Characterization of bovine ileal epithelial cell line for lectin binding, susceptibility to enteric pathogens, and TLR mediated immune responses

Pratik Katwal; Tirth Uprety; Faten Okda; Linto Antony; Milton Thomas; Christopher Chase; Diego G. Diel; Eric Nelson; Alan Young; Feng Li; Joy Scaria; Radhey S. Kaushik

doi:10.1016/j.cimid.2020.101581

Characterization of bovine ileal epithelial cell line for lectin binding, susceptibility to enteric pathogens, and TLR mediated immune responses

Pratik Katwal
, Tirth Uprety
, Faten Okda
, Linto Antony
, Milton Thomas
, Christopher Chase
, Diego G. Diel
, Eric Nelson
, Alan Young
, Feng Li
, Joy Scaria
, Radhey S. Kaushik

Producción científica: Article › revisión exhaustiva

9 Citas (Scopus)

Resumen

In this study, primary and immortalized bovine intestinal epithelial cells (BIECs) were characterized for the expression of surface carbohydrate moieties. Primary BIEC-c4 cells showed staining greater than 90 % for 16 lectins but less than 50 % staining for four lectins. Immortalized BIECs showed significantly different lectin binding profile for few lectins compared to BIEC-c4 cells. BIEC-c4 cells were studied for infectivity to E. coli, Salmonella enterica, bovine rotavirus, bovine coronavirus, and bovine viral diarrhea virus. Bovine strain E. coli B41 adhered to BIEC-c4 cells and Salmonella strains S. Dublin and S. Mbandaka showed strong cell invasion. BIEC-c4 cells were susceptible to bovine rotavirus. LPS stimulation upregulated IL-10, IL-8, and IL-6 expression and Poly I:C upregulated TLR 8 and TLR 9 expression. This study provides important knowledge on the glycoconjugate expression profile of primary and immortalized BIECs and infectivity and immune responses of primary BIECs to bacterial and viral pathogens or ligands.

Idioma original	English
Número de artículo	101581
Publicación	Comparative Immunology, Microbiology and Infectious Diseases
Volumen	74
DOI	https://doi.org/10.1016/j.cimid.2020.101581
Estado	Published - feb 2021

Nota bibliográfica

Publisher Copyright:
© 2020 Elsevier Ltd

Financiación

Radhey S. Kaushik, Pratik Katwal, Tirth Uprety, and Milton Thomas, and this research project were funded and supported by USDA , NIFA , SDSU Agricultural Experiment Station Hatch grants # SD00H326-09 , and SD00H547-15 . This study was also funded by USDA/CSREES through project title JDIP: Johne’s Disease Integrated Program in Research, Education, and Extension , grant number # 2004-35605-14243 ; Sub-award No. Q6286224171. We acknowledge use of the SDSU-FGCF supported in part by NSF/EPSCoR Grant No. 0091948 and by the State of South Dakota.

Financiadores	Número del financiador
Milton Thomas
NSF-Kentucky EPSCoR cluster	0091948
USDA-CSREES	2004-35605-14243, Q6286224171
U.S. Department of Agriculture
US Department of Agriculture National Institute of Food and Agriculture, Agriculture and Food Research Initiative
https://aaes.auburn.edu/about/	SD00H326-09, SD00H547-15
https://aaes.auburn.edu/about/

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

Good health and well being

ASJC Scopus subject areas

Microbiology
Immunology and Allergy
Immunology
General Veterinary
Infectious Diseases

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Katwal, P., Uprety, T., Okda, F., Antony, L., Thomas, M., Chase, C., Diel, D. G., Nelson, E., Young, A., Li, F., Scaria, J., & Kaushik, R. S. (2021). Characterization of bovine ileal epithelial cell line for lectin binding, susceptibility to enteric pathogens, and TLR mediated immune responses. Comparative Immunology, Microbiology and Infectious Diseases, 74, Artículo 101581. https://doi.org/10.1016/j.cimid.2020.101581

