For people with a damaged liver or too much iron in their blood,
enjoying raw oysters from the Gulf of Mexico is a deadly gamble. Most of
the oysters harbor Vibrio vulnificus, a bacterium responsible for almost
all seafood-related deaths in the United States. Healthy people shrug
off the microbe, but susceptible folks who get a full-blown infection
have more than a 50 percent chance of dying. "You can be dead
within 24 hours," says Paul A. Gulig of the University of Florida
College of Medicine in Gainesville. Seeking a treatment that works
faster than antibiotics do, he and his colleagues recently isolated a
bacteria-killing virus, or bacteriophage, that targets V. vulnificus and
can prevent the deaths of mice infected with it.
Gulig's report was one of a handful on bacteriophage therapy
presented last week at the American Society for Microbiology (ASM)
meeting in Los Angeles. Other scientists described phages that attack
bacteria that cause anthrax, wound and burn infections, and meat and
poultry contamination.
Although U.S. physicians today don't embrace the strategy, phage
therapy dates back almost a century (SN: 6/1/96, p. 350). The viruses
infect, reproduce within, and eventually burst bacteria. Since phages
reproduce only as long as they have target bacteria to infect, Elizabeth
M. Kutter of Evergreen State College in Olympia, Wash., calls the
viruses "self-replicating, self-limiting antibiotics."
In the V. vulnificus work, Gulig and his colleagues sampled muck from
oyster beds and isolated phages that destroy the bacterium. They
simultaneously infected mice with V. vulnificus and enriched the
rodents' blood with iron, which helps the bacterium thrive. When given
phages at the time of infection, five of eight mice remained healthy.
Without such treatment, all mice succumbed within 18 hours.
Gulig cautions that his team has just begun to examine phage therapy
for V. vulnificus. The scientists plan to test a cocktail of phages and
to find out whether phages can help rodents when treatment comes a few
hours after infection.
Like Gulig, Michael H. Walter of the University of Northern Iowa in
Cedar Falls has turned to phages to defeat a deadly bacterium. His enemy
is Bacillus anthracis, the germ responsible for anthrax.
Since the anthrax bacterium is dangerous to handle, Walter's group
has begun characterizing phages that infect a harmless relative,
Bacillus cereus. Such viruses may prove useful in anthrax therapy, says
Walter, or in destroying stockpiles of B. anthracis captured from
terrorists or rogue countries.
As bacteria increasingly develop antibiotic resistance, several U.S.
companies have also taken an interest in phage therapy. One, the
Baltimore firm Intralytix, works closely with the Eliava Institute of
Bacteriophage, Microbiology, and Virology in Tbilisi, Georgia, which has
developed phages for medical use since 1934. Physicians in the former
Soviet Union regularly turn to phages.
At the ASM meeting, Intralytix cofounder and Georgian scientist
Alexander Sulakvelidze described his firm's progress in identifying
phages that destroy the Salmonella bacteria that commonly infect meat,
poultry, and eggs. One phage alone kills 90 percent of common Salmonella
strains, and a cocktail of phages eliminates 95 percent, he says.
Intralytix scientists bought chicken in groceries and seeded it with
Salmonella. Spraying the poultry with phages dramatically reduced
contamination, the researchers report. Sulakvelidze predicts that the
poultry industry will begin testing this disinfection strategy in their
processing plants within a year.
Moreover, Intralytix plans to bring to market a U.S. version of a
bacteriophage-impregnated, biodegradable polymer originally created by
Georgian scientists. Intended to prevent infections in burns and wounds,
the skinlike dressing has passed clinical testing in Georgia. Kutter
calls it "the most exciting new phage-therapy product in recent
years."
Intralytix and several other firms are also studying whether phages
can help people infected with strains of Enterococcus and Staphylococcus
that are resistant to all antibiotics, including vancomycin, currently
the drug of last resort. "There's nothing else we can use to treat
these patients," says Sulakvelidze.