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Prepared by Suzette B. Doctolero: Pseudomonas, Burkholderia

This chapter discusses Pseudomonas aeruginosa, Burkholderia cepacia, B. pseudomallei, and B. mallei. P. aeruginosa is an opportunistic pathogen found in moist environments. It produces several virulence factors and can cause community-acquired or hospital-acquired infections. B. cepacia can colonize the lungs of cystic fibrosis patients. B. pseudomallei causes melioidosis and is found in tropical areas. Identification involves examining colony morphology, biochemical tests, and antibiotic resistance patterns. Therapies exist but resistance is a concern, particularly for B. cepacia and B. pseudomallei.

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0% found this document useful (0 votes)
137 views31 pages

Prepared by Suzette B. Doctolero: Pseudomonas, Burkholderia

This chapter discusses Pseudomonas aeruginosa, Burkholderia cepacia, B. pseudomallei, and B. mallei. P. aeruginosa is an opportunistic pathogen found in moist environments. It produces several virulence factors and can cause community-acquired or hospital-acquired infections. B. cepacia can colonize the lungs of cystic fibrosis patients. B. pseudomallei causes melioidosis and is found in tropical areas. Identification involves examining colony morphology, biochemical tests, and antibiotic resistance patterns. Therapies exist but resistance is a concern, particularly for B. cepacia and B. pseudomallei.

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Chapter 22

Pseudomonas, Burkholderia,
and Similar Organisms

PREPARED BY SUZETTE B. DOCTOLERO


Objectives
 Describe the normal sources (habitat) for Pseudomonas aeruginosa,
Burkholderia cepacia, B. pseudomallei, and B. mallei, including the routes
of transmission.
 Identify the factors that contribute to the pathogenicity of P. aeruginosa,
and explain the physiologic mechanism for each.
 List the various disease states associated with P. aeruginosa and
Burkholderia sp.
 Compare and contrast the Gram-stain appearance of the gram-
negative bacilli discussed in this chapter.
 List the appropriate identification scheme for identifying P. aeruginosa.
 Describe the media and chemical principle of each media used,
including differential and selective agars that aid in the cultivation of
Pseudomonas, Brevundimonas, and Ralstonia.
 Describe the potential therapies for B. cepacia and B. pseudomallei and
the concerns regarding optimal therapy.
 Describe and identify the patterns of antibiotic resistance in P.
aeruginosa.
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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonads
gram-_________ bacilli
strictly aerobic,
catalase-________
oxidase-______
Some are motile

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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas spp.
grow on MacConkey agar
oxidize glucose.
found in moist environments

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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas aeruginosa
UBIQUITOUS: env’t, domestic
env’t, hospital:
uncommon normal flora
MOT: ingestion or exposure to
contaminated food, water, or
medical devices.
opportunistic pathogen that can
cause CA or HA
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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas aeruginosa
Virulence factors include:
 Exotoxin
A:_____________________________________
 Endotoxins
 Proteolytic enzymes:
_______________________________________
 Pili
:_______________________________________

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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas aeruginosa
Virulence factors include:
Alginate:
__________________________________
__________________________________
Pyocyanin:
____________________________
Catalase:_________________________
Intrinsic resistance to many
antimicrobial agents
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PREPARED BY SUZETTE B. DOCTOLERO
P. aeruginosa Infections
Community-Acquired
 Folliculitis
 Otitisexternal
 Eye infections
 Osteomyelitis
 Endocarditis in intravenous (IV) drug users
 Respiratory tract infections in patients with
cystic fibrosis

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PREPARED BY SUZETTE B. DOCTOLERO
P. aeruginosa Infections
Hospital-Acquired

Respiratory
tract
Urinary tract
Wounds
Bacteremia
CNS
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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas aeruginosa Identification
Spreading, flat
colony with metallic
sheen
Beta-hemolytic
musty grape-like (or
corn tortilla) odor
May also be mucoid

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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas aeruginosa Identification
Denitrification of nitrates and
nitrites,
Arginine dihydrolase positive
Oxidizes glucose and xylose
__________: selective and
differential for P. aeruginosa

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PREPARED BY SUZETTE B. DOCTOLERO
P. aeruginosa on MH

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PREPARED BY SUZETTE B. DOCTOLERO
P. aeruginosa
NLF in MAC
Oxidase ________
Citrate __________
TSI:K/NC
Grows well at 42°C