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title = "Characterization of bovine ileal epithelial cell line for lectin binding, susceptibility to enteric pathogens, and TLR mediated immune responses",

abstract = "In this study, primary and immortalized bovine intestinal epithelial cells (BIECs) were characterized for the expression of surface carbohydrate moieties. Primary BIEC-c4 cells showed staining greater than 90 \% for 16 lectins but less than 50 \% staining for four lectins. Immortalized BIECs showed significantly different lectin binding profile for few lectins compared to BIEC-c4 cells. BIEC-c4 cells were studied for infectivity to E. coli, Salmonella enterica, bovine rotavirus, bovine coronavirus, and bovine viral diarrhea virus. Bovine strain E. coli B41 adhered to BIEC-c4 cells and Salmonella strains S. Dublin and S. Mbandaka showed strong cell invasion. BIEC-c4 cells were susceptible to bovine rotavirus. LPS stimulation upregulated IL-10, IL-8, and IL-6 expression and Poly I:C upregulated TLR 8 and TLR 9 expression. This study provides important knowledge on the glycoconjugate expression profile of primary and immortalized BIECs and infectivity and immune responses of primary BIECs to bacterial and viral pathogens or ligands.",

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doi = "10.1016/j.cimid.2020.101581",

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Katwal, P, Uprety, T, Okda, F, Antony, L, Thomas, M, Chase, C, Diel, DG, Nelson, E, Young, A, Li, F, Scaria, J & Kaushik, RS 2021, 'Characterization of bovine ileal epithelial cell line for lectin binding, susceptibility to enteric pathogens, and TLR mediated immune responses', Comparative Immunology, Microbiology and Infectious Diseases, vol. 74, 101581. https://doi.org/10.1016/j.cimid.2020.101581

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AU - Katwal, Pratik

AU - Uprety, Tirth

AU - Okda, Faten

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AU - Thomas, Milton

AU - Chase, Christopher

AU - Diel, Diego G.

AU - Nelson, Eric

AU - Young, Alan

AU - Li, Feng

AU - Scaria, Joy

AU - Kaushik, Radhey S.

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N2 - In this study, primary and immortalized bovine intestinal epithelial cells (BIECs) were characterized for the expression of surface carbohydrate moieties. Primary BIEC-c4 cells showed staining greater than 90 % for 16 lectins but less than 50 % staining for four lectins. Immortalized BIECs showed significantly different lectin binding profile for few lectins compared to BIEC-c4 cells. BIEC-c4 cells were studied for infectivity to E. coli, Salmonella enterica, bovine rotavirus, bovine coronavirus, and bovine viral diarrhea virus. Bovine strain E. coli B41 adhered to BIEC-c4 cells and Salmonella strains S. Dublin and S. Mbandaka showed strong cell invasion. BIEC-c4 cells were susceptible to bovine rotavirus. LPS stimulation upregulated IL-10, IL-8, and IL-6 expression and Poly I:C upregulated TLR 8 and TLR 9 expression. This study provides important knowledge on the glycoconjugate expression profile of primary and immortalized BIECs and infectivity and immune responses of primary BIECs to bacterial and viral pathogens or ligands.

AB - In this study, primary and immortalized bovine intestinal epithelial cells (BIECs) were characterized for the expression of surface carbohydrate moieties. Primary BIEC-c4 cells showed staining greater than 90 % for 16 lectins but less than 50 % staining for four lectins. Immortalized BIECs showed significantly different lectin binding profile for few lectins compared to BIEC-c4 cells. BIEC-c4 cells were studied for infectivity to E. coli, Salmonella enterica, bovine rotavirus, bovine coronavirus, and bovine viral diarrhea virus. Bovine strain E. coli B41 adhered to BIEC-c4 cells and Salmonella strains S. Dublin and S. Mbandaka showed strong cell invasion. BIEC-c4 cells were susceptible to bovine rotavirus. LPS stimulation upregulated IL-10, IL-8, and IL-6 expression and Poly I:C upregulated TLR 8 and TLR 9 expression. This study provides important knowledge on the glycoconjugate expression profile of primary and immortalized BIECs and infectivity and immune responses of primary BIECs to bacterial and viral pathogens or ligands.

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KW - Bovine intestinal epithelial cells

KW - Bovine rotavirus

KW - Bovine viral diarrhea virus

KW - Cytokines

KW - Enterotoxigenic E. coli

KW - Lectin binding profile

KW - Salmonella

KW - Toll-like receptors

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VL - 74

JO - Comparative Immunology, Microbiology and Infectious Diseases

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M1 - 101581

ER -

Characterization of bovine ileal epithelial cell line for lectin binding, susceptibility to enteric pathogens, and TLR mediated immune responses

Resumen

Nota bibliográfica

Financiación

ODS de las Naciones Unidas

ASJC Scopus subject areas

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