Immunoglobulin T from sea bass (Dicentrarchus labrax L.): molecular characterization, tissue localization and expression after nodavirus infection
- Francesco Buonocore†1Email authorView ORCID ID profile,
- Valentina Stocchi†1,
- Noelia Nunez-Ortiz1,
- Elisa Randelli1,
- Marco Gerdol2,
- Alberto Pallavicini2,
- Angelo Facchiano3,
- Chiara Bernini1,
- Laura Guerra1,
- Giuseppe Scapigliati1 and
- Simona Picchietti1
© The Author(s) 2017
Received: 21 November 2016
Accepted: 11 March 2017
Published: 15 March 2017
Immunoglobulins (Igs) are fundamental components of the adaptive immune system of vertebrates, with the IgT/IgZ isotype specific of Teleosts. In this paper we describe the identification of an IgT heavy chain from the European sea bass (Dicentrarchus labrax L.), its molecular characterization and tissue mRNA localization by in situ hybridization.
Sea bass IgT consists of 552 aa (Accession Number KM410929) and it contains a putative 19 amino acids long signal peptide and one potential N-glycosylation site. The C-region consists of four CH domains; each contains the cysteine and tryptophan residues required for their correct folding. Based on the recent sequencing of sea bass genome, we have identified five different genomic contigs bearing exons unequivocally pertaining to IgT (CH2, CH3 and CH4), but none corresponded to a complete IgH locus as IgT sequences were found in the highly fragmented assembled genomic regions which could not be assigned to any major scaffold. The 3D structure of sea bass IgT has been modelled using the crystal structure of a mouse Ig gamma as a template, thus showing that the amino acid sequence is suitable for the expected topology referred to an immunoglobulin-like architecture. The basal expression of sea bass IgT and IgM in different organs has been analysed: gut and gills, important mucosal organs, showed high IgT transcripts levels and this was the first indication of the possible involvement of sea bass IgT in mucosal immune responses. Moreover, sea bass IgT expression increased in gills and spleen after infection with nodavirus, highlighting the importance of IgT in sea bass immune responses. In situ hybridization confirmed the presence of IgT transcripts in the gut and it revealed a differential expression along the intestinal tract, with a major expression in the posterior intestine, suggesting the hindgut as a site for the recruitment of IgT+ cells in this species. IgT transcripts were also found in gill filaments and parallel lamellae and, for the first time, we identified scattered IgT positive cells in the liver, with a strong signal in the hepatic parenchyma.
In conclusion, we performed a full molecular characterization of IgT in sea bass that points out its possible involvement in mucosal immune responses of this species.
Immunoglobulins (Igs) are critical factors of the adaptive immune system and they have been found in all vertebrates with jaws (gnathostomes) investigated to date . Igs are composed of two heavy (H) and two light (L) chains and their repertoire is obtained through the recombination of variable (V), diversity (D) and joining (J) gene segments . Different Igs isotypes have been identified in vertebrates, like: IgM, that is considered the most present within all species ; IgD, one of the less studied ; IgW, found in cartilaginous fish and in lungfish [5, 6]; IgY, found in amphibians, reptiles and birds ; IgG, IgE and IgA, found in mammals , and IgF, only found in amphibians .
In teleost fish only the presence of two Ig isotypes was recognized until about 10 years ago: IgM, a tetrameric molecule highly used to verify the specific immune-response against pathogens being the most abundant Ig in the serum , and IgD, a monomeric immunoglobulin whose function still needs to be fully characterized . But in 2005 a new Ig was found at the same time in rainbow trout (Onchorynchus mykiss) and in zebrafish (Danio rerio) and named in two different ways: IgT (from trout, ) and IgZ (from zebrafish, ), respectively. After that, other IgT/IgZ sequences have been identified in different fish species such as in fugu (Fugu rubripes) , carp (Cyprinus carpio) , stickleback (Gasterosteus aculeatus) , Atlantic salmon (Salmo salar) [16, 17], Pacific bluefin tuna (Thunnus orientalis)  and, recently, in the emerald rockcod (Trematomus bernacchii)  and in the Atlantic salmon (Salmo salar) . Only in catfish (Ictalurus punctatus) and medaka (Oryzias latipes), until now, appear to lack IgT orthologous genes [21, 22]. The functional characterization of IgT has been first performed in rainbow trout, where it has been considered mainly involved in mucosal immunity, thanks to the production of both polyclonal and monoclonal antibodies against this molecule . The trout IgT was found in serum as a monomer, but not in gut mucus where it was identified as a tetramer with the different IgT monomers associated by non-covalent bonds [24, 25]. Moreover, IgT levels in gut mucus were double compared to serum IgT and even the ratio IgT/IgM was much higher in gut mucus compared to serum . Another important finding was that IgT+ B cells could be considered as a new B cell lineage as they did not express either IgM or IgD transcripts . Finally, with regard to the response against pathogens, IgT was demonstrated to be specifically involved in gut response against the parasite Ceratomyxa shasta  and in gills and skin response against the parasitic ciliate Ichthyophthirius multifiliis [26, 27] in rainbow trout and in head kidney response against the ectoparasite Argulus siamensis in rohu (Labeo rohita) . Moreover, using homozygous isogenic rainbow trout, it was demonstrated that the variable heavy chain domain repertoires of IgT in spleen are induced in spleen after viral infection , whereas in the Chines perch (Siniperca chuatsi) IgT expression in different tissues was modulated in a different way compared to IgM and IgD after vaccination with Flavobacterium columnare .
In the present work we identified an IgT from sea bass (Dicentrarchus labrax L.) and we characterized this immunoglobulin from a molecular point of view even by analysing in detail its 3D structure and by investigating its basal expression and distribution in mucosal and not-mucosal tissues by real-time PCR and in situ hybridization. The obtained results are of high interest for a view on the possible function of IgT in sea bass especially taking into consideration the involvement of the mucosal tissues in the immune response against pathogens and the high impact and economic value of this species in the Mediterranean aquaculture.
