Microsoft Word - ISJ385 ISJ 12: 188-194, 2015 ISSN 1824-307X REVIEW Presence and conservation of the immunoglobulin superfamily in insects: current perspective and future challenges M Mandrioli1, M Monti2, R Tedeschi2 1Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy 2Department of Agricultural, Forest and Food Sciences, University of Turin, Turin, Italy Accepted July 6, 2015 Abstract Numerous proteins that contain a bona fide immunoglobulin domain have been identified in the last decade showing that immunoglobulin-like proteins are quite common in metazoans. In particular, recent surveys identified more than 140 immunoglobulin-like proteins in Drosophila melanogaster, Anopheles gambiae and Bombyx mori. A well-studied example of immunoglobulin-like protein is the Drosophila Down syndrome cell adhesion molecule (Dscam) that, accordingly to comparative molecular analyses, showed a high conservation in Diptera, Hymenoptera and Coleoptera, together with a conserved presence of alternative splicing that permitted insects to possess an unsuspected molecular complexity of their innate immune system. At a functional level, immunoglobulin-like proteins seem to be capable of reacting to pathogen challenges and may contribute to the defense against infection so that they are candidates as immune effector molecules in insects. Preliminary findings on insect-borne plant and animal diseases suggest a possible role of the immunoglobulin-like proteins in the vectorial capacity. Key Words: immunoglobulin-like proteins; insects; innate immunity; non-self recognition   Introduction The evolution of immunity has been frequently regarded as a sort of tinkering resulting in jawed vertebrates (gnathostomes) in the presence of conserved “building blocks”, including immunoglobulins, T-cell receptors (TCRs) and polymorphic MHC class I and class II molecules, as well as a thymus and compartmentalized secondary lymphoid tissues (Zapata and Amemiya, 2000). A relevant role has been also played by the evolution of the recombination-activating gene (RAG)- mediated V(D)J recombination and the somatic hypermutation of immunoglobulin genes that brought to the synthesis of hypervariable immunoglobulins (Igs) that can bind to their nominal antigens with exquisite specificity and neutralize the harmful effects of non-self antigens (Zouali, 2001; Flajnik, 2002). Urochordates and cephalochordates do not have an adaptive immune system involving the somatic rearrangement of the antigen receptor genes so that the status of their immune system ___________________________________________________________________________ Corresponding author: Mauro Mandrioli Department of Life Sciences University of Modena and Reggio Emilia via Campi 213/D, 41125 Modena, Italy E-mail: mauro.mandrioli@unimore.it seems to reflect a “primitive” pre-RAG stage. In particular, an immunological “big bang” of the adaptive immunity occurred in an ancestor of jawed vertebrates, where the insertion of a transposon into an immunoglobulin superfamily gene member initiated the antigen receptor gene rearrangement via the RAG recombinase (Bernstein et al., 1996; Agrawal et al., 1998; Hiom et al., 1998; Schatz, 1999; Flajnik, 2002, 2014). Interestingly, numerous proteins that contain bona fide immunoglobulin domains have been identified in invertebrates confirming that gnathostome Igs evolved from previously present molecules that gained a primary role in immunity (Pancer et al., 1998; Blumbach et al., 1999; Azumi et al., 2003). Indeed, proteins containing immunoglobulin-like domains are frequently involved in activities other than defense in invertebrates, and just some of them participate to immune responses, as already reported in cephalochordates (Cannon et al., 2002; Haire et al., 2004) and for the “molluscan defense molecules” identified in the pond snail Lymnaea stagnalis (Sun et al., 1990; Hoek et al., 1996). Even though none of the invertebrate molecules that bear an immunoglobulin-like domain resembles gnathostome antibodies, the fibrinogen-related proteins (FREP) from the freshwater snail Biomphalaria glabrata can recognize through its Ig- 188   like domain a wide range of pathogens (from prokaryotes to eukaryotes) and different categories of FREPs seem to exhibit a functional specialization with respect to the encountered pathogens (Zhang et al., 2008). In the last years, the publication of the wholly