In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci

Detalhes bibliográficos
Autor(a) principal: Sader, Helio S. [UNIFESP]
Data de Publicação: 2004
Outros Autores: Johnson, D. M., Jones, R. N.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1128/AAC.48.1.53-62.2004
http://repositorio.unifesp.br/handle/11600/27523
Resumo: LB 11058 is a novel parenteral cephalosporin with a C-3 pyrimidinyl-substituted vinyl sulfide group and a C-7 2-amino-5-chloro-1,3-thiazole group. This study evaluated the in vitro activity and spectrum of LB 11058 against 1,245 recent clinical isolates, including a subset of gram-positive strains with specific resistant phenotypes. LB 11058 was very active against Streptococcus pneumoniae. the novel cephalosporin was 8- to 16-fold more potent than ceftriaxone, cefepime, or amoxicillin-clavulanate against both penicillin-intermediate and -resistant S. pneumoniae. LB 11058 was also very active against both beta-hemolytic streptococci (MIC at which 90% of isolates were inhibited [MIC90], less than or equal to0.008 mug/ml) and viridans group streptococci (MIC90, 0.03 to 0.5 mug/ml), including penicillin-resistant strains. Among oxacillin-susceptible Staphylococcus aureus, LB 11058 MIC results varied from 0.06 to 0.25 mug/ml (MIC50, 0.12 mug/ml), while among oxacillin-resistant strains LB 11058 MICs varied from 0.25 to 1 mug/ml (MIC50, 1 mug/ml). Coagulase-negative staphylococci showed an LB 11058 susceptibility pattern similar to that of S. aureus, with all isolates being inhibited at less than or equal to1 mug/ml. LB 11058 also showed reasonable in vitro activity against Enterococcus faecalis, including vancomycin-resistant strains (MIC50, 1 mug/ml), and Bacillus spp. (MIC50, 0.25 mug/ml); however, it was less active against Enterococcus faecium (MIC50, >64 mug/ml) and Corynebacterium spp. (MIC50, 32 mug/ml). Against gram-negative pathogens, LB 11058 showed activity against Haemophilus influenzae (MIC90, 0.25 to 0.5 mug/ml) and Moraxella catarrhalis (MIC90, 0.25 mug/ml), with MICs not influenced by beta-lactamase production. in conclusion, LB 11058 demonstrated a broad antibacterial spectrum and was highly active against gram-positive bacteria, particularly against multidrug-resistant staphylococci and streptococci.
id UFSP_e38dd819a3259be654b83987d9dec4e0
oai_identifier_str oai:repositorio.unifesp.br/:11600/27523
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococciLB 11058 is a novel parenteral cephalosporin with a C-3 pyrimidinyl-substituted vinyl sulfide group and a C-7 2-amino-5-chloro-1,3-thiazole group. This study evaluated the in vitro activity and spectrum of LB 11058 against 1,245 recent clinical isolates, including a subset of gram-positive strains with specific resistant phenotypes. LB 11058 was very active against Streptococcus pneumoniae. the novel cephalosporin was 8- to 16-fold more potent than ceftriaxone, cefepime, or amoxicillin-clavulanate against both penicillin-intermediate and -resistant S. pneumoniae. LB 11058 was also very active against both beta-hemolytic streptococci (MIC at which 90% of isolates were inhibited [MIC90], less than or equal to0.008 mug/ml) and viridans group streptococci (MIC90, 0.03 to 0.5 mug/ml), including penicillin-resistant strains. Among oxacillin-susceptible Staphylococcus aureus, LB 11058 MIC results varied from 0.06 to 0.25 mug/ml (MIC50, 0.12 mug/ml), while among oxacillin-resistant strains LB 11058 MICs varied from 0.25 to 1 mug/ml (MIC50, 1 mug/ml). Coagulase-negative staphylococci showed an LB 11058 susceptibility pattern similar to that of S. aureus, with all isolates being inhibited at less than or equal to1 mug/ml. LB 11058 also showed reasonable in vitro activity against Enterococcus faecalis, including vancomycin-resistant strains (MIC50, 1 mug/ml), and Bacillus spp. (MIC50, 0.25 mug/ml); however, it was less active against Enterococcus faecium (MIC50, >64 mug/ml) and Corynebacterium spp. (MIC50, 32 mug/ml). Against gram-negative pathogens, LB 11058 showed activity against Haemophilus influenzae (MIC90, 0.25 to 0.5 mug/ml) and Moraxella catarrhalis (MIC90, 0.25 mug/ml), with MICs not influenced by beta-lactamase production. in conclusion, LB 11058 demonstrated a broad antibacterial spectrum and was highly active against gram-positive bacteria, particularly against multidrug-resistant staphylococci and streptococci.JONES Grp JMI Labs, N Liberty, IA 52317 USAUniversidade Federal de São Paulo, São Paulo, BrazilTufts Univ, Sch Med, Boston, MA 02111 USAUniversidade Federal de São Paulo, EPM, São Paulo, BrazilWeb of ScienceAmer Soc MicrobiologyJONES Grp JMI LabsUniversidade Federal de São Paulo (UNIFESP)Tufts UnivSader, Helio S. [UNIFESP]Johnson, D. M.Jones, R. N.2016-01-24T12:34:10Z2016-01-24T12:34:10Z2004-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion53-62application/pdfhttp://dx.doi.org/10.1128/AAC.48.1.53-62.2004Antimicrobial Agents and Chemotherapy. Washington: Amer Soc Microbiology, v. 48, n. 1, p. 53-62, 2004.10.1128/AAC.48.1.53-62.2004WOS000187728500007.pdf0066-4804http://repositorio.unifesp.br/handle/11600/27523WOS:000187728500007engAntimicrobial Agents and Chemotherapyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-07T12:17:24Zoai:repositorio.unifesp.br/:11600/27523Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-07T12:17:24Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
title In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
spellingShingle In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
Sader, Helio S. [UNIFESP]
title_short In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
title_full In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
title_fullStr In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
title_full_unstemmed In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
title_sort In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
author Sader, Helio S. [UNIFESP]
author_facet Sader, Helio S. [UNIFESP]
Johnson, D. M.
