Professional Documents
Culture Documents
OF URINARY RTACT
By
Dr. Marwa Salah
Learning objectives
1.
2.
3.
References
Major
structur
al
features
pathogenes
is
Clinical
significa
nce
Lab
diagnosis
Escherichi G ve
a coli
motile
bacilli
Adhesins
Haemolysin
s
K antigen
UTI
M/E
Quantitative
urine culture
Klebsiella G ve
pneumoni nona
motile
bacilli
Capsule
UTI
M/E
Quantitative
urine culture
Proteus
mirabilis
G ve
motile
bacilli
Adherence
Urease
Motility
UTI
M/E
Quantitative
urine culture
Serratia
G-ve
Adherence
UTI
M/E
S aureus
Other coagulase negative staphylococci
B fragilis
M tuberculosis
Escherichia coli
Enterobacteriacaea (General
Features)
1. Facultative anaerobes
2. Oxidase negative
3. Ferment D-glucose (lactose fermentation is
an important differential character)
4. Reduce nitrate to nitrite
Morphology:
Gram -ve bacilli, motile, some
are capsulated
Cultural Characters:
Facultative anaerobic, 24h, 37oC
Selective indicator medium:
MacConkey agar rose pink
colonies due to lactose
fermentation
Biochemical Reactions:
1. Oxidase negative
2. Ferments glucose, lactose,
maltose, mannite, sucrose &
salicin with production of acid &
gas
3. Urease negative
4. Indole +ve, methyl red (MR)
+ve, Voges-Proskauer (VP) ve,
citrate -ve (IMVC ++--)
Antigenic structure:
Serological classification of E. coli is based on:
1. O (somatic) antigen of the cell wall lipopolysaccharide
(LPS)
2. H (flagellar) antigen
3. Capsular (K) antigen in capsulated strains
Pathogenesis
Most predominant facultative anaerobe in large intestine of man
Provides protection against harmful microorganisms
One of the important indicators of faecal pollution of water;
since it is constantly found in human & animal faeces (besides E.
faecalis & Cl. Perfringens)
Hospital-acquired UTI:
Associated with urinary catheters &
caused by multi-drug resistant strains
Laboratory Diagnosis
A. Specimen: urine
Urine Sample collection
B. Direct detection:
Microscopy:
Wet mount: pus cells, motility test
Gram-stained smear
C. Culture:
Urine should be quantitatively
cultured to determine significant
bacteruria (105 CFU/ml)
D. Identification:
1.
2.
3.
4.
Colony morphology
Gram stain
Oxidase test
Biochemical reactions
KLEBSIELLA
Enterobacteriacaea
Important members are K. pneumoniae,
K. ozaenae, K. rhinoscleromatis & K. oxytoca
(K. pneumoniae is the medically most
important species)
Morphology:
Gram-negative bacilli, non-motile,
capsulated (capsule is the most important
virulence factor)
Culture:
Facultative anaerobic, 24h, 37oC
Selective indicator medium:
MacConkey agar rose pink
colonies due to lactose
fermentation
Colonies are usually mucoid
Biochemical Reactions:
Klebsiella ferments sugars with production
of acid & gas
IMVC is --++
Pathogenesis
habitats:
(1) the environment: in surface water, sewage, soil
& on plants
(2) mucosal surfaces of intestinal & respiratory
tracts
Multi-drug resistant Klebsiella strains may
Laboratory Diagnosis
A.Specimens: urine
B. Direct detection:
Microscopy:
Wet mount: pus cells, motility test
Gram-stained smear
Proteus mirabilis
Morphology
Gram-negative bacilli, motile,
usually pleomorphic
Cultural characters
FA, 37oC, 24h
Simple media: nutrient agar
swarming (due to high motility)
Selective indicator media:
MacConkey NLF
Biochemical reactions
Lactose non-fermenter (LNF)
H2S +ve
Phenylalanine deaminase +ve
Urease +ve
Pathogenesis
Serratia marcescence
Enterobacteriacaea
Morphology
G-ve bacilli
Culture
Some strains produce red pigment & are used for
testing efficiency of bacterial filters
PSEUDOMONAS
AERUGINOSA
Morphology
G ve motile bacilli
Cultural characters
Aerobic, 24h, 37oC (can grow
in 42oC)
Simple media: nutrient
agar greenish exopigment
(yellow pyoverdin+blue
pyocyanin), grape-like odour
Some are -haemolytic
MacConkey agar: NLF
Biocemical reactions
Non-fermentative (acid is
produced from glucose only
oxidatively)
Oxidase +ve
Pseudomonas is not an
Entrobacteriacaea as it is
aerobic, non-fermentative &
oxidase +ve
Pathogenicity
Worldwide, part of normal flora
Grows in moist environments
Highly resistant to antibiotics & disinfectants
In hospitals (nosocomial infection)
Significant human pathogen particularly in
immunocompromised
Virulence factors: invasive, toxigenic & pyogenic
1.Pili: attachment
2.LPS: endotoxin
3.Enzymes: elastase, protease, two haemolysins
4.Exotoxin A: tissue necrosis
P. aeruginosa Infections
Community-acquired
infections
Folliculitis
External ear infections
Eye infections
Osteomyelitis
Endocarditis
Nosocomial
infections
Respiratory
infections
Urinary tract
infections
Wound infections
Meningitis
following lumbar
puncture
Chronic lung
infection in cystic
Laboratory Diagnosis
A. Specimen: urine
B. Direct detection
C. Culture:
D. Identification:
1.Colony morphology
2.Gram stain
3.Oxidase test & other
biochemical reactions
4.Phage & pyocin typing for
epidemiological purposes
In vitro susceptibility to
antibiotics
Staphylococcus
saprophyticus
Coagulase ve staphylococci
Mannitol fermentation is
variable, usually fermenter on
mannitol-salt agar
Non-haemolytic on blood agar
Differentiated from S
epidermidis in being
novobiocin resistant
Second to E coli as a cause of
UTI in sexually active young
female
Enterococcus faecalis
Biochemical reactions
Hydrolyse esculin in presence of
bile salts
Catalase ve
PYR +ve
Antigenic structure
Most strains react with Lancefield
group D antibodies
Pathogenesis
Part of normal intestinal flora
Antibiotic resistant: resistant to
penicillin & vancomycin, lactamase production
Clinical diseases
Hospital acquired rather than community
acquired (particularly in ICU)
Urinary tract infection: the most
common
Intra-abdominal or pelvic wound
infection
Bacteremia, endocarditis, meningitis,
peritonitis, osteomyelitis, abscesses,
wound infection