TY - JOUR
T1 - Directed evolution of the rRNA methylating enzyme Cfr reveals molecular basis of antibiotic resistance
AU - Tsai, Kaitlyn
AU - Stojković, Vanja
AU - Noda-Garcia, Lianet
AU - Young, Iris D.
AU - Myasnikov, Alexander G.
AU - Kleinman, Jordan
AU - Palla, Ali
AU - Floor, Stephen N.
AU - Frost, Adam
AU - Fraser, James S.
AU - Tawfik, Dan S.
AU - Fujimori, Danica Galonić
N1 - Funding Information: The authors thank members of the Fujimori lab for discussion and comments on the manuscript. The authors thank the UCSF Center for Advanced CryoEM, which is supported by the National Institutes of Health (S10OD020054 and 1S10OD021741) and the Howard Hughes Medical Institute (HHMI). The authors thank Professor Kim Lewis and Dr. Yu Imai of Northeastern University for kindly providing hygromycin A. Publisher Copyright: © Tsai et al.
PY - 2022/1/11
Y1 - 2022/1/11
N2 - Alteration of antibiotic binding sites through modification of ribosomal RNA (rRNA) is a common form of resistance to ribosome-targeting antibiotics. The rRNA-modifying enzyme Cfr methylates an adenosine nucleotide within the peptidyl transferase center, resulting in the C-8 methylation of A2503 (m8A2503). Acquisition of cfr results in resistance to eight classes of ribosome-targeting antibiotics. Despite the prevalence of this resistance mechanism, it is poorly understood whether and how bacteria modulate Cfr methylation to adapt to antibiotic pressure. Moreover, direct evidence for how m8A2503 alters antibiotic binding sites within the ribosome is lacking. In this study, we performed directed evolution of Cfr under antibiotic selection to generate Cfr variants that confer increased resistance by enhancing methylation of A2503 in cells. Increased rRNA methylation is achieved by improved expression and stability of Cfr through transcriptional and post-transcriptional mechanisms, which may be exploited by pathogens under antibiotic stress as suggested by natural isolates. Using a variant that achieves near-stoichiometric methylation of rRNA, we determined a 2.2 Å cryo-electron microscopy structure of the Cfr-modified ribosome. Our structure reveals the molecular basis for broad resistance to antibiotics and will inform the design of new antibiotics that overcome resistance mediated by Cfr.
AB - Alteration of antibiotic binding sites through modification of ribosomal RNA (rRNA) is a common form of resistance to ribosome-targeting antibiotics. The rRNA-modifying enzyme Cfr methylates an adenosine nucleotide within the peptidyl transferase center, resulting in the C-8 methylation of A2503 (m8A2503). Acquisition of cfr results in resistance to eight classes of ribosome-targeting antibiotics. Despite the prevalence of this resistance mechanism, it is poorly understood whether and how bacteria modulate Cfr methylation to adapt to antibiotic pressure. Moreover, direct evidence for how m8A2503 alters antibiotic binding sites within the ribosome is lacking. In this study, we performed directed evolution of Cfr under antibiotic selection to generate Cfr variants that confer increased resistance by enhancing methylation of A2503 in cells. Increased rRNA methylation is achieved by improved expression and stability of Cfr through transcriptional and post-transcriptional mechanisms, which may be exploited by pathogens under antibiotic stress as suggested by natural isolates. Using a variant that achieves near-stoichiometric methylation of rRNA, we determined a 2.2 Å cryo-electron microscopy structure of the Cfr-modified ribosome. Our structure reveals the molecular basis for broad resistance to antibiotics and will inform the design of new antibiotics that overcome resistance mediated by Cfr.
UR - http://www.scopus.com/inward/record.url?scp=85123459601&partnerID=8YFLogxK
U2 - https://doi.org/10.7554/eLife.70017
DO - https://doi.org/10.7554/eLife.70017
M3 - Article
C2 - 35015630
SN - 2050-084X
VL - 11
JO - eLife
JF - eLife
M1 - e70017
ER -