Evidence map›Paper›PMID 31963512›Full record

ArticleMicroorganisms2020

Inter- Versus Intra-Host Sequence Diversity of pH1N1 and Associated Clinical Outcomes.

Hebah A Al Khatib, Muna A Al Maslamani, Peter V Coyle, I Richard Thompson, Elmoubasher A Farag, Asmaa A Al Thani, Hadi M Yassine

Abstract read
In one paragraph

Article in Microorganisms, 2020. 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

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.

  1. Article
  2. Article
  3. Article
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.

Hebah A Al KhatibLife Science Division, College of Science and Engineering, Hamad Ben Khalifah University, Doha 34110; Qatar.
Muna A Al MaslamaniCommunicable Diseases Center, Hamad Medical Corporation, Doha 3050, Qatar.
Peter V CoyleVirology Laboratory, Hamad Medical Corporation, Doha 3050, Qatar.
I Richard ThompsonQatar Biomedical Research Institute, Hamad Ben Khalifah University, Doha 5825, Qatar.
Elmoubasher A FaragPublic Health Department, Ministry of Public Health, Doha 42, Qatar.
Asmaa A Al ThaniBiomedical Research Center, Qatar University, Doha 2713, Qatar.
Hadi M YassineBiomedical Research Center, Qatar University, Doha 2713, Qatar.ORCID 0000-0001-7592-2788

Funding

Hamad Medical Corporation‎ ‎16335/16‎Qatar University QUCG-BRC-2018/2019-1‎
6 · The paper itself

Abstract

The diversity of RNA viruses dictates their evolution in a particular host, community or environment. Here, we reported within- and between-host pH1N1virus diversity at consensus and sub-consensus levels over a three-year period (2015-2017) and its implications on disease severity. A total of 90 nasal samples positive for the pH1N1 virus were deep-sequenced and analyzed to detect low-frequency variants (LFVs) and haplotypes. Parallel evolution of LFVs was seen in the hemagglutinin (HA) gene across three scales: among patients (33%), across years (22%), and at global scale. Remarkably, investigating the emergence of LFVs at the consensus level demonstrated that within-host virus evolution recapitulates evolutionary dynamics seen at the global scale. Analysis of virus diversity at the HA haplotype level revealed the clustering of low-frequency haplotypes from early 2015 with dominant strains of 2016, indicating rapid haplotype evolution. Haplotype sharing was also noticed in all years, strongly suggesting haplotype transmission among patients infected during a specific influenza season. Finally, more than half of patients with severe symptoms harbored a larger number of haplotypes, mostly in patients under the age of five. Therefore, patient age, haplotype diversity, and the presence of certain LFVs should be considered when interpreting illness severity. In addition to its importance in understanding virus evolution, sub-consensus virus diversity together with whole genome sequencing is essential to explain variabilities in clinical outcomes that cannot be explained by either analysis alone.

Indexed as

deep sequencing technologyhaplotype reconstruction.inter-host diversityintra-host diversitylow-frequency variantvirus diversity

Identifiers

PMID31963512
PMCPMC7022955

What OpenQuestion holds

Textmetadata
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.