4.6 Article

Expression and functional analysis of the BCL2-Associated agonist of cell death (BAD) gene in grass carp (Ctenopharyngodon idella) during bacterial infection

Journal

DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
Volume 123, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dci.2021.104160

Keywords

Ctenopharyngodon idella; BAD1; Immune response; Mitochondrial apoptosis pathway

Funding

  1. National Natural Science Foundation of China [31902409, 31872606, 31572657, U1701233]
  2. Foundation of Guangdong Provincial Marine and Fisheries Bureau [GDME-2018C006, D21822202]
  3. Foundation of China-ASEAN Maritime Cooperation [CAMC-2018F]
  4. Guangdong Provincial Special Fund For Modern Agriculture Industry Technology Innovation Teams [2019KJ141]
  5. Pearl River Scholarship from Guangdong Province

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In this study, the BAD gene GcBAD1 was cloned and characterized for the first time in grass carp, showing widespread expression in various tissues and significant up-regulation during infection. Overexpression of GcBAD1 also activated apoptosis-related genes and played a role in the mitochondrial apoptosis pathway of grass carp's innate immunity.
The BCL2-associated agonist of cell death protein is a key participant in apoptosis dependent on mitochondria and in disease progression that involves the regulation of cell death, such as tumorigenesis, diabetes, sepsis shock, and epilepsy. Nevertheless, the mechanisms underlying the immune responses to teleost BAD bacterial infection and mitochondrial-dependent apoptosis remains unclear. In order to elucidate the mechanisms involved, in this study, a Ctenopharyngodon idella (grass carp) BAD gene named GcBAD1 was firstly cloned and characterized. The results indicated that the ORF (open reading frame) of GcBAD1 was 438 bp in length, encoding a 145-amino acid putative protein of 16.66 kDa. This deduced amino acid sequence has a better identity than another teleost species according to a phylogenetic analysis, and contains a Bcl2-BAD-1 domain. In healthy grass carp fish, the mRNA transcripts of GcBAD1 were widely present in the studied tissues, which could be ranked as follows; spleen > brain > middle-kidney > head-kidney > liver > gills > intestines > heart and muscle. In addition, during infection by Aeromonas hydrophila and Staphylococcus aureus, the mRNA transcription and protein levels expression of GcBAD1 in the head-kidney, spleen, and liver tissues of the fish were significantly up-regulated. Moreover, when the C. idellus kidney cell line (CIK) cells were incubated with Lipopolysaccharide (LPS) and lipoteichoic acid (LTA), the GcBAD1 expression transcripts were also significantly up-regulated. Additionally, overexpression of GcBAD1 in CIK cells was able to activate apoptosis-related genes, including those encoding p53, Cytochrome C (CytoC), caspase-3, and caspase-9. Besides, in the TUNEL assays, when pEGFPBAD1 was over-expressed, the number of red signals associated with apoptosis were significantly increased in the CIK cells infected with LPS or LTA at 12 h. This study demonstrates that GcBAD1 has a significant role in the mitochondrial apoptosis pathway of grass carp's innate immunity. Our findings provide new insight into the potential mechanisms of teleost antibacterial immunity.

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