DNA stable isotope probing on soil treated by plant biostimulation and flooding revealed the bacterial communities involved in PCB degradation
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
Decreto ERSAF n. III/5426 del 09.12.2013
Ente Regionale per i Servizi all'Agricoltura e alle Foreste (ERSAF)
LTAUSA19013
INTER-EXCELLENCE program of the Ministry of Education, Youth and Sports of the Czech Republic
841317
UE Horizon 2020 Marie Sklodowska-Curie
PubMed
36357494
PubMed Central
PMC9649793
DOI
10.1038/s41598-022-23728-2
PII: 10.1038/s41598-022-23728-2
Knihovny.cz E-zdroje
- MeSH
- Actinomycetales * genetika MeSH
- Bacteria MeSH
- biodegradace MeSH
- DNA bakterií genetika metabolismus MeSH
- DNA metabolismus MeSH
- ekosystém MeSH
- izotopy metabolismus MeSH
- látky znečišťující půdu * metabolismus MeSH
- polychlorované bifenyly * metabolismus MeSH
- půda chemie MeSH
- půdní mikrobiologie MeSH
- RNA ribozomální 16S genetika metabolismus MeSH
- rostliny metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA bakterií MeSH
- DNA MeSH
- izotopy MeSH
- látky znečišťující půdu * MeSH
- polychlorované bifenyly * MeSH
- půda MeSH
- RNA ribozomální 16S MeSH
Polychlorinated biphenyl (PCB)-contaminated soils represent a major treat for ecosystems health. Plant biostimulation of autochthonous microbial PCB degraders is a way to restore polluted sites where traditional remediation techniques are not sustainable, though its success requires the understanding of site-specific plant-microbe interactions. In an historical PCB contaminated soil, we applied DNA stable isotope probing (SIP) using 13C-labeled 4-chlorobiphenyl (4-CB) and 16S rRNA MiSeq amplicon sequencing to determine how the structure of total and PCB-degrading bacterial populations were affected by different treatments: biostimulation with Phalaris arundinacea subjected (PhalRed) or not (Phal) to a redox cycle and the non-planted controls (Bulk and BulkRed). Phal soils hosted the most diverse community and plant biostimulation induced an enrichment of Actinobacteria. Mineralization of 4-CB in SIP microcosms varied between 10% in Bulk and 39% in PhalRed soil. The most abundant taxa deriving carbon from PCB were Betaproteobacteria and Actinobacteria. Comamonadaceae was the family most represented in Phal soils, Rhodocyclaceae and Nocardiaceae in non-planted soils. Planted soils subjected to redox cycle enriched PCB degraders affiliated to Pseudonocardiaceae, Micromonosporaceae and Nocardioidaceae. Overall, we demonstrated different responses of soil bacterial taxa to specific rhizoremediation treatments and we provided new insights into the populations active in PCB biodegradation.
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