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Biology subjects

Jacob, L.

Publications and source records attributed to Jacob, L..

At least 19 recordsLinked to original sources

Fox: Predicting rates of host-symbiont co-evolution events with association-aware attention

Motivation: Hosts and their symbionts share a history of associations in which lineages cospeciate, switch hosts, duplicate, or are lost. Quantifying the relative frequencies of these four events is a central goal of cophylogenetics, but existing tools typically require a fully resolved, correctly rooted host tree, often alongside a symbiont tree, propagating tree-inference errors into the reconciliation and scaling poorly to large systems. Results: We introduce Fox, a transformer neural network architecture that infers the relative frequencies of the four cophylogenetic events directly from a pair of host and symbiont multiple sequence alignments (MSAs) and their sequence mapping, with no tree-reconstruction or reconciliation step. Fox is trained under a simulation-based inference scheme: it learns event frequencies from alignments generated by a coevolutionary process, paying its computational cost once at training time and processing any new system in a single forward pass. On held-out data from its training simulator, Fox recovers event frequencies accurately and with near-zero bias. On additional synthetic data from an independent cophylogeny simulator, its error roughly doubled, but is still very low allowing to track the true frequencies. Most importantly, when compared to the Approximate Bayesian Computation (ABC)-based method AmoCoala on these data, it reduces mean absolute error by 45-76% for cospeciations, host switches and duplications and shows similar error for losses, while running more than three orders of magnitude faster. Applied to the empirical cockroach-Blattabacterium system, Fox recovers the expected cospeciation-dominated profile, showing that behaviour learned on simulated data transfers to real sequences. These results confirm that the coevolutionary signal usually extracted from trees can be read directly, accurately, and fast in the alignments themselves

bioinformatics↗

Teddy: neural inference of epidemiological parameters from viral sequences

Estimating how fast infections spread or how long they last is essential to control outbreaks. Phylodynamics methods enable the inference of key epidemiological pa-rameters from viral genomic data but remain limited in terms of biological realism and speed because they need to derive and compute likelihoods. We address this is-sue using simulation-based inference and introduce a deep learning-based framework directly trained on alignments of viral genetic sequences. Our neural posterior estima-tion matches the accuracy of leading Bayesian likelihood-based methods while running a thousand times faster and avoiding a phylogeny reconstruction step. This perfor-mance can be harnessed to analyze large datasets and opens new perspectives to tackle biologically realistic models in terms of pathogen life histories or genomic evolution.

genomics↗

Graph Neural Networks for Likelihood-Free Inference in Diversification Models

A common approach to infer the processes that gave rise to past speciation and extinction rates across taxa, space and time is to formulate hypotheses in the form of probabilistic diversification models and estimate their parameters from extant phylogenies using Maximum Likelihood or Bayesian inference. A drawback of this approach is that likelihoods can easily become computationally intractable, limiting our ability to extend current diversification models with new hypothesized mechanisms. Neural networks have been proposed as a likelihood-free alternative for parameter inference of stochastic models, but so far there is little experience in using this method for diversification models, and the quality of the results is likely to depend on finding the right network architecture and data representation. As phylogenies are essentially graphs, graph neural networks (GNNs) appear to be the most natural architecture but previous results on their performance are conflicting, with some studies reporting poor accuracy of GNNs in practice. Here, we show that this underperformance was likely caused by optimization issues and inappropriate pooling operations that flatten the information along the phylogeny and make it harder to extract relevant information about the diversification parameters. When equipped with PhyloPool, a new time-informed pooling procedure, GNNs show similar or better performance compared to all other architectures and data representations (including Maximum Likelihood Estimation) that we tested for two common diversification models, the Constant Rate Birth-Death and the Binary State Speciation and Extinction. We conclude that GNNs could serve as a generic tool for estimating diversification parameters of complex diversification models with intractable likelihoods.

