Abstract

Aquatic nodulation on the tropical legume Sesbania rostrata occurs at lateral root bases via intercellular crack-entry invasion. A gene was identified (Srprx1) that is transiently up-regulated during the nodulation process and codes for a functional class III plant peroxidase. The expression strictly depended on bacterial nodulation factors (NFs) and could be modulated by hydrogen peroxide, a downstream signal for crack-entry invasion. Expression was not induced after wounding or pathogen attack, indicating that the peroxidase is a symbiosis-specific isoform. In situ hybridization showed Srprx1 transcripts around bacterial infection pockets and infection threads until they reached the central tissue of the nodule. A root nodule extensin (SrRNE1) colocalized with Srprx1 both in time and space and had the same NF requirement, suggesting a function in a similar process. Finally, in mixed inoculation nodules that were invaded by NF-deficient bacteria and differed in infection thread progression, infection-associated peroxidase transcripts were not observed. Lack of Srprx1 gene expression could be one of the causes for the aberrant structure of the infection threads.

Highlights

  • Aquatic nodulation on the tropical legume Sesbania rostrata occurs at lateral root bases via intercellular crack-entry invasion

  • A complex signal exchange between the macrosymbiont and the microsymbiont initiates the nodulation process: Upon perception of flavonoids exuded by host roots, rhizobia switch on their nodulation genes, forming lipochitooligosaccharide molecules, designated nodulation factors (NFs; D’Haeze and Holsters, 2002)

  • When S. rostrata roots are grown under aerated conditions, invasion switches from intercellular crack-entry or lateral root base (LRB) invasion to the intracellular root hair curling (RHC) mode (Goormachtig et al, 2004b)

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Summary

Introduction

Aquatic nodulation on the tropical legume Sesbania rostrata occurs at lateral root bases via intercellular crack-entry invasion. The expression strictly depended on bacterial nodulation factors (NFs) and could be modulated by hydrogen peroxide, a downstream signal for crack-entry invasion. In M. truncatula roots, recognition of compatible NFs rapidly stimulates localized production of superoxide. This response is absent in the non-nodulating plant mutant does not make infections (dmi1-1), which is impaired in the NF signal transduction pathway. Transcripts of a Rhizobium-induced peroxidase (Rip1) identified in M. truncatula (Cook et al, 1995) have a tissue-specific localization pattern similar to that of ROS and accumulate upon addition of exogenous H2O2 (Ramu et al, 2002)

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