Rapid regrowth and detection of microbial contaminants in equine fecal microbiome samples

• Published in: PloS one 2017-11, Vol.12 (11), p.e0187044-e0187044
• Main Authors: Beckers, Kalie F, Schulz, Christopher J, Childers, Gary W
• Format: Article
• Language: English
• Subjects: Animals; Bacteria; Bacteria - classification; Bacteria - genetics; Bacteria - isolation & purification; Biodiversity; Bioinformatics; Biology and Life Sciences; Communities; Community composition; Composition effects; Contaminants; Crowdsourcing; Defecation; Deoxyribonucleic acid; DNA; Ecology and Environmental Sciences; Fecal microflora; Feces; Feces - microbiology; High-Throughput Nucleotide Sequencing; Horses; Laboratories; Libraries; Medicine and Health Sciences; Methods; Microbial contamination; Microbiota; Microbiota (Symbiotic organisms); Microorganisms; Nutrition; Pellets; Phylogenetics; Polymerase Chain Reaction; Regrowth; Research and analysis methods; RNA, Ribosomal, 16S - genetics; rRNA 16S; Sampling; Studies; Taxa
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0187044

Advances have been made to standardize 16S rRNA gene amplicon based studies for inter-study comparisons, yet there are many opportunities for systematic error that may render these comparisons improper and misleading. The fecal microbiome of horses has been examined previously, however, no universal horse fecal collection method and sample processing procedure has been established. This study was initialized in large part to ensure that samples collected by different individuals from different geographical areas (i.e., crowdsourced) were not contaminated due to less than optimal sampling or holding conditions. In this study, we examined the effect of sampling the surface of fecal pellets compared to homogenized fecal pellets, and also the effect of time of sampling after defecation on 'bloom' taxa (bloom taxa refers to microbial taxa that can grow rapidly in horse feces post-defecation) using v4 16S rRNA amplicon libraries. A total of 1,440,171 sequences were recovered from 65 horse fecal samples yielding a total of 3,422 OTUs at 97% similarity. Sampling from either surface or homogenized feces had no effect on diversity and little effect on microbial composition. Sampling at various time points (0, 2, 4, 6, 12 h) had a significant effect on both diversity and community composition of fecal samples. Alpha diversity (Shannon index) initially increased with time as regrowth taxa were detected in the amplicon libraries, but by 12 h the diversity sharply decreased as the community composition became dominated by a few bloom families, including Bacillaceae, Planococcaeae, and Enterococcaceae, and other families to a lesser extent. The results show that immediate sampling of horse feces must be done in order to ensure accurate representation of horse fecal samples. Also, several of the bloom taxa found in this study are known to occur in human and cattle feces post defecation. The dominance of these taxa in feces shortly after defecation suggests that the feces is an important habitat for these organisms, and horse fecal samples that were improperly stored can be identified by presence of bloom taxa.