The kinetics of cellular and humoral immune responses of common carp to presporogonic development of the myxozoan Sphaerospora molnari
Language English Country Great Britain, England Media electronic
Document type Journal Article
Grant support
634429 ParaFishControl
Horizon 2020 Framework Programme
19-28399X
Grantová Agentura České Republiky
19-25589Y
Grantová Agentura České Republiky
TG02010016
Technologická Agentura České Republiky
CENAKVA No. CZ.1.05/2.1.00/01.0024
Ministerstvo Školství, Mládeže a Tělovýchovy
QK1820354
Národní agentura pro zemědělský výzkum (CZ)
PubMed
31060624
PubMed Central
PMC6501462
DOI
10.1186/s13071-019-3462-3
PII: 10.1186/s13071-019-3462-3
Knihovny.cz E-resources
- Keywords
- B cells, Cyprinus carpio, Cytokines, Host–parasite interaction, IgM, Myxozoa, Sphaerospora molnari, Teleost,
- MeSH
- Immunity, Cellular MeSH
- Cytokines metabolism MeSH
- Head Kidney metabolism MeSH
- Immunity, Humoral MeSH
- Host-Parasite Interactions MeSH
- Carps immunology parasitology MeSH
- Disease Models, Animal MeSH
- Myxozoa growth & development immunology MeSH
- Fish Diseases immunology parasitology MeSH
- Parasitic Diseases, Animal immunology parasitology MeSH
- Spores MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Cytokines MeSH
BACKGROUND: Sphaerospora molnari is a myxozoan parasite causing skin and gill sphaerosporosis in common carp (Cyprinus carpio) in central Europe. For most myxozoans, little is known about the early development and the expansion of the infection in the fish host, prior to spore formation. A major reason for this lack of information is the absence of laboratory model organisms, whose life-cycle stages are available throughout the year. RESULTS: We have established a laboratory infection model for early proliferative stages of myxozoans, based on separation and intraperitoneal injection of motile and dividing S. molnari stages isolated from the blood of carp. In the present study we characterize the kinetics of the presporogonic development of S. molnari, while analyzing cellular host responses, cytokine and systemic immunoglobulin expression, over a 63-day period. Our study shows activation of innate immune responses followed by B cell-mediated immune responses. We observed rapid parasite efflux from the peritoneal cavity (< 40 hours), an initial covert infection period with a moderate proinflammatory response for about 1-2 weeks, followed by a period of parasite multiplication in the blood which peaked at 28 days post-infection (dpi) and was associated with a massive lymphocyte response. Our data further revealed a switch to a massive anti-inflammatory response (up to 1456-fold expression of il-10), a strong increase in the expression of IgM transcripts and increased number of IgM+ B lymphocytes, which produce specific antibodies for the elimination of most of the parasites from the fish at 35 dpi. However, despite the presence of these antibodies, S. molnari invades the liver 42 dpi, where an increase in parasite cell number and indistinguishable outer cell membranes are indicative of effective exploitation and disguise mechanisms. From 49 dpi onwards, the acute infection changes to a chronic one, with low parasite numbers remaining in the fish. CONCLUSIONS: To our knowledge, this is the first time myxozoan early development and immune modulation mechanisms have been analyzed along with innate and adaptive immune responses of its fish host, in a controlled laboratory system. Our study adds important information on host-parasite interaction and co-evolutionary adaptation of early metazoans (Cnidaria) with basic vertebrate (fish) immune systems and the evolution of host adaptation and parasite immune evasion strategies.
Faculty of Engineering and Natural Sciences Johannes Kepler University Linz Austria
Faculty of Science University of South Bohemia in České Budějovice České Budějovice Czech Republic
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