Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model

Ceftobiprole is a novel broad-spectrum cephalosporin with good in vitro activity against methicillin-resistant Staphylococcus aureus and Enterococcus faecalis. The objective of this study was to assess the in vivo activity of ceftobiprole against four strains of E. faecalis, including β-lactamase- p...

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Autores:
Arias, Cesar A.
Singh, Kavindra V.
Panesso, Diana
Murray, Barbara E.
Tipo de recurso:
Article of journal
Fecha de publicación:
2007
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/5169
Acceso en línea:
http://hdl.handle.net/20.500.12495/5169
https://doi.org/10.1093/jac/dkm237
https://repositorio.unbosque.edu.co
Palabra clave:
Enterococci
Cephalosporins
Animal model
Rights
openAccess
License
Acceso abierto
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dc.title.spa.fl_str_mv Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
dc.title.translated.spa.fl_str_mv Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
title Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
spellingShingle Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
Enterococci
Cephalosporins
Animal model
title_short Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
title_full Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
title_fullStr Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
title_full_unstemmed Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
title_sort Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis model
dc.creator.fl_str_mv Arias, Cesar A.
Singh, Kavindra V.
Panesso, Diana
Murray, Barbara E.
dc.contributor.author.none.fl_str_mv Arias, Cesar A.
Singh, Kavindra V.
Panesso, Diana
Murray, Barbara E.
dc.contributor.orcid.none.fl_str_mv Panesso, Diana [0000-0002-4049-9702]
dc.subject.keywords.spa.fl_str_mv Enterococci
Cephalosporins
Animal model
topic Enterococci
Cephalosporins
Animal model
description Ceftobiprole is a novel broad-spectrum cephalosporin with good in vitro activity against methicillin-resistant Staphylococcus aureus and Enterococcus faecalis. The objective of this study was to assess the in vivo activity of ceftobiprole against four strains of E. faecalis, including β-lactamase- producing (Bla+) and vancomycin-resistant strains. Mice were infected intraperitoneally with strains of E. faecalis: (i) the Bla+ strain HH22; (ii) two vancomycin-resistant strains (TX2484 and V583); and (iii) OG1RF (a laboratory strain), using 10 × the LD50 for each strain. Ceftobiprole doses of 25, 12.5 and 6.25 mg/kg (single doses) and ampicillin 50, 25, 12.5 and 6.25 mg/kg (single and double doses) were administered subcutaneously immediately after bacterial challenge and mice were monitored for 96 h. All four E. faecalis had ceftobiprole MICs ≤0.5 mg/L. Despite being susceptible in vitro at the standard inoculum, ampicillin (single and double doses) did not protect mice against intraperitoneal challenge with Bla+ E. faecalis HH22, with a 50% protective dose (PD50) of >100 mg/kg, whereas ceftobiprole was protective (PD50 of 2 mg/kg). Ceftobiprole PD50s for vancomycin-resistant isolates TX2484 and V583 were 7.7 and 5.2 mg/kg, respectively, similar to those of single dose ampicillin (12.5 and 16.4 mg/kg, respectively). For OG1RF, both ampicillin and ceftobiprole protected all mice at doses of 25 and 12.5 mg/kg, respectively, with a PD50 of 4.2 and 8 mg/kg for ceftobiprole and ampicillin, respectively. Ceftobiprole had comparable in vivo activity to that of ampicillin against vancomycin-resistant and ampicillin-susceptible strains of E. faecalis in the mouse peritonitis model. Ceftobiprole was superior in vivo to ampicillin against the Bla+ strain HH22. Our data support the further study of ceftobiprole as a therapeutic agent in humans infected with E. faecalis.
