HbpA from Glaesserella parasuis induces an inflammatory response in 3D4/21 cells by activating the MAPK and NF-κB signalling pathways and protects mice against G. parasuis when used as an immunogen.


Journal

Veterinary research
ISSN: 1297-9716
Titre abrégé: Vet Res
Pays: England
ID NLM: 9309551

Informations de publication

Date de publication:
29 Jul 2024
Historique:
received: 22 01 2024
accepted: 17 06 2024
medline: 30 7 2024
pubmed: 30 7 2024
entrez: 29 7 2024
Statut: epublish

Résumé

Glaesserella parasuis is usually a benign swine commensal in the upper respiratory tract, but virulent strains can cause systemic infection characterized by pneumonia, meningitis, and fibrinous polyserositis. The intensive pulmonary inflammatory response following G. parasuis infection is the main cause of lung injury and death in pigs. Vaccination has failed to control the disease due to the lack of extended cross-protection. Accumulating evidence indicates that the heme-binding protein A (HbpA) is a potential virulence determinant and a promising antigen candidate for the development of a broader range of vaccines. However, it is not yet known whether HbpA contributes to G. parasuis virulence or has any potential immune protective effects against G. parasuis. Here, we show that HbpA can induce the transcription and secretion of proinflammatory cytokines (IL-6, TNF-α, and MCP-1) in porcine alveolar macrophages (PAM, 3D4/31). The HbpA protein is recognized by Toll-like receptors 2 and 4 on 3D4/21 macrophages, resulting in the activation of MAP kinase and NF-κB signalling cascades and the transcription and secretion of proinflammatory cytokines. HbpA contributes to virulence and bacterial pulmonary colonization in C57BL/6 mice and plays a role in adhesion to host cells and evasion of the bactericidal effect of pulmonary macrophages. In addition, mice immunized with HbpA were partially protected against challenge by G. parasuis SC1401. The results suggest that HbpA plays an important role in the pathogenesis of disease caused by G. parasuis and lay a foundation for the development of a subunit or chimeric anti-G. parasuis vaccine.

Identifiants

pubmed: 39075605
doi: 10.1186/s13567-024-01344-4
pii: 10.1186/s13567-024-01344-4
doi:

Substances chimiques

NF-kappa B 0
Bacterial Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

93

Subventions

Organisme : Key R & D support plan of Chengdu Science and Technology Bureau
ID : 2022-YF05-00817-SN

Informations de copyright

© 2024. The Author(s).

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Auteurs

Zhen Yang (Z)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Yiwen Zhang (Y)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Qin Zhao (Q)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Senyan Du (S)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Xiaobo Huang (X)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Rui Wu (R)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Qigui Yan (Q)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Xinfeng Han (X)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.

Yiping Wen (Y)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China. wyp@sicau.edu.cn.

San-Jie Cao (SJ)

Research Center of Swine Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China. csanjie@sicau.edu.cn.

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