Biology subjects

Smith, J.

Publications and source records attributed to Smith, J..

At least 55 records · Page 3Linked to original sources

bioRxiv2025

The herpetofauna of Despotiko Island (Cyclades, Greece)

The Aegean islands are a known hotspot for herpetofauna and have been extensively studied in this area. However, there are still numerous islands that lack this research. This includes the uninhabited islet of Despotiko found in the Paros archipelago, Cyclades. It is known for its importance in archaeology, which in turn attracts tourism. However, there is not yet a complete understanding on the presence of herpetofauna there, with the last published records written in 1977. In an effort to address this, a combination of past ad-hoc sightings and visual surveys were carried out during summer 2024. These yielded two new records of reptile species, Eryx jaculus and Lacerta citrovittata. Furthermore, the enclosed archaeological site had greater reptile diversity and richness than outside the site. This highlights the potential importance of the archaeological site as a key reptile habitat. Our findings help to improve our understanding of reptilian diversity in the archipelago, providing avenues for further research into the potential interactions between archaeological sites and reptile diversity.

ecology↗

bioRxiv2024

Structure-Based Design of Small-Molecule Inhibitors of Human Interleukin-6

Human Interleukin-6 (hIL-6) is a pro inflammatory cytokine that binds to its receptor, IL-6R followed by binding to gp130 and subsequent dimerization to form a hexamer signaling complex. A critical inflammation mediator, hIL-6 is associated with a diverse range of diseases and monoclonal antibodies are in clinical use that either target IL-6R or hIL-6 to inhibit signaling. Here, we perform high throughput structure-based computational screening using ensemble docking for small molecule antagonists for which the target conformations were taken from 600 ns long molecular dynamics simulations of the apo protein. Prior knowledge of the contact sites from binary complex studies and experimental work was incorporated into the docking studies. The top 20 scored ligands from the in silico studies after post analysis were subjected to in vitro functional assays. Among these compounds, the ligand with second-highest calculated binding affinity showed experimentally [~]84% inhibitory effect on IL6-induced STAT3 reporter activity at 10-5 molar concentration. This finding may pave the way for designing small molecule inhibitors of hIL-6 of therapeutic significance.

bioinformatics↗

bioRxiv2024

Remarkable diversity of alkaloid scaffolds in Piper fimbriulatum

Plant specialized metabolites play key roles in diverse physiological processes and ecological interactions. Identifying structurally novel metabolites, as well as discovering known compounds in new species, is often crucial for answering broader biological questions. The Piper genus (Piperaceae family) is known for its special phytochemistry and has been extensively studied over the past decades. Here, we investigated the alkaloid diversity of Piper fimbriulatum, a myrmecophytic plant native to Central America, using a metabolomics workflow that combines untargeted LC-MS/MS analysis with a range of recently-developed computational tools. Specifically, we leverage open MS/MS spectral libraries and metabolomics data repositories for metabolite annotation, guiding isolation efforts towards structurally-new compounds (i.e., dereplication). As a result, we identified several alkaloids belonging to 5 different classes and isolated one novel seco-benzylisoquinoline alkaloid featuring a linear quaternary amine moiety that we named fimbriulatumine. Notably, many of the identified compounds were never reported in Piperaceae plants. Our findings expand the known alkaloid diversity of this family, and demonstrate the value of revisiting well-studied plant families using state-of-the-art computational metabolomics workflows to uncover previously overlooked chemodiversity. To contextualize our findings into a broader biological context, we employed a workflow for automated mining of literature reports of the identified alkaloid scaffolds and mapped the results onto the angiosperm tree of life. By doing so, we highlight the remarkable alkaloid diversity within the Piper genus and provide a framework for generating hypotheses on the biosynthetic evolution of these specialized metabolites. Many of the computational tools and data resources used in this study remain underutilized within the plant science community. This manuscript demonstrates their potential through a practical application and aims to promote broader accessibility to untargeted metabolomics approaches. Significance StatementWe combine untargeted metabolomics with a range of recently developed computational tools to uncover a previously overlooked diversity of alkaloid scaffolds in Piper fimbriulatum. Our findings demonstrate the potential of revisiting well-studied plant families using state-of-the-art computational metabolomics workflows to uncover previously overlooked chemodiversity.

