VapD in Xylella fastidiosa Is a Thermostable Protein with Ribonuclease Activity

PLoS One. 2015 Dec 22;10(12):e0145765. doi: 10.1371/journal.pone.0145765. eCollection 2015.

Abstract

Xylella fastidiosa strain 9a5c is a gram-negative phytopathogen that is the causal agent of citrus variegated chlorosis (CVC), a disease that is responsible for economic losses in Brazilian agriculture. The most well-known mechanism of pathogenicity for this bacterial pathogen is xylem vessel occlusion, which results from bacterial movement and the formation of biofilms. The molecular mechanisms underlying the virulence caused by biofilm formation are unknown. Here, we provide evidence showing that virulence-associated protein D in X. fastidiosa (Xf-VapD) is a thermostable protein with ribonuclease activity. Moreover, protein expression analyses in two X. fastidiosa strains, including virulent (Xf9a5c) and nonpathogenic (XfJ1a12) strains, showed that Xf-VapD was expressed during all phases of development in both strains and that increased expression was observed in Xf9a5c during biofilm growth. This study is an important step toward characterizing and improving our understanding of the biological significance of Xf-VapD and its potential functions in the CVC pathosystem.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics
  • Enzyme Stability
  • Hot Temperature*
  • Membrane Glycoproteins / chemistry*
  • Membrane Glycoproteins / genetics
  • Ribonucleases / chemistry*
  • Ribonucleases / genetics
  • Xylella / enzymology*
  • Xylella / genetics
  • Xylella / pathogenicity

Substances

  • Bacterial Proteins
  • Membrane Glycoproteins
  • VapD protein, Bacteria
  • Ribonucleases

Grants and funding

The authors gratefully acknowledge the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP, Process 2012/51580-4 and 2001/07533-7) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES, Computational Biology Program). JSM received a Ph.D. fellowship from CAPES, ASS was partially supported by a Ph.D. fellowship from FAPESP (Process 2011/50268-4) and CAPES (Computational Biology Program); CAS is the recipient of a post-doctoral fellowship from the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). APS and AAS are the recipients of a research fellowship from CNPq.