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

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26 BACTERIOSESpened in the 1974 epizootic in Texas (USA), during which 218 cattle, 6 horses, <strong>and</strong>1 mule died. Eighty-three percent of the fields where the outbreak <strong>to</strong>ok place hadacid pH soil <strong>and</strong> 94% had subsoil with an alkaline pH (Whitford, 1979).Contaminated animal by-products, especially bone meal <strong>and</strong> blood meal used asfood supplements, can also give rise <strong>to</strong> distant foci of infection.Another mode of transmission is cutaneous entry through insect bites, but this isconsidered of minor epidemiologic importance.Role of Animals in the Epidemiology of the Disease: Animals are essential.Anthrax is transmitted <strong>to</strong> humans by animals or animal products. Transmissionbetween humans is exceptional.Diagnosis: The presence of the etiologic agent must be confirmed by microscopicexamination of stained smears of vesicular fluid (in man), edemas (in swine), <strong>and</strong>blood (in other animals); by culturing the microorganism from the liquid aspiratedfrom malignant pustules or from blood samples of a dead or dying animal; <strong>and</strong> byinoculation of labora<strong>to</strong>ry animals (guinea pigs <strong>and</strong> mice). If the material is contaminated,cutaneous inoculation (by scarification) should be used. The use of antibioticsquickly reduces the possibility of isolating the etiologic agent.The fluorescent antibody technique applied <strong>to</strong> fresh stains or blood smears canprove useful for presumptive diagnosis. Smears of blood or other bodily fluids canalso be stained using the Giemsa or Wright method <strong>to</strong> make the pink capsule thatsurrounds the bacillus st<strong>and</strong> out. The Ascoli precipitation test has limited value due<strong>to</strong> its limited specificity, but is still used in some labora<strong>to</strong>ries for animal products,from which the agent cannot be isolated.The ELISA <strong>and</strong> Western Blot tests can be used <strong>to</strong> detect antibodies <strong>to</strong> the protectiveantigen in individuals who have had anthrax <strong>and</strong> from whom the agent cannotbe isolated, i.e., in retrospective studies (Thurnbull et al., 1986; Sirisanthana et al.,1988; Harrison et al., 1989). Antibodies have also been found in people living nearanimal reserves in Africa who have been exposed <strong>to</strong> anthrax in wild animals withoutbecoming ill themselves (Thurnbull et al., 1991).Control: In man, the prevention of anthrax is based mainly on: (a) control of theinfection in animals; (b) prevention of contact with infected animals <strong>and</strong> contaminatedanimal products; (c) environmental <strong>and</strong> personal hygiene in places whereproducts of animal origin are h<strong>and</strong>led (adequate ventilation <strong>and</strong> work clothing); (d)medical care for cutaneous lesions; <strong>and</strong> (e) disinfection of fur <strong>and</strong> wool with hotformaldehyde. Occupational groups at risk may benefit from vaccination with theprotective antigen.The human vaccine used in the US <strong>and</strong> Great Britain is acellular <strong>and</strong> consists ofa filtrate of B. anthracis culture from a nonencapsulated strain that is adsorbed withaluminum hydroxide. This vaccine is not very potent <strong>and</strong> may not protect against allfield strains. In the countries of Eastern Europe <strong>and</strong> in China, a live attenuated sporevaccine is administered by scarification.In animals, anthrax control is based on systematic vaccination in enzootic areas.Sterne’s avirulent spore vaccine is indicated because of its effectiveness <strong>and</strong> safety.The vaccine consists of spores from the nonencapsulated 34F2 strain with an adjuvant—usuallya saponin—<strong>and</strong> is currently used worldwide, with a few exceptions.It is suitable for all domestic animal species. However, goats sometimes have severe

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