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Biology subjects

Thomas, G.

Publications and source records attributed to Thomas, G..

At least 19 recordsLinked to original sources

Stainless Steel vs Calcium Fluoride for biomedical Raman Spectroscopy

Raman spectroscopy (RS) has been shown to differentiate various disease states in tissue samples, yet the impact of sample substrate on spectral quality and downstream machine-learning (ML) performance is under-explored. We collected 960 spectra from 36 formalin-fixed, paraffin-embedded colonic specimens mounted in parallel on calcium fluoride (CaF2) and mirrored stainless-steel (SS) slides. Raw SS spectra were more intense than CaF2, and routine dewaxing left prominent paraffin peaks on CaF2 that were largely absent on SS. Extending CaF2 xylene immersion to 48 h reduced key paraffin peaks by 11 to 23%, aligning its biochemical profile with SS. Nested cross-validated classifiers were built to distinguish true disease (T1) from epithelial misplacement (EM). The highest accuracies were observed on SS (0.65 - 0.66), while CaF2 improved from 0.41 - 0.57 to 0.65 - 0.69 after extended dewaxing, chiefly via gains in recall. Although optimal dewaxing renders CaF2 diagnostically non-inferior, SS still offers superior accuracy, faster preparation, at approximately 4% of the cost, supporting its integration into scalable, AI-enabled RS pathology workflows.

molecular biology↗

PlumageParts: A fine-grained avian plumage segmentation dataset and benchmark for ecological image analysis

Fine-grained localisation of plumage regions is a prerequisite for computational analyses of avian colouration, patterning and visual traits in ecological and evolutionary research. Progress is limited by the scarcity of image resources with annotations aligned to biologically meaningful anatomical units: existing avian benchmarks provide either landmark points or coarse part categories that do not capture ornithologically defined plumage regions. We present a curated dataset of 4,705 bird images annotated for nine plumage regions: head, throat, breast, belly, vent, back, coverts, remiges and tail. Spanning 39 avian orders and 222 families, the dataset provides a taxonomically broad resource for fine-grained avian image analysis. The dataset was built through an iterative model-assisted annotation workflow, in which model predictions were reviewed and corrected rather than drawn from scratch, improving the efficiency of region-level annotation. We benchmark classical segmentation architectures, SAM-based models and self-supervised foundation-model encoders on this task. A frozen DINOv3 encoder with a lightweight decoder achieved the highest performance on the held-out test set, reaching 84.01% mean Intersection over Union while requiring substantially less memory than end-to-end fine-tuning. The model generalised to external avian benchmarks, including the bird subset of PartImageNet and CUB-200-2011, and achieved competitive performance on the full PartImageNet part-segmentation benchmark, which includes diverse animal taxa. We provide a modular detect-track-segment pipeline as a proof-of-concept extension to video data. Together, these results show that anatomically grounded avian annotations can serve both as a resource for plumage phenotyping and as a benchmark for efficient, transferable biological part segmentation. Author SummaryBirds vary enormously in colour and pattern, but studying this variation at large scales requires more than identifying the bird in a photograph. Researchers often need to know where each colour or pattern occurs on the body, such as on the head, throat, breast, wing or tail. We created PlumageParts to make this kind of region-level analysis easier. The dataset contains 4,705 bird images annotated into nine biologically meaningful plumage regions, covering a wide range of bird families and orders. To build the dataset efficiently, we used a model-assisted workflow in which computer-generated masks were checked and corrected by researchers rather than drawn entirely by hand. We then tested several image-segmentation approaches and found that a frozen self-supervised vision model, combined with a lightweight decoder, provided accurate plumage-region predictions while requiring relatively modest computing resources. The same approach also performed well on a broader animal part-segmentation benchmark, suggesting that it may be useful beyond birds when suitable annotations are available. By releasing the annotations, code and trained model, we aim to support future studies of bird plumage and biologically meaningful image segmentation.

ecology↗

Dual-antigen Doggybone DNA vaccine induces potent anti-tumor immunity against immunosuppressive oral cancer

