Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples

Detalhes bibliográficos
Autor(a) principal: Colavite-Machado, Priscila M. [UNESP]
Data de Publicação: 2013
Outros Autores: Ishikawa, Larissa Lumi W. [UNESP], Donegá França, Thaís G. [UNESP], Zorzella-Pezavento, Sofia Fernanda G. [UNESP], da Rosa, Larissa C. [UNESP], Chiuso-Minicucci, Fernanda [UNESP], da Cunha, Maria de Lourdes Ribeiro de Souza [UNESP], Garlet, Gustavo P., Sartori, Alexandrina [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/1471-2334-13-400
http://hdl.handle.net/11449/76365
Resumo: Background: Staphylococcus aureus is the most common agent of septic arthritis that is a severe, rapidly progressive and destructive joint disease. Superantigens produced by S. aureus are considered the major arthritogenic factors. In this study, we compared the arthritogenic potential of five superantigen-producing staphylococcal strains.Methods: Male C57BL/6 mice were intravenously infected with ATCC 19095 SEC+, N315 ST5 TSST-1+, S-70 TSST-1+, ATCC 51650 TSST-1+ and ATCC 13565 SEA+ strains. Clinical parameters as body weight, arthritis incidence and clinical score were daily evaluated. Joint histopathological analysis and spleen cytokine production were evaluated at the 14th day after infection.Results: Weight loss was observed in all infected mice. ATCC 19095 SEC+, N315 ST5 TSST-1+ and S-70 TSST-1+ were arthritogenic, being the highest scores observed in ATCC 19095 SEC+ infected mice. Intermediate and lower clinical scores were observed in N315 ST5 TSST-1+ and S-70 TSST-1+ infected mice, respectively. The ATCC 13565 SEA+ strain caused death of 85% of the animals after 48 h. Arthritis triggered by the ATCC 19095 SEC+ strain was characterized by accentuated synovial hyperplasia, inflammation, pannus formation, cartilage destruction and bone erosion. Similar joint alterations were found in N315 ST5 TSST-1+ infected mice, however they were strikingly more discrete. Only minor synovial proliferation and inflammation were triggered by the S-70 TSST-1+ strain. The lowest levels of TNF-α, IL-6 and IL-17 production in response to S. aureus stimulation were found in cultures from mice infected with the less arthritogenic strains (S-70 TSST-1+ and ATCC 51650 TSST-1+). The highest production of IL-17 was detected in mice infected with the most arthritogenic strains (ATCC 19095 SEC+ and N315 ST5 TSST-1+).Conclusions: Together these results demonstrated that S. aureus strains, isolated from biological samples, were able to induce a typical septic arthritis in mice. These results also suggest that the variable arthritogenicity of these strains was, at least in part, related to their differential ability to induce IL-17 production. © 2013 Colavite-Machado et al.; licensee BioMed Central Ltd.
