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Small-Molecule Inhibitors of the Type III Secretion System

Journal

MOLECULES
Volume 20, Issue 9, Pages 17659-17674

Publisher

MDPI AG
DOI: 10.3390/molecules200917659

Keywords

type III secretion system; pathogens; small-molecule inhibitors; effector proteins; Gram-negative bacteria; virulence; antibacterial agents

Funding

  1. National Science Foundation of China [21272029]
  2. 333 High-level Talent Training Program of Jiangsu Province of China
  3. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
  4. International Collaboration Program of Changzhou City [CZ20130024]

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Drug-resistant pathogens have presented increasing challenges to the discovery and development of new antibacterial agents. The type III secretion system (T3SS), existing in bacterial chromosomes or plasmids, is one of the most complicated protein secretion systems. T3SSs of animal and plant pathogens possess many highly conserved main structural components comprised of about 20 proteins. Many Gram-negative bacteria carry T3SS as a major virulence determinant, and using the T3SS, the bacteria secrete and inject effector proteins into target host cells, triggering disease symptoms. Therefore, T3SS has emerged as an attractive target for antimicrobial therapeutics. In recent years, many T3SS-targeting small-molecule inhibitors have been discovered; these inhibitors prevent the bacteria from injecting effector proteins and from causing pathophysiology in host cells. Targeting the virulence of Gram-negative pathogens, rather than their survival, is an innovative and promising approach that may greatly reduce selection pressures on pathogens to develop drug-resistant mutations. This article summarizes recent progress in the search for promising small-molecule T3SS inhibitors that target the secretion and translocation of bacterial effector proteins.

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