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Biology subjects

Bals, J.

Publications and source records attributed to Bals, J..

3 recordsLinked to original sources

Transformer-Based Phenotyping of Rice Root Aerenchyma Across Environments Enables Climate-Smart Rice Selection

Quantification of root anatomical traits such as cortical aerenchyma is key to understanding rice adaptation to diverse water regimes. Recently, the role of aerenchyma in regulating methane emissions has been demonstrated, making it a target for climate change mitigation. Despite its importance, breeding for root anatomical traits remains limited because manual analysis of root cross-sections is labor-intensive, inconsistent, and poorly scalable, and analysis pipelines do not generalize across heterogeneous imaging conditions. We present a deep learning pipeline based on a recent vision transformer architecture to automatically segment rice root anatomical structures and quantify aerenchyma. The model was trained on a multi-environment dataset of 1,760 annotated rice root cross-sections acquired across growth stages, cultivation systems, and countries, using a collaboratively defined annotation protocol. The model achieved high segmentation performance (mean Intersection-over-Union > 0.92) and near-perfect aerenchyma ratio quantification (R2 = 0.98), and was evaluated by two experts as performing on par with, and in some cases better than, expert annotators. Delivered as open-source software with an online interactive demonstrator, the pipeline revealed differences in aerenchyma across genotypes, water regimes, environments, and developmental stages. Overall, this work demonstrates that transformer-based segmentation enables high-throughput anatomical phenotyping, supporting scalable and climate-smart rice breeding. HIGHLIGHTSO_LITransformer-based segmentation enables robust aerenchyma phenotyping across environments C_LIO_LIA SegFormer model achieves expert-level accuracy on diverse rice root cross-sections C_LIO_LIAutomated analysis delivers near-perfect lacuna-to-cortex ratio quantification (R2 {approx} 0.98) C_LIO_LIOur online demonstrator supports scalable, climate-smart rice breeding applications C_LI

physiology↗

HCF101 is a novel component of the CIA cytosolic iron-sulfur synthesis pathway in the human pathogen Toxoplasma gondii

Several key cellular functions depend on proteins harboring an iron-sulfur (Fe-S) cofactor. As these Fe-S proteins localize to several subcellular compartments, they require a dedicated machinery for cofactor assembly. For instance, in plants and algae there are Fe-S cluster synthesis pathways localizing to the cytosol, but also present in the mitochondrion and in the chloroplast, two organelles of endosymbiotic origin. Toxoplasma gondii is a plastid-bearing parasitic protist responsible for a pathology affecting humans and other warm-blooded vertebrates. We have characterized the Toxoplasma homologue of HCF101, originally identified in plants as a protein transferring Fe-S clusters to photosystem I subunits in the chloroplast. Contrarily to plants, we have shown that HCF101 does not localize to the plastid in parasites, but instead is an important component of the cytosolic Fe-S assembly (CIA) pathway which is vital for Toxoplasma. While the CIA pathway is widely conserved in eukaryotes, it is the first time the involvement of HCF101 in this pan-eukaryotic machinery is established. Moreover, as this protein is essential for parasite viability and absent from its mammalian hosts, it constitutes a novel and promising potential drug target.

microbiology↗

Naive human B cells can neutralize SARS-CoV-2 through recognition of its receptor binding domain

Exposure to a pathogen elicits an adaptive immune response aimed to control and eradicate. Interrogating the abundance and specificity of the naive B cell repertoire contributes to understanding how to potentially elicit protective responses. Here, we isolated naive B cells from 8 seronegative human donors targeting the SARS-CoV-2 receptor-binding domain (RBD). Single B cell analysis showed diverse gene usage with no restricted complementarity determining region lengths. We show that recombinant antibodies engage SARS-CoV-2 RBD, circulating variants, and pre-emergent coronaviruses. Representative antibodies signal in a B cell activation assay and can be affinity matured through directed evolution. Structural analysis of a naive antibody in complex with spike shows a conserved mode of recognition shared with infection-induced antibodies. Lastly, both naive and affinity-matured antibodies can neutralize SARS-CoV-2. Understanding the naive repertoire may inform potential responses recognizing variants or emerging coronaviruses enabling the development of pan-coronavirus vaccines aimed at engaging germline responses. One Sentence SummaryIsolation of antibody germline precursors targeting the receptor binding domain of coronaviruses.

immunology↗