Sea bass IgT cloning
A partial secretory IgT nucleotide sequence was identified after the analysis of a sea bass gills transcriptome . From this sequence two primers were designed (IGTFW 5′-GACCAACTGTGTTTCCTCTGATGC-3′ and IGTRV 5′-GCCATCCTTATAGATGCCAGGGGA-3′) and used in RT-PCR on total RNA extracted with Trisure (Bio-line) solution from gills of a juvenile sea bass (200 g of weight). Leukocytes from sea bass gills were obtained following previously described procedures . RT-PCR was performed using Ready-To-Go RT-PCR Beads (GE Healthcare) and an amplicon of 1034 bp was obtained. The cycling protocol was one cycle of 94 °C for 5 min, 35 cycles of 94 °C for 45 s, 55 °C for 45 s, 72 °C for 45 s, followed by one cycle of 72 °C for 10 min. PCR products (10 μl) were visualised on 1% (w/v) agarose gels containing Gel Red stain (Biotium) and using hyperladder IV (Bioline) as size marker. Controls for the presence of DNA contamination were performed using the RNA samples as template in the PCR cycle. The DNA amplified by PCR was purified using the QIAquick Gel Extraction Kit (QIAgen), inserted into the pGEM-T Easy vector (Promega) and transformed into competent JM109 Escherichia coli cells. Plasmid DNA from at least three independent clones was purified using the Wizard Plus SV Minipreps DNA Purification System (Promega) and sequenced using MWG DNA Sequencing Services. The generated sequence was analysed for similarity with other known sequences using the BLAST program .
A RACE-PCR using the FirstChoice RLM-RACE kit (Ambion) was performed to obtain the complete secretory IgT sequence. For 5′ RACE, first stand cDNA was synthesized from total gills RNA after adding the 5′ RACE adapter to RNA following the manufacturer’s instruction. A PCR was performed using this cDNA with the IGT1RV1 primer (5′-GAGTGAGTAGACAGGACTGGG-3′), designed on the already known partial IgT sequence, and the 5′ RACE Outer primer of the RLM-RACE kit (5′-GCTGATGGCGATGAATGAACACTG-3′). A 709 bp amplicon containing the 5′ end of the IgT sequence was obtained. For 3′ RACE, first-strand cDNA was obtained using the 3′ RACE adapter following the manufacturer’s instruction. A PCR was performed using this cDNA with the IGT1FW primer (5′-CTCCCTGCCACTCAGTGCG-3′), designed on the already known partial IgT sequence, and the 3′ RACE Outer primer of the kit (5′-GCGAGCACAGAATTAATACGACT-3′). A 701 bp amplicon containing the 5′ end of the IgT sequence was obtained.
The full-length secretory IgT sequence was analysed for the presence of a signal peptide, using SignalP software , and of N-glycosylation sites (with the NetNGlyc 1.0 Server). Alignment of the sea bass IgT amino acid sequences to other known molecules from other species and phylogenetic tree with IgT, IgM and IgD sequences were carried out using MEGA 4.1 Software .
Three-dimensional modelling of sea bass IgT
Molecular modelling of sea bass IgT has been performed by comparative modelling technique. The search for template structures has been performed by means of BLAST (http://www.blast.ncbi.lnm.nih.gov) by selecting the Protein Data Bank archive. The results suggested the structure of mouse IgG as a template. The crystallographic structure is deposited with PDB id code 1IGT . The 1IGT structure includes four Ig chains: B chain has been used as template for the modelling of 3D structure of sea bass IgT.
Modelling has been performed by using Modeller 9.12 . The modelling protocol used, as assessed in our lab from previous studies (see  as an example), implies firstly the generation of ten models, and, successively, the selection of the best one in terms of structural quality. Stereochemistry analyses and energy evaluations have been obtained by Vadar web server  and ProsaWeb . Further structural analyses and visualization have been performed by Discovery Studio (Dassault Systèmes BIOVIA, Discovery Studio Modelling Environment, Release 4.5, San Diego: Dassault Systèmes, 2015).
Sea bass IgT basal expression analysis
To study the IgT basal expression, four sea bass juveniles were sampled and leucocytes from different tissues [brain, spleen, gut, head kidney (HK), gills, thymus and liver] obtained as described before . Total RNA was isolated from each tissue separately with Trisure (Bioline), suspended in DEPC treated water and used for real-time quantitative PCR without pooling the tissue samples coming from the different fishes. For reverse transcription, the BioScript RNase H minus (Bioline) enzyme was used following the manufacturer’s instruction. The expression level of IgT transcript was determined with a Mx3000PTM real time PCR system (Stratagene) equipped with version 4.1 software and using the Brilliant SYBR Green Q-PCR Master Mix (Agilent Technologies) following the manufacturer’s instructions, with ROX as internal passive reference dye. Specific PCR primers were designed for the amplification of 200 bp products from IgT (IgTFW2 5′-CGGACTTCATTCAGTACCCTG-3′ and IgTRV2 5′-CAACTGTACACATCAGGGCC-3′) and 18S ribosomal RNA (18SFW: 5′-CCAACGAGCTGCTGACC-3′; 18SRV: 5′-CCGTTACCCGTGGTCC-3′), used as house-keeping gene. The primers were selected to amplify a region of the IgT conserved domain that was present in all cloned IgT isoforms. The expression of IgM (Accession Number FN908858) in the same samples was monitored using the primers: IGFW 5′-GAGCTGCAGAAGGACAGTG-3′ and IGRV 5′-TCAGACTGGCCTCACAGCT-3′). 10 ng of cDNA template was used in each PCR reaction. The PCR conditions were 95 °C for 10 min, followed by 35 cycles of 95 °C for 45 s, 52 °C for 45 s and 72 °C for 45 s. Triplicate reactions were performed for each template cDNA and the template was replaced with water in all blank control reactions. The analysis was carried out using the endpoints method option that causes the collection of the fluorescence data at the end of each extension stage of amplification. A relative quantitation has been performed, comparing the levels of the target transcripts (IgT and IgM) to a reference transcript (calibrator, in this case the IgT and IgM expression in the brain, respectively). A normalizer target (18S ribosomal RNA) is included to correct for differences in total cDNA input between samples. The results are expressed as the mean ± SD of the results obtained from the four considered fishes.
