TY - JOUR
T1 - Targeting of interaction between BB0323-BB0238 informs new paradigms in Lyme disease therapeutics
AU - Bista, Sandhya
AU - Brangulis, Kalvis
AU - Bhattachan, Bibek
AU - Foor, Shelby D
AU - Ronzetti, Michael H
AU - Jain, Sankalp
AU - Miller, Jenna
AU - Subramanion, Jothy Lachumy
AU - Kitsou, Chrysoula
AU - Rana, Vipin S
AU - Rai, Ganesha
AU - Zakharov, Alexey V
AU - Simeonov, Anton
AU - Baljinnyam, Bolormaa
AU - Pal, Utpal
N1 - Publisher Copyright:
Copyright: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
PY - 2026/1
Y1 - 2026/1
N2 - Borrelia burgdorferi, one of the most prevalent tick-borne pathogens, can cause a complex and multisystem illness called Lyme disease, where there has been an unmet need for novel therapeutic or preventive strategies. We previously identified an essential protein-protein interaction (PPI) event in B. burgdorferi involving two unique proteins, BB0323 and BB0238; herein, we show that this PPI is indispensable for long-term borrelial survival in mammals and explore its potential as a novel target for small molecule therapeutics. Using X-ray crystallography, we solved the structure of the BB0238-BB0323 complex and identified the hotspot residues that form the biomolecular PPI interface area of ~1000 square Ångstroms. We then performed quantitative high-throughput drug screens of 62,740 diverse small molecules utilizing an amplified luminescent proximity homogeneous assay linked immunosorbent assay (AlphaLISA). Following a comprehensive pipeline to confirm small molecule hits, we short-listed three distinct PPI inhibitors of BB0238-BB0323. One of these inhibitors, called lomibuvir (VX-222, VCH-222), displayed robust PPI inhibition inside B. burgdorferi cells and was shown to affect pathogen persistence in a tick-borne murine model of Lyme disease. Our study highlights targeted PPI disruption as a new therapeutic strategy against B. burgdorferi and may foster future antimicrobial discovery efforts to resolve clinical complications associated with Lyme disease.
AB - Borrelia burgdorferi, one of the most prevalent tick-borne pathogens, can cause a complex and multisystem illness called Lyme disease, where there has been an unmet need for novel therapeutic or preventive strategies. We previously identified an essential protein-protein interaction (PPI) event in B. burgdorferi involving two unique proteins, BB0323 and BB0238; herein, we show that this PPI is indispensable for long-term borrelial survival in mammals and explore its potential as a novel target for small molecule therapeutics. Using X-ray crystallography, we solved the structure of the BB0238-BB0323 complex and identified the hotspot residues that form the biomolecular PPI interface area of ~1000 square Ångstroms. We then performed quantitative high-throughput drug screens of 62,740 diverse small molecules utilizing an amplified luminescent proximity homogeneous assay linked immunosorbent assay (AlphaLISA). Following a comprehensive pipeline to confirm small molecule hits, we short-listed three distinct PPI inhibitors of BB0238-BB0323. One of these inhibitors, called lomibuvir (VX-222, VCH-222), displayed robust PPI inhibition inside B. burgdorferi cells and was shown to affect pathogen persistence in a tick-borne murine model of Lyme disease. Our study highlights targeted PPI disruption as a new therapeutic strategy against B. burgdorferi and may foster future antimicrobial discovery efforts to resolve clinical complications associated with Lyme disease.
KW - Lyme Disease/drug therapy
KW - Borrelia burgdorferi/metabolism
KW - Animals
KW - Mice
KW - Anti-Bacterial Agents/pharmacology
KW - Bacterial Proteins/metabolism
KW - Humans
KW - Crystallography, X-Ray
UR - https://www.scopus.com/pages/publications/105026525877
U2 - 10.1371/journal.ppat.1013805
DO - 10.1371/journal.ppat.1013805
M3 - Article
C2 - 41481600
SN - 1553-7366
VL - 22
SP - e1013805
JO - PLoS Pathogens
JF - PLoS Pathogens
IS - 1
ER -