An ELISA immunoassay employing a conserved Leishmania hypothetical protein for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans

[Display omitted] •Antigens used in the serodiagnosis of leishmaniasis present problems.•A conserved Leishmania hypothetical protein was identified.•It was employed in ELISA experiments for serodiagnosis of leishmaniasis.•Both sera from visceral and tegumentary leishmaniasis patients recognized rLiH...

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Published inCellular immunology Vol. 318; pp. 42 - 48
Main Authors Carvalho, Ana Maria R.S., Costa, Lourena E., Salles, Beatriz C.S., Santos, Thaís T.O., Ramos, Fernanda F., Lima, Mariana P., Chávez-Fumagalli, Miguel A., Silvestre, Bruna T., Portela, Áquila S.B., Roatt, Bruno M., Silveira, Julia A.G., Gonçalves, Denise U., Magalhães-Soares, Danielle F., Duarte, Mariana C., Menezes-Souza, Daniel, Coelho, Eduardo A.F.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Inc 01.08.2017
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Abstract [Display omitted] •Antigens used in the serodiagnosis of leishmaniasis present problems.•A conserved Leishmania hypothetical protein was identified.•It was employed in ELISA experiments for serodiagnosis of leishmaniasis.•Both sera from visceral and tegumentary leishmaniasis patients recognized rLiHypA.•This antigen can be considered for the diagnosis of human and canine leishmaniasis. In the present study, a conserved Leishmania hypothetical protein, namely LiHypA, was evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans. This protein showed a high amino acid sequence homology between viscerotropic and cutaneotropic Leishmania species. An enzyme-linked immunosorbent assay (ELISA) was developed using the recombinant antigen (rLiHypA), in addition to the A2 protein and two parasite antigenic preparations, which were used as controls. Regarding human diagnosis, results showed that rLiHypA was more sensitive and specific than ELISA-L. braziliensis SLA in detecting both cutaneous or mucosal leishmaniasis patients, but not those from Chagas disease patients or healthy subjects. Regarding canine diagnosis, this recombinant antigen showed higher sensitivity and specificity values, as well as a perfect accuracy to identify asymptomatic and symptomatic visceral leishmaniasis (VL) in dogs, but not those from vaccinated animals or those developing babesiosis, ehrlichiosis, or Chagas disease. However, using the rA2 protein or L. braziliensis SLA as controls, significant cross-reactivity was found when these samples were used, hampering their sensitivity and specificity values for the diagnosis. In this context, LiHypA could be considered a candidate to be evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans.
AbstractList In the present study, a conserved Leishmania hypothetical protein, namely LiHypA, was evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans. This protein showed a high amino acid sequence homology between viscerotropic and cutaneotropic Leishmania species. An enzyme-linked immunosorbent assay (ELISA) was developed using the recombinant antigen (rLiHypA), in addition to the A2 protein and two parasite antigenic preparations, which were used as controls. Regarding human diagnosis, results showed that rLiHypA was more sensitive and specific than ELISA-L. braziliensis SLA in detecting both cutaneous or mucosal leishmaniasis patients, but not those from Chagas disease patients or healthy subjects. Regarding canine diagnosis, this recombinant antigen showed higher sensitivity and specificity values, as well as a perfect accuracy to identify asymptomatic and symptomatic visceral leishmaniasis (VL) in dogs, but not those from vaccinated animals or those developing babesiosis, ehrlichiosis, or Chagas disease. However, using the rA2 protein or L. braziliensis SLA as controls, significant cross-reactivity was found when these samples were used, hampering their sensitivity and specificity values for the diagnosis. In this context, LiHypA could be considered a candidate to be evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans.In the present study, a conserved Leishmania hypothetical protein, namely LiHypA, was evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans. This protein showed a high amino acid sequence homology between viscerotropic and cutaneotropic Leishmania species. An enzyme-linked immunosorbent assay (ELISA) was developed using the recombinant antigen (rLiHypA), in addition to the A2 protein and two parasite antigenic preparations, which were used as controls. Regarding human diagnosis, results showed that rLiHypA was more sensitive and specific than ELISA-L. braziliensis SLA in detecting both cutaneous or mucosal leishmaniasis patients, but not those from Chagas disease patients or healthy subjects. Regarding canine diagnosis, this recombinant antigen showed higher sensitivity and specificity values, as well as a perfect accuracy to identify asymptomatic and symptomatic visceral leishmaniasis (VL) in dogs, but not those from vaccinated animals or those developing babesiosis, ehrlichiosis, or Chagas disease. However, using the rA2 protein or L. braziliensis SLA as controls, significant cross-reactivity was found when these samples were used, hampering their sensitivity and specificity values for the diagnosis. In this context, LiHypA could be considered a candidate to be evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans.