Sea bass IgT expression after infection with nodavirus
The in vivo IgT and IgM expression was investigated on larvae sea bass specimens experimentally infected with viral encephalopathy and retinopathy virus (VERv) or nervous necrosis virus (NNV), a virus belonging to the Nodaviridae family, genus Betanodavirus, that is one of the most significant viral pathogens for finfish (see ). Briefly, 200 sea bass individuals (30–40 g) were injected intramuscularly (i.m.) with PBS, whereas all fish from other tanks (200 + 200 individuals) were injected i.m. with VERv (104 TCID50/ml-1). The virus dose was tested to induce low mortality in sea bass. For gene expression analyses, fish fish/group/time points (0, 24, 48 and 72 h after injection) were sampled and from each individual fish spleen, gills and muscle were removed. RNA extraction, cDNA preparation and real time PCR analysis were performed as described above using as calibrator one muscle from the time 0 control. The results were expressed as the mean ± SD of the results obtained from four fishes and the differences from the control were considered significant if p < 0.05 using the two-way ANOVA analysis following by Bonferroni’s post-test.
In situ hybridization (ISH) for sea bass IgT
Synthesis of RNA probes
Cells from gills, gut and liver of sea bass juveniles (20–30 g) were obtained by tissue teasing and suspended in Tripure (Roche). Total RNA was extracted following manufacturer’s instructions and isolated in DEPC treated water. RT-PCR was performed with Ready-To-Go RT-PCR beads (Amersham) using 1 μg total RNA and 0.5 μg random primers [pd(N)6] in a total 50 μl volume. The primers IgTISHFW (5′-GATGTAGCTGGCACTACCT-3′) and IgTISHRW (5′-TCTCTAGCAGCAGAACAGC-3′) were designed to amplify a 426 bp product corresponding to the constant region of sea bass IgT. Reactions were run using the Mastercycler personal (Eppendorf). The cycling protocol was: 1 cycle of 94 °C for 5 min, 35 cycles of 94 °C for 45 s, 55 °C for 45 s, 72 °C for 45 s, followed by 1 cycle of 72 °C for 10 min. PCR products (15 ml) were visualised on 1% agarose gels containing ethidium bromide (10 ng/ml) using Hyperladder IV (Bioline) as size marker. DNA amplified by PCR was purified using the QIAquick Gel Extraction Kit (QIAgen), inserted into the pGEM-T Easy vector (Promega) and transfected into competent JM109 E. coli cells. Plasmid DNA from three independent clones was purified using the Wizard Plus SV Minipreps DNA Purification System (Promega) and sequenced using MWG DNA Sequencing Services. Sequences generated were analysed for similarity with other known sequences using the BLAST program.
The anti-sense probe was obtained using the selected plasmid clone as target in a PCR reaction with primers IgTISHFW and SP6 (5′-GCATTTAGGTGACACTATAGAATAG-3′). The cycling protocol was: 1 cycle of 94 °C for 5 min, 35 cycles of 94 °C for 45 s, 48 °C for 45 s, 72 °C for 45 s, followed by 1 cycle of 72 °C for 10 min. The sense probe (for negative control of ISH) was obtained using the selected plasmid clone as target in a PCR reaction with primers T7 (5′-TAATACGACTCACTATAGGG-3′) and IgTISHRW. The cycling protocol was: 1 cycle of 94 °C for 5 min, 35 cycles of 94 °C for 45 s, 54 °C for 45 s, 72 °C for 45 s, followed by 1 cycle of 72 °C for 10 min. The fragments obtained were purified by Quick Clean Kit (Bioline) and used to synthesize digoxigenin-labeled RNA probes with the DIG-RNA Labeling Kit (Roche) following manufacturer′s instructions.
Dissected gills, gut (anterior, middle and posterior portions) and liver from 1 year-old specimens (N = 20) were fixed overnight at room temperature in 4% paraformaldehyde in 0.01 M, pH 7.4 phosphate-buffered saline (PBS) and gradually dehydrated before paraffin wax embedding. Serial sections (5 μm) were collected on poly-l-lysine coated slides, air-dried overnight at 37 °C and stored at room temperature for subsequent investigation. Sections were dewaxed with xylene, rehydrated in graded ethanol series and DEPC treated water, and then washed with water before proteinase K (Sigma-Aldrich) digestion. The concentration of proteinase K was 1 μg/ml. The digestion was stopped by immersion in cold DEPC water. Acetylation was performed by incubating sections in 0.25% acetic anhydride in 85 mM Tris–HCl buffer containing 0.2% acetic acid and 0.02 M ethylenediaminetetraacetic acid (EDTA) for 10 min. The sections were washed with DEPC water and gradually dehydrated. A dilution profile was performed for the probes with concentrations varying from 0.3 to 0.6 ng/μl and the optimal one resulted 0.45 ng/μl. Following overnight incubation at 45 °C, the sections were washed with 2× saline-sodium citrate (SSC) buffer at room temperature, then with 0.2× SSC at 55 °C for 90 min and incubated in 20 μg/ml RNAaseA in 0.01 M Tris–HCl containing 0.5 M NaCl and 1 mM EDTA for 30 min. Sections were transferred to Buffer 1 (0.1 M Tris containing 0.15 M NaCl and 1% blocking reagent) for 1 h, then to Buffer 2 (0.1 M Tris containing 0.15 M NaCl, 0.5% BSA and 0.3% Triton X-100) for 30 min. The sections were incubated for 2 h at room temperature with alkaline phosphatase-conjugated anti-digoxigenin antibody (Fab fragment; Roche Diagnostic, Germany) diluted 1:1000 in Buffer 2, then washed with 0.1 M Tris containing 0.15 M NaCl and Buffer 3 (0.1 M Tris containing 0.1 M NaCl and 50 mM MgCl2). Bound antibody was localized using nitro blue tetrazolium chloride and 5-bromo-4-chloro-3-indolyl-phosphate (Roche Diagnostic, Germany) incubating the sections overnight at room temperature. Thereafter, sections were washed in distilled water and mounted with 50% glycerol. Light microscopy images were captured using a computer-assisted image analysis system which includes a Zeiss microscope equipped with a colour video camera (Axio Cam MRC, Arese, Milano Italy) and a software package (KS 300 and AxioVision).
