Decoding The Gut-Brain Axis
Earlier this week, a newly published study made headlines for showing a direct link between the gut microbiome and depression. For the past several years, scientists have suspected a link between bugs in the gut and neurological health. However, most of the evidence for the association has come from animal studies. Researchers from the Flanders Institute for Biotechnology (Flanders, Belgium) discovered that two different strains of bacteria, Coprococcus and Dialister, are depleted in the gut microbiome of people with depression.
This research, as well as other recent work, has made it clear that the gut microbiome also impacts neurological health, leading to the phrase “the gut-brain axis.” Let’s explore this connection and examine the early efforts by a few innovative biotechs to translate these new discoveries into the clinic.
Gut Microbiome Primer
The human microbiome is the complex collection of microbes (mostly bacteria, but also includes small numbers of fungi and viruses) that reside on and inside the human body, including our skin, mouth, nose, respiratory tract, and digestive tract (gut). The microbiome is huge — microbial cells outnumber human cells by a ten to one ratio! Human cells are much larger than bacteria cells, however, so don’t worry — you’re still mostly human. For every 100 pounds that you weigh, it is estimated that about two pounds of that weight come from bacteria.
Most of us think of bacteria as harmful and certainly some types are; however, those that have evolved with humans to become part of the human microbiome are either neutral — causing no harm — or beneficial. Scientists are busy trying to better understand and characterize these beneficial bacteria and the role that they play in human health.
The gut contains the largest number of bacteria, as well as the greatest diversity of bacteria, when compared to other parts of the body. Thus much of the attention directed towards the human microbiome has been focused on the gut microbiome in particular, which continues to surprise us with its influence on diseases such as obesity, diabetes, and, increasingly, brain disorders.
In order to determine if there is a link between variations in the gut microbiome and depression, The Flanders Institute for Biotechnology researchers analyzed the microbiomes of 1,054 people who are part of the Flemish Gut Flora Project. Researchers also had access to physician-diagnosed depression data on the same subjects. Analysis showed different bacteria strains are negatively or positively correlated with mental health.
To find out whether the link applies to humans, Raes and his colleagues analyzed the microbiomes of 1,054 people enrolled in a study known as the Flemish Gut Flora project, as well as self-reported and physician-diagnosed depression data on the same subjects. The results revealed several types of bacteria that are negatively or positively correlated with mental health.
Of course, this study is only the first step. Further work will be required to answer questions related to how these bacterial strains are impacting mental health, and if they may one day form the basis of a new treatment. (Article continues below)
Axial Biotherapeutics (Cambridge, MA) is focusing much of its initial attention on work originally done at microbiologist Sarkis Mazmanian’s lab in the California Institute of Technology (Pasadena, CA) — mostly relating to the gut-brain axis’ role in Parkinson’s disease (PD) and autism.
Parkinson’s disease (PD) is a chronic and progressive movement disorder, according to the Parkinson’s Disease Foundation. Symptoms include tremor of the hands, arms, legs, jaw, and face; slowness of movement; rigidity of the limbs and trunk; and impaired balance and coordination. These symptoms are caused by the malfunction and death of neurons that produce the neurotransmitter dopamine. PD affects nearly one million people in the U.S., and the cause is unknown. About 75% of PD cases are accompanied by gastrointestinal disorders such as constipation, which provided an initial impetus to examine a possible connection between gut health and the disease.
A key molecular characteristic of PD is the aggregation of a protein called alpha-synuclein (αSyn) within cells of the brain and gut. Researchers in the Mazmanian lab used a strain of mice that overproduce αSyn to study the disease. One group of the αSyn mice were bred in a completely sterile environment to create “germ-free” (GF) αSyn mice. The other αSyn mice had the normal collection of gut bacteria. On a series of tests designed to assess motor skills, the GF αSyn mice performed significantly better — suggesting that even in mice that overproduced the αSyn protein, the presence of certain microbes are required for the disease to progress. Further work suggested that a molecule called butyrate, produced by certain gut bacteria, can enter the brain and activate an immune response, leading neurons to malfunction or die.
There is reason to believe that this connection is also at work in humans with PD. In collaboration with Rush University (Chicago, IL) gastroenterologists, Mazmanian lab researchers transferred fecal samples from PD patients into the GF αSyn mice. Fecal transplants are an established way to “reset” the gut microbiome of the recipient to make it match that of the donor. After transplantation, the mice began exhibiting symptoms of PD. Transfer of fecal matter from healthy people did not trigger these symptoms. These experiments suggest that the gut microbiome is a major contributor to the disease process in PD patients.
Of course, these promising early stage findings still need to be translated into human therapeutics. This may be easier than traditional neurological approaches because it is much easier to deliver drugs to the gut than to get them to cross the blood-brain barrier. Following up with a targeted approach to modulate the production of butyrate and other inflammatory compounds produced in the gut may bring the first truly effective PD therapy into the clinics.
Autism Spectrum Disorder
Autism spectrum disorder (ASD) is a developmental brain disorder characterized by impaired social interaction, communication, and restrictive and repetitive behavior. These symptoms impact a child’s educational, social, emotional, and physical development. More than 3.5 million Americans live with an autism spectrum disorder according to the Autism Society. The cause is unknown, although genetics is thought to play a role.
Similar to PD, a significant portion of ASD patients exhibit gastrointestinal problems. The Mazmanian lab demonstrated that feeding ASD mice a specific strain of bacteria called B. fragilis — a part of the human microbiome — altered the mouse microbiome and reduced some of the ASD-like behaviors such as anxiety and repetitive behavior, and increased levels of communication with other mice. These experiments suggest a possible probiotic therapy for autism.
Carb Loading With Symbiotix
Another early-stage company making headlines in the gut-brain axis space is Symbiotix (Boston, MA). Focusing on multiple sclerosis (MS), their lead candidate is a carbohydrate molecule produced by B. fragilis. This therapy increases the production of regulatory T-cells, which are a class of T-cells that “turn down” an overactive immune response by releasing anti-inflammatory signaling molecules. Symbiotix is preparing to enter clinical trials with an orally-administered product for the treatment of MS and inflammatory bowel disease.
The emerging work described here gives credence to the old expression “think with your gut.” As the story continues to unfold, we are likely to see new therapeutics based on restoring the balance that millions of years of human-microbe co-evolution has fine-tuned.