Myxozoans are microscopic, metazoan, obligate parasites, belonging to the phylum Cnidaria. In contrast to the free-living lifestyle of most members of this taxon, myxozoans have complex life cycles alternating between vertebrate and invertebrate hosts. Vertebrate hosts are primarily fish, although they are also reported from amphibians, reptiles, trematodes, mollusks, birds and mammals. Invertebrate hosts include annelids and bryozoans. Most myxozoans are not overtly pathogenic to fish hosts, but some are responsible for severe economic losses in fisheries and aquaculture. In both scenarios, the interaction between the parasite and the host immune system is key to explain such different outcomes of this relationship. Innate immune responses contribute to the resistance of certain fish strains and species, and the absence or low levels of some innate and regulatory factors explain the high pathogenicity of some infections. In many cases, immune evasion explains the absence of a host response and allows the parasite to proliferate covertly during the first stages of the infection. In some infections, the lack of an appropriate regulatory response results in an excessive inflammatory response, causing immunopathological consequences that are worse than inflicted by the parasite itself. This review will update the available information about the immune responses against Myxozoa, with special focus on T and B lymphocyte and immunoglobulin responses, how these immune effectors are modulated by different biotic and abiotic factors, and on the mechanisms of immune evasion targeting specific immune effectors. The current and future design of control strategies for myxozoan diseases is based on understanding this myxozoan-fish interaction, and immune-based strategies such as improvement of innate and specific factors through diets and additives, host genetic selection, passive immunization and vaccination, are starting to be considered.

• MeSH
• Adaptive Immunity * MeSH
• Antiparasitic Agents pharmacology   MeSH
• B-Lymphocytes immunology   metabolism   parasitology   MeSH
• Immune Evasion MeSH
• Immunoglobulins immunology   metabolism   MeSH
• Host-Parasite Interactions MeSH
• Myxozoa drug effects   immunology   pathogenicity   MeSH
• Fish Diseases immunology   metabolism   parasitology   prevention & control   MeSH
• Parasitic Diseases, Animal immunology   metabolism   parasitology   prevention & control   MeSH
• Immunity, Innate * MeSH
• Fishes immunology   metabolism   parasitology   MeSH
• T-Lymphocytes immunology   metabolism   parasitology   MeSH
• Vaccines pharmacology   MeSH
• Aquaculture MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Review MeSH
• Research Support, U.S. Gov't, Non-P.H.S. MeSH

Two genotypes of the intestinal parasite Ceratonova shasta infect Oncorhynchus mykiss: genotype 0 results in a chronic infection with low mortality while genotype IIR causes disease with high mortality. We determined parasite load and the relative expression of six immune factors (IgT, IgM, IL-6, IL-8, IL-10, IFNG) in fish infected with either genotype over 29 days post-exposure. In genotype IIR infections the host responded with upregulation of inflammatory and regulatory cytokines. In contrast, genotype 0 infection did not elicit an inflammatory response and expression of IFNG and IL-10 was lower. Antibody expression was upregulated in both infections but appeared to have limited efficacy in the virulent genotype IIR infections. Histologically, in genotype 0 infections the parasite migrated through the tissue layers causing inflammation but minimal damage to the mucosal epithelium, which contrasts with the severe pathology found in genotype IIR infections.

• MeSH
• Cytokines genetics   metabolism   MeSH
• Genotype * MeSH
• Immunoglobulin M blood   MeSH
• Immunoglobulins blood   MeSH
• Host-Parasite Interactions MeSH
• Myxozoa genetics   pathogenicity   MeSH
• Fish Diseases immunology   MeSH
• Oncorhynchus mykiss immunology   MeSH
• Parasitic Diseases, Animal immunology   MeSH
• Parasite Load MeSH
• Cell Movement MeSH
• Fish Proteins blood   MeSH
• Mucous Membrane immunology   MeSH
• Virulence MeSH
• Inflammation immunology   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Research Support, N.I.H., Extramural MeSH
• Research Support, U.S. Gov't, Non-P.H.S. MeSH

Myxozoans are highly diverse and globally distributed cnidarian endoparasites in freshwater and marine habitats. They have adopted a heteroxenous life cycle, including invertebrate and fish hosts, and have been associated with diseases in aquaculture and wild fish stocks. Despite their importance, genomic resources of myxozoans have proven difficult to obtain due to their miniaturized and derived genome character and close associations with fish tissues. The first 'omic' datasets have now become the main resource for a better understanding of host-parasite interactions, virulence, and diversity, but also the evolutionary history of myxozoans. In this review, we discuss recent genomic advances in the field and outline outstanding questions to be answered with continuous and improved efforts of generating myxozoan genomic data.

