The presence of Trichinella pseudospiralis has been increasingly reported in Europe in the last decade. The parasite was recorded for the first time in Central Europe in 2003-2004, in eastern Slovakia, in pigs, rats and a cat from a pig breeding farm. In the following years, it was also repeatedly diagnosed in co-infection with T. britovi in sylvatic animals from this area. Molecular analyses revealed a distinctive genetic relationship of the Slovak isolate with those from Finland and Sweden, suggesting the potential role of migratory birds of prey in the transmission of the parasite. Thus, potential host species, including mammals and birds, were investigated for the presence of T. pseudospiralis. During 2006-2018, a total of 360 carcasses of raptorial, carrion-feeding and scavenging birds were collected and examined using artificial digestion of pectoral muscle samples. Muscle larvae were detected in muscle of one golden eagle (Aquila chrysaetos), two common kestrels (Falco tinnunculus) and one peregrine falcon (F. peregrinus). Molecular analyses confirmed the presence of T. pseudospiralis. These findings in diurnal raptorial species represent new host records for Trichinella spp. In 2017, a mandatory examination of pigs (Sus scrofa domesticus), red foxes (Vulpes vulpes) and wild boars (Sus scrofa) revealed one wild boar from the central part of territory to be infected with T. pseudospiralis. Our data confirm that the parasite has already established itself in Slovakia, and thus adequate veterinary measures and public education are needed to prevent its transmission to the food chain and the risk of human infection.
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http://dx.doi.org/10.1016/j.vetpar.2020.109129 | DOI Listing |
Iran J Parasitol
January 2024
Department of Parasitology and Parasitic Diseases, Faculty of Veterinary Sciences, University of Buenos Aires, Buenos Aires, Argentina.
Background: The aim of this study was to investigate the survival of and in decaying wild boar tissue and assess their freezing tolerance in experimentally infected animals.
Methods: The present study was conducted in Buenos Aires City, Argentina during the 2018-2019 period. Two wild boars were used, one infected with 20,000 muscle larvae (ML) of and the other with .
Cytokine
December 2024
Department of Translational Research, N.T.M.S., Università di Pisa, Pisa, Italy. Electronic address:
Introduction: We studied the cellular immune response in a patient infected since 10 months (along with other 51 people) during a trichinellosis outbreak caused by Trichinella spp.
Methods: A 46 years old female resulted serologically positive for trichinellosis. We isolated peripheral blood mononuclear cells (PBMCs) and incubated them with excretory/secretory antigens (ESA) of Trichinella spiralis (T1) or Trichinella pseudospiralis (T4) to produce antigen specific T cell lines and clones, analysed for the phenotype (T helper or cytotoxic cells), for their T4 or T1 antigens specificity and for their cytokine profile (IFNγ, IL-17A, IL-4) by flow cytometry, thymidine incorporation assay and ELISpot.
Vet Parasitol
January 2025
Institute of Parasitology, Slovak Academy of Sciences, Hlinkova 3, Košice 040 01, Slovak Republic.
Trichinella pseudospiralis belongs to the non-encapsulated clade of the genus and its epidemiology is influenced by various biotic and abiotic factors. The role of different animal species in the spread and epidemiology of the parasite is still not well understood and further research is needed in the areas where its occurrence has been recorded. In Slovakia, T.
View Article and Find Full Text PDFVet Parasitol
January 2025
German Federal Institute for Risk Assessment (BfR), Department for Biological Safety, Max-Dohrn-Str. 8-10, Berlin 10589, Germany. Electronic address:
Int J Mol Sci
July 2024
Department of Veterinary Biosciences, Melbourne Veterinary School, Faculty of Science, The University of Melbourne, Parkville, VIC 3010, Australia.
Nematodes of the genus are important pathogens of humans and animals. This study aimed to enhance the genomic and transcriptomic resources for (non-encapsulated phenotype) and (encapsulated phenotype) and to explore transcriptional profiles. First, we improved the assemblies of the genomes of (code ISS13) and (code ISS534), achieving genome sizes of 56.
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