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3 - The HIV–AIDS vaccine and the disadvantage of natural selection: the yellow fever vaccine and the advantage of artificial selection

Published online by Cambridge University Press:  24 November 2009

Gerald Esch
Affiliation:
Wake Forest University, North Carolina
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Summary

Cruel as death, and hungry as the grave.

The Seasons: Winter, James Thomson (1700–1748)

One of the things I have always been curious about is why vaccines are effective for certain viruses and not others. The major viral scourge of today is, of course, HIV, with influenza probably a close second. Yellow fever was a major problem in the world until the early 1930s. In the case of HIV, a vaccine has not yet been created, despite an investment of hundreds of millions of dollars. An effective yellow fever vaccine was developed some 75 years ago, in the early 1930s. In fact, since then, nearly 300 000 000 doses of the latter vaccine have been administered without adverse effect. The question I am going to ask in this essay is, why has there been a vaccine success for one of these viruses, but not the other? In a curious way, the answer is decidedly ecological.

The primary sources for my information came from several very good virology books, discussions with a virologist colleague, plus some literature searches in our library. The first tome I used was Topley and Wilson's Volume I of Microbiology and Microbial Infections: Virology, edited by Brian Mahy and Leslie Collier (1998). A second was a popular general ecology textbook, Evolutionary Analysis, written by Scott Freeman and Jon Herron (2004). I also had a series of very productive discussions with Pat Lord, a very solid virologist in our Biology Department here at Wake Forest University.

Type
Chapter
Information
Parasites and Infectious Disease
Discovery by Serendipity and Otherwise
, pp. 150 - 163
Publisher: Cambridge University Press
Print publication year: 2007

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References

Collier, L. H. and Mahy, B. W. J. (eds.). 1998. Topley and Wilson's Microbiology and Microbial Infections. Vol. I: Virology. London: Hodder Arnold.Google Scholar
Freeman, S., and Herron, J. C.. 2004. Evolutionary Analysis. Pearson Education, Inc., Upper Saddle River, New Jersey, 802 p.Google Scholar
Gubler, D. J., and J. T. Roehing. 1998. Arboviruses (Togaviridae and Flavoviridae). In Topley and Wilson's Microbiology and Microbial Infections, Vol. I: Virology, ed. Mahy, B. W. J. and Collier, L., pp. 579–600. London: Arnold.Google Scholar
Hubner, A., Kruhoffer, M., Grosse, F., and Krauss, G.. 1992. Fidelity of human immunodeficiency vurus type 1 reverse transcriptase in copying natural RNA. Journal of Molecular Biology 223: 595–600.CrossRefGoogle Scholar
Larder, B. A., Darby, G., and Richman, D. D.. 1989. HIV with reduced sensitivity to Zidovudine (AZT) isolated during prolonged therapy. Science 243: 1731–1734.CrossRefGoogle ScholarPubMed
Shankarappa, R., Margolick, J. B., Gange, S. J.et al. 1999. Consistent viral evolutionary changes associated with the progression of human immunodeficiency virus type 1 infection. Journal of Virology 73: 10489–10502.Google ScholarPubMed
Wain-Hobson, S. 1993. The fastest genome evolution ever described: HIV variation in situ. Current Opinion in Genetics and Development 3: 878–883.CrossRefGoogle ScholarPubMed

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