A C-type lectin from Bothrops jararacussu venom disrupts Staphylococcal biofilms

PLoS One. 2015 Mar 26;10(3):e0120514. doi: 10.1371/journal.pone.0120514. eCollection 2015.

Abstract

Bovine mastitis is a major threat to animal health and the dairy industry. Staphylococcus aureus is a contagious pathogen that is usually associated with persistent intramammary infections, and biofilm formation is a relevant aspect of the outcome of these infections. Several biological activities have been described for snake venoms, which led us to screen secretions of Bothrops jararacussu for antibiofilm activity against S. aureus NRS155. Crude venom was fractionated by size-exclusion chromatography, and the fractions were tested against S. aureus. Biofilm growth, but not bacterial growth, was affected by several fractions. Two fractions (15 and 16) showed the best activities and were also assayed against S. epidermidis NRS101. Fraction 15 was identified by TripleTOF mass spectrometry as a galactose-binding C-type lectin with a molecular weight of 15 kDa. The lectin was purified from the crude venom by D-galactose affinity chromatography, and only one peak was observed. This pure lectin was able to inhibit 75% and 80% of S. aureus and S. epidermidis biofilms, respectively, without affecting bacterial cell viability. The lectin also exhibited a dose-dependent inhibitory effect on both bacterial biofilms. The antibiofilm activity was confirmed using scanning electron microscopy. A pre-formed S. epidermidis biofilm was significantly disrupted by the C-type lectin in a time-dependent manner. Additionally, the lectin demonstrated the ability to inhibit biofilm formation by several mastitis pathogens, including different field strains of S. aureus, S. hyicus, S. chromogenes, Streptococcus agalactiae, and Escherichia coli. These findings reveal a new activity for C-type lectins. Studies are underway to evaluate the biological activity of these lectins in a mouse mastitis model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biofilms*
  • Bothrops*
  • Dose-Response Relationship, Drug
  • Lectins, C-Type* / chemistry
  • Mass Spectrometry
  • Snake Venoms / chemistry*
  • Staphylococcus / drug effects*
  • Staphylococcus / physiology*
  • Staphylococcus / ultrastructure
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / physiology
  • Staphylococcus epidermidis / drug effects
  • Staphylococcus epidermidis / physiology

Substances

  • Lectins, C-Type
  • Snake Venoms

Grants and funding

AOBR was supported by Fundação de Amparo a Pesquisa do Estado de Minas Gerais (Fapemig)CBB-APQ-01054-10. http://www.fapemig.br/. FM was supported by Natural Sciences and Engineering Research Council of Canada. Grant 89758-2010. http://www.nserc-crsng.gc.ca/. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.