Comparative proteomic analysis reveals drug resistance of Staphylococcus xylosus ATCC700404 under tylosin stress

BMC Vet Res. 2019 Jul 2;15(1):224. doi: 10.1186/s12917-019-1959-9.

Abstract

Background: As a kind of opportunist pathogen, Staphylococcus xylosus (S. xylosus) can cause mastitis. Antibiotics are widely used for treating infected animals and tylosin is a member of such group. Thus, the continuous use of antibiotics in dairy livestock enterprise will go a long way in increasing tylosin resistance. However, the mechanism of tylosin-resistant S. xylosus is not clear. Here, isobaric tag for relative and absolute quantitation (iTRAQ)-based quantitative proteomics methods was used to find resistance-related proteins.

Results: We compared the differential expression of S. xylosus in response to tylosin stress by iTRAQ. A total of 155 proteins (59 up-regulated, 96 down-regulated) with the fold-change of >1.2 or <0.8 (p value ≤0.05) were observed between the S. xylosus treated with 1/2 MIC (0.25 μg/mL) tylosin and the untreated S. xylosus. Bioinformatic analysis revealed that these proteins play important roles in stress-response and transcription. Then, in order to verify the relationship between the above changed proteins and mechanism of tylosin-resistant S. xylosus, we induced the tylosin-resistant S. xylosus, and performed quantitative PCR analysis to verify the changes in the transcription proteins and the stress-response proteins in tylosin-resistant S. xylosus at the mRNA level. The data displayed that ribosomal protein L23 (rplw), thioredoxin(trxA) and Aldehyde dehydrogenase A(aldA-1) are up-regulated in the tylosin-resistant S. xylosus, compared with the tylosin-sensitive strains.

Conclusion: Our findings demonstrate the important of stress-response and transcription in the tylosin resistance of S. xylosus and provide an insight into the prevention of this resistance, which would aid in finding new medicines .

Keywords: Aldehyde dehydrogenase a;; Drug-resistance; Ribosomal protein L23; Staphylococcus xylosus; Thioredoxin; Tylosin; iTRAQ.

Publication types

  • Comparative Study

MeSH terms

  • Aldehyde Dehydrogenase / genetics
  • Aldehyde Dehydrogenase / metabolism
  • Anti-Bacterial Agents / pharmacology
  • Bacterial Proteins / isolation & purification
  • Bacterial Proteins / metabolism*
  • Drug Resistance, Bacterial / drug effects*
  • Drug Resistance, Bacterial / genetics
  • Gene Expression Regulation, Bacterial / drug effects
  • Microbial Sensitivity Tests
  • Proteome / analysis*
  • Proteomics / methods
  • Ribosomal Proteins / genetics
  • Ribosomal Proteins / metabolism
  • Staphylococcus / drug effects*
  • Staphylococcus / genetics
  • Staphylococcus / metabolism
  • Thioredoxins / genetics
  • Thioredoxins / metabolism
  • Tylosin / pharmacology*

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Proteome
  • Ribosomal Proteins
  • Thioredoxins
  • Aldehyde Dehydrogenase
  • Tylosin