Abstract

We used sensitive rRNA-targeted reverse transcription-quantitative PCR (RT-qPCR) to quantify the Clostridium coccoides group, which is a major anaerobic population in the human intestine. For this purpose, the C. coccoides group was classified into 3 subgroups and 19 species for expediency in accordance with the existing database, and specific primers were newly developed to evaluate them. Population levels of the C. coccoides group in human feces determined by RT-qPCR were equivalent to those determined by fluorescence in situ hybridization. RT-qPCR analysis of fecal samples from 96 volunteers (32 young children, 32 adults and 32 elderly) by using the 22 new primer sets together with the C. coccoides group-specific primer setm revealed that (i) total counts obtained as the sum of the 3 subgroups and 19 species were equivalent to the results obtained by using the C. coccoides group-specific primer set; (ii) total C. coccoides-group counts in the elderly were significantly lower than those in young children and adults; (iii) genus Blautia was the most common subgroup in the human intestinal C. coccoides-group populations at all age populations tested; (iv) the prevalences of Fusicatenibacter saccharivorans and genus Dorea were significantly higher in adults than in young children and the elderly; and (v) the prevalences of C. scindens and C. hylemonae, both of which produce secondary bile acid in the human intestine, were significantly higher in the elderly than in young children and adults. Hierarchical clustering and principal component analysis showed clear separation of the bacterial components between adult and elderly populations. Taken together, these data suggest that aging plays an important role in the diversity of C. coccoides-group populations in human intestinal microbiota; changes in this diversity likely influence the health of the host.

Highlights

  • The human intestine is inhabited by more than 1000 bacterial species, with a total of 1011 to 1012 bacterial cells per gram of feces [1]

  • The population levels of C. coccoides group determined by reverse transcription-quantitative PCR (RT-qPCR) using the C. coccoides group-specific primer set were statistically equivalent to the results obtained by using fluorescence in situ hybridization (FISH)

  • The population levels determined by qPCR were significantly higher than those determined by using RT-qPCR (Steel-Dwass test, P

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Summary

Introduction

The human intestine is inhabited by more than 1000 bacterial species, with a total of 1011 to 1012 bacterial cells per gram of feces [1]. Certain commensal C. coccoides-group species induce regulatory T-cell production in the mouse colon, suggesting that these bacteria play critical roles in immune homeostasis [11,12] Taken together, these findings show that C. coccoides group play important roles in immunology, nutrition, and pathological processes, and in the health of their hosts. YIF-SCAN (Yakult Intestinal Flora-SCAN), a highly sensitive and rapid system that uses reverse transcription-quantitative PCR (RT-qPCR), has been developed to quantify a variety of bacterial populations in the intestinal microbiota [13,14,15,16,17] The sensitivity of this technique has been shown to be 100 to 1000 times higher than that of qPCR, because the rRNA copy number per cell (approximately 104 copies per actively growing cell) is higher than that of rRNA genes (approximately 10 copies in a genome) [13,14,16]. We analyzed the intestinal C. coccoide-group populations in 96 Japanese volunteers (32 young children, 32 adults, and 32 elderly) by using RT-qPCR to evaluate bacterial population diversity in the different age groups

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