Collectin-K1 Plays a Role in the Clearance of Streptococcus agalactiae in Nile Tilapia ( Oreochromis niloticus ).
Jinfeng MoJiadong LiLi QiuYiqing WangLiangliang MuJian-Min YePublished in: International journal of molecular sciences (2024)
Collectin-K1 (CL-K1) is a multifunctional C-type lectin that has been identified as playing a crucial role in innate immunity. It can bind to carbohydrates on pathogens, leading to direct neutralization, agglutination, and/or opsonization, thereby inhibiting pathogenic infection. In this study, we investigated a homolog of CL-K1 ( On CL-K1) in Nile tilapia ( Oreochromis niloticus ) and its role in promoting the clearance of the pathogen Streptococcus agalactiae ( S. agalactiae ) and enhancing the antibacterial ability of the fish. Our analysis of bacterial load displayed that OnCL-K1 substantially reduced the amount of S. agalactiae in tissues of the liver, spleen, anterior kidney, and brain in Nile tilapia. Furthermore, examination of tissue sections revealed that On CL-K1 effectively alleviated tissue damage and inflammatory response in the liver, anterior kidney, spleen, and brain tissue of tilapia following S. agalactiae infection. Additionally, OnCL-K 1 was found to decrease the expression of the pro-inflammatory factor IL-6 and migration inhibitor MIF , while increasing the expression of anti-inflammatory factor IL-10 and chemokine IL-8 in the spleen, anterior kidney, and brain tissues of tilapia. Moreover, statistical analysis of survival rates demonstrated that On CL-K1 significantly improved the survival rate of tilapia after infection, with a survival rate of 90%. Collectively, our findings suggest that On CL-K1 plays a vital role in the innate immune defense of resisting bacterial infection in Nile tilapia. It promotes the removal of bacterial pathogens from the host, inhibits pathogen proliferation in vivo, reduces damage to host tissues caused by pathogens, and improves the survival rate of the host.
Keyphrases
- candida albicans
- inflammatory response
- innate immune
- gene expression
- poor prognosis
- resting state
- white matter
- free survival
- anti inflammatory
- signaling pathway
- gram negative
- oxidative stress
- biofilm formation
- functional connectivity
- antimicrobial resistance
- drug delivery
- binding protein
- escherichia coli
- cystic fibrosis
- cerebral ischemia
- staphylococcus aureus
- multidrug resistant
- lipopolysaccharide induced
- single cell
- mass spectrometry
- cancer therapy
- lps induced
- wound healing