Evidence map›Paper›PMID 35917402›Full record

ArticleClinical and translational medicine2022

Screening of cell-virus, cell-cell, gene-gene crosstalk among animal kingdom at single cell resolution.

Dongsheng Chen, Zhihua Ou, Jiacheng Zhu, Haoyu Wang, Peiwen Ding, Lihua Luo, Xiangning Ding, Chengcheng Sun, Tianming Lan, Sunil Kumar Sahu and 26 more

Abstract read
In one paragraph

Article in Clinical and translational medicine, 2022. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Mapping Cell Atlases at the Single-Cell Level.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  4. Article
  5. 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

36 authors.

Dongsheng ChenBGI-Shenzhen, Shenzhen, China.ORCID https://orcid.org/0000-0003-2400-0315
Zhihua OuBGI-Shenzhen, Shenzhen, China.
Jiacheng ZhuBGI-Shenzhen, Shenzhen, China.
Haoyu WangBGI-Shenzhen, Shenzhen, China.
Peiwen DingBGI-Shenzhen, Shenzhen, China.
Lihua LuoBGI-Shenzhen, Shenzhen, China.ORCID https://orcid.org/0000-0002-2129-4226
Xiangning DingBGI-Shenzhen, Shenzhen, China.
Chengcheng SunBGI-Shenzhen, Shenzhen, China.
Tianming LanBGI-Shenzhen, Shenzhen, China.
Sunil Kumar SahuBGI-Shenzhen, Shenzhen, China.
Weiying WuThe MOE Frontier Science Center for Brain Research and Brain-Machine Integration, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou, China.
Yuting YuanDepartment of Physiology, School of Basic Medical Sciences, Binzhou Medical University, Yantai, China.
Wendi WuBGI-Shenzhen, Shenzhen, China.
Jiaying QiuBGI-Shenzhen, Shenzhen, China.
Yixin ZhuBGI-Shenzhen, Shenzhen, China.
Qizhen YueBGI-Shenzhen, Shenzhen, China.
Yi JiaBGI-Shenzhen, Shenzhen, China.
Yanan WeiBGI-Shenzhen, Shenzhen, China.
Qiuyu QinBGI-Shenzhen, Shenzhen, China.
Runchu LiBGI-Shenzhen, Shenzhen, China.
Wandong ZhaoBGI-Shenzhen, Shenzhen, China.
Zhiyuan LvBGI-Shenzhen, Shenzhen, China.
Mingyi PuBGI-Shenzhen, Shenzhen, China.
Boqiong LvBGI-Shenzhen, Shenzhen, China.
Shangchen YangCollege of Life Sciences, Zhejiang University, Hangzhou, China.
Ashley ChangBGI-Shenzhen, Shenzhen, China.ORCID https://orcid.org/0000-0002-3439-9457
Xiaofeng WeiChina National GeneBank, Shenzhen, China.
Fengzhen ChenChina National GeneBank, Shenzhen, China.
Tao YangChina National GeneBank, Shenzhen, China.ORCID https://orcid.org/0000-0003-4211-5183
Zhenyong WeiChina National GeneBank, Shenzhen, China.
Fan YangChina National GeneBank, Shenzhen, China.
Peijing ZhangCenter for Stem Cell and Regenerative Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Guoji GuoCenter for Stem Cell and Regenerative Medicine, Zhejiang University School of Medicine, Hangzhou, China.
Yuejiao LiBGI-Shenzhen, Shenzhen, China.
Yan HuaGuangdong Provincial Key Laboratory of Silviculture, Protection and Utilization, Guangdong Academy of Forestry, Guangzhou, China.
Huan LiuBGI-Shenzhen, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe exact animal origin of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains obscure and understanding its host range is vital for preventing interspecies transmission.

methodsHerein, we applied single-cell sequencing to multiple tissues of 20 species (30 data sets) and integrated them with public resources (45 data sets covering 26 species) to expand the virus receptor distribution investigation. While the binding affinity between virus and receptor is essential for viral infectivity, understanding the receptor distribution could predict the permissive organs and tissues when infection occurs.

resultsBased on the transcriptomic data, the expression profiles of receptor or associated entry factors for viruses capable of causing respiratory, blood, and brain diseases were described in detail. Conserved cellular connectomes and regulomes were also identified, revealing fundamental cell-cell and gene-gene cross-talks from reptiles to humans.

conclusionsOverall, our study provides a resource of the single-cell atlas of the animal kingdom which could help to identify the potential host range and tissue tropism of viruses and reveal the host-virus co-evolution.

Indexed as

COVID-19Spike Glycoprotein, CoronavirusAnimalsHost SpecificityHumansReceptors, VirusSARS-CoV-2Receptors, VirusSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2crosstalksingle cell sequencing

Identifiers

PMID35917402
PMCPMC9345398

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.