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Published on: October 4, 2024
Lipopolysaccharide elicits expression of immune-related genes in the silkworm, Bombyx mori
H Tanaka1, A Sagisaka, K Fujita
1Innate Immunity Research Unit, National Institute of Agrobiological Sciences, Ibaraki, Japan.
Abstract:
Lipopolysaccharide (LPS), a major cell wall component of gram-negative bacteria, was found to be unable to activate immune-related genes in Drosophila melanogaster. In contrast, highly purified LPS elicited immune-related gene expression in the fat body of Bombyx mori. However, the level of activation by highly purified LPS was lower than crude LPS and peptidoglycan. Furthermore, synthetic lipid A also activated these genes, suggesting that B. mori possesses unknown signal pathways to activate immune-related genes by LPS. Up-regulation of antimicrobial peptide genes by highly purified LPS was not confirmed in the immune-responsive cell line, NIAS-Bm-aff3, suggesting that some factors necessary for signal transduction activated by LPS are deficient in this cell line.
Insights
Lipopolysaccharide (LPS) activates immune genes in silkworms (Bombyx mori) but not fruit flies (Drosophila melanogaster), indicating unique insect immune pathways. Further research is needed to identify the specific signaling mechanisms in B. mori.
Area of Science:
- Insect immunology
- Molecular biology
- Biochemistry
Background:
- Lipopolysaccharide (LPS) is a key component of gram-negative bacterial cell walls.
- LPS recognition is crucial for innate immunity in many organisms.
- Previous studies have shown varied responses to LPS across different insect species.
Purpose of the Study:
- To investigate the immune response of Bombyx mori (silkworm) to lipopolysaccharide (LPS).
- To compare LPS-induced immune gene expression in B. mori with Drosophila melanogaster.
- To explore potential novel signaling pathways involved in LPS recognition in insects.
Main Methods:
- Treatment of B. mori with highly purified LPS, crude LPS, and peptidoglycan.
- Analysis of immune-related gene expression in the fat body of B. mori.
- Treatment of the NIAS-Bm-aff3 immune-responsive cell line with highly purified LPS.
- Investigation of synthetic lipid A's effect on gene expression.
Main Results:
- Highly purified LPS induced immune-related gene expression in B. mori fat body, unlike in D. melanogaster.
- The activation level by purified LPS was lower than crude LPS and peptidoglycan.
- Synthetic lipid A also activated immune genes in B. mori.
- No significant up-regulation of antimicrobial peptide genes was observed in the NIAS-Bm-aff3 cell line upon LPS treatment.
Conclusions:
- Bombyx mori possesses distinct signaling pathways for LPS-mediated immune gene activation.
- The immune-deficient cell line NIAS-Bm-aff3 may lack essential factors for LPS signal transduction.
- Further studies are required to elucidate the specific molecular mechanisms of LPS recognition and signaling in B. mori.

