Abstract

Here we describe the first application of transient gene silencing in Saprolegnia parasitica, a pathogenic oomycete that infects a wide range of fish, amphibians, and crustaceans. A gene encoding a putative tyrosinase from S. parasitica, SpTyr, was selected to investigate the suitability of RNA-interference (RNAi) to functionally characterize genes of this economically important pathogen. Tyrosinase is a mono-oxygenase enzyme that catalyses the O-hydroxylation of monophenols and subsequent oxidation of O-diphenols to quinines. These enzymes are widely distributed in nature, and are involved in the melanin biosynthesis. Gene silencing was obtained by delivering in vitro synthesized SpTyr dsRNA into protoplasts. Expression analysis, tyrosinase activity measurements, and melanin content analysis confirmed silencing in individual lines. Silencing of SpTyr resulted in a decrease of tyrosinase activity between 38 % and 60 %, dependent on the level of SpTyr-expression achieved. The SpTyr-silenced lines displayed less pigmentation in developing sporangia and occasionally an altered morphology. Moreover, developing sporangia from individual silenced lines possessed a less electron dense cell wall when compared to control lines, treated with GFP-dsRNA. In conclusion, the tyrosinase gene of S. parasitica is required for melanin formation and transient gene silencing can be used to functionally characterize gene S in S. parasitica. (C) 2014 The British Mycological Society. Published by Elsevier Ltd. All rights reserved.

Keywords

Melanin; Cell wall; Gene expression; Transient transformation; Oomycete

Published in

Fungal Biology
2014, Volume: 118, number: 7, pages: 621-629

SLU Authors

• Grenville-Briggs Didymus, Laura

  • Royal Institute of Technology (KTH)
  • University of Aberdeen

UKÄ Subject classification

Microbiology
Genetics


Publication Identifiers

DOI: https://doi.org/10.1016/j.funbio.2014.01.011

Permanent link to this page (URI)

https://res.slu.se/id/publ/69016