sequenced genomes of different insect species allowed a deep analysis of the evolution of their immune systems. In particular, proteins containing immunoglobulin-like domains seem to be quite common and, at least part of them, play relevant roles in the immune response making insects valuable models to understand the extent of roles played by the immunoglobulin superfamily (IgSF) in the insect immunity. From one to thousand: current state of the art of the insect immunoglobulin superfamily Immunoglobulins have been considered as typical molecules of gnathostomes since the identification of hemolin (previously called P4), an immune protein isolated from the lepidopterans Hyalophora cecropia and Manduca sexta (Sun et al., 1990; Ladendorff and Kanost, 1991; Lindström- Dinnetz et al., 1995). Indeed hemolin has been the first Ig-like molecule isolated in invertebrates and it has been assessed that it was also involved in the immune response (Sun et al., 1990; Ladendorff and Kanost, 1991; Lindström-Dinnetz et al., 1995). Hemolin is present in low, but significant, amounts in the hemolymph of untreated larvae and pupae, and its level increases 18 - 30-fold after injection of live bacteria into the insect body, as a consequence of an increased synthesis at the fat bodies (Rasmuson and Boman, 1979; Faye and Wyatt, 1980; Ladendorff and Kanost, 1991). Functional analyses clearly assessed that H. cecropia hemolin was able to bind to bacterial cell wall components in vitro, forming a complex with two other hemolymph proteins (Sun et al., 1990), whereas M. sexta hemolin was able to bind not only to bacteria (triggering a protective response involving humoral and cellular reactions), but also to hemocytes inhibiting their aggregation in vitro (Ladendorff and Kanost, 1991; Eleftherianos et al., 2006, 2007). As a whole, hemolin was not only belonging to the immunoglobulin superfamily, but also played a relevant role in immunity, probably as a pattern recognition molecule, which discriminates between self and infectious non-self by the recognition of molecules unique to microorganisms, such as LPS (Schmidt et al., 1993). Since this first identification, the immunoglobulin superfamily has been greatly enriched in insect genes encoding proteins with at least one immunoglobulin domain. The Ig domain is highly conserved and it has a representative sandwich structure of two opposing antiparallel β- pleated sheets, stabilized by a disulphide bridge, that make it easily identified by bioinformatics analyses (Bork et al., 1994; Halaby et al., 1999). Indeed, searches of the InterPro and Pfam databases showed several types of Ig domains such as I-subtype, I-subtype 2, C2-set_2, V-set, V-type, Ig, I-set and Ig-like (Huang et al., 2009). These domains are found in cell adhesion molecules, cell receptors, antigens, cell surface glycoproteins and other proteins (Wang and Springer, 1998; Ossiboff and Parker, 2007; Soroka et al., 2010) and they are at the basis of specific adhesion and recognition capability, including cell-cell adhesion, cell-surface recognition and pathogen recognition (Hutter et al., 2000; Hynes and Zhao, 2000). Recent surveys identified more than 140 IgSF proteins in Drosophila melanogaster (Vogel et al., 2003), 138 IgSF proteins in Anopheles gambiae, with 85 of them increasing their amount after induction with Plasmodium, gram-negative or gram- positive bacteria (Garver et al., 2008), and more than 150 IgSF genes containing at least one immunoglobulin domain have been predicted in Bombyx mori (He et al., 2014). At a functional level, recent reports showed that insect IgSF proteins are essential for the immune response (i.e., Garver et al., 2008). For instance, in A. gambiae, the IgSF protein Down syndrome cell adhesion molecule (Dscam) is involved in the defense against bacteria and Plasmodium (Dong et al., 2006) and hemolin-like proteins have been also isolated in the silk glands of Galleria mellonella in response to bacterial challenge and might mark apoptotic cells for elimination by hemocytes (Shaik and Sehnal, 2009). Multiple sequence alignments and phylogenetic analyses indicated that, despite IgSFs evolved rapidly, 58 % of Anopheles IgSF genes has orthologues in D. melanogaster and Aedes aegypti even if they tended to share more sequence similarity with Aedes than with Drosophila (Garver et al., 2008). For instance, 10 genes are homologous between