"Doctor Schnabel von Rom" (English: "Doctor Beak of Rome") engraving by Paul Fürst (after J Columbina). The beak is a primitive gas mask, stuffed with substances (such as spices and herbs) thought to ward off the plague.Worldwide distribution of plague infected animals 1998
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Bubonic plague

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Types

ICD-10 codes are provided below.

  • (A20.0) Bubonic plague is an infectious disease that is believed to have caused several epidemics or pandemics throughout history. The disease is caused by the bacterium Yersinia pestis. Bubonic plague is the most common form of plague, and is characterized by swollen, tender, inflamed lymph glands (called buboes).
  • (A20.7) Septicemic plague occurs when plague bacteria multiply in the blood.
  • (A20.2) Pneumonic plague occurs when the lungs are infected.

Infection/transportation

Bubonic plague is primarily a disease of rodents, particularly marmots (in which the most virulent strains of plague are primarily found), but also black rats, prairie dogs, chipmunks, squirrels and other similar large rodents. Human infection most often occurs when a person is bitten by a rat flea (Xenopsylla cheopsis) that has fed on an infected rodent. The bacillus multiplies in the stomach of the flea, blocking it. When the flea next bites a mammal, blood consumed by the flea is regurgitated along with the bacillus into the bloodstream of the bitten animal. Any serious outbreak of plague is started by other disease outbreaks in the rodent population. During these outbreaks, infected fleas that have lost their normal hosts seek other sources of blood.

In 1894, bacteriologists Alexandre Yersin and Shibasaburo Kitasato independently isolated the responsible bacterium and Yersin further determined that rodents were the likely common mode of transmission. The disease is caused by the bacterium Yersinia pestis.

Symptoms and treatment

The disease becomes evident 2–7 days after infection. Initial symptoms are chills, fever, headaches, and the formation of buboes. The buboes are formed by the infection of the lymph nodes, which swell and become prominent. If unchecked, the bacteria infects the bloodstream (septicemic plague), and can progress to the lungs (pneumonic plague).

In septicemic plague there is bleeding into the skin and other organs, which creates black patches on the skin. Untreated septicemic plague is universally fatal, but early treatment with antibiotics (usually streptomycin or gentamicin) is effective, reducing the mortality rate to around 15% (USA 1980s). People who die from this form of plague often die on the same day symptoms first appear.

With pneumonic plague infecting lungs comes the possibility of person-to-person transmission through respiratory droplets. The incubation period for pneumonic plague is usually between two and four days, but can be as little as a few hours. The initial symptoms of headache, weakness, and coughing with hemoptysis are indistinguishable from other respiratory illnesses. Without diagnosis and treatment, the infection can be fatal in one to six days; mortality in untreated cases may be as high as 95%. The disease can be effectively treated with antibiotics.

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Plague from eating raw camel liver
From Emerging Infectious Diseases, 9/1/05 by Abdulaziz A. Bin Saeed

We investigated a cluster of 5 plague cases; the patients included 4 with severe pharyngitis and submandibular lymphadenitis. These 4 case-patients had eaten raw camel liver. Yersinia pestis was isolated from bone marrow of the camel and from jirds (Meriones libycus) and fleas Xenopsylla cheopis captured at the camel corral.

**********

Human plague is acquired most often from the bites of infected fleas that leave their rodent hosts. Sporadic plague has also been attributed to domestic dogs and cats that may transport either Yersinia pestis in their mouths or infected fleas from rodent hosts to humans (1). Bubonic, pneumonic, or pharyngeal plague may develop in domestic cats and infect humans directly (2). However, humans rarely become infected when handling and preparing the carcasses of wild animals (3). Although domestic cats and other carnivores may be infected by eating infected animals, only 1 previous report raises the possibility of human plague infection from eating meat of an infected animal (4).

The Study

In February 1994, we investigated a cluster of 5 plague cases in Goriat, a town of 50,000 persons in a remote desert area in northwestern Saudi Arabia. On February 18, a 26 year-old-woman was admitted to the provincial hospital for severe pharyngitis and tonsillitis. Given the striking swelling of her neck, local clinicians suspected diphtheria. Since 2 of the patient's relatives had also been hospitalized in the previous 2 days with similar illnesses, the hospital called for assistance from the local preventive medicine specialist. He had seen similar cases in 1984 and suspected pharyngeal plague.

Through interviews with physicians and review of hospital admissions, we identified 5 patients, including the index case, who had been hospitalized with suspected plague or plague pharyngitis. The patients included a 9-year-old girl and 4 adults (2 men and 2 women, age range 18-35 years). Symptoms developed in 1 patient on February 15 and in 4 patients on February 16. All had fever (39[degrees]-40[degrees]C), chills, malaise, myalgias, vomiting, headache, and delirium. Leukocyte counts ranged from 11,000 to 88,000/[micro]L. Chest radiographs were normal in all 5 patients. Four had severe pharyngitis; 3 of them had dysphagia, tender submandibular lymphadenitis, and tonsillar enlargement. The fourth patient, the 9-year-old girl, had severe abdominal pain and tenderness on abdominal palpation, profound hypotension (blood pressure 60/30 mm Hg), and a generalized hemorrhagic rash. This patient and the 26-year-old index patient (blood pressure 90/60 mm Hg) died. These 4 patients with pharyngitis did not have buboes or lymphadenitis at any other site. The patient without pharyngitis had axillary lymphadenitis and cellulitis of his right arm; he had cut his arm while killing a sick camel on February 13. None of the patients had skin lesions that suggested recent flea bites.