• MeSH
• Genome genetics   MeSH
• Genomics trends   MeSH
• Myxozoa classification   genetics   pathogenicity   MeSH
• Parasitic Diseases parasitology   transmission   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Review MeSH

Kudoid parasites are known to infect a large variety of fish. A significant proportion of Kudoa species have relatively low host specificity, with a single species able to infect multiple host species representing various host families even from different host orders. Since DNA sequences have been associated with myxosporean species characterisations, it has become far easier to determine host range of new species and validate host records from earlier descriptions. This study investigated the host specificity of a kudoid parasite, Kudoa thalassomi Adlard, Bryant, Whipps et Kent, 2005, from the Great Barrier Reef in Australia using DNA sequence analysis and morphology. The results revealed the host specificity to be broad, with K. thalassomi identified in 18 different fish species representing six different fish families. This study also compares current genetic information from different host isolates of Kudoa Meglitsch, 1947 to their host ranges recorded in existing literature. From this analysis, only half of the Kudoa species with multiple host records (27 Kudoa species) have half or more isolates that are genetically characterised, and thus specifically identified with a high confidence, from their known hosts. Only five kudoid species have genetically characterised isolates from all of their recorded hosts.

• MeSH
• Financing, Organized MeSH
• Phylogeny MeSH
• Genetic Variation MeSH
• Host-Parasite Interactions genetics   MeSH
• Molecular Sequence Data MeSH
• Myxozoa isolation & purification   classification   pathogenicity   MeSH
• Fish Diseases parasitology   MeSH
• Parasitic Diseases, Animal parasitology   MeSH
• DNA, Ribosomal chemistry   MeSH
• RNA, Ribosomal, 18S genetics   MeSH
• RNA, Ribosomal, 28S genetics   MeSH
• Fishes MeSH
• Base Sequence MeSH
• Sequence Analysis, DNA MeSH
• Spores genetics   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Geographicals
• Queensland MeSH

In South Bohemia, Czech Republic, 178 shrews, including 98 common shrews, Sorex araneus L., 70 pygmy shrews, Sorex minutus L., and 10 lesser white-toothed shrews, Crocidura suaveolens (Pallas), were examined for Soricimyxum fegati Prunescu, Prunescu, Pucek et Lom, 2007 infections, using squash preparations of unfixed tissues, histological sections and molecular methods. The infection was found in 51 (52%) S. araneus, 14 (20%) S. minutus and 1 (10%) C. suaveolens. The records of the latter two species extend host range of S. fegati. Lesions associated with S. fegati infections in the liver, the organ of specific localisation of the parasite, were found to be induced by proliferative stages migrating toward lumina of bile ducts. In other organs of these three host species, xenoma-like formations (XLFs) were found that severely injured blood vessels. XLFs contained presporogonic stages of S. fegati, whose species identity was evidenced using molecular methods.

• MeSH
• Blood Vessels parasitology   pathology   MeSH
• Species Specificity MeSH
• Host Specificity MeSH
• Liver parasitology   pathology   MeSH
• Molecular Sequence Data MeSH
• Myxozoa genetics   isolation & purification   classification   pathogenicity   MeSH
• Organ Specificity MeSH
• Parasitic Diseases, Animal parasitology   pathology   MeSH
• Shrews classification   parasitology   MeSH
• RNA, Ribosomal analysis   MeSH
• Base Sequence MeSH
• Sequence Analysis, DNA MeSH
• Bile Ducts parasitology   pathology   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Research Support, Non-U.S. Gov't MeSH
• Geographicals
• Czech Republic MeSH