A. gambiae and D. melanogaster, but not with A. aegypti, 28 genes are orthologues between the two mosquito species only, 23 IgSF genes are uniquely present in anopheline and two of these share similarity with Apis mellifera only (Garver et al., 2008). Gene ontology annotation indicated that insect IgSF members are involved as cellular components and in different molecular functions and biological processes (Garver et al., 2008; He et al., 2014). Indeed IgSF proteins were implicated in signal transduction and cell communication and they can be expressed in a wide range of tissue, such as testis, ovary, fat bodies, midgut, integument, hemocytes, malpighian tubules and head, as clearly assessed in B. mori (He et al., 2014). A well-studied example of a member of the Ig superfamily is the Drosophila Dscam, whose gene comprises clusters of variable exons flanked by constant exons (Schmucker et al., 2000) (Fig. 1). Interestingly, fly cells can combine Dscam constant and variable exons by mutually exclusive alternative splicing potentially generating more than 19,000 different extracellular domains (Watson et al., 2005; Brites et al., 2008, 2013). Despite the absence of a somatic rearrangement similar to that of gnathostome immunoglobulins, Dscam is at the basis of a large protein isoform repertoire with the potential for recognizing diverse ligands and epitopes (Schmucker et al., 2000). Secreted Dscam isoforms have been detected in the hemolymph and hemocyte-specific loss of Dscam impaired the efficiency of phagocytic uptake of bacteria, possibly due to reduced bacterial 189   http://www.sciencedirect.com/science/article/pii/S0378111914008130#bb0005 http://www.sciencedirect.com/science/article/pii/S0378111914008130#bb0015 http://www.sciencedirect.com/science/article/pii/S0378111914008130#bb0020 Fig. 1 The Dscam gene contains four variable exon blocks (indicated in red, blue, green and yellow) (A) and multiple isoforms are assembled using single variants from each block through an elaborate process of alternative splicing (B). Each generated protein contain 10 immunoglobulin domain, 6 fibronectin type III repeats, a transmembrane domain (TM) and a cytoplasmic tail. The Dscam proteins show a isoform-specific homophilic binding (C) where the Ig2, Ig3, and Ig7 variable domains match in two opposing isoforms (as represented by the same shape) at all three variable domains is required for protein binding. Modified from Schmucker et al. (2000). binding. Furthermore, Dscam is upregulated after infection in numerous arthropods (Armitage et al., 2014). Importantly, comparative analyses of Dscam- like sequences show high conservation of orthologous Dscam genes in Diptera, Hymenoptera and Coleoptera (Graveley et al., 2004; Watson et al., 2005), together with a conserved expression of diverse Dscam isoforms in immune-competent fat body cells and immunocytes among highly diverged insect species (Watson et al., 2005). Lastly, the molecular diversity of Dscam transcripts generated through alternative splicing is highly conserved across the major insect orders suggesting a common (and unsuspected) molecular complexity of the innate immune system of insects. Interestingly, the availability of numerous genomes and transcriptomes belonging to different insects could allow to deeply explore Dscam presence, expression and alternative splicing in insects (Palmer and Jiggins, 2015). As a whole, insect IgSF members seem to be capable of reacting to pathogen challenges and to control events that contribute to the defence against infection so that they are intriguing candidates as immune effector molecules in insects. Immunoglobulin-like proteins and the insect vectorial capacity: from theory to the field Several insects are involved in the transmission of pathogens to both animal and plant species. Some of these insect-borne pathogens may circulate within the vector body after acquisition and eventually be inoculated into new hosts during insect salivation event (circulative pathogens), while others may bind to various sections of the foregut of vectors without host internalization (Killiny et al., 2012). Biological and molecular interactions in both of these models are very complex leading to a high specificity between a pathogen and insect vectors and determining transmission success and different efficiency. For instance, it has been demonstrated that the gut microbiota is