Anti-PD1 blockade benefits only a subset of patients with head and neck squamous cell carcinoma (HNSCC), highlighting the need for approaches that overcome tumor immune resistance. Here, using the doggybone DNA (dbDNATM) platform, we developed CaVac OPT, an optimized dual-antigen DNA vaccine targeting MAGED4B and FJX1, which are overexpressed in most HPV-negative HNSCC and multiple solid tumors. In the MOC-2 oral cancer model, CaVac OPT significantly reduced tumor growth and when combined with anti-PD1 therapy, further delayed progression and improved survival. Immune profiling showed increased infiltration of CD4+ and CD8+ T cells, expansion of stem-like Tcf1+ populations, without increase in regulatory T cells, a reduced M2/M1 macrophage ratio and activation of interferon gamma associated pathways with suppression of tumor-promoting signals. These findings demonstrate that CaVac OPT reprograms the tumor microenvironment, converting cold HNSCC into T cell-inflamed responsive tumors. CaVac OPT represents a promising strategy for achieving durable control of aggressive, immunotherapy-resistant head and neck cancer.

cancer biology↗

Defects in the DNA Damage Response of Patient-derived Endometriosis Stromal Cells

With each menstrual cycle, endometrial cells rapidly proliferate and decidualize in preparation for pregnancy. Such rapid proliferation generates replication stress and results in DNA damage with irreparable cells undergoing senescence. Here, we examine the DNA damage response (DDR) of patient-derived stromal cell lines from menstrual effluent (MenSC) of healthy donors and donors with endometriosis. We found that proliferating MenSCs from endometriosis patients (Endo) have a defective DDR that is also present when these cells reach confluence. In G1, these cells contain more 53BP1-nuclear bodies (NBs) and are less senescent than healthy samples. We also treated with hydroxyurea (Hu) to generate replication stress and found that Endo MenSCs responded to this treatment by activating the DDR and generating more 53BP1-NBs. We examined the MRN complex, upstream of the ATM-dependent DDR. Hu treatment of our cell lines resulted in downregulation of all genes encoding the MRN complex, and RAD50 and NBS1 proteins. In a scRNA-seq dataset of endometriosis stromal tissue, we also identified downregulation of RAD50 and NBS1. To evaluate the growth potential of MenSCs, we decidualized cells after Hu treatment and then replated them in growing medium. Untreated endometriosis MenSCs formed more colonies than healthy MenSCs; neither sample type formed colonies after Hu treatment. Together, our studies suggest that endometriosis MenSCs have a defective DDR that may be exploited therapeutically.

cell biology↗

Fair-weather friends: Unequal partnerships between Parastagonospora nodorum and Pyrenophora tritici-repentis define disease dynamics in wheat

Parastagonospora nodorum and Pyrenophora tritici-repentis are the causal agents of septoria nodorum blotch and tan spot of wheat, respectively. Though these fungal phytopathogens have been found to frequently cohabitate the same leaf, their interaction dynamics in the manifestation of disease remain poorly understood due to limitations in species-specific detection methods. We developed a digital PCR based model targeting conserved regions of the -tubulin gene, enabling biomass quantification of both pathogens during infection. Field surveys revealed up to two in three symptomatic infections involved both pathogens, with co-infected plants showing significantly higher individual pathogen biomass than single-species infections. Host plants in the field with moderate resistance to both pathogens were found to be significantly more necrotic under co-infection, with individual pathogen biomass up to twice that observed value for single infections. However, like fair-weather friends the partnership between these two pathogens seems to be conditional.When P. tritici-repentisestablished first, secondary P. nodorumcolonisationled to a breakdown of host resistance. Conversely, when P. nodorum established on the host first, it suppressed P. tritici-repentis colonisation regardless of host resistance. To our knowledge this is the first description of asymmetric priority effects overcoming host resistance in a plant pathosystem. Resistance breeding strategies evaluating single pathogen challenges may inadvertently select for cultivars vulnerable to sequential co-infection, necessitating integrated disease complex approaches for durable resistance development.

microbiology↗

Therapeutic Blockade of Type 2 Cytokines and PD1 Unleashes Anti-Tumor Immunity Through Coordinated Reprogramming of Innate and Adaptive Immune Surveillance

