TY - JOUR
T1 - Structural studies of ribosome from an anaerobic Bacteroidetes human pathogen Porphyromonas gingivalis
AU - Hiregange, Disha Gajanan
AU - Samiya, Sarit
AU - Mizgalska, Danuta
AU - Ben-Zeev, Efrat
AU - Waghalter, Miriam
AU - Rivalta, Andre
AU - Rajan, K. Shanmugha
AU - Halfon, Yehuda
AU - Breiner-Goldstein, Elinor
AU - Kaczmarczyk, Igor
AU - Sroka, Aneta
AU - Taoka, Masato
AU - Nobe, Yuko
AU - Isobe, Toshiaki
AU - Paukner, Susanne
AU - Zimmerman, Ella
AU - Bashan, Anat
AU - Potempa, Jan
AU - Yonath, Ada
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/5/22
Y1 - 2025/5/22
N2 - 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 erm∆porN. 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 erm∆porN 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.
AB - 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 erm∆porN. 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 erm∆porN 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.
UR - https://www.scopus.com/pages/publications/105007087426
U2 - 10.1093/nar/gkaf458
DO - 10.1093/nar/gkaf458
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C2 - 40444637
AN - SCOPUS:105007087426
SN - 0305-1048
VL - 53
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 10
M1 - gkaf458
ER -