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Toll-Like Receptor 22 in Labeo rohita: Molecular Cloning, Characterization, 3D Modeling, and Expression Analysis Following Ligands Stimulation and Bacterial Infection

Toll-like receptors (TLRs) are a class of innate immune receptors that sense pathogens or their molecular signatures and activate signaling cascades to induce a quick and non-specific immune response in the host. Among various types of TLRs, TLR22 is exclusively present in teleosts and amphibians an...

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Published in:Applied biochemistry and biotechnology 2014-09, Vol.174 (1), p.309-327
Main Authors: Samanta, Mrinal, Swain, Banikalyan, Basu, Madhubanti, Mahapatra, Girishbala, Sahoo, Bikash R, Paichha, Mahismita, Lenka, Saswati S, Jayasankar, Pallipuram
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creator Samanta, Mrinal
Swain, Banikalyan
Basu, Madhubanti
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Sahoo, Bikash R
Paichha, Mahismita
Lenka, Saswati S
Jayasankar, Pallipuram
description Toll-like receptors (TLRs) are a class of innate immune receptors that sense pathogens or their molecular signatures and activate signaling cascades to induce a quick and non-specific immune response in the host. Among various types of TLRs, TLR22 is exclusively present in teleosts and amphibians and is expected to play the distinctive role in innate immunity. This report describes molecular cloning, three-dimensional (3D) modeling, and expression analysis of TLR22 in rohu (Labeo rohita), the most commercially important freshwater fish species in the Indian subcontinent. The open reading frame (ORF) of rohu TLR22 (LrTLR22) comprised of 2,838 nucleotides (nt), encoding 946 amino acid (aa) residues with the molecular mass of ∼107.6 kDa. The secondary structure of deduced LrTLR22 exhibited the presence of signal peptide (1–22 aa), 18 leucine-rich repeat (LRR) regions (79–736 aa), and TIR domain (792–935 aa). The 3D model of LrTLR22-LRR regions together elucidated the horse-shoe-shaped structure having parallel β-strands at the concave surface and few α-helices at the convex surface. The TIR domain structure revealed alternate presence of five α-helices and β-sheets. Phylogenetically, LrTLR22 was closely related to common carp and exhibited significant similarity (92.2 %) and identity (86.1 %) in their amino acids. In rohu, TLR22 was constitutively expressed in all embryonic developmental stages, and tissue-specific analysis illustrated its expression in all examined tissues, highest was in liver and lowest in brain. In vivo modulation of TLR22 gene expression was analyzed by quantitative real-time PCR (qRT-PCR) assay following stimulation with lipopolysaccharide (LPS), synthetic double stranded RNA (polyinosinic-polycytidylic acid), and bacterial (Aeromonas hydrophila) RNA. Among these ligands, bacterial RNA most significantly (p 
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Among various types of TLRs, TLR22 is exclusively present in teleosts and amphibians and is expected to play the distinctive role in innate immunity. This report describes molecular cloning, three-dimensional (3D) modeling, and expression analysis of TLR22 in rohu (Labeo rohita), the most commercially important freshwater fish species in the Indian subcontinent. The open reading frame (ORF) of rohu TLR22 (LrTLR22) comprised of 2,838 nucleotides (nt), encoding 946 amino acid (aa) residues with the molecular mass of ∼107.6 kDa. The secondary structure of deduced LrTLR22 exhibited the presence of signal peptide (1–22 aa), 18 leucine-rich repeat (LRR) regions (79–736 aa), and TIR domain (792–935 aa). The 3D model of LrTLR22-LRR regions together elucidated the horse-shoe-shaped structure having parallel β-strands at the concave surface and few α-helices at the convex surface. The TIR domain structure revealed alternate presence of five α-helices and β-sheets. Phylogenetically, LrTLR22 was closely related to common carp and exhibited significant similarity (92.2 %) and identity (86.1 %) in their amino acids. In rohu, TLR22 was constitutively expressed in all embryonic developmental stages, and tissue-specific analysis illustrated its expression in all examined tissues, highest was in liver and lowest in brain. In vivo modulation of TLR22 gene expression was analyzed by quantitative real-time PCR (qRT-PCR) assay following stimulation with lipopolysaccharide (LPS), synthetic double stranded RNA (polyinosinic-polycytidylic acid), and bacterial (Aeromonas hydrophila) RNA. Among these ligands, bacterial RNA most significantly (p &lt; 0.05) induced TLR22 gene expression in most of the tested tissues. In A. hydrophila infection, induction of TLR22 gene expression was also observed in majority of the tested tissues. Together, these data suggested that in addition to sensing other microbial signatures, TLR22 can recognize bacterial RNA and may play the important role in augmenting innate immunity in fish.