Evidence map›Paper›PMID 27186639›Full record

ArticlePloS one2016

In-Depth Analysis of HA and NS1 Genes in A(H1N1)pdm09 Infected Patients.

Claudia Caglioti, Marina Selleri, Gabriella Rozera, Emanuela Giombini, Paola Zaccaro, Maria Beatrice Valli, Maria Rosaria Capobianchi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. 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
0.2field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Claudia CagliotiLaboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", I.R.C.C.S., Rome, Italy.
Marina SelleriLaboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", I.R.C.C.S., Rome, Italy.
Gabriella RozeraLaboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", I.R.C.C.S., Rome, Italy.
Emanuela GiombiniLaboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", I.R.C.C.S., Rome, Italy.
Paola ZaccaroLaboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", I.R.C.C.S., Rome, Italy.
Maria Beatrice ValliLaboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", I.R.C.C.S., Rome, Italy.
Maria Rosaria CapobianchiLaboratory of Virology, National Institute for Infectious Diseases "L. Spallanzani", I.R.C.C.S., Rome, Italy.
Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In March/April 2009, a new pandemic influenza A virus (A(H1N1)pdm09) emerged and spread rapidly via human-to-human transmission, giving rise to the first pandemic of the 21th century. Influenza virus may be present in the infected host as a mixture of variants, referred to as quasi-species, on which natural and immune-driven selection operates. Since hemagglutinin (HA) and non-structural 1 (NS1) proteins are relevant in respect of adaptive and innate immune responses, the present study was aimed at establishing the intra-host genetic heterogeneity of HA and NS1 genes, applying ultra-deep pyrosequencing (UDPS) to nasopharyngeal swabs (NPS) from patients with confirmed influenza A(H1N1)pdm09 infection. The intra-patient nucleotide diversity of HA was significantly higher than that of NS1 (median (IQR): 37.9 (32.8-42.3) X 10(-4) vs 30.6 (27.4-33.6) X 10(-4) substitutions/site, p = 0.024); no significant correlation for nucleotide diversity of NS1 and HA was observed (r = 0.319, p = 0.29). Furthermore, a strong inverse correlation between nucleotide diversity of NS1 and viral load was observed (r = - 0.74, p = 0.004). For both HA and NS1, the variants appeared scattered along the genes, thus indicating no privileged mutation site. Known polymorphisms, S203T (HA) and I123V (NS1), were observed as dominant variants (>98%) in almost all patients; three HA and two NS1 further variants were observed at frequency >40%; a number of additional variants were detected at frequency <6% (minority variants), of which three HA and four NS1 variants were novel. In few patients multiple variants were observed at HA residues 203 and 222. According to the FLUSURVER tool, some of these variants may affect immune recognition and host range; however, these inferences are based on H5N1, and their extension to A(H1N1)pdm09 requires caution. More studies are necessary to address the significance of the composite nature of influenza virus quasi-species within infected patients.

Indexed as

AdolescentAdultAgedFemaleGenes, ViralGenetic VariationHemagglutinin Glycoproteins, Influenza VirusHumansInfluenza A Virus, H1N1 SubtypeInfluenza, HumanMaleMiddle AgedRNA, ViralSequence Analysis, RNAViral Nonstructural ProteinsYoung AdultH1N1 virus hemagglutininHemagglutinin Glycoproteins, Influenza VirusINS1 protein, influenza virusRNA, ViralViral Nonstructural Proteins

Identifiers

PMID27186639
PMCPMC4871468
OpenAlexW2403360770

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.