able to decrease viral and parasitic infections in mosquito and tsetse fly vectors by activating their immune responses or directly inhibiting pathogen development (Cirimotich et al., 2011a). In particular, Cirimotich et al. (2011b) identified an enterobacterium that confers total refractoriness to P. falciparum through the production of reactive oxygen molecules. However, the mechanisms responsible for bacteria-mediated reduction in vectorial capacity can also be indirect. In this case, the bacteria seem to impede the development of malaria by priming the mosquito immune system (Lefèvre et al., 2013). Intrinsic factors of the vectors such as age, reproductive status, and body size can have important consequences on vectorial capacity, as well. For example, the host immune system may weaken with age, resulting in an increased susceptibility to pathogens (Lefèvre et al., 2013). 190   Moreover, genetic variability of both vectors and pathogen strains can differently act on these interactions, as reported for phytoplasmas (Seemüller and Schneider, 2007; Suzuki et al., 2006). This could be translated in the insect capacity to only acquire the pathogen or transmit it with low or high efficiency (Galetto et al., 2009). Recent gene expression analyses of infected and non-infected insect vectors of plant and animal pathogens offer novel opportunities to exploit new knowledge about host-parasite interactions in the different pathosystems. In particular, this approach pointed out the activation of particular genes encoding antimicrobial peptides, such as defensin and cecropin. However, genes involved in pathogen recognition, such as those encoding lectins, and those encoding receptors that activate the innate immune response, such as Toll-3 have been studied, together with genes encoding for members of the signal transduction pathways activated by Toll-like receptors, such as JNK kinase (Medeiros et al., 2004; Fisher et al., 2014; Vyas et al., 2014; Padrón et al., 2014; Colpitts et al., 2011; Shigihara et al., 2008). Concerning immunoglobulin-like proteins, so far little is known about their direct correlation with the vectorial capacity. It is reported for examples in Anopheles gambiae an interplay between AgDscam and the resistance to Plasmodium infection. In the specific, this study demonstrated that a RNAi- mediated AgDscam depletion in mosquitoes, which fed on mice infected with GFP-expressing P. bergei parasites, resulted in a statistically significant increase of oocystis numbers on the midgut as well as at 13d of feeding (Dong et al., 2006). As well, in A. gambiae it has been reported that the immunoglobulin domain 6 gene (IRID 6) seems to be involved in limiting Plasmodium infection, and so in the resistance to the pathogen invasion, since it was strongly down-regulated in the gut during P. berghei ookinete invasion (Garver et al., 2008). On the other hand, the plant virus Tomato Spotted Wilt Tospovirus (TSWV) activates the immune system of its main insect vector, Frankliniella occidentalis and homologues of gene members of the immunoglobulin superfamily of proteins, such as hemolin are among the genes activated after TSWV infection (Medeiros et al., 2004). In the light of these findings, it could be interesting to verify if the large protein isoform repertoire related to the Ig superfamily is involved in the establishment of the different insect vectorial capacity (Fig. 2). This role could be particularly intriguing since it could allow us to disrupt some pathogen-vector interactions leading to the blockage of transmission. In particular, it would be the starting point to guide strategies in order to block the transmission of vector-borne pathogens to plants or animals altering gene expression. However, deep analyses of insect vector transcripts under infected and non-infected conditions prove to be a pivotal tool for identification of genes involved in the host immunity response to pathogen infection and transmission. Fig. 2 Despite the conservation of the Dscam genes, the repertoire of proteins that may be assembled is different among diverse species so that two phylogenetically related species may have very similar (but not identical) Dscam repertoire. As a consequence, some pathogen genotypes could be detected in one species, but 191   undetected in the other (indicated by the arrow in each species) explaining the different vectorial capacity