4.7 Article

Arsenic accumulation in Pteris vittata: Time course, distribution, and arsenic-related gene expression in fronds and whole plantlets

Journal

ENVIRONMENTAL POLLUTION
Volume 309, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2022.119773

Keywords

Arsenic; Pteris vittata; Phytoextraction; As-related genes; As distribution; ?-XRF

Funding

  1. Regione Lazio, Italy [POR FESR 2014-2020-85-2017 FONDI LISPA 15067 CUP B56C18000870002]

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This study investigated the accumulation and distribution of arsenic (As) in young fronds of Pteris vittata using mu-XRF technique. It was found that the As content in young fronds increased linearly up to 60 days and gradually distributed from the apex to the base of the fronds. In whole plantlets, As was detectable in the apex of a few fronds and fiddleheads from 9 to 20 days, and later localized in all fronds, the rhizome, and the basal part of the roots. The study also revealed the correlation between As content and the expression of As-related genes.
In this work, arsenic (As) accumulation and distribution over time in Pteris vittata young fronds from adult plants and in whole plantlets, grown on a highly contaminated As-soil, was determined by mu-XRF. A linear increase in As content up to 60 days was found in young fronds at different times, and a progressive distribution from the apex to the base of the fronds was observed. In whole plantlets, As signal was detectable from 9 to 20 days in the apex of a few fronds and fiddleheads. Later, up to 60 days, As was localized in all fronds, in the rhizome and in basal part of the roots. The dynamics of expression of As-related genes revealed a good correlation between As content and the level of the As (III)-antiporter PvACR3 transcript in plantlets roots and fronds and in young fronds. Moreover, the transcription of As (V)-related gametophytic genes PvGAPC1, PvOCT4 increases over time during As accumulation while PvGSTF1 is expressed only in roots. Here, we demonstrate the suitability of the mu-XRF technique to monitor As accumulation, which allowed us to propose that As is initially directly transported to fiddleheads and apex of fronds, is later distributed to the whole fronds and simultaneously accumulated in the rhizome and roots. We also provide indications on the expression of candidate genes possibly involved in As (hyper)accumulation.

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