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Intestinal Microbial Diversity in Female Rhesus () at Different Physiological Periods

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Journal Front Microbiol
Specialty Microbiology
Date 2022 Oct 13
PMID 36225360
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Abstract

To explore the relationship between the changes in the physiological period and the fecal microbial population of female rhesus monkeys by measuring microbial composition of fecal samples and the serum hormones. Blood and fecal samples were collected from six female adult rhesus monkeys during the menstrual period (MP), ovulation period (OP), and Luteal period (LP). Serum estradiol (E2) and progesterone (P) levels were determined by the chemiluminescence method and the stool samples were subjected to high-throughput 16S rRNA sequencing. The highest level of E2 and P secretions were during the MP, and LP, respectively. Stool samples produced valid sequences and the number of operational taxonomic unit/OTU was: 810056/3756 (MP), 845242/4159 (OP), 881560/3970 (LP). At the phylum level, the three groups of Firmicutes and Bacteroides accounted for > 95%. The dominant flora at the LP was Bacteroides (53.85%), the dominant flora at the MP and OP was Firmicutes, 64.08 and 56.53%, respectively. At the genus level, the dominant genus at the LP was , the dominant genera at the MP were , and . The dominant genera at OP were and . At the phylum level, P levels were negatively correlated to Firmicutes, Actinomycetes Actinobacteria, and Fibrobacteres, but positively correlated to Bacteroidetes. Likewise, E2 was positively correlated to Proteobacteria but negatively correlated to Euryarchaeota. At the genus level, P hormone showed a significant correlation with 16 bacterial species, and E2 was significantly correlated to seven bacterial species. Function prediction analysis revealed a high similarity between the MP and OP with six differentially functional genes (DFGs) between them and 11 DFGs between OP and LP ( < 0.05). Fecal microbiota types of female rhesus monkeys varied with different stages of the menstrual cycle, possibly related to changes in hormone levels.

References
1.
. Structure, function and diversity of the healthy human microbiome. Nature. 2012; 486(7402):207-14. PMC: 3564958. DOI: 10.1038/nature11234. View

2.
Ochman H, Worobey M, Kuo C, Ndjango J, Peeters M, Hahn B . Evolutionary relationships of wild hominids recapitulated by gut microbial communities. PLoS Biol. 2010; 8(11):e1000546. PMC: 2982803. DOI: 10.1371/journal.pbio.1000546. View

3.
Bouguen G, Langlois A, Djouina M, Branche J, Koriche D, Dewaeles E . Intestinal steroidogenesis controls PPARγ expression in the colon and is impaired during ulcerative colitis. Gut. 2014; 64(6):901-10. DOI: 10.1136/gutjnl-2014-307618. View

4.
Ley R, Backhed F, Turnbaugh P, Lozupone C, Knight R, Gordon J . Obesity alters gut microbial ecology. Proc Natl Acad Sci U S A. 2005; 102(31):11070-5. PMC: 1176910. DOI: 10.1073/pnas.0504978102. View

5.
Wahlstrom A, Sayin S, Marschall H, Backhed F . Intestinal Crosstalk between Bile Acids and Microbiota and Its Impact on Host Metabolism. Cell Metab. 2016; 24(1):41-50. DOI: 10.1016/j.cmet.2016.05.005. View