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免疫表位的自然变异揭示了细菌内拮抗作用。

Natural variation of immune epitopes reveals intrabacterial antagonism.

作者信息

Stevens Danielle M, Moreno-Pérez Alba, Weisberg Alexandra J, Ramsing Charis, Fliegmann Judith, Zhang Ning, Madrigal Melanie, Martin Gregory, Steinbrenner Adam, Felix Georg, Coaker Gitta

机构信息

Integrative Genetics and Genomics Graduate Group, University of California, Davis, Davis CA 95616, USA.

Department of Plant Pathology, University of California, Davis, Davis CA 95616, USA.

出版信息

bioRxiv. 2024 Mar 1:2023.09.21.558511. doi: 10.1101/2023.09.21.558511.

Abstract

Plants and animals detect biomolecules termed Microbe-Associated Molecular Patterns (MAMPs) and induce immunity. Agricultural production is severely impacted by pathogens which can be controlled by transferring immune receptors. However, most studies use a single MAMP epitope and the impact of diverse multi-copy MAMPs on immune induction is unknown. Here we characterized the epitope landscape from five proteinaceous MAMPs across 4,228 plant-associated bacterial genomes. Despite the diversity sampled, natural variation was constrained and experimentally testable. Immune perception in both and tomato depended on both epitope sequence and copy number variation. For example, Elongation Factor Tu is predominantly single copy and 92% of its epitopes are immunogenic. Conversely, 99.9% of bacterial genomes contain multiple Cold Shock Proteins and 46% carry a non-immunogenic form. We uncovered a new mechanism for immune evasion, intrabacterial antagonism, where a non-immunogenic Cold Shock Protein blocks perception of immunogenic forms encoded in the same genome. These data will lay the foundation for immune receptor deployment and engineering based on natural variation.

摘要

植物和动物能够检测被称为微生物相关分子模式(MAMPs)的生物分子并诱导免疫反应。农业生产受到病原体的严重影响,而通过转移免疫受体可以控制这些病原体。然而,大多数研究仅使用单一的MAMP表位,不同多拷贝MAMPs对免疫诱导的影响尚不清楚。在此,我们对4228个植物相关细菌基因组中的五种蛋白质类MAMPs的表位图谱进行了表征。尽管样本具有多样性,但自然变异受到限制且可通过实验进行测试。在本氏烟草和番茄中的免疫识别均取决于表位序列和拷贝数变异。例如,延伸因子Tu主要为单拷贝,其92%的表位具有免疫原性。相反,99.9%的细菌基因组含有多个冷休克蛋白,46%携带非免疫原性形式。我们发现了一种新的免疫逃避机制——细菌内拮抗作用,即非免疫原性冷休克蛋白会阻断对同一基因组中编码的免疫原性形式的识别。这些数据将为基于自然变异的免疫受体部署和工程改造奠定基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b983/10913959/d1d352f8b24b/nihpp-2023.09.21.558511v2-f0001.jpg

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