Molecular and functional characterization of two IgM subclasses in large yellow croaker (Larimichthys crocea)

As the predominant immunoglobulin (Ig) isotype, IgM plays a crucial role in the acquired immunity of vertebrates. There is only one Igμ gene in mammals, except cattle, while the number of Igμ gene varies among teleost fish. In the current study, we found two functional Igμ genes (Igμ1 and Igμ2) and...

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Veröffentlicht in:Fish & shellfish immunology 2023-03, Vol.134, p.108581-108581, Article 108581
Hauptverfasser: Cui, Zhengwei, Zhao, Han, Chen, Xinhua
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Chen, Xinhua
description As the predominant immunoglobulin (Ig) isotype, IgM plays a crucial role in the acquired immunity of vertebrates. There is only one Igμ gene in mammals, except cattle, while the number of Igμ gene varies among teleost fish. In the current study, we found two functional Igμ genes (Igμ1 and Igμ2) and a pseudo Cμ gene (ψIgμ) in large yellow croaker (Larimichthys crocea). Both Igμ1 and Igμ2 genes possessed two transcript variants, which encoded the heavy chains of secreted (sIgM1 and sIgM2) and membrane-bound IgM1 and IgM2 (mIgM1 and mIgM2), respectively. Both the heavy chains of sIgM1 and sIgM2 consisted of a variable Ig domain, four constant Ig domains (CH1, CH2, CH3 and CH4) and a secretory tail, while those of mIgM1 and mIgM2 consisted of a variable Ig domain, three constant Ig domains (CH1, CH2 and CH3), a transmembrane domain and a short cytoplasmic tail. Cysteine residues that are necessary for the formation of intrachain and interchain disulfide bonds and tryptophan residues that are important for the folding of the Ig superfamily domain were well conserved in large yellow croaker IgM1 and IgM2. Interestingly, large yellow croaker IgM2 had an extra cysteine (C94) in the CH1 domain compared with IgM1, which may cause the structural difference between IgM1 and IgM2. A liquid chromatography–tandem mass spectrometry analysis revealed that both IgM1 and IgM2 were present at the protein level in large yellow croaker serum. Both the Igμ1 and Igμ2 genes were mainly expressed in systemic immune tissues, such as head kidney and spleen, but the expression level of Igμ2 was much lower than that of Igμ1. After Pseudomonas plecoglossicida infection, the expression levels of Igμ1 and Igμ2 in both the spleen and head kidney were significantly upregulated, with a higher upregulation of Igμ2 than that of Igμ1. These results suggested that Igμ1 and Igμ2 may play a differential role in the immune response of large yellow croaker against bacterial infection. •Two functional IgM subclasses in large yellow croaker were identified at the genome, mRNA and protein levels.•The expression level of Igμ2 in all tested tissues was much lower than that of Igμ1.•Igμ1 and Igμ2 can be induced by Pseudomonas plecoglossicida.
