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来自单一存档样本的染色体连续参考基因组阐明了人类钩虫生物学及宿主-寄生虫相互作用。

Chromosome-Contiguous Reference Genome from a Single Archived Specimen Elucidates Human Hookworm Biology and Host-Parasite Interactions.

作者信息

Young Neil D, Zheng Yuanting, Sumanam Sunita B, Wang Tao, Song Jiangning, Chang Bill C H, Gasser Robin B

机构信息

Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Parkville, VIC 3010, Australia.

Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Clayton, VIC 3800, Australia.

出版信息

Int J Mol Sci. 2025 Jun 11;26(12):5576. doi: 10.3390/ijms26125576.

Abstract

Soil-transmitted helminths (STHs) are parasitic nematodes that infect humans, particularly in tropical and subtropical regions, where they contribute substantially to neglected tropical diseases (NTDs). Among them, hookworms (, and ) cause substantial morbidity, leading to anaemia, malnutrition, and developmental impairment. Despite the global impact of hookworm disease, genomic research on has lagged behind that of other hookworms, limiting comparative and molecular biological investigations. Here, we report the first chromosome-level reference genome of , assembled from a single adult specimen archived in ethanol at -20 °C for more than 27 years. Using third-generation sequencing (PacBio Revio, Menlo Park, CA, USA, Oxford Nanopore, Oxford, UK), Hi-C scaffolding, and advanced computational tools, we produced a high-quality 319 Mb genome, filling a critical gap in hookworm genomics. Comparative analyses with and the related, free-living nematode provided new insights into genome organisation, synteny, and specific adaptations. While exhibited strong chromosomal synteny with , its limited synteny with highlights its distinct parasitic adaptations. We identified 20,015 protein-coding genes, including conserved single-copy orthologues (SCOs) linked to host-pathogen interactions, immune evasion and essential biological processes. The first comprehensive secretome analysis of revealed a diverse repertoire of excretory/secretory (ES) proteins, including immunomodulatory candidates predicted to interact with host structural and immune-related proteins. This study advances hookworm genomics, establishes a basis for the sequencing of archival specimens, and provides fundamental insights into the molecular biology of . The genomic resource for this hookworm species creates new opportunities for diagnostic, therapeutic, and vaccine development within a framework. It complements recent epidemiological work and aligns with the WHO NTD roadmap (2021-2030) and Sustainable Development Goal 3.3.

摘要

土源性蠕虫(STHs)是感染人类的寄生线虫,特别是在热带和亚热带地区,它们是被忽视的热带病(NTDs)的主要病因。其中,钩虫( 、 和 )会导致严重发病,引发贫血、营养不良和发育障碍。尽管钩虫病具有全球影响,但对 的基因组研究却落后于其他钩虫,限制了比较生物学和分子生物学研究。在此,我们报告了 的首个染色体水平参考基因组,该基因组由保存在-20°C乙醇中超过27年的单个成年标本组装而成。利用第三代测序技术(美国加利福尼亚州门洛帕克的PacBio Revio、英国牛津的Oxford Nanopore)、Hi-C支架构建技术和先进的计算工具,我们生成了一个高质量的319 Mb基因组,填补了钩虫基因组学的关键空白。与 和相关的自由生活线虫 进行的比较分析,为基因组组织、同线性和特定适应性提供了新的见解。虽然 与 表现出很强的染色体同线性,但其与 的同线性有限,突出了其独特的寄生适应性。我们鉴定出20,015个蛋白质编码基因,包括与宿主-病原体相互作用、免疫逃避和基本生物学过程相关的保守单拷贝直系同源基因(SCOs)。对 的首次全面分泌蛋白组分析揭示了丰富多样的排泄/分泌(ES)蛋白,包括预测与宿主结构和免疫相关蛋白相互作用的免疫调节候选蛋白。本研究推动了钩虫基因组学的发展,为存档标本的测序奠定了基础,并为 的分子生物学提供了基本见解。该钩虫物种的基因组资源为在 框架内进行诊断、治疗和疫苗开发创造了新机会。它补充了近期的流行病学工作,并与世界卫生组织的NTD路线图(2021 - 2030年)和可持续发展目标3.3保持一致。

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