Evidence map›Paper›PMID 38260375›Full record

ArticlebioRxiv : the preprint server for biology2024

Neu5Gc binding loss of subtype H7 influenza A virus facilitates adaptation to gallinaceous poultry following transmission from waterbirds but restricts spillback.

Minhui Guan, Thomas J Deliberto, Aijing Feng, Jieze Zhang, Tao Li, Shuaishuai Wang, Lei Li, Mary Lea Killian, Beatriz Praena, Emily Giri and 7 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 8 institutions in 2 countries.

Minhui GuanCenter for Influenza and Emerging Infectious Diseases (CIEID), University of Missouri, Columbia, MO, USA.
Thomas J DelibertoUS Department of Agriculture Animal and Plant Health Inspection Service, Fort Collins, Colorado, USA.
Aijing FengCenter for Influenza and Emerging Infectious Diseases (CIEID), University of Missouri, Columbia, MO, USA.
Jieze ZhangDepartment of Bioengineering, Rice University, Houston, TX, 77030 USA.
Tao LiViral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Shuaishuai WangDepartment of Chemistry and Center for Diagnostics & Therapeutics, Georgia State University, Atlanta, Georgia, USA.
Lei LiDepartment of Chemistry and Center for Diagnostics & Therapeutics, Georgia State University, Atlanta, Georgia, USA.
Mary Lea KillianNational Veterinary Services Laboratories, Veterinary Services, U.S. Department of Agriculture, Ames, Iowa, USA.
Beatriz PraenaCenter for Influenza and Emerging Infectious Diseases (CIEID), University of Missouri, Columbia, MO, USA.
Emily GiriCenter for Influenza and Emerging Infectious Diseases (CIEID), University of Missouri, Columbia, MO, USA.
Shelagh T DelibertoUS Department of Agriculture Animal and Plant Health Inspection Service, Fort Collins, Colorado, USA.
Jun HangViral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.ORCID 0000-0002-6597-7045
Alicia OlivierDepartment of Pathobiology and Population Medicine, College of Veterinary Medicine, Mississippi State University, Mississippi State, Mississippi, USA.
Mia Kim TorchettiNational Veterinary Services Laboratories, Veterinary Services, U.S. Department of Agriculture, Ames, Iowa, USA.
Yizhi Jane TaoDepartment of BioSciences, Rice University, Houston, TX 77251, USA.
Colin ParrishDepartment of Microbiology and Immunology, College of Veterinary Medicine, Baker Institute for Animal Health, Cornell University, Ithaca, NY, USA.
Xiu-Feng WanCenter for Influenza and Emerging Infectious Diseases (CIEID), University of Missouri, Columbia, MO, USA.ORCID 0000-0003-2629-9234
University of Missouri · USAnimal and Plant Health Inspection Service · USGeorgia State University · USRice University · USUnited States Department of Agriculture · USWalter Reed Army Institute of Research · USCornell University · USMississippi State University · US

Funding

Use of Clinical Samples to Identify Influenza Virus Antigenic VariantsR01AI147640 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI WAN, XIUFENG HENRY · 2019 to 2024
$2.8M
Influenza host specific glycan motif identification through systems biologyR21AI144433 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI WAN, XIUFENG HENRY · 2020 to 2021
$440k
NIAID NIH HHS R01 AI147640NIAID NIH HHS R21 AI144433
6 · The paper itself

Abstract

Migratory waterfowl, gulls, and shorebirds serve as natural reservoirs for influenza A viruses, with potential spillovers to domestic poultry and humans. The intricacies of interspecies adaptation among avian species, particularly from wild birds to domestic poultry, are not fully elucidated. In this study, we investigated the molecular mechanisms underlying avian species barriers in H7 transmission, particularly the factors responsible for the disproportionate distribution of poultry infected with A/Anhui/1/2013 (AH/13)-lineage H7N9 viruses. We hypothesized that the differential expression of N-glycolylneuraminic acid (Neu5Gc) among avian species exerts selective pressure on H7 viruses, shaping their evolution and enabling them to replicate and transmit efficiently among gallinaceous poultry, particularly chickens. Our glycan microarray and biolayer interferometry experiments showed that AH/13-lineage H7N9 viruses exclusively bind to Neu5Ac, in contrast to wild waterbird H7 viruses that bind both Neu5Ac and Neu5Gc. Significantly, reverting the V179 amino acid in AH/13-lineage back to the I179, predominantly found in wild waterbirds, expanded the binding affinity of AH/13-lineage H7 viruses from exclusively Neu5Ac to both Neu5Ac and Neu5Gc. When cultivating H7 viruses in cell lines with varied Neu5Gc levels, we observed that Neu5Gc expression impairs the replication of Neu5Ac-specific H7 viruses and facilitates adaptive mutations. Conversely, Neu5Gc deficiency triggers adaptive changes in H7 viruses capable of binding to both Neu5Ac and Neu5Gc. Additionally, we assessed Neu5Gc expression in the respiratory and gastrointestinal tissues of seven avian species, including chickens, Canada geese, and various dabbling ducks. Neu5Gc was absent in chicken and Canada goose, but its expression varied in the duck species. In summary, our findings reveal the crucial role of Neu5Gc in shaping the host range and interspecies transmission of H7 viruses. This understanding of virus-host interactions is crucial for developing strategies to manage and prevent influenza virus outbreaks in diverse avian populations.

Identifiers

PMID38260375
PMCPMC10802348
OpenAlexW4390649588

What OpenQuestion holds

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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.