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| 70. |  | BATISTA, A. C.; OLIVEIRA, E. C. A.; MENDES, R. A. Germinação de sementes de Catasetum sp. (Orchidaceae) em meio líquido e sólido, com e sem agitação. In: ENCONTRO DO TALENTO ESTUDANTIL DA EMBRAPA RECURSOS GENÉTICOS E BIOTECNOLOGIA, 5., 2000, Brasília, DF. Anais: resumos dos trabalhos. Brasília, DF: Embrapa Recursos Genéticos e Biotecnologia, 2000. p. 64.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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Registro Completo
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Biblioteca(s): |
Embrapa Meio Ambiente. |
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Data corrente: |
15/03/2024 |
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Data da última atualização: |
15/03/2024 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
NISHISAKA, C. S.; VENTURA, J. P.; BAIS, H.; MENDES, R. |
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Afiliação: |
CAROLINE S. NISHISAKA, BOLSISTA EMBRAPA MEIO AMBIENTE; JOÃO PAULO VENTURA, BOLSISTA EMBRAPA MEIO AMBIENTE; HARSH BAIS, UNIVERSITY OF DELAWARE, NEWARK; RODRIGO MENDES, CNPMA. |
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Título: |
Impact of Bacillus subtilis eps and TasA genes defective on rhizosphere microbiome assembly of tomato. |
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Ano de publicação: |
2023 |
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Fonte/Imprenta: |
In: PLANT MICROBIOME SYMPOSIUM, 4., 2023, Quito. Abstracts... Quito, Equador: Universidad San Francisco de Quito, 2023. Ref. 3-C. |
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Páginas: |
1 p. |
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Idioma: |
Português |
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Conteúdo: |
Bacillus subtilis holds significant agricultural and ecological importance as one of the most extensively studied plant growth promoters. To better understand Bacillus genetic traits associated with plant fitness, we used a mutant gene-defective model to analyze itsimpact on tomato development and on rhizosphere microbiome under a gradient of soil microbial diversity. We used B. subtilis strain UD1022 and its mutant (UD1022eps-TasA- ) defective for biofilm formation. Control treatments and plants inoculated with wild or mutant Bacillus strains were used in the bioassay. Soil DNA isolation was followed by qPCR targeting B. subtilis gyrB gene, and 16S rRNA and ITS amplicon sequencing. Data analysis included comparisons of plant growth performance, gyrB quantification, and amplicon sequence variants processing using Dada2 pipeline, followed by exploratory, permutational variance, and covariance analysis. UD1022 strain significantly increased shoot and root dry masses when tomato was grown in soils with lower microbial diversity. UD1022 inoculation significantly changed soil bacterial and fungal communities’assembly in low microbial diverse soil (autoclaved soil), compared to UD1022epsTasAand control in the same soil. On the other hand, in high microbial diversity (natural soil) the rhizosphere microbiome is less affected by the inoculants. Bacterial network analysis showed that the UD1022 inoculation also impacted the relationship among bacteria phyla, by increasing the network’s modularity and number of nodes, compared to control and UD1022eps-TasA- treatments. For fungal network, the UD1022eps-TasAinoculation caused higher changes on network’s modularity, number of nodes and edges, compared to control and UD1022 treatments. In conclusion, knocking down genes associated with biofilm formation in Bacillus, impacts not only the ability of plant colonization, but also the assembly of the rhizosphere microbiome during plant development. MenosBacillus subtilis holds significant agricultural and ecological importance as one of the most extensively studied plant growth promoters. To better understand Bacillus genetic traits associated with plant fitness, we used a mutant gene-defective model to analyze itsimpact on tomato development and on rhizosphere microbiome under a gradient of soil microbial diversity. We used B. subtilis strain UD1022 and its mutant (UD1022eps-TasA- ) defective for biofilm formation. Control treatments