Scientists have discovered that its evolutionary path was eerily simple
All it took for
flesh-eating bacteria to go from harmless organisms to gruesome
infectious pathogens was four mutations and about 35 years. That's what
an international group of researchers announced today in a study that outside experts are calling the largest bacterial genome paper ever published.
"One of the major proteins is an active ingredient in Adolphe's meat tenderizer."
Despite its name, flesh-eating
bacteria — a type of streptococcus — doesn't consume flesh. What it does
do is produce proteins that break down human skin, fat, and muscle — a
process that causes flesh to die rather quickly. "One of the major
proteins is an active ingredient in Adolph's meat tenderizer,"
says James Musser, an infectious disease expert at Houston Methodist
Research Institute and co-author of the study published today in Proceedings of the National Academy of Sciences.
The ensuing disease, called necrotizing fasciitis, is very difficult to
treat; although antibiotics can do the trick, skin-grafting and
amputations are not uncommon. Worse yet, the disease causes death in 70 percent
of cases if left untreated. And the infection is actually
human-specific, so other animals can't get the disease. These
characteristics, Musser says, make it a particularly interesting beast
with which to work.
To find out how the
bacteria mutated, the researchers analyzed the genomes of over 3,615
population-based strains of streptococcus. For the most part, these
organisms don't make humans sick, but some can result in pink eye,
meningitis and pneumonia. The most notorious strep strain, however, is
probably Group A streptococcus — the group that tends to cause the most
epidemics of flesh-eating disease. "We needed this magnitude of data,"
Musser says, "to be clear about what transpired to create this thug
pathogen."
"there were four key genetic changes."
Once the researchers
had gathered all the historical genomic data, they set about building a
molecular clock where each change in the bacterial genome brought them
closer to finding out exactly what genetic changes allowed the pathogen
to become this successful. "By working backward, we were able to
determine that there were four key genetic changes," Musser says. The
first two mutations — changes that took place prior to 1960 — arose
after a single progenitor cell line became infected with two different
types of viruses. "Bacteria can get viral infections too," Musser says,
"and the viruses that they got infected with carried genes encoding
novel toxins," which the bacteria were then able to integrate into their
own DNA.
The third mutation
involved a change in a single nucleotide — nucleotides are subunits of
DNA and RNA — that Musser says allowed the bacteria to produce a better
toxin than the one that previously existed. "It was just a change in one
amino acid in the toxin around the 1960s or 1970s," Musser says.
Finally, the last mutation event was gene transfer with another
bacterium that took place around 1983. And according to Musser, it gave
the bacteria the ability to encode two cell-killing toxins in far
greater quantities that they could before. "The whole game that the
organism plays is to figure out how to make more toxins or how to make
them in increasing amounts." Flesh-eating bacteria actually produce over
90 different types of toxins, Musser says, but this combination of four
mutations is what makes them particularly devastating.
A single progenitor cell line
Yet what's most
surprising about the study's results, Musser says, is that all four
mutations occurred in a single progenitor cell line — no other cell line
mutated in this way. "Over time, there was a cell that sequentially
acquired these various additional parts so that at the end of the day,
when it acquired that fourth event, it created that souped-up
streptococcus." Musser equates this to one super-customized car, where
sequentially adding a new engine, exhaust, and sound-system eventually
makes it stand out like no other.
"A new strain of strep will emerge in 35 years from 1987."
Now, Musser's team is delving
even deeper into the origins of flesh-eating bacteria. He says that
researchers still need to know precisely why this organism spread so
rapidly, and globally. Yet, that these scientists were able to construct
such a detailed mutation timeline is pretty remarkable, says David
Morens, an epidemiologist at the National Institutes of Health who did
not participate in the study. "Nothing like this has ever been done
before," he says. "This is a pathogenic organism that evolved from
something that wasn't pathogenic, and then morphed into something
extremely infectious — and now we know how it happened." Morens says
this study won't help anyone cure disease, but it will help in
surveillance because "now we know which steps are bad."
Patrick Schlievert, a
microbiologist at the University of Iowa who co-authored the first
paper to describe flesh-eating bacteria in 1987, agrees with Morens. He
told The Verge that Musser's study shows that future mutations
will depend on gene movement by viruses, and that they will occur along
the same timeline as they did with flesh-eating bacteria. "I will tell
you that a new strain of strep will emerge in 35 years from 1987," he
wrote, "but I cannot tell you what it will look like or where it will
begin... just that it will happen." If scientists are to stop the
emergence of super-successful pathogens, Schlievert said, they will have
to find a way to halt those viruses from spreading. Perhaps then, "they
might be able to stop these epidemics."
No comments:
Post a Comment