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There is only one Igμ gene in mammals, except cattle, while the number of Igμ gene varies among teleost fish. In the current study, we found two functional Igμ genes (Igμ1 and Igμ2) and a pseudo Cμ gene (ψIgμ) in large yellow croaker (Larimichthys crocea). Both Igμ1 and Igμ2 genes possessed two transcript variants, which encoded the heavy chains of secreted (sIgM1 and sIgM2) and membrane-bound IgM1 and IgM2 (mIgM1 and mIgM2), respectively. Both the heavy chains of sIgM1 and sIgM2 consisted of a variable Ig domain, four constant Ig domains (CH1, CH2, CH3 and CH4) and a secretory tail, while those of mIgM1 and mIgM2 consisted of a variable Ig domain, three constant Ig domains (CH1, CH2 and CH3), a transmembrane domain and a short cytoplasmic tail. Cysteine residues that are necessary for the formation of intrachain and interchain disulfide bonds and tryptophan residues that are important for the folding of the Ig superfamily domain were well conserved in large yellow croaker IgM1 and IgM2. Interestingly, large yellow croaker IgM2 had an extra cysteine (C94) in the CH1 domain compared with IgM1, which may cause the structural difference between IgM1 and IgM2. A liquid chromatography–tandem mass spectrometry analysis revealed that both IgM1 and IgM2 were present at the protein level in large yellow croaker serum. Both the Igμ1 and Igμ2 genes were mainly expressed in systemic immune tissues, such as head kidney and spleen, but the expression level of Igμ2 was much lower than that of Igμ1. After Pseudomonas plecoglossicida infection, the expression levels of Igμ1 and Igμ2 in both the spleen and head kidney were significantly upregulated, with a higher upregulation of Igμ2 than that of Igμ1. These results suggested that Igμ1 and Igμ2 may play a differential role in the immune response of large yellow croaker against bacterial infection. •Two functional IgM subclasses in large yellow croaker were identified at the genome, mRNA and protein levels.•The expression level of Igμ2 in all tested tissues was much lower than that of Igμ1.•Igμ1 and Igμ2 can be induced by Pseudomonas plecoglossicida.</description><identifier>ISSN: 1050-4648</identifier><identifier>EISSN: 1095-9947</identifier><identifier>DOI: 10.1016/j.fsi.2023.108581</identifier><identifier>PMID: 36754157</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>adaptive immunity ; Animals ; Bacterial infection ; bacterial infections ; blood serum ; Cattle ; Cattle Diseases ; Cysteine ; disulfides ; domain ; fish ; Fish Diseases ; Fish Proteins - genetics ; genes ; IgM ; immune response ; Immunoglobulin M - genetics ; immunoglobulins ; kidneys ; Large yellow croaker ; Larimichthys crocea ; liquid chromatography ; Mammals - metabolism ; Perciformes ; Phylogeny ; protein content ; Pseudomonas plecoglossicida ; shellfish ; spleen ; superfamily ; tandem mass spectrometry ; tryptophan</subject><ispartof>Fish &amp; shellfish immunology, 2023-03, Vol.134, p.108581-108581, Article 108581</ispartof><rights>2023 Elsevier Ltd</rights><rights>Copyright © 2023 Elsevier Ltd. 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There is only one Igμ gene in mammals, except cattle, while the number of Igμ gene varies among teleost fish. In the current study, we found two functional Igμ genes (Igμ1 and Igμ2) and a pseudo Cμ gene (ψIgμ) in large yellow croaker (Larimichthys crocea). Both Igμ1 and Igμ2 genes possessed two transcript variants, which encoded the heavy chains of secreted (sIgM1 and sIgM2) and membrane-bound IgM1 and IgM2 (mIgM1 and mIgM2), respectively. Both the heavy chains of sIgM1 and sIgM2 consisted of a variable Ig domain, four constant Ig domains (CH1, CH2, CH3 and CH4) and a secretory tail, while those of mIgM1 and mIgM2 consisted of a variable Ig domain, three constant Ig domains (CH1, CH2 and CH3), a transmembrane domain and a short cytoplasmic tail. Cysteine residues that are necessary for the formation of intrachain and interchain disulfide bonds and tryptophan residues that are important for the folding of the Ig superfamily domain were