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A new virus emerges and
spreads like wildfire.
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In order to contain it, researchers must
first collect data about who’s been infected.
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Two main viral testing techniques are
critical:
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one tells you if you have the virus and
the other shows if you’ve already had it.
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So, how exactly do these tests work?
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PCR, or polymerase chain reaction testing,
targets the virus’s genetic material in the body
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and is used to diagnose someone who is currently infected.
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Yet, this genetic material may be present
in such imperceptible amounts
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that actually detecting it is difficult.
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This is where PCR comes in:
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it’s widely used to amplify genetic
information to large enough quantities
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that it can be readily observed.
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To develop a PCR test for a
never-before-seen virus,
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researchers first sequence its genetic
material, or genome,
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and identify regions that are unique
to that specific virus.
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PCR then targets these
particular segments.
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A PCR test begins by collecting a sample:
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this can be blood for hepatitis viruses,
feces for poliovirus,
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and samples from the nose or throat
for coronaviruses.
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The sample is taken to a
central laboratory
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where PCR is performed to test for the
presence of the virus’ genome.
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Genetic information can be encoded
via DNA or RNA.
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HPV, for example, uses DNA, while
SARS-CoV-2, the cause of COVID-19,
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uses RNA. Before running the PCR,
the viral RNA—if present—
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must be reverse transcribed to make
a strand of complementary DNA.
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Researchers then run the PCR.
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If the virus is present in the sample,
its unique regions of genetic code
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will be identified by complementary
primers and copied by enzymes.
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One strand of DNA becomes hundreds
of millions,
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which are detected using probes marked
with fluorescent dye.
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If the PCR machine senses fluorescence,
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the sample has tested positive
for the virus,
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meaning the individual is infected.
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Immunoassays, on the other hand,
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tap into the immune system’s
memory of the virus,
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showing if someone has previously
been infected.
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They work by targeting virus-specific
antibodies generated by the immune system
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during infection.
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These are specialized classes of proteins
that identify and fight foreign substances,
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like viruses.
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Immunoassays may detect IgG antibodies,
the most abundant class,
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and IgM antibodies, the type that’s first
produced in response to a new infection.
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The presence of IgM antibodies suggests
a recent infection,
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but since it can take the body over a week
to produce a detectable amount,
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they’re unreliable in diagnosing
current infections.
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Meanwhile, IgG antibodies circulate for
an extended period after infection;
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their presence usually indicates that
someone was exposed and recovered.
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Before the immunoassay,
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health professionals draw blood
from an individual.
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This sample then comes into contact
with a portion of the virus of interest.
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If the body has, in fact, been exposed to
the virus in the past,
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the body’s virus-specific antibodies
will bind to it during the test.
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This reaction produces a change in color,
indicating that the sample tested positive
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and the individual has been
exposed to the virus.
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Immunoassays are especially important
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when it comes to retroactively diagnosing
people who were infected but went untested.
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And there’s exciting potential for those
who have developed immunity to a virus:
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in some cases, their blood plasma could
be used as treatment
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in people who are currently fighting it.
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PCR and immunoassays are always in the
process of becoming more accurate and efficient.
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For example, innovations in PCR have led
to the use of self-contained testing devices
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that relay results within one hour.
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Digital PCR, which quantifies individual pieces
of target DNA,
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shows promise in further boosting accuracy.
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And although immunoassays are difficult
to develop quickly,
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researchers in Singapore were able to
create one for SARS-CoV-2
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even before COVID-19 was declared a
pandemic.
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These tests – along with the scientists
who develop them
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and the health professionals who
administer them –
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are absolutely essential.
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And when deployed early, they
can save millions lives.