Evidence map›Paper›PMID 39471134›Full record

ArticlePloS one2024

Genetic and pathogenic potential of highly pathogenic avian influenza H5N8 viruses from live bird markets in Egypt in avian and mammalian models.

Yassmin Moatasim, Basma Emad Aboulhoda, Mokhtar Gomaa, Ahmed El Taweel, Omnia Kutkat, Mina Nabil Kamel, Mohamed El Sayes, Mohamed GabAllah, Amany Elkhrsawy, Hend AbdAllah and 4 more

Abstract read
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Article in PloS one, 2024. 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

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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.

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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

14 authors.

Yassmin MoatasimCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Basma Emad AboulhodaDepartment of Anatomy and Embryology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Mokhtar GomaaCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Ahmed El TaweelCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Omnia KutkatCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Mina Nabil KamelCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Mohamed El SayesCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Mohamed GabAllahCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Amany ElkhrsawyCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Hend AbdAllahDepartment of Anatomy and Embryology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Ahmed KandeilCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.ORCID 0000-0003-3253-6961
Mohamed Ahmed AliCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.
Ghazi KayaliHuman Link DMCC, Dubai, United Arab Emirates.ORCID 0000-0002-5387-1622
Rabeh El-SheshenyCenter of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt.ORCID 0000-0002-8798-2240

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since its first isolation from migratory birds in Egypt in 2016, highly pathogenic avian influenza (HPAI) H5N8 has caused several outbreaks among domestic poultry in various areas of the country affecting poultry health and production systems. However, the genetic and biological properties of the H5N8 HPAI viruses have not been fully elucidated yet. In this study, we aimed to monitor the evolution of circulating H5N8 viruses and identify the pathogenicity and mammalian adaptation in vitro and in vivo. Three H5N8 HPAI viruses were used in this study and were isolated in 2021-2022 from poultry and wild birds during our routine surveillance. RNA extracts were subjected to full genome sequencing. Genetic, phylogenetic, and antigenic analyses were performed to assess viral characteristics and similarities to previously isolated viruses. Phylogenetic analysis showed that the hemagglutinin genes of the three isolates belonged to clade 2.3.4.4b and grouped with the 2019 viruses from G3 with high similarity to Russian and European lineages. Multiple basic amino acids were observed at cleavage sites in the hemagglutinin proteins of the H5N8 isolates, indicating high pathogenicity. In addition, several mutations associated with increased virulence and polymerase activity in mammals were observed. Growth kinetics assays showed that the H5N8 isolate is capable of replicating efficiently in mammalian cells lines. In vivo studies were conducted in SPF chickens (White Leghorn), mice, and hamsters to compare the virological characteristics of the 2022 H5N8 isolates with previous H5N8 viruses isolated in 2016 from the first introduction. The H5N8 viruses caused lethal infection in all tested chickens and transmitted by direct contact. However, we showed that the 2016 H5N8 virus causes a higher mortality in chickens compared to 2022 H5N8 virus. Moreover, the 2022 virus can replicate efficiently in hamsters and mice without preadaptation causing systemic infection. These findings underscore the need for continued surveillance of H5 viruses to identify circulating strains, determine the commercial vaccine's effectiveness, and identify zoonotic potential.

Indexed as

Influenza A Virus, H5N8 SubtypeInfluenza in BirdsPhylogenyAnimalsBirdsChickensDogsEgyptMadin Darby Canine Kidney CellsMicePoultryPoultry DiseasesVirulence

Identifiers

PMID39471134
PMCPMC11521303

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LicenceCC BY
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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.