</description><identifier>ISSN: 0273-2289</identifier><identifier>EISSN: 1559-0291</identifier><identifier>DOI: 10.1007/s12010-014-1058-0</identifier><identifier>PMID: 25064133</identifier><identifier>CODEN: ABIBDL</identifier><language>eng</language><publisher>Boston: Springer-Verlag</publisher><subject>Aeromonas hydrophila ; Amino acids ; Amphibians ; Animals ; Bacteria ; Bacterial diseases ; Bacterial infections ; Biochemistry ; Biological and medical sciences ; Biotechnology ; brain ; Chemistry ; Chemistry and Materials Science ; Cloning ; Cloning, Molecular ; Cyprinidae - genetics ; Cyprinidae - immunology ; Cyprinidae - metabolism ; Cyprinidae - microbiology ; Cyprinus carpio ; Developmental stages ; embryogenesis ; Fish Diseases - genetics ; Fish Diseases - immunology ; Fish Diseases - microbiology ; Fish Proteins - biosynthesis ; Fish Proteins - chemistry ; Fish Proteins - genetics ; Fish Proteins - immunology ; Freshwater fish ; Fundamental and applied biological sciences. Psychology ; gene expression ; Gene Expression Regulation - genetics ; Gene Expression Regulation - immunology ; Immune response ; Immune system ; innate immunity ; Labeo rohita ; Ligands ; lipopolysaccharides ; liver ; Models, Molecular ; molecular cloning ; molecular weight ; open reading frames ; Pathogens ; phylogeny ; polyinosinic-polycytidylic acid ; Protein Structure, Tertiary ; quantitative analysis ; quantitative polymerase chain reaction ; receptors ; reverse transcriptase polymerase chain reaction ; Ribonucleic acid ; RNA ; signal peptide ; Signal transduction ; Teleostei ; Toll-Like Receptors - biosynthesis ; Toll-Like Receptors - chemistry ; Toll-Like Receptors - genetics ; Toll-Like Receptors - immunology</subject><ispartof>Applied biochemistry and biotechnology, 2014-09, Vol.174 (1), p.309-327</ispartof><rights>Springer Science+Business Media New York 2014</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-c69387176c38ccae9c48d70335a73953652d7fa5c64cece2bce5c62b3f1096ba3</citedby><cites>FETCH-LOGICAL-c529t-c69387176c38ccae9c48d70335a73953652d7fa5c64cece2bce5c62b3f1096ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28799899$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25064133$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Samanta, Mrinal</creatorcontrib><creatorcontrib>Swain, Banikalyan</creatorcontrib><creatorcontrib>Basu, Madhubanti</creatorcontrib><creatorcontrib>Mahapatra, Girishbala</creatorcontrib><creatorcontrib>Sahoo, Bikash R</creatorcontrib><creatorcontrib>Paichha, Mahismita</creatorcontrib><creatorcontrib>Lenka, Saswati S</creatorcontrib><creatorcontrib>Jayasankar, Pallipuram</creatorcontrib><title>Toll-Like Receptor 22 in Labeo rohita: Molecular Cloning, Characterization, 3D Modeling, and Expression Analysis Following Ligands Stimulation and Bacterial Infection</title><title>Applied biochemistry and biotechnology</title><addtitle>Appl Biochem Biotechnol</addtitle><addtitle>Appl Biochem Biotechnol</addtitle><description>Toll-like receptors (TLRs) are a class of innate immune receptors that sense pathogens or their molecular signatures and activate signaling cascades to induce a quick and non-specific immune response in the host. Among various types of TLRs, TLR22 is exclusively present in teleosts and amphibians and is expected to play the distinctive role in innate immunity. This report describes molecular cloning, three-dimensional (3D) modeling, and expression analysis of TLR22 in rohu (Labeo rohita), the most commercially important freshwater fish species in the Indian subcontinent. The open reading frame (ORF) of rohu TLR22 (LrTLR22) comprised of 2,838 nucleotides (nt), encoding 946 amino acid (aa) residues with the molecular mass of ∼107.6 kDa. The secondary structure of deduced LrTLR22 exhibited the presence of signal peptide (1–22 aa), 18 leucine-rich repeat (LRR) regions (79–736 aa), and TIR domain (792–935 aa). The 3D model of LrTLR22-LRR regions together elucidated the horse-shoe-shaped structure having parallel β-strands at the concave surface and few α-helices at the convex surface. The TIR domain structure revealed alternate presence of five α-helices and β-sheets. 