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Background <p>The genetic susceptibility of halitosis is unclear, challenging its precise management in high-risk population. Here we investigated the association of <i>hTAS2R38</i> polymorphisms with the prevalence and treatment outcome of halitosis, with a particular focus on oral microbiota.</p> Methods <p>A cross-sectional study including 689 participants was conducted to investigate the association between <i>hTAS2R38</i> polymorphisms and halitosis. A 6-month cohort including 60 halitosis patients was established to explore the relationship between <i>hTAS2R38</i> polymorphisms and treatment outcome of halitosis. Salivary microbiota was further analyzed and its correlation with <i>hTAS2R38</i> polymorphisms was investigated.</p> Results <p>In the cross-sectional study, a higher prevalence of halitosis was observed in individuals with AVI/AVI genotype as compared to non-AVI/AVI genotype (PAV/PAV + PAV/AVI) (OR = 2.380, 95% CI = 1.493–3.807). 16S rRNA sequencing revealed the enrichment of <i>Prevotella</i> in the saliva of AVI/AVI individuals. In the prospective study, halitosis patients with AVI/AVI genotype exhibited poor treatment outcome relative to non-AVI/AVI individuals during the 6-month follow-up after halitosis intervention (RR = 2.077, 95% CI = 1.382–3.339). <i>Tannerella</i>, <i>Filifactor</i>, and <i>Mycoplasma</i> were identified to be the major persistent genus in the saliva of AVI/AVI patients over the 6-month period after treatment. Furthermore, the human gingival fibroblasts with AVI/AVI genotype exhibited reduced inhibition against the growth and volatile sulfur compounds production of periodontal pathogens<i>.</i></p> Conclusions <p>Our work demonstrates that <i>hTAS2R38</i> polymorphisms contribute to the development and treatment outcome of halitosis via modulating oral microbiota, providing new insights to the better management of halitosis.</p> <p><MediaObject ID="MOESM2"> <VideoObject FileRef="MediaObjects/40168_2025_2087_MOESM2_ESM.mp4" VideoID="D5U2bXM-3veDLfL8au3xfZ"> <Caption Language="En" xml:lang="en"> <CaptionContent> <p>Video Abstract</p> </CaptionContent> </Caption> </VideoObject> </MediaObject></p>

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hTAS2R38 polymorphisms modulate oral microbiota and influence the prevalence and treatment outcome of halitosis

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年3月28日

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  • Hongxiang Mei,
  • Cai Qi,
  • Jinchi Liu,
  • Sirui Yang,
  • Jiajia Zhou,
  • Yangyu Lu,
  • Liwei Zheng,
  • Juan Li,
  • Lei Zhao,
  • Xin Xu

摘要

Background

The genetic susceptibility of halitosis is unclear, challenging its precise management in high-risk population. Here we investigated the association of hTAS2R38 polymorphisms with the prevalence and treatment outcome of halitosis, with a particular focus on oral microbiota.

Methods

A cross-sectional study including 689 participants was conducted to investigate the association between hTAS2R38 polymorphisms and halitosis. A 6-month cohort including 60 halitosis patients was established to explore the relationship between hTAS2R38 polymorphisms and treatment outcome of halitosis. Salivary microbiota was further analyzed and its correlation with hTAS2R38 polymorphisms was investigated.

Results

In the cross-sectional study, a higher prevalence of halitosis was observed in individuals with AVI/AVI genotype as compared to non-AVI/AVI genotype (PAV/PAV + PAV/AVI) (OR = 2.380, 95% CI = 1.493–3.807). 16S rRNA sequencing revealed the enrichment of Prevotella in the saliva of AVI/AVI individuals. In the prospective study, halitosis patients with AVI/AVI genotype exhibited poor treatment outcome relative to non-AVI/AVI individuals during the 6-month follow-up after halitosis intervention (RR = 2.077, 95% CI = 1.382–3.339). Tannerella, Filifactor, and Mycoplasma were identified to be the major persistent genus in the saliva of AVI/AVI patients over the 6-month period after treatment. Furthermore, the human gingival fibroblasts with AVI/AVI genotype exhibited reduced inhibition against the growth and volatile sulfur compounds production of periodontal pathogens.

Conclusions

Our work demonstrates that hTAS2R38 polymorphisms contribute to the development and treatment outcome of halitosis via modulating oral microbiota, providing new insights to the better management of halitosis.

Video Abstract