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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas fluorescens and
Pseudomonas putida
low virulence, rarely causing clinical
disease.
Both species can grow at 4 °C but not
at 42 °C
Both produce pyoverdin, but not
pyocyanin
Differentiated by gelatin hydrolysis

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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas stutzeri
 rareisolate
 Colonies are wrinkled, leathery colonies

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PREPARED BY SUZETTE B. DOCTOLERO
Burkholderia
These organisms are found in the
environment in water, in soil, and
on plants.
Not Normal flora
Two important human pathogens
Burkholderia __________
 Burkholderia ___________

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PREPARED BY SUZETTE B. DOCTOLERO
Burkholderia cepacia
May colonize respiratory tract
of patients with cystic fibrosis.
Assoc. with contaminated
equipment, medications, and
disinfectants,
MOT: _____________________

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PREPARED BY SUZETTE B. DOCTOLERO
Burkholderia cepacia
Includes fulminant lung
infections and bacteremia.
Cystic fibrosis
Chronic granulomatous
disease

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PREPARED BY SUZETTE B. DOCTOLERO
Burkholderia cepacia
May result from exposure to
contaminated medical
solutions or devices.
Septicemia
Urinarytract infections
Respiratory tract infections

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PREPARED BY SUZETTE B. DOCTOLERO
B. pseudomallei
found in tropical and
subtropical areas.
MOT: inhalation or direct
inoculation through
mucosa.

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PREPARED BY SUZETTE B. DOCTOLERO
B. pseudomallei
can survive within
phagocytes
Causes m______________

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PREPARED BY SUZETTE B. DOCTOLERO
B. mallei
Is an agent of glanders in
horses.
Is associated with close
animal contact.

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PREPARED BY SUZETTE B. DOCTOLERO
Gram-Stain Appearance
Medium-size
straight rods
Burkholderia mallei
Coccobacillus
Pseudomonas
pseudomallei
Small with bi-polar
staining
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PREPARED BY SUZETTE B. DOCTOLERO
Burkholderia
gram-___________ BACILLI
aerobic,
non–spore-forming,
Allare motile except for
_________________
catalase positive
most are oxidase positive.
NLF on On MacConkey’s agar

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PREPARED BY SUZETTE B. DOCTOLERO
Cultivation
5% sheep blood and
chocolate agars
MacConkey agar
Pseudomonas cepacia (PC)
agar

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PREPARED BY SUZETTE B. DOCTOLERO
Cultivation
Oxidative-fermentative base-polymyxin
B-bacitracin-lactose (OFPBL) agar
 B.
_________ ferments lactose and appears
___________

Ashdown medium
For the isolation of
_____________ w/c turns red
on this medium.
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PREPARED BY SUZETTE B. DOCTOLERO
Therapy: DON’t copy
 Antimicrobialtherapy for B. cepacia and
B. pseudomallei rarely eradicates B.
cepacia, and therapy for melioidosis
remains controversial.
 Burkholderia cepacia
• Chloramphenicol
 Piperacillin
• Trimethoprim-sulfamethoxazole
 Ceftazidime
 Ciprofloxacin
 B. pseudomallei
• Amoxicillin-clavulanate
 Ceftazidime
 Piperacillin-tazobactam• Imipenem
 Ticarcillin-clavulanate • Trimethoprim-
sulfamethoxazole
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PREPARED BY SUZETTE B. DOCTOLERO
Pseudomonas aeruginosa
Therapy: DON’t copy
 P.aeruginosa is intrinsically resistant to
various antimicrobial agents.
 P. aeruginosa readily acquires resistance
to active agents.
 Therapeutic options include:
• Imipenem
 Antipseudomonal beta-lactam
• Meropenem
with or without an aminoglycoside
• Gentamicin
 Quinolones
• Tobramycin
 Piperacillin-tazobactam
• Amikacin-netilmicin
 Ceftazidime
• Ciprofloxacin
 Cefepime
• Levofloxacin
 Aztreonam
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PREPARED BY SUZETTE B. DOCTOLERO
References:

 Henry, J. B. (2010). Henry’s Clinical Diagnosis


and Management by Laboratory Methods
21st ed. Philadelphia: W.B Saunders
 Mahon, C., Lehman, D., & Manuselis,G.
(2015). Textbook of Diagnostic Microbiology.
Elsevier
 Tille, P. (2014). Bailey and Scott’s Diagnostic
Microbiology. 13th ed. Elsevier Mosby.
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PREPARED BY SUZETTE B. DOCTOLERO

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