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Trichinella spiralis - New method for sample preparation and objective detection of specific antigens using a chemiluminescence immunoassay.
Braasch, Jana; Ostermann, Stefanie; Mackiewicz, Monika; Bardot, Catherine; Pagneux, Caroline; Borchardt-Lohölter, Viola; Lattwein, Erik.
Afiliação
  • Braasch J; Institute for Experimental Immunology, affiliated to EUROIMMUN Medizinische Labordiagnostika AG, Seekamp 31, 23560 Lübeck, Germany.
  • Ostermann S; Institute for Experimental Immunology, affiliated to EUROIMMUN Medizinische Labordiagnostika AG, Seekamp 31, 23560 Lübeck, Germany.
  • Mackiewicz M; Institute for Experimental Immunology, affiliated to EUROIMMUN Medizinische Labordiagnostika AG, Seekamp 31, 23560 Lübeck, Germany.
  • Bardot C; EUROFINS Laboratory in Moulins, Boulevard De Nomazy - BP 1707, 03017 Moulins, France.
  • Pagneux C; EUROFINS Laboratory in Moulins, Boulevard De Nomazy - BP 1707, 03017 Moulins, France.
  • Borchardt-Lohölter V; Institute for Experimental Immunology, affiliated to EUROIMMUN Medizinische Labordiagnostika AG, Seekamp 31, 23560 Lübeck, Germany.
  • Lattwein E; Institute for Experimental Immunology, affiliated to EUROIMMUN Medizinische Labordiagnostika AG, Seekamp 31, 23560 Lübeck, Germany.
Vet Parasitol X ; 4: 100033, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33305254
The parasitic roundworm Trichinella spiralis is most commonly transmitted to humans through consumption of raw or undercooked meat of infected pigs or game. To prevent human infection, slaughterhouses perform meat safety surveillance using the gold standard "Magnetic Stirrer Method". We introduce a fast and objective method using automated detection of specific Trichinella spiralis antigens by a newly developed immunoassay based on chemiluminescence (ChLIA). Panel A comprised muscle tissue samples from non-infected pigs (n = 37). Panel B comprised muscle tissue samples from non-infected pigs spiked with different amounts of Trichinella larvae without collagen capsules (n = 56). Panel C contained muscle tissue samples from experimentally infected pigs including Trichinella larvae encapsulated in collagen (n = 32). Each sample was shredded with PBS buffer in a knife mill, destroying Trichinella larvae. Following centrifugation, the supernatant (muscle tissue extract containing released excretory and secretory Trichinella spiralis antigens) was used for Trichinella-specific antigen detection by the new Trichinella ChLIA. The overall accuracy of the Trichinella ChLIA was 97.6 %. The specificity of the Trichinella ChLIA was 100 % (panel A). The sensitivity in samples from experimentally infected pigs was 100 % representing a detection limit of 0.01 larvae per gram. Cross-reactivity with parasites other than Trichinella spp. was not observed. This new meat inspection method for the detection of Trichinella spiralis antigens presents high specificity and high sensitivity, especially in truly infected samples. In contrast to the gold standard, this new approach to meat safety surveillance does not require longsome digestion or microscopy by trained personnel.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Vet Parasitol X Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Vet Parasitol X Ano de publicação: 2020 Tipo de documento: Article