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ChimLeish, a new recombinant chimeric protein evaluated as a diagnostic and prognostic marker for visceral leishmaniasis and human immunodeficiency virus coinfection

ChimLeish, a new recombinant chimeric protein evaluated as a diagnostic and prognostic marker for visceral leishmaniasis and human immunodeficiency virus coinfection
ChimLeish, a new recombinant chimeric protein evaluated as a diagnostic and prognostic marker for visceral leishmaniasis and human immunodeficiency virus coinfection

Visceral leishmaniasis (VL) is a neglected tropical disease of global importance caused by parasites of the genus Leishmania, and coinfection with human immunodeficiency virus (HIV) is common in countries where both diseases are endemic. In particular, widely used immunological tests for VL diagnosis have impaired sensitivity (Se) and specificity (Sp) in VL/HIV coinfected patients and there is also cross-reactivity with other endemic diseases, e.g., Chagas disease, malaria, and tuberculosis. To develop new antigens to improve the diagnosis of VL and VL/HIV coinfection, we predicted eight specific B-cell epitopes of four Leishmania infantum antigens and constructed a recombinant polypeptide chimera antigen called ChimLeish. A serological panel of 195 serum samples was used to compare the diagnostic capabilities of ChimLeish alongside the individual synthetic peptides. ChimLeish reacted with sera from all VL and VL/HIV coinfected patients [Se = 100%; Sp = 100%; area under the curve (AUC) = 1.0]. Peptides showed lower reactivities (Se = 76.8 to 99.2%; Sp = 67.1 to 95.7%; AUC between 0.87 and 0.98) as did a L. infantum antigenic preparation used as an antigen control (Se = 56.8%; Sp = 69.5%: AUC = 0.45). Notably, ChimLeish demonstrated a significant reduction (p < 0.05) of anti-ChimLeish antibodies after treatment and cure of a small number of patients. Although only a limited serological panel was tested, preliminary data suggest that ChimLeish should be evaluated in larger sample studies for the diagnosis of VL and VL/HIV coinfection.

Diagnosis, ELISA, Prognosis, Recombinant chimera, Synthetic peptides, Visceral leishmaniasis
0932-0113
4037-4047
Galvani, Nathalia C.
bd9c76e0-caf2-46ca-a7eb-1fced08c5c57
Machado, Amanda S.
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Lage, Daniela P.
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Freitas, Camila S.
de050131-f325-4793-920c-db2bc3b13c5d
Vale, Danniele L.
f29a8048-fd51-462f-9b05-99391c418faa
de Oliveira, Daysiane
ae379cce-737b-4f4b-b04a-41f2bfd94fcd
Ludolf, Fernanda
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Ramos, Fernanda F.
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Fernandes, Bruna B.
5d4772db-eefb-46db-8911-221e244587d4
Luiz, Gabriel P.
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Mendonça, Débora V.C.
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Oliveira-da-Silva, João A.
cafe61b3-a3b0-4516-a3bf-76587a110e2c
Reis, Thiago A.R.
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Tavares, Grasiele S.V.
fc7d96b8-844a-4ed9-8828-a3b97c891e05
Chaves, Ana T.
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Guimarães, Nathalia S.
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Tupinambás, Unaí
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Cota, Gláucia F.
97a31251-3859-4db9-ae47-11ac55fd5f2c
Humbert, Maria V.
82134d25-24b8-4fdd-bd1c-461683b5322e
Martins, Vívian T.
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Christodoulides, Myron
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Coelho, Eduardo A.F.
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Machado-de-Ávila, Ricardo A.
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Galvani, Nathalia C.
bd9c76e0-caf2-46ca-a7eb-1fced08c5c57
Machado, Amanda S.
c8ade693-7d20-4447-be3f-cde9b9784bc1
Lage, Daniela P.
7748210f-98a7-4cc0-8d81-a06157865ab7
Freitas, Camila S.
de050131-f325-4793-920c-db2bc3b13c5d
Vale, Danniele L.
f29a8048-fd51-462f-9b05-99391c418faa
de Oliveira, Daysiane
ae379cce-737b-4f4b-b04a-41f2bfd94fcd
Ludolf, Fernanda
0e932908-e3e2-4d45-8c76-b2d860dcc115
Ramos, Fernanda F.
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Fernandes, Bruna B.
5d4772db-eefb-46db-8911-221e244587d4
Luiz, Gabriel P.
b89e7e01-1c6b-4032-b198-f9dd2619df54
Mendonça, Débora V.C.
9e62c2c7-b5f3-466d-9415-20228131ab6a
Oliveira-da-Silva, João A.
cafe61b3-a3b0-4516-a3bf-76587a110e2c
Reis, Thiago A.R.
d686af7d-6970-47ba-ac0c-fe4d796edb23
Tavares, Grasiele S.V.
fc7d96b8-844a-4ed9-8828-a3b97c891e05
Chaves, Ana T.
50f56642-6bb2-43be-8dd0-1fd3805023f3
Guimarães, Nathalia S.
5852b418-1e1a-4b51-bef3-719e54ad9b7c
Tupinambás, Unaí
50b75eb7-b46f-4de1-88eb-7998cb771627
Cota, Gláucia F.
97a31251-3859-4db9-ae47-11ac55fd5f2c
Humbert, Maria V.
82134d25-24b8-4fdd-bd1c-461683b5322e
Martins, Vívian T.
e78dc578-9d04-451d-aa4e-6cd471acd034
Christodoulides, Myron
eba99148-620c-452a-a334-c1a52ba94078
Coelho, Eduardo A.F.
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Machado-de-Ávila, Ricardo A.
092a70ab-eda8-4db7-817d-62aaefaf7877