evolutionary biology↗

Phyloformer: Fast, accurate and versatile phylogenetic reconstruction with deep neural networks

Phylogenetic inference aims at reconstructing the tree describing the evolution of a set of sequences descending from a common ancestor. The high computational cost of state-of-the-art Maximum likelihood and Bayesian inference methods limits their usability under realistic evolutionary models. Harnessing recent advances in likelihood-free inference and geometric deep learning, we introduce Phyloformer, a fast and accurate method for evolutionary distance estimation and phylogenetic reconstruction. Sampling many trees and sequences under an evolutionary model, we train the network to learn a function that enables predicting the former from the latter. Under a commonly used model of protein sequence evolution and exploiting GPU acceleration, it outpaces fast distance methods while matching maximum likelihood accuracy on simulated and empirical data. Under more complex models, some of which include dependencies between sites, it outperforms other methods. Our results pave the way for the adoption of sophisticated realistic models for phylogenetic inference.

bioinformatics↗

A conserved fertilization complex of Izumo1, Spaca6, and Tmem81 mediates sperm-egg interaction in vertebrates

Fertilization, the fusion of sperm and egg, is essential for sexual reproduction. While several proteins have been demonstrated to be essential for the binding and fusion of gametes in vertebrates, the molecular mechanisms driving this key process are poorly understood. Here, we performed a protein interaction screen using AlphaFold-Multimer to uncover protein-protein interactions in fertilization. This screen resulted in the prediction of a trimeric complex composed of the essential fertilization factors Izumo1 and Spaca6, and Tmem81, a protein previously not implicated in fertilization. We show that Tmem81 is a conserved, testis-expressed transmembrane protein that is evolutionarily related to Izumo1 and Spaca6 and is essential for male fertility in fish and mice. Consistent with trimer formation in vivo, zebrafish izumo1-/-, spaca6-/-, and tmem81-/- mutants exhibit the same sperm-egg binding defect and show co-depletion of all three proteins in sperm. Moreover, we provide experimental evidence that Izumo1, Spaca6, and Tmem81 interact in zebrafish sperm. Strikingly, the Izumo1-Spaca6 interaction is predicted to form a cleft that serves as a binding site for Bouncer, the only identified egg protein essential for fertilization in zebrafish. Together, these results provide compelling evidence for a conserved sperm factor complex in vertebrates that forms a specific interface for the sperm-egg interaction required for successful fertilization.

developmental biology↗

Simulations of sequence evolution: how (un)realistic they really are and why

MotivationSimulating Multiple Sequence Alignments (MSAs) using probabilistic models of sequence evolution plays an important role in the evaluation of phylogenetic inference tools, and is crucial to the development of novel learning-based approaches for phylogenetic reconstruction, for instance, neural networks. These models and the resulting simulated data need to be as realistic as possible to be indicative of the performance of the developed tools on empirical data and to ensure that neural networks trained on simulations perform well on empirical data. Over the years, numerous models of evolution have been published with the goal to represent as faithfully as possible the sequence evolution process and thus simulate empirical-like data. In this study, we simulated DNA and protein MSAs under increasingly complex models of evolution with and without insertion/deletion (indel) events using a state-of-the-art sequence simulator. We assessed their realism by quantifying how accurately supervised learning methods are able to predict whether a given MSA is simulated or empirical. ResultsOur results show that we can distinguish between empirical and simulated MSAs with high accuracy using two distinct and independently developed classification approaches across all tested models of sequence evolution. Our findings suggest that the current state-of-the-art models fail to accurately replicate several aspects of empirical MSAs, including site-wise rates as well as amino acid and nucleotide composition. Data and Code AvailabilityAll simulated and empirical MSAs, as well as all analysis results, are available at https://cme.h-its.org/exelixis/material/simulation_study.tar.gz. All scripts required to reproduce our results are available at https://github.com/tschuelia/SimulationStudy and https://github.com/JohannaTrost/seqsharp. Contactjulia.haag@h-its.org

bioinformatics↗

BRCA1 expression, its correlation with clinicopathological features and response to neoadjuvant chemotherapy in high grade serous ovarian cancer from an Indian centre