and plants inoculated with wild or mutant Bacillus strains were used in the bioassay. Soil DNA isolation was followed by qPCR targeting B. subtilis gyrB gene, and 16S rRNA and ITS amplicon sequencing. Data analysis included comparisons of plant growth performance, gyrB quantification, and amplicon sequence variants processing using Dada2 pipeline, followed by exploratory, permutational variance, and covariance analysis. UD1022 strain significantly increased shoot and root dry masses when tomato was grown in soils with lower microbial diversity. UD1022 inoculation significantly changed soil bacterial and fungal communities’assembly in low microbial diverse soil (autoclaved soil), compared to UD1022epsTasAand control in the same soil. On the other hand, in high microbial diversity (natural soil) the rhizosphere microbiome is less affected by the inoculants. Bacterial network analysis showed that the UD1022 inoculation also impacted the relationship among bacteria phyla, by increasing the network... Mostrar Tudo |
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Palavras-Chave: |
eps; PGPR; Rhizosphere microbiome; Soil diversity. |
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Thesagro: |
Tomate. |
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Thesaurus NAL: |
Bacillus subtilis; Mutants. |
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Categoria do assunto: |
G Melhoramento Genético |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1162857/1/RA-MendesR-4thPlantMicrobiomeSymposium-2023-Ref3-C.pdf
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Marc: |
LEADER 02732nam a2200241 a 4500
001 2162857
005 2024-03-15
008 2023 bl uuuu u00u1 u #d
100 1 $aNISHISAKA, C. S.
245 $aImpact of Bacillus subtilis eps and TasA genes defective on rhizosphere microbiome assembly of tomato.$h[electronic resource]
260 $aIn: PLANT MICROBIOME SYMPOSIUM, 4., 2023, Quito. Abstracts... Quito, Equador: Universidad San Francisco de Quito, 2023. Ref. 3-C.$c2023
300 $a1 p.
520 $aBacillus subtilis holds significant agricultural and ecological importance as one of the most extensively studied plant growth promoters. To better understand Bacillus genetic traits associated with plant fitness, we used a mutant gene-defective model to analyze itsimpact on tomato development and on rhizosphere microbiome under a gradient of soil microbial diversity. We used B. subtilis strain UD1022 and its mutant (UD1022eps-TasA- ) defective for biofilm formation. Control treatments and plants inoculated with wild or mutant Bacillus strains were used in the bioassay. Soil DNA isolation was followed by qPCR targeting B. subtilis gyrB gene, and 16S rRNA and ITS amplicon sequencing. Data analysis included comparisons of plant growth performance, gyrB quantification, and amplicon sequence variants processing using Dada2 pipeline, followed by exploratory, permutational variance, and covariance analysis. UD1022 strain significantly increased shoot and root dry masses when tomato was grown in soils with lower microbial diversity. UD1022 inoculation significantly changed soil bacterial and fungal communities’assembly in low microbial diverse soil (autoclaved soil), compared to UD1022epsTasAand control in the same soil. On the other hand, in high microbial diversity (natural soil) the rhizosphere microbiome is less affected by the inoculants. Bacterial network analysis showed that the UD1022 inoculation also impacted the relationship among bacteria phyla, by increasing the network’s modularity and number of nodes, compared to control and UD1022eps-TasA- treatments. For fungal network, the UD1022eps-TasAinoculation caused higher changes on network’s modularity, number of nodes and edges, compared to control and UD1022 treatments. In conclusion, knocking down genes associated with biofilm formation in Bacillus, impacts not only the ability of plant colonization, but also the assembly of the rhizosphere microbiome during plant development.
650 $aBacillus subtilis
650 $aMutants
650 $aTomate
653 $aeps
653 $aPGPR
653 $aRhizosphere microbiome
653 $aSoil diversity
700 1 $aVENTURA, J. P.
700 1 $aBAIS, H.
700 1 $aMENDES, R.
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Embrapa Meio Ambiente (CNPMA) |
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