4.7 Article

The tongue biofilm metatranscriptome identifies metabolic pathways associated with the presence or absence of halitosis

Journal

NPJ BIOFILMS AND MICROBIOMES
Volume 8, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41522-022-00364-2

Keywords

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Funding

  1. APOSTD grant by Generalitat Valenciana (Conselleria d'Educacio, Investigacio, Cultura y Esport) [2018/081]
  2. European Union (Fondo Social Europeo)
  3. Spanish Ministry of Science, Innovation and Universities [BIO2015-68711-R]

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Intra-oral halitosis is usually caused by volatile sulfur compounds produced by tongue microbiota. This study revealed that halitosis-free individuals had higher activity of Streptococcus, Veillonella, and Rothia, while halitosis was associated with Prevotella, Fusobacterium, and Leptotrichia. Additionally, the gene expression profiles showed differences in genes related to L-cysteine and L-homocysteine synthesis and cysteine degradation.
Intra-oral halitosis usually results from the production of volatile sulfur compounds, such as methyl mercaptan and hydrogen sulfide, by the tongue microbiota. There are currently no reports on the microbial gene-expression profiles of the tongue microbiota in halitosis. In this study, we performed RNAseq of tongue coating samples from individuals with and without halitosis. The activity of Streptococcus (including S. parasanguinis), Veillonella (including V. dispar) and Rothia (including R. mucilaginosa) was associated with halitosis-free individuals while Prevotella (including P. shahi), Fusobacterium (including F. nucleatum) and Leptotrichia were associated with halitosis. Interestingly, the metatranscriptome of patients that only had halitosis levels of methyl mercaptan was similar to that of halitosis-free individuals. Finally, gene expression profiles showed a significant over-expression of genes involved in L-cysteine and L-homocysteine synthesis, as well as nitrate reduction genes, in halitosis-free individuals and an over-expression of genes responsible for cysteine degradation into hydrogen sulfide in halitosis patients.

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