Differential arthritogenicity of Staphylococcus aureus strains isolated from biological samples
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , , |
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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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 2.620 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) |
repository.mail.fl_str_mv |
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1808129465686949888 |