What is the difference between innate and adaptive defences
B lymphocytes from early vertebrates have potent phagocytic and microbicidal abilities. Nat Immunol. Nitric oxide production by nurse shark Ginglymostoma cirratum and clearnose skate Raja eglanteria peripheral blood leucocytes.
Recent advances on the complement system of teleost fish. Noris M, Remuzzi G. Overview of complement activation and regulation.
Semin Nephrol. Complement and its role in innate and adaptive immune responses. Cell Res. The complement system of elasmobranches revealed by liver transcriptome analysis of a hammerhead shark, Sphyrna zygaena. Smith SL, Nonaka M. Shark complement: genes, proteins and function. Identification and characterization of a variant of the third component of complement C3 in rainbow trout Salmo gairdneri serum.
PubMed Abstract Google Scholar. Diversity of the third form of complement, C3, in fish: functional characterization of five forms of C3 in the diploid fish Sparus aurata. Biochem J. Complement activity in the egg cytosol of zebrafish Danio rerio : evidence for the defense role of maternal complement components. Opsonic effect of the alternative complement pathway on channel catfish peripheral blood phagocytes.
Rebl A, Goldammer T. Under control: the innate immunity of fish from the inhibitors' perspective. Isolation and initial characterisation of complement components C3 and C4 of the nurse shark and the channel catfish.
Molecular and expression analysis of complement component C5 in the nurse shark Ginglymostoma cirratum and its predicted functional role. Molecular characterization of the alpha subunit of complement component C8 GcC8alpha in the nurse shark Ginglymostoma cirratum. Kimura A, Nonaka M. Scand J Immunol. Differential gene expression in the liver of the African lungfish, Protopterus annectens , after 6 days of estivation in air.
J Comp Physiol B. Molecular cloning and protein analysis of divergent forms of the complement component C3 from a bony fish, the common carp Cyprinus carpio : presence of variants lacking the catalytic histidine. Eur J Immunol. Saurabh S, Sahoo PK. Lysozyme: an important defence molecule of fish innate immune system. Grinde B. A lysozyme isolated from rainbow trout acts on mastitis pathogens.
Jolles P, Jolles J. What's new in lysozyme research? Always a model system, today as yesterday. Mol Cell Biochem.
Molecular cloning, expression and evolution of the Japanese flounder goose-type lysozyme gene, and the lytic activity of its recombinant protein. Biochim Biophys Acta. Enzyme characterisation and gene expression profiling of Atlantic salmon chicken- and goose-type lysozymes. Molecular cloning, expression of orange-spotted grouper goose-type lysozyme cDNA, and lytic activity of its recombinant protein. Dis Aquat Organ. Molecular characterization, gene structure and antibacterial activity of a g-type lysozyme from the European sea bass Dicentrarchus labrax L.
Multiple specialised goose-type lysozymes potentially compensate for an exceptional lack of chicken-type lysozymes in Atlantic cod. Mar Biol. Isolation and characterization of a c-type lysozyme from the nurse shark. Irwin DM. Evolution of the vertebrate goose-type lysozyme gene family. BMC Evol Biol. Purification and pore-forming activity of two hydrophobic polypeptides from the secretion of the Red Sea Moses sole Pardachirus marmoratus.
Characterization and ion channel activities of novel antibacterial proteins from the skin mucosa of carp Cyprinus carpio. Eur J Biochem. Characterization and expression studies of Gaduscidin-1 and Gaduscidin-2; paralogous antimicrobial peptide-like transcripts from Atlantic cod Gadus morhua. Naturally concurrent infections of bacterial and viral pathogens in disease outbreaks in cultured Nile tilapia Oreochromis niloticus farms. Two cathelicidin genes are present in both rainbow trout Oncorhynchus mykiss and Atlantic salmon Salmo salar.