In high grade serous ovarian cancers (HG-SOC), BRCA1/2 mutations have been reported as the most predominant mutations by various studies. However, the non-mutational mechanisms of BRCA pathway inactivation in HG-SOC are unclear. We aimed to evaluate BRCA1 inactivation by estimating its expression along with its repressor in primary and neoadjuvant chemotherapy (NACT) treated HG-SOC tumors with known therapeutic response. The expression pattern of BRCA1 protein was evaluated by immunohistochemistry (IHC) in 119 cases of HG-SOC from a hospital cohort consisting of primary (N= 69) and NACT treated (N=50) tumors. Histological patterns (SET), stromal infiltration by lymphocytes (sTILs) and chemotherapy response score (CRS) were estimated by microscopic examination. Gene expression levels of BRCA1, and its repressor ID4 was estimated by qPCR. Association of BRCA1 protein and mRNA with clinicopathological features was studied. Relevance of the BRCA1/ID4 ratio was evaluated in tumors with different CRS. BRCA1 protein expression was observed in 12% of primary and 19% of NACT treated HG-SOC tumors. Moderate concordance was observed between BRCA1 protein and mRNA expression (AUC-0.677). High BRCA1 mRNA expression was significantly associated with more frequent SET pattern (p=0.024), higher sTILs density (p=0.042), increased mitosis (p=0.028). BRCA1 negative tumors showed higher expression of ID4 though not statistically significant. Higher BRCA1/ID4 ratio was associated with high sTILs density in primary (p=0.042) and NACT treated tumors (p=0.040). Our findings show the utility of BRCA1/ID4 ratio to predict neoadjuvant therapy response, which needs further evaluation in larger cohort with long term outcomes.

cancer biology↗

Neural Networks beyond explainability: Selective inference for sequence motifs

Over the past decade, neural networks have been successful at making predictions from biological sequences, especially in the context of regulatory genomics. As in other fields of deep learning, tools have been devised to extract features such as sequence motifs that can explain the predictions made by a trained network. Here we intend to go beyond explainable machine learning and introduce SEISM, a selective inference procedure to test the association between these extracted features and the predicted phenotype. In particular, we discuss how training a one-layer convolutional network is formally equivalent to selecting motifs maximizing some association score. We adapt existing sampling-based selective inference procedures by quantizing this selection over an infinite set to a large but finite grid. Finally, we show that sampling under a specific choice of parameters is sufficient to characterize the composite null hypothesis typically used for selective inference--a result that goes well beyond our particular framework. We illustrate the behavior of our method in terms of calibration, power and speed and discuss its power/speed trade-off with a simpler data-split strategy. SEISM paves the way to an easier analysis of neural networks used in regulatory genomics, and to more powerful methods for genome wide association studies (GWAS).

bioinformatics↗

Phyloformer: towards fast and accurate phylogeny estimation with self-attention networks

AO_SCPLOWBSTRACTC_SCPLOWAn important problem in molecular evolution is that of phylogenetic reconstruction, that is, given a set of sequences descending from a common ancestor, the reconstruction of the binary tree describing their evolution from the latter. State-of-the-art methods for the task, namely Maximum likelihood and Bayesian inference, have a high computational cost, which limits their usability on large datasets. Recently researchers have begun investigating deep learning approaches to the problem but so far these attempts have been limited to the reconstruction of quartet tree topologies, addressing phylogenetic reconstruction as a classification problem. We present here a radically different approach with a transformer-based network architecture that, given a multiple sequence alignment, predicts all the pairwise evolutionary distances between the sequences, which in turn allow us to accurately reconstruct the tree topology with standard distance-based algorithms. The architecture and its high degree of parameter sharing allow us to apply the same network to alignments of arbitrary size, both in the number of sequences and in their length. We evaluate our network Phyloformer on two types of simulations and find that its accuracy matches that of a Maximum Likelihood method on datasets that resemble training data, while being significantly faster.

