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Critical Roles of Spätzle5 in Antimicrobial Peptide Production Against Escherichia coli in Tenebrio molitor Malpighian Tubules.

Authors :
Ali Mohammadie Kojour, Maryam
Edosa, Tariku Tesfaye
Jang, Ho Am
Keshavarz, Maryam
Jo, Yong Hun
Han, Yeon Soo
Source :
Frontiers in Immunology; 12/16/2021, Vol. 12, p1-18, 18p
Publication Year :
2021

Abstract

The dimeric cytokine ligand Spätzle (Spz) is responsible for Toll pathway activation and antimicrobial peptide (AMP) production upon pathogen challenge in Tenebrio molitor. Here, we indicated that Tm Spz5 has a functional role in response to bacterial infections. We showed that the highest expression of TmSpz5 is induced by Candida albicans. However, TmSpz5 knockdown reduced larval survival against Escherichia coli and Staphylococcus aureus. To evaluate the molecular mechanism underlying the observed survival differences, the role of TmSpz5 in AMP production was examined by RNA interference and microbial injection. T. molitor AMPs that are active against Gram-negative and -positive bacteria, including Tm tenecins, Tm attacins, Tm coleoptericins, Tm taumatin-like-proteins, and Tm cecropin-2, were significantly downregulated by TmSpz-5 RNAi in the Malpighian tubules (MTs) following a challenge with E. coli and S. aureus. However, upon infection with C. albicans the mRNA levels of most AMPs in the ds TmSpz5 -injected group were similar to those in the control groups. Likewise, the expression of the transcription factors NF-κB, TmDorX2 , and TmRelish were noticeably suppressed in the MTs of TmSpz5 -silenced larvae. Moreover, E. coli -infected TmSpz5 knockdown larvae showed decreased antimicrobial activity in the MTs and hindgut compared with the control group. These results demonstrate that Tm Spz5 has a defined role in T. molitor innate immunity by regulating AMP expression in MTs in response to E. coli. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16643224
Volume :
12
Database :
Complementary Index
Journal :
Frontiers in Immunology
Publication Type :
Academic Journal
Accession number :
154181897
Full Text :
https://doi.org/10.3389/fimmu.2021.760475