plant biology↗

bioRxiv2024

Discovery and isolation of novel capsaicinoids and their TRPV1-related activity

Chilis contain capsaicin and other structurally related molecules known as capsaicinoids. Capsaicins target protein, the transient receptor potential cation channel subfamily V member 1 (TRPV1), has been linked to many post-activation effects, including changes in metabolism and pain sensation. Capsaicinoids also bind to TRPV1, but current studies often disregard non-capsaicin interactions. To fill in these gaps, we screened 40 different chili varieties derived from four Capsicum species by means of untargeted metabolomics and a rat TRPV1 (rTRPV1) calcium influx activation assay. The resulting capsaicinoid profiles were specific to each variety but only partially corresponded with species delimitations. Based on rTRPV1 activation elicited by crude chili extracts, capsaicinoids act in an additive manner and a capsaicinoid profile can serve as a gauge of this activation. In addition, we isolated eighteen capsaicinoids, including five previously unreported ones, and confirmed their structure by NMR and MS/MS. We then tested rTRPV1 activation by 23 capsaicinoids and three related compounds. This testing revealed that even slight deviations from the structure of capsaicin reduce the ability to activate the target, with a mere single hydroxylation on the acyl tail reducing potency towards rTRPV1 by more than 100-fold. In addition, we tested how rTRPV1 activity changes in the presence of capsaicin together with non-activating capsaicin analogs and weakly activating capsaicinoids and found both classes of molecules to positively modulate the effects of capsaicin. This demonstrates that even such compounds have measurable pharmacological effects, making a case for the use and study of natural chili extracts. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=76 SRC="FIGDIR/small/620944v2_ufig1.gif" ALT="Figure 1"> View larger version (17K): org.highwire.dtl.DTLVardef@1d56d02org.highwire.dtl.DTLVardef@e7a66dorg.highwire.dtl.DTLVardef@5f409forg.highwire.dtl.DTLVardef@18b88f7_HPS_FORMAT_FIGEXP M_FIG C_FIG Created in BioRender. Smith, J. (2025) https://BioRender.com/a61h668 HighlightsO_LI5 novel capsaicinoids (vanilloids) and 13 other capsaicinoids were isolated from chilis. C_LIO_LIThe slightest deviation in the capsaicin structure results in decreased TRPV1 activity. C_LIO_LIA single hydroxylation can reduce potency to TRPV1 100-fold. C_LIO_LINon-pungent vanilloids modulate capsaicin-TRPV1 activity. C_LI

pharmacology and toxicology↗

bioRxiv2024

Genomic evidence suggests the balanced lethal system in Triturus newts originated in an instantaneous speciation event.

Triturus newts are afflicted by a balanced lethal system causing the spontaneous death of half of their offspring. How could such a maladaptive trait evolve? We construct genetic maps for Triturus and its sister genus Lissotriton, identifying genes involved in the balanced lethal system. Triturus chromosome 1 has diverged into two versions, which each carry a single massive deletion that is compensated for by duplication of the same region in the alternate version - indicating that the balanced lethal system arose instantaneously, in a single macromutation. Simulations show that, counterintuitively, the deleterious nature of the rearranged chromosomes protects them against competition with the ancestral arrangement via reproductive isolation. We conclude that the origin of the Triturus balanced lethal system also led to instantaneous speciation.

evolutionary biology↗

bioRxiv2024

Targeting the acetyltransferase NAT10 corrects pathologies in human frontotemporal neurons and extends lifespan in an in vivo Drosophila tauopathy model

Disruption of the neuronal nuclear membrane and perturbation of nucleocytoplasmic transport are features of neurodegenerative diseases, including Alzheimers disease, that involve the microtubule-associated protein tau (MAPT). We previously identified that missense and splicing mutations in the MAPT gene, causal for frontotemporal dementia, result in nuclear envelope deformation and disrupted nucleocytoplasmic transport in human neurons. This is most likely due to microtubule mechanical stress, similar to that observed in Hutchinson-Gilford Progeria Syndrome (HGPS). A small molecule inhibitor of the acetyltransferase NAT10 has been shown to correct nuclear membrane defects in HGPS by modulating microtubule dynamics. We report here that NAT10 inhibition alters microtubule dynamics and corrects nuclear lamina defects and aberrant nucleocytoplasmic transport in human iPSC-derived FTD-MAPT neurons. Similarly, NAT10 inhibition and haploinsufficiency correct neuronal nuclear shape defects and extend lifespan in vivo in a Drosophila model of tauopathy. Our results show that NAT10 mediates neuronal pathologies in tauopathies and is a promising new therapeutic target in these diseases.

