Mostrar el registro sencillo del ítem

dc.date.available
2024-05-06T13:19:40Z  
dc.identifier.citation
Bontempi, Iván; Arias, Diego Gustavo; Marcipar, Iván Sergio; (2024): Improved Serodiagnosis of Trypanosoma vivax Infections in Cattle Reveals High Infection Rates in the Livestock Regions of Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. (dataset). http://hdl.handle.net/11336/234547  
dc.identifier.uri
http://hdl.handle.net/11336/234547  
dc.description.abstract
Bovine trypanosomosis, caused by Trypanosoma vivax, currently affects cattle and has a significant economic impact in sub-Saharan Africa and South America. The development of new diagnostic antigens is essential to improve and refine existing methods. Our study evaluated the efficacy of two recombinant antigens in detecting specific antibodies in cattle. These antigens are derivatives of an invariant surface glycoprotein (ISG) from T. vivax. A fraction of a previously described antigen (TvY486_0045500), designated TvISGAf, from an African strain was evaluated, and a new ISG antigen from an American isolate, TvISGAm, was identified. The two antigens were expressed as fusion proteins in Escherichia coli: TvISGAf was fused to the MBP-His-tag, and TvISGAm was obtained as a His-tag fused protein. An ELISA evaluation was conducted using these antigens on 149 positive and 63 negative bovine samples. The diagnostic performance was enhanced by the use of a combination of both antigens (referred to as TvISG-based ELISA), achieving a sensitivity of 89.6% and specificity of 93.8%. Following the validation of the TvISG-based ELISA, the seroprevalence of T. vivax infection in 892 field samples from cattle in the central region of Argentina was determined. The mean seroprevalence of T. vivax was 53%, with variation ranging from 21% to 69% among the six departments studied. These results support the use of the TvISG ELISA as a valuable serological tool for the detection and monitoring of T. vivax infection in cattle. Furthermore, we report for the first time the seroprevalence of T. vivax in Argentina, which highlights the widespread endemic nature of the disease in the region. In order to effectively manage the increasing spread of T. vivax in the vast livestock production areas of South America, it is essential to implement consistent surveillance programs and to adopt preventive strategies.  
dc.rights
info:eu-repo/semantics/embargoedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.title
Improved Serodiagnosis of Trypanosoma vivax Infections in Cattle Reveals High Infection Rates in the Livestock Regions of Argentina  
dc.type
dataset  
dc.date.updated
2024-04-30T13:16:57Z  
dc.description.fil
Fil: Bontempi, Iván. Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas. Laboratorio de Tecnología Inmunológica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Arias, Diego Gustavo. Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas. Laboratorio de Enzimología Molecular; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.description.fil
Fil: Marcipar, Iván Sergio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas. Laboratorio de Tecnología Inmunológica; Argentina  
dc.rights.embargoDate
2024-06-01  
dc.datacite.PublicationYear
2024  
dc.datacite.Creator
Bontempi, Iván  
dc.datacite.Creator
Arias, Diego Gustavo  
dc.datacite.Creator
Marcipar, Iván Sergio  
dc.datacite.affiliation
Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas. Laboratorio de Tecnología Inmunológica  
dc.datacite.affiliation
Consejo Nacional de Investigaciones Científicas y Técnicas  
dc.datacite.affiliation
Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas. Laboratorio de Enzimología Molecular  
dc.datacite.affiliation
Consejo Nacional de Investigaciones Científicas y Técnicas  
dc.datacite.affiliation
Consejo Nacional de Investigaciones Científicas y Técnicas  
dc.datacite.affiliation
Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas. Laboratorio de Tecnología Inmunológica  
dc.datacite.publisher
Consejo Nacional de Investigaciones Científicas y Técnicas  
dc.datacite.subject
Otras Ciencias Veterinarias  
dc.datacite.subject
Ciencias Veterinarias  
dc.datacite.subject
CIENCIAS AGRÍCOLAS  
dc.datacite.date
02/01/2021-05/01/2023  
dc.datacite.DateType
Recolectado  
dc.datacite.language
eng  
dc.datacite.version
1.0  
dc.datacite.description
resumir: Immunodetection experiments were adapted from a previously described method for T. cruzi (31). Briefly, polyclonal antibodies against TvISGAf and TvISGAm were obtained by immunizing mice with 10 µg of purified recombinant protein at two-week intervals, as previously described (32). T. vivax cells of the Y486 strain, obtained from mice infected for four days, were pelleted and washed twice for 15 minutes at room temperature with sterile PBS buffer and then fixed in 4% (v/v) formaldehyde. After washing, they were permeabilized and blocked for 30 minutes in a medium containing PBS with the addition of 0.1% (v/v) Triton X-100 and 3% (w/v) BSA. The primary antibodies used were either mouse anti-TvISAf sera (1/100) or mouse anti-TvISGAm sera (1/100), along with rabbit anti-TccPx polyclonal antibodies (1/100 dilution). Slide wells were washed three times with blocking solution (3x50 µl). Secondary antibodies diluted 1/100 in blocking buffer (20 µl) were added to the slide wells and incubated for 60 minutes. FITC-conjugated goat anti-rabbit or Alexa 680-conjugated goat anti-mouse antibodies were used as secondary antibodies. DAPI (20 µl/slide well), diluted in PBS (final concentration 0.5 µg/ml), was added to each slide well. Slides were examined with a confocal microscope (Leica).  
dc.datacite.DescriptionType
Métodos  
dc.datacite.FundingReference
PICT-2020-SERIEA-025 92  
dc.datacite.FunderName
Ministerio de Ciencia, Tecnología e Innovación Productiva. Agencia Nacional de Promoción Científica y Tecnológica. Fondo para la Investigación Científica y Tecnológica  
dc.subject.keyword
T. vivax seroprevalence  
dc.subject.keyword
Dairy cattle  
dc.subject.keyword
Endemic disease  
dc.subject.keyword
Parasite spreading  
dc.datacite.resourceTypeGeneral
dataset  
dc.conicet.datoinvestigacionid
15254  
dc.datacite.awardTitle
DESARROLLO DE UNA INMUNOCROMATOGRAFÍA DE FLUJO LATERAL PARA EL DIAGNÓSTICO RÁPIDO DE TRYPANOSOMIASIS BOVINA CARÁTULA DE PROYECTO  
dc.datacite.geolocation
Santa Fe  
dc.datacite.geolocation
Córdoba  
dc.datacite.formatedDate
2021-2023