In vitro activities of the novel cephalosporin LB 11058 against multidrug-resistant staphylococci and streptococci
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , |
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. |
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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 |
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1814268294004211712 |