Cargando…

Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor

Although Toll-like receptors have been widely identified and functionally characterized in mammalian models and Drosophila, the immunological function of these receptors in other insects remains unclear. Here, we explored the relevant innate immune response of Tenebrio molitor (T. molitor) Toll-3 ag...

Descripción completa

Detalles Bibliográficos
Autores principales: Ali Mohammadie Kojour, Maryam, Jang, Ho Am, Lee, Yong Seok, Jo, Yong Hun, Han, Yeon Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095136/
https://www.ncbi.nlm.nih.gov/pubmed/37047723
http://dx.doi.org/10.3390/ijms24076751
_version_ 1785024010498605056
author Ali Mohammadie Kojour, Maryam
Jang, Ho Am
Lee, Yong Seok
Jo, Yong Hun
Han, Yeon Soo
author_facet Ali Mohammadie Kojour, Maryam
Jang, Ho Am
Lee, Yong Seok
Jo, Yong Hun
Han, Yeon Soo
author_sort Ali Mohammadie Kojour, Maryam
collection PubMed
description Although Toll-like receptors have been widely identified and functionally characterized in mammalian models and Drosophila, the immunological function of these receptors in other insects remains unclear. Here, we explored the relevant innate immune response of Tenebrio molitor (T. molitor) Toll-3 against Gram-negative bacteria, Gram-positive bacteria, and fungal infections. Our findings indicated that TmToll-3 expression was mainly induced by Candida albicans infections in the fat bodies, gut, Malpighian tubules, and hemolymph of young T. molitor larvae. Surprisingly, Escherichia coli systemic infection caused mortality after TmToll-3 knockdown via RNA interference (RNAi) injection, which was not observed in the control group. Further analyses indicated that in the absence of TmToll-3, the final effector of the Toll signaling pathway, antimicrobial peptide (AMP) genes and relevant transcription factors were significantly downregulated after E. coli challenge. Our results indicated that the expression of almost all AMP genes was suppressed in silenced individuals, whereas the expression of relevant genes was positively regulated after fungal injection. Therefore, this study revealed the immunological involvement of TmToll-3 in T. molitor in response to systematic infections.
format Online
Article
Text
id pubmed-10095136
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-100951362023-04-13 Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor Ali Mohammadie Kojour, Maryam Jang, Ho Am Lee, Yong Seok Jo, Yong Hun Han, Yeon Soo Int J Mol Sci Article Although Toll-like receptors have been widely identified and functionally characterized in mammalian models and Drosophila, the immunological function of these receptors in other insects remains unclear. Here, we explored the relevant innate immune response of Tenebrio molitor (T. molitor) Toll-3 against Gram-negative bacteria, Gram-positive bacteria, and fungal infections. Our findings indicated that TmToll-3 expression was mainly induced by Candida albicans infections in the fat bodies, gut, Malpighian tubules, and hemolymph of young T. molitor larvae. Surprisingly, Escherichia coli systemic infection caused mortality after TmToll-3 knockdown via RNA interference (RNAi) injection, which was not observed in the control group. Further analyses indicated that in the absence of TmToll-3, the final effector of the Toll signaling pathway, antimicrobial peptide (AMP) genes and relevant transcription factors were significantly downregulated after E. coli challenge. Our results indicated that the expression of almost all AMP genes was suppressed in silenced individuals, whereas the expression of relevant genes was positively regulated after fungal injection. Therefore, this study revealed the immunological involvement of TmToll-3 in T. molitor in response to systematic infections. MDPI 2023-04-04 /pmc/articles/PMC10095136/ /pubmed/37047723 http://dx.doi.org/10.3390/ijms24076751 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ali Mohammadie Kojour, Maryam
Jang, Ho Am
Lee, Yong Seok
Jo, Yong Hun
Han, Yeon Soo
Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor
title Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor
title_full Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor
title_fullStr Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor
title_full_unstemmed Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor
title_short Innate Immune Response of TmToll-3 Following Systemic Microbial Infection in Tenebrio molitor
title_sort innate immune response of tmtoll-3 following systemic microbial infection in tenebrio molitor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095136/
https://www.ncbi.nlm.nih.gov/pubmed/37047723
http://dx.doi.org/10.3390/ijms24076751
work_keys_str_mv AT alimohammadiekojourmaryam innateimmuneresponseoftmtoll3followingsystemicmicrobialinfectionintenebriomolitor
AT janghoam innateimmuneresponseoftmtoll3followingsystemicmicrobialinfectionintenebriomolitor
AT leeyongseok innateimmuneresponseoftmtoll3followingsystemicmicrobialinfectionintenebriomolitor
AT joyonghun innateimmuneresponseoftmtoll3followingsystemicmicrobialinfectionintenebriomolitor
AT hanyeonsoo innateimmuneresponseoftmtoll3followingsystemicmicrobialinfectionintenebriomolitor