of insect for similar pathogenic species. Conclusions Most animals, including insects, have not acquired adaptive immunity, but present a large receptor diversity that increases the effectiveness of immune responses of individual animals. In view of the absence of the adaptive immunity, the insect immune system has been described as simple, term that has been often misinterpreted as evolutionarily inferior to the complex vertebrate immune system. This is a viewpoint that falsely equates the phylogenetic position with a sort of functional inferiority. Insects are the most successful class of organism on the planet (e.g., Gullan and Cranston, 2000) and their simple immune system plays an important role in that success. At this regard, the insect open hemocel provides some advantages in terms of the function of the immune system in contrast to the closed circulatory networks of higher vertebrates, since mediators, effector systems and immunocytes can be more rapidly disseminated and organised. However, the open architecture also presents a problem when the insect is faced with systemic immune insult. Indeed, an open body cavity facilitates rapid movement of infective agents through the host so that selection may have favoured the evolution of effector systems that rapidly and efficiently localise and neutralize invaders. As a consequence, any acquired, or acquired-like, immune response could be not effectives, since such responses are also characterised by a relatively slow response time. A better knowledge of genes involved in insect immune system by means of the study of vector transcriptomes can therefore lead to a deeper understanding of the mechanisms at the base of the insect-mediated pathogen transmission. References Agrawal A, Eastman QM, Schatz DG. Transposition mediated by RAG1 and RAG2 and its implications for the evolution of the immune system. Nature 394: 744-751, 1998. Anselme C, Vallier A, Balmand S, Fauvarque MO, Heddi A. Host PGR gene expression and bacterial release in endosymbiosis of the weevil Sitophilus zeamais. Appl. Environ. Microbiol. 72: 6766-6772, 2006. Armitage SAO, Sun W, You X, Kurtz J, Schmucker D, Chen W. Quantitative profiling of Drosophila melanogaster Dscam1 isoforms reveals no changes in splicing after bacterial exposure. PLoS One 9: e108660, 2014. Azumi K, De Santis R, De Tomaso A, Rigoutsos I, Yoshizaki F, Pinto MR, et al. Genomic analysis of immunity in a urochordate and the emergence of the vertebrate immune system: "Waiting for Godot". Immunogenetics 55: 570- 581, 2003. Bernstein RM, Schluter SF, Bernstein H, Marchalonis JJ. Primordial emergence of the recombination-activating gene 1 (RAG1): sequence of the complete shark gene indicates homology to microbial integrases. Proc. Natl. Acad. Sci. USA 93: 9454-9459, 1996. Blumbach B, Diehl-Seifert D, Seack J, Steffen R, Müller IM, Müller WEG. Cloning and expression of new receptors to the immunoglobulin superfamily from the marine sponge Geodia cydonium. Immunogenetics 49: 751-763, 1999. Bork P, Holm L, Sander C. The immunoglobulin fold-structural classification, sequence patterns and common core. J. Mol. Biol. 242: 309-320, 1994. Brites D, McTaggart S, Morris K, Anderson J, Thomas K, Colson I, et al. The Dscam homologue of the crustacean Daphnia is diversified by alternative splicing like in insects. Mol. Biol. Evol. 25:1429-1439, 2008. Brites D, Brena C, Ebert D, Du Pasquier L. More than one way to produce protein diversity: duplication and limited alternative splicing of an adhesion molecule gene in basal arthropods. Evol. Int. J. Org. Evol. 67: 2999-3011, 2013. Cannon JP, Haire RN, Litman GW. Identification of diversified genes that contain immunoglobulin- like variable regions in a protochordate. Nat. Immunol. 3: 1200-1207, 2002. Cirimotich CM, Ramirez JL, Dimopoulos G. Native microbiota shape insect vector competence for human pathogens. Cell Host Microbe 10: 307- 310 2011a. Cirimotich CM, Dong Y, Clayton AM, Sandiford SL, Souza-Neto JA, Mulenga M, et al. Natural microbe-mediated refractoriness to Plasmodium infection in Anopheles gambiae. Science 332: 855-858, 2011b. Colpitts TM, Cox J, Vanlandingham DL, Feitosa FM, Cheng G, Kurscheid S, et al. Alterations in the Aedes aegypti transcriptome during infection with West Nile, dengue and yellow fever viruses. PLoS Pathog. 