Chapter 16 - Enterobacteriaceae
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Transcript Chapter 16 - Enterobacteriaceae
Chapter 22 –
Mycobacterium
tuberculosis & Other
Nontuberculous
Mycobacteria
MLAB 2434 – Clinical Microbiology
Cecile Sanders & Keri Brophy-Martinez
General Characteristics
Slender, slightly curved or straight
rod-shaped organisms
Non-motile
Do not form spores
Cell wall with extremely high lipid
content
Staining requires longer time or
application of heat
Once stained, resist decolorization
with acid-alcohol (acid-fast)
General Characteristics
(cont’d)
Strictly aerobic
Grow more slowly than most bacteria
Traditional characteristics used to
identify Mycobacterium
Rate of growth
Colony morphology
Pigment production
Nutritional requirements
Optimum incubation temperature
Biochemical test results
General Characteristics
(cont’d)
Newer techniques
Automated culture system, such
as BACTEC
Nucleic acid probes with PCR
Thin-layer chromatography
GLC
High-performance liquid
chromatography
Safety Considerations
Mycobacteriology workers are three
times more likely to seroconvert
(develop positive skin test)
Adequate safety equipment
Safe laboratory procedures training
Information on hazards
Preparations for unexpected accidents
Staff must be monitored regularly by
medical personnel
Safety Considerations
(cont’d)
Skin test
Also called “Mantoux test” and PPD
Those with positive skin test must
be advised to have chest X-ray
Proper Ventilation
Separate from other parts of lab
Negative air pressure (6 to 12 room
air changes/hour)
Safety Considerations
(cont’d)
Biological Safety Cabinet
Use of Proper Disinfectant
Bactericidal for mycobacteria
Also called “tuberculocidal”
Other precautions
Disposables
Protective clothing, face masks
Specimen Collection and
Processing
Variety of clinical specimens,
including respiratory, urine, feces,
blood, CSF, tissues, and aspirations
Should be collected before
antibiotic therapy and processed
ASAP
Sputum is most common; should be
collected in a wide-mouth container
to avoid aerosols
Specimen Collection and
Processing (cont’d)
Sputum
Number of specimens needed is
inversely related to the frequency
of smear positivity
Should be from a deep cough or
expectorated sputum induced by
neubulization
Bronchial washings or lavages may
be collected
Specimen Collection and
Processing (cont’d)
Gastric aspirates
Used to recover mycobacterium
that may have been swallowed
during the night
Only used when patient is unable to
produce a good quality sputum
specimen
Urine – First morning preferred
Specimen Collection and
Processing (cont’d)
Stools – primarily collected from AIDS
patients to determine Mycobacterium
avium complex (MAC)
Blood – most commonly from AIDS and
other immunosuppressed patients
Tissues and other body fluids – need a
fairly large volume of CSF, since number
of organisms in that site are rare
Digestion & Decontamination
of Specimens
Because Mycobacterium grow so slowly
and are often collected from non-sterile
body sites, they are easily overgrown by
other bacteria
Specimens from non-sterile sites,
therefore, must be “decontaminated”
Sputums or other viscous specimens also
must be “digested”
Specimens from sterile sites (CSF, etc.)