Sea bass IgT cloning
Moreover, we analysed the organization of the sea bass IgT CH exons based on its recently sequenced genome . Despite this chromosome-scale effort was able to place about 85% of the assembled genomic regions to the 24 sea bass chromosomes, about 15% of the genome sequence consists of relatively small contigs which could not be placed to any major scaffold. Curiously, all the IgT CH exons we identified in sea bass are confined to this portion of the genome, suggesting that they may be present in multiple, nearly identical copies, or surrounded by highly repetitive DNA regions which makes quite complicated the assembly of these genomic regions in larger scaffolds. As a matter of fact, we could identify at least five different genomic contigs bearing exons unequivocally pertaining to IgT (CH2, CH3 and CH4), and none of these contigs corresponded to a complete IgH locus. Due to the high apparent fragmentation of IgH loci in the sea bass genome, it remains impossible to establish, based on the data currently available, whether these assembled genomic sequences correspond to five distinct IgT genes and how many IgH loci are actually present in sea bass. The presence of multiple IgT genes, organized in different IgH loci, has been previously reported in other teleosts fish, including salmon (8 genes in two distinct loci)  and even in Eupercaria, such as, stickleback (4 genes in four distinct loci) . The complete cloned sequence of the sea bass IgT corresponds almost perfectly to one of the identified IgT genes, with the exception of a few SNPs located at the 3′ of the coding sequence.
Three-dimensional modelling of sea bass IgT
IgT basal expression analysis
Sea bass IgT expression after infection with nodavirus
In situ hybridization (ISH) for sea bass IgT
In this paper we described the identification of an IgT heavy chain from sea bass (D. labrax L.) and we performed its molecular characterization, its expression analysis in different un-stimulated organs and tissues and after in vivo infection with nodavirus and, finally, its localization by in situ hybridisation to preliminary investigate the functional activities of this molecule.
The complete sequence of the secreted IgT heavy chain, obtained from gills cDNA, is composed of 552 aa and its conserved region is constituted of four domains as it happens in all Teleost sequences identified until now except for Fugu  and stickleback . In all sequences the CH1, which shows high similarity with the CH1 region of IgM, and the CH4 are conserved; this aspect may be related to their possible role in binding to Ig light chains (CH1) or to other Ig heavy chains (CH4) through inter-chain disulphide bonds . In the recent identified IgT from an Antarctic fish, the Trematomus bernacchii, we have a peculiar situation with the lack of most of the second constant domain that maintained only few amino acid residues . The performed phylogenetic analysis (Fig. 2) showed that sea bass IgT sequence clustered with IgT sequence from other Perciformes, whereas the sequences from Cypriniformes resulted quite different from the other teleost IgT and were located in a different clade.
The 3D structure of sea bass IgT has been generated with the template structure of a mouse Ig, which results best template available in PDB. Intra-chain S–S bonds are similarly located in the four domains, while differences are found between the two sequences for the position of other cysteines not involved in intra-chain S–S bonds. In mouse Ig gamma, Cys128 forms an inter-chain S–S bond with Cys214 of the light chain (A chain in the PDB file). In similar position, sea bass IgT has Cys123 in the CH1 domain, not involved in intra-chain bonds that could be suitable for an inter-chain bond. Cys19 and Cys20 residues in sea bass IgT do not appear able to form intra-chain bonds, and they have no corresponding Cys residue in the mouse sequence. On the contrary, mouse Ig gamma has three Cys residues in position 237, 240, and 242, not involved in intra-chain bonds, for which there is no corresponding Cys residue in sea bass IgT. These residues in mouse IgG form inter-chain S–S bonds with the corresponding residue (i.e., Cys237 of B chain linked to Cys237 of D chain) of another Ig gamma heavy chain in the crystallographic structure. The modelling of the multimeric structure of sea bass IgT was not possible in the absence of the light chain sequence; therefore, for the same reason, it was not possible to more deeply check the suitability of the model to form inter-chain S–S bonds.