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spelling Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samplesIL-17Septic arthritisStaphylococcus aureusBackground: Staphylococcus aureus is the most common agent of septic arthritis that is a severe, rapidly progressive and destructive joint disease. Superantigens produced by S. aureus are considered the major arthritogenic factors. In this study, we compared the arthritogenic potential of five superantigen-producing staphylococcal strains.Methods: Male C57BL/6 mice were intravenously infected with ATCC 19095 SEC+, N315 ST5 TSST-1+, S-70 TSST-1+, ATCC 51650 TSST-1+ and ATCC 13565 SEA+ strains. Clinical parameters as body weight, arthritis incidence and clinical score were daily evaluated. Joint histopathological analysis and spleen cytokine production were evaluated at the 14th day after infection.Results: Weight loss was observed in all infected mice. ATCC 19095 SEC+, N315 ST5 TSST-1+ and S-70 TSST-1+ were arthritogenic, being the highest scores observed in ATCC 19095 SEC+ infected mice. Intermediate and lower clinical scores were observed in N315 ST5 TSST-1+ and S-70 TSST-1+ infected mice, respectively. The ATCC 13565 SEA+ strain caused death of 85% of the animals after 48 h. Arthritis triggered by the ATCC 19095 SEC+ strain was characterized by accentuated synovial hyperplasia, inflammation, pannus formation, cartilage destruction and bone erosion. Similar joint alterations were found in N315 ST5 TSST-1+ infected mice, however they were strikingly more discrete. Only minor synovial proliferation and inflammation were triggered by the S-70 TSST-1+ strain. The lowest levels of TNF-α, IL-6 and IL-17 production in response to S. aureus stimulation were found in cultures from mice infected with the less arthritogenic strains (S-70 TSST-1+ and ATCC 51650 TSST-1+). The highest production of IL-17 was detected in mice infected with the most arthritogenic strains (ATCC 19095 SEC+ and N315 ST5 TSST-1+).Conclusions: Together these results demonstrated that S. aureus strains, isolated from biological samples, were able to induce a typical septic arthritis in mice. These results also suggest that the variable arthritogenicity of these strains was, at least in part, related to their differential ability to induce IL-17 production. © 2013 Colavite-Machado et al.; licensee BioMed Central Ltd.Department of Microbiology and Immunology Biosciences Institute Univ. Estadual Paulista (UNESP), Distrito de Rubião Júnior s/n, 18618-070 Botucatu, São PauloDepartment of Biological Sciences School of Dentistry of Bauru São Paulo University-FOB/USP, Bauru, São PauloDepartment of Microbiology and Immunology Biosciences Institute Univ. Estadual Paulista (UNESP), Distrito de Rubião Júnior s/n, 18618-070 Botucatu, São PauloUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Colavite-Machado, Priscila M. [UNESP]Ishikawa, Larissa Lumi W. [UNESP]Donegá França, Thaís G. [UNESP]Zorzella-Pezavento, Sofia Fernanda G. [UNESP]da Rosa, Larissa C. [UNESP]Chiuso-Minicucci, Fernanda [UNESP]da Cunha, Maria de Lourdes Ribeiro de Souza [UNESP]Garlet, Gustavo P.Sartori, Alexandrina [UNESP]2014-05-27T11:30:30Z2014-05-27T11:30:30Z2013-08-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1186/1471-2334-13-400BMC Infectious Diseases, v. 13, n. 1, 2013.1471-2334http://hdl.handle.net/11449/7636510.1186/1471-2334-13-400WOS:0003242625000012-s2.0-848849588222-s2.0-84884958822.pdf4977572416129527Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Infectious Diseases2.6201,576info:eu-repo/semantics/openAccess2024-01-13T06:30:46Zoai:repositorio.unesp.br:11449/76365Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:49:08.589414Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
title Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
spellingShingle Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
Colavite-Machado, Priscila M. [UNESP]
IL-17
Septic arthritis
Staphylococcus aureus
title_short Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
title_full Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
title_fullStr Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
title_full_unstemmed Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
title_sort Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
author Colavite-Machado, Priscila M. [UNESP]
author_facet Colavite-Machado, Priscila M. [UNESP]
Ishikawa, Larissa Lumi W. [UNESP]
Donegá França, Thaís G. [UNESP]
Zorzella-Pezavento, Sofia Fernanda G. [UNESP]
da Rosa, Larissa C. [UNESP]
Chiuso-Minicucci, Fernanda [UNESP]
da Cunha, Maria de Lourdes Ribeiro de Souza [UNESP]
Garlet, Gustavo P.
Sartori, Alexandrina [UNESP]
author_role author
author2 Ishikawa, Larissa Lumi W. [UNESP]
Donegá França, Thaís G. [UNESP]
Zorzella-Pezavento, Sofia Fernanda G. [UNESP]
da Rosa, Larissa C. [UNESP]
Chiuso-Minicucci, Fernanda [UNESP]
da Cunha, Maria de Lourdes Ribeiro de Souza [UNESP]
Garlet, Gustavo P.
