intestinal symbiont known to improve the gut barrier function in mice and humans. Various cell envelope components have been identified to play a critical role in the immune signaling of A. muciniphila, but the chemical composition and role of peptidoglycan (PG) remained elusive. Here, we isolated PG fragments from A. muciniphila MucT (ATCC BAA-835), analyzed their composition and evaluated their immune signaling capacity. Structurally, the PG of A. muciniphila was found to be noteworthy due of the presence of some nonacetylated glucosamine residues, which presumably stems from deacetylation of N-acetylglucosamine. Some of the N-acetylmuramic acid (MurNAc) subunits were O-acetylated. The immunological assays revealed that muropeptides released from the A. muciniphila PG could both activate the intracellular NOD1 and NOD2 receptors to a comparable extent as muropeptides from Escherichia coli BW25113. These data challenge the hypothesis that non-N-acetylattion of PG can be used as a NOD-1 evasion mechanism. Our results provide new insights into the diversity of cell envelope structures of key gut microbiota members and their role in steering host–microbiome interactions.",
author = "Pilar Garcia-Vello and Tytgat, {Hanne L P} and Joe Gray and Janneke Elzinga and Lorenzo, {Flaviana Di} and Jacob Biboy and Daniela Vollmer and Castro, {Cristina De} and Waldemar Vollmer and Vos, {Willem M de} and Antonio Molinaro",
year = "2022",
doi = "10.1093/glycob/cwac027",
language = "English",
volume = "32",
pages = "712–719",
journal = "Glycobiology",
issn = "0959-6658",
publisher = "Oxford University Press",
number = "8",

}

RIS

TY - JOUR

T1 - Peptidoglycan from Akkermansia muciniphila MucT: chemical structure and immunostimulatory properties of muropeptides

AU - Garcia-Vello, Pilar

AU - Tytgat, Hanne L P

AU - Gray, Joe

AU - Elzinga, Janneke

AU - Lorenzo, Flaviana Di

AU - Biboy, Jacob

AU - Vollmer, Daniela

AU - Castro, Cristina De

AU - Vollmer, Waldemar

AU - Vos, Willem M de

AU - Molinaro, Antonio

PY - 2022

Y1 - 2022

N2 - Akkermansia muciniphila is an intestinal symbiont known to improve the gut barrier function in mice and humans. Various cell envelope components have been identified to play a critical role in the immune signaling of A. muciniphila, but the chemical composition and role of peptidoglycan (PG) remained elusive. Here, we isolated PG fragments from A. muciniphila MucT (ATCC BAA-835), analyzed their composition and evaluated their immune signaling capacity. Structurally, the PG of A. muciniphila was found to be noteworthy due of the presence of some nonacetylated glucosamine residues, which presumably stems from deacetylation of N-acetylglucosamine. Some of the N-acetylmuramic acid (MurNAc) subunits were O-acetylated. The immunological assays revealed that muropeptides released from the A. muciniphila PG could both activate the intracellular NOD1 and NOD2 receptors to a comparable extent as muropeptides from Escherichia coli BW25113. These data challenge the hypothesis that non-N-acetylattion of PG can be used as a NOD-1 evasion mechanism. Our results provide new insights into the diversity of cell envelope structures of key gut microbiota members and their role in steering host–microbiome interactions.

AB - Akkermansia muciniphila is an intestinal symbiont known to improve the gut barrier function in mice and humans. Various cell envelope components have been identified to play a critical role in the immune signaling of A. muciniphila, but the chemical composition and role of peptidoglycan (PG) remained elusive. Here, we isolated PG fragments from A. muciniphila MucT (ATCC BAA-835), analyzed their composition and evaluated their immune signaling capacity. Structurally, the PG of A. muciniphila was found to be noteworthy due of the presence of some nonacetylated glucosamine residues, which presumably stems from deacetylation of N-acetylglucosamine. Some of the N-acetylmuramic acid (MurNAc) subunits were O-acetylated. The immunological assays revealed that muropeptides released from the A. muciniphila PG could both activate the intracellular NOD1 and NOD2 receptors to a comparable extent as muropeptides from Escherichia coli BW25113. These data challenge the hypothesis that non-N-acetylattion of PG can be used as a NOD-1 evasion mechanism. Our results provide new insights into the diversity of cell envelope structures of key gut microbiota members and their role in steering host–microbiome interactions.

U2 - 10.1093/glycob/cwac027

DO - 10.1093/glycob/cwac027

M3 - Journal article

C2 - 35452117

VL - 32

SP - 712

EP - 719

JO - Glycobiology

JF - Glycobiology

SN - 0959-6658

IS - 8

ER -

ID: 359858130