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Structure · collection · 2018

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

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Coevolution of the human host and its associated microbiota has led to sophisticated interactions to maintain a delicate homeostasis.

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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.

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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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DataCite10.25384/sage.c.4095620.v111 d agoJSON v1
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