Evidence map›Paper›PMID 38139214›Full record

ArticleInternational journal of molecular sciences2023

The Effect of Mice Adaptation Process on the Pathogenicity of Influenza A/South Africa/3626/2013 (H1N1)pdm09 Model Strain.

Mohammad Al Farroukh, Irina Kiseleva, Ekaterina Stepanova, Ekaterina Bazhenova, Elena Krutikova, Artem Tkachev, Anna Chistyakova, Andrey Rekstin, Ludmila Puchkova, Larisa Rudenko

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 68% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. 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

10 authors at 2 institutions in 1 country.

Mohammad Al FarroukhFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
Irina KiselevaFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.ORCID 0000-0002-3892-9873
Ekaterina StepanovaFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.ORCID 0000-0002-8670-8645
Ekaterina BazhenovaFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.ORCID 0000-0003-3280-556X
Elena KrutikovaFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
Artem TkachevInstitute of Biomedical Systems and Biotechnology, Peter the Great St. Petersburg Polytechnic University, St. Petersburg 194021, Russia.
Anna ChistyakovaFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.ORCID 0000-0001-9541-5636
Andrey RekstinFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
Ludmila PuchkovaFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.ORCID 0000-0003-0958-2812
Larisa RudenkoFederal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
Institute of Experimental Medicine · RUPeter the Great St. Petersburg Polytechnic University · RU

Funding

Institute of Experimental Medicine 122020300200-8
6 · The paper itself

Abstract

Influenza virus strain A/South Africa/3626/2013 (H1N1)pdm09 (SA-WT) is a non-mouse-adapted model strain that has naturally high pathogenic properties in mice. It has been suggested that the high pathogenicity of this strain for mice could be due to the three strain-specific substitutions in the polymerase complex (Q687R in PB1, N102T in PB2, and E358E/K heterogeneity in PB2). To evaluate the role of these replacements, SA-WT was passaged five times in mouse lungs, and the genome of the mouse-adapted version of the SA-WT strain (SA-M5) was sequenced. SA-M5 lost E358E/K heterogeneity and retained E358, which is the prevalent amino acid at this position among H1N1pdm09 strains. In addition, in the hemagglutinin of SA-M5, two heterogeneous substitutions (G155G/E and S190S/R) were identified. Both viruses, SA-M5 and SA-WT, were compared for their toxicity, ability to replicate, pathogenicity, and immunogenicity in mice. In mice infected with SA-M5 or SA-WT strains, toxicity, virus titer in pulmonary homogenates, and mouse survival did not differ significantly. In contrast, an increase in the immunogenicity of SA-M5 compared to SA-WT was observed. This increase could be due to the substitutions G155G/E and S190S/R in the HA of SA-M5. The prospects for using SA-M5 in studying the immunogenicity mechanisms were also discussed.

Indexed as

Influenza A Virus, H1N1 SubtypeInfluenza, HumanHemagglutinin Glycoproteins, Influenza VirusHumansPhylogenyVirulenceHemagglutinin Glycoproteins, Influenza VirusA/South Africa/3626/2013 (H1N1)pdm09H1N1pdm09 model strainimmunogenicityinfluenza A virusmutations in polymerase complex and hemagglutininpathogenicitytoxicity

Identifiers

PMID38139214
PMCPMC10743444
OpenAlexW4389618085

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.