7: e1002189, 2011 Dong Y, Aguilar R, Xi Z, Warr E, Mongin E, Dimopoulos G. Anopheles gambiae immune responses to human and rodent Plasmodium parasite species. PLoS Pathog. 2: e52, 2006. Eleftherianos I, Millichap PJ, Ffrench-Constant RH, Reynolds SE. RNAi suppression of recognition protein mediated immune responses in the tobacco hornworm Manduca sexta causes increased susceptibility to the insect pathogen Photorhabdus. Dev. Comp. Immunol. 30: 1099- 1107, 2006. Eleftherianos I, Boundy S, Joyce S, Aslam S, Marshall J, Cox R, et al. An antibiotic produced by an insect-pathogenic bacterium suppresses host defenses through phenoloxidase inhibition. Proc. Natl. Acad. Sci. USA 104: 2419-2424, 2007. Faye I, Wyatt GR. The synthesis of antibacterial proteins in isolated fat body from Cecropia silkmoth pupae. Experentia 36: 1325-1326, 1980. Fisher TW, Vyas M, He R, Nelson W, Cicero JM, Willer M, et al. Comparison of potato and asian citrus psyllid adult and nymph transcriptomes identified vector transcripts with potential involvement in circulative, propagative 192   http://www.sciencemag.org/search?author1=Musapa+Mulenga&sortspec=date&submit=Submit http://www.sciencemag.org/search?author1=George+Dimopoulos&sortspec=date&submit=Submit Liberibacter transmission. Pathogens 3: 875- 907, 2014. Flajnik MF. Comparative analyses of immunoglobulin genes: surprises and portents. Nat. Rev. Immunol. 2: 688-98, 2002. Flajnik MF. Re-evaluation of the immunological Big Bang. Curr. Biol. 24: R1060-5, 2014. Galetto L, Nardi M, Saracco P, Bressan A, Marzachì C, Bosco D. Variation in vector competency depends on chrysanthemum yellows phytoplasma distribution within Euscelidius variegatus. Entomol. Exp. Appl. 131: 200-207, 2009. Garver LS, Xi Z, Dimopoulos G. Immunoglobulin superfamily members play an important role in the mosquito immune system. Dev. Comp. Immunol. 32: 519-531, 2008. Graveley BR, Kaur A, Gunning D, Zipursky SL, Rowen L, Clemens JC. The organization and evolution of the dipteran and hymenopteran Down syndrome cell adhesion molecule (Dscam) genes. RNA 10: 1499-1506, 2004. Gullan PJ, Cranston PS. The insects, Oxford: Blackwell, 2000. Haire RN, Schnitker N, Mueller MG, Litman GW. Individual protochordates possess unique immune-type receptor repertoires. Curr. Biol. 14: 465-466, 2004. Halaby DM, Poupon A, Mornon JP. The immunoglobulin fold family: sequence analysis and 3D structure comparisons. Protein Eng. 12: 563-571, 1999. He L, Cao G, Huang M, Xue R, Hu X, Gong C. Expression pattern of immunoglobulin superfamily members in the silkworm, Bombyx mori. Gene 548: 198-209, 2014. Hiom K, Melek M and Gellert M. Transposition by the RAG1 and RAG2 proteins: a possible source of oncogenic translocations. Cell 94: 463-470, 1998. Hoek RM, Smit AB, Frings H, Vink JM, de Jong- Brink M, Geraerts WP. A new Ig-superfamily member, molluscan defence molecule (MDM) from Lymnaea stagnalis, is down-regulated during parasitosis. Eur. J. Immunol. 26: 939- 944, 1996. Huang L, Cheng T, Xu P, Duan J, Fang T, Xia Q. Immunoglobulin superfamily is conserved but evolved rapidly and is active in the silkworm, Bombyx mori. Insect Mol. Biol. 18: 517-530, 2009. Hughes GL, Ren X, Ramirez JL, Sakamoto JM, Bailey JA, Jedlicka AE, et al. Wolbachia infections in Anopheles gambiae cells: transcriptomic characterization of novel host- symbiont interaction. PLoS Pathog. 7:e1001296, 2011. Hutter H, Vogel BE, Plenefisch JD, Norris CR, Proenca RB, Spieth J, et al. Conservation and novelty in the evolution of cell adhesion and extracellular matrix genes. Science 287: 989- 994, 2000. Hynes RO, Zhao Q. The evolution of cell adhesion. J. Cell Biol. 150: 89-96, 2000. Ladendorff NE, Kanost MR. Bacteria induced protein P4 (hemolin) from Manduca sexta: a member of the immunoglobulin superfamily, which can inhibit hemocyte aggregation. Arch. Insect Biochem. Physiol. 18: 285-300, 1991. Lefevre T, Vantaux A, Dabire KR, Mouline K, Cohuet A. Non-genetic determinants of mosquito competence for malaria parasites. PLoS Pathog. 9: e1003365, 2013. Kampen H. What makes an insect a vector? Berl. Munch. Tierarztl. Wochenschr. 122: 451-457, 2009. Killiny N, Rashed A, Almeida RPP. Disrupting the transmission of a vector-borne plant pathogen. Appl. Environ. Microbiol. 78: 638-643, 2012. Lindström-Dinnetz I, Sun SC, Faye I. Structure and expression of hemolin, an insect member of the immunoglobulin gene superfamily. Eur. J. Biochem. 