Suppr超能文献

建立并标准化基于杆状病毒表达的阿根廷正汉坦病毒核衣壳蛋白的酶联免疫吸附试验用于检测阿根廷正汉坦病毒感染

Development and standardization of an enzyme-linked inmunosorbent for the detection of orthohantavirus infection in Argentina based on its bacterial-expressed nucleocapside protein.

机构信息

Instituto Nacional de Enfermedades Virales Humanas Dr. "Julio Maiztegui ", INEVH-ANLIS, Pergamino, 2700, Argentina.

Laboratorio de Virología, Instituto de Biotecnología, Universidad Nacional de Hurlingham (UNAHUR), Hurlingham, 1688, Argentina.

出版信息

Braz J Microbiol. 2024 Sep;55(3):2683-2691. doi: 10.1007/s42770-024-01412-z. Epub 2024 Jun 14.

Abstract

We conducted a development and standardization of an IgG ELISA assay for serological detection of human orthohantavirus infections using the recombinant antigen rLECH13 produced in bacterial and derived from the LECHV. The evaluation and standardization were carried out by analyzing serum samples from a total of 50 patients with confirmed Hantavirus Pulmonary Syndrome (HPS) diagnosis through the reference technique, 50 negative sera, and 53 patients with other medical conditions. The data from the assay analysis showed a diagnostic sensitivity value of 95% and a diagnostic specificity of 80%. The high sensitivity of this novel assay leads us to conclude that rLECH13 is a feasible option for use in the immunodiagnostic of orthohantavirus infection. Additionally, it is crucial to have an antigen that can be produced under conditions that do not require highly complex laboratories. Furthermore, the new assay is cost-effective, reproducible, and demonstrates excellent performance.

摘要

我们使用从 LECHV 衍生而来的重组抗原 rLECH13 开发并标准化了一种 IgG ELISA 检测法,用于检测人类正布尼亚病毒感染的血清学。通过参考技术、50 份阴性血清和 53 份其他病症患者的血清样本,对总共 50 份经确诊的汉坦病毒肺综合征 (HPS) 患者血清样本进行了评估和标准化。该检测分析的数据显示,该检测方法的诊断灵敏度值为 95%,诊断特异性为 80%。该新型检测方法具有较高的灵敏度,这使我们得出结论,rLECH13 是用于正布尼亚病毒感染免疫诊断的一种可行选择。此外,拥有一种可在无需高度复杂实验室条件下生产的抗原至关重要。此外,新检测方法具有成本效益、可重复性,并且性能优异。

相似文献

6
Novel serological tools for detection of Thottapalayam virus, a Soricomorpha-borne hantavirus.
Arch Virol. 2012 Nov;157(11):2179-87. doi: 10.1007/s00705-012-1405-9. Epub 2012 Jul 25.
9
Hantavirus infection in Brazil: development and evaluation of an enzyme immunoassay and immunoblotting based on N recombinant protein.
Diagn Microbiol Infect Dis. 2007 May;58(1):89-97. doi: 10.1016/j.diagmicrobio.2006.11.012. Epub 2007 Mar 26.

本文引用的文献

2
Hantavirus Replication Cycle-An Updated Structural Virology Perspective.
Viruses. 2021 Aug 6;13(8):1561. doi: 10.3390/v13081561.
3
MEGA11: Molecular Evolutionary Genetics Analysis Version 11.
Mol Biol Evol. 2021 Jun 25;38(7):3022-3027. doi: 10.1093/molbev/msab120.
5
Hantaviral Proteins: Structure, Functions, and Role in Hantavirus Infection.
Front Microbiol. 2015 Nov 27;6:1326. doi: 10.3389/fmicb.2015.01326. eCollection 2015.
6
Diagnosis of hantavirus infection in humans.
Expert Rev Anti Infect Ther. 2015 Aug;13(8):939-46. doi: 10.1586/14787210.2015.1047825. Epub 2015 Jun 19.
7
Antigenic properties of N protein of hantavirus.
Viruses. 2014 Aug 13;6(8):3097-109. doi: 10.3390/v6083097.
8
Serological diagnosis with recombinant N antigen for hantavirus infection.
Virus Res. 2014 Jul 17;187:77-83. doi: 10.1016/j.virusres.2013.12.040. Epub 2014 Jan 31.
9
Hantaviruses in the americas and their role as emerging pathogens.
Viruses. 2010 Dec;2(12):2559-86. doi: 10.3390/v2122559. Epub 2010 Nov 25.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验