» Articles » PMID: 26966006

Changes of Diet and Dominant Intestinal Microbes in Farmland Frogs

Overview
Journal BMC Microbiol
Publisher Biomed Central
Specialty Microbiology
Date 2016 Mar 12
PMID 26966006
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Agricultural activities inevitably result in anthropogenic interference with natural habitats. The diet and the gut microbiota of farmland wildlife can be altered due to the changes in food webs within agricultural ecosystems. In this work, we compared the diet and intestinal microbiota of the frog Fejervarya limnocharis in natural and farmland habitats in order to understand how custom farming affects the health of in vivo microbial ecosystems.

Results: The occurrence, abundance, and the numbers of prey categories of stomach content were significantly different between the frogs inhabiting natural and farmland habitats. In addition, differences in the abundance, species richness, and alpha-diversity of intestinal microbial communities were also statistically significant. The microbial composition, and particularly the composition of dominant microbes living in intestines, indicated that the land use practices might be one of factors affecting the gut microbial community composition. Although the first three dominant microbial phyla Bacteroidetes, Firmicutes, and Proteobacteria found in the intestines of frogs were classified as generalists among habitats, the most dominant gut bacterial phylum Bacteroidetes in natural environments was replaced by the microbial phylum Firmicutes in farmland frogs. Increased intestinal microbial richness of the farmland frogs, which is mostly contributed by numerous microbial species of Proteobacteria, Actinobacteria, Acidobacteria, and Planctomycetes, not only reflects the possible shifts in microbial community composition through the alteration of external ecosystem, but also indicates the higher risk of invasion by disease-related microbes.

Conclusions: This study indicates that anthropogenic activities, such as the custom farming, have not only affected the food resources of frogs, but also influenced the health and in vivo microbial ecosystem of wildlife.

Citing Articles

Spatiotemporal differences induced changes in the structure and function of the gut microbiota in an endangered ungulate.

Ma X, Hu X, Liu K, Wang W, Jia W, Gao H Anim Microbiome. 2024; 6(1):74.

PMID: 39707511 PMC: 11662579. DOI: 10.1186/s42523-024-00362-z.


From Skin to Gut: Understanding Microbial Diversity in Rana amurensis and R. dybowskii.

Yang M, Liu H, Wang H, Lu Z, Han X, Luo Z Curr Microbiol. 2024; 81(11):354.

PMID: 39269482 DOI: 10.1007/s00284-024-03868-6.


Significant Differences in Intestinal Bacterial Communities of Sympatric Bean Goose, Hooded Crane, and Domestic Goose.

Yin J, Yuan D, Xu Z, Wu Y, Chen Z, Xiang X Animals (Basel). 2024; 14(11).

PMID: 38891737 PMC: 11170997. DOI: 10.3390/ani14111688.


The Circadian Rhythm of the Behavior and Gut Microbiota in Dybowski's Frogs () during the Autumn Migration Period.

Hu N, Li Y, Wang M, Ji H, Zhang X, San B Life (Basel). 2024; 14(3).

PMID: 38541648 PMC: 10971735. DOI: 10.3390/life14030322.


Are fecal samples an appropriate proxy for amphibian intestinal microbiota?.

Lam I, Fong J Ecol Evol. 2024; 14(2):e10862.

PMID: 38304268 PMC: 10828907. DOI: 10.1002/ece3.10862.


References
1.
Tsai S, Chen C, Shu K, Wu M . Peritonitis caused by Roseomonas in a patient undergoing automated peritoneal dialysis: case report and literature review. Intern Med. 2012; 51(13):1721-4. DOI: 10.2169/internalmedicine.51.6737. View

2.
Suau A, Bonnet R, Sutren M, Godon J, Gibson G, Collins M . Direct analysis of genes encoding 16S rRNA from complex communities reveals many novel molecular species within the human gut. Appl Environ Microbiol. 1999; 65(11):4799-807. PMC: 91647. DOI: 10.1128/AEM.65.11.4799-4807.1999. View

3.
Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S . MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011; 28(10):2731-9. PMC: 3203626. DOI: 10.1093/molbev/msr121. View

4.
Bresciano J, Salvador C, Paz-Y-Mino C, Parody-Merino A, Bosch J, Woodhams D . Variation in the Presence of Anti-Batrachochytrium dendrobatidis Bacteria of Amphibians Across Life Stages and Elevations in Ecuador. Ecohealth. 2015; 12(2):310-9. DOI: 10.1007/s10393-015-1010-y. View

5.
Berthrong S, Buckley D, Drinkwater L . Agricultural management and labile carbon additions affect soil microbial community structure and interact with carbon and nitrogen cycling. Microb Ecol. 2013; 66(1):158-70. DOI: 10.1007/s00248-013-0225-0. View