Y. pestis was isolated from the blood of the patient with pharyngitis who died and from the spinal fluid of the patient with abdominal pain. Identification was confirmed by phage lysis and direct fluorescent antibody staining. Indirect hemagglutination for plague was positive in convalescent-phase sera from the 3 survivors from whom Y. pestis was not isolated.

The patients were from 4 related families, 2 from Goriat and 2 from a village 20 km from this town. The adult family members denied seeing rodents around their homes or being bitten by fleas or other biting insects. All families owned camels. The male head of each family traveled to the desert daily to allow his camels to graze. These men reported that several of their camels had recently died. We observed 3 camel carcasses in the desert near a corral where the camels were fed grain and hay to supplement their grazing.

The meat from the sick camel that had been butchered on February 13 was shared among 11 families (106 members). No other food was shared among these families. The 4 patients with pharyngeal plague were among 37 people who had eaten this camel meat; 1 patient with bubonic plague (the man who slaughtered the camel) was among the 69 people who had not eaten the meat (risk ratio [RR] 7.7, p<0.05, Fisher exact test). Moreover, pharyngeal plague developed in 4 of 6 patients who had eaten raw camel liver, but not in 31 persons who had eaten only cooked camel meat or liver (RR not defined, p<0.01, Fisher exact test).

We isolated Y. pestis from a sample of leftover camel meat containing bone and marrow. Jirds (Meriones libycus), jird carcasses, rodent burrows, and rodent excreta were found at the camel corral. Y. pestis was isolated from the blood and liver of live jirds collected from the camel corral and from fleas (Xenopsylla cheopis) combed from these jirds.

Conclusions

This investigation confirms that human plague with pharyngeal and gastrointestinal symptoms can result from eating infected raw camel liver. Only 1 published report has proposed this method of infection. In 1976, in a small, remote Libyan village, 13 plague cases occurred after a sick camel was slaughtered and its meat eaten (4). However, as a source of infection eating camel meat could not be distinguished from droplet transmission, percutaneous exposure during camel killing or handling fresh meat, or flea bites. Moreover, plague infection was not found in the camel, and the human pharyngeal plague might have resulted from crushing fleas between the teeth while grooming (5).

The 4 patients with pharyngeal plague had symptoms similar to those of domestic cats with plague in New Mexico, where 46% of plague-infected cats had submandibular lymphadenitis (2). These feline cases were thought to result from eating infected prey. Similarly, since human plague patients had submandibular lymphadenitis, tonsillitis, pharyngitis and dysphagia, or severe gastrointestinal symptoms, this suggests ingestion as the route of exposure.

Christie et al. suggested that among domestic animals, camels may be an important plague host because their wide-ranging behavior increases the chance of coming into contact with natural plague loci (4). Our investigation indicates another scenario, with evidence of a plague epizootic at a fixed site where camels were corralled. Russian investigators have proposed several methods of natural infection of camels: bites from rodent fleas, mechanical transmission from ticks, eating feed contaminated with excreta of infected rodents, and eating dead rodents along with their feed (6). All of these possibilities existed in this outbreak.

This unusual profile of human plague was recognized because several related patients with life-threatening illnesses were seen at a hospital over a 2-day period and a medical officer recognized the illness. Sporadic cases of pharyngeal or gastrointestinal plague would be less likely to attract the attention of medical or public health workers. Clinicians and public health officers, particularly in the Middle East, North Africa, and Central Asia, should be alert for sporadic cases of pharyngeal or gastrointestinal plague so that curative and preventive measures can be promptly initiated.

Dr Bin Saeed is a graduate of the Saudi Arabian Field Epidemiology Training Program, where he performed this investigation. He has a doctorate in epidemiology from the University of Texas. His current research interest is the epidemiology of infectious diseases.

References

(1.) Mann JM, Martone W J, Boyce JM, Kaufmann AF, Barnes AM, Weber NS. Endemic plague in New Mexico: risk factors associated with infection. J Infect Dis. 1979;140:397-401.

(2.) Eidson M, Tierney LA, Rollag O J, Becker T, Brown T, Hull HF. Feline plague in New Mexico: risk factors and transmission to humans. Am J Public Health. 1988;78:1333-5.

(3.) Von Reyn CF, Barnes AM, Weber NS, Hodgin UG. Bubonic plague from exposure to a rabbit: a documented case, and a review of rabbit-associated cases in the United States. Am J Epidemiol. 1976;104:81-7.

(4.) Christie AB, Chen TH, Elberg SS. Plague in camels and goats: their role in human epidemics. J infect Dis. 1980;141:724-6.

(5.) Conrad FG, LeCocq FR, Krain R. A recent epidemic of plague in Vietnam. Arch Intern Med. 1968:122:193-7.

(6.) Federov VN. Plague in camels and its prevention in the USSR. Bull World Health Organ. 1960;23:275-81.

Abdulaziz A. Bin Saeed,* ([dagger])([double dagger]) Nasser A. Al-Hamdan, ([dagger]) and Robert E. Fontaine ([dagger])([section])

* King Saud University College of Medicine, Riyadh, Saudi Arabia; ([dagger]) Ministry of Health, Riyadh, Saudi Arabia; ([double dagger]) King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia; and ([section]) Centers for Disease Control and Prevention, Atlanta, Georgia, USA

Address for correspondence: Abdulaziz A. Bin Saeed, Department of Family and Community Medicine, King Saud University College of Medicine, PO Box 2925, Riyadh 11461, Saudi Arabia; fax: 966-1-4671967; email: abinsaeed2001@yahoo.com

COPYRIGHT 2005 U.S. National Center for Infectious Diseases
COPYRIGHT 2005 Gale Group

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