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Together, these data suggested that in addition to sensing other microbial signatures, TLR22 can recognize bacterial RNA and may play the important role in augmenting innate immunity in fish.</description><subject>Aeromonas hydrophila</subject><subject>Amino acids</subject><subject>Amphibians</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Bacterial diseases</subject><subject>Bacterial infections</subject><subject>Biochemistry</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>brain</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Cloning</subject><subject>Cloning, Molecular</subject><subject>Cyprinidae - genetics</subject><subject>Cyprinidae - immunology</subject><subject>Cyprinidae - metabolism</subject><subject>Cyprinidae - microbiology</subject><subject>Cyprinus carpio</subject><subject>Developmental stages</subject><subject>embryogenesis</subject><subject>Fish Diseases - genetics</subject><subject>Fish Diseases - immunology</subject><subject>Fish Diseases - microbiology</subject><subject>Fish Proteins - biosynthesis</subject><subject>Fish Proteins - chemistry</subject><subject>Fish Proteins - genetics</subject><subject>Fish Proteins - immunology</subject><subject>Freshwater fish</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gene expression</subject><subject>Gene Expression Regulation - genetics</subject><subject>Gene Expression Regulation - immunology</subject><subject>Immune response</subject><subject>Immune system</subject><subject>innate immunity</subject><subject>Labeo rohita</subject><subject>Ligands</subject><subject>lipopolysaccharides</subject><subject>liver</subject><subject>Models, Molecular</subject><subject>molecular cloning</subject><subject>molecular weight</subject><subject>open reading frames</subject><subject>Pathogens</subject><subject>phylogeny</subject><subject>polyinosinic-polycytidylic acid</subject><subject>Protein Structure, Tertiary</subject><subject>quantitative analysis</subject><subject>quantitative polymerase chain reaction</subject><subject>receptors</subject><subject>reverse transcriptase polymerase chain reaction</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>signal peptide</subject><subject>Signal transduction</subject><subject>Teleostei</subject><subject>Toll-Like Receptors - biosynthesis</subject><subject>Toll-Like Receptors - chemistry</subject><subject>Toll-Like Receptors - genetics</subject><subject>Toll-Like Receptors - immunology</subject><issn>0273-2289</issn><issn>1559-0291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkc1uEzEUhS1ERUPgAdiAJYTEogPX9njGZldCWyoFIdF2PbpxPKmLM07tGUF5IJ4TJxN-xALhjS3f75x77UPIEwavGED9OjEODApgZcFAqgLukQmTUhfANbtPJsBrUXCu9CF5mNINAONK1g_IIZdQlUyICfl-Gbwv5u6zpZ-ssZs-RMo5dR2d48IGGsO16_EN_RC8NYPHSGc-dK5bHdHZNUY0vY3uG_YudEdUvMvc0vpdGbslPfm6iTalXKTHHfq75BI9zQ3Dl4zQuVtlKNGL3q2z9dZjp3o7uqKn511rzfb-ETlo0Sf7eL9PydXpyeXsfTH_eHY-O54XRnLdF6bSQtWsroxQxqDVplTLGoSQWAstRSX5sm5Rmqo0-bV8YWw-84VoGehqgWJKXo6-mxhuB5v6Zu2Ssd5jZ8OQGiarSgmtOfsPVGoApcsqo8__Qm_CEPOH7CglapB5yClhI2ViSCnattlEt8Z41zBotnk3Y95NzrvZ5t1sNU_3zsNibZe_FD8DzsCLPYDJoG8jdsal35yqtVZaZ46PXMqlbmXjHyP-o_uzUdRiaHAVs_HVRYYk5CWhLMUPSrvLdw</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Samanta, Mrinal</creator><creator>Swain, Banikalyan</creator><creator>Basu, Madhubanti</creator><creator>Mahapatra, Girishbala</creator><creator>Sahoo, Bikash R</creator><creator>Paichha, Mahismita</creator><creator>Lenka, Saswati S</creator><creator>Jayasankar, Pallipuram</creator><general>Springer-Verlag</general><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>IQODW</scope><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>3V.