Structural studies of ribosome from an anaerobic Bacteroidetes human pathogen Porphyromonas gingivalis

Author:

Hiregange Disha-Gajanan1,Samiya Sarit1,Mizgalska Danuta2,Ben-Zeev Efrat3,Waghalter Miriam1,Rivalta Andre1,Rajan K Shanmugha1,Halfon Yehuda1,Breiner-Goldstein Elinor1,Kaczmarczyk Igor124ORCID,Sroka Aneta24,Taoka Masato5ORCID,Nobe Yuko5,Isobe Toshiaki5,Paukner Susanne6,Zimmerman Ella1,Bashan Anat1ORCID,Potempa Jan27,Yonath Ada1

Affiliation:

1. Weizmann Institute of Science Department of Chemical and Structural Biology, , Rehovot 7610001 ,

2. Faculty of Biochemistry, Biophysics, and Biotechnology, Jagiellonian University Department of Microbiology, , Krakow 30-387,

3. Nancy and Stephen Grand Israel National Center for Personalized Medicine, Mantoux Institute for Bioinformatics, Weizmann Institute of Science , Rehovot 7610001 ,

4. Doctoral School of Exact and Natural Sciences, Jagiellonian University , Krakow 30-387 ,

5. Graduate School of Science, Tokyo Metropolitan University Department of Chemistry, , Minami-Osawa 1-1, Hachioji -shi, Tokyo 192-0397 ,

6. Nabriva Therapeutics GmbH , Vienna 1110 ,

7. University of Louisville Department of Oral Immunology and Infectious Diseases, , Louisville , KY 40292,

Abstract

Abstract Porphyromonas gingivalis, an anaerobic pathogen in chronic periodontitis, belongs to the Bacteroidota phylum and is associated with various virulence factors. Its antibiotic-resistant strains and its propensity to form biofilms pose a challenge to effective treatment. To explore therapeutic avenues, we studied the high-resolution cryogenic electron microscope structures of ribosomes from the wild-type P. gingivalis W83 and the macrolide-resistant mutant strain ermΔporN. The structural analysis revealed unique features primarily at the ribosome periphery. Together with the distinctive distribution of ribosomal RNA modifications, these findings offer insights into the therapeutical potential, such as creation of novel therapeutic compounds inhibiting the specific cellular functions of the P. gingivalis ribosomes. Moreover, the high-resolution structure of the ermΔporN ribosome in its complex with the approved antibiotic lefamulin suggests its repurposing against P. gingivalis. Furthermore, we provide a foundation for additional effective strategies to treat periodontitis and associated systemic diseases.

Funder

Kimmelman Center for Macromolecular Assemblies

National Institutes of Health

Strategic Programme Excellence Initiative

Publisher

Oxford University Press (OUP)

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