The collection of microbes that inhabits the human gastrointestinal tract is known as
intestinal microbiota, and an enormous body of work has shown that their activities
contribute to health and disease. Ulcerative colitis (UC), which is a type of inflammatory
bowel disease, is considered to arise due to a disruption in the balance between the
immune system and microbiota. However, there is little consensus on the mechanism
of action and microbes involved in the disease manifestation. In this work, I applied
culture-enriched metagenomics (CEMG) to characterize the dynamics of gut microbiota
in healthy individuals and UC patients. I showed that CEMG provides a higher resolution
to study these microbial communities, and we used this approach to understand
microbial colonization after fecal microbiota transplantation (FMT) therapy in UC patient.
I showed that sequencing approaches alone did not reveal consistent engraftment
across FMT responders. Using CEMG and a collection of bacterial whole-genome sequences,
I showed patient-specific microbial strain transfer and a signature of commonly
engrafted genes only in patients who responded to FMT. In this work, I also investigated
the dynamics of a highly abundant bacteriophage, crAssphage, in an FMT donor
and implemented a new method to detect bacteriophage engraftment post-FMT using
SNP analysis. Finally, it has been suggested that antibiotic treatment before FMT may
increase the efficacy of FMT. However, in this work, I show that while antibiotics alter
the microbiome, there was no difference in the composition of the microbiome of antibiotic
vs placebo group post-FMT. This is consistent with the randomized controlled trial
results that shows pretreatment with antibiotics does not improve FMT outcome. Together,
this work demonstrate the importance of in-depth microbiome analysis applied
to culture-dependent and -independent sequencing to characterize microbial changes
post-FMT. / Dissertation / Doctor of Philosophy (PhD) / Many bacteria reside in the human gut, and they are essential in our health and in
disease. It is evident that these bacteria are associated with inflammatory bowel disease,
but we do not yet know how and what bacteria are involved in this disease. In this
work, I describe a method to study these bacteria from stool that relies on growing
them and investigating their DNA. I showed that our approach helped us recover a
greater diversity of these bacteria and their genetic content in healthy individuals and
patients with inflammatory bowel disease compared to methods that use only DNA
based approaches. Using this method, we could better understand why some patients
responded to a treatment consisting of transferring stool content from healthy donor to
patient. I also investigated a group of viruses that infect bacteria and implemented a new
computational method based on DNA sequencing to test whether these viruses transfer
to the patient after receiving the fecal therapy. We also found that antibiotic treatment
before fecal therapy in patients with inflammatory bowel disease does not improve the
patient’s recovery.
| Identifer | oai:union.ndltd.org:mcmaster.ca/oai:macsphere.mcmaster.ca:11375/27919 |
| Date | 11 1900 |
| Creators | Shekarriz, Shahrokh |
| Contributors | Surette, Michael G, Biochemistry and Biomedical Sciences |
| Source Sets | McMaster University |
| Language | English |
| Detected Language | English |
| Type | Thesis |
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