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IKKβ regulates antimicrobial innate immune responses in the yellow mealworm, Tenebrio molitor

Toll and IMD pathways regulate antimicrobial innate immune responses in insect model systems. The transcriptional activation of antimicrobial peptides (AMPs) confers humoral immunity in the host against invaded pathogens. The IKK kinase complex (IKKα, IKKβ, and the regulatory subunit IKKγ/NEMO) cent...

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Published in:Developmental and comparative immunology 2023-10, Vol.147, p.104761-104761, Article 104761
Main Authors: Ko, Hye Jin, Jang, Ho Am, Park, Ki Beom, Kim, Chang Eun, Patnaik, Bharat Bhusan, Lee, Yong Seok, Han, Yeon Soo, Jo, Yong Hun
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container_title Developmental and comparative immunology
container_volume 147
creator Ko, Hye Jin
Jang, Ho Am
Park, Ki Beom
Kim, Chang Eun
Patnaik, Bharat Bhusan
Lee, Yong Seok
Han, Yeon Soo
Jo, Yong Hun
description Toll and IMD pathways regulate antimicrobial innate immune responses in insect model systems. The transcriptional activation of antimicrobial peptides (AMPs) confers humoral immunity in the host against invaded pathogens. The IKK kinase complex (IKKα, IKKβ, and the regulatory subunit IKKγ/NEMO) centrally regulates the NF-κB response to various stimuli. It triggers an appropriate antimicrobial immune response in the host. In this study, a TmIKKβ (or TmIrd5) homolog was screened from the RNA-seq database of the coleopteran beetle, Tenebrio molitor. A single exon characterizes the TmIKKβ gene, and the open reading frame (ORF) comprises of 2112 bp that putatively encodes a polypeptide of 703 amino acid residues. TmIKKβ contains a serine/threonine kinase domain and is phylogenetically close to Tribolium castaneum IKKβ homolog (TcIKKβ). TmIKKβ transcripts were highly expressed in the early pupal (P1) and adult (A5) stages. Among the tissues, TmIKKβ showed higher expression in the integument of the last instar larvae and the fat body and hemocytes of 5-day-old adults. TmIKKβ mRNA was upregulated post-E. coli challenge to the host. Moreover, RNAi-based TmIKKβ mRNA silencing increased host larvae’ susceptibility against E. coli, S. aureus and C. albicans. TmIKKβ RNAi in the fat body led to a downregulation in mRNA expression of ten out of fourteen AMP genes, including TmTenecin1, -2, and -4; TmDefensin, and -like; TmColeoptericinA, and -B; and TmAttacin1a, -1b, and -2, suggesting the requirement of the gene in antimicrobial innate immune responses. Further, a decrease in the mRNA expression of NF-κB factors such as TmRelish, TmDorsal1, and TmDorsal2 in the fat body of T. molitor larvae was observed post-microorganisms challenge. Thus, TmIKKβ regulates antimicrobial innate immune responses in T. molitor. •We have newly identified IκB kinase β gene from the Tenebrio molitor, named TmIKKβ and domain analysis indicated that it contains one Serine/Threonine protein kinase catalytic domain, suggesting that TmIKKβ may regulate cell signaling by phosphorylation.•The temporal and spatial expression patterns of TmIKKβ transcripts and its induction patterns in responses to microbial challenges indicated that the TmIKKβ may have important roles in development as well as immune responses against microbial challenges.•We have investigated the effects of TmIKKβ RNAi on larval survivability, and expression patterns of antimicrobial peptide (AMP) genes and transcription factors for
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The transcriptional activation of antimicrobial peptides (AMPs) confers humoral immunity in the host against invaded pathogens. The IKK kinase complex (IKKα, IKKβ, and the regulatory subunit IKKγ/NEMO) centrally regulates the NF-κB response to various stimuli. It triggers an appropriate antimicrobial immune response in the host. In this study, a TmIKKβ (or TmIrd5) homolog was screened from the RNA-seq database of the coleopteran beetle, Tenebrio molitor. A single exon characterizes the TmIKKβ gene, and the open reading frame (ORF) comprises of 2112 bp that putatively encodes a polypeptide of 703 amino acid residues. TmIKKβ contains a serine/threonine kinase domain and is phylogenetically close to Tribolium castaneum IKKβ homolog (TcIKKβ). TmIKKβ transcripts were highly expressed in the early pupal (P1) and adult (A5) stages. Among the tissues, TmIKKβ showed higher expression in the integument of the last instar larvae and the fat body and hemocytes of 5-day-old adults. TmIKKβ mRNA was upregulated post-E. coli challenge to the host. Moreover, RNAi-based TmIKKβ mRNA silencing increased host larvae’ susceptibility against E. coli, S. aureus and C. albicans. TmIKKβ RNAi in the fat body led to a downregulation in mRNA expression of ten out of fourteen AMP genes, including TmTenecin1, -2, and -4; TmDefensin, and -like; TmColeoptericinA, and -B; and TmAttacin1a, -1b, and -2, suggesting the requirement of the gene in antimicrobial innate immune responses. Further, a decrease in the mRNA expression of NF-κB factors such as TmRelish, TmDorsal1, and TmDorsal2 in the fat body of T. molitor larvae was observed post-microorganisms challenge. Thus, TmIKKβ regulates antimicrobial innate immune responses in T. molitor. •We have newly identified IκB kinase β gene from the Tenebrio molitor, named TmIKKβ and domain analysis indicated that it contains one Serine/Threonine protein kinase catalytic domain, suggesting that TmIKKβ may regulate cell signaling by phosphorylation.