NOD-like receptor repertoire in the chromosome-level genome of the demosponge Dysidea avara (Schmidt, 1862)

Porifera, one of the earliest diverging metazoans, have shown a surprisingly complex immune repertoire. However, most information to date is based on <i>de novo</i> transcriptome assemblies, limiting our knowledge regarding the presence and evolution of poriferan immune repertoire. Here, we generated the chromosome-level genome of the demosponge <i>Dysidea avara</i>, a target species in studies on symbiosis and differential expression of immune genes. We examined the presence and the number of common immune protein domains in the annotated genome of <i>D. avara</i>, and we further focused on NOD-like Receptors (NLRs), which are one of the most expanded immune receptors in Porifera according to previous reports on draft genomes and transcriptome assemblies. <i>Dysidea avara</i> has a 575 Mb genome with N50 41Mb, 162 scaffolds, and 15 chromosomes. We additionally recovered 37 sequences corresponding to microbial genomes, including complete bacterial and viral genomes. Based on the presence of conserved domains, we detected a large number of immune receptors and other immune genes in <i>D. avara</i> genome, such as 14 TIR, 39 CARD, 128 DEATH, and 230 NACHT domain-containing genes. Based on their architecture, we identified a large expansion of <i>bona fide</i> NLRs (i.e., 126 NACHT+LRR domain-containing genes); of which, 20 included a N-terminal CARD domain (NLRC), and 25 included a N-terminal DEATH domain (NLRD). In <i>D. avara</i>, the different NLR categories (i.e., NLRX, NLRC and NLRD) formed distinct phylogenetic clusters, while the NLR phylogenetic analysis across sponge chromosome-level genomes indicated that NLRs were mainly grouped by species rather than category. The NLRX category was the most expanded, while the NLRC category was absent in 7 out of 11 studied sponge genomes. These observations indicate that the diversification of NLRs in sponges, most likely derived from the ancestor NLRX, responds to species-specific selective pressures related to their immunity. This is the first study characterizing sponge NLR diversity in a chromosome-level genome, enhancing our knowledge of NLR evolution in the ancient phylum Porifera.

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Journal
Frontiers in Immunology
Published
2026-02-03
DOI
https://doi.org/10.3389/fimmu.2026.1725140
Primary Topic
Invertebrate Immune Response Mechanisms
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article
Field-Weighted Citation Impact
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article

NOD-like receptor repertoire in the chromosome-level genome of the demosponge Dysidea avara (Schmidt, 1862)

U Hentschel, Montserrat Torres-Oliva, André Franke, Ángela M. Marulanda-Gómez et al.
Frontiers in Immunology
Invertebrate Immune Response Mechanisms
article

NOD-like receptor repertoire in the chromosome-level genome of the demosponge Dysidea avara (Schmidt, 1862)

U Hentschel, Montserrat Torres-Oliva, André Franke, Ángela M. Marulanda-Gómez, Vasiliki Koutsouveli, Janina Fuß, Ruth A. Schmitz, Lucía Pita, Thorsten B. H. Reusch
article en

Abstract

Porifera, one of the earliest diverging metazoans, have shown a surprisingly complex immune repertoire. However, most information to date is based on <i>de novo</i> transcriptome assemblies, limiting our knowledge regarding the presence and evolution of poriferan immune repertoire. Here, we generated the chromosome-level genome of the demosponge <i>Dysidea avara</i>, a target species in studies on symbiosis and differential expression of immune genes. We examined the presence and the number of common immune protein domains in the annotated genome of <i>D. avara</i>, and we further focused on NOD-like Receptors (NLRs), which are one of the most expanded immune receptors in Porifera according to previous reports on draft genomes and transcriptome assemblies. <i>Dysidea avara</i> has a 575 Mb genome with N50 41Mb, 162 scaffolds, and 15 chromosomes. We additionally recovered 37 sequences corresponding to microbial genomes, including complete bacterial and viral genomes. Based on the presence of conserved domains, we detected a large number of immune receptors and other immune genes in <i>D. avara</i> genome, such as 14 TIR, 39 CARD, 128 DEATH, and 230 NACHT domain-containing genes. Based on their architecture, we identified a large expansion of <i>bona fide</i> NLRs (i.e., 126 NACHT+LRR domain-containing genes); of which, 20 included a N-terminal CARD domain (NLRC), and 25 included a N-terminal DEATH domain (NLRD). In <i>D. avara</i>, the different NLR categories (i.e., NLRX, NLRC and NLRD) formed distinct phylogenetic clusters, while the NLR phylogenetic analysis across sponge chromosome-level genomes indicated that NLRs were mainly grouped by species rather than category. The NLRX category was the most expanded, while the NLRC category was absent in 7 out of 11 studied sponge genomes. These observations indicate that the diversification of NLRs in sponges, most likely derived from the ancestor NLRX, responds to species-specific selective pressures related to their immunity. This is the first study characterizing sponge NLR diversity in a chromosome-level genome, enhancing our knowledge of NLR evolution in the ancient phylum Porifera.

Frontiers in ImmunologyVol. 17
Carl von Ossietzky Universität Oldenburg (DE), Christian-Albrechts-Universität zu Kiel (DE), GEOMAR Helmholtz Centre for Ocean Research Kiel (DE), National Research Council (LK)
Deutsche Forschungsgemeinschaft, Agencia Estatal de Investigación, European Social Fund
Openalex Percentile: Top 68%
Invertebrate Immune Response Mechanisms
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