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Abstract

The asexual multinucleated sporangia of Phytophthora infestans can germinate directly through a germ tube or indirectly by releasing zoospores. The molecular mechanisms controlling sporangial cytokinesis or sporangial cleavage, and zoospore release are largely unknown. Sporangial cleavage is initiated by a cold shock that eventually compartmentalizes single nuclei within each zoospore. Comparison of EST representation in different cDNA libraries revealed a putative ATP-dependent DEAD-box RNA-helicase gene in P. infestans, Pi-RNH1, which has a 140-fold increased expression level in young zoospores compared to uncleaved sporangia. RNA interference was employed to determine the role of Pi-RNH1 in zoospore development. Silencing efficiencies of up to 99% were achieved in some transiently-silenced lines. These Pi-RNH1-silenced lines produced large aberrant zoospores that had undergone partial cleavage and often had multiple flagella on their surface. Transmission electron microscopy revealed that cytoplasmic vesicles fused in the silenced lines, resulting in the formation of large vesicles. The Pi-RNH1-silenced zoospores were also sensitive to osmotic pressure and often ruptured upon release from the sporangia. These findings indicate that Pi-RNH1 has a major function in zoospore development and its potential role in cytokinesis is discussed. (c) 2008 Elsevier Inc. All rights reserved.

Keywords

Phytophthora infestans; oomycete; RNA-helicase; zoospore; pathogen; development

Published in

Fungal Genetics and Biology
2008, volume: 45, number: 6, pages: 954-962
Publisher: ACADEMIC PRESS INC ELSEVIER SCIENCE

SLU Authors

UKÄ Subject classification

Microbiology

Publication identifier

  • DOI: https://doi.org/10.1016/j.fgb.2008.03.004

Permanent link to this page (URI)

https://res.slu.se/id/publ/52521