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Lusutrombopag as a Repurposing Drug in Combination with Aminoglycosides against Vancomycin-Resistant Enterococcus.
She, Pengfei; Li, Linhui; Yang, Yifan; Zhou, Linying; Huang, Guanqing; Xiao, Dan; Wu, Yong.
Affiliation
  • She P; Department of Laboratory Medicine, The Third Xiangya Hospital of Central South University, Changsha 410013, China.
  • Li L; Department of Laboratory Medicine, The Third Xiangya Hospital of Central South University, Changsha 410013, China.
  • Yang Y; Department of Laboratory Medicine, The Third Xiangya Hospital of Central South University, Changsha 410013, China.
  • Zhou L; Department of Laboratory Medicine, The Affiliated Changsha Hospital of Xiangya School of Medicine (The First Hospital of Changsha), Central South University, Changsha 410005, China.
  • Huang G; Department of Laboratory Medicine, The Affiliated Changsha Hospital of Xiangya School of Medicine (The First Hospital of Changsha), Central South University, Changsha 410005, China.
  • Xiao D; Department of Laboratory Medicine, The Affiliated Changsha Hospital of Xiangya School of Medicine (The First Hospital of Changsha), Central South University, Changsha 410005, China.
  • Wu Y; Department of Laboratory Medicine, The Affiliated Changsha Hospital of Xiangya School of Medicine (The First Hospital of Changsha), Central South University, Changsha 410005, China.
ACS Infect Dis ; 10(4): 1327-1338, 2024 04 12.
Article in En | MEDLINE | ID: mdl-38567846
ABSTRACT
Due to the widespread abuse of antibiotics, drug resistance in Enterococcus has been increasing. However, the speed of antibiotic discovery cannot keep pace with the acquisition of bacterial resistance. Thus, drug repurposing is a proposed strategy to solve the crises. Lusutrombopag (LP) has been approved as a thrombopoietin receptor agonist by the Food and Drug Administration. This study demonstrated that LP exhibited significant antimicrobial activities against vancomycin-resistant Enterococcus in vitro with rare resistance occurrence. Further, LP combined with tobramycin exhibited synergistic antimicrobial effects in vitro and in vivo against Enterococcus. No in vitro or in vivo detectable toxicity was observed when using LP. Mechanism studies indicated that the disrupted proton motive force may account for LP's antimicrobial activity. In summary, these results demonstrate that LP has the previously undocumented potential to serve as an antibacterial agent against refractory infections caused by Enterococcus.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thiazoles / Cinnamates / Vancomycin-Resistant Enterococci / Aminoglycosides Country/Region as subject: America do norte Language: En Journal: ACS Infect Dis Year: 2024 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thiazoles / Cinnamates / Vancomycin-Resistant Enterococci / Aminoglycosides Country/Region as subject: America do norte Language: En Journal: ACS Infect Dis Year: 2024 Document type: Article Affiliation country: China Country of publication: United States