Noninvasive sampling of the small intestinal chyme for microbiome, metabolome and antimicrobial resistance genes in dogs, a proof of concept.

IF 4.9 Q1 MICROBIOLOGY
Julie Menard, Sahar Bagheri, Sharanya Menon, Y Tina Yu, Laura B Goodman
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Abstract

Background: The gastrointestinal microbiome and metabolome vary greatly throughout the different segments of the gastrointestinal tract, however current knowledge of gastrointestinal microbiome and metabolome in health and disease is limited to fecal samples due to ease of sampling. The engineered Small Intestinal MicroBiome Aspiration (SIMBA™) capsule allows specific sampling of the small intestine in humans. We aimed to determine whether administration of SIMBA™ capsules to healthy beagle dogs could reliably and safely sample the small intestinal microbiome and metabolome when compared to their fecal microbiome and metabolome.

Results: Eleven beagle dogs were used for the study. Median transit time of capsules was 29.93 h (range: 23.83-77.88). Alpha diversity, as measured by the Simpson diversity, was significantly different (P = 0.048). Shannon diversity was not different (P = 0.114). Beta diversity results showed a significant difference between capsule and fecal samples regarding Bray-Curtis, weighted and unweighted unifrac (P = 0.002) and ANOSIM distance metric s (R = 0.59, P = 0.002). In addition to observing a statistically significant difference in the microbial composition of capsules and feces, distinct variation in the metabolite profiles was seen between the sample types. Heat map analysis showed 16 compounds that were significantly different between the 2 sampling modes (adj-P value ranged between 0.004 and 0.036) with 10 metabolites more abundant in the capsule than in the feces and 6 metabolites more abundant in the feces compared to the capsules.

Conclusions: The engineered Small Intestinal MicroBiome Aspiration (SIMBA™) capsule was easy and safe to administer to dogs. Microbiome and metabolome analysis from the capsule samples were significantly different than that of the fecal samples and were like previously published small intestinal microbiome and metabolome composition.

对狗的小肠食糜进行无创采样,以检测微生物组、代谢组和抗菌药耐药性基因,这是一项概念验证。
背景:胃肠道微生物组和代谢组在胃肠道的不同部分存在很大差异,但由于取样方便,目前对健康和疾病中胃肠道微生物组和代谢组的了解仅限于粪便样本。工程化的小肠微生物组抽吸(SIMBA™)胶囊可对人体小肠进行特定采样。我们的目的是确定健康小猎犬服用 SIMBA™ 胶囊是否能可靠、安全地采集小肠微生物组和代谢组样本,并与它们的粪便微生物组和代谢组进行比较:研究使用了 11 只小猎犬。胶囊的中位运输时间为 29.93 小时(范围:23.83-77.88)。以辛普森多样性衡量的阿尔法多样性有显著差异(P = 0.048)。香农多样性没有差异(P = 0.114)。Beta 多样性结果显示,胶囊样本和粪便样本在 Bray-Curtis、加权和非加权 unifrac(P = 0.002)以及 ANOSIM 距离指标(R = 0.59,P = 0.002)方面存在显著差异。除了观察到胶囊和粪便中微生物组成的显著统计学差异外,还发现不同类型样本之间的代谢物特征也存在明显差异。热图分析显示,16种化合物在两种取样方式之间存在显著差异(adj-P值介于0.004和0.036之间),其中10种代谢物在胶囊中的含量高于粪便,6种代谢物在粪便中的含量高于胶囊:结论:工程化小肠微生物组抽吸术(SIMBA™)胶囊给狗用药简单、安全。胶囊样本的微生物组和代谢组分析结果与粪便样本的分析结果有显著差异,与之前公布的小肠微生物组和代谢组组成相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
0.00%
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0
审稿时长
13 weeks
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