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In this manuscript, we discuss a novel method to sample and analyze the duodenal microbiome. This method provides an accurate depiction of microbial diversity and composition in the duodenum and could be useful for further investigation of the duodenal microbiome.
Shifts in the microbiome have been correlated with the physiology and pathophysiology of many organ systems both in humans and in mouse models. The gut microbiome has been typically studied through fecal specimen collections. The ease of obtaining fecal samples has resulted in many studies that have revealed information concerning the distal luminal gastrointestinal tract. However, few studies have addressed the importance of the microbiome in the proximal gut. Given that the duodenum is a major site for digestion and absorption, its microbiome is relevant to nutrition and liver disease and warrants further investigation. Here we detail a novel method for sampling the proximal luminal and mucosal gut microbiome in human subjects undergoing upper endoscopy by obtaining duodenal aspirate and biopsies. Specimen procurement is facile and unaffected by artifacts such as patient preparatory adherence, as might be the case in obtaining colonic samples during colonoscopy. The preliminary results show that the luminal and mucosal microbiomes differ significantly, which is likely related to environmental conditions and barrier functions. Therefore, a combination of duodenal aspirate and biopsies reveal a more comprehensive picture of the microbiome in the duodenum. Biopsies are obtained from the descending and horizontal segments of the duodenum, which are anatomically close to the liver and biliary tree. This is important in studying the role of bile acid biology and the gut-liver axis in liver disease. Biopsies and aspirate can be used for 16S ribosomal RNA sequencing, metabolomics, and other similar applications.
The intestinal microbiome has become an area of increased interest in recent years. It is now understood that the diverse bacterial population in the gut can differ based on a variety of factors, including genetics, diet, medication, and environmental influences1. Studies have also identified unique microbial profiles linked to varying gastrointestinal diseases, such as obesity, inflammatory bowel disease, and liver disease2,3. The majority of studies focus on profiling the microbiome of the large intestine through the analysis of fecal and distal mucosal samples4
Duodenal samples were obtained at the Veteran Affairs Greater Los Angeles Healthcare System, Cedars-Sinai Medical Center, and the Ronald Reagan UCLA Medical Center after the clinical protocol for the Microbiome, Microbial Markers and Liver Disease (M3LD) study was accepted by the institutional review board of the local ethics review committee. Written informed consent was obtained from all participating patients.
1. Consent of participants
Population differences between mucosal and luminal microbiome of proximal gut
Previous studies have found differences in the microbial populations of luminal and mucosal colon specimens4,5,18. The preliminary results show that duodenal aspirate and biopsy specimens can measure for both luminal and mucosal microbiota in the proximal gut. Furthermore, we have found that these microbiome populations are disti.......
Studies of the microbiome are incredibly important, as this complex ecosystem has a critical role in energy homeostasis, immunologic responses, and metabolism19. Regional microbiome differences exist that may reflect the distinct physiological functions of various regions of the gastrointestinal tract, which may affect different disease states20. The fecal microbiome is most commonly studied but more recently the small intestine microbiome has come under investigation
This research was funded by the National Institutes of Health/National Cancer Institute grant number RO1CA204145.
....Name | Company | Catalog Number | Comments |
2 mL cryovials | Corning | 430659 | |
96-well plates | Applied Biosystems | 4306737 | |
dNTPs | Sigma | D7295 | |
Dry ice | Provided by institution | ||
EG29-i10 endoscope | Pentax | N/A | Endoscope size may vary depending on patient physiology |
Epoch microplate spectrophotometer | Biotek | N/A | |
Ethanol | Sigma Aldrich | 676829 | |
HiSeq 2500 | Illumina | N/A | |
IL_806r reverse primer | IDT DNA technologies | custom | custom primers |
ILHS_515f forward primer | IDT DNA technologies | custom | custom primers |
JumpStart Taq DNA | Sigma | D4184 | |
Mucus specimen trap | Busse Hospital Disposables | 405 | 40 cc specimen trap with transport cap |
Nanodrop Gen5 software | ThermoFisher Scientific | ||
PCR buffer | Sigma | P2192 | |
PCR cleanup kit | Zymo Research | D4204 | |
Radial Jaw 4 Jumbo Forceps | Boston Scientific | M00513343 | 2.8mm Jaw OD |
Vioscreen dietary questionnaire | VioCare | N/A | |
ZymoBIOMICS DNA Microprep Kit | Zymo Research | D4300 | 25 ug binding capacity |
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