Evidence map›Paper›PMID 36674845›Full record

ArticleInternational journal of molecular sciences2023

Single-Cell Transcriptome Identifies the Renal Cell Type Tropism of Human BK Polyomavirus.

Feng Yang, Xutao Chen, Hui Zhang, Guo-Dong Zhao, Huifei Yang, Jiang Qiu, Siyan Meng, Penghan Wu, Liang Tao, Qin Wang and 1 more

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Feng YangOrgan Transplant Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.ORCID 0000-0002-7976-1640
Xutao ChenOrgan Transplant Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.
Hui ZhangOrgan Transplant Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.
Guo-Dong ZhaoOrgan Transplant Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.
Huifei YangDepartment of Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou 510080, China.
Jiang QiuOrgan Transplant Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.
Siyan MengDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou 510080, China.
Penghan WuDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou 510080, China.
Liang TaoDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou 510080, China.
Qin WangDepartment of Pharmacology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou 510080, China.
Gang HuangOrgan Transplant Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.
Sun Yat-sen University · CNGuangzhou University of Chinese Medicine · CN

Funding

National Natural Science Foundation of China 82270786the Basic and Applied Basic Research Foundation of Guangdong Province 2020A1515110075
6 · The paper itself

Abstract

BK polyomavirus (BKPyV) infection is the main factor affecting the prognosis of kidney transplant recipients, as no antiviral agent is yet available. A better understanding of the renal-cell-type tropism of BKPyV can serve to develop new treatment strategies. In this study, the single-cell transcriptomic analysis demonstrated that the ranking of BKPyV tropism for the kidney was proximal tubule cells (PT), collecting duct cells (CD), and glomerular endothelial cells (GEC) according to the signature of renal cell type and immune microenvironment. In normal kidneys, we found that BKPyV infection-related transcription factors P65 and CEBPB were PT-specific transcription factors, and PT showed higher glycolysis/gluconeogenesis activities than CD and GEC. Furthermore, in the BKPyV-infected kidneys, the percentage of late viral transcripts in PT was significantly higher than in CD and GEC. In addition, PT had the smallest cell-cell interactions with immune cells compared to CD and GEC in both normal and BKPyV-infected kidneys. Subsequently, we indirectly demonstrated the ranking of BKPyV tropism via the clinical observation of sequential biopsies. Together, our results provided in-depth insights into the renal cell-type tropism of BKPyV in vivo at single-cell resolution and proposed a novel antiviral target.

Indexed as

BK VirusKidney TransplantationPolyomavirus InfectionsAntiviral AgentsEndothelial CellsHumansKidneyTranscriptomeAntiviral AgentsBK polyomavirusimmune microenvironmentmetabolismmulti-omicssingle-cell transcriptomicstropism

Identifiers

PMID36674845
PMCPMC9861348
OpenAlexW4315497969

What OpenQuestion holds

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LicenceCC BY
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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.