evolutionary biology↗

Mycobacterium tuberculosis genetic features associated with pulmonary tuberculosis severity

Mycobacterium tuberculosis (Mtb) infections result in a wide spectrum of clinical presentations but without proven Mtb genetic determinants. Herein, 234 pulmonary tuberculosis (TB) patients were stratified according to TB disease severity and Mtb genetic features were explored using whole genome sequencing, including heterologous single nucleotide polymorphism (SNP) calling to explore micro-diversity. Clinical isolates from patients with mild TB carried mutations in genes associated with host-pathogen interaction, while those from patients with moderate/severe TB carried mutations associated with regulatory mechanisms. Genome-wide association study identified a SNP in the promoter of the gene coding for the virulence regulator EspR associated with moderate/severe disease. Structural equation modelling and model comparisons indicated that TB severity was associated with the detection of Mtb micro-diversity within clinical isolates and to the espR SNP. Taken together, these results provide a new insight to better understand TB pathophysiology and could provide new prognosis tool for pulmonary TB severity.

microbiology↗

3D-imaging reveals conserved cerebrospinal fluid drainage via meningeal lymphatic vasculature in mice and humans

Meningeal lymphatic vessels (MLVs) contribute to waste product elimination and immune surveillance in brain tissues. MLVs were identified in the dorsal and caudo-basal regions of the dura mater, where they ensure the clearance of cerebrospinal fluid (CSF). Whether MLVs exist in the complex anterior part of the murine and human skull, and how they connect with the glymphatic system and extracranial lymphatic vasculature remained unclear. Here, we generated three-dimensional (3D) maps of MLV drainage by light-sheet fluorescence microscopy (LSFM) imaging of mouse whole-head preparations following fluorescent OVA-A555 tracer injections into the CSF. In humans, we performed real-time magnetic resonance vessel wall imaging (MR-VWI) after systemic gadobutrol injections. We observed a conserved 3D-anatomy of MLVs in mice and humans, and we discovered an extended anterior network around the dural cavernous sinus including multiple capillary beds and exit routes through the foramina of emissary veins. MR-VWI may provide a diagnostic tool for patients with CSF drainage defects and neurological diseases. Short abstractWe established the 3D-anatomy of meningeal lymphatic vasculature and associated CSF drainage by postmortem light-sheet imaging in mice and by real-time magnetic resonance imaging in humans, demonstrating conserved lymphatic circuitries in contact with dural venous sinuses.

neuroscience↗

CALDERA: Finding all significant de Bruijn subgraphs for bacterial GWAS

Genome wide association studies (GWAS), aiming to find genetic variants associated with a trait, have widely been used on bacteria to identify genetic determinants of drug resistance or hypervirulence. Recent bacterial GWAS methods usually rely on k-mers, whose presence in a genome can denote variants ranging from single nucleotide polymorphisms to mobile genetic elements. Since many bacterial species include genes that are not shared among all strains, this approach avoids the reliance on a common reference genome. However, the same gene can exist in slightly different versions across different strains, leading to diluted effects when trying to detect its association to a phenotype through k-mer based GWAS. Here we propose to overcome this by testing covariates built from closed connected subgraphs of the De Bruijn graph defined over genomic k-mers. These covariates are able to capture polymorphic genes as a single entity, improving k-mer based GWAS in terms of power and interpretability. As the number of subgraphs is exponential in the number of nodes in the DBG, a method naively testing all possible subgraphs would result in very low statistical power due to multiple testing corrections, and the mere exploration of these subgraphs would quickly become computationally intractable. The concept of testable hypothesis has successfully been used to address both problems in similar contexts. We leverage this concept to test all closed connected subgraphs by proposing a novel enumeration scheme for these objects which fully exploits the pruning opportunity offered by testability, resulting in drastic improvements in computational efficiency. We illustrate this on both real and simulated datasets and also demonstrate how considering subgraphs leads to a more powerful and interpretable method. Our method integrates with existing visual tools to facilitate interpretation. We also provide an implementation of our method, as well as code to reproduce all results at https://github.com/HectorRDB/Caldera_Recomb.