neuroscience↗

bioRxiv2024

The G3BP Stress-Granule Proteins Reinforce the Translation Program of the Integrated Stress Response

When mammalian cells are exposed to stress, they coordinate the condensation of stress granules (SGs) through the action of proteins G3BP1 and G3BP2 (G3BPs) and, simultaneously, undergo a massive reduction in translation. Although SGs and G3BPs have been linked to this translation response, their overall impact has been unclear. Here, we investigate the question of how, and indeed whether, G3BPs and SGs shape the stress translation response. We find that SGs are enriched for mRNAs that are resistant to the stress-induced translation shutdown. Although the accurate recruitment of these stress-resistant mRNAs does require the context of stress, a combination of optogenetic tools and spike-normalized ribosome profiling demonstrates that G3BPs and SGs are necessary and sufficient to both help prioritize the translation of their enriched mRNAs and help suppress cytosolic translation. Together these results support a model in which G3BPs and SGs reinforce the stress translation program by prioritizing the translation of their resident mRNAs.

molecular biology↗

bioRxiv2024

The Platinum Pedigree: A long-read benchmark for genetic variants

Recent advances in genome sequencing have improved variant calling in complex regions of the human genome. However, it is difficult to quantify variant calling performance since existing standards often focus on specificity, neglecting completeness in difficult to analyze regions. To create a more comprehensive truth set, we used Mendelian inheritance in a large pedigree (CEPH-1463) to filter variants across Illumina, PacBio high-fidelity (HiFi), and Oxford Nanopore Technologies platforms. This generated a variant map with over 4.7 million single-nucleotide variants, 767,795 indels, 537,486 tandem repeats, and 24,315 structural variants, covering 2.77 Gb of the GRCh38 genome. This work adds [~]200 Mb of high-confidence regions, including 8% more small variants, and introduces the first tandem repeat and structural variant truth sets for NA12878. As an example of the value of this improved benchmark, we retrained DeepVariant using this data to reduce genotyping errors by [~]34%.

genomics↗

bioRxiv2024

Neural Encoding of Direction and Distance across Reference Frames in Visually Guided Reaching

Goal-directed actions require transforming sensory information into motor plans defined across multiple parameters and reference frames. Substantial evidence supports the encoding of target direction in gaze- and body-centered coordinates within parietal and premotor regions. However, how the brain encodes the equally critical parameter of target distance remains less understood. Here, using Bayesian pattern component modeling of fMRI data during a delayed reach-to-target task, we dissociated the neural encoding of both target direction and the relative distances between target, gaze, and hand at early and late stages of motor planning. This approach revealed independent representations of direction and distance along the human dorsomedial reach pathway. During early planning, most premotor and superior parietal areas encoded a targets distance in single or multiple reference frames and encoded its direction. In contrast, distance encoding was magnified in gaze- and body-centric reference frames during late planning. These results emphasize a flexible and efficient human central nervous system that achieves goals by remapping sensory information related to multiple parameters, such as distance and direction, in the same brain areas. Significance statementMotor plans specify various parameters, e.g., target direction and distance, each of which can be defined in multiple reference frames relative to gaze, limb, or head. Combining fMRI, a delayed reach-to-target task, and Bayesian pattern component modeling, we present evidence for independent goal-relevant representations of direction and distance in multiple reference frames across early and late planning along the dorsomedial reach pathway. Initially, areas encoding distance also encode direction, but later in planning, distance encoding in multiple reference frames was magnified. These results emphasize central nervous system flexibility in transforming movement parameters in multiple reference frames crucial for successful goal-directed actions and have important implications for brain-computer interface technology advances with sensory integration.

neuroscience↗

bioRxiv2024

IFT and BBSome proteins are required for Leishmania mexicana pathogenicity, but flagellar motility is dispensable

