Research into how Clostridioides difficile causes excessive inflammation in the gut
Research led by scientists from UCLA and Harvard University has uncovered details about how the bacterium Clostridioides difficile (C. diff) causes excessive inflammation in the gut that can lead to potentially deadly colitis, according to a news release from UCLA.
The study is published online in the journal Gastroenterology.
The researchers pinpointed which part of the toxic protein can permeate cell membranes to gain entry to cellular structures called endosomes, demonstrating that even fragments of the protein that contain the key segment are capable of accessing endosomes.
In addition, they showed how the toxin molecule causes inflammation, which has been a long-standing mystery because such molecules are generally quickly digested in the gut. The scientists found that toxin A – and surprisingly even fragments of the toxin – can organize DNA into ordered crystalline particles that amplify an immune response by binding to multiple TLR9 receptors, which are normally part of the body’s early detection system for microbial DNA. The findings demonstrate that this mechanism causes the body’s natural defenses to produce excessive inflammation.
Infection from C. difficile in the gut can cause life-threatening colitis, with nearly 500,000 cases and 29,000 deaths in the United States alone each year, according to the Centers for Disease Control and Prevention (CDC).
Older patients who have been treated with antibiotics are at particular risk from C. diff, which is resistant to a number of antibiotics. The bacterium is usually harmless when it is kept in check by symbiotic microbes normally found in the human gut. However, when the gut microbiome is suppressed by antibiotics, C. diff can take over: Its toxins can spur a severe autoimmune response that causes symptoms such as diarrhea, cramping, fever and nausea.
The research at UCLA and Harvard combined machine learning, experiments with a technique called small-angle X-ray scattering at the Stanford Synchrotron Radiation Lightsource (a Department of Energy laboratory), and experiments using human cell lines, mouse cell lines and mice.