[Display omitted] •Antigens used in the serodiagnosis of leishmaniasis present problems.•A conserved Leishmania hypothetical protein was identified.•It was employed in ELISA experiments for serodiagnosis of leishmaniasis.•Both sera from visceral and tegumentary leishmaniasis patients recognized rLiHypA.•This antigen can be considered for the diagnosis of human and canine leishmaniasis. In the present study, a conserved Leishmania hypothetical protein, namely LiHypA, was evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans. This protein showed a high amino acid sequence homology between viscerotropic and cutaneotropic Leishmania species. An enzyme-linked immunosorbent assay (ELISA) was developed using the recombinant antigen (rLiHypA), in addition to the A2 protein and two parasite antigenic preparations, which were used as controls. Regarding human diagnosis, results showed that rLiHypA was more sensitive and specific than ELISA-L. braziliensis SLA in detecting both cutaneous or mucosal leishmaniasis patients, but not those from Chagas disease patients or healthy subjects. Regarding canine diagnosis, this recombinant antigen showed higher sensitivity and specificity values, as well as a perfect accuracy to identify asymptomatic and symptomatic visceral leishmaniasis (VL) in dogs, but not those from vaccinated animals or those developing babesiosis, ehrlichiosis, or Chagas disease. However, using the rA2 protein or L. braziliensis SLA as controls, significant cross-reactivity was found when these samples were used, hampering their sensitivity and specificity values for the diagnosis. In this context, LiHypA could be considered a candidate to be evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans.
In the present study, a conserved Leishmania hypothetical protein, namely LiHypA, was evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans. This protein showed a high amino acid sequence homology between viscerotropic and cutaneotropic Leishmania species. An enzyme-linked immunosorbent assay (ELISA) was developed using the recombinant antigen (rLiHypA), in addition to the A2 protein and two parasite antigenic preparations, which were used as controls. Regarding human diagnosis, results showed that rLiHypA was more sensitive and specific than ELISA-L. braziliensis SLA in detecting both cutaneous or mucosal leishmaniasis patients, but not those from Chagas disease patients or healthy subjects. Regarding canine diagnosis, this recombinant antigen showed higher sensitivity and specificity values, as well as a perfect accuracy to identify asymptomatic and symptomatic visceral leishmaniasis (VL) in dogs, but not those from vaccinated animals or those developing babesiosis, ehrlichiosis, or Chagas disease. However, using the rA2 protein or L. braziliensis SLA as controls, significant cross-reactivity was found when these samples were used, hampering their sensitivity and specificity values for the diagnosis. In this context, LiHypA could be considered a candidate to be evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans.
Author Ramos, Fernanda F.
Lima, Mariana P.
Portela, Áquila S.B.
Silvestre, Bruna T.
Menezes-Souza, Daniel
Chávez-Fumagalli, Miguel A.
Duarte, Mariana C.
Roatt, Bruno M.
Magalhães-Soares, Danielle F.
Salles, Beatriz C.S.
Gonçalves, Denise U.
Silveira, Julia A.G.
Carvalho, Ana Maria R.S.
Santos, Thaís T.O.
Costa, Lourena E.
Coelho, Eduardo A.F.
