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First published online April 27, 2018

Human tRNA-Derived Small RNAs Modulate Host–Oral Microbial Interactions

Abstract

Coevolution of the human host and its associated microbiota has led to sophisticated interactions to maintain a delicate homeostasis. Emerging evidence suggests that in addition to small molecules, peptides, and proteins, small regulatory noncoding RNAs (sRNAs) might play an important role in cross-domain interactions. In this study, we revealed the presence of diverse host transfer RNA–derived small RNAs (tsRNAs) among human salivary sRNAs. We selected 2 tsRNAs (tsRNA-000794 and tsRNA-020498) for further study based on their high sequence similarity to specific tRNAs from a group of Gram-negative oral bacteria, including Fusobacterium nucleatum, a key oral commensal and opportunistic pathogen. We showed that the presence of F. nucleatum triggers exosome-mediated release of tsRNA-000794 and tsRNA-020498 by human normal oral keratinocyte cells. Furthermore, both tsRNA candidates exerted a growth inhibition effect on F. nucleatum, likely through interference with bacterial protein biosynthesis, but did not affect the growth of Streptococcus mitis, a health-associated oral Gram-positive bacterium whose genome does not carry sequences bearing high similarity to either tsRNA. Our data provide the first line of evidence for the modulatory role of host-derived tsRNAs in the microbial-host interaction.

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Published In

Article first published online: April 27, 2018
Issue published: October 2018

Keywords

  1. tsRNAs
  2. cross-domain interactions
  3. oral microbiome
  4. antimicrobials
  5. microbial-host interaction
  6. sRNAs

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© International & American Associations for Dental Research 2018.
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PubMed: 29702004

Authors

Affiliations

X. He*
The Forsyth Institute, Cambridge, MA, USA
F. Li*
School of Dentistry, University of California, Los Angeles, Los Angeles, CA, USA
Institute of Diagnostic in Chinese Medicine, Hunan University of Chinese Medicine, Changsha, China
B. Bor#
The Forsyth Institute, Cambridge, MA, USA
K. Koyano#
Department of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, CA, USA
Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, USA
L. Cen
The Forsyth Institute, Cambridge, MA, USA
X. Xiao
Department of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, CA, USA
Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, USA
W. Shi
The Forsyth Institute, Cambridge, MA, USA
D.T.W. Wong
School of Dentistry, University of California, Los Angeles, Los Angeles, CA, USA
Department of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, CA, USA
Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, USA

Notes

W. Shi, The Forsyth Institute, 245 First St., Cambridge, MA 02142, USA. Email: [email protected]
D. Wong, School of Dentistry, University of California, Los Angeles, 10833 Le Conte Ave., Rm. 73-017 CHS, Los Angeles, CA 90095, USA. Email: [email protected]
*
Authors contributing equally as first authors.
#
Authors contributing equally as third authors.

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