BackgroundCheckpoint inhibitors improve survival in patients with several types of tumors. However, resistance to checkpoint inhibitors creates an opportunity for patients to benefit from novel immunotherapies. The type 2 cytokines IL-4, IL-13 and TSLP have been implicated in suppressing anti-tumor immune responses through T and myeloid cells. Our current study tested whether combined therapeutic blockade of IL-4, IL-13 and TSLP improved anti-tumor immunity alone and in combination with PD1 antagonism. MethodsWe used in vitro experiments with primary cells to identify cell types likely to participate in controlling tumors upon IL-4, IL-13, TSLP and PD1 blockade. Therapeutic blockade in the subcutaneous CT26 model tested in vivo tumor growth inhibition and associated immunological changes. Bioinformatic analysis of human tumor bulk RNA sequencing data probed for survival associations with IL-4/IL-13 and TSLP transcriptional responses. ResultsIn vitro, IL-4 suppressed T cell-mediated tumor growth inhibition and reduced monocyte-derived dendritic cell expression of proteins associated with anti-tumor immunity. In vivo, blocking IL-4, IL-13, TSLP and PD1 improved tumor growth inhibition by creating "hotter" tumors. This was associated with repolarization of CD4 and CD8 T cells and shifts in monocyte, conventional type 1 and type 2 (or monocyte-derived) dendritic cell programs. Transcriptional responses to IL-4/IL-13 and TSLP were associated with poor survival outcomes across patients with several types of cancers. ConclusionTherapeutic blockade of IL-4, IL-13 and TSLP may drive immunological tumor growth inhibition in subsets of cancer patients alone and in combination with checkpoint inhibitors. Improved tumor growth inhibition was likely driven through augmented cytotoxic T cell priming in secondary lymphoid organs and improved reactivation by repolarized monocytes and dendritic cells in tumors.

cancer biology↗

Integrative proteomics and metabolomics map reveals key sectors of defense metabolism in ginger against Pythium myriotylum

Ginger (Zingiber officinale) cultivation is severely threatened by rhizome rot caused by Pythium myriotylum. Hitherto, detail molecular machineries and metabolic pathways of defense against P. myriotylum in edible ginger are elusive. To elucidate the defense mechanisms, we employed integrative quantitative proteomics (TMT labelling) and high resolution untargeted metabolomics to investigate temporal defense responses of ginger during infection. Proteomics analysis revealed enrichment of cellular detoxification and secondary metabolism pathways indicating co-activation of oxidative stress management and its mediated defense metabolite biosynthesis. Key phenylpropanoid enzymes (PAL, C4H, CAD) and LOX, a regulator of jasmonic acid (JA) biosynthesis, were significantly up-regulated, correlating JA signaling with secondary metabolic defenses. Metabolomics profiling confirmed accumulation of phenylpropanoids, flavonoids, and terpenoids, including known antimicrobial metabolites such as gingerol, shogaol, curcumin, and gingerdione, alongside expression of their key regulatory enzyme was also induced. Notably, machine learning identified the monoterpenoid TGA as the top defense-associated metabolite. Functional assays demonstrated strong anti-P. myriotylum activity of TGA, which inhibited mycelial growth and suppressed expression of key pathogenicity-related genes (NIP1, GHs, cellulase). These findings highlight coordinated activation of detoxification and secondary metabolic pathways in ginger defense and establish TGA as a promising bio-control agent against P. myriotylum.

plant biology↗

MiroSCOPE: An AI-driven digital pathology platform for annotating functional tissue units

Cancer tissue analysis in digital pathology is typically conducted across different spatial scales, ranging from high-resolution cell-level modeling to lower-resolution tile-based assessments. However, these perspectives often overlook the structural organization of functional tissue units (FTUs), the small, repeating structures which are crucial to tissue function and key factors during pathological assessment. The incorporation of FTU information is hindered by the need for detailed manual annotations, which are costly and time-consuming to obtain. While artificial intelligence (AI)-based solutions hold great promise to accelerate this process, there is currently no comprehensive workflow for building the large, annotated cohorts required. To remove these roadblocks and advance the development of more interpretable approaches, we developed MiroSCOPE, an end-to-end AI-assisted platform for annotating FTUs at scale, built on QuPath. MiroSCOPE integrates a fine-tunable multiclass segmentation model and curation-specific usability features to enable a human-in-the-loop system that accelerates AI annotation by a pathologist. The system is used to efficiently annotate over 71,900 FTUs on 184 prostate cancer hematoxylin and eosin (H&E)-stained tissue samples and demonstrates ready translation to breast cancer. Furthermore, we publicly release a dataset named Miro-120, consisting of 120 prostate cancer H&E with 30,568 annotations, which can be used by the community as a high-quality resource for FTU-level machine learning aims. In summary, MiroSCOPE provides an adaptable AI-driven platform for annotating functional tissue units, facilitating the use of structural information in digital pathology analyses.

bioinformatics↗

Inducible volatile chemical signalling drives antifungal activity of Trichoderma hamatum GD12 during confrontation with the pathogen Sclerotinia sclerotiorum