IgT/IgZ ontogeny has been studied in zebrafish, trout and Fugu and it seemed evident that transcripts related to these molecules are expressed from the very early developmental stages (as an example 4 days post-fertilization in Fugu and 22 days in rainbow trout) [11, 13] . In zebrafish two IgZ isoforms were detected which showed different expression times: IgZ1 was detected few days post-fertilization, whereas IgZ2 only 14 days post-fertilization . In sea bass we analysed the basal expression of IgT and IgM in different organs and tissues and we found that gut and gills, important mucosal organs, showed high IgT transcripts levels and this was for us the first evidence of the possible involvement of sea bass IgT in mucosal immune responses as already demonstrated in rainbow trout . Moreover, we have observed expression, but at a lesser extent, in other important organs linked to the immune responses, like thymus, head kidney and liver. IgM levels, on the contrary, were high in head kidney, spleen and liver, organs that are involved in systemic immune responses. In general, however, the basal expression seems an aspect peculiar in relation to the investigated fish species. We have examples, like zebrafish, where IgT transcripts are found only in primary lymphoid organs (head kidney and thymus) in adult individuals, while IgM expression is widespread in both primary and secondary lymphoid organs . On the other hand in other species, such as trout, fugu and Atlantic salmon the two expression patterns are very similar [11, 13, 17]. Moreover, in carp IgT is expressed even in non-lymphoid organs  and, after specific infection with fish parasites, in carp and trout IgT becomes highly over-expressed in mucosal organs (gut and gills) [23, 48]. Sea bass IgT expression was modulated, even if the variations were not statistically significant although not considering the response of single fishes, after i.m. infection with nodavirus both in spleen and gills. The IgT increase was more evident in gills, an important mucosal tissue, and less in spleen. The involvement of sea bass IgT in the immune response against bacterial  and virus  pathogens has been previous evidenced in gut, but this is the first time of a similar investigation in gills and spleen. It has to be noted that in rainbow trout a robust clonal response involving few variable heavy chain domain repertories has been evidenced in spleen after challenge with a rhabdovirus  and that it has been demonstrated that in rainbow trout, after pathogen exposure, IgT+ B cells proliferate and generate specific IgT in the gills and in the skin [27, 51].
However, while extensive studies have been performed on the distribution of IgM-producing cells in lymphoid tissues , little information is available on the distribution of IgT/IgZ producing cells in fish species. To this purpose we performed in situ hybridization to detect IgT-producing cells in sea bass mucosal tissues, gills and gut. IgT transcripts were localized in gill filaments and parallel lamellae showing strong positive signals, while in Fugu a strong expression of IgZ was seen in the gill epithelial cells  and in mandarin fish a moderate expression of IgZ positive cells was detected loosely located along gill filaments , with a similar distribution to that of IgM transcripts. Functional studies in mandarin fish, that measured the levels of specific transcripts for IgM, IgD and IgZ in mucosal secretions after vaccination with the inactivated bacteria Flavobacterium columnare, demonstrated an increase of Igs in gills, although with different kinetics for the three Ig isotypes, suggesting that in the gill associated lymphoid tissue B cells could play important roles in protecting fish from pathogens . In accordance with this, data obtained in sea bass showed that antibody production was early induced in the gills of juveniles after immersion in Photobacterium damselae ssp. piscicida bacterin demonstrating that the gill is a major organ for antibody secreting cell production .
In situ hybridization with a IgT-mRNA probe confirmed the presence of IgT transcripts also in the sea bass gut. To notice, sea bass IgT expression was regionalized with a major expression in the posterior intestine, data that points to the hindgut as the segment in which the recruitment of IgT+ cells is most significant in this species. Also in rainbow trout gut IgT+ cells distribution was regionalized, although in this species the pyloric caeca was the area with a major recruitment of B cells in response to oral vaccination, as demonstrated through both real time PCR and immune-histochemistry . In sea bass IgT+ cells were mostly intra-epithelial leukocytes (IELs) in anterior and middle segments, while they were localized in the lamina propria (LP) in all segments. However, the location of IgT-producing cells is not coincident among different fish species. In fact, although in rainbow trout IgT+ cells were mostly IELs in all segments and rarely they were localized in the LP in the midgut and hindgut regions , after vaccination, the cells found in the LP can infiltrate the epithelium . Interestingly, in mandarin fish no IgZ positive cells could be detected in intestine, while numerous IgM positive cells were located abundantly in both submucosa and lamina propria of posterior intestine and sometimes nearing the goblet cells. In sea bass, IgM+ cells were more common in the epithelium than in lamina propria and T cells were mainly found in the posterior intestine . The presence of T cells and IgM + and IgT + cells in the mucosa of the sea bass posterior intestine seems one of the factors that could account for its capacity to respond to immune stimuli.
Overall, numerous observations, recently reviewed by Parra et al. , indicated that, similarly to IgA and IgM in mammals, the transportation of polymeric IgT and IgM in teleost fish is mediated by pIgR. However, as demonstrated in mouse, rat and rabbit, only a small proportion of IgA synthesized in the lamina propria of intestinal mucosa enters the gut lumen directly. The majority goes through the mesenteric lymph, then in the bloodstream, and is finally transported into bile by hepatocytes to protect the intestinal epithelium. Finally, in sea bass IgT transcripts were also found in the liver. In particular, the IgT mRNA probe allowed identifying scattered IgT positive cells, showing a strong positive signal, in the hepatic parenchyma, providing clear evidence in support of the existence of a resident immune cell population in this tissue. The result validates previous data obtained in trout that provided evidence for the existence of an intrahepatic immune cells population which is 15–29% of the non-hepatocyte cells in the liver . However, the present study, to the best of our knowledge, demonstrates for the first time the existence of an intraparenchymal lymphocyte IgT population in sea bass liver. In rainbow trout it has been evidenced the presence of IgT+ cells and the liver immune response after infection with the viral hemorrhagic septicemia virus has been assessed .
From this analysis we could conclude that sea bass IgT presents different molecular aspects in agreement with previously identified homologs from other Teleost fish species and that expression and localization data strongly suggest its possible involvement in mucosal immune responses against pathogens. Much work needs to be addressed to study more in detail this last aspect, for the importance of mucosal antibodies as a target to study the efficacy of oral vaccines (via feed) that are used in fish immersion vaccination, an ideal method for the aquaculture sector [58, 59], and to investigate the importance of the IgT population evidenced in the sea bass liver.
VS and NNO were responsible for most of the experimental work and handling of fishes. ER and CB performed real-time experiments. LG and SP worked on in situ hybridisation. MG and AP were involved in genomic studies. AF performed the 3D analysis. FB, GS and SP are the principal investigators who conceived the study; FB wrote the paper and critically reviewed the manuscript with GS and SP. All authors read and approved the final manuscript.
