Polymorphism of the cysteine protease YopT from Yersinia pestis

Mikhail E. Platonov, Tat'yana E. Svetoch, Vera V. Evseeva, Anastasiya I. Knyazeva, Svetlana V. Dentovskaya, Vladimir L. Motin, Vladimir N. Uversky, Andrey P. Anisimov

Research output: Contribution to journalArticlepeer-review


Antibiotic therapy of plague is hampered by the recent isolation of Yersinia pestis strain Andrey P. Anisimov resistant to all of antibiotics recommended for cure. This has constrained a quest for new antimicrobials taking aim at alternative targets. Recently Y. pestis cysteine protease YopT has been explored as a potential drug target. Targets conserved in the pathogen populations should be more efficacious; therefore, we evaluated intraspecies variability in yopT genes and their products. 114 Y. pestis isolates were screened. Only two YopT full-size isoforms were found among them. The endemic allele (N149) was present in biovar caucasica from Dagestan-highland natural plague focus # 39. The biovar caucasica strains from Transcaucasian-highland (# 4-6) and Pre-Araks (# 7) plague foci also contained the N149 allele. These strains from foci # 4-7 possessed truncated versions of YopT that were a consequence of a frame-shift due to the deletion of a single nucleotide at position 71 bp. Computational analyses showed that although the SNP at the position 149 has a very minimal effect of the intrinsic disorder propensity of YopT proteins, the N-terminal truncations of the YopT detected in bv. caucasica strains Pestoides F, and Pestoides G generated isoforms with the significantly modified intrinsic disorder propensities and with reduced capability to interact with lost ability to utilize their N-terminal tail for the disorder-based interactions with biological partners. Considering that representatives of biovar caucasica were reported to be the reason of sporadic cases of human plague, this study supports the necessity of additional testing of globally disseminated YopT (S149) isoform as a potential target for treatment of plague caused by the strains producing different YopT isoforms.

Original languageEnglish (US)
Pages (from-to)379-385
Number of pages7
JournalProtein and Peptide Letters
Issue number4
StatePublished - Feb 1 2016


  • Drug target
  • Intrinsic disorder
  • Pathogen variability
  • Plague
  • Type 3 secretion system
  • YopT

ASJC Scopus subject areas

  • Structural Biology
  • Biochemistry


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