well conserved in large yellow croaker IgM1 and IgM2. Interestingly, large yellow croaker IgM2 had an extra cysteine (C94) in the CH1 domain compared with IgM1, which may cause the structural difference between IgM1 and IgM2. A liquid chromatography–tandem mass spectrometry analysis revealed that both IgM1 and IgM2 were present at the protein level in large yellow croaker serum. Both the Igμ1 and Igμ2 genes were mainly expressed in systemic immune tissues, such as head kidney and spleen, but the expression level of Igμ2 was much lower than that of Igμ1. After Pseudomonas plecoglossicida infection, the expression levels of Igμ1 and Igμ2 in both the spleen and head kidney were significantly upregulated, with a higher upregulation of Igμ2 than that of Igμ1. These results suggested that Igμ1 and Igμ2 may play a differential role in the immune response of large yellow croaker against bacterial infection. •Two functional IgM subclasses in large yellow croaker were identified at the genome, mRNA and protein levels.•The expression level of Igμ2 in all tested tissues was much lower than that of Igμ1.•Igμ1 and Igμ2 can be induced by Pseudomonas plecoglossicida.</description><subject>adaptive immunity</subject><subject>Animals</subject><subject>Bacterial infection</subject><subject>bacterial infections</subject><subject>blood serum</subject><subject>Cattle</subject><subject>Cattle Diseases</subject><subject>Cysteine</subject><subject>disulfides</subject><subject>domain</subject><subject>fish</subject><subject>Fish Diseases</subject><subject>Fish Proteins - genetics</subject><subject>genes</subject><subject>IgM</subject><subject>immune response</subject><subject>Immunoglobulin M - genetics</subject><subject>immunoglobulins</subject><subject>kidneys</subject><subject>Large yellow croaker</subject><subject>Larimichthys crocea</subject><subject>liquid chromatography</subject><subject>Mammals - metabolism</subject><subject>Perciformes</subject><subject>Phylogeny</subject><subject>protein content</subject><subject>Pseudomonas plecoglossicida</subject><subject>shellfish</subject><subject>spleen</subject><subject>superfamily</subject><subject>tandem mass spectrometry</subject><subject>tryptophan</subject><issn>1050-4648</issn><issn>1095-9947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtv2zAUhYkiRZ24_QFdAo7JIJcUH5KQKQjyMGCjSzsTfFzZdGQxIaUE7q8vBbsd24nkxTkHPPdD6CslC0qo_LZbtMkvSlKy_K5FTT-gc0oaUTQNr86muyAFl7yeoYuUdoQQyST5hGZMVoJTUZ2j_Tp0YMdOR6x7h9uxt4MPve6w3eqo7QDR_9LTCIcWD-8BLzdrnEZjO50SJOx7nM0bwAfouvCObQz6GSK-Wuno995uh-0hTVML-voz-tjqLsGX0zlHPx_uf9w9Favvj8u721VhWS2HwohW0kqWRjgrmJECuHM2l2mIpi0VpmwcUE00VMY4lrtY00hWMkJryQRnc3R1zH2J4XWENKi9TzZ_UPcQxqTKmvGS8mkf_5VWFa8bSSqWpfQozW1SitCql1xRx4OiRE1A1E5lIGoCoo5AsufyFD-aPbi_jj8EsuDmKIC8jzcPUSXrobfgfAQ7KBf8P-J_A0K3m6s</recordid><startdate>202303</startdate><enddate>202303</enddate><creator>Cui, Zhengwei</creator><creator>Zhao, Han</creator><creator>Chen, Xinhua</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0003-0020-6829</orcidid></search><sort><creationdate>202303</creationdate><title>Molecular and functional characterization of two IgM subclasses in large yellow croaker (Larimichthys crocea)</title><author>Cui, Zhengwei ; Zhao, Han ; Chen, Xinhua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-b5f61762b5dc53b65e4ddc05090a1f15b29de1a0ae7bbd3754cb9632301863543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>adaptive immunity</topic><topic>Animals</topic><topic>Bacterial infection</topic><topic>bacterial infections</topic><topic>blood serum</topic><topic>Cattle</topic><topic>Cattle Diseases</topic><topic>Cysteine</topic><topic>disulfides</topic><topic>domain</topic><topic>fish</topic><topic>Fish Diseases</topic><topic>Fish Proteins - genetics</topic><topic>genes</topic><topic>IgM</topic><topic>immune response</topic><topic>Immunoglobulin M - genetics</topic><topic>immunoglobulins</topic><topic>kidneys</topic><topic>Large yellow croaker</topic><topic>Larimichthys crocea</topic><topic>liquid chromatography</topic><topic>Mammals - metabolism</topic><topic>Perciformes</topic><topic>Phylogeny</topic><topic>protein