Antimicrob Agents Chemother. Evidence of an antimicrobial-immunomodulatory role of Atlantic salmon cathelicidins during infection with Yersinia ruckeri. J Mol Evol. Squalamine: an aminosterol antibiotic from the shark. Antimicrobial peptide isolated from the skin of the fermented skate, Raja kenojei. Acute phase proteins and their potential role as an indicator for fish health and in diagnosis of fish diseases.
Protein Pept Lett. Acute-phase proteins during inflammatory reaction by bacterial infection: fish-model. Bayne CJ, Gerwick L. The acute phase response and innate immunity of fish.
Pentraxins at the crossroads between innate immunity, inflammation, matrix deposition, and female fertility. Annu Rev Immunol. Biochemical and functional characterization of the interaction between pentraxin 3 and C1q. Plasma proteins of rainbow trout Oncorhynchus mykiss isolated by binding to lipopolysaccharide from Aeromonas salmonicida. Lund V, Olafsen JA. A comparative study of pentraxin-like proteins in different fish species. The analysis of the acute phase response during the course of Trypanosoma carassii infection in the goldfish Carassius auratus L.
Changes of C-reactive protein levels in rainbow trout Oncorhynchus mykiss sera after exposure to anti-ectoparasitic chemicals used in aquaculture.
Serum CRP-like protein profile in common carp Cyprinus carpio challenged with Aeromonas hydrophila and Escherichia coli lipopolysaccharide.
Isolation and characterization of two major serum proteins from the dogfish, Mustelus canis , C-reactive protein and amyloid P component. Plasma proteins and selected acute-phase proteins in the whitespotted bamboo shark Chiloscyllium plagiosum. J Zoo Wildl Med. Mar Environ Res. Analysis of the transcriptome of the Indonesian coelacanth Latimeria menadoensis. Mashoof S, Criscitiello MF. Fish immunoglobulins.
Immunoglobulin genes and their transcriptional control in teleosts. Intraclass diversification of immunoglobulin heavy chain genes in the African lungfish. J chain in the nurse shark: implications for function in a lower vertebrate. An evolutionarily mobile antigen receptor variable region gene: doubly rearranging NAR-TcR genes in sharks. The many important facets of T-cell repertoire diversity.
Function and control of recombination-activating gene activity. Ann N Y Acad Sci. Hsu E. V D J recombination: of mice and sharks. Adv Exp Med Biol. Lymphocyte differentiation in sea bass thymus: CD4 and CD8-alpha gene expression studies. The immunoglobulin heavy-chain locus in zebrafish: identification and expression of a previously unknown isotype, immunoglobulin Z.
Evolution of duplicated IgH loci in Atlantic salmon, Salmo salar. A shark antibody heavy chain encoded by a nonsomatically rearranged VDJ is preferentially expressed in early development and is convergent with mammalian IgG.
The evolution of multiple isotypic IgM heavy chain genes in the shark. Comparative analyses of immunoglobulin genes: surprises and portents. The African coelacanth genome provides insights into tetrapod evolution.
Genome complexity in the coelacanth is reflected in its adaptive immune system. Structural and functional characterization of complement C4 and C1s-like molecules in teleost fish: insights into the evolution of classical and alternative pathways. Fc receptor for shark IgM. Clem LW. Phylogeny of immunoglobulin structure and function. Immunoglobulins of the giant grouper, Epinephelus itaira. Evolution of antibody structure and effector functions: comparative hemolytic activities of monomeric and tetrameric IgM from rainbow trout, Salmo gairdnerii.
Comp Biochem Physiol B. Evolutionary variation of immunoglobulin mu heavy chain RNA processing pathways: origins, effects, and implications. Immunol Rev. B cell receptor accessory molecules in the channel catfish, Ictalurus punctatus. Putting J chain back on the map: how might its expression define plasma cell development? Analysis of two IgM isotypes in Atlantic salmon and brown trout. Cloning and sequence analysis of two isotypic IgM heavy chain genes from Atlantic salmon, Salmo salar L.
Dooley H, Flajnik MF. Shark immunity bites back: affinity maturation and memory response in the nurse shark, Ginglymostoma cirratum.
