» Articles » PMID: 33329438

Gut Microbiota in Dholes During Estrus

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2020 Dec 17
PMID 33329438
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

The co-evolution of gut microbes and the host plays a vital role in the survival and reproduction of the host. The dhole () has been listed as endangered species by the International Union for Conservation of Nature; therefore, conservation and effective breeding of dholes are essential. Effective estrus can promote reproduction. However, little is known about the relative contribution of estrus in shaping the structure and the functions of fecal microbiota. Here, we investigated the potential association between estrus and the fecal microbiota in dholes using shotgun metagenomic sequencing. We found that the estrus stages in dholes vary significantly in terms of gut bacterial composition and microbiome metabolism and function. Compared with that of non-estrus, adult dholes, the microbiome of estrus adult dholes had a significantly higher abundance of and , which play a key role in the synthesis of sex hormones and nucleic acids, energy production, and reproductive cell division. The insulin and energy metabolism-related pathways are significantly enhanced in the gut microbes and the related gluconeogenic enzymes are significantly enriched during estrus. These findings suggest that the structure and metagenome of the fecal microbiome during estrus have a significant effect in promoting estrus in dholes, thus providing a new perspective for dhole conservation.

Citing Articles

Distribution Patterns and Ecological Determinants of Suitable Habitats for the Dhole () in China.

Yang Y, Luo P, Zhao Y, Zhang T, Jiang F, You Z Animals (Basel). 2025; 15(4).

PMID: 40002945 PMC: 11852048. DOI: 10.3390/ani15040463.


Seasonal Variations in the Structure and Function of the Gut Flora in Adult Male Rhesus Macaques Reared in Outdoor Colonies.

Lv L, Zhang F, Zhou H, Xiao W, Hu Y, Wang W Microorganisms. 2025; 13(1).

PMID: 39858885 PMC: 11767529. DOI: 10.3390/microorganisms13010117.


Characteristics of Microbiota in Different Segments of the Digestive Tract of .

Shang Y, Zhong H, Liu G, Wang X, Wu X, Wei Q Animals (Basel). 2023; 13(4).

PMID: 36830518 PMC: 9952230. DOI: 10.3390/ani13040731.


Growth Stages and Inter-Species Gut Microbiota Composition and Function in Captive Red Deer () and Blue Sheep ().

Zhao Y, Sun J, Ding M, Khattak R, Teng L, Liu Z Animals (Basel). 2023; 13(4).

PMID: 36830340 PMC: 9951700. DOI: 10.3390/ani13040553.


Uncovering the Fecal Bacterial Communities of Sympatric Sika Deer () and Wapiti ().

Yan J, Wu X, Wang X, Shang Y, Zhang H Animals (Basel). 2022; 12(18).

PMID: 36139327 PMC: 9495088. DOI: 10.3390/ani12182468.


References
1.
Gonzales G, Cordova A, Vega K, Chung A, Villena A, Gonez C . Effect of Lepidium meyenii (Maca), a root with aphrodisiac and fertility-enhancing properties, on serum reproductive hormone levels in adult healthy men. J Endocrinol. 2003; 176(1):163-8. DOI: 10.1677/joe.0.1760163. View

2.
Shepherd E, DeLoache W, Pruss K, Whitaker W, Sonnenburg J . An exclusive metabolic niche enables strain engraftment in the gut microbiota. Nature. 2018; 557(7705):434-438. PMC: 6126907. DOI: 10.1038/s41586-018-0092-4. View

3.
Qin N, Yang F, Li A, Prifti E, Chen Y, Shao L . Alterations of the human gut microbiome in liver cirrhosis. Nature. 2014; 513(7516):59-64. DOI: 10.1038/nature13568. View

4.
Kanehisa M, Goto S, Sato Y, Kawashima M, Furumichi M, Tanabe M . Data, information, knowledge and principle: back to metabolism in KEGG. Nucleic Acids Res. 2013; 42(Database issue):D199-205. PMC: 3965122. DOI: 10.1093/nar/gkt1076. View

5.
Lynch J, Hsiao E . Microbiomes as sources of emergent host phenotypes. Science. 2019; 365(6460):1405-1409. DOI: 10.1126/science.aay0240. View