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| Main Authors: | , , , , , , |
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| Format: | Artículo científico |
| Language: | en |
| Published: |
Biology
2025
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| Online Access: | https://pubmed.ncbi.nlm.nih.gov/40906104/ |
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| _version_ | 1868266157464616962 |
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| author | Yang, Yanjian Zhang, Guanrong Xu, Ruilong Deng, Yiyang Mo, Zequan Li, Yanwei Dan, Xueming |
| author_facet | Yang, Yanjian Zhang, Guanrong Xu, Ruilong Deng, Yiyang Mo, Zequan Li, Yanwei Dan, Xueming Yang, Yanjian Zhang, Guanrong Xu, Ruilong Deng, Yiyang Mo, Zequan Li, Yanwei Dan, Xueming |
| collection | PubMed - marine biology |
| contents | Proteomic and Functional Analysis Reveals Temperature-Driven Immune Evasion Strategies of in Yellowfin Seabream (). Yang, Yanjian Zhang, Guanrong Xu, Ruilong Deng, Yiyang Mo, Zequan Li, Yanwei Dan, Xueming () is a globally significant aquatic pathogen responsible for severe economic losses in aquaculture. While the infection often exhibits distinct seasonal patterns strongly correlated with water temperature, there is limited knowledge regarding the temperature-dependent immune evasion strategies of . Our results demonstrated a striking temperature-dependent virulence phenotype, with significantly higher mortality rates observed at high temperature (HT, 33 °C) compared to low temperature (LT, 23 °C). Proteomic analysis revealed temperature-dependent upregulation of key virulence factors, including streptolysin S-related proteins (SagG, SagH), antioxidant-related proteins (SodA), and multiple capsular polysaccharide (cps) synthesis proteins (cpsD, cpsH, cpsL, cpsY). Flow cytometry analysis showed that HT infection significantly reduced the percentage of lymphocyte and myeloid cell populations in the head kidney leukocytes of , which was associated with elevated expression and increased apoptosis. In addition, HT infection significantly inhibited the release of reactive oxygen species (ROS) but not nitric oxide (NO) production. Using cps-deficient mutant, Δcps, we demonstrated that the cps is essential for temperature-dependent phagocytosis resistance in , as phagocytic activity against Δcps remained unchanged across temperatures, while NS-1 showed significantly reduced uptake at HT. These findings provide new insights into the immune evasion of under thermal regulation, deepening our understanding of the thermal adaptation of aquatic bacterial pathogens. |
| format | Artículo científico |
| id | pubmed_40906104 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | Biology |
| record_format | pubmed |
| spellingShingle | Proteomic and Functional Analysis Reveals Temperature-Driven Immune Evasion Strategies of in Yellowfin Seabream (). Yang, Yanjian Zhang, Guanrong Xu, Ruilong Deng, Yiyang Mo, Zequan Li, Yanwei Dan, Xueming Proteomic and Functional Analysis Reveals Temperature-Driven Immune Evasion Strategies of in Yellowfin Seabream (). Yang, Yanjian Zhang, Guanrong Xu, Ruilong Deng, Yiyang Mo, Zequan Li, Yanwei Dan, Xueming () is a globally significant aquatic pathogen responsible for severe economic losses in aquaculture. While the infection often exhibits distinct seasonal patterns strongly correlated with water temperature, there is limited knowledge regarding the temperature-dependent immune evasion strategies of . Our results demonstrated a striking temperature-dependent virulence phenotype, with significantly higher mortality rates observed at high temperature (HT, 33 °C) compared to low temperature (LT, 23 °C). Proteomic analysis revealed temperature-dependent upregulation of key virulence factors, including streptolysin S-related proteins (SagG, SagH), antioxidant-related proteins (SodA), and multiple capsular polysaccharide (cps) synthesis proteins (cpsD, cpsH, cpsL, cpsY). Flow cytometry analysis showed that HT infection significantly reduced the percentage of lymphocyte and myeloid cell populations in the head kidney leukocytes of , which was associated with elevated expression and increased apoptosis. In addition, HT infection significantly inhibited the release of reactive oxygen species (ROS) but not nitric oxide (NO) production. Using cps-deficient mutant, Δcps, we demonstrated that the cps is essential for temperature-dependent phagocytosis resistance in , as phagocytic activity against Δcps remained unchanged across temperatures, while NS-1 showed significantly reduced uptake at HT. These findings provide new insights into the immune evasion of under thermal regulation, deepening our understanding of the thermal adaptation of aquatic bacterial pathogens. |
| title | Proteomic and Functional Analysis Reveals Temperature-Driven Immune Evasion Strategies of in Yellowfin Seabream (). |
| url | https://pubmed.ncbi.nlm.nih.gov/40906104/ |