BACKGROUNDThe use of beneficial soil fungi or their natural products offers a more sustainable alternative to synthetic fungicides for pathogen management in crops. Volatile organic compounds (VOCs) produced by such fungi act as semiochemicals that inhibit pathogens, with VOC production influenced by physical interactions between competing fungi. This study explores the interaction between the beneficial soil fungus Trichoderma hamatum GD12 strain (GD12), previously shown to antagonize crop pathogens such as Sclerotinia sclerotiorum, to test the hypothesis that its antagonistic effect is mediated by volatile chemical signalling. A GD12 mutant deficient in the chitinolytic enzyme N-acetyl-{beta}-glucosaminidase ({Delta}Thnag : : hph), which shows reduced biocontrol activity, was also examined. RESULTSIn dual-culture confrontation assays, co-inoculation of GD12 and S. sclerotiorum led to fungistatic interactions after 7 days, whereas{Delta} Thnag : : hph showed no antagonism, indicating a loss of antagonistic function. VOCs collected from individual and co-cultures were analysed by gas chromatography - flame ionization detector (GC-FID) analysis and coupled GC-mass spectrometry (GC-MS), revealing significant differences in VOC production between treatments, with VOC production notably upregulated in the GD12 + S. sclerotiorum co-culture. Peak production of 6-pentyl-2H-pyran-2-one occurred 17 days post-inoculation. This upregulation was absent in the{Delta} Thnag : : hph co-culture, suggesting VOCs may drive antagonism. Synthetic VOC assays revealed several compounds inhibitory to S. sclerotiorum, including 1-octen-3-one, which also arrested the growth of key fungal pathogens (Botrytis cinerea, Pyrenopeziza brassicae, and Gaeumannomyces tritici). Structural insights into 1-octen-3-ones antifungal activity against S. sclerotiorum are also presented. CONCLUSIONSThese findings support the hypothesis that the antagonistic properties of T. hamatum GD12 against crop fungal pathogens can, in part, be attributed to VOC production. Further research is needed to assess the potential of these semiochemicals as tools for pathogen management in agriculture.

microbiology↗

Long-term editing of brain circuits in mice using an engineered electrical synapse

Electrical signaling across distinct populations of brain cells underpins cognitive and emotional function; however, approaches that selectively regulate electrical signaling between two cellular components of a mammalian neural circuit remain sparse. Here, we engineered an electrical synapse composed of two connexin proteins found in Morone americana (white perch fish) - connexin34.7 and connexin35 - to accomplish mammalian circuit modulation. By exploiting protein mutagenesis, devising a new in vitro system for assaying connexin hemichannel docking, and performing computational modeling of hemichannel interactions, we uncovered a structural motif that contributes to electrical synapse formation. Targeting these motifs, we designed connexin34.7 and connexin35 hemichannels that dock with each other to form an electrical synapse, but not with other major connexins expressed in the mammalian central nervous system. We validated this electrical synapse in vivo using C. elegans and mice, demonstrating that it can strengthen communication across neural circuits composed of pairs of distinct cell types and modify behavior accordingly. Thus, we establish Long-term integration of Circuits using connexins (LinCx) for precision circuit-editing in mammals.

neuroscience↗

Deciphering the molecular landscape of human peripheral nerves: implications for diabetic peripheral neuropathy

Diabetic peripheral neuropathy (DPN) is a prevalent complication of diabetes mellitus that is caused by metabolic toxicity to peripheral axons. We aimed to gain deep mechanistic insight into the disease process using bulk and spatial RNA sequencing on tibial and sural nerves recovered from lower leg amputations in a mostly diabetic population. First, our approach comparing mixed sensory and motor tibial and purely sensory sural nerves shows key pathway differences in affected nerves, with distinct immunological features observed in sural nerves. Second, spatial transcriptomics analysis of sural nerves reveals substantial shifts in endothelial and immune cell types associated with severe axonal loss. We also find clear evidence of neuronal gene transcript changes, like PRPH, in nerves with axonal loss suggesting perturbed RNA transport into distal sensory axons. This motivated further investigation into neuronal mRNA localization in peripheral nerve axons generating clear evidence of robust localization of mRNAs such as SCN9A and TRPV1 in human sensory axons. Our work gives new insight into the altered cellular and transcriptomic profiles in human nerves in DPN and highlights the importance of sensory axon mRNA transport as an unappreciated potential contributor to peripheral nerve degeneration.

