Bacterial genomics offers new approaches to better health
Bacteria are single-celled microorganisms abundant in nature that
can’t be seen with the naked eye. In fact, there are approximately five
multiplied by 10³¹ bacteria on the earth, constituting 90% of its
biomass.
These microorganisms are found everywhere in our environment and are
vitally important to maintaining a balanced ecosystem. They cycle
carbon, nitrogen, sulphur, hydrogen and oxygen, regulate and affect the
growth of plants and animals, and are at the base of most food chains.
Microorganisms also play a pivotal role in human health, as most
areas of our body that come in contact with the outside environment,
such as the skin and gastrointestinal tract, harbour resident
(colonising) bacteria. In fact, there are about ten times as many
bacterial cells inside and on you than there are human cells.
These colonising bacteria don’t cause disease under normal
conditions. They actually protect us by preventing the growth of harmful
bacteria. But sometimes colonising bacteria can get past the body’s
defence mechanisms, invade underlying tissue and cause an infection.
This occurs most often when people are unwell and their immunity (or
ability to fight infection) is diminished.
In addition to environmental sources, bacteria are also able to
spread from person to person through close contact. This is generally
not problematic as we are able to remove these transient bacteria with
natural defence mechanisms and regular washing. But when we’re ill, the
ability to clear transient bacteria from our hands or skin is reduced.
These bacteria can then invade and cause infections.
Not surprisingly, this phenomenon is most commonly seen in hospitals
where many ill people are close to each other. When bacteria are spread
to multiple patients over a short period of time, there’s an outbreak of
disease.
Antibiotics are generally used to fight these infections, but
bacteria are able to fight back and evolve resistance, making the
medicines ineffective. They do this by getting DNA that confers
resistance from other bacteria through cell-to-cell transfer (or
conjugation), bacterial viruses or natural uptake of DNA released from
other cells.
A bacterium’s own DNA can also randomly change due to errors that
occur when cells make copies of themselves. Sometimes these changes can
also confer resistance by mechanisms such as changing the site the
antibiotic targets.
Bacteria are masters of adaptation in this respect and, in some
cases, have become resistant to all known antibiotics. Worryingly, the
development of new antibiotics is slow and without more prudent use of
existing ones, it’s likely that the number of people with untreatable
infections will steadily increase.
The complete DNA makeup of an organism is referred to as its genome,
and its constituent part, the DNA-helix, is made up of subunits called
nucleotides (or bases). The human genome is composed of approximately
three billion bases. In contrast, bacterial genomes can range in size
from 0.1 to 13 million bases.
All functions in bacteria (as in humans) are determined by the
genome, and being able to determine a bacterium’s DNA sequence enables
us to gain many important insights. This has not been possible on a
large scale until quite recently. The development of
whole-genome-sequencing technologies means we are now able to sequence
several bacterial genomes in one or two days.
This is useful information because it allows us to understand changes
in bacteria that enable them to invade the body. Bacterial genome
information shows us DNA alterations or mutations that allow bacteria to
switch from being a coloniser to an invader.
It can also provide us with an understanding of which strain or type
of bacteria is dominant within a specific hospital setting, such as an
intensive care unit.
Together, these factors help researchers and medical professionals
develop ways of preventing life-threatening infections. Understanding
the genome dynamics of the bacterium Neiserria meningitidis
(meningococcus), for instance, facilitated development of the meningitis
vaccine. This vaccine now forms part of the general immunisation
schedule and saves numerous lives each year.
Bacterial genome sequencing also allows us to study how bacteria
develop antibiotic resistance. This provides opportunities such as
developing more effective drugs. In other words, we can alter
antibiotics to overcome identified mechanisms of resistance.
And it allows us to understand how bacteria cause outbreaks and track
the spread from person to person, ultimately preventing patients from
developing associated infections.
Being able to readily determine the DNA sequence of bacteria can
facilitate disease prevention in many different ways. And that
dramatically improves the potential for positive patient outcomes.
The field of bacterial genomics (and genome sequencing in general) is
inspired and driven by landmark achievements, such as completion of the
first Human Genome Project. It is now conceivable that, in the not too
distant future, bacterial genome sequencing will be routinely used by
infectious disease specialists to guide patient care
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