genetics↗

Endothelial Unc5B controls blood-brain barrier integrity

Blood-brain barrier (BBB) integrity is critical for proper function of the central nervous system (CNS). Here, we showed that the endothelial Netrin1 receptor Unc5B controls BBB integrity by maintaining Wnt/{beta}-catenin signaling. Inducible endothelial-specific deletion of Unc5B in adult mice led to region and size-selective BBB opening. Loss of Unc5B decreased BBB Wnt/{beta}-catenin signaling, and {beta}-catenin overexpression rescued Unc5B mutant BBB defects. Mechanistically, Netrin1 enhanced Unc5B interaction with the Wnt co-receptor LRP6, induced its phosphorylation and activated Wnt/{beta}-catenin downstream signaling. Intravenous delivery of antibodies blocking Netrin1 binding to Unc5B caused a transient disruption of Wnt signaling and BBB breakdown, followed by neurovascular barrier resealing. These data identify Netrin-Unc5B signaling as a novel regulator of BBB integrity with potential therapeutic utility for CNS diseases.

cell biology↗

SLIT2-ROBO signaling in tumor-associated microglia/macrophages drives glioblastoma immunosuppression and vascular dysmorphia

SLIT2 is a secreted polypeptide that guides migration of cells expressing ROBO1&2 receptors. Herein, we investigated SLIT2/ROBO signaling effects in gliomas. In patients with glioblastoma (GBM), SLIT2 expression increased with malignant progression and correlated with poor survival and immunosuppression. Knockdown of SLIT2 in mouse glioma cells and patient derived GBM xenografts reduced tumor growth and synergized with immunotherapy to prolong survival. Tumor cell SLIT2 knockdown inhibited macrophage invasion and promoted a cytotoxic gene expression profile, which improved tumor vessel function and enhanced efficacy of chemotherapy and immunotherapy. Mechanistically, SLIT2 promoted microglia/macrophage chemotaxis and tumor-supportive polarization via ROBO1&2-mediated PI3K{gamma} activation. Macrophage Robo1&2 deletion and systemic SLIT2 trap delivery mimicked SLIT2 knockdown effects on tumor growth and the tumor microenvironment (TME), revealing SLIT2 signaling through macrophage ROBOs as a novel regulator of the GBM microenvironment and a potential immunotherapeutic target for brain tumors.

cancer biology↗

Within-host genetic micro-diversity of Mycobacterium tuberculosis and the link with tuberculosis disease features

Tuberculosis (TB), caused by Mycobacterium tuberculosis (Mtb) complex, is still the number one deadly contagious disease. Mtb infection results in a wide spectrum of clinical presentations and severity symptoms, but without proven Mtb genetic determinants. Thanks to a collection of 355 clinical isolates with associated patients clinical data, we showed that Mtb micro-diversity within patient isolates is strongly correlated with TB-associated severity scores. Interestingly, this diversity is driven by a selection pressure to adapt to different lifestyles related to the infection site. Taken together, these results provide a new insight to better understand TB pathophysiology. Furthermore, Mtb micro-diversity could be envisioned as a new prognostic tool to improve the management of TB patients.

microbiology↗

Mass Spectrometric Characterization of Narcolepsy-Associated Pandemic 2009 Influenza Vaccines.

