by foxypar4
Promising Antibiotic Could Spawn the Next Superbug:
[Via Discover Magazine | RSS]
Bacteria-killing viruses called bacteriophages can rapidly accelerate the evolution of pathogens by transferring genes from one bacterial species to another. The recipient “could literally bypass a billion years of evolution in a single event”—and could spread genes for toxic shock syndrome toxin.
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The really interesting aspect of the paper is that bacteriophages may be able to interact with a wider variety of bacteria than first believed. Many bacteriophages only infect a specific type of virus.
These researchers demonstrated that in some cases the bacterial viruses could not only infect different species of bacteria, but could also drag along bits of bacterial chromosomes with them.
Thus the possibility that bacteriophage could move genes between bacterial species. An unexpected result but the words ’spawn the next superbug’ may be a little hyperbolic.
Bacteria exchange genetic material all the time. It is one of the ways that antibiotic resistance genes move between bacteria anyway. It is often how specific strains become superbugs (i.e. by picking up a multitude of genetic elements providing antibiotic resistance).
The bacteriophage described exist in nature, as do the two bacterial strains. So this same sort of genetic exchange is able to occur by itself in the wild.
That is what I would be worried about. Normal use of antibiotics puts selective pressure on Listeria to gain the resistance genes. In the wild, these genes could be transferred by regular bacteriophages from Staphlyococcus.
So, is hits a worry if we use bacteriophage as an engineered antibiotic? Maybe but the references I could find do not indicate that it is a very sucessful treatment. Here is the relevant part from a paper published in 2006 in Antimicrobial Agents and Chemotherapy entitled Efficacy and Pharmacokinetics of Bacteriophage Therapy in Treatment of Subclinical Staphylococcus aureus Mastitis in Lactating Dairy Cattle:
In conclusion, the efficacy of bacteriophage in the treatment of bovine mastitis caused by S. aureus appears to be limited under the treatment conditions studied.
The phage were fairly rapidly degraded in the mammary glands of the cattle and had little ability to get rid of bacteria. So, this may require a lot of work to become useful, with many really big hurdles to overcome (i.e. the cattle generate an immune response to the phage which may render them useless).
Right now, I am more worried about Listeria picking up the genes from Staph via a natural route rather than an engineered one. Just another reason for us to rethink our pretty poorly conceptualized approach to antibiotics in livestock.
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