S A F Jégouzo
Mammalian lectin arrays for screening host-microbe interactions
Jégouzo, S A F; Nelson, C; Hardwick, T; Wong, S T A; Lau, N K K; Neoh, G K E; Castellanos-Rueda, R; Huang, Z; Mignot, B; Hirdaramani, A; Howitt, A; Frewin, K; Shen, Z; Fox, R J; Wong, R; Ando, M; Emony, L; Zhu, H; Holder, A L; Werling, D; Krishnan, N; Robertson, B D; Clements, A; Taylor, M E; Drickamer, K
Authors
C Nelson
T Hardwick
S T A Wong
N K K Lau
G K E Neoh
R Castellanos-Rueda
Z Huang
B Mignot
A Hirdaramani
A Howitt
K Frewin
Z Shen
R J Fox
R Wong
M Ando
L Emony
H Zhu
A L Holder
D Werling
N Krishnan
B D Robertson
A Clements
M E Taylor
K Drickamer
Abstract
Many members of the C-type lectin family of glycan-binding receptors have been ascribed roles in the recognition of microorganisms and serve as key receptors in the innate immune response to pathogens. Other mammalian receptors have become targets through which pathogens enter target cells. These receptor roles have often been documented with binding studies involving individual pairs of receptors and micro-organisms. To provide a systematic overview of interactions between microbes and the large complement of C-type lectins, here we developed a lectin array and suitable protocols for labeling of microbes that could be used to probe this array. The array contains C-type lectins from cow, chosen as a model organism of agricultural interest for which the relevant pathogen–receptor interactions have not been previously investigated in detail. Screening with yeast cells and various strains of both Gram-positive and -negative bacteria revealed distinct binding patterns, which in some cases could be explained by binding to lipopolysaccharides or capsular polysaccharides, but in other cases suggested the presence of novel glycan targets on many of the microorganisms. These results are consistent with interactions previously ascribed to the receptors, but also highlight binding to additional sugar targets that have not previously been recognized. Our findings indicate that mammalian lectin arrays represent unique discovery tools for identifying both novel ligands and new receptor functions.
Citation
Jégouzo, S. A. F., Nelson, C., Hardwick, T., Wong, S. T. A., Lau, N. K. K., Neoh, G. K. E., Castellanos-Rueda, R., Huang, Z., Mignot, B., Hirdaramani, A., Howitt, A., Frewin, K., Shen, Z., Fox, R. J., Wong, R., Ando, M., Emony, L., Zhu, H., Holder, A. L., Werling, D., …Drickamer, K. (2020). Mammalian lectin arrays for screening host-microbe interactions. Journal of Biological Chemistry, 295(14), 4541-4555. https://doi.org/10.1074/jbc.RA120.012783
Journal Article Type | Article |
---|---|
Acceptance Date | Feb 24, 2020 |
Publication Date | Feb 24, 2020 |
Deposit Date | Mar 11, 2020 |
Publicly Available Date | Mar 11, 2020 |
Journal | JOURNAL OF BIOLOGICAL CHEMISTRY |
Print ISSN | 0021-9258 |
Electronic ISSN | 1083-351X |
Publisher | American Society for Biochemistry and Molecular Biology |
Peer Reviewed | Peer Reviewed |
Volume | 295 |
Issue | 14 |
Pages | 4541-4555 |
DOI | https://doi.org/10.1074/jbc.RA120.012783 |
Public URL | https://rvc-repository.worktribe.com/output/1378516 |
Files
12600_Mammalian-lectin-arrays-for-screening-host–microbe-interactions.pdf
(867 Kb)
PDF
12600_Mammalian-lectin-arrays-for-screening-host-microbe-interactions_Accepted.pdf
(465 Kb)
PDF
You might also like
First detection and characterisation of Eimeria zaria in Europe
(2023)
Journal Article