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Performance of recombinant proteins in diagnosis and differentiation of canine visceral leishmaniasis infected and vaccinated dogs.

作者信息

Pereira Ingrid E, Silva Kyssia P, Menegati Laura M, Pinheiro Aimara C, Assunção Elaine A O, Araújo Maria De Lourdes P, Abass Elfadil, Duthie Malcolm S, Steinhoff Ulrich, Teixeira Henrique C

机构信息

1Department of Parasitology, Microbiology and Immunology, Institute of Biological Sciences, Federal University of Juiz de Fora, 36036-900, Juiz de Fora, Brazil.

2Zoonosis Control Center, Municipal Health Secretariat, 35022-280, Governador Valadares, Brazil.

出版信息

Eur J Microbiol Immunol (Bp). 2020 Aug 27;10(3):165-171. doi: 10.1556/1886.2020.00018.


DOI:10.1556/1886.2020.00018
PMID:32857712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7592511/
Abstract

Control of canine visceral leishmaniasis (CVL), a major zoonotic disease in Brazil and many other tropical and subtropical countries, remains difficult as an accurate and reliable diagnosis is still missing. In endemic regions, infected dogs are the main parasitic reservoir host of human Visceral leishmaniasis (VL) infection. Vaccination of dogs against Leishmania infection constitutes an important strategy to prevent or to better control CVL, thus, a serological test that can discriminate between antibodies induced by immunization versus infection is highly desirable in order to improve and simplify diagnosis. Here, four recombinant proteins were evaluated for their ability to detect and differentiate between dogs that are infected with Leishmania or have been immunized with the anti-Leishmania vaccine Leish-Tec®. Receiver operating characteristic (ROC) curve analysis of the four Leishmania-specific IgG ELISA revealed superior performance of rK28, followed by rKLO8, rK39 and rLb6H. The rK28-based ELISA revealed not only the best accuracy against CVL, but also the lowest cross-reactivity with sera from Leish-Tec® immunized dogs. Our data show that the rK28-based ELISA is highly suitable for CVL screening as it shows high sensitivity with simultaneous low cross-reactivity. Further, the high specificity of the rKLO8 indicates its suitability for the confirmation of CVL diagnosis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/df3a95c34252/eujmi-10-165-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/72cf53fd2e95/eujmi-10-165-s001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/d8c200d8ddd4/eujmi-10-165-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/e7d751d2fb27/eujmi-10-165-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/df3a95c34252/eujmi-10-165-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/72cf53fd2e95/eujmi-10-165-s001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/d8c200d8ddd4/eujmi-10-165-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/e7d751d2fb27/eujmi-10-165-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b50/7592511/df3a95c34252/eujmi-10-165-g003.jpg

相似文献

[1]
Performance of recombinant proteins in diagnosis and differentiation of canine visceral leishmaniasis infected and vaccinated dogs.

Eur J Microbiol Immunol (Bp). 2020-8-27

[2]
Antibody responses induced by Leish-Tec®, an A2-based vaccine for visceral leishmaniasis, in a heterogeneous canine population.

Vet Parasitol. 2014-8-29

[3]
Comparison of two commercial vaccines against visceral leishmaniasis in dogs from endemic areas: IgG, and subclasses, parasitism, and parasite transmission by xenodiagnosis.

Vaccine. 2014-1-6

[4]
Field randomized trial to evaluate the efficacy of the Leish-Tec® vaccine against canine visceral leishmaniasis in an endemic area of Brazil.

Vaccine. 2016-4-27

[5]
High Performance of ELISA test using recombinant rLiNTPDase2 from Leishmania infantum: a Phase II diagnosis of Canine Visceral Leishmaniasis.

Acta Trop. 2020-5-22

[6]
Virulence Factor A2 Protein: Linear B-Cell Epitope Mapping and Identification of Three Main Linear B-Cell Epitopes in Vaccinated and Naturally Infected Dogs.

Front Immunol. 2018-7-25

[7]
A new Leishmania-specific hypothetical protein and its non-described specific B cell conformational epitope applied in the serodiagnosis of canine visceral leishmaniasis.

Parasitol Res. 2016-4

[8]
Diagnostic accuracy of rKLO8 versus rK26 ELISAs for screening of canine visceral leishmaniasis.

Acta Trop. 2017-2

[9]
Canine visceral leishmaniasis follow-up: a new anti-IgG serological test more sensitive than ITS-1 conventional PCR.

Vet Parasitol. 2017-12-15

[10]
Heterogeneity of Leishmania donovani parasites complicates diagnosis of visceral leishmaniasis: comparison of different serological tests in three endemic regions.

PLoS One. 2015-3-3

引用本文的文献

[1]
Performance of Extracellular Vesicles From () for Serological Diagnosis of Human and Canine Visceral Leishmaniasis.

J Parasitol Res. 2025-1-21

[2]
Comparative Study of a Novel Lateral Flow Rapid Test with Conventional Serological Test Systems for the Diagnosis of Canine Leishmaniosis in Croatia and Brazil.

Pathogens. 2024-1-26

[3]
The immune response in canine and human leishmaniasis and how this influences the diagnosis- a review and assessment of recent research.

Front Cell Infect Microbiol. 2023

[4]
Reporter gene systems: A powerful tool for studies.

Curr Res Microb Sci. 2022-9-29

[5]
Validation of a mixture of rK26 and rK39 antigens from Iranian strain of Leishmania infantum to detect anti-Leishmania antibodies in human and reservoir hosts.

Sci Rep. 2022-6-21

[6]
Emergent canine visceral leishmaniasis in Argentina: Comparative diagnostics and relevance to proliferation of human disease.

PLoS Negl Trop Dis. 2021-7

[7]
Serum antibodies blocked by glycan antigens in canine visceral leishmaniasis serology are mostly IgA immune complexes.

Parasitology. 2021-10

[8]
Validation of ELISA with recombinant antigens in serological diagnosis of canine Leishmania infantum infection.

Mem Inst Oswaldo Cruz. 2021

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