neuroscience↗

Novel inhibitors of acute, axonal DLK palmitoylation are neuroprotective and avoid the deleterious side effects of cell-wide DLK inhibition

Dual leucine-zipper kinase (DLK) drives acute and chronic forms of neurodegeneration, suggesting that inhibiting DLK signaling could ameliorate diverse neuropathological conditions. However, direct inhibition of DLKs kinase domain in human patients and conditional knockout of DLK in mice both cause unintended side effects, including elevated plasma neurofilament levels, indicative of neuronal cytoskeletal disruption. Indeed, we found that a DLK kinase domain inhibitor acutely disrupted the axonal cytoskeleton and caused vesicle aggregation in cultured dorsal root ganglion (DRG) neurons, further cautioning against this therapeutic strategy. In seeking a more precise intervention, we found that retrograde (axon-to-soma) pro-degenerative signaling requires acute, axonal palmitoylation of DLK and hypothesized that modulating this post-translational modification might be more specifically neuroprotective than cell-wide DLK inhibition. To address this possibility, we screened >28,000 compounds using a high-content imaging assay that quantitatively evaluates DLKs palmitoylation-dependent subcellular localization. Of the 33 hits that significantly altered DLK localization in non-neuronal cells, several reduced DLK retrograde signaling and protected cultured DRG neurons from DLK-dependent neurodegeneration. Mechanistically, the two most neuroprotective compounds selectively prevent stimulus-dependent palmitoylation of axonal pools of DLK, a process crucial for DLKs recruitment to axonal vesicles. In contrast, these compounds minimally impact DLK localization and signaling in healthy neurons and avoid the cytoskeletal disruption associated with direct DLK inhibition. Importantly, our hit compounds also reduce pro-degenerative retrograde signaling in vivo, suggesting that modulating DLKs palmitoylation-dependent localization could be a novel neuroprotective strategy.

neuroscience↗

DACIT: Device for Axon - Cancer cell Interaction Testing in 2D and 3D

There is increasing interest in studying the role of peripheral innervation in tumor growth and metastasis. However, in vitro studies of interactions between cancer cells and axonal projections are technically challenging. To address this, we have developed a microfluidic Device for Axon-Cancer cell Interaction Testing in 2D and 3D (DACIT). We show that DACIT successfully separates neuronal soma from the axons and cancer cells into two compartments, which can be exposed to similar, or different growth conditions, depending on the experimental needs. We compare neoaxonogenesis using either the PC-12 cell line or primary embryonic or adult sensory neurons, demonstrating superior neurite growth in primary cells. Additionally, we show that DACIT can accommodate assessing growth and 3D invasion of tumor spheroids, due to its unique height profile. Hence, DACIT can be used to analyze cancer cell interactions with axons in most typical cell biology assays such as proliferation, invasion, and calcium activity which we demonstrate on examples of imaging transients in GCaMP6-labeled neurons, invadopodia assay, and 3D cancer spheroid invasion.

cancer biology↗

Bait, not reward: CO2-enriched Nepenthes pitchers secrete toxic nectar

Nepenthes pitchers are leaf-evolved biological traps holding high levels of CO2 within them. Extrafloral nectar (EFN) secreted by these pitchers has long been regarded as the major reward to visiting arthropods, but its chemical constituents and their role in prey capture are least explored. Here we demonstrate Nepenthes EFN as a sugar (glucose-fructose-sucrose) mix with high C:N ratio, minimal amino acids, proteins, and vitamin C. Nepenthes khasiana peristome and lid EFNs displayed strong acetylcholinesterase (AChE) inhibition; the naphthoquinone derivative, (+)-isoshinanolone, has been identified as the AChE inhibitor. Plumbagin, the major volatile naphthoquinone in Nepenthes, also showed strong AChE inhibition. Direct EFN- and (+)-isoshinanolone-feeding bioassays demonstrated symptoms of cholinergic toxicity in ants. We testify that Nepenthes EFN is a toxic bait which hinders neuronal activity in visiting arthropods. These unique traps adopt various deceptive strategies for prey capture, and our discovery abolishes the notion that Nepenthes EFN is a reward to visiting ants and other arthropods. Moreover, our findings infer elevated CO2 within their pitchers as the key factor influencing the growth, metabolism, herbivory, and carnivory in Nepenthes. HighlightNepenthes extrafloral nectar has high content of carbohydrates and minimal nitrogenous metabolites. It is laced with (+)-isoshinanolone, an acetylcholinesterase inhibitor, and acts as a toxic bait, aiding prey capture.

