The Complexity of erm-Mediated Resistance: Structural and Functional Perspectives From β-Hemolytic Streptococci
Lillie M Powell1, Rita Berisio2, P Rocco LaSala3
1Department of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, USA.
Abstract:
Macrolide overuse and resulting resistance crippled the applicability of one of the most important and successful classes of antibiotics. The rising incidence of invasive infections caused by β-hemolytic group A and group B streptococci have been paralleled with marked increases in erythromycin and clindamycin resistance. As a result, resistant invasive group A and group B Streptococcus infections have been classified by the CDC as a concerning level threat since 2019. Acquisition of erythromycin resistance methylase (erm) genes is a major contributor of the MLSB [macrolide (i.e., erythromycin), lincosamide (i.e., clindamycin), and streptogramin B] resistance phenotype in US isolates. The erm-encoded enzymes utilize the methyl-group from S-adenosyl-L-methionine (SAM) to methylate the adenosine A2058 residue of bacterial ribosomal RNA, which serves as the overlapping rRNA target site for the three MLSB classes of antibiotics. The major mechanism that regulates Erm methyltransferase production is translational attenuation in the 5' regulatory region upstream of the erm coding sequence. The 5' regulatory region of erm includes at least one short leader peptide ermL, with the leader peptide ribosome binding site (SD1), non-translational stem-loop structures, and the erm start codon with its ribosome binding site (SD2). Binding of a macrolide antibiotic to the ribosome causes stalling during translation of the ermL peptide, which disrupts and alters the formation of inhibitory mRNA hairpins in the erm 5' regulatory region, thereby releasing the erm SD2-site from the posterior stem-loop hairpin, thus allowing Erm protein translation. The streptococcal ErmA, ErmB, and ErmT proteins have conserved structures with primary sequence conservation of residues involved in SAM- and rRNA-binding activity, as well as a high-level of structural conservation. However, the observed variation in the erm 5' regulatory region sequences, transcript expression, and ribosome methylation levels associated with these genes and proteins underscore the regulatory complexity of Erm expression. This review aims to present insights into mechanisms of Erm-mediated resistance, trends in streptococcal epidemiology and treatment, and progress in the development of improved MLSB drugs that effectively block erm-mediated resistance.
Insights
Macrolide resistance in streptococci is increasing due to erm genes, threatening antibiotic effectiveness. Understanding Erm-mediated resistance mechanisms is crucial for developing new MLSB drugs to combat these infections.
Area of Science:
- Microbiology and Infectious Diseases
- Molecular Biology
- Pharmacology
Background:
- Overuse of macrolide antibiotics has led to widespread resistance, diminishing the effectiveness of this critical drug class.
- Invasive infections caused by β-hemolytic group A and B streptococci are rising, with increasing resistance to erythromycin and clindamycin.
- The Centers for Disease Control and Prevention (CDC) has classified resistant invasive streptococcal infections as a concerning threat since 2019.
Purpose of the Study:
- To review the mechanisms of Erm-mediated macrolide, lincosamide, and streptogramin B (MLSB) resistance in streptococci.
- To examine epidemiological trends and treatment challenges associated with resistant streptococcal infections.
- To highlight progress in developing novel MLSB drugs that overcome erm-mediated resistance.
Main Methods:
- Analysis of the molecular mechanisms of translational attenuation regulating Erm methyltransferase production.
- Review of conserved structural and sequence features of streptococcal ErmA, ErmB, and ErmT proteins.
- Examination of variations in erm 5' regulatory regions, transcript expression, and ribosome methylation levels.
Main Results:
- Erythromycin resistance methylase (erm) genes are a primary driver of the MLSB resistance phenotype in US streptococcal isolates.
- Erm-encoded enzymes methylate bacterial ribosomal RNA at the A2058 adenosine residue, the shared target site for MLSB antibiotics.
- Macrolide binding to ribosomes stalls translation of the leader peptide, altering mRNA hairpin formation and enabling Erm protein synthesis.
Conclusions:
- Erm-mediated resistance presents a significant challenge to treating streptococcal infections, necessitating a deeper understanding of regulatory complexity.
- Conserved structural elements in Erm proteins suggest a common mechanism of action, despite variations in regulatory regions.
- Developing new MLSB drugs that circumvent Erm-mediated resistance is essential for effective clinical management of invasive streptococcal diseases.
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