Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach

Detalhes bibliográficos
Autor(a) principal: Lessa-Aquino, Carolina
Data de Publicação: 2013
Outros Autores: Rodrigues, Camila Borges, Ribeiro, Guilherme S. et al.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFBA
Texto Completo: http://repositorio.ufba.br/ri/handle/ri/14363
Resumo: Leptospirosis is a widespread zoonotic disease worldwide. The lack of an adequate laboratory test is a major barrier for diagnosis, especially during the early stages of illness, when antibiotic therapy is most effective. Therefore, there is a critical need for an efficient diagnostic test for this life threatening disease. Methodology: In order to identify new targets that could be used as diagnostic makers for leptopirosis, we constructed a protein microarray chip comprising 61% of Leptospira interrogans proteome and investigated the IgG response from 274 individuals, including 80 acute-phase, 80 convalescent-phase patients and 114 healthy control subjects from regions with endemic, high endemic, and no endemic transmission of leptospirosis. A nitrocellulose line blot assay was performed to validate the accuracy of the protein microarray results. Principal findings: We found 16 antigens that can discriminate between acute cases and healthy individuals from a region with high endemic transmission of leptospirosis, and 18 antigens that distinguish convalescent cases. Some of the antigens identified in this study, such as LipL32, the non-identical domains of the Lig proteins, GroEL, and Loa22 are already known to be recognized by sera from human patients, thus serving as proof-of-concept for the serodiagnostic antigen discovery approach. Several novel antigens were identified, including the hypothetical protein LIC10215 which showed good sensitivity and specificity rates for both acute- and convalescent-phase patients. Conclusions:Our study is the first large-scale evaluation of immunodominant antigens associated with naturally acquired leptospiral infection, and novel as well as known serodiagnostic leptospiral antigens that are recognized by antibodies in the sera of leptospirosis cases were identified. The novel antigens identified here may have potential use in both the development of new tests and the improvement of currently available assays for diagnosing this neglected tropical disease. Further research is needed to assess the utility of these antigens in more deployable diagnostic platforms.
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spelling Lessa-Aquino, CarolinaRodrigues, Camila BorgesRibeiro, Guilherme S. et al.Lessa-Aquino, CarolinaRodrigues, Camila BorgesRibeiro, Guilherme S. et al.2014-01-15T13:45:22Z2014-01-15T13:45:22Z2013-101935-2735http://repositorio.ufba.br/ri/handle/ri/14363v.7, n.10, p.1-13.Leptospirosis is a widespread zoonotic disease worldwide. The lack of an adequate laboratory test is a major barrier for diagnosis, especially during the early stages of illness, when antibiotic therapy is most effective. Therefore, there is a critical need for an efficient diagnostic test for this life threatening disease. Methodology: In order to identify new targets that could be used as diagnostic makers for leptopirosis, we constructed a protein microarray chip comprising 61% of Leptospira interrogans proteome and investigated the IgG response from 274 individuals, including 80 acute-phase, 80 convalescent-phase patients and 114 healthy control subjects from regions with endemic, high endemic, and no endemic transmission of leptospirosis. A nitrocellulose line blot assay was performed to validate the accuracy of the protein microarray results. Principal findings: We found 16 antigens that can discriminate between acute cases and healthy individuals from a region with high endemic transmission of leptospirosis, and 18 antigens that distinguish convalescent cases. Some of the antigens identified in this study, such as LipL32, the non-identical domains of the Lig proteins, GroEL, and Loa22 are already known to be recognized by sera from human patients, thus serving as proof-of-concept for the serodiagnostic antigen discovery approach. Several novel antigens were identified, including the hypothetical protein LIC10215 which showed good sensitivity and specificity rates for both acute- and convalescent-phase patients. Conclusions:Our study is the first large-scale evaluation of immunodominant antigens associated with naturally acquired leptospiral infection, and novel as well as known serodiagnostic leptospiral antigens that are recognized by antibodies in the sera of leptospirosis cases were identified. The novel antigens identified here may have potential use in both the development of new tests and the improvement of currently available assays for diagnosing this neglected tropical disease. Further research is needed to assess the utility of these antigens in more deployable diagnostic platforms.Submitted by Maria Creuza Silva (mariakreuza@yahoo.com.br) on 2014-01-15T13:45:22Z No. of bitstreams: 1 Guilherme Ribeiro. 