4.6 Article

The selective regulation of immune responses by matrix metalloproteinase MMP14 in Ostrinia furnacalis

Journal

INSECT SCIENCE
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1111/1744-7917.13202

Keywords

antimicrobial peptide; cecropin; lysozyme; MMP14; phenoloxidase; RNAi

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This study investigates the role of MMP14 in immune responses and antimicrobial activity in Ostrinia furnacalis larvae. The knockdown of MMP14 in the larvae reduces phenoloxidase (PO) activity and Cecropin expression, while enhancing the expressions of Lysozyme, Attacin, Gloverin, and Moricin. The knockdown of MMP14 also decreases larvae survival to bacterial infections.
Matrix metalloproteinases (MMPs) are crucial for tissue remodeling and immune responses in insects, yet it remains unclear how MMPs affect the various immune processes against pathogenic infections and whether the responses vary among insects. In this study, we used the lepidopteran pest Ostrinia furnacalis larvae to address these questions by examining the changes of immune-related gene expression and antimicrobial activity after the knockdown of MMP14 and bacterial infections. We identified MMP14 in O. furnacalis using the rapid amplification of complementary DNA ends (RACE), and found that it was conserved and belonged to the MMP1 subfamily. Our functional investigations revealed that MMP14 is an infection-responsive gene, and its knockdown reduces phenoloxidase (PO) activity and Cecropin expression, while the expressions of Lysozyme, Attacin, Gloverin, and Moricin are enhanced after MMP14 knockdown. Further PO and lysozyme activity determinations showed consistent results with gene expression of these immune-related genes. Finally, the knockdown of MMP14 decreased larvae survival to bacterial infections. Taken together, our data indicate that MMP14 selectively regulates the immune responses, and is required to defend against bacterial infections in O. furnacalis larvae. Conserved MMPs may serve as a potential target for pest control using a combination of double-stranded RNA and bacterial infection.

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