Literature DB >> 32687668

Molecular detection of 7SL-derived small RNA is a promising alternative for trypanosomosis diagnosis.

Mylène Verney1, Finn Grey2, Charlène Lemans1, Tristan Géraud1, David Berthier3,4, Sophie Thévenon3,4, Alain Rincé5, Aymeric Hans1, Liam Morrison2, Laurent Hébert1.   

Abstract

Equine trypanosomosis comprises different parasitic diseases caused by protozoa of the subgenus Trypanozoon: Trypanosoma equiperdum (causative agent of dourine), Trypanosoma brucei (nagana) and Trypanosoma evansi (surra). Due to the absence of a vaccine and the lack of efficacy of the few available drugs, these diseases represent a major health and economic problem for international equine trade. Development of affordable, sensitive and specific diagnostic tests is therefore crucial to ensure the control of these diseases. Recently, it has been shown that a small RNA derived from the 7SL gene (7SL-sRNA) is produced in high concentrations in sera of cattle infected with Trypanosoma congolense, Trypanosoma vivax and Trypanosoma brucei. Our objective was to determine whether 7SL-sRNA could serve as a marker of active infection in equids experimentally infected with Trypanosoma equiperdum by analysing the sensitivity, specificity and stability of the 7SL-sRNA. Using a two-step RT-qPCR, we were able to detect the presence of 7SL-sRNA between 2 and 7 days post-infection, whereas seroconversion was detected by complement fixation test between 5 and 14 days post-infection. There was a rapid loss of 7SL-sRNA signal from the blood of infected animals one day post-trypanocide treatment. The 7SL-sRNA RT-qPCR allowed an early detection of a treatment failure revealed by glucocorticoid-induced immunosuppression. In addition, the 7SL-sRNA remains detectable in positive sera after 7 days of storage at either 4°C, room temperature or 30°C, suggesting that there is no need to refrigerate serum samples before analysis. Our findings demonstrate continual detection of 7SL-sRNA over an extended period of experimental infection, with signals detected more than six weeks after inoculation. The detection of a strong and consistent 7SL-sRNA signal even during subpatent parasitemia and the early detection of treatment failure highlight the very promising nature of this new diagnostic method.
© 2020 Blackwell Verlag GmbH.

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Keywords:  zzm321990Trypanosoma equiperdumzzm321990; 7SL-sRNA; RT-qPCR; diagnosis; equine trypanosomosis

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Year:  2020        PMID: 32687668     DOI: 10.1111/tbed.13744

Source DB:  PubMed          Journal:  Transbound Emerg Dis        ISSN: 1865-1674            Impact factor:   5.005


  2 in total

1.  Comparative Sensitivity and Specificity of the 7SL sRNA Diagnostic Test for Animal Trypanosomiasis.

Authors:  Maria Contreras Garcia; Emily Walshe; Pieter C Steketee; Edith Paxton; Javier Lopez-Vidal; Michael C Pearce; Keith R Matthews; Fatima Ezzahra-Akki; Alec Evans; Karen Fairlie-Clark; Jacqueline B Matthews; Finn Grey; Liam J Morrison
Journal:  Front Vet Sci       Date:  2022-04-05

Review 2.  Diagnosis of animal trypanosomoses: proper use of current tools and future prospects.

Authors:  Marc Desquesnes; Alireza Sazmand; Marisa Gonzatti; Alain Boulangé; Géraldine Bossard; Sophie Thévenon; Geoffrey Gimonneau; Philippe Truc; Stéphane Herder; Sophie Ravel; Denis Sereno; Etienne Waleckx; Vincent Jamonneau; Philippe Jacquiet; Sathaporn Jittapalapong; David Berthier; Philippe Solano; Laurent Hébert
Journal:  Parasit Vectors       Date:  2022-06-27       Impact factor: 4.047

  2 in total

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