Evidence map›Paper›PMID 36409124›Full record

ArticlemBio2022

Restriction of Influenza A Virus by SERINC5.

Kin Kui Lai, James B Munro, Guoli Shi, Saliha Majdoul, Alex A Compton, Alan Rein

Open access · goldAbstract read
In one paragraph

Article in mBio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. IFITM1 and IFITM3 cooperate to restrict virus entry in endolysosomes.bioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. SERINC5 counters retroviruses and non-retroviruses.Frontiers in cellular and infection microbiology · 2024
    Review
  9. Review
  10. Review
  11. 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

6 authors at 2 institutions in 1 country.

Kin Kui LaiHIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institutegrid.48336.3a, Frederick, Maryland, USA.ORCID 0000-0003-2694-6243
James B MunroDepartment of Microbiology and Physiological Systems, UMass Chan Medical School, Worcester, Massachusetts, USA.ORCID 0000-0001-7634-4633
Guoli ShiHIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institutegrid.48336.3a, Frederick, Maryland, USA.
Saliha MajdoulHIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institutegrid.48336.3a, Frederick, Maryland, USA.
Alex A ComptonHIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institutegrid.48336.3a, Frederick, Maryland, USA.ORCID 0000-0002-7508-4953
Alan ReinHIV Dynamics and Replication Program, Center for Cancer Research, National Cancer Institutegrid.48336.3a, Frederick, Maryland, USA.ORCID 0000-0002-8273-546X
National Cancer Institute · USUniversity of Massachusetts Chan Medical School · US

Funding

Biophysical studies of viral membrane fusion proteinsR01GM143773 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MUNRO, JAMES B, SOMASUNDARAN, MOHAN · 2022 to 2025
$2.1M
NIGMS NIH HHS R01 GM143773
6 · The paper itself

Abstract

Serine incorporator 5 (Ser5), a transmembrane protein, has recently been identified as a host antiviral factor against human immunodeficiency virus (HIV)-1 and gammaretroviruses like murine leukemia viruses (MLVs). It is counteracted by HIV-1 Nef and MLV glycogag. We have investigated whether it has antiviral activity against influenza A virus (IAV), as well as retroviruses. Here, we demonstrated that Ser5 inhibited HIV-1-based pseudovirions bearing IAV hemagglutinin (HA); as expected, the Ser5 effect on this glycoprotein was antagonized by HIV-1 Nef protein. We found that Ser5 inhibited the virus-cell and cell-cell fusion of IAV, apparently by interacting with HA proteins. Most importantly, overexpressed and endogenous Ser5 inhibited infection by authentic IAV. Single-molecular fluorescent resonance energy transfer (smFRET) analysis further revealed that Ser5 both destabilized the pre-fusion conformation of IAV HA and inhibited the coiled-coil formation during membrane fusion. Ser5 is expressed in cultured small airway epithelial cells, as well as in immortal human cell lines. In summary, Ser5 is a host antiviral factor against IAV which acts by blocking HA-induced membrane fusion.

Indexed as

Influenza A virusAnimalsCell LineHemagglutininsHumansLeukemia Virus, MurineMembrane ProteinsMiceHemagglutininsMembrane ProteinsSERINC5 protein, humanhemagglutinininfluenza A virusrestrictionSERINC5virus entry

Identifiers

PMID36409124
PMCPMC9765469
OpenAlexW4309511013

What Socratic holds

Textmetadata
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 Socratic graph.