Galvani, Nathalia C., Machado, Amanda S., Lage, Daniela P., Freitas, Camila S., Vale, Danniele L., de Oliveira, Daysiane, Ludolf, Fernanda, Ramos, Fernanda F., Fernandes, Bruna B., Luiz, Gabriel P., Mendonça, Débora V.C., Oliveira-da-Silva, João A., Reis, Thiago A.R., Tavares, Grasiele S.V., Chaves, Ana T., Guimarães, Nathalia S., Tupinambás, Unaí, Cota, Gláucia F., Humbert, Maria V., Martins, Vívian T., Christodoulides, Myron, Coelho, Eduardo A.F. and Machado-de-Ávila, Ricardo A. (2021) ChimLeish, a new recombinant chimeric protein evaluated as a diagnostic and prognostic marker for visceral leishmaniasis and human immunodeficiency virus coinfection. Parasitology Research, 120 (12), 4037-4047. (doi:10.1007/s00436-021-07342-1).

Record type: Article

Abstract

Visceral leishmaniasis (VL) is a neglected tropical disease of global importance caused by parasites of the genus Leishmania, and coinfection with human immunodeficiency virus (HIV) is common in countries where both diseases are endemic. In particular, widely used immunological tests for VL diagnosis have impaired sensitivity (Se) and specificity (Sp) in VL/HIV coinfected patients and there is also cross-reactivity with other endemic diseases, e.g., Chagas disease, malaria, and tuberculosis. To develop new antigens to improve the diagnosis of VL and VL/HIV coinfection, we predicted eight specific B-cell epitopes of four Leishmania infantum antigens and constructed a recombinant polypeptide chimera antigen called ChimLeish. A serological panel of 195 serum samples was used to compare the diagnostic capabilities of ChimLeish alongside the individual synthetic peptides. ChimLeish reacted with sera from all VL and VL/HIV coinfected patients [Se = 100%; Sp = 100%; area under the curve (AUC) = 1.0]. Peptides showed lower reactivities (Se = 76.8 to 99.2%; Sp = 67.1 to 95.7%; AUC between 0.87 and 0.98) as did a L. infantum antigenic preparation used as an antigen control (Se = 56.8%; Sp = 69.5%: AUC = 0.45). Notably, ChimLeish demonstrated a significant reduction (p < 0.05) of anti-ChimLeish antibodies after treatment and cure of a small number of patients. Although only a limited serological panel was tested, preliminary data suggest that ChimLeish should be evaluated in larger sample studies for the diagnosis of VL and VL/HIV coinfection.

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More information

Accepted/In Press date: 4 October 2021
Published date: 19 October 2021
Keywords: Diagnosis, ELISA, Prognosis, Recombinant chimera, Synthetic peptides, Visceral leishmaniasis

Identifiers

Local EPrints ID: 453920
URI: http://eprints.soton.ac.uk/id/eprint/453920
ISSN: 0932-0113
PURE UUID: e3ca5869-cd54-46bf-bae4-d69028545474
ORCID for Maria V. Humbert: ORCID iD orcid.org/0000-0002-5728-6981
ORCID for Myron Christodoulides: ORCID iD orcid.org/0000-0002-9663-4731

Catalogue record

Date deposited: 25 Jan 2022 18:10
Last modified: 06 Jun 2024 01:53

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Contributors

Author: Nathalia C. Galvani
Author: Amanda S. Machado
Author: Daniela P. Lage
Author: Camila S. Freitas
Author: Danniele L. Vale
Author: Daysiane de Oliveira
Author: Fernanda Ludolf
Author: Fernanda F. Ramos
Author: Bruna B. Fernandes
Author: Gabriel P. Luiz
Author: Débora V.C. Mendonça
Author: João A. Oliveira-da-Silva
Author: Thiago A.R. Reis
Author: Grasiele S.V. Tavares
Author: Ana T. Chaves
Author: Nathalia S. Guimarães
Author: Unaí Tupinambás
Author: Gláucia F. Cota
Author: Maria V. Humbert ORCID iD
Author: Vívian T. Martins
Author: Eduardo A.F. Coelho
Author: Ricardo A. Machado-de-Ávila

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