This aspect does not apply to the manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
The original data of the real-time PCR experiments will be available upon request.
Consent for publication
This aspect does not apply to the manuscript.
Ethics approval and consent to participate
All fishes were handled complying with the Guidelines of the European Union Council and of the Ethical Committee of the Tuscia University (Prof. Giuseppe Scapigliati, Prof. Nicola Lacetera, Prof. Nicla Romano) for the use of live laboratory animals.
This research was funded by the European Commission under the 7th Framework Programme for Research and Technological Development (FP7) of the European Union (Grant Agreement 311993 TARGETFISH).
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- Flajnik MF, Kasahara M. Origin and evolution of the adaptive immune system: genetic events and selective pressures. Nat Rev Genet. 2010;11:47–59.View ArticlePubMedGoogle Scholar
- Tonegawa S. Somatic generation of antibody diversity. Nature. 1983;302:575–81.View ArticlePubMedGoogle Scholar
- Flajnik MF. Comparative analyses of immunoglobulin genes: surprises and portents. Nat Rev Immunol. 2002;2:688–98.View ArticlePubMedGoogle Scholar
- Chen K, Cerutti A. New insights into the enigma of immunoglobulin D. Immunol Rev. 2010;237:160–79.View ArticlePubMedPubMed CentralGoogle Scholar
- Berstein RM, Schluter SF, Shen S, Marchalonis JJ. A new high molecular weight immunoglobulin class from the carcharhine shark: implications for the properties of the primordial immunoglobulin. Proc Natl Acad Sci USA. 1996;93:3289–93.View ArticlePubMedPubMed CentralGoogle Scholar
- Ota T, Rast JP, Litman GW, Amemiya CT. Lineage-restricted retention of a primitive immunoglobulin heavy chain isotype within the Dipnoi reveals an evolutionary paradox. Proc Natl Acad Sci USA. 2003;100:2501–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Warr GW, Magor KE, Higgins DA. IgY: clues to the origins of modern antibodies. Immunol Today. 1995;16:392–8.View ArticlePubMedGoogle Scholar
- Zhao Y, Pan-Hammarström Q, Yu S, Wertz N, Zhang X, Li N, Butler JE, Hammarström L. Identification of IgF, a hinge-region-containing Ig class, and IgD in Xenopus tropicalis. Proc Natl Acad Sci. 2006;103:12087–92.View ArticlePubMedPubMed CentralGoogle Scholar
- Sunyer JO. Evolutionary and functional relationships of B cells from fish and mammals: insights into their novel roles in phagocytosis and presentation of particulate antigen. Infect Disord Drug Targets. 2012;12:200–12.View ArticlePubMedPubMed CentralGoogle Scholar
- Edholm ES, Bengten E, Wilson M. Insights into the function of IgD. Dev Comp Immunol. 2011;35:1309–16.View ArticlePubMedGoogle Scholar
- Hansen JD, Landis ED, Phillips RB. Discovery of a unique Ig heavy-chain isotype (IgT) in rainbow trout: implications for a distinctive B cell developmental pathway in teleost fish. Proc Natl Acad Sci USA. 2005;102:6919–24.View ArticlePubMedPubMed CentralGoogle Scholar
- Danilova N, Bussmann J, Jekosch K, Steiner LA. The immunoglobulin heavy-chain locus in zebrafish: identification and expression of a previously unknown isotype, immunoglobulin Z. Nat Immunol. 2005;6:295–302.View ArticlePubMedGoogle Scholar
- Savan R, Aman A, Sato K, Yamaguchi R, Sakai M. Discovery of a new class of immunoglobulin heavy chain from fugu. Eur J Immunol. 2005;35:3320–31.View ArticlePubMedGoogle Scholar
- Savan R, Aman A, Nakao M, Watanuki H, Sakai M. Discovery of a novel immunoglobulin heavy chain gene chimera from common carp (Cyprinus carpio L.). Immunogenetics. 2005;57:458–63.View ArticlePubMedGoogle Scholar
- Gambon-Deza F, Sanchez-Espinel C, Magadan-Mompo S. Presence of an unique IgT on the IGH locus in three-spined stickleback fish (Gasterosteus aculeatus) and the very recent generation of a repertoire of VH genes. Dev Comp Immunol. 2010;34:114–22.View ArticlePubMedGoogle Scholar
- Yasuike M, de Boer J, von Schalburg KR, Cooper GA, McKinnel L, Messmer A, So S, Davidson WS, Koop BF. Evolution of duplicated IgH loci in Atlantic salmon, Salmo salar. BMC Genom. 2011;11:486.View ArticleGoogle Scholar
- Tadiso TM, Lie KK, Hordvik I. Molecular cloning of IgT from Atlantic salmon, and analysis of the relative expression of τ, μ, and δ in different tissues. Vet Immunol Immunopathol. 2011;139:17–26.View ArticlePubMedGoogle Scholar
- Mashoof S, Pohlenz C, Chen PL, Deiss TC, Gatlin D III, Buentello A, Criscitiello MF. Expressed IgH μ and τ transcripts share diversity segment in ranched Thunnus orientalis. Dev Comp Immunol. 2014;43:76–86.View ArticlePubMedGoogle Scholar
- Giacomelli S, Buonocore F, Albanese F, Scapigliati G, Gerdol M, Oreste U, Coscia MR. New insights into evolution of IgT genes coming from Antarctic teleosts. Mar Genom. 2015;24:55–68.View ArticleGoogle Scholar
- Hordvik I. Immunoglobulin isotypes in Atlantic salmon, Salmo salar. Biomolecules. 2015;5:166–77.View ArticlePubMedPubMed CentralGoogle Scholar
