Evidence map›Paper›PMID 26460183›Full record

ArticleThe Analyst2015

Detection of neuraminidase stalk motifs associated with enhanced N1 subtype influenza A virulence via Raman spectroscopy.

JooYoung Choi, Sharon J H Martin, Ralph A Tripp, S Mark Tompkins, Richard A Dluhy

Abstract read
In one paragraph

Article in The Analyst, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

JooYoung ChoiDepartment of Chemistry, University of Georgia, Athens, GA 30602, USA. dluhy@uga.edu.
Sharon J H MartinDepartment of Chemistry, University of Georgia, Athens, GA 30602, USA. dluhy@uga.edu.
Ralph A TrippDepartment of Infectious Disease, University of Georgia, Athens, GA 30602, USA.
S Mark TompkinsDepartment of Infectious Disease, University of Georgia, Athens, GA 30602, USA.
Richard A DluhyDepartment of Chemistry, University of Georgia, Athens, GA 30602, USA. dluhy@uga.edu.

Funding

Determination of Markers of High Pathogenicity in InfluenzaR01GM102546 · NIGMS · UNIVERSITY OF GEORGIA · PI DLUHY, RICHARD A. · 2012 to 2015
$1.1M
NIGMS NIH HHS GM102546NIGMS NIH HHS R01 GM102546
6 · The paper itself

Abstract

Oligonucleotides corresponding to neuraminidase (NA) stalk motifs that have been associated with enhanced influenza virulence have been identified using surface-enhanced Raman spectroscopy (SERS). 5'-Thiolated ssDNA oligonucleotides were immobilized onto a hexadecyltrimethylammonium bromide (CTAB) coated Au nanoparticles (AuNP). Three synthetic RNA sequences corresponding to specific amino acid deletions in the influenza NA stalk region were attached to the CTAB-modified AuNPs. Two of these sequences were specific to sequences with amino acid deletions associated with increased virulence, and one was a low virulence sequence with no amino acid deletions. Hybridization of synthetic matched and mismatched DNA-RNA complexes were detected based on the intrinsic SERS spectra. In addition, this platform was used to analyze RNA sequences isolated from laboratory grown influenza viruses having the NA stalk motif associated with enhanced virulence, including A/WSN/33/H1N1, A/Anhui/1/2005/H5N, and A/Vietnam/1203/2004/H5N1 strains. Multivariate feature selection methods were employed to determine the specific wavenumbers in the Raman spectra that contributed the most information for class discrimination. A one-way analysis of variance (ANOVA) test identified 884 and 1196 wavenumbers as being highly significant in the high and low virulence spectra, respectively (p < 0.01). A post-hoc Tukey Honestly Significance Difference (HSD) test identified the wavenumbers that played a major role in differentiating the DNA-RNA hybrid classes. An estimate of the spectral variability, based on the Wilcoxon rank sum test, found the major source of variation to be predominately between the different classes, and not within the classes, thus confirming that the spectra reflected real class differences and not sampling artifacts. The multivariate classification methods partial least squares discriminant analysis (PLS-DA) and support vector machine discriminant analysis (SVM-DA) were able to distinguish between different NA stalk-motifs linked to NA-enhanced influenza virus virulence (NA-EIV) with >95% sensitivity and specificity in both synthetic RNA sequences as well as the isolated viral RNA. This study demonstrates the feasibility of SERS for direct identification of influenza NA stalk mutations associated with virulence without sample amplification or labeling.

Indexed as

Amino Acid SequenceBase SequenceCetrimoniumCetrimonium CompoundsDNA ProbesGoldHumansImmobilized Nucleic AcidsInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H5N1 SubtypeInfluenza, HumanMetal NanoparticlesMutationNeuraminidaseRNA, ViralSpectrum Analysis, RamanCetrimoniumCetrimonium CompoundsDNA ProbesGoldImmobilized Nucleic AcidsNeuraminidaseRNA, Viral

Identifiers

PMID26460183
PMCPMC4687448

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.