Gut microbiota community adaption during young children fecal microbiota transplantation by 16s rDNA sequencing
Introduction
The human gut is colonized by a highly diverse community of microorganisms that play a critical symbiosis with their host, including energy metabolism, immunity and nervous system [1], [2]. Studies of the intestinal microbiota imply that an unbalanced microbial community is associated with the pathogenesis of gastrointestinal symptoms. Growing evidence supported that fecal microbiota transplantation could reestablish the balance of gut microbiota community and is an effective treatment against several gastrointestinal symptoms, best known as a treatment for recurrent Clostridium difficile infection (CDI) [3], current studies suggested it is also promising results with many other digestive or auto-immune disease, including inflammatory bowel disease (IBD), Irritable Bowel Syndrome (IBS), and Ulcerative Colitis (UC) [4]. It is reported that intestinal gut microbiota appears various bacterial richness and diversity among different diseases [5], [6]. The microbiota community studies in CDI indicated that compared with healthy controls, the patients had an initial CDI appears a progressive decrease in species diversity and reduction of Bacteroidetes and Firmicutes phylum in their fecal samples [3]. A larger cohort study of pediatric Crohn׳s Disease imply that a set of microorganism taxa associated with disease status, it is might be a bacterial biomarker for early diagnosis [7].
Fecal microbiota transplantation (FMT) is transplantation of a fecal suspension from a healthy donor into the gastrointestinal tract of patient, and to reestablish the balance of intestinal microbiota community of patient. Although FMT has been most accepted treatment for the intestinal microbiota dysbiosis, but the mechanism is still not entirely clear. More research is needed to investigate and understand the dynamic changes of intestinal microbiota community during the FMT treatment, and especially in children patients because children is more impressionable to environmental factors than adult. Gut microbiota studies are commonly performed by analyzing the 16s ribosomal DNA gene (16s rDNA), and it is also current golden standard for microbial community analysis [8], [9]. In present study, we applied 16s rDNA sequencing analysis to profile the fecal microbiota community from 3 young children with Juvenile idiopathic arthritis, Ulcerative colitis or Hemophagocytic syndrome. The aim of this study was to characterize the changes of microbiota community before and after the FMT for these young children.
Section snippets
Patient information and feces sample process
Three young children (1 female, 2 male; aged 19–40 months) with immune-imbalance related chronic diseases were planning to undergo FMT surgery at Department of Gastroenterology at Shanghai Children׳s Hospital, and invited to participate in this study. The Shanghai Children׳s Hospital review board approved this study and we obtained written informed consent for this study from their guardians. Before donating the feces, the two healthy adult donors were screened following test: HIV1/2
Results and discussion
Using Illumina Hiseq 2000 sequencing platform, a total of 1.4 Gb clean data was generated from 14 samples involving 3 young children patients with different sampling time-point for each patient covered pre-FMT to post-FMT treatment and 2 healthy adult donors, the detailed information of samples listed in Table 1. After removing low quality reads, 776 Mb clean sequencing data were produced. These sequencing reads were pre-assembled and then clustered into operational taxonomic units (OTUs) that
Conclusion
From this study, some results have shown that FMT surgeries can change the species richness of the gut microbial community, but the bacterial spectrum of fecal samples exhibit strong stability along with the FMT surgeries. 16s rDNA sequencing reports displayed that some species may change sharply after FMT surgeries. However, only with the 16s rDNA data, the results can’t tell what had happened after FMT surgeries. A number of important questions are also raised by these findings. For example,
Acknowledgments
This work is supported in part by the National Natural Science Foundation of China (Nos. 31071167 and 31370751), Shanghai Municipal Commission of Health and Family Planning (Grant nos. 201440434, 20144Y0179 and 20144Y0175), Shanghai Key Projects for Basic Scientific Research (14JC1405700), Research and Innovation Project of High Level Talents in Putuo District of Shanghai (2014-A-20) and Natural Science Foundation of Shanghai (14ZR1434200), China.
Jianlei Gu is an Assistant Research Fellow at Shanghai Children′s Hospital, Shanghai Jiao Tong University. He obtained his Master degree in Microbiology Science from Fudan University (2008.9–2011.7) and Bachelor degree in Biological Engineering from the China University of Mining and Technology (2004.09–2008.7).
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Jianlei Gu is an Assistant Research Fellow at Shanghai Children′s Hospital, Shanghai Jiao Tong University. He obtained his Master degree in Microbiology Science from Fudan University (2008.9–2011.7) and Bachelor degree in Biological Engineering from the China University of Mining and Technology (2004.09–2008.7).
Yizhong Wang, Ph.D., is an Assistant Professor at Shanghai Children′s Hospital, Shanghai Jiao Tong University. He was a Postdoctoral fellow at Division of Gastroenterology, University of Utah School of Medicine (2009.09–2010.06) and at the Department of Pathology and Laboratory Medicine, Temple University School of Medicine (2010.07–2014.02).
Shiyi Liu is a graduate student at Shanghai Jiaotong University.
Guangjun Yu, Ph.D., is a Professor and the President of Shanghai Children׳s Hospital, Shanghai Jiaotong University.
Ting Zhang, M.D., is the Director of Gastroenterology Department, Shanghai Children׳s Hospital, Shanghai Jiaotong University.
Hui Lu Ph.D. Shanghai Jiao Tong University and Shanghai Children’s Hospital.
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These authors contributed equally to this work.