A Pectate Lyase-Coding Gene Abundantly Expressed during Early Stages of Infection Is Required for Full Virulence in Alternaria brassicicola

PLoS One. 2015 May 21;10(5):e0127140. doi: 10.1371/journal.pone.0127140. eCollection 2015.

Abstract

Alternaria brassicicola causes black spot disease of Brassica species. The functional importance of pectin digestion enzymes and unidentified phytotoxins in fungal pathogenesis has been suspected but not verified in A. brassicicola. The fungal transcription factor AbPf2 is essential for pathogenicity and induces 106 genes during early pathogenesis, including the pectate lyase-coding gene, PL1332. The aim of this study was to test the importance and roles of PL1332 in pathogenesis. We generated deletion strains of the PL1332 gene, produced heterologous PL1332 proteins, and evaluated their association with virulence. Deletion strains of the PL1332 gene were approximately 30% less virulent than wild-type A. brassicicola, without showing differences in colony expansion on solid media and mycelial growth in nutrient-rich liquid media or minimal media with pectins as a major carbon source. Heterologous PL1332 expressed as fusion proteins digested polygalacturons in vitro. When the fusion proteins were injected into the apoplast between leaf veins of host plants the tissues turned dark brown and soft, resembling necrotic leaf tissue. The PL1332 gene was the first example identified as a general toxin-coding gene and virulence factor among the 106 genes regulated by the transcription factor, AbPf2. It was also the first gene to have its functions investigated among the 19 pectate lyase genes and several hundred putative cell-wall degrading enzymes in A. brassicicola. These results further support the importance of the AbPf2 gene as a key pathogenesis regulator and possible target for agrochemical development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternaria / genetics*
  • Alternaria / pathogenicity*
  • Brassica / microbiology
  • Enzyme Activation
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Fungal Proteins / genetics
  • Gene Deletion
  • Gene Expression Regulation, Fungal*
  • Necrosis / genetics
  • Phenotype
  • Plant Diseases / microbiology*
  • Polysaccharide-Lyases / genetics*
  • Virulence / genetics

Substances

  • Fungal Proteins
  • Polysaccharide-Lyases
  • pectate lyase

Grants and funding

This research was supported by the World Class Institute ((WCI) NRF-2009-002) program, global R&D center (GRDC) program (NRF-2010-0079), Bio & Medical Technology Development Program (NRF-2014M3A9B5073938), and KRIBB Research Initiative Program funded by the Ministry of Science, ICT and Future Planning (MSIP), Republic of Korea. The research was also supported by grants from the Chuncheongbuk-do and the KRIBB Research Initiative Program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.