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1.
Front Immunol ; 12: 673692, 2021.
Article in English | MEDLINE | ID: mdl-34305903

ABSTRACT

In a perspective entitled 'From plant survival under severe stress to anti-viral human defense' we raised and justified the hypothesis that transcript level profiles of justified target genes established from in vitro somatic embryogenesis (SE) induction in plants as a reference compared to virus-induced profiles can identify differential virus signatures that link to harmful reprogramming. A standard profile of selected genes named 'ReprogVirus' was proposed for in vitro-scanning of early virus-induced reprogramming in critical primary infected cells/tissues as target trait. For data collection, the 'ReprogVirus platform' was initiated. This initiative aims to identify in a common effort across scientific boundaries critical virus footprints from diverse virus origins and variants as a basis for anti-viral strategy design. This approach is open for validation and extension. In the present study, we initiated validation by experimental transcriptome data available in public domain combined with advancing plant wet lab research. We compared plant-adapted transcriptomes according to 'RegroVirus' complemented by alternative oxidase (AOX) genes during de novo programming under SE-inducing conditions with in vitro corona virus-induced transcriptome profiles. This approach enabled identifying a major complex trait for early de novo programming during SARS-CoV-2 infection, called 'CoV-MAC-TED'. It consists of unbalanced ROS/RNS levels, which are connected to increased aerobic fermentation that links to alpha-tubulin-based cell restructuration and progression of cell cycle. We conclude that anti-viral/anti-SARS-CoV-2 strategies need to rigorously target 'CoV-MAC-TED' in primary infected nose and mouth cells through prophylactic and very early therapeutic strategies. We also discuss potential strategies in the view of the beneficial role of AOX for resilient behavior in plants. Furthermore, following the general observation that ROS/RNS equilibration/redox homeostasis is of utmost importance at the very beginning of viral infection, we highlight that 'de-stressing' disease and social handling should be seen as essential part of anti-viral/anti-SARS-CoV-2 strategies.


Subject(s)
Cellular Reprogramming/genetics , Multifactorial Inheritance/genetics , SARS-CoV-2/pathogenicity , Acetylserotonin O-Methyltransferase/genetics , Arabidopsis/genetics , Arabidopsis/growth & development , Cell Cycle/genetics , Databases, Genetic , Daucus carota/genetics , Daucus carota/growth & development , Fermentation , Gene Expression Profiling , Humans , Mitochondrial Proteins/genetics , Mitochondrial Proteins/metabolism , Oxidoreductases/genetics , Oxidoreductases/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Reactive Nitrogen Species/metabolism , Reactive Oxygen Species/metabolism , Tubulin/genetics , Viruses/pathogenicity
2.
Braz J Microbiol ; 50(3): 593-601, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31250404

ABSTRACT

Arbuscular mycorrhizal (AM) fungi show high promiscuity in terms of host. Effector proteins expressed by AM fungi are found important in establishing interaction with host. However, the mechanistic underlying host-specific interactions of the fungi remain unknown. The present study aimed (i) to identify effectors encoded by Rhizophagus proliferus and (ii) to understand molecular specificity encoded in effectors for interaction with specific plant species. The effectors predicted from the whole genome sequence were annotated by homology search in NCBI non-redundant protein, Interproscan, and pathogen-host interaction (PHI) databases. In total, 416 small secreted peptides (SSPs) were predicted, which were effector peptides with presence of nuclear localization signal, small cysteine-rich, and repeat-containing proteins domains. Similar to the functionally validated SP7 effectors in Rhizophagus irregularis, two proteins (RP8598 and RP23081) were identified in R. proliferus. To understand whether interaction between SP7 and the plant target protein, ERF19, is specific in nature, we examined protein-peptide interaction using in silico molecular docking. Pairwise interaction of RP8598 and RP23081 with the ethylene-responsive factors (ERF19) coded by five different plant species (Lotus japonicus, Solanum lycopersicum, Ocimum tenuiflorum, Medicago truncatula, Diospyros kaki) was investigated. Prediction of high-quality interaction of SP7 effector with ERF19 protein expressed only by specific plant species was observed in in silico molecular docking, which may reiterate the role of effectors in host specificity. The outcomes from our study indicated that sequence precision encoded in the effector peptides of AM fungi and immunomodulatory proteins of host may regulate host specificity in these fungi.


Subject(s)
Fungal Proteins/chemistry , Fungal Proteins/metabolism , Glomeromycota/physiology , Plants/microbiology , Fungal Proteins/genetics , Glomeromycota/chemistry , Glomeromycota/genetics , Host Specificity , Host-Pathogen Interactions , Molecular Docking Simulation , Mycorrhizae/chemistry , Mycorrhizae/genetics , Mycorrhizae/physiology , Plant Proteins/chemistry , Plant Proteins/genetics , Plant Proteins/metabolism , Plants/chemistry , Plants/genetics , Plants/metabolism , Protein Domains
3.
Res Microbiol ; 166(3): 174-85, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25700632

ABSTRACT

Production of nitric oxide (NO) and the presence of NO metabolism genes, nitrous oxide reductase (nosZ), nitrous oxide reductase regulator (nosR) and nitric oxide reductase (norB) were identified in the plant-associated bacterium (PAB) Azospirillum brasilense SM. NO presence was confirmed in all overexpressing strains, while improvement in the plant growth response of these strains was mediated by increased NO and indole-3-acetic acid (IAA) levels in the strains. Electron microscopy showed random distribution to biofilm, with surface colonization of pleiomorphic Azospirilla. Quantitative IAA estimation highlighted a crucial role of nosR and norBC in regulating IAA biosynthesis. The NO quencher and donor reduced/blocked IAA biosynthesis by all strains, indicating their common regulatory role in IAA biosynthesis. Tryptophan (Trp) and l-Arginine (Arg) showed higher expression of NO genes tested, while in the case of ipdC, only Trp and IAA increased expression, while Arg had no significant effect. The highest nosR expression in SMnosR in the presence of IAA and Trp, along with its 2-fold IAA level, confirmed the relationship of nosR overexpression with Trp in increasing IAA. These results indicate a strong correlation between IAA and NO in A. brasilense SM and suggest the existence of cross-talk or shared signaling mechanisms in these two growth regulators.


Subject(s)
Azospirillum brasilense/genetics , Azospirillum brasilense/metabolism , Indoleacetic Acids/metabolism , Nitric Oxide/metabolism , Sorghum/microbiology , Arginine/metabolism , Azospirillum brasilense/growth & development , Bacterial Proteins/genetics , Biofilms/growth & development , Gene Expression Regulation, Bacterial , Membrane Proteins/genetics , Microscopy, Electron, Scanning , Nitric Oxide/isolation & purification , Plant Roots/microbiology , Plant Roots/ultrastructure , Signal Transduction , Sorghum/growth & development , Tryptophan/metabolism
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