Chitinolytic microbes confer Meloidogyne incognita resistance and augment secondary metabolites in Bacopa monnieri (L.) Pennell

Abstract The secondary metabolites, 3,5-dihydroxy-4-isopropylstilbene (ST) and indole, from the culture filtrate of Photorhabdus luminescens MD, were shown to have nematicidal properties. ST caused nearly 100% mortality of J4 and adults of Aphelenchoides rhytium , Bursaphelenchus spp. and Caenorhabditis elegans at 100 mu g/ml, but had no effect on J2 of Meloidogyne incognita or infective juveniles (IJ) of Heterorhabditis megidis at 200 mu g/ml. Indole was lethal to several nematode species at 300 mu g/ml, and caused a high percentage of Bursaphelenchus spp. (J4 and adults), M. incognita (J2) and Heterorhabditis spp. (IJ) to be paralysed at 300, 100 and 400 mu g/ml, respectively. Both ST and indole inhibited egg hatch of M. incognita . ST repelled IJ of some Steinernema spp. but not IJ of Heterorhabditis spp., and indole repelled IJ of some species of both Steinernema and Heterorhabditis . ST, but not indole, was produced in nematode-infected larval Galleria mellonella after 24 h infection. Von Photorhabdus luminescens (Enterobacteriaceae), einem Symbionten entomopathogener Nematoden gebildete nematizide Metaboliten - Es wurde gezeigt, dass die Sekundarmetaboliten 3,5-Dihydroxy-4-isopropylstilben (ST) und Indol aus dem Kulturfiltrat von Photorhabdus luminescens MD nematizide Eigenschaften besassen. In einer Konzentration von 100 mu g/ml verursachte ST eine fast 100%ige Sterblichkeit bei J4 und Adulten von Aphelenchoides rhytium , Bursaphelenchus spp. und Caenorhabditis elegans , hatte aber bei 200 mu g/ml keine Wirkung auf J2 von Meloidogyne incognita oder auf Infektionsjuvenile (IJ) von Heterorhabditis megidis . Bei 300 mu g/ml war Indol fur etliche Nematodenarten todlich und fuhrte dazu, dass Bursaphelenchus spp. (J4 and Adulte) bei 300, M. incognita (J2) bei 100, und Heterorhabditis spp. (IJ) bei 400 mu g/ml zu einem grossen Teil gelahmt wurden. ST und Indol behinderten beide das Schlupfen von M. incognita . ST wirkte abstossend auf IJ einiger Steinernema -Arten aber nicht auf IJ von Heterorhabditis spp., und Indol wirkte abstossend auf IJ einiger Arten der beiden Gattungen Steinernema und Heterorhabditis . ST wurde in nematoden-befallenen Larven von Galleria mellonella 24 h nach der Infektion gebildet, Indol dagegen nicht.

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Effects associated with insertion of cryptogein gene utilizing Ri and Ti plasmids on morphology and secondary metabolites are stable in Bacopa monnieri-transformed plants grown in vitro and ex vitro

Plant Biotechnology Reports ◽

10.1007/s11816-015-0360-9 ◽

2015 ◽

Vol 9 (4) ◽

pp. 231-245 ◽

Cited By ~ 12

Author(s):

Pijush Paul ◽

Sayantika Sarkar ◽

Sumita Jha

Keyword(s):

Secondary Metabolites ◽

Bacopa Monnieri ◽

Ex Vitro ◽

Transformed Plants ◽

Ti Plasmids ◽

Cryptogein Gene

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Intergrated Metagenomics and Metabolomics Analysis Discovers Nematicidal Microbes, Enzymes and Metabolites From the Plant Rhizosphere Microbiota

10.21203/rs.3.rs-187899/v1 ◽

2021 ◽

Author(s):

Xiuyun Zhao ◽

Changchun Lin ◽

Wenfang Yuan ◽

Song Ruan ◽

Gaofu Qi

Keyword(s):

Secondary Metabolites ◽

Meloidogyne Incognita ◽

Crop Production ◽

Root Systems ◽

Rhizosphere Soils ◽

Microbial Network ◽

Infected Tobacco ◽

Culture Dependent ◽

Metabolomics Analysis ◽

Volatile Materials

Abstract BackgroundRoot-knot nematode Meloidogyne incognita infects root systems of many crops resulting in huge decrease of crop production. Nematicidal microorganisms provides a safe and effective strategy to control M. incognita infection. In order to find more microorganisms with high activity and new nematicidal metabolites, we collected the M. incognita infected tobacco rhizosphere soils (RNI) and non-infected tobacco rhizosphere soils (NS), and investigated their microbial community and network via metagenomics and metabolomics analysis. ResultsMicrobial networks of RNI soils were very different from the NS soils. Many nematicidal microorganisms were enriched in the NS soils, including some isolates such as Aspergillus , Achromobacter , Acinetobacter , Bacillus , Burkholderia , Comamonas , Enterobacter , Lysobacter , Microbacterium , Paenibacillus , Pantoea , Pseudomonas , Streptomyces and Variovorax. Enzymes analysis showed these nematicidal microorganisms can produce proteases, chitinase and lipases. The functions genes belonging to pathways of secondary metabolites biosynthesis and carbohydrate transport and metabolism were overrepresented in the rhizophere microbiota of NS soils comparing with the RNI soils. 102 metabolites contents were significantly different between the RNI and NS rhizosphere microbiota. 35 metabolites were overrepresented in the NS soils comparing the RNI samples, including acetophenone. Acetophenone showed high nematicidal (LC 50 = 0.66 μg/ml) and avoidance activity against M. incognita . A isolate of Bacillus amyloliquefaciens W1 with production of acetophenone can kill 98.8% of M . incognita . ConclusionsIn general, the rhizophere microbiota of NS soils could produce volatile materials, multiple enzymes and secondary metabolites against nematode. Collectively, the microbiota of NS and RNI rhizophere differed significantly in microbial network structure, community composition, function genes and metabolites. Collectively, combination of multi-omics analysis and culture-dependent technology is powerful for finding nematicidal microorganisms and metabolites from soil.

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