The onset of narcolepsy, an irreversible sleep disorder, has been associated with 2009 influenza pandemic (pH1N1) infections in China, and with ASO3-adjuvanted pH1N1 vaccinations using Pandemrix in Europe. Intriguingly, however, the increased incidence was only observed following vaccination with Pandemrix but not Arepanrix in Canada. In this study, the mutational burden of actual vaccine lots of Pandemrix (n=6) and Arepanrix (n=5) sourced from Canada, and Northern Europe were characterized by mass spectrometry. The four most abundant influenza proteins across both vaccines were nucleoprotein NP, hemagglutinin HA, matrix protein M1, with the exception that Pandemrix harbored a significantly increased proportion of neuraminidase NA (7.5%) as compared to Arepanrix (2.6%). Most significantly, 17 motifs in HA, NP, and M1 harbored mutations, which significantly differed in Pandemrix versus Arepanrix. Among these, a 6-fold higher deamidation of HA146 (N to D) in Arepanrix was found relative to Pandemrix, while NP257 (T to A) and NP424 (T to I) were increased in Pandemrix. DQ0602 binding and tetramer analysis with mutated epitopes were conducted in Pandemrix-vaccinated cases versus controls but were unremarkable. Pandemrix harbored lower mutational burden than Arepanrix, indicating higher similarity to wild-type 2009 pH1N1, which could explain differences in narcolepsy susceptibility amongst the vaccines.

immunology↗

A fast and agnostic method for bacterial genome-wide association studies: bridging the gap between kmers and genetic events

MotivationGenome-wide association study (GWAS) methods applied to bacterial genomes have shown promising results for genetic marker discovery or fine-assessment of marker effect. Recently, alignment-free methods based on kmer composition have proven their ability to explore the accessory genome. However, they lead to redundant descriptions and results which are hard to interpret.\n\nMethodsHere, we introduce DBGWAS, an extended kmer-based GWAS method producing interpretable genetic variants associated with pheno-types. Relying on compacted De Bruijn graphs (cDBG), our method gathers cDBG nodes identified by the association model into subgraphs defined from their neighbourhood in the initial cDBG. DBGWAS is fast, alignment-free and only requires a set of contigs and phenotypes. It produces annotated subgraphs representing local polymorphisms as well as mobile genetic elements (MGE) and offers a graphical framework to interpret GWAS results.\n\nResultsWe validated our method using antibiotic resistance phenotypes for three bacterial species. DBGWAS recovered known resistance determinants such as mutations in core genes in Mycobacterium tuberculosis and genes acquired by horizontal transfer in Staphylococcus aureus and Pseudomonas aeruginosa - along with their MGE context. It also enabled us to formulate new hypotheses involving genetic variants not yet described in the antibiotic resistance literature.\n\nConclusionOur novel method proved its efficiency to retrieve any type of phenotype-associated genetic variant without prior knowledge. All experiments were computed in less than two hours and produced a compact set of meaningful subgraphs, thereby outperforming other GWAS approaches and facilitating the interpretation of the results.\n\nAvailabilityOpen-source tool available at https://gitlab.com/leoisl/dbgwas

bioinformatics↗

Predicting Transcription Factor Binding Sites with Convolutional Kernel Networks

The growing number of annotated biological sequences available makes it possible to learn genotype-phenotype relationships from data with increasingly high accuracy. When large quantities of labeled samples are available for training a model, convolutional neural networks can be used to predict the phenotype of unannotated sequences with good accuracy. Unfortunately, their performance with medium- or small-scale datasets is mitigated, which requires inventing new data-efficient approaches. In this paper, we introduce a hybrid approach between convolutional neural networks and kernel methods to model biological sequences. Our method enjoys the ability of convolutional neural networks to learn data representations that are adapted to a specific task, while the kernel point of view yields algorithms that perform significantly better when the amount of training data is small. We illustrate these advantages for transcription factor binding prediction and protein homology detection, and we demonstrate that our model is also simple to interpret, which is crucial for discovering predictive motifs in sequences. The source code is freely available at https://gitlab.inria.fr/dchen/CKN-seq.

bioinformatics↗