content</topic><topic>Pseudomonas plecoglossicida</topic><topic>shellfish</topic><topic>spleen</topic><topic>superfamily</topic><topic>tandem mass spectrometry</topic><topic>tryptophan</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cui, Zhengwei</creatorcontrib><creatorcontrib>Zhao, Han</creatorcontrib><creatorcontrib>Chen, Xinhua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Fish &amp; shellfish immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cui, Zhengwei</au><au>Zhao, Han</au><au>Chen, Xinhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular and functional characterization of two IgM subclasses in large yellow croaker (Larimichthys crocea)</atitle><jtitle>Fish &amp; shellfish immunology</jtitle><addtitle>Fish Shellfish Immunol</addtitle><date>2023-03</date><risdate>2023</risdate><volume>134</volume><spage>108581</spage><epage>108581</epage><pages>108581-108581</pages><artnum>108581</artnum><issn>1050-4648</issn><eissn>1095-9947</eissn><abstract>As the predominant immunoglobulin (Ig) isotype, IgM plays a crucial role in the acquired immunity of vertebrates. There is only one Igμ gene in mammals, except cattle, while the number of Igμ gene varies among teleost fish. In the current study, we found two functional Igμ genes (Igμ1 and Igμ2) and a pseudo Cμ gene (ψIgμ) in large yellow croaker (Larimichthys crocea). Both Igμ1 and Igμ2 genes possessed two transcript variants, which encoded the heavy chains of secreted (sIgM1 and sIgM2) and membrane-bound IgM1 and IgM2 (mIgM1 and mIgM2), respectively. Both the heavy chains of sIgM1 and sIgM2 consisted of a variable Ig domain, four constant Ig domains (CH1, CH2, CH3 and CH4) and a secretory tail, while those of mIgM1 and mIgM2 consisted of a variable Ig domain, three constant Ig domains (CH1, CH2 and CH3), a transmembrane domain and a short cytoplasmic tail. Cysteine residues that are necessary for the formation of intrachain and interchain disulfide bonds and tryptophan residues that are important for the folding of the Ig superfamily domain were well conserved in large yellow croaker IgM1 and IgM2. Interestingly, large yellow croaker IgM2 had an extra cysteine (C94) in the CH1 domain compared with IgM1, which may cause the structural difference between IgM1 and IgM2. A liquid chromatography–tandem mass spectrometry analysis revealed that both IgM1 and IgM2 were present at the protein level in large yellow croaker serum. Both the Igμ1 and Igμ2 genes were mainly expressed in systemic immune tissues, such as head kidney and spleen, but the expression level of Igμ2 was much lower than that of Igμ1. After Pseudomonas plecoglossicida infection, the expression levels of Igμ1 and Igμ2 in both the spleen and head kidney were significantly upregulated, with a higher upregulation of Igμ2 than that of Igμ1. These results suggested that Igμ1 and Igμ2 may play a differential role in the immune response of large yellow croaker against bacterial infection. •Two functional IgM subclasses in large yellow croaker were identified at the genome, mRNA and protein levels.•The expression level of Igμ2 in all tested tissues was much lower than that of Igμ1.•Igμ1 and Igμ2 can be induced by Pseudomonas plecoglossicida.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>36754157</pmid><doi>10.1016/j.fsi.2023.108581</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-0020-6829</orcidid></addata></record>
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subjects adaptive immunity
Animals
Bacterial infection
bacterial infections
blood serum
Cattle
Cattle Diseases
Cysteine
disulfides
domain
fish
Fish Diseases
Fish Proteins - genetics
genes
IgM
immune response
Immunoglobulin M - genetics
immunoglobulins
kidneys
Large yellow croaker
Larimichthys crocea
liquid chromatography
Mammals - metabolism
Perciformes
Phylogeny
protein content
Pseudomonas plecoglossicida
shellfish
spleen
superfamily
tandem mass spectrometry
tryptophan
title Molecular and functional characterization of two IgM subclasses in large yellow croaker (Larimichthys crocea)
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