Biology subjects

Sivaprakasam Padmanaban, P. B.

Publications and source records attributed to Sivaprakasam Padmanaban, P. B..

4 recordsLinked to original sources

bioRxiv2026

Fungal volatiles drive lifestyle-dependent, systemic metabolic reprogramming in poplar

O_LIRationale: Although trees encounter diverse fungal communities, it is unclear how they adjust their physiology in response to fungal ecological strategies before physical contact. We tested whether volatile organic compounds (VOCs) emitted by fungi are sufficient to induce systemic, lifestyle-consistent metabolic states in poplar roots and leaves. C_LIO_LIMethods: Populus x canescens roots were exposed to VOCs from a pathogen (Heterobasidion annosum), a saprotroph (Postia placenta) or an ectomycorrhizal mutualist (Laccaria bicolor) for six weeks in a contact-free pot-in-pot system. Untargeted LC-MS metabolomics characterized VOC-induced metabolic reprogramming in roots and leaves. C_LIO_LIKey results: Fungal VOC exposure alone reconfigured the metabolomes of roots and leaves, with strong discrimination between treatments despite belowground exposure. Poplar revealed a shared VOC-responsive component, but also fungus-specific programmes: pathogen VOCs produced a suppression-dominated systemic phenotype; saprotroph VOCs promoted lipid-centred metabolic activation; and mutualist VOCs elicited restrained, compatibility-consistent shifts with targeted pathway modulation. C_LIO_LIMain conclusion: Volatile-mediated surveillance allows trees to anticipate fungal lifestyle-associated cues and adjust systemic metabolism before physical contact occurs. This links airborne fungal cues to whole-plant physiological configuration and extends plant-fungal recognition beyond contact-dependent mechanisms. C_LI One-sentence summaryVolatile-mediated surveillance allows trees to anticipate fungal lifestyle and adjust systemic metabolism before physical contact occurs.

plant biology↗

bioRxiv2025

Provenance Legacies Override Species Effects in Shaping Oak Rhizosphere Microbiomes and Metabolomes

As climate change drives more frequent and intense drought-heat extremes, selecting drought-tolerant trees is crucial for future forest resilience. However, the role of tree-microbial associations for this key trait remains largely unclear. In this study, we investigated how geographic origin, species identity, and intrinsic water-use efficiency (iWUE) shape the rhizosphere microbiome and root-rhizosphere metabolome of pedunculate (Quercus robur) and sessile (Q. petraea) oaks. In a six-year common garden experiment, we analyzed trees from both species, each grown from seeds from two distinct geographic origins, the upper Rhine basin (URB) and the north-east German lowlands (NGL), differing in water availability, using 16S and ITS rRNA gene based metabarcoding and untargeted metabolomics. We found a consistent legacy effect of seed origin on the composition of the prokaryotic rhizosphere microbiome and the metabolome, whereas tree species had no significant impact. The bacterial family Pseudonocardiaceae was enriched at trees from the drier origin NGL, while Blastocatellaceae and Micromonosporaceae were positively associated with iWUE across samples. Higher iWUE was furthermore significantly correlated with lower prokaryotic diversity and shifts in {beta}-diversity, thereby linking a drought-adaptive host trait to the assembly of the belowground environment. Ellagic acid, a plant derived polyphenol associated with drought tolerance, was enriched in the drier origin NGL and linked to several prokaryotic taxa in correlation networks. The rhizosphere fungal community, however, was largely unaffected by origin or species. Solely fungal community evenness declined with increasing iWUE. Together, our findings suggest that ecotypic adaptation linked to origin can outweigh the effect of species-level traits in shaping the oak rhizosphere microbiome and metabolome. These findings emphasize that provenance-driven ecotypic adaptation can strongly influence plant-microbe interactions and underscore the need for provenance-aware selection and microbiome-informed assisted migration as strategies to strengthen forest drought resilience under global climate change.

ecology↗

bioRxiv2024

Deciphering plant-beneficial fungal interactions: Unravelling metabolic diversity that underpins communication between Laccaria bicolor and Trichoderma

With over 250 known species, the genus Trichoderma (Ascomycota, Hypocreaceae) is found in various soils, on plant surfaces and as plant endophytes. While Trichoderma species are known as mycoparasites, their antagonistic behaviour can also negatively affect other beneficial fungi, such as mycorrhizal fungi. To gain insight into the metabolic signals involved in the interactions between the ectomycorrhizal fungus (ECM) Laccaria bicolor (Basidomycota, Hydnangiaceae), and different mycoparasitic Trichoderma spp. (T. harzianum strains WM24a1, MS8a1 and ES8g1, and T. atrobrunneum), we performed in vitro dual-confrontation experiments. We studied the volatile organic compounds (VOCs), hyphal metabolomes and soluble metabolites released by each of the fungi in various co-cultivation scenarios. The results revealed an altered growth of the mycelia depending on the degree of contact: When Trichoderma spp. and L. bicolor shared only the same headspace, Trichoderma spp. growth was at least partially inhibited, whereas in direct contact the growth of L. bicolor was impaired. Distinct strain- and species-specific changes in hyphal metabolites, in exudates and volatile emission were revealed from each of the studied fungi. We identified both core metabolite profiles and interaction-specific metabolic responses that were related to carbohydrate, lipid, nucleotide, energy and amino acid metabolisms. Volatile and soluble metabolites revealed temporal and spatial adjustments in dual cultures compared to solitary cultures, suggesting rapid contact-dependent adaptations and demonstrating the dynamic communication mechanisms between Trichoderma spp. and the ECM. These results suggest a central role for both emitted and secreted fungal metabolites in the fungal non-self-recognition and in interaction with each other.

microbiology↗

bioRxiv2024

Lifestyle-specific responses of Trichoderma spp. in mycoparasitic confrontations and implications for biocontrol of Populus x canescens

O_LITrichoderma spp. are gaining popularity in agriculture and forestry due to their multifaceted roles in promoting plant growth through e.g. nutrient translocation, hormone production, induction of plant systemic resistance, but also direct antagonism of other fungi. However, the mycotrophic nature of the genus bears the risk of possible interference with other native plant-beneficial fungi, such as ectomycorrhiza, in the rhizosphere. Such interference could yield unpredictable consequences for the host plants of these ecosystems. C_LIO_LIWe investigated whether Trichoderma spp. can differentiate between beneficial ectomycorrhizal fungi (represented by Laccaria bicolor and Hebeloma cylindrosporum) and pathogenic fungi (represented by Fusarium graminearum and Alternaria alternata) in different confrontation scenarios, including a newly developed olfactometer "race tube"-like system. C_LIO_LIUsing two independent species, T. harzianum, and T. atrobrunneum, with plant-growth-promoting and immune-stimulating properties towards Populus x canescens, our study revealed robustly accelerated growth towards phytopathogens, while showing a contrary response to ectomycorrhizal fungi. Transcriptomic analyses identified distinct genetic programs during interaction corresponding to the lifestyles, emphasizing the expression of mycoparasitism-related genes only in the presence of phytopathogens. C_LIO_LIThe findings reveal a critical mode of fungal community interactions belowground and suggest that Trichoderma spp. can distinguish between fungal partners of different lifestyles already at a distance. C_LI

microbiology↗