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A colorized electron microscope image captures a Staphylococcus aureus bacteria
colony. PHOTOGRAPH BY MARTIN OEGGERLI, NATIONAL GEOGRAPHIC
PUBLISHED JULY 27, 2016
On Wednesday, a team of
German microbiologists unveiled a new kind of antibiotic from an unlikely
source: bacteria that call the human body home. Got questions about how they
sniffed out the discovery? Here’s everything you need to know.
In a nutshell, what did
the researchers find?
The team found a
first-of-its-kind antibiotic, called lugdunin, that’s extremely effective
against the bacterium Staphylococcus aureus, which can be resistant
to many common antibiotics and can cause serious infections. For instance, Staphylococcus
aureus is the species behind the notorious MRSA infections.
And, as the team points
out in Nature, the drugmaker is all-natural: A bacterium called Staphylococcus
lugdunensis secretes the antibiotic.
That sounds like a useful
species! Where did they find it?
Here’s the cool part: S.
lugdunensis lives in the human nose.
Um … why were researchers
looking for antibiotics in their noses?
Well, technically, they
weren’t looking in their noses. They were looking through
massive libraries of bacterial cultures that they had collected from other
people’s noses. Previous work has identified promising antibiotics within the
human microbiome, so the researchers were looking for more by seeing if some
bacterial cultures inhibited the growth of others. It’s the same basic method
that Alexander Fleming accidentally used to discover penicillin in 1928.
Wait, what’s the microbiome?
Your body is an ecosystem
unto itself, home to a bewilderingly vast array of microorganisms that
co-evolved with us and, depending on when you had your last bowel movement, may or may not outnumber your body’s cells. Microorganisms
living in and on your body play important roles in regulating immune responses,
aiding digestion, and crowding out nefarious pathogens. For instance, human
breast milk contains sugarsthat specifically nourish the bacterium that populates babies’ guts,
a strategy that defends babies’ intestines against pathogenic viruses and
bacteria. (Read more about our relationship with microbes in National
Geographic magazine.)
So is this nasal
bacterium producing the antibiotic to help us?
Strictly speaking, no. It
turns out that the bacterium naturally wields the antibiotic to defend its turf
against invading hordes of S. aureus. Even when outnumbered ten to
one in a petri dish, S. lugdunensis managed to kill off
encroaching S. aureus, an upset that researchers confirmed by
inoculating the noses of lab rats with mixtures of the two bacteria. However, a
strain of S. lugdunensis with a broken lugdunin gene couldn’t
pull off the comeback, strongly suggesting that lugdunin was its weapon of choice
against S. aureus.
Is lugdunin the first
antibiotic discovered in the human microbiome?
No, but it’s special
nonetheless. In the last few years, we’ve learned that bacteria in the human
microbiome can produce powerful compounds that have good and bad effects on
people. Bacteria in the vaginal cavity, for instance, secrete an antibiotic called lactocillin, while some gut
bacteria make a DNA-damaging toxin called colibactin that seems to
increase the risk of colorectal cancer.
But all told, these sorts
of secreted compounds, called secondary metabolites, are rare within the human
microbiome—and it’s even more uncommon to learn how and why bacteria use them,
as researchers did with lugdunin. By contrast, scientists are still
trying to pin down how bacteria use lactocillin in the vaginal ecosystem, and
they’re not even entirely sure how the Penicillium mold uses
penicillin in the wild.
Got it. So how does the
new antibiotic work?
Lugdunin’s discoverers
don’t know for sure, but after S. aureus is exposed to
lugdunin, it stops taking in all sorts of vital building blocks, suggesting
that the compound somehow breaks the bacterium’s overall metabolism, mirroring
the general effects of the antibiotic daptomycin.
Antibiotics generally
work in one of a few ways: Some ravage bacteria’s cell membranes or their outer
cell walls, while others gum up their protein-making machinery or prevent
bacteria from repairing their DNA. Surprisingly, researchers often struggle to
nail down precisely how individual ones work, even once they’re successfully
commercialized. Daptomycin was discovered in the late 1980s—but scientists
still aren’t totally sure how it does the job.
Well, no matter what, a
new antibiotic sounds great! When will humans start using it?
Not so fast. It’ll be
years before human clinical trials begin, and even then, there’s no guarantee
that lugdunin will be deemed safe and effective. Daptomycin, for instance, took
more than a decade to obtain approval from the U.S. Food and Drug
Administration, getting the formal sign-off in September 2003.
But as it stands, plenty
of people probably have reaped the advantages of the antibiotic without even
knowing it. The researchers checked the nasal microbiomes of 187 hospital
patients, and only one of the 17 patients withS. lugdunensis colonies
also carried S. aureus. By contrast, nearly two-thirds of the
people without S. lugdunensis carried S. aureus.
And sure enough, all of the hospital patients’ S. lugdunensis colonies
produced lugdunin.
In other words, a helpful
bacterium was hiding under our noses the whole time—by hiding in them.
CREDIT: FEEDSPOT
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