Protists of the order Kinetoplastida possess a single multifunctional flagellum, which powers cellular displacement and mediates attachment to tissues of the arthropod vector. The kinetoplastid flagellar cytoskeleton consists of a nine-microtubule doublet axoneme; further structural elaborations, which can vary between species and life cycle stages, include the assembly of axonemal dynein complexes, a pair of singlet microtubules and the extra-axonemal paraflagellar rod. The intracellular amastigote forms of Leishmania spp. build a short, non-motile cilium whose function has remained enigmatic. Here we used a panel of 25 barcoded promastigote cell lines, including mutants lacking genes encoding flagellar assembly proteins, cytoskeletal proteins required for normal motility, or flagellar membrane proteins to examine how these defects impact on their virulence in macrophages and mice. Mutants lacking intraflagellar transport (IFT) protein 88 were severely attenuated indicating that assembly of a flagellum is necessary to allow for Leishmania survival in a mammalian host. A similarly severe loss of virulence was observed upon deletion of BBS2, a core component of the BBSome complex, which may act as a cargo adapter for IFT. By contrast, promastigotes that were unable to beat their flagella due to loss of PF16 could establish an infection and only showed a small reduction of parasite burden in vivo compared to the parental cell lines. These results confirm that flagellar motility is not necessary for mammalian infection but flagellum assembly and the integrity of the BBSome are essential for pathogenicity.

cell biology↗

bioRxiv2024

Sensory context of initiation-cue modulates action goal-relevant neural representations

The ability to produce goal-directed movement relies on the integration of diverse sources of sensory information specific to the task goal. Neural representations of goal-relevant features, such as target location and gaze direction, have been well studied in sensorimotor areas. It remains less clear whether goal-relevant motor representations are influenced by sensory changes to initiation-relevant information, such as a go-cue that provides no information about target location. We used Bayesian pattern component modelling of fMRI data during a delayed reach task with either visual or audiovisual go-cues to explore whether neural representations of goal-related features in sensorimotor areas are modulated by changes to initiation-relevant sensory information. We found that representations of target direction and gaze direction in the primary sensory areas, motor areas, and posterior parietal cortex, were sensitive to whether a reach was cued with a visual or audiovisual go-cue. These findings indicate that the central nervous system flexibly delegates the tasks of where to move and when to move based on available sensory context, even if initiation-relevant stimuli provide no additional information about target location.

neuroscience↗

bioRxiv2024

Inhibition of Soluble Epoxide Hydrolase Ameliorates Cerebral Blood Flow Autoregulation and Cognition in Alzheimer's Disease and Diabetes-Related Dementia Rat Models

Alzheimers Disease and Alzheimers Disease-related dementias (AD/ADRD) pose major global healthcare challenges, with diabetes mellitus (DM) being a key risk factor. Both AD and DM-related ADRD are characterized by reduced cerebral blood flow, although the exact mechanisms remain unclear. We previously identified compromised cerebral hemodynamics as early signs in TgF344-AD and type 2 DM-ADRD (T2DN) rat models. Genome-wide studies have linked AD/ADRD to SNPs in soluble epoxide hydrolase (sEH). This study explored the effects of sEH inhibition with TPPU on cerebral vascular function and cognition in AD and DM-ADRD models. Chronic TPPU treatment improved cognition in both AD and DM-ADRD rats without affecting body weight. In DM-ADRD rats, TPPU reduced plasma glucose and HbA1C levels. Transcriptomic analysis of primary cerebral vascular smooth muscle cells from AD rats treated with TPPU revealed enhanced pathways related to cell contraction, alongside decreased oxidative stress and inflammation. Both AD and DM-ADRD rats exhibited impaired myogenic responses and autoregulation in the cerebral circulation, which were normalized with chronic sEH inhibition. Additionally, TPPU improved acetylcholine-induced vasodilation in the middle cerebral arteries (MCA) of DM-ADRD rats. Acute TPPU administration unexpectedly caused vasoconstriction in the MCA of DM-ADRD rats at lower doses. In contrast, higher doses or longer durations were required to induce effective vasodilation at physiological perfusion pressure in both control and ADRD rats. Additionally, TPPU decreased reactive oxygen species production in cerebral vessels of AD and DM-ADRD rats. These findings provide novel evidence that chronic sEH inhibition can reverse cerebrovascular dysfunction and cognitive impairments in AD/ADRD, offering a promising avenue for therapeutic development.

molecular biology↗

bioRxiv2024

Insect size responses to climate changes vary across elevations according to seasonal timing

