Disrupting Bacterial Communications

Disrupting Bacterial Communications

Brian Trumbore just dropped off an interesting article on head

lice. It seems that perhaps one in every five children in Britain

have these creatures roaming around in their hair. Getting rid of

them is no easy task and there is a good deal of controversy over

the best procedures. As widespread as it is, the lice problem

seems rather low on the scale of problems that need solutions,

especially in these times of anthrax and other deadly diseases

that terrorists might employ. I found an article in the July 2001

issue of Scientific American that seems more relevant now than

it was back in July.

The article, by J. W. Costerton and Philip S. Stewart, is titled

“Battling Biofilms”. The opening paragraph notes the similarity

between the Pentagon”s “information warfare” and a developing

approach by researchers fighting harmful bacteria. As we”ve

now seen in Afghanistan, a major objective of the Pentagon”s

strategy has been to destroy the Taliban”s ability to communicate.

Within the past decade or so, communication among bacteria has

also been recognized as playing an important role in spreading

disease.

We”re all familiar with the work of those who culture bacteria in

dishes and then add an antibiotic or some other drug to see if the

drug kills the bacteria. We often hear of some promising drug

that seems to be the solution to curing a certain disease, based on

such experiments. Yet, years later we don”t seem to hear

anything more about that drug. What”s the problem? The drug

doesn”t work the same way in the human body. Sometimes the

drug is unacceptable because of serious side effects. However,

scientists now realize that there”s another problem – biofilms.

What do your teeth, contact lenses, metal piping in steam-driven

electric power plants and the Washington, D.C. water supply

have in common? All present surfaces for the growth of

biofilms. Dental plaque is a biofilm, as is the growth on your

lens that could cause corneal infection. Biofilms in power plants

speed up corrosion, the cause of half their unscheduled outages.

Biofilms resistant to chlorination have apparently on several

occasions degraded the quality of water supplies below the

Federal standards in Washington.

What is a biofilm? Ever since the germ theory of disease was

proved, virtually everybody looked at these bacteria swimming

around in various fluids as single cells. That”s how they are

studied in those cultures, as single cells in a watery liquid.

Overlooked was all that slimy stuff that is found all around us.

Or, in the case of dental plaque, inside us. What the slimes were

showing us was something we”ve known for thousands of years.

The solitary life isn”t as good as a life in a family or a

community. Bacteria are no different. They like to get together

to form a biofilm.

When the individual bacterium plops down on a surface, it first

grabs onto the surface, then begins making and sending out

signaling molecules. If there are other bacteria in the region,

they”re also sending out these signaling molecules. When the

concentration of these molecules gets high enough, it”s a signal

that there are enough bacteria in the area to form a “quorum”.

It”s time for the bacteria to come together and form a little

community by clumping together. If enough bacteria are around

there will be a number of these little communities and the

bacteria begin making a gooey, liquidy stuff that keeps the

clumps together. When things are just right, the cells start

multiplying and this biofilm grows, like a mushroom.

Now we have a network of these clumps of bacteria held together

in this porous gooey stuff, with channels in it that allow water

and nutrients to flow. But, while the outer clumps get a full share

of nutrients, the clumps deeper in the biofilm don”t get the same

share. As a result, the bacteria within the biofilm are in different

stages. The well-fed bacteria may be very active and multiplying

while the undernourished inner bacteria are sluggish or even

dormant. Sometimes, other kinds of bacteria passing by decide

the biofilm looks attractive and they jump in to join in the fun.

This can prove to be a beneficial immigration for the original

bacteria, which may thrive on the waste products of the new

arrivals or vice versa. So, now you have a multicultural biofilm

with different “races” and different stages of the same bacteria.

This diversity within the biofilm is not good if you”re trying to

kill the bacteria. For example, some drugs such as penicillin go

after reproducing bacteria but may be ineffective against the

dormant bacteria. Thus you might kill the outer bacteria but the

inner dormant ones are still unaffected and ready to spring into

action to rebuild the biofilm when the time is ripe. Those

bacteria that have become resistant to penicillin may have the

ability to manufacture a chemical that fights the penicillin. A

single cell, however, may still succumb to the penicillin but a

biofilm colony of the same bacteria will produce enough of the

chemical to mount an effective defense.

You may have an example of this benefit to a bacterial

community in a biofilm in that slimy stuff that forms in your

shower. You may reach for the chlorine bleach and a brush to

scrub the area clean. But that biofilm has stuff in it that tends to

neutralize the bleach and you may think you”ve killed the

buggers. However, the inner bacteria are still quite alive, if

dormant. You may find it takes a lot more scrubbing and a lot

more bleach to do the job than you had thought.

As with any community, there are some individuals who prefer

to strike out on their own and as the biofilm ages, some of the

bacteria revert to their single cell behavior and wander off to

establish new biofilms of their own.

Now that medical researchers know that the real challenge posed

by bacteria is in biofilms, they are starting to target various

stages in the biofilm”s development. We”ve seen that a key to

forming the biofilm is those signaling molecules. Disrupting the

communications is one approach. Accordingly, efforts are being

made to find drugs that will inhibit the signaling molecules from

being formed or released or even being sensed. Workers are also

trying to find compounds to apply to medical implants that will

stop the production of that gooey stuff that holds the biofilm

together. There is also the possibility of finding something that

will inhibit the bacteria from sticking to the surface in the first

place. All sorts of things can now be tried.

Biofilms have now been implicated in a number of maladies as

varied as periodontal disease, prostate infections, tuberculosis

and Legionnaire”s disease. Wouldn”t it be great if something

could be found that would either prevent the formation of the

hurtful biofilms or break them up after they formed? A few

years ago, workers by the names of Kjelleberg and Steinberg in

an Australian university made a discovery that has prompted a

new field of work on just such a compound. They found that the

fronds of a certain red alga in the waters of Botany Bay hardly

ever were covered with biofilms. Yet other types of algae in the

same waters harbored biofilms routinely.

Kjelleberg and Steinberg found that the “clean” red alga

produced a chemical in the class known as furanones. I have no

idea what furanones are – let”s call then Fury for short. The other

algae did not have Fury associated with them. Obviously, it was

hoped that it was Fury that was preventing or killing the

biofilms. Remember those signaling molecules I mentioned

earlier? It turns out that Fury is similar to the molecules used by

bacteria in signaling and detecting when they have the “quorum”

to begin a biofilm. Speculation is that, because of the similarity,

Fury grabs onto the sites on the bacteria where the signaling

molecules normally attach. By beating those signaling molecules

to the punch, Fury prevents the bacteria from finding out there”s a

quorum and the biofilm doesn”t form.

Experiments have shown that Fury can prevent or even break up

biofilms in mice. However, it doesn”t appear that that the Fury

compounds tested so far are safe for human use. Nevertheless,

Fury has stimulated a major effort to find other, safer compounds

that can mimic those signaling molecules and carry out the same

strategy as the Pentagon -disrupt the communications. Let”s hope

both the military and the biological strategies prove wildly

successful!

Allen F. Bortrum