<i>In vitro</i> activity of MRS-2541, a novel MetRS inhibitor, against a selection of resistant gram-positive organisms associated with serious hospital infections

Infections caused by antibiotic-resistant bacteria are inherently challenging to treat. Poor outcomes, including higher death rates, are associated with infections caused by antibiotic-resistant organisms. As a result, there is an urgent need for new antibiotics, particularly ones that act via novel mechanisms that evade established resistance mechanisms. In this paper, we provide new data about MRS-2541, a preclinical antibiotic that acts by inhibiting the bacterial methionyl-tRNA synthetase. We show that MRS-2541 has potent in vitro activity against diverse strains of <i>Staphylococcus</i>, <i>Streptococcus</i>, and <i>Enterococcus</i>. For example, all 115 strains of <i>Staphylococcus</i> spp. (including 27 methicillin-resistant <i>Staphylococcus aureus</i> strains and 12 vancomycin-intermediate <i>S. aureus</i> strains) were fully susceptible to MRS-2541 with MICs of <0.25 μg/mL. The specific activity against gram-positive bacteria and sparing of gram-negative flora indicates that MRS-2541 may be less disruptive of intestinal microbiota than broad-spectrum antibiotics. MRS-2541 is a promising preclinical candidate for infections due to resistant gram-positive organisms.

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Publication Details

Journal
Microbiology Spectrum
Published
2026-03-11
DOI
https://doi.org/10.1128/spectrum.03615-25
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
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article

In vitro activity of MRS-2541, a novel MetRS inhibitor, against a selection of resistant gram-positive organisms associated with serious hospital infections

Dawn Reyna, David Hufnagel, Elke Lipka, Frederick S. Buckner et al.
Microbiology Spectrum
RNA and protein synthesis mechanisms
article

In vitro activity of MRS-2541, a novel MetRS inhibitor, against a selection of resistant gram-positive organisms associated with serious hospital infections

Dawn Reyna, David Hufnagel, Elke Lipka, Frederick S. Buckner, Nora M. R. Molasky, Andrea Marra, Chris M. Pillar, John M. Domagala, Angela K Mendez, Erkang Fan, Seyedhameneh Jahanbakhsh, Zhongsheng Zhang
article en

Abstract

Infections caused by antibiotic-resistant bacteria are inherently challenging to treat. Poor outcomes, including higher death rates, are associated with infections caused by antibiotic-resistant organisms. As a result, there is an urgent need for new antibiotics, particularly ones that act via novel mechanisms that evade established resistance mechanisms. In this paper, we provide new data about MRS-2541, a preclinical antibiotic that acts by inhibiting the bacterial methionyl-tRNA synthetase. We show that MRS-2541 has potent in vitro activity against diverse strains of <i>Staphylococcus</i>, <i>Streptococcus</i>, and <i>Enterococcus</i>. For example, all 115 strains of <i>Staphylococcus</i> spp. (including 27 methicillin-resistant <i>Staphylococcus aureus</i> strains and 12 vancomycin-intermediate <i>S. aureus</i> strains) were fully susceptible to MRS-2541 with MICs of <0.25 μg/mL. The specific activity against gram-positive bacteria and sparing of gram-negative flora indicates that MRS-2541 may be less disruptive of intestinal microbiota than broad-spectrum antibiotics. MRS-2541 is a promising preclinical candidate for infections due to resistant gram-positive organisms.

Microbiology Spectrum
University of Washington (US), Office of Infectious Diseases (US), Mycologie et Sécurité des Aliments (FR), Therapeutics Systems Research Laboratories (United States) (US)
Good health and well-being
Openalex Percentile: Top 27%
RNA and protein synthesis mechanisms
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