TY - JOUR
T1 - New Insights into the Mechanism of Action of the Thienopyrimidine Antitubercular Prodrug TP053
AU - Chiarelli, Laurent R.
AU - Salina, Elena G.
AU - Mori, Giorgia
AU - Azhikina, Tatyana
AU - Riabova, Olga
AU - Lepioshkin, Alexander
AU - Grigorov, Artem
AU - Forbak, Martin
AU - Madacki, Jan
AU - Orena, Beatrice Silvia
AU - Manfredi, Marcello
AU - Gosetti, Fabio
AU - Buzzi, Arianna
AU - Degiacomi, Giulia
AU - Sammartino, José Camilla
AU - Marengo, Emilio
AU - Korduláková, Jana
AU - Riccardi, Giovanna
AU - Mikušová, Katarína
AU - Makarov, Vadim
AU - Pasca, Maria Rosalia
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2020/2/14
Y1 - 2020/2/14
N2 - The thienopyrimidine TP053 is an antitubercular prodrug active against both replicating and nonreplicating Mycobacterium tuberculosis (M. tuberculosis) cells, which requires activation by the mycothiol-dependent nitroreductase Mrx2. The investigation of the mechanism of action of TP053 revealed that Mrx2 releases nitric oxide from this drug both in the enzyme assays with purified Mrx2 and in mycobacterial cultures, which can explain its activity against nonreplicating bacilli, similar to pretomanid activated by the nitroreductase Ddn. In addition, we identified a highly reactive metabolite, 2-(4-mercapto-6-(methylamino)-2-phenylpyrimidin-5-yl)ethan-1-ol, which can contribute to the antimycobacterial effects on replicating cells as well as on nonreplicating cells. In summary, we explain the mechanism of action of TP053 on both replicating and nonreplicating M. tuberculosis and report a novel activity for Mrx2, which in addition to Ddn, represents another example of nitroreductase releasing nitric oxide from its substrate. These findings are particularly relevant in the context of drugs targeting nonreplicating M. tuberculosis, which is shown to be killed by increased levels of nitric oxide.
AB - The thienopyrimidine TP053 is an antitubercular prodrug active against both replicating and nonreplicating Mycobacterium tuberculosis (M. tuberculosis) cells, which requires activation by the mycothiol-dependent nitroreductase Mrx2. The investigation of the mechanism of action of TP053 revealed that Mrx2 releases nitric oxide from this drug both in the enzyme assays with purified Mrx2 and in mycobacterial cultures, which can explain its activity against nonreplicating bacilli, similar to pretomanid activated by the nitroreductase Ddn. In addition, we identified a highly reactive metabolite, 2-(4-mercapto-6-(methylamino)-2-phenylpyrimidin-5-yl)ethan-1-ol, which can contribute to the antimycobacterial effects on replicating cells as well as on nonreplicating cells. In summary, we explain the mechanism of action of TP053 on both replicating and nonreplicating M. tuberculosis and report a novel activity for Mrx2, which in addition to Ddn, represents another example of nitroreductase releasing nitric oxide from its substrate. These findings are particularly relevant in the context of drugs targeting nonreplicating M. tuberculosis, which is shown to be killed by increased levels of nitric oxide.
KW - Mycobacterium tuberculosis
KW - mechanism of action
KW - nitric oxide
KW - thienopyrimidine
KW - tuberculosis
UR - http://www.scopus.com/inward/record.url?scp=85076313212&partnerID=8YFLogxK
U2 - 10.1021/acsinfecdis.9b00388
DO - 10.1021/acsinfecdis.9b00388
M3 - Article
SN - 2373-8227
VL - 6
SP - 313
EP - 323
JO - ACS Infectious Diseases
JF - ACS Infectious Diseases
IS - 2
ER -