Medicilon Logo
|
search icon search icon language icon contact icon menu icon
Medicilon Logo
|
search icon close search icon language icon contact icon menu icon
logo icon CN
Contact Us
Close Button
Message
Back To Top
Online Message×
Click switch
Close Button
News information

Bacteria-Killing Bacteria Study May Open Door to Fighting Microbial Resistance

2015-12-07
|
Page View:

    Scientists from the Universities of Nottingham and Birmingham report that they have discovered how a potentially useful predatory bacterium called Bdellovibrio protects itself against its own weapons when it invades other bacteria. The researchers say their work offers insights into early steps in the evolution of bacterial predators and will help to inform new ways to fight antimicrobial resistance. Their study (“Ankyrin-mediated self-protection during cell invasion by the bacterial predator Bdellovibrio bacteriovorus”) is published in Nature Communications.


    B. bacteriovorus eats other bacteria, including important pathogens of humans, animals and crops. It attacks them from inside out using DD-endopeptidases that first loosen the cell walls of prey bacteria and then cause them to round up like a pufferfish, providing space as a temporary home for the predator. However, Bdellovibrio have similar cell walls so why they don’t fall victim of their own attack has been a conundrum, until now.


    The project, funded by the Biotechnology and Biological Sciences Research Council, found that the bacterium uses the Bd3460 ankyrin-type protein as a shield. It binds to the tip of the enzyme weapons, nullifying their action until they are safely secreted out of the Bdellovibrio and into the prey bacteria.


    Andrew Lovering, Ph.D., lecturer in structural biology, school of biosciences, and Ian Cadby at the University of Birmingham determined the structure of the ankyrin protein using X-ray crystallography and found that it attaches to two DD-endopeptidase weapons to temporarily deactivate them. Colleagues at the University of Nottingham, including Liz Sockett, Ph.D. professor, faculty of medicine & health sciences, confirmed the antidote protein’s use when the gene responsible for its production was deleted.


    “When I first showed this to Liz, she hit the nail on the head by describing it as a decorative ‘quiff’ on top of the endopeptidase” said Dr. Lovering. “This covers up the active site of the enzymes that are used to cut cell walls and offers protection to the Bdellovibrio until these weapons are excreted into the prey.”


    “When the bd3460 gene responsible for antidote production was deleted, the Bdellovibrio had no way of protecting itself from its own weapons,” noted Dr. Sockett. “When it attacked harmful bacteria with its cell-wall-damaging enzymes it also felt the effects. The Bdellovibrio bacteria lacking the bd3460 gene tried to invade the bacteria but suddenly rounded up like pufferfish and couldn’t complete the invasion. The fatter predator cell could not enter the prey cell.”


    Pointing out that this is the first paper to discover a ‘self-protection’ protein in predatory bacteria, Dr. Sockett added that “Most bacteria are not predatory and so understanding these mechanisms gives us a glimpse of how predation evolved. In this case it seems that the bd3460 gene was transferred into ancestors of Bdellovibrio, probably when they were beginning to develop as predators.”


    “If we are to use Bdellovibrio as a therapeutic in the future, we need to understand the mechanisms underpinning prey killing and be sure that any self-protective genes couldn’t be acquired by pathogens, causing resistance,” commented Dr. Lovering. “Brilliantly, Liz and Carey have demonstrated this did not happen with the bd3460 antidote protein, and Ian and I showed how the mechanism works on predator enzymes only. This is a great inter-university collaboration.”

Relevant newsRelevant news