MadSci Network: Virology |
That is a good question. There are those who would speculate that 1,400,000 people would
die during the acute epidemic. This would be a simple extrapolation of
proportional deaths based on the percent of the population 600,000
represented in 1918 - 1919. Of course that would be a terrifying event but
it also would be very unlikely because of present knowledge about
influenza, epidemiology and medical treatment.
There were several coincidences in 1981 that converged on the beginnings
of this epidemic that might never occur this way again.
One rare coincidence was the fact that two or more genes encoding proteins
responsible for the infectivity and virulence mutated and those mutations
resulted in increased infectivity and virulence. Mutations occur in these
proteins but often they reduce infectivity and virulence rather than
increase it. If a protein responsible for virulence is changed the change
is usually only a slight shift. In the case of the 1918 Flu the two
antigens known to have changed, changed so dramatically that there was
little or no cross reactive immunity from other Flu infections to reduce
the disease.
The other rare coincidence was that the epidemic started just as the world
was involved with World War I and huge numbers of military recruits were
housed in cramped quarters at training camps, aboard ships, and in
trenches in the battlefield. Since influenza spreads by aerosol, which is
comprised of tiny droplets of moisture containing shed viruses that can
remain airborne long enough to enter the nose, throat and lungs of
neighbors who breath the contaminated air. The huge outbreaks of Flu among
young soldiers who then mobilized all over the country and all over Europe
served as a human Trojan horse that amplified the magnitude of spread of
the epidemic. The likelihood that such a massive troop mobilization would
be happening at the onset of a Flu epidemic would be very small today.
Furthermore, we now monitor (The CDC
Monitors) serious cases of influenza and the specific antigens are
determined so that the next year's vaccine can contain antigens from the most serious or infectious cases.
The epidemic of 1918 occurred when the fields of immunology and virology
were in infancy and few hospitals had the ability to do serology for
influenza and few could isolate and characterize a virus. Today, molecular
biology has given us tools that supplement serological diagnoses and we
anticipate will revolutionize viral diagnosis as these tools become
licensed for use in hospital clinical laboratories.
The news that scientists at the Armed
Forces Institute of Pathology had recovered and analyzed the RNA for
the 1918 Flu virus from autopsy tissues archived since 1918, and
scientists collected similar specimens from human cases that had been
under permafrost above the arctic circle indicates that Gene probes could
be available that would enable diagnosis of a Flu infection like the 1918
Flu within moments of its testing by this experimental system. The
prototype system benefits from Polymerase Chain Reaction PCR technology
and other linked technologies that allow identification of the PCR product
in real-time. It took days to weeks in 1918 to even determine that the
infection was caused by a virus and not a bacterium. The shortening of
time for diagnosis by itself could be a significant reason to suspect
reduced mortality from such an epidemic.
Availability of gene sequence information about the genes encoding
proteins of influenza virus that were responsible for high virulence in
1918 could enable quick development of novel anti-viral drugs that inhibit
attachment, uncoating, gene activation or replication would nip this
influenza in the bud. The potential to make such claims frankly did not
exist in 1918.
OK, so I am an optimist. The truth is an epidemic often starts before
anyone becomes aware of it. There is often a period of time when people
first realize something is wrong when numerous theories about what is
wrong often interferes with the systematic process of isolating the agent,
collecting specimens from sick people and analyzing both to determine what
it is. Often the knowledge, skill and experience to do this effectively
exists in a small poorly funded laboratory in an institute or university,
maybe even a place that isn't known in every household. This is why quick
effective communication about infectious diseases is as important as the
technology in reducing morbidity (sickness) and mortality (death).
I hope these answers were useful to you and anyone interested in the
topic.
Art Anderson
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