TY - JOUR
T1 - Rapidly processed stool swabs approximate stool microbiota profiles
AU - Bokulich, Nicholas A.
AU - Maldonado, Juan
AU - Kang, Dae Wook
AU - Krajmalnik-Brown, Rosa
AU - Caporaso, J. Gregory
N1 - Publisher Copyright:
© 2019 Bokulich et al.
PY - 2019/3/1
Y1 - 2019/3/1
N2 - Studies of the intestinal microbiome commonly utilize stool samples to measure the microbial composition in the distal gut. However, collection of stool can be difficult from some subjects under certain experimental conditions. Sampling of fecal material using sterile swabs can streamline sample collection, handling, and processing. In this study, we validate the use of swabs of fecal matter to approximate measurements of microbiota in stool using 16S rRNA gene Illumina amplicon sequencing and evaluate the effects of shipping time at ambient temperatures on accuracy. The results indicate that swab samples reliably replicate the stool microbiota bacterial composition, alpha diversity, and beta diversity when swabs are processed quickly (≤2 days) but that sample quality quickly degrades after this period and is accompanied by increased abundances of Enterobacteriaceae. Fresh swabs appear to be a viable alternative to stool sampling when standard collection methods are challenging, but extended exposure to ambient temperatures prior to processing threatens sample integrity.
AB - Studies of the intestinal microbiome commonly utilize stool samples to measure the microbial composition in the distal gut. However, collection of stool can be difficult from some subjects under certain experimental conditions. Sampling of fecal material using sterile swabs can streamline sample collection, handling, and processing. In this study, we validate the use of swabs of fecal matter to approximate measurements of microbiota in stool using 16S rRNA gene Illumina amplicon sequencing and evaluate the effects of shipping time at ambient temperatures on accuracy. The results indicate that swab samples reliably replicate the stool microbiota bacterial composition, alpha diversity, and beta diversity when swabs are processed quickly (≤2 days) but that sample quality quickly degrades after this period and is accompanied by increased abundances of Enterobacteriaceae. Fresh swabs appear to be a viable alternative to stool sampling when standard collection methods are challenging, but extended exposure to ambient temperatures prior to processing threatens sample integrity.
KW - 16S rRNA genes
KW - Gut microbiome
KW - Sample collection
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U2 - 10.1128/mSphere.00208-19
DO - 10.1128/mSphere.00208-19
M3 - Article
C2 - 30971445
AN - SCOPUS:85064431791
SN - 2379-5042
VL - 4
JO - mSphere
JF - mSphere
IS - 2
M1 - e00208-19
ER -