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. 2006 Mar;12(3):460-7.
doi: 10.3201/eid1203.051051.

Pneumonic plague cluster, Uganda, 2004

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Pneumonic plague cluster, Uganda, 2004

Elizabeth M Begier et al. Emerg Infect Dis. 2006 Mar.

Abstract

The public and clinicians have long-held beliefs that pneumonic plague is highly contagious; inappropriate alarm and panic have occurred during outbreaks. We investigated communicability in a naturally occurring pneumonic plague cluster. We defined a probable pneumonic plague case as an acute-onset respiratory illness with bloody sputum during December 2004 in Kango Subcounty, Uganda. A definite case was a probable case with laboratory evidence of Yersinia pestis infection. The cluster (1 definite and 3 probable cases) consisted of 2 concurrent index patient-caregiver pairs. Direct fluorescent antibody microscopy and polymerase chain reaction testing on the only surviving patient's sputum verified plague infection. Both index patients transmitted pneumonic plague to only 1 caregiver each, despite 23 additional untreated close contacts (attack rate 8%). Person-to-person transmission was compatible with transmission by respiratory droplets, rather than aerosols, and only a few close contacts, all within droplet range, became ill.

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Figures

Figure 1
Figure 1
A) Grossly bloody sputum sample obtained from the surviving patient (caregiver B2) 30 h after onset of primary pneumonic plague. B) Polymerase chain reaction results of sputum sample from caregiver B2. Lanes 1–3, caf1; lanes 4–6, repA1; lanes 7–9, pla. Lanes 1, 4, and 7 are positive controls; lanes 2, 5, and 8 are patient samples; lanes 3, 6, and 9 are negative controls. C) Anti-F1 direct fluorescent antibody staining of sputum sample from caregiver B2. Numerous bacteria with classic halo structures are characteristic of Yersinia pestis. The circled bacterium classically depicts this halo.
Figure 2
Figure 2
Three serial frontal chest radiographs from surviving caregiver B2 with primary pneumonic plague obtained on illness days 2, 3, and 18 showing bilateral lower lung zone predominant airspace disease associated with bilateral (right > left) pleural effusions. The radiographs have artifacts related to hand-dipping of the films, which account for multiple densities that move between images and the areas of apparent lucency.

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