Institute of Food Research (IFR) microbiologists are reinvigorating a way of battling C. difficile infections that they hope will help overcome the growing problem of antibiotic-resistant superbugs in hospitals.
Our digestive system is home to trillions of bacteria, which are crucial to our overall health, through helping us digest food and battling potentially harmful microbes. When we take antibiotics to combat bacterial infections these beneficial bacteria can also be killed off, leaving us at risk of infection by harmful bacteria. Clostridium difficile is one of these harmful bacteria and is the leading cause of hospital infections in England and Wales. Although the number of C. difficile infections is dropping, treating them is becoming harder as it becomes more resistant to antibiotics. New ways of controlling C. difficile infections are desperately needed to replace ineffective antibiotics, and bacteriophages are one such technology being investigated.
Bacteriophages are naturally occurring viruses that target bacteria. Bacteriophage therapy is not a new idea; it was being developed not long after their discovery at the start of the 20th century. However, after the discovery of penicillin and other antibiotics the research into the use of phages was abandoned in the West but its application continues in Eastern Europe, particularly in Georgia. Now that the bacterial resistance to antibiotics is becoming such a large problem, there is renewed interest in developing bacteriophage therapy.
For use as a therapy, the bacteriophage must not affect any of the hundreds of different bacterial species that make up a healthy human microbiota. Researchers at the IFR had previously discovered and isolated a bacteriophage that specifically targets C. difficile. The new study, published in the journal Anaerobe, looked to assess how effective using this phage might be in combatting C. difficile infections.
The researchers used a model of the human colon, set up to mimic that of an elderly person in hospital. Antibiotics were given in the same way as in hospital, disrupting the normal balance of bacteria and allowing C. difficile to establish itself, and then produce the toxins that make C. difficile infections so dangerous.
The study showed that the administration of a specific bacteriophage significantly reduced the number of C. difficile cells and also the amount of toxin produced, without significantly affecting the other members of the gut microbiota. This suggests that bacteriophages could have great potential for use to combat C. difficile infections in hospital settings.
The phage wasnt, however, able to kill off all of the C. difficile cells. This was because this bacteriophage, like many others, is able to insert its own DNA into the bacterial chromosome a process known as lysogeny. This makes the bacteria resistant to further bacteriophage attack.
Interestingly, in some cases the lysogeny seemed to prevent the C difficile cells from producing the toxin. So although all of the cells arent killed, those that survive are a lot less dangerous. This may give clinicians more time to get C. difficile infections under control.
This research was carried out by Dr. Emma Meader as part of her PhD studentship at the IFR, under the supervision of Dr. Arjan Narbad. This article is one of a series highlighting the work of IFRs PhD students who received their doctorates at UEAs congregation ceremony in July 2013.
Reference: Evaluation of bacteriophage therapy to control Clostridium difficile and toxin production in an in vitro human colon model system, Emma Meader et al, Anaerobe S1075-9964(13)00082-6. doi: 10.1016/j.anaerobe.2013.05.001