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BmPGPR-L4 is a negative regulator of the humoral immune response in the silkworm Bombyx mori.

Authors :
Yang W
Lin Y
He Y
Li Q
Chen W
Lin Q
Swevers L
Liu J
Source :
Archives of insect biochemistry and physiology [Arch Insect Biochem Physiol] 2024 Feb; Vol. 115 (2), pp. e22093.
Publication Year :
2024

Abstract

Toll, immune deficiency and prophenoloxidase cascade represent vital immune signaling pathways in insects. Peptidoglycan recognition proteins (PGRPs) are innate immune receptors that activate and regulate the immune signaling pathways. Previously, we reported that BmPGPR-L4 was induced in the silkworm Bombyx mori larvae by bacteria and peptidoglycan challenges. Here, we focused on the function of BmPGRP-L4 in regulating the expression of antimicrobial peptides (AMPs). The hemolymph from BmPGRP-L4-silenced larvae exhibited an enhanced inhibitory effect on the growth of Escherichia coli, either by growth curve or inhibitory zone experiments. Coincidentally, most of the AMP genes were upregulated after RNAi of BmPGRP-L4. Oral administration of heat-inactivated E. coli and Staphylococcus aureus after RNAi of BmPGRP-L4 resulted in the increased expression of BmPGRP-L4 in different tissues of the silkworm larvae, revealing an auto-regulatory mechanism. By contrast, the expression of most AMP genes was downregulated by oral bacterial administration after RNAi of BmPGRP-L4. The above results demonstrate that BmPGRP-L4 recognizes bacterial pathogen-associated molecular patterns and negatively regulates AMP expression to achieve immunological homeostasis. As a negative regulator, BmPGPR-L4 is proposed to be involved in the feedback regulation of the immune signaling pathways of the silkworm to prevent excessive activation of the immune response.<br /> (© 2024 Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1520-6327
Volume :
115
Issue :
2
Database :
MEDLINE
Journal :
Archives of insect biochemistry and physiology
Publication Type :
Academic Journal
Accession number :
38409870
Full Text :
https://doi.org/10.1002/arch.22093