SECTION I - INFECTIOUS AGENT


NAME: Yersinia pestis


SYNONYM OR CROSS REFERENCE: Plague, Peste, Bubonic plague


CHARACTERISTICS: Gram negative rod, ovoid, bipolar staining (safety pin appearance), facultative intracellular parasite.

SECTION II - HEALTH HAZARD

PATHOGENICITY: Zoonotic disease; bubonic plague with lymphadenitis in nodes receiving drainage from site of flea bite, occurring in lymph nodes and inguinal areas, fever, 50% case fatality if untreated; may progress to systemic plague with dissemination by blood to meninges; secondary pneumonic plague with pneumonia, mediastinitis, and pleural effusion; untreated pneumonic and septicemic cases are fatal.


EPIDEMIOLOGY: Wild rodent plague in North America, South America, Africa, Near and Middle East, Central and Southeast Asia, Indonesia; plague foci in USSR; urban plague controlled in most areas; human plague occurred recently in Africa; endemic in Burma and Vietnam; sporadic cases in North and South America following exposure to wild rodents or their fleas (no human-to-human transmission in USA since 1924).


HOST RANGE: Humans, various animals.


INFECTIOUS DOSE: Unknown.


MODE OF TRANSMISSION: Result of human intrusion into zoonotic (sylvatic) cycle or by entry of rodents or infected fleas into human's habitat and bite of infected fleas; domestic pets can carry plague-infected fleas; contact of commensal rodents and their fleas with sylvatic rodents may result in epizootic and epidemic plague; handling of infected tissues; airborne droplets from humans or pets with plague pneumonia; careless manipulation of laboratory cultures; person-to-person transmission by human fleas.


INCUBATION PERIOD: From 2-6 days; may be a few days longer in vaccinated individuals; for primary plague pneumonia, 1-6 days, usually short.


COMMUNICABILITY: Fleas may remain infective for months; bubonic plague not usually transmitted directly from person to person; pneumonic plague may be highly communicable under appropriate climatic conditions (overcrowding facilitates transmission).

SECTION III - DISSEMINATION

RESERVOIR: Wild rodents (rats) are the natural reservoir; lagomorphs (rabbits, hares) and carnivores (especially cats via aerosol) may be a source of infection to humans.


ZOONOSIS: Yes - bites of fleas from an infected animal; contact (especially aerosol) or being bitten by an infected animal.


VECTORS: Wild rodent fleas, especially the oriental rat flea (Xenopsylla cheopis); occasionally by human fleas (Pulex irritans).

SECTION IV - VIABILITY

DRUG SUSCEPTIBILITY: Sensitive to streptomycin, tetracycline, chloramphenicol.


SUSCEPTIBILITY TO DISINFECTANTS: Susceptible to many disinfectants - 1% sodium hypochlorite (20% commercial bleach), 70% ethanol, 2% glutaraldehyde, iodines, phenolics, formaldehyde.


PHYSICAL INACTIVATION: Sensitive to moist heat (121o C for at least 15 min.) and dry heat (160o - 170o C for at least 1 hour).


SURVIVAL OUTSIDE HOST: Blood - 100 days; human bodies - up to 270 days.

SECTION V - MEDICAL

SURVEILLANCE: Monitor for symptoms; presumptive diagnosis by visualizing bipolar staining, ovoid, gram-negative organisms in sputum or material aspirated from bubo; FA and ELISA test; PHA using Fraction-1 antigen.


FIRST AID/TREATMENT: Antibiotic therapy in early stages (8-24 hours after onset of pneumonic plague) typically tetracycline or streptomycin; secondary infection or suppurative bubo may require incision and drainage.


IMMUNIZATION: Although field trials have not been conducted to determine the efficacy of licensed vaccines, experience has been favorable; immunization is recommended for personnel working regularly with cultures of Y pestis or infected rodents.


PROPHYLAXIS: Chemoprophylaxis using tetracyclines or sulfonamides; for close contacts of pneumonic cases.

SECTION VI - LABORATORY HAZARDS

LABORATORY-ACQUIRED INFECTIONS: 10 reported laboratory acquired infections with 4 deaths.


SOURCES/SPECIMENS: Bubo fluid, blood, sputum, CSF, feces, urine.


PRIMARY HAZARDS: Direct contact with cultures and infectious materials from humans or rodents; infectious aerosols or droplets generated during manipulation of cultures and infected tissues and in the necropsy of rodents-, accidental auto-inoculation; ingestion.


SPECIAL HAZARDS: Bites by infected fleas collected from rodents.

SECTION VII - RECOMMENDED PRECAUTIONS

CONTAINMENT REQUIREMENTS: Biosafety level 2 practices, containment equipment and facilities for all activities involving the handling of potentially infectious clinical materials and cultures. Additional primary containment and personnel precautions as described for BL3 are recommended for activities with high potential for droplet or aerosol production, for work with antibiotic-resistant strains, and for activities involving production, large quantities, or high concentrations of infectious materials.


PROTECTIVE CLOTHING: Gloves should be worn when handling field-collected or infected laboratory rodents and when there is the likelihood of direct skin contact with infectious materials; gown with tight cuffs and ties in back should be worn when manipulating cultures and specimens.


OTHER PRECAUTIONS: Special care should be taken to avoid the generation of aerosols during the necropsy of animals- necropsy should be conducted in a biological safety cabinet.

SECTION VIII - HANDLING INFORMATION

SPILLS: Allow aerosols to settle; wearing protective clothing, gently cover spill with paper towels and apply 1% sodium hypochlorite (20% commercial bleach), starting at perimeter and working towards the center, allow sufficient contact time (30 min) before clean up.


DISPOSAL: Decontaminate before disposal; steam sterilization, incineration (animal carcasses).


STORAGE: In scaled containers that are appropriately labeled.

Date prepared: October 11, 19 97 Prepared by: Canadian Office of Biosafety Information edited by the Colorado State University Office of Biosafety; June 16, 1998.

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