Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1007/s00284-017-1319-6 https://repositorio.unifesp.br/handle/11600/58288 |
Resumo: | Acanthamoeba is a free-living amoeba that causes severe corneal infection (Acanthamoeba keratitis) and produces a variety of extracellular enzymes, called exoproteome. Since physicochemical characters are suggested being associated with therapeutic profile and clinical severity of the infection, we investigated the physicochemical properties of proteolysis mediated by amoebic exoproteome. Corneal scraping was collected from a patient who showed typical symptoms of acute Acanthamoeba keratitis. Axenic amoeba was phylogenetically identified by 18S rDNA sequencing analysis. Effects of pH, temperature and diamidines on proteolysis mediated by exoproteome were assessed using zymography assays. Proteolytic enzymes were most active at pH 7.0 and 37 A degrees C. Calcium ions decreased enzymatic activity. The main components of amoebic exoproteome were characterized as serine proteases. We demonstrated for the first time that commercial antimicrobial diamidines used for Acanthamoeba keratitis therapy inhibit enzymatic activity of amoebic exoproteome. Results showed the thermostability of Acanthamoeba proteases, which suggest a long-term effect of these virulence factors at the central and peripheral cornea with possible role in degradation of extracellular matrix components. Our findings open new perspectives about the complementary and unreported properties of antimicrobial compounds of the diamidine class on the inhibition of enzymatic activity and presumptive control of amoebic infection in the cornea. |
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Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical ParametersAcanthamoeba is a free-living amoeba that causes severe corneal infection (Acanthamoeba keratitis) and produces a variety of extracellular enzymes, called exoproteome. Since physicochemical characters are suggested being associated with therapeutic profile and clinical severity of the infection, we investigated the physicochemical properties of proteolysis mediated by amoebic exoproteome. Corneal scraping was collected from a patient who showed typical symptoms of acute Acanthamoeba keratitis. Axenic amoeba was phylogenetically identified by 18S rDNA sequencing analysis. Effects of pH, temperature and diamidines on proteolysis mediated by exoproteome were assessed using zymography assays. Proteolytic enzymes were most active at pH 7.0 and 37 A degrees C. Calcium ions decreased enzymatic activity. The main components of amoebic exoproteome were characterized as serine proteases. We demonstrated for the first time that commercial antimicrobial diamidines used for Acanthamoeba keratitis therapy inhibit enzymatic activity of amoebic exoproteome. Results showed the thermostability of Acanthamoeba proteases, which suggest a long-term effect of these virulence factors at the central and peripheral cornea with possible role in degradation of extracellular matrix components. Our findings open new perspectives about the complementary and unreported properties of antimicrobial compounds of the diamidine class on the inhibition of enzymatic activity and presumptive control of amoebic infection in the cornea.Univ Fed Sao Paulo, Dept Ophthalmol & Visual Sci, Paulista Sch Med, Botucatu St,821 Vila Clementino, BR-04023062 Sao Paulo, SP, BrazilCtr Univ Espirito Santo UNESC, Colatina, Espirito Santo, BrazilUniv Fed Sao Paulo, Dept Ophthalmol & Visual Sci, Paulista Sch Med, Botucatu St,821 Vila Clementino, BR-04023062 Sao Paulo, SP, BrazilWeb of ScienceSao Paulo Research FoundationCoordination for the Improvement of Higher Education PersonnelFAPESP: 2008/53969-0FAPESP: 2014/18926-02FAPESP: 2011/51626-1FAPESP: 2012/15603-0CAPES: 23038.001063/2012-01, PNPDSpringer2020-09-01T13:21:28Z2020-09-01T13:21:28Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1316-1323http://dx.doi.org/10.1007/s00284-017-1319-6Current Microbiology. New York, v. 74, n. 11, p. 1316-1323, 2017.10.1007/s00284-017-1319-60343-8651https://repositorio.unifesp.br/handle/11600/58288WOS:000413002800010engCurrent MicrobiologyNew Yorkinfo:eu-repo/semantics/openAccessSant'Ana, Viviane P. [UNIFESP]Foronda, Annette S. [UNIFESP]de Freitas, Denise [UNIFESP]Carrijo-Carvalho, Linda C. [UNIFESP]de Souza Carvalho, Fabio Ramos [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-02-07T21:54:05Zoai:repositorio.unifesp.br/:11600/58288Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-02-07T21:54:05Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters |
title |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters |
spellingShingle |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters Sant'Ana, Viviane P. [UNIFESP] |
title_short |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters |
title_full |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters |
title_fullStr |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters |
title_full_unstemmed |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters |
title_sort |
Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters |
author |
Sant'Ana, Viviane P. [UNIFESP] |
author_facet |
Sant'Ana, Viviane P. [UNIFESP] Foronda, Annette S. [UNIFESP] de Freitas, Denise [UNIFESP] Carrijo-Carvalho, Linda C. [UNIFESP] de Souza Carvalho, Fabio Ramos [UNIFESP] |
author_role |
author |
author2 |
Foronda, Annette S. [UNIFESP] de Freitas, Denise [UNIFESP] Carrijo-Carvalho, Linda C. [UNIFESP] de Souza Carvalho, Fabio Ramos [UNIFESP] |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Sant'Ana, Viviane P. [UNIFESP] Foronda, Annette S. [UNIFESP] de Freitas, Denise [UNIFESP] Carrijo-Carvalho, Linda C. [UNIFESP] de Souza Carvalho, Fabio Ramos [UNIFESP] |
description |
Acanthamoeba is a free-living amoeba that causes severe corneal infection (Acanthamoeba keratitis) and produces a variety of extracellular enzymes, called exoproteome. Since physicochemical characters are suggested being associated with therapeutic profile and clinical severity of the infection, we investigated the physicochemical properties of proteolysis mediated by amoebic exoproteome. Corneal scraping was collected from a patient who showed typical symptoms of acute Acanthamoeba keratitis. Axenic amoeba was phylogenetically identified by 18S rDNA sequencing analysis. Effects of pH, temperature and diamidines on proteolysis mediated by exoproteome were assessed using zymography assays. Proteolytic enzymes were most active at pH 7.0 and 37 A degrees C. Calcium ions decreased enzymatic activity. The main components of amoebic exoproteome were characterized as serine proteases. We demonstrated for the first time that commercial antimicrobial diamidines used for Acanthamoeba keratitis therapy inhibit enzymatic activity of amoebic exoproteome. Results showed the thermostability of Acanthamoeba proteases, which suggest a long-term effect of these virulence factors at the central and peripheral cornea with possible role in degradation of extracellular matrix components. Our findings open new perspectives about the complementary and unreported properties of antimicrobial compounds of the diamidine class on the inhibition of enzymatic activity and presumptive control of amoebic infection in the cornea. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 2020-09-01T13:21:28Z 2020-09-01T13:21:28Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1007/s00284-017-1319-6 Current Microbiology. New York, v. 74, n. 11, p. 1316-1323, 2017. 10.1007/s00284-017-1319-6 0343-8651 https://repositorio.unifesp.br/handle/11600/58288 WOS:000413002800010 |
url |
http://dx.doi.org/10.1007/s00284-017-1319-6 https://repositorio.unifesp.br/handle/11600/58288 |
identifier_str_mv |
Current Microbiology. New York, v. 74, n. 11, p. 1316-1323, 2017. 10.1007/s00284-017-1319-6 0343-8651 WOS:000413002800010 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Current Microbiology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1316-1323 |
dc.coverage.none.fl_str_mv |
New York |
dc.publisher.none.fl_str_mv |
Springer |
publisher.none.fl_str_mv |
Springer |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268351396970496 |