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探索与急性发热疾病和不明原因严重神经疾病相关的微生物:一种纳米孔宏基因组学方法。

Exploring Microorganisms Associated to Acute Febrile Illness and Severe Neurological Disorders of Unknown Origin: A Nanopore Metagenomics Approach.

机构信息

Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte 31270-901, Brazil.

Eduardo de Menezes Hospital, Belo Horizonte 30622-020, Brazil.

出版信息

Genes (Basel). 2024 Jul 15;15(7):922. doi: 10.3390/genes15070922.

Abstract

Acute febrile illness (AFI) and severe neurological disorders (SNDs) often present diagnostic challenges due to their potential origins from a wide range of infectious agents. Nanopore metagenomics is emerging as a powerful tool for identifying the microorganisms potentially responsible for these undiagnosed clinical cases. In this study, we aim to shed light on the etiological agents underlying AFI and SND cases that conventional diagnostic methods have not been able to fully elucidate. Our approach involved analyzing samples from fourteen hospitalized patients using a comprehensive nanopore metagenomic approach. This process included RNA extraction and enrichment using the SMART-9N protocol, followed by nanopore sequencing. Subsequent steps involved quality control, host DNA/cDNA removal, de novo genome assembly, and taxonomic classification. Our findings in AFI cases revealed a spectrum of disease-associated microbes, including , sp., Human Immunodeficiency Virus 1 (Subtype B), and Human Pegivirus. Similarly, SND cases revealed the presence of pathogens such as , sp., and Dengue virus type 2 (Genotype-II lineage). This study employed a metagenomic analysis method, demonstrating its efficiency and adaptability in pathogen identification. Our investigation successfully identified pathogens likely associated with AFI and SNDs, underscoring the feasibility of retrieving near-complete genomes from RNA viruses. These findings offer promising prospects for advancing our understanding and control of infectious diseases, by facilitating detailed genomic analysis which is critical for developing targeted interventions and therapeutic strategies.

摘要

急性发热性疾病(AFI)和严重神经障碍(SND)常因潜在的多种感染源而导致诊断困难。纳米孔宏基因组学作为一种强大的工具,可用于识别可能导致这些未确诊临床病例的微生物。在这项研究中,我们旨在阐明常规诊断方法未能充分阐明的 AFI 和 SND 病例的病因。我们的方法包括使用综合纳米孔宏基因组学方法分析 14 名住院患者的样本。该过程包括使用 SMART-9N 方案进行 RNA 提取和富集,然后进行纳米孔测序。后续步骤包括质量控制、宿主 DNA/cDNA 去除、从头基因组组装和分类学分类。我们在 AFI 病例中的发现揭示了一系列与疾病相关的微生物,包括, sp.,人类免疫缺陷病毒 1(亚型 B)和人类 Pegivirus。同样,SND 病例中也发现了病原体的存在,如, sp.和登革热病毒 2(基因型-II 谱系)。本研究采用了宏基因组分析方法,证明了其在病原体鉴定中的效率和适应性。我们的调查成功地确定了可能与 AFI 和 SND 相关的病原体,这突出了从 RNA 病毒中获取近乎完整基因组的可行性。这些发现为深入了解和控制传染病提供了有前景的前景,通过促进关键的靶向干预和治疗策略的详细基因组分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc3e/11276239/fab9fbe3db88/genes-15-00922-g001.jpg

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