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Perspective

The Origins of Pandemic Influenza — Lessons from the 1918 Virus

Robert B. Belshe, M.D.

N Engl J Med 2005; 353:2209-2211November 24, 2005

Article

Audio Interview

Interview with Dr. Robert Belshe on the origins of pandemic influenza.

Interview with Dr. Robert Belshe on the origins of pandemic influenza. (7:14)

The completion of the genetic sequencing of the 1918 influenza A virus by Taubenberger et al.1 and the subsequent recovery of the virus by Tumpey et al.2 using reverse genetic techniques are spectacular achievements of contemporary molecular biology and provide important insights into the origin of pandemic influenza. The three pandemic viruses that emerged in the 20th century — the 1918 (“Spanish influenza”) H1N1 virus, the 1957 (“Asian influenza”) H2N2 virus, and the 1968 (“Hong Kong influenza”) H3N2 virus — all spread rapidly around the world, but only the 1918 virus was associated with mortality measured in the thousands per 100,000 population.

In both 1957 and 1968, a new influenza virus emerged because of reassortment events involving two influenza viruses. The segmented genome allows each influenza A virus to exchange genetic material with other influenza A viruses. In 1957, dual infection of an individual animal — probably a human, but possibly another species, such as a pig — with an avian H2N2 influenza and a human H1N1 influenza resulted in the emergence of a new influenza virus containing the hemagglutinin, the neuraminidase, and the gene for one of the polymerase proteins (PB1) from the avian virus, along with the remaining five genetic segments from the human H1N1 influenza virus.

The new reassortant virus circulated in humans until 1968, when it was replaced by another reassortant virus, the H3N2 Hong Kong virus — created by the replacement of the hemagglutinin (H2) and polymerase (PB1) genes of the H2N2 virus with two new avian genes, H3 and a new PB1. Today, the descendants of this virus continue to cause the majority of influenza infections in humans (see diagramThe Two Mechanisms whereby Pandemic Influenza Originates.). Five of the genes of today's H3N2 influenza virus have their origin in the 1918 pandemic.

The startling observation of Taubenberger et al. was that the 1918 virus did not originate through a reassortment event involving a human influenza virus: all eight genes of the H1N1 virus are more closely related to avian influenza viruses than to influenza from any other species, indicating that an avian virus must have infected humans and adapted to them in order to spread from person to person. Thus, pandemic influenza may originate through at least two mechanisms: reassortment between an animal influenza virus and a human influenza virus that yields a new virus, and direct spread and adaptation of a virus from animals to humans.

The concern at present relates to the widespread epidemic of avian H5N1 influenza in domestic fowl, as well as wild birds, with sporadic transmission to humans. In the past decade, numerous instances of bird-to-human transmission have been recognized (see tableExamples of Transmission of Avian Influenza Viruses to Humans.); although we have only recently become aware of them, these events are surely not new. What is new is the broadening of the range of avian and nonavian species that have become infected with the current H5N1 virus.3

The characterization of the recovered 1918 virus in tissue culture and mice reveals at least two unique qualities. This virus is able to replicate and form plaques on tissue-culture monolayers in the absence of the protease trypsin. Normally, a protease such as trypsin is required to activate the hemagglutinin in order to initiate the infection of tissue culture, but the 1918 virus can activate its own hemagglutinin through the action of neuraminidase, either directly or indirectly (possibly by neuraminidase's binding of a host protease). The exact mechanism by which the neuraminidase takes on the protease activity has not been determined.

In addition, the 1918 virus is 100 times as lethal in mice as any other human influenza virus; the median lethal dose (LD50, or 103.5 to 3.75 median egg infectious doses [EID50]) is low, and the virus replicates rapidly so that high titers (>107 EID50 per milliliter) are found in the lungs of infected mice. High virus inocula result in the death of mice as early as three days after they have been infected. The 1918 virus was susceptible to the adamantine compounds (amantadine and rimantadine) and neuraminidase inhibitors (oseltamivir and zanamivir), and the availability of the recovered virus will facilitate studies of other therapeutics. For example, the vigorous release of cytokines in mice infected with the 1918 influenza virus is associated with rapid onset of pulmonary disease and death. Compounds that block the action of specific cytokines can now be evaluated as therapeutics that might help to reduce the mortality associated with pandemic influenza.

It is not possible to know whether the current H5N1 is capable of adapting to humans so that it can spread with high efficiency through low-titer aerosol transmission to initiate an influenza pandemic. However, Taubenberger et al. provide some guidance on the genetic changes that might be required for such an event. The role of PB1 must be critical, since in both 1957 and 1968, this polymerase gene was transferred along with the hemagglutinin during reassortment. By comparing the consensus sequence of the three avian influenza polymerase genes PA, PB1, and PB2 with the 1918 sequence, as well as with more contemporary influenza viruses, Taubenberger et al. have identified four amino acids of PA, one of PB1, and five of PB2 that are found in human influenza viruses (including the 1918 virus) but generally not in avian influenza viruses. In two instances, these amino acids are found in nuclear localization signaling regions, suggesting that some or all of these amino acid differences are critical for the virus to adapt to humans.

The genetic sequences of the 1997 Hong Kong H5N1 virus and the 2004 Vietnam H5N1 virus reveal that several human isolates of these viruses contain one of the five amino acid changes in PB2 that have been identified as important to the ability of the 1918 virus to infect humans. This finding suggests that several additional genetic changes must occur before these viruses will begin to spread efficiently from person to person. The genetic sequences of avian viruses may provide a window through which to monitor these sporadic transmissions for the potential of the viruses to adapt to humans. The occurrence of additional genetic changes in the avian H5N1 virus circulating in birds that match the consensus sequence for PA, PB1, or PB2 in human influenza would be cause for heightened concern.

On the basis of the rates of replacement of amino acids, Taubenberger et al. estimated that avian influenza polymerase genes had been circulating in humans as early as 1900. If this estimate is correct, then monitoring of the sequences of viruses isolated in instances of bird-to-human transmission for genetic changes in key regions may enable us to track viruses years before they develop the capacity to replicate with high efficiency in humans. Knowledge of the genetic sequences of influenza viruses that predate the 1918 pandemic would be extremely helpful in determining the events that may lead to the adaptation of avian viruses to humans before the occurrence of pandemic influenza. We could then conduct worldwide surveillance for similar events involving contemporary avian viruses.

An interview with Dr. Belshe can be heard at www.nejm.org.

Source Information

Dr. Belshe is a professor of medicine, pediatrics, and molecular microbiology in the Division of Infectious Diseases and Immunology, Department of Internal Medicine, Saint Louis University, St. Louis.

References

References

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    Taubenberger JK, Reid AH, Lourens RM, Wang R, Jin G, Fanning TG. Characterization of the 1918 influenza virus polymerase genes. Nature 2005;437:889-893
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    The Writing Committee of the World Health Organization (WHO) Consultation on Human Influenza A/H5. Avian influenza A (H5N1) infection in humans. N Engl J Med 2005;353:1374-1385
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