Jones, R. N.
author_role author
author2 Johnson, D. M.
Jones, R. N.
author2_role author
author
dc.contributor.none.fl_str_mv JONES Grp JMI Labs
Universidade Federal de São Paulo (UNIFESP)
Tufts Univ
dc.contributor.author.fl_str_mv Sader, Helio S. [UNIFESP]
Johnson, D. M.
Jones, R. N.
description LB 11058 is a novel parenteral cephalosporin with a C-3 pyrimidinyl-substituted vinyl sulfide group and a C-7 2-amino-5-chloro-1,3-thiazole group. This study evaluated the in vitro activity and spectrum of LB 11058 against 1,245 recent clinical isolates, including a subset of gram-positive strains with specific resistant phenotypes. LB 11058 was very active against Streptococcus pneumoniae. the novel cephalosporin was 8- to 16-fold more potent than ceftriaxone, cefepime, or amoxicillin-clavulanate against both penicillin-intermediate and -resistant S. pneumoniae. LB 11058 was also very active against both beta-hemolytic streptococci (MIC at which 90% of isolates were inhibited [MIC90], less than or equal to0.008 mug/ml) and viridans group streptococci (MIC90, 0.03 to 0.5 mug/ml), including penicillin-resistant strains. Among oxacillin-susceptible Staphylococcus aureus, LB 11058 MIC results varied from 0.06 to 0.25 mug/ml (MIC50, 0.12 mug/ml), while among oxacillin-resistant strains LB 11058 MICs varied from 0.25 to 1 mug/ml (MIC50, 1 mug/ml). Coagulase-negative staphylococci showed an LB 11058 susceptibility pattern similar to that of S. aureus, with all isolates being inhibited at less than or equal to1 mug/ml. LB 11058 also showed reasonable in vitro activity against Enterococcus faecalis, including vancomycin-resistant strains (MIC50, 1 mug/ml), and Bacillus spp. (MIC50, 0.25 mug/ml); however, it was less active against Enterococcus faecium (MIC50, >64 mug/ml) and Corynebacterium spp. (MIC50, 32 mug/ml). Against gram-negative pathogens, LB 11058 showed activity against Haemophilus influenzae (MIC90, 0.25 to 0.5 mug/ml) and Moraxella catarrhalis (MIC90, 0.25 mug/ml), with MICs not influenced by beta-lactamase production. in conclusion, LB 11058 demonstrated a broad antibacterial spectrum and was highly active against gram-positive bacteria, particularly against multidrug-resistant staphylococci and streptococci.
publishDate 2004
dc.date.none.fl_str_mv 2004-01-01
2016-01-24T12:34:10Z
2016-01-24T12:34:10Z
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/10.1128/AAC.48.1.53-62.2004
Antimicrobial Agents and Chemotherapy. Washington: Amer Soc Microbiology, v. 48, n. 1, p. 53-62, 2004.
10.1128/AAC.48.1.53-62.2004
WOS000187728500007.pdf
0066-4804
http://repositorio.unifesp.br/handle/11600/27523
WOS:000187728500007
url http://dx.doi.org/10.1128/AAC.48.1.53-62.2004
http://repositorio.unifesp.br/handle/11600/27523
identifier_str_mv Antimicrobial Agents and Chemotherapy. Washington: Amer Soc Microbiology, v. 48, n. 1, p. 53-62, 2004.
10.1128/AAC.48.1.53-62.2004
WOS000187728500007.pdf
0066-4804
WOS:000187728500007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Antimicrobial Agents and Chemotherapy
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 53-62
application/pdf
dc.publisher.none.fl_str_mv Amer Soc Microbiology
publisher.none.fl_str_mv Amer Soc Microbiology
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_ 1814268294004211712