•The temporal and spatial expression patterns of TmIKKβ transcripts and its induction patterns in responses to microbial challenges indicated that the TmIKKβ may have important roles in development as well as immune responses against microbial challenges.•We have investigated the effects of TmIKKβ RNAi on larval survivability, and expression patterns of antimicrobial peptide (AMP) genes and transcription factors for Toll and Imd pathways to understand the critical function of TmIKKβ in antimicrobial immune responses.</description><identifier>ISSN: 0145-305X</identifier><identifier>EISSN: 1879-0089</identifier><identifier>DOI: 10.1016/j.dci.2023.104761</identifier><identifier>PMID: 37331676</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Antimicrobial peptides ; IKK ; Imd pathway ; Innate immunity ; RNAi ; Tenebrio molitor</subject><ispartof>Developmental and comparative immunology, 2023-10, Vol.147, p.104761-104761, Article 104761</ispartof><rights>2023</rights><rights>Copyright © 2023. 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The transcriptional activation of antimicrobial peptides (AMPs) confers humoral immunity in the host against invaded pathogens. The IKK kinase complex (IKKα, IKKβ, and the regulatory subunit IKKγ/NEMO) centrally regulates the NF-κB response to various stimuli. It triggers an appropriate antimicrobial immune response in the host. In this study, a TmIKKβ (or TmIrd5) homolog was screened from the RNA-seq database of the coleopteran beetle, Tenebrio molitor. A single exon characterizes the TmIKKβ gene, and the open reading frame (ORF) comprises of 2112 bp that putatively encodes a polypeptide of 703 amino acid residues. TmIKKβ contains a serine/threonine kinase domain and is phylogenetically close to Tribolium castaneum IKKβ homolog (TcIKKβ). TmIKKβ transcripts were highly expressed in the early pupal (P1) and adult (A5) stages. Among the tissues, TmIKKβ showed higher expression in the integument of the last instar larvae and the fat body and hemocytes of 5-day-old adults. TmIKKβ mRNA was upregulated post-E. coli challenge to the host. Moreover, RNAi-based TmIKKβ mRNA silencing increased host larvae’ susceptibility against E. coli, S. aureus and C. albicans. TmIKKβ RNAi in the fat body led to a downregulation in mRNA expression of ten out of fourteen AMP genes, including TmTenecin1, -2, and -4; TmDefensin, and -like; TmColeoptericinA, and -B; and TmAttacin1a, -1b, and -2, suggesting the requirement of the gene in antimicrobial innate immune responses. Further, a decrease in the mRNA expression of NF-κB factors such as TmRelish, TmDorsal1, and TmDorsal2 in the fat body of T. molitor larvae was observed post-microorganisms challenge. 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The transcriptional activation of antimicrobial peptides (AMPs) confers humoral immunity in the host against invaded pathogens. The IKK kinase complex (IKKα, IKKβ, and the regulatory subunit IKKγ/NEMO) centrally regulates the NF-κB response to various stimuli. It triggers an appropriate antimicrobial immune response in the host. In this study, a TmIKKβ (or TmIrd5) homolog was screened from the RNA-seq database of the coleopteran beetle, Tenebrio molitor. A single exon characterizes the TmIKKβ gene, and the open reading frame (ORF) comprises of 2112 bp that putatively encodes a polypeptide of 703 amino acid residues. TmIKKβ contains a serine/threonine kinase domain and is phylogenetically close to Tribolium castaneum IKKβ homolog (TcIKKβ). TmIKKβ transcripts were highly expressed in the early pupal (P1) and adult (A5) stages. Among the tissues, TmIKKβ showed higher expression in the integument of the last instar larvae and the fat body and hemocytes of 5-day-old adults. TmIKKβ mRNA was upregulated post-E. coli challenge to the host. Moreover, RNAi-based TmIKKβ mRNA silencing increased host larvae’ susceptibility against E. coli, S. aureus and C. albicans. TmIKKβ RNAi in the fat body led to a downregulation in mRNA expression of ten out of fourteen AMP genes, including TmTenecin1, -2, and -4; TmDefensin, and -like; TmColeoptericinA, and -B; and TmAttacin1a, -1b, and -2, suggesting the requirement of the gene in antimicrobial innate immune responses. Further, a decrease in the mRNA expression of NF-κB factors such as TmRelish, TmDorsal1, and TmDorsal2 in the fat body of T. molitor larvae was observed post-microorganisms challenge. Thus, TmIKKβ regulates antimicrobial innate immune responses in T. molitor. •We have newly identified IκB kinase β gene from the Tenebrio molitor, named TmIKKβ and domain analysis indicated that it contains one Serine/Threonine protein kinase catalytic domain, suggesting that TmIKKβ may regulate cell signaling by phosphorylation.•The temporal and spatial expression patterns of TmIKKβ transcripts and its induction patterns in responses to microbial challenges indicated that the TmIKKβ may have important roles in development as well as immune responses against microbial challenges.•We have investigated the effects of TmIKKβ RNAi on larval survivability, and expression patterns of antimicrobial peptide (AMP) genes and transcription factors for Toll and Imd pathways to understand the critical function of TmIKKβ in antimicrobial immune responses.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>37331676</pmid><doi>10.1016/j.dci.2023.104761</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9277-5772</orcidid></addata></record>
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subjects Antimicrobial peptides
IKK
Imd pathway
Innate immunity
RNAi
Tenebrio molitor
title IKKβ regulates antimicrobial innate immune responses in the yellow mealworm, Tenebrio molitor
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