Evidence map›Paper›PMID 38288510›Full record

ArticleInfluenza and other respiratory viruses2024

Genome characterization of influenza A and B viruses in New South Wales, Australia, in 2019: A retrospective study using high-throughput whole genome sequencing.

Xinye Wang, Ki Wook Kim, Gregory Walker, Sacha Stelzer-Braid, Matthew Scotch, William D Rawlinson

Open access · goldAbstract read
In one paragraph

Article in Influenza and other respiratory viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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  5. Improved influenza A whole-genome sequencing protocol.Frontiers in cellular and infection microbiology · 2024
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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

6 authors at 2 institutions in 2 countries.

Xinye WangSchool of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.ORCID 0000-0003-2703-5505
Ki Wook KimVirology Research Laboratory, Serology and Virology Division (SAViD), NSW Health Pathology Prince of Wales Hospital Sydney New South Wales Australia.
Gregory WalkerSchool of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.
Sacha Stelzer-BraidSchool of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.
Matthew ScotchBiodesign Center for Environmental Health Engineering, Biodesign Institute Arizona State University Phoenix Arizona USA.ORCID 0000-0001-5100-9724
William D RawlinsonSchool of Biomedical Sciences, Faculty of Medicine and Health University of New South Wales Sydney New South Wales Australia.
New South Wales Department of Health · AUCenter for Environmental Health · US

Funding

Juvenile Diabetes Research Foundation (JDRF) Career Development Award 5-CDA-2023-1332-S-BUniversity of New South Wales
6 · The paper itself

Abstract

backgroundDuring the 2019 severe influenza season, New South Wales (NSW) experienced the highest number of cases in Australia. This study retrospectively investigated the genetic characteristics of influenza viruses circulating in NSW in 2019 and identified genetic markers related to antiviral resistance and potential virulence.

methodsThe complete genomes of influenza A and B viruses were amplified using reverse transcription-polymerase chain reaction (PCR) and sequenced with an Illumina MiSeq platform.

resultsWhen comparing the sequencing data with the vaccine strains and reference sequences, the phylogenetic analysis revealed that most NSW A/H3N2 viruses (n = 68; 94%) belonged to 3C.2a1b and a minority (n = 4; 6%) belonged to 3C.3a. These viruses all diverged from the vaccine strain A/Switzerland/8060/2017. All A/H1N1pdm09 viruses (n = 20) showed genetic dissimilarity from vaccine strain A/Michigan/45/2015, with subclades 6B.1A.5 and 6B.1A.2 identified. All B/Victoria-lineage viruses (n = 21) aligned with clade V1A.3, presenting triple amino acid deletions at positions 162-164 in the hemagglutinin protein, significantly diverging from the vaccine strain B/Colorado/06/2017. Multiple amino acid substitutions were also found in the internal proteins of influenza viruses, some of which have been previously reported in hospitalized influenza patients in Thailand. Notably, the oseltamivir-resistant marker H275Y was present in one immunocompromised patient infected with A/H1N1pdm09 and the resistance-related mutation I222V was detected in another A/H3N2-infected patient.

conclusionsConsidering antigenic drift and the constant evolution of circulating A and B strains, we believe continuous monitoring of influenza viruses in NSW via the high-throughput sequencing approach provides timely and pivotal information for both public health surveillance and clinical treatment.

Indexed as

Herpesvirus 1, CercopithecineInfluenza, HumanInfluenza VaccinesAustraliaHemagglutinin Glycoproteins, Influenza VirusHumansInfluenza A Virus, H3N2 SubtypeNew South WalesPhylogenyRetrospective StudiesSeasonsWhole Genome SequencingHemagglutinin Glycoproteins, Influenza VirusInfluenza Vaccinesdrug resistance, viralhigh-throughput nucleotide sequencinginfluenza, humanNew South Wales

Identifiers

PMID38288510
PMCPMC10824601
OpenAlexW4391328552

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.