Antibody repertoire development in cartilaginous fish. Lineage-restricted retention of a primitive immunoglobulin heavy chain isotype within the Dipnoi reveals an evolutionary paradox. Discovery of J chain in African lungfish Protopterus dolloi , Sarcopterygii using high throughput transcriptome sequencing: implications in mucosal immunity.
A second class of immunoglobulin other than IgM present in the serum of a cartilaginous fish, the skate, Raja kenojei: isolation and characterization. Identification of sturgeon IgD bridges the evolutionary gap between elasmobranchs and teleosts.
Ohta Y, Flajnik M. IgD, like IgM, is a primordial immunoglobulin class perpetuated in most jawed vertebrates. Insights into the function of IgD. Discovery and characterization of secretory IgD in rainbow trout: secretory IgD is produced through a novel splicing mechanism. B cells and their role in the teleost gut. The IgH locus of the channel catfish, Ictalurus punctatus , contains multiple constant region gene sequences: different genes encode heavy chains of membrane and secreted IgD.
Stenvik J, Jorgensen TO. Immunoglobulin D IgD of Atlantic cod has a unique structure. Genes of the constant regions of functional immunoglobulin heavy chain of Japanese flounder, Paralichthys olivaceus. Ig heavy chain genes and their locus in grass carp Ctenopharyngodon idella. The astonishing diversity of Ig classes and B cell repertoires in teleost fish. Discovery of a unique Ig heavy-chain isotype IgT in rainbow trout: implications for a distinctive B cell developmental pathway in teleost fish.
Characterization of the immunoglobulin repertoire of the spiny dogfish Squalus acanthias. Unprecedented multiplicity of Ig transmembrane and secretory mRNA forms in the cartilaginous fish.
Assembly and expression of shark Ig genes. Mucosal immunoglobulins and B cells of teleost fish. Discovery of a novel immunoglobulin heavy chain gene chimera from common carp Cyprinus carpio L.
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. IgT, a primitive immunoglobulin class specialized in mucosal immunity. B cell heterogeneity in the teleost kidney: evidence for a maturation gradient from anterior to posterior kidney.
Zwollo P. Dissecting teleost B cell differentiation using transcription factors. Plasmablast and plasma cell production and distribution in trout immune tissues. The cellular context of AID expressing cells in fish lymphoid tissues. Lymphomyeloid tissues and blood cell morphology in elasmobranchs. Arch Biol.
The development of primary and secondary lymphoid tissues in the nurse shark Ginglymostoma cirratum: B-cell zones precede dendritic cell immigration and T-cell zone formation during ontogeny of the spleen. Evolutionary origins of lymphocytes: ensembles of T cell and B cell transcriptional regulators in a cartilaginous fish. Structure of the lymphoid organs of elasmobranchs.
Development of immunological memory in rainbow trout Oncorhynchus mykiss. An immunochemical and cellular analysis of the B cell response. Vaccination of turbot, Psetta maxima L. J Fish Dis. Association between plasma antibody response and protection in rainbow trout Oncorhynchus mykiss immersion vaccinated against Yersinia ruckeri. Why is the antibody response of Atlantic cod so poor? The search for a genetic explanation. Fish Sci. Star B, Jentoft S. Stavnezer J, Amemiya CT. Evolution of isotype switching.
Semin Immunol. Magor BG. Antibody affinity maturation in fishes-our current understanding. Cloning and expression of the AID gene in the channel catfish. Identification of the activation-induced cytidine deaminase gene from zebrafish: an evolutionary analysis.
Evolution of class switch recombination function in fish activation-induced cytidine deaminase, AID. Zebrafish AID is capable of deaminating methylated deoxycytidines.
Nucleic Acids Res. Biochemical regulatory features of activation-induced cytidine deaminase remain conserved from lampreys to humans. Mol Cell Biol. African lungfish reveal the evolutionary origins of organized mucosal lymphoid tissue in vertebrates. Curr Biol. The strength of B cell interaction with antigen determines the degree of IgM polymerization. Binding properties of shark immunoglobulins. First molecular and biochemical analysis of an in vivo affinity maturation in an ectothermic vertebrate.