publishDate 2007
dc.date.issued.none.fl_str_mv 2007
dc.date.accessioned.none.fl_str_mv 2020-12-03T19:31:04Z
dc.date.available.none.fl_str_mv 2020-12-03T19:31:04Z
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dc.type.local.none.fl_str_mv Artículo de revista
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dc.identifier.issn.none.fl_str_mv 1460-2091
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12495/5169
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1093/jac/dkm237
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
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identifier_str_mv 1460-2091
instname:Universidad El Bosque
reponame:Repositorio Institucional Universidad El Bosque
url http://hdl.handle.net/20.500.12495/5169
https://doi.org/10.1093/jac/dkm237
https://repositorio.unbosque.edu.co
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Journal of Antimicrobial Chemotherapy, 1460-2091, Vol. 60, Nro. 3, 2007 p. 594-598
dc.relation.uri.none.fl_str_mv https://academic.oup.com/jac/article/60/3/594/734011
dc.rights.local.spa.fl_str_mv Acceso abierto
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rights_invalid_str_mv Acceso abierto
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eu_rights_str_mv openAccess
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dc.publisher.journal.spa.fl_str_mv Journal of Antimicrobial Chemotherapy
institution Universidad El Bosque
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spelling Arias, Cesar A.Singh, Kavindra V.Panesso, DianaMurray, Barbara E.Panesso, Diana [0000-0002-4049-9702]2020-12-03T19:31:04Z2020-12-03T19:31:04Z20071460-2091http://hdl.handle.net/20.500.12495/5169https://doi.org/10.1093/jac/dkm237instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengJournal of Antimicrobial Chemotherapy, 1460-2091, Vol. 60, Nro. 3, 2007 p. 594-598https://academic.oup.com/jac/article/60/3/594/734011Evaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis modelEvaluation of ceftobiprole medocaril against Enterococcus faecalis in a mouse peritonitis modelArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85EnterococciCephalosporinsAnimal modelJournal of Antimicrobial ChemotherapyCeftobiprole is a novel broad-spectrum cephalosporin with good in vitro activity against methicillin-resistant Staphylococcus aureus and Enterococcus faecalis. The objective of this study was to assess the in vivo activity of ceftobiprole against four strains of E. faecalis, including β-lactamase- producing (Bla+) and vancomycin-resistant strains. Mice were infected intraperitoneally with strains of E. faecalis: (i) the Bla+ strain HH22; (ii) two vancomycin-resistant strains (TX2484 and V583); and (iii) OG1RF (a laboratory strain), using 10 × the LD50 for each strain. Ceftobiprole doses of 25, 12.5 and 6.25 mg/kg (single doses) and ampicillin 50, 25, 12.5 and 6.25 mg/kg (single and double doses) were administered subcutaneously immediately after bacterial challenge and mice were monitored for 96 h. All four E. faecalis had ceftobiprole MICs ≤0.5 mg/L. Despite being susceptible in vitro at the standard inoculum, ampicillin (single and double doses) did not protect mice against intraperitoneal challenge with Bla+ E. faecalis HH22, with a 50% protective dose (PD50) of >100 mg/kg, whereas ceftobiprole was protective (PD50 of 2 mg/kg). Ceftobiprole PD50s for vancomycin-resistant isolates TX2484 and V583 were 7.7 and 5.2 mg/kg, respectively, similar to those of single dose ampicillin (12.5 and 16.4 mg/kg, respectively). For OG1RF, both ampicillin and ceftobiprole protected all mice at doses of 25 and 12.5 mg/kg, respectively, with a PD50 of 4.2 and 8 mg/kg for ceftobiprole and ampicillin, respectively. Ceftobiprole had comparable in vivo activity to that of ampicillin against vancomycin-resistant and ampicillin-susceptible strains of E. faecalis in the mouse peritonitis model. Ceftobiprole was superior in vivo to ampicillin against the Bla+ strain HH22. Our data support the further study of ceftobiprole as a therapeutic agent in humans infected with E. faecalis.Acceso abiertohttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto2007ORIGINALArias_Cesar_A._2007.pdfArias_Cesar_A._2007.pdfapplication/pdf171147https://repositorio.unbosque.edu.co/bitstreams/40d2bdf8-1b0b-4cd2-b773-e1ff412f6d1e/download7f8b68ef4518bee51aa0e3f88e5fbc07MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.unbosque.edu.co/bitstreams/88f3f01e-f62e-4ecd-977b-0a8c7ad7a3ba/download8a4605be74aa9ea9d79846c1fba20a33MD52THUMBNAILArias_Cesar_A._2007.pdf.jpgArias_Cesar_A._2007.pdf.jpgimage/jpeg5775https://repositorio.unbosque.edu.co/bitstreams/e0154619-2442-4a36-95b4-8d06ba594057/download7210a811635d1799e7c05fee5d259be7MD53TEXTArias_Cesar_A._2007.pdf.txtArias_Cesar_A._2007.pdf.txtExtracted texttext/plain26426https://repositorio.unbosque.edu.co/bitstreams/25a1b9d2-737d-4e16-a383-4604410cf10c/download7e4cbb115a0a313f6f90dbf0c19d6f36MD5420.500.12495/5169oai:repositorio.unbosque.edu.co:20.500.12495/51692024-02-07 06:51:13.283restrictedhttps://repositorio.unbosque.edu.coRepositorio Institucional Universidad El Bosquebibliotecas@biteca.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