Widespread plastic and evolutionary responses to temperature have led to body size declines being proposed as a universal response to warming, but the high degree of variation in terrestrial ectotherms has challenged this view. We investigate whether temperature dependent development and growth rates in ectothermic organisms drive departures from universal size responses. Leveraging a long-term study of montane grasshoppers, we detect size shifts over recent decades that depend on elevation and species seasonal timing. Size shifts have been focused at low elevations with the earliest emerging species (those that overwinter as juveniles) getting bigger, and later season species getting smaller. The shifts correspond to warmer temperatures at low elevation increasing the sizes of the earliest season species but decreasing the sizes of the later season species. This is consistent with our hypothesis that the earliest season species may be able to take advantage of warmer conditions accelerating growth during early spring development, whereas warm temperatures may adversely impact later season species via mechanisms such as increased rates of energy use or thermal stress. Grasshoppers tend to capitalize on warm conditions by both getting bigger and reaching adulthood earlier. Our analysis further reinforces the need to move beyond expectations of universal responses to climate change to consider how environmental exposure and sensitivity varies across elevations and life histories.

ecology↗

bioRxiv2024

A single-nucleus census of immune and non-immune cell types for the major immune organ systems of chicken.

In the avian host, comprehensively cataloging immune cell types, their transcriptome profiles, and varying molecular responses to pathogen challenges are necessary steps toward a better understanding of the interplay between genetics and disease resilience. We present a first nuclei atlas of immune cell types derived from the three main immune organs of layer chickens, including spleen, bursa, and thymus. In bursa we also present, an accounting of cell type activation with the bacterial toxin lipopolysaccharide (LPS). Our analysis includes 36,370 total nuclei and 16, 12, and 12 transcriptionally distinct clusters for spleen, bursa, and thymus, respectively. We discover nuclei molecular profiles that uniquely distinguish states of the transcriptome within cell type that could serve as new means to characterize avian immune subtypes. We further subcluster refined immune cell type classifications, specifically highlighting the transcriptomic diversity of B and T cell subtypes. In the bursa, inferred intercellular communication and signaling pathway enrichment analyses across immune and non-immune cell types demonstrate the unappreciated complexity of the B cell repertoire in a model mimicking systemic bacterial infection. This census of all cell types in both primary and one major secondary avian immune organ system, although preliminary, provides a first review of how nuclei transcribe numerous genes, known and unknown, a critical prerequisite for the study avian immunogenetics by cell type.

immunology↗

bioRxiv2024

Protein interactions, calcium, phosphorylation, and cholesterol modulate CFTR cluster formation on membranes

The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is a chloride channel whose dysfunction leads to intracellular accumulation of chloride ions, dehydration of cell surfaces, and subsequent damage to airway and ductal organs. Beyond its function as a chloride channel, interactions between CFTR, ENaC, and SLC transporter family membrane proteins and cytoplasmic proteins, including calmodulin and NHERF-1, co-regulate ion homeostasis. CFTR has also been observed to form mesoscale membrane clusters. However, the biophysical mechanisms that regulate the formation of CFTR clusters are unknown. Using a combination of computational modeling and complex biochemical reconstitution assays, we demonstrate that multivalent protein-protein interactions with CFTR binding partners, calcium, and membrane cholesterol can induce CFTR cluster formation on model membranes. Phosphorylation of the intracellular domains of CFTR also promotes cluster formation in the absence of calcium, indicating that multiple mechanisms can regulate CFTR cluster formation. Our findings reveal that coupling of multivalent protein and lipid interactions promote CFTR cluster formation consistent with membrane-associated biological phase separation. SIGNIFICANCE STATEMENTMutations in the cystic fibrosis transmembrane conductance regulator (CFTR) membrane protein underlie cystic fibrosis. It is thought that molecular "hubs" of CFTR and its binding partners co-regulate ion homeostasis and that disruption of these clusters can result in disease. However, the physical basis for molecular hub formation is unclear. In this study, we present evidence that multivalent protein and lipid interactions drive the formation of mesoscale CFTR-containing clusters or "hubs" on model membranes in a manner consistent with biological phase separation. These data provide important insights into physical mechanisms that modulate CFTR membrane organization and offer a new lens for the development of corrective therapeutics.

