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zoonoses and communicable diseases common to ... - PAHO/WHO

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PLAGUE 207PLAGUEICD-10 A20.0 bubonic plague; A20.2 pneumonic plague;A20.7 septicaemic plagueSynonyms: Black death, pestilential fever, pest.Etiology: The etiologic agent of plague is Yersinia pestis, a gram-negative, nonmotilebacterium, coccobacillary <strong>to</strong> bacillary in form <strong>and</strong> showing bipolar stainingthat is not very resistant <strong>to</strong> physical <strong>and</strong> chemical agents. DNA hybridization studiesdemonstrated the close genetic relationship between Yersinia pestis <strong>and</strong> Y.pseudotuberculosis (Bercovier et al., 1980). On the basis of this, the authors suggestedcalling the etiologic agent of plague Y. pseudotuberculosis subsp. pestis(International Committee on Systemic Bacteriology, List 7, 1981). However, theCommittee’s Judicial Commission (1985) decided <strong>to</strong> reject this nomenclature <strong>and</strong>retain the name Y. pestis in order, among other reasons, <strong>to</strong> avoid possible confusion.Three biological varieties are distinguished: Orientalis (oceanic), Antiqua (continental),<strong>and</strong> Mediaevalis. This distinction has a certain epidemiological significance,principally for nosography, but there is no difference in the biotypes’ pathogenicity.Some virulence fac<strong>to</strong>rs of Y. pestis were defined in the 1980s. Apparently, theprincipal fac<strong>to</strong>r is a 45-megadal<strong>to</strong>n plasmid. This plasmid encodes calcium dependencyfor growth at 37°C, but not at lower temperatures, as well as the virulence antigensV <strong>and</strong> W. The two proteins on the outer membranes that are assumed <strong>to</strong> beimportant in virulence (E <strong>and</strong> K) are also plasmid dependent. The precise role ofeach of these fac<strong>to</strong>rs is not yet well defined (Butler, 1989).Geographic Distribution: Natural foci of infection persist on nearly all continents;they do not exist in Australia, New Zeal<strong>and</strong>, or New Guinea. In the Americas,sylvatic plague is maintained in rodents in the western third of the United States, theborder region of Ecuador <strong>and</strong> Peru, southeastern Bolivia, <strong>and</strong> northeastern Brazil.Similarly, there are foci in north-central, eastern, <strong>and</strong> southern Africa, includingMadagascar; the Near East; the border area between Yemen <strong>and</strong> Saudi Arabia;Kurdistan province (Iran); <strong>and</strong> central <strong>and</strong> Southeast Asia, in Myanmar (Burma) <strong>and</strong>Vietnam. There are also several natural foci in the former Soviet Union <strong>and</strong> inIndonesia (Benenson, 1990).Occurrence in Man: Since the dawn of the Christian era, there have been threegreat p<strong>and</strong>emics: the first began in 542 (Justinian plague) <strong>and</strong> is estimated <strong>to</strong> havecaused 100 million deaths; the second began in 1346, lasted three centuries, <strong>and</strong>claimed 25 million victims; <strong>and</strong> the last began in 1894 <strong>and</strong> continued until the1930s. However, the data on incidence in the Middle Ages are very approximate <strong>and</strong>difficult <strong>to</strong> verify. As a result of the last p<strong>and</strong>emic, natural foci of infection wereestablished in South America, West Africa, South Africa, Madagascar, <strong>and</strong>Indochina.Urban plague has been brought under control in almost the entire world, <strong>and</strong> ruralplague of murine origin is also on the decline. Nevertheless, epidemics haveoccurred in Indonesia, Nepal, <strong>and</strong> southern Vietnam. In this last country, there were5,274 cases in 1967 due <strong>to</strong> contact with domestic rats <strong>and</strong> their fleas.

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