Professional Documents
Culture Documents
By
Dr. R.Jayaprada, M.D
Assistant Professor,
Dept of Microbiology
Introduction
The name, Acinetobacter, comes from the
Latin word for "motionless," because
they lack cilia or flagella with which to
move.
Have 32 species, A. baumanii and A.
lwoffii have greatest clinical importance.
Introduction
Most species are not significant sources of infection.
However,one
opportunistic
species,
Acinetobacter
Acinetobacter
Gram-Negative
Coccobacilli
Strictly aerobic
Nonmotile
Nonfermenting
Nonfastidious
Catalase positive
Oxidase negative
Acinetobacter
It has DNA G+C content of 39% to 47%.
Based on more recent taxonomic data, it
was proposed that members of the genus
Acinetobacter should be classified in the
new family Moraxellaceae within the order.
Acinetobacter baumannii
Pinkish colonies on MacConkey agar, acid is
formed without gas in glucose, arabinose, xylose
and occasionally rhamnose
Grows at 44oC
Forms acid in 10% lactose and not in 1% lactose
Final identification done only by DNA
hybridisation
Acinetobacter lwoffi
Yellow colonies on MacConkey agar
Does not acidify sugars
Some strains are oxidase positive
Epidemiology
Environmental reservoirs
Soil
Fresh water
Vegetables
Animals
Body lice, fleas, ticks
Source of Acinetobacter:
Where do these organisms reside?
Dr.T.V.Rao MD
10
Environmental Contamination
with Acinetobacter
Hands
Bed rails
Bedside tables
Ventilators
Infusion pumps
Mattresses
Pillows
Air humidifiers
Patient monitors
Growth Requirment
Aerobic
Grow at 44 C
Differential Media
MacConky Agar
Selective Media
CHROM Agar
Leeds Acinetobacter Agar
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MacConky Agar
CHROM Agar
13
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Colony Characters
Colonies are 1 to 2
mm, nonpigmented,
domed, and muciod,
with smooth to pitted
surfaces.
They can't reduce
nitrate or to grow
anaerobically
(different from
Enterobacteriaceae).
15
Biochemical Profile
Both A.baumannii and A.lwofii
are Catalase positive and
Oxidase Negative (opposite to
Neisseria spp. or Moraxella
spp.)
A.baumannii ferment glucose,
xylose and lactose but A.lwofii
cannot ferment.
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17
Rapid Detection
Rapid detection of Acinetobacter can be
done by RapID ONE Panel (remel) and
Api 20 E strips. These can differentiate up
to species level.
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Molecular Detection
A.baumannii and A.lwofii can be detected
by PCR.
recA specific primers are used to detect
recA gene in A.baumannii, giving a 382 bp
fragment
est specific primers are used to detect est
gene in A.lwofii, giving a 309 bp product.
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Pathogenesis
Opportunistic pathogen
Survive under dry conditions
Virulence Factors
Polysaccharide capsule, prevent complement
activation, delay phagocytosis
Fimbriae (adhere to human bronchial epithelium)
Pili (colonization of environmental surface to form
biofilms)
20
Transmission
Acinetobacter can be
spread from person to
person (infected or
colonized patients), contact
with contaminated surfaces
of exposure to the
environment.
21
22
Ventilator-associated pneumonia
Urinary tract infection
Bloodstream infection
Secondary meningitis
Skin/wound infections
Endocarditis
CAPD-associated peritonitis
Ventriculitis
23
The respiratory
tract is an
important
reservoir for
Acinetobacter
bloodstream
infections
Abdominal
infection
19%
Respiratory tract
71%
Central venous
line 8%
N=37
Garcia-Garmendia J-L et al. Clin Infect Dis 2001;33:939-946.
Antibiotic Resistance
Acinetobacter
capable
of
species
are
accumulating
leading
development
of
to
the
multidrug-
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Antibiotic Resistance
Mechanisms
26
Treatment
27
28
Summary
Opportunistic pathogen
Nosocomial infection
Grow best at aerobic conditions
Can be transmitted by contact
Possessing multi antibiotic resistance.
29
Acinetobacter pakistanensis
30
General Measures
Hand hygiene
Use of alcohol-based hand sanitizers
Contact precautions
Gowns/gloves
Dedicate non-critical devices to patient room
Environmental decontamination
Prudent use of antibiotics
Avoidance of transfer of patients to Burn Unit from
other ICUs
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