Sartori, Alexandrina [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Colavite-Machado, Priscila M. [UNESP]
Ishikawa, Larissa Lumi W. [UNESP]
Donegá França, Thaís G. [UNESP]
Zorzella-Pezavento, Sofia Fernanda G. [UNESP]
da Rosa, Larissa C. [UNESP]
Chiuso-Minicucci, Fernanda [UNESP]
da Cunha, Maria de Lourdes Ribeiro de Souza [UNESP]
Garlet, Gustavo P.
Sartori, Alexandrina [UNESP]
dc.subject.por.fl_str_mv IL-17
Septic arthritis
Staphylococcus aureus
topic IL-17
Septic arthritis
Staphylococcus aureus
description Background: Staphylococcus aureus is the most common agent of septic arthritis that is a severe, rapidly progressive and destructive joint disease. Superantigens produced by S. aureus are considered the major arthritogenic factors. In this study, we compared the arthritogenic potential of five superantigen-producing staphylococcal strains.Methods: Male C57BL/6 mice were intravenously infected with ATCC 19095 SEC+, N315 ST5 TSST-1+, S-70 TSST-1+, ATCC 51650 TSST-1+ and ATCC 13565 SEA+ strains. Clinical parameters as body weight, arthritis incidence and clinical score were daily evaluated. Joint histopathological analysis and spleen cytokine production were evaluated at the 14th day after infection.Results: Weight loss was observed in all infected mice. ATCC 19095 SEC+, N315 ST5 TSST-1+ and S-70 TSST-1+ were arthritogenic, being the highest scores observed in ATCC 19095 SEC+ infected mice. Intermediate and lower clinical scores were observed in N315 ST5 TSST-1+ and S-70 TSST-1+ infected mice, respectively. The ATCC 13565 SEA+ strain caused death of 85% of the animals after 48 h. Arthritis triggered by the ATCC 19095 SEC+ strain was characterized by accentuated synovial hyperplasia, inflammation, pannus formation, cartilage destruction and bone erosion. Similar joint alterations were found in N315 ST5 TSST-1+ infected mice, however they were strikingly more discrete. Only minor synovial proliferation and inflammation were triggered by the S-70 TSST-1+ strain. The lowest levels of TNF-α, IL-6 and IL-17 production in response to S. aureus stimulation were found in cultures from mice infected with the less arthritogenic strains (S-70 TSST-1+ and ATCC 51650 TSST-1+). The highest production of IL-17 was detected in mice infected with the most arthritogenic strains (ATCC 19095 SEC+ and N315 ST5 TSST-1+).Conclusions: Together these results demonstrated that S. aureus strains, isolated from biological samples, were able to induce a typical septic arthritis in mice. These results also suggest that the variable arthritogenicity of these strains was, at least in part, related to their differential ability to induce IL-17 production. © 2013 Colavite-Machado et al.; licensee BioMed Central Ltd.
publishDate 2013
dc.date.none.fl_str_mv 2013-08-30
2014-05-27T11:30:30Z
2014-05-27T11:30:30Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1186/1471-2334-13-400
BMC Infectious Diseases, v. 13, n. 1, 2013.
1471-2334
http://hdl.handle.net/11449/76365
10.1186/1471-2334-13-400
WOS:000324262500001
2-s2.0-84884958822
2-s2.0-84884958822.pdf
4977572416129527
url http://dx.doi.org/10.1186/1471-2334-13-400
http://hdl.handle.net/11449/76365
identifier_str_mv BMC Infectious Diseases, v. 13, n. 1, 2013.
1471-2334
10.1186/1471-2334-13-400
WOS:000324262500001
2-s2.0-84884958822
2-s2.0-84884958822.pdf
4977572416129527
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Infectious Diseases
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1,576
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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