Author_xml – sequence: 1
  givenname: Ana Maria R.S.
  surname: Carvalho
  fullname: Carvalho, Ana Maria R.S.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 2
  givenname: Lourena E.
  surname: Costa
  fullname: Costa, Lourena E.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 3
  givenname: Beatriz C.S.
  surname: Salles
  fullname: Salles, Beatriz C.S.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 4
  givenname: Thaís T.O.
  surname: Santos
  fullname: Santos, Thaís T.O.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 5
  givenname: Fernanda F.
  surname: Ramos
  fullname: Ramos, Fernanda F.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 6
  givenname: Mariana P.
  surname: Lima
  fullname: Lima, Mariana P.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 7
  givenname: Miguel A.
  surname: Chávez-Fumagalli
  fullname: Chávez-Fumagalli, Miguel A.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 8
  givenname: Bruna T.
  surname: Silvestre
  fullname: Silvestre, Bruna T.
  organization: Departamento de Parasitologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, 31270-901 Belo Horizonte, Minas Gerais, Brazil
– sequence: 9
  givenname: Áquila S.B.
  surname: Portela
  fullname: Portela, Áquila S.B.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 10
  givenname: Bruno M.
  surname: Roatt
  fullname: Roatt, Bruno M.
  organization: Departamento de Patologia Clínica, COLTEC, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Minas Gerais, Brazil
– sequence: 11
  givenname: Julia A.G.
  surname: Silveira
  fullname: Silveira, Julia A.G.
  organization: Departamento de Parasitologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, 31270-901 Belo Horizonte, Minas Gerais, Brazil
– sequence: 12
  givenname: Denise U.
  surname: Gonçalves
  fullname: Gonçalves, Denise U.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 13
  givenname: Danielle F.
  surname: Magalhães-Soares
  fullname: Magalhães-Soares, Danielle F.
  organization: Departamento de Medicina Veterinária Preventiva, Escola de Veterinária, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Minas Gerais, Brazil
– sequence: 14
  givenname: Mariana C.
  surname: Duarte
  fullname: Duarte, Mariana C.
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 15
  givenname: Daniel
  surname: Menezes-Souza
  fullname: Menezes-Souza, Daniel
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
– sequence: 16
  givenname: Eduardo A.F.
  surname: Coelho
  fullname: Coelho, Eduardo A.F.
  email: eduardoferrazcoelho@yahoo.com.br
  organization: Programa de Pós-Graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte 30130-100, Minas Gerais, Brazil
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Keywords Sensitivity
Specificity
Hypothetical proteins
Leishmaniasis
Diagnosis
ELISA
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SSID ssj0011490
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Snippet [Display omitted] •Antigens used in the serodiagnosis of leishmaniasis present problems.•A conserved Leishmania hypothetical protein was identified.•It was...
In the present study, a conserved Leishmania hypothetical protein, namely LiHypA, was evaluated for the serodiagnosis of visceral and tegumentary leishmaniasis...
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SubjectTerms Animals
Antigens, Protozoan - genetics
Antigens, Protozoan - immunology
Antigens, Protozoan - metabolism
Chagas Disease - diagnosis
Chagas Disease - immunology
Conserved Sequence - genetics
Cross Reactions
Diagnosis
Dogs
ELISA
Enzyme-Linked Immunosorbent Assay - methods
Humans
Hypothetical proteins
Leishmania - immunology
Leishmaniasis
Leishmaniasis, Cutaneous - diagnosis
Leishmaniasis, Cutaneous - immunology
Leishmaniasis, Visceral - diagnosis
Leishmaniasis, Visceral - immunology
Predictive Value of Tests
Recombinant Proteins - genetics
Recombinant Proteins - immunology
Recombinant Proteins - metabolism
Reproducibility of Results
Sensitivity
Sensitivity and Specificity
Specificity
Title An ELISA immunoassay employing a conserved Leishmania hypothetical protein for the serodiagnosis of visceral and tegumentary leishmaniasis in dogs and humans
URI https://dx.doi.org/10.1016/j.cellimm.2017.06.001
https://www.ncbi.nlm.nih.gov/pubmed/28602279
https://www.proquest.com/docview/1908797953
Volume 318
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