Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Jan 30;8(2):191.
doi: 10.3390/microorganisms8020191.

Emerging Treatment Options for Infections by Multidrug-Resistant Gram-Positive Microorganisms

Affiliations
Review

Emerging Treatment Options for Infections by Multidrug-Resistant Gram-Positive Microorganisms

Despoina Koulenti et al. Microorganisms. .

Abstract

Antimicrobial agents are currently the mainstay of treatment for bacterial infections worldwide. However, due to the increased use of antimicrobials in both human and animal medicine, pathogens have now evolved to possess high levels of multi-drug resistance, leading to the persistence and spread of difficult-to-treat infections. Several current antibacterial agents active against Gram-positive bacteria will be rendered useless in the face of increasing resistance rates. There are several emerging antibiotics under development, some of which have been shown to be more effective with an improved safety profile than current treatment regimens against Gram-positive bacteria. We will extensively discuss these antibiotics under clinical development (phase I-III clinical trials) to combat Gram-positive bacteria, such as Staphylococcus aureus, Enterococcus faecium and Streptococcus pneumoniae. We will delve into the mechanism of actions, microbiological spectrum, and, where available, the pharmacokinetics, safety profile, and efficacy of these drugs, aiming to provide a comprehensive review to the involved stakeholders.

Keywords: clinical trials; defensin mimetics; dihydrofolate reductase inhibitors; emerging anti gram-positive antibiotics; ketolides; multi-drug resistance organisms; oxazolidinones; quinolones; topoisomerase II inhibitors; β-lactams.

PubMed Disclaimer

Conflict of interest statement

Author J.L. reports: Advisory Board with MSD and honorarium for lectures from Pfizer and MSD. All other authors declare no conflicts of interest related to the manuscript.

References

    1. Tanwar J., Das S., Fatima Z., Hameed S. Multidrug resistance: An emerging crisis. Interdiscip. Perspect. Infect. Dis. 2014 doi: 10.1155/2014/541340. - DOI - PMC - PubMed
    1. Gelband H., Molly Miller P., Pant S., Gandra S., Levinson J., Barter D., White A., Laxminarayan R. The state of the world’s antibiotics 2015. Wound Heal. South. Afr. 2015;8:30–34.
    1. Fair R.J., Tor Y. Antibiotics and bacterial resistance in the 21st century. Perspect. Med. Chem. 2014;6:25–64. doi: 10.4137/PMC.S14459. - DOI - PMC - PubMed
    1. Koulenti D., Xu E., Yin Sum Mok I., Song A., Karageorgopoulos D.E., Armaganidis A., Lipman J., Tsiodras S. Novel antibiotics for multidrug-resistant gram-positive microorganisms. Microorganisms. 2019;7:270. doi: 10.3390/microorganisms7080270. - DOI - PMC - PubMed
    1. Koulenti D., Xu E., Yin Sum Mok I., Song A., Karageorgopoulos D.E., Armaganidis A., Lipman J., Tsiodras S. Lefamulin. Comment on: “Novel Antibiotics for Multidrug-Resistant Gram-Positive Microorganisms. Microorganisms. 2019;7:386. doi: 10.3390/microorganisms7100386. - DOI - PMC - PubMed

LinkOut - more resources