Evidence map›Paper›PMID 41453891›Full record

ArticleNature communications2025

Non-parasite genome encoded virus-like RNAs reprogram the pathogenicity of human blood flukes.

Tongling Shan, Zhigang Lu, Tianqi Xia, Xiaoxu Wang, Lu Liu, Chuantao Fang, Shun Li, Yameng Zheng, Guofeng Cheng

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. NResearch (Washington, D.C.) · 2026
    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

9 authors.

Tongling Shan *Shanghai Tenth People's Hospital, Institute for Infectious Diseases and Vaccine Development, Clinical Center for Brain and Spinal Cord Research of Tongji University, Affiliated Shanghai Blue Cross Brain hospital, Tongji University School of Medicine, Shanghai, China.ORCID http://orcid.org/0000-0002-5329-6349
Zhigang Lu *Faculty of Natural Sciences, University of Hohenheim, Stuttgart, Germany.
Tianqi Xia *Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.
Xiaoxu Wang *Shanghai Tenth People's Hospital, Institute for Infectious Diseases and Vaccine Development, Clinical Center for Brain and Spinal Cord Research of Tongji University, Affiliated Shanghai Blue Cross Brain hospital, Tongji University School of Medicine, Shanghai, China.
Lu Liu *Shanghai Tenth People's Hospital, Institute for Infectious Diseases and Vaccine Development, Clinical Center for Brain and Spinal Cord Research of Tongji University, Affiliated Shanghai Blue Cross Brain hospital, Tongji University School of Medicine, Shanghai, China.
Chuantao Fang *Shanghai Tenth People's Hospital, Institute for Infectious Diseases and Vaccine Development, Clinical Center for Brain and Spinal Cord Research of Tongji University, Affiliated Shanghai Blue Cross Brain hospital, Tongji University School of Medicine, Shanghai, China.
Shun LiShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.
Yameng ZhengShanghai Tenth People's Hospital, Institute for Infectious Diseases and Vaccine Development, Clinical Center for Brain and Spinal Cord Research of Tongji University, Affiliated Shanghai Blue Cross Brain hospital, Tongji University School of Medicine, Shanghai, China.
Guofeng ChengShanghai Tenth People's Hospital, Institute for Infectious Diseases and Vaccine Development, Clinical Center for Brain and Spinal Cord Research of Tongji University, Affiliated Shanghai Blue Cross Brain hospital, Tongji University School of Medicine, Shanghai, China. chengguofeng@tongji.edu.cn.ORCID http://orcid.org/0000-0001-5249-1065

Funding

National Natural Science Foundation of China (National Science Foundation of China) 31672550
6 · The paper itself

Abstract

Non-parasite genome encoded RNAs (ngRNAs) are often overlooked in their roles, especially their functions in shaping the biology of organisms. Here we show four non-parasite genome encoded virus-like RNAs that present in Schistosoma japonicum, a human blood fluke responsible for significant morbidity and mortality. These ngRNAs are predominantly localized in the germ cells that play crucial roles in oogenesis and egg production, pivotal processes contributing to host pathology. The ngRNA encode RNA-dependent RNA polymerase (RdRp) that synthesize complementary RNA strands, governing embryo viability and egg production. Notably, similar virus-like ngRNAs are also found in the planarian Dugesia japonica, where RdRp sustains worm survival. In this work, we integrate metatranscriptomics, single-cell RNA sequencing, RNA interference and various molecular methods to comprehensively identify ngRNAs and then characterize their functions. We further demonstrate the mechanism by which ngRNAs shape critical biological traits in parasitic helminths, providing novel insights into potential therapeutic targets for schistosomiasis control and advancing our understanding of ngRNA functions in certain organisms.

Indexed as

RNA, HelminthRNA, ViralSchistosoma japonicumAnimalsFemaleGenome, HelminthHumansOogenesisPlanariansRNA-Dependent RNA PolymeraseRNA InterferenceRNA-Dependent RNA PolymeraseRNA, HelminthRNA, Viral

Identifiers

PMID41453891
PMCPMC13036067

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.