Abstract

Although this book’s title promises the excitement of a 21st-century computer game, the cover photograph of Robert Koch in 1883 provides a better clue to the contents. The general plan is a survey of 20th-century genetics, illustrated by insights into human coevolution with microbial pathogens. Early chapters focus on familiar examples, including G6PD deficiency and sickle cell trait as adaptations to malaria, as evidence for pathogen-driven natural selection. Later chapters discuss more recent research findings, varying from female preference for the scent of males with dissimilar human leukocyte antigen types to the role of human CFTR membrane protein in infection with Salmonella Typhi. All of these are such good stories that science writer Matt Ridley included briefer versions in Chapter 9 of his popular book Genome: The Autobiography of a Species in 23 Chapters (1). Battle of the Genomes: The Struggle for Survival in a Microbial World discusses in some detail how catastrophic epidemics of cholera, bubonic plague, and smallpox could explain the emergence of certain common human genetic mutations. Some of these mutations are deleterious; for example, CFTR ΔF508, which reduces the risk for typhoid, causes cystic fibrosis in persons who inherit 2 copies. Other mutations are beneficial, such as CCR5 Δ32, which may have protected carriers from smallpox and now reduces the risk for HIV infection. In general, the author’s review of the evidence for and against these hypotheses, which remain speculative, is evenhanded and up-to-date. His accounts of the human and social effects of epidemic diseases and the origins of public health are full of lively anecdotes and colorful detail. Interspersed throughout are personal asides, clinical pearls, and lengthy tutorials on basic science topics, such as DNA replication and gene splicing. Although this book is far more information dense than are popular books for the lay public, its many shortcomings in terms of organization, depth, and documentation (including surprisingly few references) diminish its value to scholarly readers. More than anything else, it resembles an intellectually inspired but somewhat disorganized professor’s medical school lecture, which would probably be more fun to hear in person than to read. Meanwhile, those who are interested in a 21st-century account of the battle of the genomes may want to wait. Rapid advances in genomic science and technology are opening the way to better understanding of biology, evolution, and medicine, but the full integration of these disciplines is still at a relatively early stage. The idea that genes of 1 species can influence whole ecosystems, described by Richard Dawkins in 1982 as the “extended phenotype” (2), is only now giving rise to new perspectives on community genetics (3).

Highlights

  • Prions are believed to be the causative agents of a group of rapidly progressive neurodegenerative diseases called transmissible spongiform encephalopathies, or prion diseases

  • Interest in prion disease research dramatically increased after the identification in the 1980s of a large international outbreak of bovine spongiform encephalopathy (BSE, known as mad cow disease) in cattle and after accumulating scientific evidence indicated the zoonotic transmission of BSE to humans causing variant Creutzfeldt-Jakob disease (CJD)

  • Secondary bloodborne transmission of variant CJD has been reported in the United Kingdom

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Summary

Claudio Soto

CRC Press, Taylor & Francis Group, Boca Raton, Florida, USA, 2005 ISBN: 9780849314421 Pages: 184; Price: US $139.95. Prions are believed to be the causative agents of a group of rapidly progressive neurodegenerative diseases called transmissible spongiform encephalopathies, or prion diseases. They are infectious isoforms of a hostencoded cellular protein known as the prion protein. The book is organized into 12 mostly brief chapters, which nicely summarize the various types of prion diseases and the challenges associated with their diagnosis and treatment. These sections review the biology of prions, the underlying hypotheses for prion replication, and the biochemical basis for strain diversity. All things considered, the book can be a valuable resource for scientists beginning to understand the world of prion diseases, the underlying biochemical mechanism of disease occurrence, and the challenges associated with the diagnosis and treatment of prion diseases

Struggle for Survival in a Microbial World
Phyllis Entis
Full Text
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