A team of US-based scientists has developed a novel bacterial community comprising 119 microbial species naturally found in the human body. The study is published in the journal Cell.
Study: Design, construction, and in vivo augmentation of a complex gut microbiome. Image Credit: Volodimir Zozulinskyi / Shutterstock
Background
The human gastrointestinal (GI) tract contains a diverse range of microorganisms, collectively called the gut microbiota. About 30 trillion microbes in the GI tract play crucial roles in regulating a wide variety of physiological functions, including digestion, metabolism, immune response, and neurological activity.
Any alteration in the gut microbial composition and diversity is called dysbiosis, a condition responsible for the onset of many inflammatory diseases and infections. However, despite advancements in knowledge, it is still uncertain how and to what extent the gut microbiota is associated with human physiology and pathophysiology.
In the current study, scientists have developed and characterized a synthetic bacterial community representing the most common microbial species found in the endogenous human gut microbiota.
Development of bacterial community
The scientists initially developed a complex microbial community containing 104 bacterial strains. They analyzed the metagenomic sequence data from the Human Microbiome Project to determine the most prevalent bacterial strains. Then, by conducting a series of experiments, they measured the accurate abundance of each bacterial strain in the formed community.
They determined the strain-strain and strain-nutrient interactions by systematically perturbing the formed community and its growth medium. In this way, nutrient competition and mutualism-dependent nutrient utilization within the community could be understood. Overall, they identified specific “keystone” amino acids that are essential in determining community composition.
Colonization of mice with bacterial community
In the next part of the study, scientists colonized this bacterial community in germ-free mice for four weeks and determined its stability. Next, they challenged the mice with a human fecal sample. This step was performed to ensure the development of a more defined bacterial community that better represents the human gut microbiota.
They determined the community composition by analyzing fecal samples collected from the mice. The findings revealed that the newly formed, more enriched community contains a total of 119 bacterial strains, of which 97 were from the initial community and 22 were new strains.
Colonization of mice with new bacterial community
Scientists first colonized this new community in germ-free mice and challenged them with the same human fecal sample. Then, by analyzing mice-derived fecal samples, they observed that the new community is more enriched and stable to fecal challenge and its colonization resistance to pathogens is significantly higher than the initial community.
Characterization of new bacterial community
Scientists conducted a series of experiments in germ-free mice colonized with the human fecal sample or the new bacterial community. The findings revealed that the composition of new community resembles that of a human fecal community in the mouse gut. The new community also exhibited a high degree of biological reproducibility, justifying its applicability as an experimental model.
The phenotypic characterization of the new community revealed a similar colonization density in the mouse gut as a normal human fecal community. Moreover, the new community exhibited comparable phenotypes to normal human fecal communities in terms of immune and metabolic responses.
Colonization resistance against Escherichia coli
To further validate the experimental utility of the new bacterial community, scientists determined its ability to resist colonization by pathogens. They selected an enterohemorrhagic E. coli for invasion as colonization of this bacterial strain is known to cause life-threatening diarrheal infections, hemolytic uremic syndrome, malnutrition, and inflammatory bowel disease.
They experimented by colonizing germ-free mice with the new bacterial community, or a previously studied 12-member community (control), or an unknown human fecal community (positive control).
The findings revealed that both new bacterial and human fecal communities exhibit similar levels of colonization resistance against pathogenic E. coli. In contrast, the 12-member community failed to resist E. coli colonization and, thus, allowed significantly higher levels of E. coli growth.
Further analysis showed that Firmicutes, a phylum of Gram-positive bacteria, play a vital role in E. coli colonization resistance.
Study significance
The study describes the development and characterization of a complex, defined bacterial community that resembles natural human gut microbiota. This novel community exhibits robust colonization resistance against pathogenic E. coli.
As mentioned by scientists, the novel bacterial community can be used as an experimental model to study the effects of gut bacterial strains on host physiology and health.
- Cheng AG. 2022. Design, construction, and in vivo augmentation of a complex gut microbiome. Cell. https://www.sciencedirect.com/science/article/abs/pii/S0092867422009904
Posted in: Medical Science News | Medical Research News
Tags: Bacteria, Cell, Digestion, Dysbiosis, E. coli, Hemolytic Uremic Syndrome, Immune Response, in vivo, Inflammatory Bowel Disease, Malnutrition, Metabolism, Microbiome, Pathophysiology, Physiology, Syndrome
Written by
Dr. Sanchari Sinha Dutta
Dr. Sanchari Sinha Dutta is a science communicator who believes in spreading the power of science in every corner of the world. She has a Bachelor of Science (B.Sc.) degree and a Master's of Science (M.Sc.) in biology and human physiology. Following her Master's degree, Sanchari went on to study a Ph.D. in human physiology. She has authored more than 10 original research articles, all of which have been published in world renowned international journals.
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