- Bengten E, Clem LW, Miller NW, Warr GW, Wilson M. Channel catfish immunoglobulins: repertoire and expression. Dev Comp Immunol. 2006;30:77–92.View ArticlePubMedGoogle Scholar
- Magadán-Mompó S, Sánchez-Espinel C, Gambón-Deza F. Immunoglobulin heavy chains in medaka (Oryzias latipes). BMC Evol Biol. 2011;11:165.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang YA, Li J, Parra D, Bjork S, Xu Z, LaPatra SE, Bartholomew J, Sunyer JO. IgT, a primitive immunoglobulin class specialized in mucosal immunity. Nat Immunol. 2010;11:827–35.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang YA, Salinas I, Sunyer OJ. Recent findings on the structure and function of teleost IgT. Fish Shellfish Immunol. 2011;31:627–34.View ArticlePubMedPubMed CentralGoogle Scholar
- Parra D, Korytar T, Takizawa F, Sunyer JO. B cells and their role in the teleost gut. Dev Comp Immunol. 2016;64:150–66.View ArticlePubMedPubMed CentralGoogle Scholar
- Olsen MM, Kania PW, Heinecke RD, Skjoedt K, Rasmussen KJ, Buchmann K. Cellular and humoral factors involved in the response of rainbow trout gills to Ichthyophthirius multifiliis infections: molecular and immunohistochemical studies. Fish Shellfish Immunol. 2011;30:859–69.View ArticlePubMedGoogle Scholar
- Xu Z, Parra D, Gomez D, Salinas I, Zhang YA, von Gersdorff Jorgensen L, Heinecke RD, Buchmann K, LaPatra S, Sunyer JO. Teleost skin, an ancient mucosal surface that elicits gut-like immune responses. Proc Natl Acad Sci USA. 2013;110:13097–102.View ArticlePubMedPubMed CentralGoogle Scholar
- Kar B, Mohapatra A, Mohanty J, Sahoo PK. Transcriptional changes in three immunoglobulin isotypes of rohu, Labeo rohita in response to Argulus siamensis infection. Fish Shellfish Immunol. 2015;47:28–33.View ArticlePubMedGoogle Scholar
- Castro R, Jouneau L, Pham HP, Bouchez O, Giudicelli V, Lefranc MP, Quillet E, Benmansour A, Cazals F, Six A, Fillatreau S, Sunyer O, Boudinot P. Teleost fish mount complex clonal IgM and IgT responses in spleen upon systemic viral infection. PLoS Pathog. 2013;9:e1003098.View ArticlePubMedPubMed CentralGoogle Scholar
- Tian JY, Sun BJ, Luo YP, Zhang YA, Nie P. Distribution of IgM, IgD and IgZ in mandarin fish, Siniperca chuatsi lymphoid tissues and their transcriptional changes after Flavobacterium columnare stimulation. Aquaculture. 2009;288:14–21.View ArticleGoogle Scholar
- Nunez Ortiz N, Gerdol M, Stocchi V, Marozzi C, Randelli E, Bernini C, Buonocore F, Picchietti S, Papeschi C, Sood N, Pallavicini A, Scapigliati G. T cell transcripts and T cell activities in the gills of the Teleost fish sea bass (Dicentrarchus labrax). Dev Comp Immunol. 2014;47:309–18.View ArticlePubMedGoogle Scholar
- Scapigliati G, Buonocore F, Bird S, Zou J, Pelegrin P, Falasca C, Prugnoli D, Secombes CJ. Phylogeny of cytokines: molecular cloning and expression analysis of sea bass Dicentrarchus labrax interleukin-1β. Fish Shellfish Immunol. 2001;11:711–26.View ArticlePubMedGoogle Scholar
- Altschul SF, Gish W, Miller W, Myers E, Lipman DJ. Best local alignment search tool. J Mol Biol. 1990;215:403–10.View ArticlePubMedGoogle Scholar
- Nielsen H, Engelbrecht J, Brunak S, von Heijne G. Identification of prokaryotic and eukaryotic signal peptides and prediction of their cleavage sites. Protein Eng. 1997;10:1–6.View ArticlePubMedGoogle Scholar
- Tamura K, Dudley J, Nei M, Kumar S. MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol. 2007;24:1596–9.View ArticlePubMedGoogle Scholar
- Harris LJ, Larson SB, Hasel KW, McPherson A. Refined structure of an intact IgG2a monoclonal antibody. Biochemistry. 1997;36:1581–97.View ArticlePubMedGoogle Scholar
- Šali A, Blundell TL. Comparative protein modelling by satisfaction of spatial restraints. J Mol Biol. 1993;234:779–815.View ArticlePubMedGoogle Scholar
- Buonocore F, Castro R, Randelli E, Lefranc M-P, Six A, Kuhl H, Reinhardt R, Facchiano A, Boudinot P, Scapigliati G. Diversity, molecular characterization and expression of T cell receptor γ in a teleost fish, the sea bass (Dicentrarchus labrax, L.). PLoS ONE. 2012;7:e47957.View ArticlePubMedPubMed CentralGoogle Scholar
- Willard L, Ranjan A, Zhang H, Monzavi H, Boyko RF, Sykes BD, Wishart DS. VADAR: a web server for quantitative evaluation of protein structure quality. Nucleic Acids Res. 2003;31:3316–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Wiederstein M, Sippl MJ. ProSA-web: interactive web service for the recognition of errors in three-dimensional structures of proteins. Nucleic Acids Res. 2007;35:W407–10.View ArticlePubMedPubMed CentralGoogle Scholar
- Scapigliati G, Buonocore F, Randelli E, Casani D, Meloni S, Zarletti G, Tiberi M, Pietretti D, Boschi I, Manchado M, Martin-Antonio B, Jimenez-Cantizano R, Bovo G, Borghesan F, Lorenzen N, Einer-Jensen K, Adams S, Thompson K, Alonso C, Bejar J, Cano I, Borrego JJ, Alvarez MC. Cellular and molecular immune responses of the sea bass (Dicentrarchus labrax) experimentally infected with betanodavirus. Fish Shellfish Immunol. 2010;28:303–11.View ArticlePubMedGoogle Scholar