biophysics↗

bioRxiv2024

Sleep deprivation and the rodent psychomotor vigilance test (rPVT): Assessing lapses in attention, the response stimulus interval effect, and time on task in rats using food reinforcement

Study objectiveSleep deprivation (SD) impairs sustained attention when assessed with the psychomotor vigilance test (PVT). Food restriction attenuates the effects of SD on sustained attention in rats, possibly limiting translation of rodent tests. Our goal was to determine if an rPVT requiring high baseline performance was sensitive to the effects of SD when using food restriction and reinforcement. MethodsrPVT-trained rats experienced SD and were tested the following day. ResultsSD significantly increased lapses, and this effect was specific to shorter response-stimulus intervals. Decreased percent correct responses and increased slow reaction times were also found following SD. ConclusionThe rPVT is sensitive to the performance impairing effects of SD in food restricted rats, a common methodology used to train and maintain performance on operant tests.

animal behavior and cognition↗

bioRxiv2024

Variability and correlations among vital rates and their influence on population growth in mule and black-tailed deer

To reverse observed range-wide population declines, managers of mule and black- tailed deer (Odocoileus hemionus) require information on the vital rates and life stages that are most influential to population growth for which to target management actions. We conducted a range-wide literature review and used hierarchical models to provide biological descriptions of mule and black-tailed deer vital rates, their variability, and how they correlate with one another. We then used matrix models and life-stage simulation analysis to determine the individual vital rates that contributed most to lambda, i.e., annual population growth rate. Adult female survival was the vital rate with the greatest ability to predict lambda and explained 62% of the variation in population growth. While annual juvenile survival explained 44% of the variation in lambda, summer and winter juvenile survival by themselves were far less explanatory than adult female survival. Winter fawn:doe ratios, a metric often collected by management agencies, only explained 10% of the variation in lambda. When adult female survival was 0.84, our simulations estimated an equal probability that a population would increase versus decrease, and correspondingly, the estimate of lambda was 1.0 with a 95% credible interval of 0.88-1.14. Simulations suggested that populations with adult survival rates less than 70% would always decline, but as survival increased beyond this value lambda increased linearly and never plateaued. In contrast, the probability of observing a stable lambda plateaued when annual juvenile survival reached approximately 0.5. The mean lambda calculated from all simulated values within the observed range of vital rate values across the species geographical distribution was 0.975, and in 61% of the simulations lambda was < 1. After 20 years, we estimated that this distribution of lambda values would cause populations to decrease in 92% of instances with a mean decrease of 44%. Our results align with the observed declines in mule deer populations throughout their range over recent decades and suggest that these trends will continue until management can improve survival of adult females.

ecology↗

bioRxiv2024

Evolutionary genomics reveals variation in structure and genetic content implicated in virulence and lifestyle in the genus Gaeumannomyces

Gaeumannomyces tritici is responsible for take-all disease, one of the most important wheat root threats worldwide. High-quality annotated genome resources are sorely lacking for this pathogen, as well as for the closely related antagonist and potential wheat take-all biocontrol agent, G. hyphopodioides. As such, we know very little about the genetic basis of the interactions in this host-pathogen-antagonist system. Using PacBio HiFi sequencing technology we have generated nine near-complete assemblies, including two different virulence lineages for G. tritici and the first assemblies for G. hyphopodioides and G. avenae (oat take-all). Genomic signatures support the presence of two distinct virulence lineages in G. tritici (types A and B), with A strains potentially employing a mechanism to prevent gene copy-number expansions. The CAZyme repertoire was highly conserved across Gaeumannomyces, while candidate secreted effector proteins and biosynthetic gene clusters showed more variability and may distinguish pathogenic and non-pathogenic lineages. A transition from self-sterility (heterothallism) to self-fertility (homothallism) may also be a key innovation implicated in lifestyle. We did not find evidence for transposable element and effector gene compartmentalisation in the genus, however the presence of Starship giant transposable elements likely contributes to genomic plasticity in the genus. Our results depict Gaeumannomyces as an ideal system to explore interactions within the rhizosphere, the nuances of intraspecific virulence, interspecific antagonism, and fungal lifestyle evolution. The foundational genomic resources provided here will enable the development of diagnostics and surveillance of understudied but agriculturally important fungal pathogens.

evolutionary biology↗