Determination of Markers of High Pathogenicity in Influenza

流感高致病性标志物的测定

• 批准号: 8534207
• 负责人: RICHARD A. DLUHY
• 金额: $ 27.23万
• 依托单位: UNIVERSITY OF GEORGIA
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-09-01 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8534207
• 关键词: Address; Affect; Amino Acids; Avian Influenza; Biochemical Markers; Biological; Biological Assay; Biological Markers; Biosensing Techniques; Cessation of life; Clinical; DNA Viruses; Deposition; Detection; Development; Diagnosis; Diagnostic; Electromagnetic Fields; Epidemic; Exhibits; Foundations; Future; Genes; Genotype; Goals; Health Professional; Hong Kong; Human; Infection; Influenza; Influenza A Virus, H5N1 Subtype; Influenza A virus; Label; Laboratories; Methods; Molecular Profiling; Molecular Virology; Mutate; Mutation; Nanotechnology; Oligonucleotides; Optical Methods; Pathogenicity; Proteins; Public Health; Publishing; RNA; RNA Viruses; Raman Spectrum Analysis; Recombinants; Research; Research Personnel; Research Project Grants; Risk Assessment; Sampling; Serotyping; Spectrum Analysis; Surface; Techniques; Technology; Virulence; Virulence Factors; Virulent; Virus; Virus Diseases; Work; base; clinical application; expectation; high risk; improved; influenza outbreak; influenza virulence; influenzavirus; innovation; mortality; nano; nanofabrication; nanorod; new technology; novel; pandemic disease; pandemic influenza; pathogen; prevent; screening; seasonal influenza; tool; vapor; viral DNA; viral detection

DESCRIPTION (provided by applicant): Specific mutated proteins in influenza A may be important diagnostic markers related to the virulence of pandemic strains. Analysis of the PB1-F2 sequence identified a single mutation (N66S) that was conserved for both the Hong Kong 1997 H5N1 highly pathogenic influenza as well as the 1918 pandemic strain. Additional studies have demonstrated that the NA stalk region of N1 influenza A viruses also affects virulence. The ability to rapidly screen for these, and other yet-to-be- discovered virulence factors, would significantly improve our ability to identify emerging strains with risk of high mortality, and allw public health professionals to effectively respond to prevent widespread infection and/or death. Unfortunately, a rapid, multiplexed method to screen for virulence factors does not exist. Recent research in our laboratories has demonstrated that a nanofabrication technique based on vapor deposition produces Ag nanorod arrays that exhibit extremely high electromagnetic field enhancements when they are used as surface-enhanced Raman spectroscopy (SERS) substrates. Our initial results suggest that these novel SERS substrates can be used as diagnostic tools to rapidly and sensitively detect the Raman spectra of RNA and DNA viruses. SERS spectra effectively act as molecular fingerprints that provide specific and quantitative information about the target. Using this method, we have shown that differentiation is possible between virus strains, serotypes, genotypes and oligonucleotides based solely on their intrinsic SERS spectra. The long-term goal of this research project is to develop a rapid, sensitive, and specific multiplexed method to detect and quantify influenza virulence factors. The objective of the current proposal is to develop an oligonucleotide-based capture array to detect influenza RNA, thus allowing for virulence assessment, without amplification or labeling. This research will provide the scientific foundation for development of new screening methods that are critically needed for risk assessment in human influenza infections. The project will: 1)develop a hybridization strategy for virulence factors using synthetic oligonucleotides, 2) identify the virulent-associated PB1-F2 mutation in laboratory viruses, 3) identify the virulent- associated NA stalk motif in laboratory viruses, and 4) validate the SERS-based assay for influenza virulence factors in clinical samples. The innovative aspect of this proposal lies in the development of a novel nanofabrication method to produce a high sensitivity, rapid and reproducible platform technology for detection of influenza virulence factors, a capability that does not currently exist The proposal will take advantage of a well-defined SERS substrate platform, proven SERS sensing technology, and the integrated expertise of physical and biological investigators. At the conclusion of this project, it is our expectation that we will have developed and validated a nano-optical method for use as a powerful tool to detect influenza virulence factors. This project will ultimately demonstrate that bio-nanotechnology combined with vibrational spectroscopy has the ability to enhance detection and diagnosis of emerging viral infections with clinical applications.

描述（由申请方提供）：甲型流感病毒中的特异性突变蛋白可能是与大流行毒株毒力相关的重要诊断标志物。对PB 1-F2序列的分析鉴定了一个单一突变（N66 S），该突变在香港1997年H5 N1高致病性流感和1918年大流行毒株中都是保守的。其他研究表明，N1甲型流感病毒的NA茎区也影响毒力。快速筛选这些和其他尚未发现的毒力因子的能力将显著提高我们识别具有高死亡率风险的新菌株的能力，并使公共卫生专业人员能够有效应对以防止广泛感染和/或死亡。不幸的是，一个快速，多重筛选毒力因子的方法并不存在。我们实验室最近的研究表明，基于气相沉积的纳米纤维技术产生的Ag纳米棒阵列，当它们用作表面增强拉曼光谱（Sers）基底时，表现出极高的电磁场增强。我们的初步结果表明，这些新的Sers基板可以用作诊断工具，快速，灵敏地检测RNA和DNA病毒的拉曼光谱。Sers光谱有效地充当分子指纹，提供关于目标的特定和定量信息。使用这种方法，我们已经表明，区分是可能的病毒株，血清型，基因型和寡核苷酸的基础上，仅根据其固有的Sers光谱。本研究项目的长期目标是开发一种快速、灵敏和特异的多重方法来检测和定量流感毒力因子。本提案的目的是开发一种基于阿托伐他汀的捕获阵列，用于检测流感RNA，从而无需扩增或标记即可进行毒力评估。这项研究将为开发人类流感感染风险评估所急需的新筛查方法提供科学基础。该项目将：1）使用合成寡核苷酸开发毒力因子的杂交策略，2）鉴定实验室病毒中的毒力相关的PB 1-F2突变，3）鉴定实验室病毒中的毒力相关的NA茎基序，以及4）验证临床样品中流感毒力因子的基于SERS的测定。该提案的创新之处在于开发一种新型的纳米芯片方法，以产生用于检测流感毒力因子的高灵敏度，快速和可重复的平台技术，该提案将利用定义明确的Sers基底平台，经过验证的Sers传感技术以及物理和生物研究人员的综合专业知识。在这个项目的结论，这是我们的期望，我们将开发和验证纳米光学方法作为一个强大的工具来检测流感毒力因子。该项目将最终证明，生物纳米技术与振动光谱学相结合，有能力提高检测和诊断新出现的病毒感染与临床应用。