230: 920-925, 1995. Medeiros RB, Resende RO, Avila AC. The plant virus tomato spotted wilt tospovirus activates the immune system of its main insect vector, Frankliniella occidentalis. J. Virol. 78, 4976- 4982, 2004. Ossiboff RJ, Parker JS. Identification of regions and residues in feline junctional adhesion molecule required for feline calicivirus binding and infection. J. Virol. 81: 13608-13621, 2007. Padrón A, Molina-Cruz A, Quinones M, Ribeiro JMC, Ramphul U, Rodrigues J, et al. In depth annotation of the Anopheles gambiae mosquito midgut transcriptome. BMC Genomics. 15: 636, 2014. Palmer WJ, Jiggins FM. Comparative genomics reveals the origins and diversity of arthropod immune systems. Mol. Biol. Evol. in press. Pancer Z, Skorokhod A, Blumbach B, Müller WEG. Multiple Ig-like featuring genes divergent within and among individuals of the marine sponge Geodia cydonium. Gene 207: 227-233, 1998. Rasmuson T, Boman HG. Insect immunity. V. Purification and some properties of immune protein P4 from haemolymph of Hyalophora cecropia pupae. Insect Biochem. 17: 133-140, 1979. Schatz DG. Transposition mediated by RAG1 and RAG2 and the evolution of the adaptive immune system. Immunol. Res. 19: 169-182, 1999. Schmidt O, Faye I, Lindstrom-Dinnetz I, Sun SC. Specific immune recognition of insect hemolin, Dev. Comp. Immunol. 17: 195-200, 1993. Schmucker D, Clemens JC, Shu H, Worby CA, Xiao J, Muda M, et al. Drosophila Dscam is an axon guidance receptor exhibiting extraordinary molecular diversity. Cell 101: 671-84, 2000. Seemüller E, Schneider B. Differences in virulence and genomic features of strains of 'Candidatus Phytoplasma mali', the apple proliferation agent. Phytopathology 97: 964-970, 2007. Shaik AH, Sehnal F. Hemolin expression in the silk glands of Galleria mellonella in response to bacterial challenge and prior to cell disintegration. J. Insect Physiol. 55: 781-787, 2009. Shigihara T, Hashimoto M, Shindo N, Aoki T. Transcriptome profile of Trypanosoma cruzi- infected cells: simultaneous up- and down- regulation of proliferation inhibitors and promoters. Parasitol. Res. 102: 715-722, 2008. 193   https://scholar.google.it/citations?view_op=view_citation&hl=it&user=ZaIqwdkAAAAJ&citation_for_view=ZaIqwdkAAAAJ:qjMakFHDy7sC https://scholar.google.it/citations?view_op=view_citation&hl=it&user=ZaIqwdkAAAAJ&citation_for_view=ZaIqwdkAAAAJ:qjMakFHDy7sC https://scholar.google.it/citations?view_op=view_citation&hl=it&user=ZaIqwdkAAAAJ&citation_for_view=ZaIqwdkAAAAJ:qjMakFHDy7sC https://scholar.google.it/citations?view_op=view_citation&hl=it&user=ZaIqwdkAAAAJ&citation_for_view=ZaIqwdkAAAAJ:qjMakFHDy7sC http://www.ncbi.nlm.nih.gov/pubmed/25073905 http://www.ncbi.nlm.nih.gov/pubmed/25073905 http://www.ncbi.nlm.nih.gov/pubmed/25073905 Soroka V, Kasper C, Poulsen FM. Structural biology of NCAM. Adv. Exp. Med. Biol. 663: 3- 22, 2010. Wang J, Springer TA. Structural specializations of immunoglobulin superfamily members for adhesion to integrins and viruses. Immunol. Rev. 163: 197-215, 1998. Sun SC, Lindstrom I, Boman HG, Faye I, Schmidt O. Hemolin: an insect-immune protein belonging to the immunoglobulin superfamily. Science 250: 1729-1732, 1990. Watson FL, Püttmann-Holgado R, Thomas F, Lamar DL, Hughes M, Kondo M, et al. Extensive diversity of Ig-superfamily proteins in the immune system of insects. Science 309: 1874- 1878, 2005. Suzuki SK, Oshima S, Kakizawa R, Arashida HY, Jung Y, Yamaji H, et al. Interaction between the membrane protein of a pathogen and insect microfilament complex determines insect-vector specificity. Proc. Natl. Acad. Sci. USA 103: 4252-4257, 2006. Zapata A, Amemiya CT. Phylogeny of lower vertebrates and their immunological structures. Curr. Opin. Microbiol. Immunol. 248: 67-107, 2000. Vyas M, Fisher TW, He R, Nelson W, Yin G, Cicero JM, et al. Asian citrus psyllid expression profiles suggest Candidatus Liberibacter asiaticus- mediated alteration of adult nutrition and metabolism. PloS One 10: e0130328, 2015. Zhang SM, Zeng Y, Loker ES. Expression profiling and binding properties of fibrinogen-related proteins (FREPs), plasma proteins from the schistosome snail host Biomphalaria glabrata. Innate Immun. 14: 175-189, 2008. Vogel C, Teichmann SA, Chothia C. The immunoglobulin superfamily in Drosophila melanogaster and Caenorhabditis elegans and the evolution of complexity. Development 130: 6317-6328, 2003. Zouali M. B cell tolerance to self in systemic autoimmunity. Arch. Immunol. Ther. Exp. 49: 361-365, 2001. 194