Linezolid: First of a new drug class for Gram-positive infections

被引:0
作者
Atanaskova N. [1 ]
Keshamouni V.G. [1 ]
Krueger J.S. [1 ]
Schwartz J.A. [2 ]
Miller F. [1 ]
Reddy K.B. [1 ]
机构
[1] Department of Pathology, Wayne State University School of Medicine, Detroit, MI 48201
[2] Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201
关键词
Adis International Limited; Linezolid; Soft Tissue Infection; Neisseria Gonorrhoeae; Chlamydial Infection;
D O I
10.2165/00042310-200117090-00001
中图分类号
学科分类号
摘要
Linezolid is an oxazolidinone-type antibacterial agent which inhibits bacterial protein synthesis by specifically binding to the 50S ribosomal subunit. Linezolid is active against Gram-positive organisms and certain anaerobes, and has shown some bactericidal activity. Methicillin-resistant staphylococci, penicillin-resistant Streptococcus pneumoniae and vancomycin-resistant Enterococcus faecalis and E. faecium are susceptible to linezolid. This agent is effective in patients with skin and soft tissue infections, community-acquired and nosocomial pneumonia, and bacteraemia, and has similar efficacy to that of other standard treatments. Resistance to linezolid has been reported in a small number of patients infected with E. faecium. Linezolid is generally well tolerated and most events (mainly GI-related) are of mild to moderate intensity, resolve during continuous linezolid treatment and are not dose-related. Linezolid is an important new drug which is likely to be of use in the treatment of serious or complicated infections due to potentially resistant Gram-positive organisms.
引用
收藏
页码:1 / 6
页数:5
相关论文
共 9 条
  • [1] Quinupristin/DalfopristinA Review of its Use in the Management of Serious Gram-Positive Infections
    Harriet M. Lamb
    David P. Figgitt
    Diana Faulds
    [J]. Drugs, 1999, 58 : 1061 - 1097
  • [2] New antimicrobial agents as therapy for resistant gram-positive cocci
    J. R. Lentino
    M. Narita
    V. L. Yu
    [J]. European Journal of Clinical Microbiology & Infectious Diseases, 2008, 27 : 3 - 15
  • [3] Type IV Pili in Gram-Positive Bacteria
    Melville, Stephen
    Craig, Lisa
    [J]. MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2013, 77 (03) : 323 - 341
  • [4] Characterization of R-pyocin activity against Gram-positive pathogens for the first time with special focus on Staphylococcus aureus
    Mohamed, A. A.
    Elshawadfy, A. M.
    Amin, G.
    Askora, A.
    [J]. JOURNAL OF APPLIED MICROBIOLOGY, 2021, 131 (06) : 2780 - 2792
  • [5] Natural Transformation in Gram-Positive Bacteria and Its Biotechnological Relevance to Lactic Acid Bacteria
    O'Connell, Laura M.
    Kelleher, Philip
    van Rijswijck, Irma M. H.
    de Waal, Paul
    van Peij, Noel N. M. E.
    Mahony, Jennifer
    van Sinderen, Douwe
    [J]. ANNUAL REVIEW OF FOOD SCIENCE AND TECHNOLOGY, 2022, 13 : 409 - 431
  • [6] CEM-101, a novel fluoroketolide: antimicrobial activity against a diverse collection of Gram-positive and Gram-negative bacteria
    Putnam, Shannon D.
    Castanheira, Mariana
    Moet, Gary J.
    Farrell, David J.
    Jones, Ronald N.
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2010, 66 (04) : 393 - 401
  • [7] Identification of Surprisingly Diverse Type IV Pili, across a Broad Range of Gram-Positive Bacteria
    Imam, Saheed
    Chen, Zhongqiang
    Roos, David S.
    Pohlschroeder, Mechthild
    [J]. PLOS ONE, 2011, 6 (12):
  • [8] In Vitro Activity of AZD0914, a Novel Bacterial DNA Gyrase/Topoisomerase IV Inhibitor, against Clinically Relevant Gram-Positive and Fastidious Gram-Negative Pathogens
    Biedenbach, Douglas J.
    Huband, Michael D.
    Hackel, Meredith
    de Jonge, Boudewijn L. M.
    Sahm, Daniel F.
    Bradford, Patricia A.
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2015, 59 (10) : 6053 - 6063
  • [9] Once-Daily High-Dose NetilmicinA New Short-Term Treatment Regimen for Patients with Moderate to Severe Gram-Negative Infections
    H. Bassaris
    G. Saroglou
    G. Petrikkos
    J. Starakis
    A. Vassiloyiannakopoulos
    A. Antoniadou
    C. Tsagaraki
    E. Skeparni
    P. Goumas
    J. Boutsikakis
    M. Lazanas
    O. Paniara
    E. Platsouka
    [J]. Clinical Drug Investigation, 1998, 15 : 205 - 216