- Lefranc M-P. The IMGT unique numbering for immunoglobulins, T cell receptors and Ig-like domains. Immunologist. 1999;7:132–6.Google Scholar
- Lefranc M-P, Pommié C, Ruiz M, Giudicelli V, Foulquier E, Truong L, Thouvenin-Contet V, Lefranc G. IMGT unique numbering for immunoglobulin and T cell receptor variable domains and Ig superfamily V-like domains. Dev Comp Immunol. 2003;27:55–77.View ArticlePubMedGoogle Scholar
- Lesk AM, Chothia C. Evolution of proteins formed by β-sheets. II. The core of the immunoglobulin domains. J Mol Biol. 1982;160:325–42.View ArticlePubMedGoogle Scholar
- Yoo EM, Coloma MJ, Trinh KR, Nguyen TQ, Vuong LU, Morrison SL, Chintalacharuvu KR. Structural requirements for polymeric immunoglobulin assembly and association with J chain. J Biol Chem. 1999;274:33771–7.View ArticlePubMedGoogle Scholar
- Tine M, Kuhl H, Gagnaire PA, Louro B, Desmarais E, Martins RS, Hecht J, Knaust F, Belkhir K, Klages S, Dieterich R, Stueber K, Piferrer F, Guinand B, Bierne N, Volckaert FA, Bargelloni L, Power DM, Bonhomme F, Canario AV, Reinhardt R. European sea bass genome and its variation provide insights into adaptation to euryhalinity and speciation. Nat Commun. 2014;5:5770.View ArticlePubMedPubMed CentralGoogle Scholar
- Hu YL, Xiang LX, Shao JZ. Identification and characterization of a novel immunoglobulin Z isotype in zebrafish: implications for a distinct B cell receptor in lower vertebrates. Mol Immunol. 2010;47:738–46.View ArticlePubMedGoogle Scholar
- Ryo S, Wijdeven RH, Tyagi A, Hermsen T, Kono T, Karunasagar I, et al. Common carp have two subclasses of bonyfish specific antibody IgZ showing differential expression in response to infection. Dev Comp Immunol. 2010;34:1183–90.View ArticlePubMedGoogle Scholar
- Galindo-Villegas J, Mulero I, García-Alcazar A, Muñoz I, Peñalver-Mellado M, Streitenberger S, Scapigliati G, Meseguer J, Mulero V. Recombinant TNFα as oral vaccine adjuvant protects European sea bass against vibriosis: insights into the role of the CCL25/CCR9 axis. Fish Shellfish Immunol. 2013;35:1260–71.View ArticlePubMedGoogle Scholar
- Valero Y, Awad E, Buonocore F, Arizcun M, Esteban MÁ, Meseguer J, Chaves-Pozo E, Cuesta A. An oral chitosan DNA vaccine against nodavirus improves transcription of cell-mediated cytotoxicity and interferon genes in the European sea bass juveniles gut and survival upon infection. Dev Comp Immunol. 2016;65:64–72.View ArticlePubMedGoogle Scholar
- Xu Z, Takizawa F, Parra D, Gomez D, von Gersdorff Jorgensen L, LaPatra SE, Sunyer JO. Mucosal immunoglobulins at respiratory surfaces mark an ancient association that predates the emergence of tetrapods. Nat Commun. 2016;7:10728.View ArticlePubMedPubMed CentralGoogle Scholar
- Salinas I. The mucosal immune system of teleost fish. Biology. 2015;4:525–39.View ArticlePubMedPubMed CentralGoogle Scholar
- dos Santos NMS, Taverne-Thiele JJ, Barnes AC, van Muiswinkel WB, Ellis AE, Rombout JHWM. The gill is a major organ for antibody secreting cell production following direct immersion of sea bass (Dicentrarchus labrax, L.) in a Photobacterium damselae ssp. piscicida bacterin: an ontogenetic study. Fish Shellfish Immunol. 2001;11:65–74.View ArticlePubMedGoogle Scholar
- Ballesteros NA, Castro R, Abos B, Rodríguez Saint-Jean SS, Perez-Prieto SI, Tafalla C. The pyloric caeca area is a major site for IgM and IgT B cell recruitment in response to oral vaccination in rainbow trout. PLoS ONE. 2013;8:e66118.View ArticlePubMedPubMed CentralGoogle Scholar
- Picchietti S, Terribili FR, Mastrolia L, Scapigliati G, Abelli L. Expression of lymphocyte antigenic determinants in developing gut-associated lymphoid tissue of the sea bass Dicentrarchus labrax (L.). Anat Embryol. 1997;196:457–63.View ArticlePubMedGoogle Scholar
- Moller AM, Korytar T, Kollner B, Schmidt-Posthaus H, Segner H. The teleostean liver as an immunological organ: intrahepatic immune cells (IHICs) in healthy and benzo[a]pyrene challenged rainbow trout (Oncorhynchus mykiss). Dev Comp Immunol. 2014;14:518–29.View ArticleGoogle Scholar
- Castro R, Abos B, Pignatelli J, von Gersdorff Jorgensen L, Gonzales Granja A, Buchmann K, Tafalla C. Early immune responses in rainbow trout liver upon viral hemorrhagic septicemia virus (VHSV) infection. PLoS ONE. 2014;9:e111084.View ArticlePubMedPubMed CentralGoogle Scholar
- Rombout JHWM, Yang G, Kiron V. Adaptive immune responses at mucosal surfaces of teleost fish. Fish Shellfish Immunol. 2014;40:634–43.View ArticlePubMedGoogle Scholar
- Parra D, Reyes-Lopez FE, Tort L. Mucosal immunity and B cells in teleosts: effect of vaccination and stress. Front Immunol. 2015;6:354.View ArticlePubMedPubMed CentralGoogle Scholar