2013.pdf: 3098624 bytes, checksum: 826a0e01117159a2da74e3d62b123c25 (MD5)Made available in DSpace on 2014-01-15T13:45:22Z (GMT). No. of bitstreams: 1 Guilherme Ribeiro. 2013.pdf: 3098624 bytes, checksum: 826a0e01117159a2da74e3d62b123c25 (MD5) Previous issue date: 2013-10San FranciscoPublic Library of ScienceLeptospirosisDiagnosisIdentification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approachPLoS Negl. Trop. Dis.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessengreponame:Repositório Institucional da UFBAinstname:Universidade Federal da Bahia (UFBA)instacron:UFBAORIGINALGuilherme Ribeiro. 2013.pdfGuilherme Ribeiro. 2013.pdfapplication/pdf3098624https://repositorio.ufba.br/bitstream/ri/14363/1/Guilherme%20Ribeiro.%20%202013.pdf826a0e01117159a2da74e3d62b123c25MD51LICENSElicense.txtlicense.txttext/plain1345https://repositorio.ufba.br/bitstream/ri/14363/2/license.txtff6eaa8b858ea317fded99f125f5fcd0MD52TEXTGuilherme Ribeiro. 2013.pdf.txtGuilherme Ribeiro. 2013.pdf.txtExtracted texttext/plain63937https://repositorio.ufba.br/bitstream/ri/14363/3/Guilherme%20Ribeiro.%20%202013.pdf.txt6eca95fff083e95fa0f2b3f205e028cbMD53ri/143632022-08-08 13:18:28.624oai:repositorio.ufba.br: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Repositório InstitucionalPUBhttp://192.188.11.11:8080/oai/requestopendoar:19322022-08-08T16:18:28Repositório Institucional da UFBA - Universidade Federal da Bahia (UFBA)false
dc.title.pt_BR.fl_str_mv Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
dc.title.alternative.pt_BR.fl_str_mv PLoS Negl. Trop. Dis.
title Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
spellingShingle Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
Lessa-Aquino, Carolina
Leptospirosis
Diagnosis
title_short Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
title_full Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
title_fullStr Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
title_full_unstemmed Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
title_sort Identification of seroreactive proteins of Leptospira interrogans serovar copenhageni using a high-density protein microarray approach
author Lessa-Aquino, Carolina
author_facet Lessa-Aquino, Carolina
Rodrigues, Camila Borges
Ribeiro, Guilherme S. et al.
author_role author
author2 Rodrigues, Camila Borges
Ribeiro, Guilherme S. et al.
author2_role author
author
dc.contributor.author.fl_str_mv Lessa-Aquino, Carolina
Rodrigues, Camila Borges
Ribeiro, Guilherme S. et al.
Lessa-Aquino, Carolina
Rodrigues, Camila Borges
Ribeiro, Guilherme S. et al.
dc.subject.por.fl_str_mv Leptospirosis
Diagnosis
topic Leptospirosis
Diagnosis
description Leptospirosis is a widespread zoonotic disease worldwide. The lack of an adequate laboratory test is a major barrier for diagnosis, especially during the early stages of illness, when antibiotic therapy is most effective. Therefore, there is a critical need for an efficient diagnostic test for this life threatening disease. Methodology: In order to identify new targets that could be used as diagnostic makers for leptopirosis, we constructed a protein microarray chip comprising 61% of Leptospira interrogans proteome and investigated the IgG response from 274 individuals, including 80 acute-phase, 80 convalescent-phase patients and 114 healthy control subjects from regions with endemic, high endemic, and no endemic transmission of leptospirosis. A nitrocellulose line blot assay was performed to validate the accuracy of the protein microarray results. Principal findings: We found 16 antigens that can discriminate between acute cases and healthy individuals from a region with high endemic transmission of leptospirosis, and 18 antigens that distinguish convalescent cases. Some of the antigens identified in this study, such as LipL32, the non-identical domains of the Lig proteins, GroEL, and Loa22 are already known to be recognized by sera from human patients, thus serving as proof-of-concept for the serodiagnostic antigen discovery approach. Several novel antigens were identified, including the hypothetical protein LIC10215 which showed good sensitivity and specificity rates for both acute- and convalescent-phase patients. Conclusions:Our study is the first large-scale evaluation of immunodominant antigens associated with naturally acquired leptospiral infection, and novel as well as known serodiagnostic leptospiral antigens that are recognized by antibodies in the sera of leptospirosis cases were identified. The novel antigens identified here may have potential use in both the development of new tests and the improvement of currently available assays for diagnosing this neglected tropical disease. Further research is needed to assess the utility of these antigens in more deployable diagnostic platforms.
publishDate 2013
dc.date.issued.fl_str_mv 2013-10
dc.date.accessioned.fl_str_mv 2014-01-15T13:45:22Z
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dc.identifier.issn.none.fl_str_mv 1935-2735
dc.identifier.number.pt_BR.fl_str_mv v.7, n.10, p.1-13.
identifier_str_mv 1935-2735
v.7, n.10, p.1-13.
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