plant biology↗

Chemical cues from beetle larvae trigger proliferation and virulence of a plant pathogen

Agricultural crop productivity and global forest biomes are coming under increasing threat from insect pests and microbial pathogens. This impact is worsened by inter- kingdom insect-microbe interactions that can increase transmission and disease severity in affected plants. Whilst bacterial chemical cues have been shown to directly influence insect behaviour, the impact of insect-derived compounds on phytopathogens is poorly understood. Here, we investigated the chemical basis for interactions between beetle larvae and bacteria in acute oak decline (AOD), a disease characterised by inner bark necrosis and involving a polymicrobial consortium including Brenneria goodwinii and larval galleries of Agrilus biguttatus. We found that A. biguttatus larval extracts contain chemical elicitors that increase bacterial growth rate and final cell density during in vitro culture, and stimulate the differential expression of [~]600 genes, including the Type III Secretion System and its effectors, which are major virulence factors in plant pathogens. Chemical compounds from closely related insect species did not have this effect. These findings highlight the importance of inter-kingdom interactions in plant disease and suggests a novel mode-of-action for insect-derived chemical elicitors in facilitating the virulence of phytopathogens.

ecology↗

Longitudinal and multimodal auditing of tumor adaptation to CDK4/6 inhibitors in HR+ metastatic breast cancers

CDK4/6 inhibitors (CDK4/6i) have transformed the treatment of hormone receptor-positive (HR+), HER2-negative (HR+) breast cancers as they are effective across all clinicopathological, age, and ethnicity subgroups for metastatic HR+ breast cancer. In metastatic ER+ breast cancer, CDK4/6i lead to strong and consistent improvement in survival across different lines of therapy. To improve understanding of how metastatic HR+ breast cancers become refractory to CDK4/6i, we have created a multimodal and longitudinal tumor atlas to investigate therapeutic adaptations in malignant cells and in the tumor immune microenvironment. This atlas is part of the NCI Cancer Moonshot Human Tumor Atlas Network and includes seven pairs of pre- and on-progression biopsies from five metastatic HR+ breast cancer patients treated with CDK4/6i. Biopsies were profiled with bulk genomics, transcriptomics, and proteomics as well as single-cell ATAC-seq and multiplex tissue imaging for spatial, single-cell resolution. These molecular datasets were then linked with detailed clinical metadata to create an atlas for understanding tumor adaptations during therapy. Analysis of our atlas datasets suggests a diverse set of tumor adaptations to CDK4/6i therapy. Malignant cells may adapt to therapy via mTORC1 activation, cell cycle bypass, and increased replication stress. The tumor immune microenvironment displayed evidence of both immune activation and immune suppression during therapy. Together, our metastatic ER+ breast cancer atlas represents a rich multimodal resource to better understand HR+ breast cancer tumor therapeutic adaptations to CDK4/6i therapy.

cancer biology↗

Fungal Pathogen Gene Selection for Predicting the Onset of Infection Using a Multi-Stage Machine Learning Approach

Phytopathogenic fungi pose a serious threat to global food security. Next-generation sequencing technologies, such as transcriptomics, are increasingly used to profile infection, assess environmental adaptation and gauge host-responses. The accumulation of these large-scale data has created the opportunity to employ new computational methods to gain greater biological insights. Machine learning approaches, that learn to identify patterns in complex data sets, have recently been applied to the field of plant-pathogen interactions. Here, we apply a machine learning approach to transcriptomics data for the fungal pathogen Zymoseptoria tritici, to predict the onset of infection as measured by timing of the appearance of necrosis. We present a method for identifying the most important genes that predict infection timings, accurately classify isolates as early and late infectors and predict the timing of infection of novel isolates using only a subset of the data. These methods and the genes identified further demonstrate the use of these tools in the field of plant-pathogen interactions and have implications for the identification of biomarkers for disease monitoring and forecasting. Fungi that infect plants pose a serious threat to global food security. Methods to study these pathogens generate vast amounts of data that create new opportunities for computational tools to analyse them. Machine learning methods can learn patterns in complex data such as when genes are turned on or off in fungal plant pathogens. In this study we use machine learning approaches to predict the onset of infection in several isolates of an important fungal pathogen. We show that these methods can identify a small group of genes that are predictive of the infection onset. We can even use these methods on novel isolates to infer the likely timing of disease development. Our work has implications for plant disease diagnosis, monitoring and forecasting.

bioinformatics↗