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

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SHIGELLOSIS 247SHIGELLOSISICD-10 A03.0 shigellosis due <strong>to</strong> Shigella dysenteriae;A03.1 shigellosis due <strong>to</strong> Shigella flexneri;A03.2 shigellosis due <strong>to</strong> Shigella boydii;A03.3 shigellosis due <strong>to</strong> Shigella sonnei; A03.8 other shigellosisSynonyms: Bacillary dysentery.Etiology: The genus Shigella belongs <strong>to</strong> the family Enterobacteriaceae. Shigellaeare small gram-negative, nonmotile, unencapsulated bacilli; they are anaerogenic(with a few exceptions) <strong>and</strong> non-lac<strong>to</strong>se fermenting (or slow fermenters).The genus Shigella may be considered genetically as a single species, closelyrelated in DNA analyses <strong>to</strong> E. coli. However, it is divided in<strong>to</strong> four species based onphenotype traits. Each species is a distinct serogroup: Shigella dysenteriae(serogroup A), S. flexneri (serogroup B), S. boydii (serogroup C), <strong>and</strong> S. sonnei(serogroup D). The four serogroups contain a <strong>to</strong>tal of 38 serotypes. Serotyping isimportant in epidemiological investigation. Diagnostic labora<strong>to</strong>ries are generallylimited <strong>to</strong> identifying the serogroup <strong>and</strong> sending cultures <strong>to</strong> a reference labora<strong>to</strong>ryfor identification of the serotype.The primary virulence fac<strong>to</strong>r of a Shigella strain is its ability <strong>to</strong> invade cells of theintestinal mucosa. The invasive capacity depends on fac<strong>to</strong>rs controlled by both chromosomic<strong>and</strong> plasmidic genes (Keusch <strong>and</strong> Bennish, 1991).The invasive capacity of a strain can be demonstrated with the Sereny test, whichconsists of inoculating a culture in a guinea pig’s conjunctival sac. Invasive strainsproduce kera<strong>to</strong>conjunctivitis in 24 <strong>to</strong> 48 hours. Cultures obtained from clinical casesalways yield a positive Sereny test result. Shigellae also produce cy<strong>to</strong><strong>to</strong>xins, particularlyin the case of S. dysenteriae serotype 1 (Shiga <strong>to</strong>xin).Geographic Distribution: Worldwide.Occurrence in Man: Shigellosis can be either epidemic or endemic. Epidemic orp<strong>and</strong>emic shigellosis is usually caused by S. dysenteriae serotype 1 (Shiga bacillus),the most virulent <strong>and</strong> <strong>to</strong>xigenic strain. In 1969–1970, a widespread epidemic causedby S. dysenteriae serotype 1 occurred in Central America <strong>and</strong> Mexico, with highmorbidity <strong>and</strong> mortality rates, particularly in children. More than 13,000 patientsdied as a result. The infection was introduced in the US, where 140 cases occurredfrom 1970 <strong>to</strong> 1972. The epidemic spread <strong>to</strong> Central Africa <strong>and</strong> Asia (India,Bangladesh, <strong>and</strong> Sri Lanka). Plasmid analysis demonstrated that the p<strong>and</strong>emic wasnot produced by a single bacterial clone. Thus, it is difficult <strong>to</strong> explain the appearanceof the disease in such distant areas. The strains isolated in all areas proved <strong>to</strong>be multiresistant <strong>to</strong> antibiotics (<strong>WHO</strong>, 1987). In Guatemala, there were 112,000cases with 10,000 deaths from 1969 <strong>to</strong> 1972. A new outbreak appeared in Guatemalain 1991 caused by S. dysenteriae serotype 1; it affected 540 people in the course ofone month, both in Guatemala City <strong>and</strong> in Verapaz, a city of 10,000 inhabitants(CDC, 1991).Endemic shigellosis is usually caused by S. flexneri <strong>and</strong> S. sonnei. The first occursprimarily in developing countries, the second, in economically advanced countries.Morbidity <strong>and</strong> mortality rates are high in developing countries, particularly in chil-

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