Evidence map›Paper›PMID 37005460›Full record

ArticleThe ISME journal2023

Targeting Fusobacterium nucleatum through chemical modifications of host-derived transfer RNA fragments.

Mengdi Yang, Pu-Ting Dong, Lujia Cen, Wenyuan Shi, Xuesong He, Jiahe Li

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 19 citations in OpenAlex.

  1. Transfer RNA Fragments in Diseases of Sensory Organs.International journal of molecular sciences · 2026
    Review
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  5. Article
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  13. Diverse plant RNAs coatProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Article
  15. Review
  16. Targeted elimination ofJournal of oral microbiology · 2024
    Article
  17. Review
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 3 institutions in 1 country.

Mengdi Yang *Department of Bioengineering, Northeastern University, Boston, MA, 02115, USA.
Pu-Ting Dong *Department of Microbiology, The Forsyth Institute, Cambridge, MA, 02142, USA.ORCID 0000-0003-2818-2021
Lujia CenDepartment of Microbiology, The Forsyth Institute, Cambridge, MA, 02142, USA.
Wenyuan ShiDepartment of Microbiology, The Forsyth Institute, Cambridge, MA, 02142, USA.
Xuesong HeDepartment of Microbiology, The Forsyth Institute, Cambridge, MA, 02142, USA. xhe@forsyth.org.ORCID 0000-0002-3333-9188
Jiahe LiDepartment of Bioengineering, Northeastern University, Boston, MA, 02115, USA. jiaheli@umich.edu.ORCID 0000-0002-9889-8546
Forsyth County Schools · USHarvard University · USNortheastern University · US

Funding

Domestication and characterization of TM7-the most elusive oral phylumR01DE023810 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Xuesong He, Jeffrey Scott McLean · 2014 to 2026
$6.6M
Host tRNA-derived small RNAs (tsRNAs) mediate interactions between host and oral microbesR01DE030943 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI Xuesong He · 2022 to 2026
$2.4M
Engineering Probiotics to Sense and Respond to the Intracellular Redox Imbalance towards Mitochondrial DysfunctionR21EB030769 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, JIAHE · 2021 to 2021
$611k
A New Class of Chemically Modified Small RNA Inhibitors against Fusobacterium nucleatumR03DE031329 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LI, JIAHE · 2022 to 2023
$341k
NIBIB NIH HHS R21 EB030769NIBIB NIH HHS R21EB030769NIDCR NIH HHS R01 DE023810NIDCR NIH HHS R01DE023810NIDCR NIH HHS R01 DE030943NIDCR NIH HHS R01DE030943NIDCR NIH HHS R03 DE031329NIDCR NIH HHS R03DE031329
6 · The paper itself

Abstract

Host mucosal barriers possess an arsenal of defense molecules to maintain host-microbe homeostasis such as antimicrobial peptides and immunoglobulins. In addition to these well-established defense molecules, we recently reported small RNAs (sRNAs)-mediated interactions between human oral keratinocytes and Fusobacterium nucleatum (Fn), an oral pathobiont with increasing implications in extra-oral diseases. Specifically, upon Fn infection, oral keratinocytes released Fn-targeting tRNA-derived sRNAs (tsRNAs), an emerging class of noncoding sRNAs with gene regulatory functions. To explore potential antimicrobial activities of tsRNAs, we chemically modify the nucleotides of the Fn-targeting tsRNAs and demonstrate that the resultant tsRNA derivatives, termed MOD-tsRNAs, exhibit growth inhibitory effect against various Fn type strains and clinical tumor isolates without any delivery vehicle in the nanomolar concentration range. In contrast, the same MOD-tsRNAs do not inhibit other representative oral bacteria. Further mechanistic studies uncover the ribosome-targeting functions of MOD-tsRNAs in inhibiting Fn. Taken together, our work provides an engineering approach to targeting pathobionts through co-opting host-derived extracellular tsRNAs.

Indexed as

MicroRNAsRNA, Small UntranslatedFusobacterium nucleatumHumansRNA, TransferMicroRNAsRNA, Small UntranslatedRNA, Transfer

Identifiers

PMID37005460
PMCPMC10202947
OpenAlexW4362506999

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.