Green Tea Liquid Consumption Alters the Human Intestinal and Oral Microbiome

Xiaojie Yuan1, Yong Long1, Zhaohua Ji1

  • 1Department of Epidemiology, School of Public Health, Fourth Military Medical University, Xi'an, Shannxi, 710032, China.

Abstract

Insights

Green tea liquid (GTL) consumption alters the gut and oral microbiome in healthy adults. GTL intake modifies microbial composition, potentially impacting colorectal cancer risk by reducing oral bacteria in the gut.

Area of Science:

  • Microbiome research
  • Gut health and oral health
  • Cancer prevention

Background:

  • Green tea polyphenols (GTPs) show anti-colorectal cancer (CRC) activity.
  • Intestinal microbiota and oral bacteria colonization are linked to CRC.
  • Green tea (GT) modulates mouse gut microbiota composition beneficially.

Purpose of the Study:

  • To investigate the effects of green tea liquid (GTL) on the gut and oral microbiome in healthy volunteers.
  • To understand how GTL consumption influences microbial diversity and composition.
  • To explore potential mechanisms linking GTL, the microbiome, and cancer prevention.

Main Methods:

  • 16S rRNA sequencing and PICRUSt analysis of fecal and saliva samples from 12 healthy volunteers.
  • Samples collected before, during (2 weeks of 400 mL/day GTL), and after a washout period.
  • Analysis included microbial diversity, core microbiota, PLS-DA, and functional pathway abundance.

Main Results:

  • GTL consumption altered fecal and salivary microbial diversity and core microbiota.
  • Increased Firmicutes to Bacteroidetes ratio (FIR:BAC), elevated SCFA-producing genera, and reduced LPS synthesis in feces.
  • Reduced abundance of carcinogenic pathways in saliva and decreased fecal Fusobacterium levels were observed.

Conclusions:

  • GTL consumption induces significant alterations in both the oral and gut microbiomes.
  • These changes include shifts in microbial composition and function relevant to carcinogenesis.
  • GTL may reduce the presence of oral-like bacteria in the gut, potentially contributing to its anti-CRC effects.

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