Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study

Detalhes bibliográficos
Autor(a) principal: Cereda, Rosângela Ferraz
Data de Publicação: 2011
Outros Autores: Azevedo, Heber Dias, Girardello, Raquel [UNIFESP], Xavier, Danilo Elias [UNIFESP], Gales, Ana Cristina [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/6544
http://dx.doi.org/10.1590/S1413-86702011000400007
Resumo: Ceftobiprole is a broad-spectrum cephalosporin with potent activity against staphylococci, including those resistant to oxacillin, as well as against most Gram-negative bacilli including Pseudomonas aeruginosa. In this study, the in vitro activity of ceftobiprole and comparator agents was tested against bacterial isolates recently collected from Brazilian private hospitals. A total of 336 unique bacterial isolates were collected from hospitalized patients between February 2008 and August 2009. Each hospital was asked to submit 100 single bacterial isolates responsible for causing blood, lower respiratory tract or skin and soft tissue infections. Bacterial identification was confirmed and antimicrobial susceptibility testing was performed using CLSI microdilution method at a central laboratory. The CLSI M100-S21 (2011) was used for interpretation of the antimicrobial susceptibility results. Among the 336 pathogens collected, 255 (75.9%) were Gram-negative bacilli and 81 (24.1%) were Gram-positive cocci. Although ceftobiprole MIC50 values for oxacillin resistant strains were two-fold higher than for methicillin susceptible S. aureus, ceftobiprole inhibited 100% of tested S. aureus at MICs < 4 µg/mL. Polymyxin B was the only agent to show potent activity against Acinetobacter spp. (MIC50/90, 0.5/1 µg/mL), and P. aeruginosa (MIC50/90, 1/2 µg/mL). Resistance to broad-spectrum cephalosporins varied from 55.3-68.5% and 14.3-28.5% among E. coli and Klebsiella spp. isolates, respectively; with ceftobiprole MIC50 > 6 µg/mL for both species. Our results showed that ceftobiprole has potent activity against staphylococci and E. faecalis, which was superior to that of vancomycin. Our data also indicates that ceftobiprole demonstrated potency comparable to that of cefepime and ceftazidime against key Gram-negative species.
id UFSP_7bd9d4e897acbfbff056c373dc6595a7
oai_identifier_str oai:repositorio.unifesp.br:11600/6544
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Cereda, Rosângela FerrazAzevedo, Heber DiasGirardello, Raquel [UNIFESP]Xavier, Danilo Elias [UNIFESP]Gales, Ana Cristina [UNIFESP]Janssen-CilagUniversidade Federal de São Paulo (UNIFESP)2015-06-14T13:43:11Z2015-06-14T13:43:11Z2011-08-01Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 15, n. 4, p. 339-348, 2011.1413-8670http://repositorio.unifesp.br/handle/11600/6544http://dx.doi.org/10.1590/S1413-86702011000400007S1413-86702011000400007.pdfS1413-8670201100040000710.1590/S1413-86702011000400007WOS:000293862800007Ceftobiprole is a broad-spectrum cephalosporin with potent activity against staphylococci, including those resistant to oxacillin, as well as against most Gram-negative bacilli including Pseudomonas aeruginosa. In this study, the in vitro activity of ceftobiprole and comparator agents was tested against bacterial isolates recently collected from Brazilian private hospitals. A total of 336 unique bacterial isolates were collected from hospitalized patients between February 2008 and August 2009. Each hospital was asked to submit 100 single bacterial isolates responsible for causing blood, lower respiratory tract or skin and soft tissue infections. Bacterial identification was confirmed and antimicrobial susceptibility testing was performed using CLSI microdilution method at a central laboratory. The CLSI M100-S21 (2011) was used for interpretation of the antimicrobial susceptibility results. Among the 336 pathogens collected, 255 (75.9%) were Gram-negative bacilli and 81 (24.1%) were Gram-positive cocci. Although ceftobiprole MIC50 values for oxacillin resistant strains were two-fold higher than for methicillin susceptible S. aureus, ceftobiprole inhibited 100% of tested S. aureus at MICs < 4 µg/mL. Polymyxin B was the only agent to show potent activity against Acinetobacter spp. (MIC50/90, 0.5/1 µg/mL), and P. aeruginosa (MIC50/90, 1/2 µg/mL). Resistance to broad-spectrum cephalosporins varied from 55.3-68.5% and 14.3-28.5% among E. coli and Klebsiella spp. isolates, respectively; with ceftobiprole MIC50 > 6 µg/mL for both species. Our results showed that ceftobiprole has potent activity against staphylococci and E. faecalis, which was superior to that of vancomycin. Our data also indicates that ceftobiprole demonstrated potency comparable to that of cefepime and ceftazidime against key Gram-negative species.Janssen-CilagUniversidade Federal de São Paulo (UNIFESP) Post-graduation Course in SciencesUNIFESPUNIFESP, Post-graduation Course in SciencesSciELO339-348engBrazilian Society of Infectious DiseasesBrazilian Journal of Infectious DiseasescephalosporinsBrazilGram-negative aerobic bacteriamethicillin-resistant Staphylococcus aureusAntimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian studyinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALS1413-86702011000400007.pdfapplication/pdf1048341${dspace.ui.url}/bitstream/11600/6544/1/S1413-86702011000400007.pdf6ede0e14a45134928ce4754b5701f6d4MD51open accessTEXTS1413-86702011000400007.pdf.txtS1413-86702011000400007.pdf.txtExtracted texttext/plain31036${dspace.ui.url}/bitstream/11600/6544/2/S1413-86702011000400007.pdf.txtf5dde6fc6603237b81d785a7e0677b11MD52open access11600/65442022-09-27 14:37:29.426open accessoai:repositorio.unifesp.br:11600/6544Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-09-27T17:37:29Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
title Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
spellingShingle Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
Cereda, Rosângela Ferraz
cephalosporins
Brazil
Gram-negative aerobic bacteria
methicillin-resistant Staphylococcus aureus
title_short Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
title_full Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
title_fullStr Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
title_full_unstemmed Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
title_sort Antimicrobial activity of ceftobiprole against Gram-negative and Gram-positive pathogens: results from INVITA-A-CEFTO Brazilian study
author Cereda, Rosângela Ferraz
author_facet Cereda, Rosângela Ferraz
Azevedo, Heber Dias
Girardello, Raquel [UNIFESP]
Xavier, Danilo Elias [UNIFESP]
Gales, Ana Cristina [UNIFESP]
author_role author
author2 Azevedo, Heber Dias
Girardello, Raquel [UNIFESP]
Xavier, Danilo Elias [UNIFESP]
Gales, Ana Cristina [UNIFESP]
author2_role author
author
author
author
dc.contributor.institution.none.fl_str_mv Janssen-Cilag
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Cereda, Rosângela Ferraz
Azevedo, Heber Dias
Girardello, Raquel [UNIFESP]
Xavier, Danilo Elias [UNIFESP]
Gales, Ana Cristina [UNIFESP]
dc.subject.eng.fl_str_mv cephalosporins
Brazil
Gram-negative aerobic bacteria
methicillin-resistant Staphylococcus aureus
topic cephalosporins
Brazil
Gram-negative aerobic bacteria
methicillin-resistant Staphylococcus aureus
description Ceftobiprole is a broad-spectrum cephalosporin with potent activity against staphylococci, including those resistant to oxacillin, as well as against most Gram-negative bacilli including Pseudomonas aeruginosa. In this study, the in vitro activity of ceftobiprole and comparator agents was tested against bacterial isolates recently collected from Brazilian private hospitals. A total of 336 unique bacterial isolates were collected from hospitalized patients between February 2008 and August 2009. Each hospital was asked to submit 100 single bacterial isolates responsible for causing blood, lower respiratory tract or skin and soft tissue infections. Bacterial identification was confirmed and antimicrobial susceptibility testing was performed using CLSI microdilution method at a central laboratory. The CLSI M100-S21 (2011) was used for interpretation of the antimicrobial susceptibility results. Among the 336 pathogens collected, 255 (75.9%) were Gram-negative bacilli and 81 (24.1%) were Gram-positive cocci. Although ceftobiprole MIC50 values for oxacillin resistant strains were two-fold higher than for methicillin susceptible S. aureus, ceftobiprole inhibited 100% of tested S. aureus at MICs < 4 µg/mL. Polymyxin B was the only agent to show potent activity against Acinetobacter spp. (MIC50/90, 0.5/1 µg/mL), and P. aeruginosa (MIC50/90, 1/2 µg/mL). Resistance to broad-spectrum cephalosporins varied from 55.3-68.5% and 14.3-28.5% among E. coli and Klebsiella spp. isolates, respectively; with ceftobiprole MIC50 > 6 µg/mL for both species. Our results showed that ceftobiprole has potent activity against staphylococci and E. faecalis, which was superior to that of vancomycin. Our data also indicates that ceftobiprole demonstrated potency comparable to that of cefepime and ceftazidime against key Gram-negative species.
publishDate 2011
dc.date.issued.fl_str_mv 2011-08-01
dc.date.accessioned.fl_str_mv 2015-06-14T13:43:11Z
dc.date.available.fl_str_mv 2015-06-14T13:43:11Z
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.citation.fl_str_mv Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 15, n. 4, p. 339-348, 2011.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/6544
http://dx.doi.org/10.1590/S1413-86702011000400007
dc.identifier.issn.none.fl_str_mv 1413-8670
dc.identifier.file.none.fl_str_mv S1413-86702011000400007.pdf
dc.identifier.scielo.none.fl_str_mv S1413-86702011000400007
dc.identifier.doi.none.fl_str_mv 10.1590/S1413-86702011000400007
dc.identifier.wos.none.fl_str_mv WOS:000293862800007
identifier_str_mv Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 15, n. 4, p. 339-348, 2011.
1413-8670
S1413-86702011000400007.pdf
S1413-86702011000400007
10.1590/S1413-86702011000400007
WOS:000293862800007
url http://repositorio.unifesp.br/handle/11600/6544
http://dx.doi.org/10.1590/S1413-86702011000400007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Brazilian Journal of Infectious Diseases
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 339-348
dc.publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
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
bitstream.url.fl_str_mv ${dspace.ui.url}/bitstream/11600/6544/1/S1413-86702011000400007.pdf
${dspace.ui.url}/bitstream/11600/6544/2/S1413-86702011000400007.pdf.txt
bitstream.checksum.fl_str_mv 6ede0e14a45134928ce4754b5701f6d4
f5dde6fc6603237b81d785a7e0677b11
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
_version_ 1802764176237527040