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dc.contributor.authorMierzejewski, Karoles_ES
dc.contributor.authorStryiński, Robertes_ES
dc.contributor.authorLopieńska-Biernat, Elzbietaes_ES
dc.contributor.authorMateos, Jesúses_ES
dc.contributor.authorBogacka, Iwonaes_ES
dc.contributor.authorCarrera, Mónicaes_ES
dc.date.accessioned2021-12-02T09:16:32Z-
dc.date.available2021-12-02T09:16:32Z-
dc.date.issued2021-
dc.identifier.citationMolecular and Cellular Proteomics 20: 100166 (2021)es_ES
dc.identifier.issn1535-9476-
dc.identifier.urihttp://hdl.handle.net/10261/255154-
dc.description18 pages, 8 figures, 1 table.-- This is an open access article under the CC BY licensees_ES
dc.description.abstractHelminths are masters at manipulating host's immune response. Especially, parasitic nematodes have evolved strategies that allow them to evade, suppress, or modulate host's immune response to persist and spread in the host's organism. While the immunomodulatory effects of nematodes on their hosts are studied with a great commitment, very little is known about nematodes' own immune system, immune response to their pathogens, and interactions between parasites and bacteria in the host's organism. To illustrate the response of the parasitic nematode Anisakis simplex s.s. during simulated interaction with Escherichia coli, different concentrations of lipopolysaccharide (LPS) were used, and the proteomic analysis with isobaric mass tags for relative and absolute quantification (tandem mass tag–based LC–MS/MS) was performed. In addition, gene expression and biochemical analyses of selected markers of oxidative stress were determined. The results revealed 1148 proteins in a group of which 115 were identified as differentially regulated proteins, for example, peroxiredoxin, thioredoxin, and macrophage migration inhibitory factor. Gene Ontology annotation and Reactome pathway analysis indicated that metabolic pathways related to catalytic activity, oxidation–reduction processes, antioxidant activity, response to stress, and innate immune system were the most common, in which differentially regulated proteins were involved. Further biochemical analyses let us confirm that the LPS induced the oxidative stress response, which plays a key role in the innate immunity of parasitic nematodes. Our findings, to our knowledge, indicate for the first time, the complexity of the interaction of parasitic nematode, A. simplex s.s. with bacterial LPS, which mimics the coexistence of helminth and gut bacteria in the host. The simulation of this crosstalk led us to conclude that the obtained results could be hugely valuable in the integrated systems biology approach to describe a relationship between parasite, host, and its commensal bacteriaes_ES
dc.description.sponsorshipThis work was funded by the GAIN-Xunta de Galicia, project number IN607D 2017/01 and the Spanish AEI/EU-FEDER PID2019-103845RB-C21 project. Part of this work was supported by “International scholarship exchange of doctoral students and academic staff (PROM)” financed by the Polish National Agency for Academic Exchange (NAWA)es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.publisherAmerican Society for Biochemistry and Molecular Biologyes_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.subjectAnisakis simplexes_ES
dc.subjectLipopolysaccharidees_ES
dc.subjectParasite–bacteria interrelationshipes_ES
dc.subjectOxidative stresses_ES
dc.subjectLC–MS/MSes_ES
dc.titleA Complex Proteomic Response of the Parasitic Nematode Anisakis simplex s.s. to Escherichia coli Lipopolysaccharidees_ES
dc.typeartículoes_ES
dc.identifier.doi10.1016/j.mcpro.2021.100166-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.mcpro.2021.100166es_ES
dc.identifier.e-issn1535-9484-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.openairetypeartículo-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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