Mycobacterium Tuberculosis, M. Bovis
Mycobacterium Tuberculosis, M. Bovis
MATERIAL SAFETY DATA SHEET – INFECTIOUS SUBSTANCES
SECTION I – INFECTIOUS AGENT
NAME: Mycobacterium tuberculosis, Mycobacterium bovis
SYNONYM OR CROSS REFERENCE: TB
CHARACTERISTICS: Gram positive rods, non-spore forming, non-motile, slightly curved, forming strands and cords, acid-fast staining, aerobic, slow-growing,
SECTION II – HEALTH HAZARD
PATHOGENICITY: Initial infection usually unnoticed, tuberculin sensitivity appears in a few weeks and lesions commonly heal; may progress to pulmonary tuberculosis (fatigue, fever, cough, chest pain, hemoptysis fibrosis, cavitation) or extrapulmonary involvement (miliary, meningeal) by lymphohematogenous dissemination; serious outcome of initial infection more frequent in infants and children; infection with bovine bacillus rare; drug resistant strains can cause irreversible damage in the lungs
EPIDEMIOLOGY: Worldwide (important cause of disability and death in many parts of the world despite downward mortality and morbidity rates); higher in males, among poor and in cities; in low incidence areas, most tuberculosis is endogenous (reactivation of initial latent foci); long exposures of some contacts leads to high risk of infection (25-50%); epidemics in enclosed areas; M. bovis infection encountered where disease in cattle has not been controlled and raw milk is still used; 11.8% of the isolates are drug resistant, 1.2% being multi-drug resistant
HOST RANGE: Primarily humans, cattle, primates, other animals (rodents)
INFECTIOUS DOSE: 10 bacilli by inhalation
MODE OF TRANSMISSION: Portal entry is the lung; pathogen is carried as airborne particles (droplet nuclei); exposure to airborne bacilli from sputum of infected persons; direct invasion of mucous membranes or breaks in skin;bovine tuberculosis from exposure to infected cattle (airborne, ingestion of raw milk or dairy products); medical personnel at risk while performing autopsies, intubation, bronchoscopies or by dermal innoculation
INCUBATION PERIOD: From infection to primary lesion or significant tuberculin reaction – 4 to 12 weeks; risk of progressive pulmonary or extrapulmonary tuberculosis is greatest within 1 to 2 years after infection; may persist for lifetime as latent infection
COMMUNICABILITY: Communicable as long as bacilli are discharged in sputum (may be years if untreated); extrapulmonary TB (except laryngeal tuberculosis) generally not communicable
SECTION III – DISSEMINATION
RESERVOIR: Primarily humans; in some areas, diseased cattle, badgers, swine and other mammals are infected (M. bovis)
ZOONOSIS: Yes – inhalation of infected droplets; direct contact with infected animals or tissues of infected animals
VECTORS: None
SECTION IV – VIABILITY
DRUG SUSCEPTIBILITY: Sensitive to combination of antimicrobial drugs – isoniazid, rifampin, streptomycin, ethambutol, pyrazinamide
DRUG RESISTANCE: Isoniazid (INH) and rifampin; multi-drug resistant isolates are resistant to first and second-line antibiotics
SUSCEPTIBILITY TO DISINFECTANTS: Greater resistant to disinfectants and require longer contact times for most disinfectants to be effective; 5% phenol, 1% sodium hypochlorite (only if low organic matter and longer contact times), iodine solutions (high concentration of available iodine required), glutaraldehyde and formaldehyde (longer contact time) are effective
PHYSICAL INACTIVATION: Sensitive to moist heat (121° C for at least 15 min), light
SURVIVAL OUTSIDE HOST: Guinea pig carcasses – 49 days; carpet – up to 70 days; dust – 90 to 120 days; cockroaches – 40 days; manure 45 days; paper book – 105 days; sputum (cool, dark location) – 6 to 8 months; clothing – 45 days
SECTION V – MEDICAL
SURVEILLANCE: Skin testing with PPD (purified protein derivative) of previously skin-tested-negative personnel; chest X-ray
FIRST AID/TREATMENT: Combination antibiotic therapy
IMMUNIZATION: Licensed attenuated live vaccine (BCG) available, but not routinely carried out
PROPHYLAXIS: Preventative treatment with INH (risk of hepatitis for those over 35 years old)
SECTION VI – LABORATORY HAZARDS
LABORATORY-ACQUIRED INFECTIONS: Incidence of tuberculosis in laboratory workers working with M. tuberculosis is three times higher than those not working with agent; fourth most commonly reported laboratory infection; 176 reported cases with 4 deaths
SOURCES/SPECIMENS: Sputum, gastric lavage fluids, cereobrospinal fluid, urine, lesions from a variety of tissues
PRIMARY HAZARDS: Inhalation of infectious aerosols; accidental parenteral inoculation, direct contact of mucous membranes, ingestion; naturally or experimentally infected non-human primates are a known cause of human infection; litter of infected animals (e.g. mice and hamsters) serve as source of infectious aerosols;
SPECIAL HAZARDS: Bacilli may survive in heat-fixed smears and may be aerosolized in the preparation of frozen sections and during manipulation of cultures; high rate of isolation of acid fast organisms from clinical specimens (>10%), sputum and other specimens, from suspected or known cases
SECTION VII – RECOMMENDED PRECAUTIONS
CONTAINMENT REQUIREMENTS: Biosafety level 2 practices, containment equipment and facilities for primary culture of sputum and preparing smears; biosafety level 3 practices, containment equipment and facilities for the propagation and manipulation of cultures of M. tuberculosis or M. bovis and for animal studies utilizing non-human primates
PROTECTIVE CLOTHING: Laboratory coat and gloves when manipulating specimens; gloves and gown with tight wrists and ties in back when manipulating cultures
OTHER PRECAUTIONS: Appropriate practices and precautions to minimize the production of infectious aerosols
SECTION VIII – HANDLING INFORMATION
SPILLS: Allow aerosols to settle; wearing protective clothing, gently cover spill with paper towels and apply 5% phenol, starting at perimeter and working towards the centre; allow sufficient contact time (30 min) before clean up
DISPOSAL: Decontaminate before disposal; steam sterilization, incineration
STORAGE: In sealed containers that are appropriately labelled
SECTION IX – MISCELLANEOUS INFORMATION
Date prepared: March, 2001
Prepared by: Office of Laboratory Security, PHAC
Although the information, opinions and recommendations contained in this Material Safety Data Sheet are compiled from sources believed to be reliable, we accept no responsibility for the accuracy, sufficiency, or reliability or for any loss or injury resulting from the use of the information. Newly discovered hazards are frequent and this information may not be completely up to date.
Copyright © Health Canada, 2001
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