Cargando…

In search of the Aplysia immunome: an in silico study

The immune repertoires of mollusks beyond commercially important organisms such as the pacific oyster Crassostrea gigas or vectors for human pathogens like the bloodfluke planorb Biomphalaria glabrata are understudied. Despite being an important model for neural aging and the role of inflammation in...

Descripción completa

Detalles Bibliográficos
Autor principal: Kron, Nicholas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334734/
https://www.ncbi.nlm.nih.gov/pubmed/35906538
http://dx.doi.org/10.1186/s12864-022-08780-6
_version_ 1784759169686962176
author Kron, Nicholas S.
author_facet Kron, Nicholas S.
author_sort Kron, Nicholas S.
collection PubMed
description The immune repertoires of mollusks beyond commercially important organisms such as the pacific oyster Crassostrea gigas or vectors for human pathogens like the bloodfluke planorb Biomphalaria glabrata are understudied. Despite being an important model for neural aging and the role of inflammation in neuropathic pain, the immune repertoire of Aplysia californica is poorly understood. Recent discovery of a neurotropic nidovirus in Aplysia has highlighted the need for a better understanding of the Aplysia immunome. To address this gap in the literature, the Aplysia reference genome was mined using InterProScan and OrthoFinder for putative immune genes. The Aplysia genome encodes orthologs of all critical components of the classical Toll-like receptor (TLR) signaling pathway. The presence of many more TLRs and TLR associated adapters than known from vertebrates suggest yet uncharacterized, novel TLR associated signaling pathways. Aplysia also retains many nucleotide receptors and antiviral effectors known to play a key role in viral defense in vertebrates. However, the absence of key antiviral signaling adapters MAVS and STING in the Aplysia genome suggests divergence from vertebrates and bivalves in these pathways. The resulting immune gene set of this in silico study provides a basis for interpretation of future immune studies in this important model organism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08780-6.
format Online
Article
Text
id pubmed-9334734
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-93347342022-07-29 In search of the Aplysia immunome: an in silico study Kron, Nicholas S. BMC Genomics Research The immune repertoires of mollusks beyond commercially important organisms such as the pacific oyster Crassostrea gigas or vectors for human pathogens like the bloodfluke planorb Biomphalaria glabrata are understudied. Despite being an important model for neural aging and the role of inflammation in neuropathic pain, the immune repertoire of Aplysia californica is poorly understood. Recent discovery of a neurotropic nidovirus in Aplysia has highlighted the need for a better understanding of the Aplysia immunome. To address this gap in the literature, the Aplysia reference genome was mined using InterProScan and OrthoFinder for putative immune genes. The Aplysia genome encodes orthologs of all critical components of the classical Toll-like receptor (TLR) signaling pathway. The presence of many more TLRs and TLR associated adapters than known from vertebrates suggest yet uncharacterized, novel TLR associated signaling pathways. Aplysia also retains many nucleotide receptors and antiviral effectors known to play a key role in viral defense in vertebrates. However, the absence of key antiviral signaling adapters MAVS and STING in the Aplysia genome suggests divergence from vertebrates and bivalves in these pathways. The resulting immune gene set of this in silico study provides a basis for interpretation of future immune studies in this important model organism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08780-6. BioMed Central 2022-07-29 /pmc/articles/PMC9334734/ /pubmed/35906538 http://dx.doi.org/10.1186/s12864-022-08780-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kron, Nicholas S.
In search of the Aplysia immunome: an in silico study
title In search of the Aplysia immunome: an in silico study
title_full In search of the Aplysia immunome: an in silico study
title_fullStr In search of the Aplysia immunome: an in silico study
title_full_unstemmed In search of the Aplysia immunome: an in silico study
title_short In search of the Aplysia immunome: an in silico study
title_sort in search of the aplysia immunome: an in silico study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334734/
https://www.ncbi.nlm.nih.gov/pubmed/35906538
http://dx.doi.org/10.1186/s12864-022-08780-6
work_keys_str_mv AT kronnicholass insearchoftheaplysiaimmunomeaninsilicostudy