do not need decontamination
Digestion & Decontamination
of Specimens (cont’d)
Decontamination
Specimen from non-sterile site is mixed
with an agent that will kill nonmycobacterium bacteria
Common decontamination agents
• NaOH is most common
• Benzalkonium chloride (Zephiran)
• Oxalic acid
After decontamination, the agent must be
neutralized so that it will not eventually
kill the Mycobacterium
Digestion & Decontamination
of Specimens
Digestion
Liquefying mucus enables the
mycobacterium to contact and use
the nutrients in the agar medium
Common digestion agents
• N-acetyl-L-cysteine – most common
• Trisodium phosphate (Z-TSP) – used
with Zephiran
Concentration
After decontamination and
digestion, the specimen is
centrifuged in a closed, vented
centrifuge to concentrate the
organisms
Acid Fast Stains
After centrifugation, the button at the bottom of
the tube is used to make a smear and to inoculate
media
Acid Fast Stains
Ziehl-Neelsen – uses heat to drive the color into
the lipids of the cell wall; decolorized with acidalcohol
Kinyoun – cold stain
Auramine or auramine-rhodamine fluorochrome
stain – more sensitive
After staining, a minimum of 300 oif are examined
Culture Media and
Isolation Methods
Mycobacterium are strictly aerobic
Slow growers; cultures held for 6
weeks before calling negative
Media
Lowenstein-Jensen (LJ) media – egg
based
Middlebrook 7H10 and 7H11 agar –
serum based
Middlebrook 7H9 broth
Culture Media and
Isolation Methods (cont’d)
Labs with large volumes of
Mycobacterium cultures use an
automated reader (BACTEC)
BACTEC broth contains 14C-labeled
substrate
When organisms grow, 14C in the
form of 14CO2 is released and
detected radiometrically
Laboratory Levels or Extents
of Service for Mycobacterium
American Thoracic Society levels
1. Specimen collection only
2. Acid-fast stains and/or
inoculation only
3. Isolation and presumptive
identification of Mycobacterium
species
4. Definitive identification and
antibiotic sensitivity testing
Identification of
Mycobacterium
Colony Morphology
Either smooth and soft or rough and
friable
Growth rate
Rapid growers – colonies in < 7 days
Slow growers – colonies in > 7 days
Temperature
Identification of
Mycobacterium (cont’d)
Photoreactivity
Photochromogens – produce
carotene pigment upon exposure to
light
Scotochromogens – produce pigment
in light or dark
Nonchromogenic – no pigment; these
colonies are a buff color
Identification of
Mycobacterium (cont’d)
Biochemical Identification
Most labs now use nucleic acid probes with
or without PCR
Older tests
•
•
•
•
•
•
Niacin accumulation
Nitrate reduction
Catalase
Hydrolysis of Tween 80
Iron uptake
Arylsulfatase
Identification of
Mycobacterium (cont’d)
Older tests (cont’d)
• Pyrainamidase
• Urease
• Inhibitory tests
•
•
•
•
•
NAP
TCH
Growth in 6.5% NaCl
Tellurite reduction
Growth on MacConkey
Antibiotic Sensitivity
Testing for Mycobacterium
These tests must be performed with great
attention to detail, because Mycobacterium is fairly
resistant and only a few organisms left can cause
reinfection
Development of drug-resistance
Common antibiotics (usually two or more are given)
Isoniazid
Rifampin
Ethambutol
Streptomycin
Pyrazinamide
Mycobacterium Infections
Truly pathogenic
Potential pathogens
M. tuberculosis
M. bovis
M. ulcerans
M. kansasii
M. marinum
Other possible pathogens and rare
pathogens listed on p. 670
Mycobacterium
tuberculosis
Primarily a pathogen of the
respiratory tract (“TB”)
One of the oldest communicable
diseases
Over 1 billion cases worldwide, with
8 to 10 new cases each year and 3
million deaths per year
Once called “consumption”
Mycobacterium
tuberculosis (cont’d)
Primary tuberculosis
Spread by coughing, sneezing, or talking
Inhaled into alveoli, where the organisms
are phagocytized
If the organism does not cause immediate
infection, the organism can be “walled off”
in a granuloma
Granulomas can break down in future and
the organisms can cause infection later
Mycobacterium
tuberculosis (cont’d)
PPD Test
Mycobacterium
tuberculosis (cont’d)
PPD Test (cont’d)
Positive Test
Mycobacterium
tuberculosis (cont’d)
Extrapulmonary tuberculosis
Spleen
Liver
Lungs
Bone marrow
Kidney
Adrenal gland
Eyes
Mycobacterium
tuberculosis (cont’d)
Identification
Slow grower
Colonies are thin, flat, spreading and
friable with a rough appearance
May exhibit characteristic “cord”
formation
Grows best at 35 to 37° C
Colonies are NOT photoreactive
Mycobacterium
tuberculosis (cont’d)
Other Mycobacteria
Mycobacterium bovis – primarily in cattle,
dogs, cats, swine, parrots and human;
disease in humans closely resembles M.
tuberculosis
MOTT (Mycobacteria Other Than
Tubercle Bacillus) or NTM
(Nontuberculous mycobacteria)
Most found in soil and water
Chronic pulmonary disease resembling TB
Other Mycobacteria
(cont’d)
NTM (cont’d)
M. avium Complex (MAC)
M. kansasii
Mycobacterium fortiutum-chelonei
Complex
M. marinum
Etc., etc.
Mycobacterium leprae
Causes leprosy or Hansen’s Disease
Infection of the skin, mucous membranes
and peripheral nerves
Most cases are from warm climates
Bacteria infect the cooler areas of the
body (ears, nose, eyebrows, fingers, toes)
Diagnosis made from finding acid-fast
bacilli in scrapings from lesions
Not culturable, except in mouse foot pads
Mycobacterium leprae
(cont’d)