Sensitivity of Enzymatic Toxins from Corneal Isolate of Acanthamoeba Protozoan to Physicochemical Parameters

Detalhes bibliográficos
Autor(a) principal: Sant'Ana, Viviane P. [UNIFESP]
Data de Publicação: 2017
Outros Autores: Foronda, Annette S. [UNIFESP], de Freitas, Denise [UNIFESP], Carrijo-Carvalho, Linda C. [UNIFESP], de Souza Carvalho, Fabio Ramos [UNIFESP]
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.
id UFSP_db462914cdfb43de0e49341d8bf1914c
oai_identifier_str oai:repositorio.unifesp.br/:11600/58288
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling 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
_version_ 1814268351396970496