</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>7QL</scope><scope>7QO</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>20140901</creationdate><title>Toll-Like Receptor 22 in Labeo rohita: Molecular Cloning, Characterization, 3D Modeling, and Expression Analysis Following Ligands Stimulation and Bacterial Infection</title><author>Samanta, Mrinal ; 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Among various types of TLRs, TLR22 is exclusively present in teleosts and amphibians and is expected to play the distinctive role in innate immunity. This report describes molecular cloning, three-dimensional (3D) modeling, and expression analysis of TLR22 in rohu (Labeo rohita), the most commercially important freshwater fish species in the Indian subcontinent. The open reading frame (ORF) of rohu TLR22 (LrTLR22) comprised of 2,838 nucleotides (nt), encoding 946 amino acid (aa) residues with the molecular mass of ∼107.6 kDa. The secondary structure of deduced LrTLR22 exhibited the presence of signal peptide (1–22 aa), 18 leucine-rich repeat (LRR) regions (79–736 aa), and TIR domain (792–935 aa). The 3D model of LrTLR22-LRR regions together elucidated the horse-shoe-shaped structure having parallel β-strands at the concave surface and few α-helices at the convex surface. The TIR domain structure revealed alternate presence of five α-helices and β-sheets. Phylogenetically, LrTLR22 was closely related to common carp and exhibited significant similarity (92.2 %) and identity (86.1 %) in their amino acids. In rohu, TLR22 was constitutively expressed in all embryonic developmental stages, and tissue-specific analysis illustrated its expression in all examined tissues, highest was in liver and lowest in brain. In vivo modulation of TLR22 gene expression was analyzed by quantitative real-time PCR (qRT-PCR) assay following stimulation with lipopolysaccharide (LPS), synthetic double stranded RNA (polyinosinic-polycytidylic acid), and bacterial (Aeromonas hydrophila) RNA. Among these ligands, bacterial RNA most significantly (p &lt; 0.05) induced TLR22 gene expression in most of the tested tissues. In A. hydrophila infection, induction of TLR22 gene expression was also observed in majority of the tested tissues. Together, these data suggested that in addition to sensing other microbial signatures, TLR22 can recognize bacterial RNA and may play the important role in augmenting innate immunity in fish.</abstract><cop>Boston</cop><pub>Springer-Verlag</pub><pmid>25064133</pmid><doi>10.1007/s12010-014-1058-0</doi><tpages>19</tpages></addata></record>
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ispartof Applied biochemistry and biotechnology, 2014-09, Vol.174 (1), p.309-327
issn 0273-2289
1559-0291
language eng
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source Springer Nature
subjects Aeromonas hydrophila
Amino acids
Amphibians
Animals
Bacteria
Bacterial diseases
Bacterial infections
Biochemistry
Biological and medical sciences
Biotechnology
brain
Chemistry
Chemistry and Materials Science
Cloning
Cloning, Molecular
Cyprinidae - genetics
Cyprinidae - immunology
Cyprinidae - metabolism
Cyprinidae - microbiology
Cyprinus carpio
Developmental stages
embryogenesis
Fish Diseases - genetics
Fish Diseases - immunology
Fish Diseases - microbiology
Fish Proteins - biosynthesis
Fish Proteins - chemistry
Fish Proteins - genetics
Fish Proteins - immunology
Freshwater fish
Fundamental and applied biological sciences. Psychology
gene expression
Gene Expression Regulation - genetics
Gene Expression Regulation - immunology
Immune response
Immune system
innate immunity
Labeo rohita
Ligands
lipopolysaccharides
liver
Models, Molecular
molecular cloning
molecular weight
open reading frames
Pathogens
phylogeny
polyinosinic-polycytidylic acid
Protein Structure, Tertiary
quantitative analysis
quantitative polymerase chain reaction
receptors
reverse transcriptase polymerase chain reaction
Ribonucleic acid
RNA
signal peptide
Signal transduction
Teleostei
Toll-Like Receptors - biosynthesis
Toll-Like Receptors - chemistry
Toll-Like Receptors - genetics
Toll-Like Receptors - immunology
title Toll-Like Receptor 22 in Labeo rohita: Molecular Cloning, Characterization, 3D Modeling, and Expression Analysis Following Ligands Stimulation and Bacterial Infection
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T19%3A45%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Toll-Like%20Receptor%2022%20in%20Labeo%20rohita:%20Molecular%20Cloning,%20Characterization,%203D%20Modeling,%20and%20Expression%20Analysis%20Following%20Ligands%20Stimulation%20and%20Bacterial%20Infection&rft.jtitle=Applied%20biochemistry%20and%20biotechnology&rft.au=Samanta,%20Mrinal&rft.date=2014-09-01&rft.volume=174&rft.issue=1&rft.spage=309&rft.epage=327&rft.pages=309-327&rft.issn=0273-2289&rft.eissn=1559-0291&rft.coden=ABIBDL&rft_id=info:doi/10.1007/s12010-014-1058-0&rft_dat=%3Cproquest_cross%3E1566839921%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c529t-c69387176c38ccae9c48d70335a73953652d7fa5c64cece2bce5c62b3f1096ba3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1558370570&rft_id=info:pmid/25064133&rfr_iscdi=true