AID from bony fish catalyzes class switch recombination. J Exp Med. Origin of immunoglobulin isotype switching. Molecular cloning, organization, expression and 3D structural analysis of the MHC class Ia gene in the whitespotted bamboo shark Chiloscyllium plagiosum.
Present yourself! Trends Immunol. The MHC class I genes of zebrafish. Comparative genomics of the MHC: glimpses into the evolution of the adaptive immune system. Major histocompatibility lineages and immune gene function in teleost fishes: the road not taken.
Crit Rev Immunol. Successive losses of central immune genes characterize the gadiformes' alternate immunity.
Genome Biol Evol. Characterization of a divergent non-classical MHC class I gene in sharks. The major histocompatibility class I locus in Atlantic salmon Salmo salar L. Innate immunity Innate immunity refers to nonspecific defense mechanisms that come into play immediately or within hours of an antigen's appearance in the body. These mechanisms include physical barriers such as skin, chemicals in the blood, and immune system cells that attack foreign cells in the body. When this happens, autoimmune diseases can develop e.
The hallmark of the adaptive immune system is clonal expansion of lymphocytes. Clonal expansion is the rapid increase of T and B lymphocytes from one or a few cells to millions. Each clone that originates from the original T or B lymphocyte has the same antigen receptor as the original and fights the same pathogen.
While the innate immune response is immediate, the adaptive immune response is not. However, the effect of the adaptive immune response is long-lasting, highly specific, and is sustained long-term by memory T cells. Natural killer cells, macrophages, neutrophils, dendritic cells, mast cells, basophils, eosinophils.
Tell us what you think about Healio. Figure 1, 2; Table 1. Innate immunity also called natural or native immunity provides the early line of defense against microbes. It consists of cellular and biochemical defense mechanisms that are in place even before infection and are poised to respond rapidly to infections. The mechanisms of innate immunity are specific for structures that are common to groups of related microbes and may not distinguish fine differences between microbes.
The principal components of innate immunity are: 1 Physical and chemical barriers, such as epithelia and antimicrobial chemicals produced at epithelial surfaces; 2 Phagocytic cells neutrophils, macrophages , dendritic cells, and natural killer NK cells and other innate lymphoid cells; 3 Blood proteins, including members of the complement system and other mediators of inflammation.
Adaptive immunity also called specific or acquired immunity system recognizes and reacts to a large number of microbial and nonmicrobial substances. The defining characteristics of adaptive immunity are the ability to distinguish different substances, called specificity, and the ability to respond more vigorously to repeated exposures to the same microbe, known as memory. The unique components of adaptive immunity are cells called lymphocytes and their secreted products, such as antibodies.
Foreign substances that induce specific immune responses or are recognized by lymphocytes or antibodies are called antigens. Figure 1. Just as resistance to disease can be innate inborn or acquired, the mechanisms mediating it can be correspondingly divided into innate left and adaptive right , each composed of both cellular lower half and humoral elements i.
Adaptive mechanisms, more recently evolved, perform many of their functions by interacting with the older innate ones. Innate immunity is activated when cells use specialized sets of receptors Pattern recognition receptor, PRR to recognize different types of microorganisms bacteria, viruses, etc. Binding to these receptors activates a limited number of basic microbial disposal mechanisms, such as phagocytosis of bacteria by macrophages and neutrophils, or the release of antiviral interferons.
Many of the mechanisms involved in innate immunity are largely the same as those responsible for non-specifically reacting to tissue damage, with the production of inflammation cover up the right-hand part of Figure 1 to appreciate this.
Adaptive mechanisms can function on their own against certain antigens cover up the left-hand part of Figure 1 , but the majority of their effects are exerted by means of the interaction of antibody with complement and the phagocytic cells of innate immunity, and of T cells with macrophages broken lines.
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