AI Article Synopsis

  • - Glaesserella parasuis is a bacterial pathogen that causes Glässer's disease in piglets, leading to potential immunosuppression, prompting researchers to study its effects on the immune response.
  • - In a controlled experiment, 20 piglets were divided into infection and control groups to analyze changes in spleen immune cell differentiation and PD-1/PD-L1 expression after being infected with the bacteria.
  • - The study discovered significant differences in protein expression in the spleen tissue of infected piglets, with 596 proteins showing changes linked to immune responses, marking the first investigation of PD-1/PD-L1 in the context of immunosuppression in piglets.

Article Abstract

Glaesserella parasuis, an important respiratory bacterial pathogen, causes Glässer's disease in piglets, with potential immunosuppression. We established a piglet infection model and explored the immunosuppression mechanism to improve our understanding of the host immune response to G. parasuis. Twenty piglets were randomly divided into two groups (n = 10). The infection group was intraperitoneally challenged with 2 × 10 CFU of G. parasuis in 2 mL TSB. The control group was intraperitoneally injected with equivalent TSB. After 72 h, the piglets were sacrificed, and spleen tissue was collected. PD-1/PD-L1 expression was determined. The splenocytes were isolated to detect CD3 T, CD3CD4 T, CD3CD8 T and CD3CD21cell differentiation. Via data-independent acquisition (DIA), we compared the proteomics of healthy and infected spleen tissues. Glaesserella parasuis modified CD3 T, CD3CD4 T, CD3CD8 T and CD3CD21 cell differentiation and PD-1/PD-L1 expression in the spleen. The infection group had 596 proteins with significant differences in expression, of which 301 were significantly upregulated and 295 downregulated. Differentially expressed proteins (DEPs) were mainly related to immune responses. This is the first study on PD-1/PD-L1 expression in the spleen associated with immunosuppression in a piglet model to explore the protein changes related to immune responses via DIA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10998357PMC
http://dx.doi.org/10.1186/s12917-024-03993-1DOI Listing

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