Detection of Microorganisms

Chapter 12
Detection and Identification of Microorganisms

Objectives
 Identify the advantages and disadvantages of
using molecular-based methods as compared to
traditional culture-based methods.
 Explain the value of controls, in particular
amplification controls, in ensuring the reliability
of PCR results.
 Compare and contrast the molecular methods
that are used to type bacterial strains in
epidemiological investigations.
Target Microorganisms for
Molecular-Based Testing
 Those that are difficult or time-consuming to
isolate
 e.g., Mycobacteria
 Hazardous organisms
 e.g., Histoplasma, Coccidiodes
 Those without reliable testing methods
 e.g., HIV, HCV
 High-volume tests
 e.g., S. pyogenes, N. gonorrhoeae, C. trachomatis
Applications of Molecular Based
Testing in Clinical Microbiology
 Rapid or high-throughput identification of
microorganisms
 Detection and analysis of resistance
genes
 Genotyping
 Classification
 Discovery of new microorganisms
Specimen Collection
 Preserve viability/nucleic acid integrity of target
microorganisms
 Avoid contamination
 Appropriate time and site of collection (blood,
urine, other)
 Use proper equipment (coagulant, wood, or
plastic swab shafts)
 Commercial collection kits are available
 The Clinical and Laboratory Standards Institute
(CLSI) has guidelines for proper specimen
handling
Sample Preparation
 Consider the specimen type (stool, plasma,
CSF)
 More rigorous lysis procedures are required to
penetrate cell walls
 Consider the number of organisms in the
sample
 Inactivate inhibitors (acidic polysaccharides in
sputum or polymerase inhibitors in CSF)
 Inactivate RNases
PCR Detection of
Microorganisms: Quality Control
 PCR and other amplification methods are
extremely sensitive and very specific. For
accurate test interpretation, use proper
controls.
 Positive control: positive template
 Negative control: negative template
 Amplification control: omnipresent
template unrelated to target
 Reagent blank: no template present
PCR Quality Control: Internal
Controls
 Homologous extrinsic Target sequence
 Controls for
amplification
 Heterologous
extrinsic
 Controls for extraction
and amplification
 Heterologous intrinsic
 Human gene control
Quality Control: False Positives
 Contamination: check reagent blank
 Dead or dying organisms: retest 3–6
weeks after antimicrobial therapy
 Detection of less than clinically significant
levels
Quality Control: False Positives
 Improper collection, specimen handling
 Extraction/amplification failure: check
internal controls
 Technical difficulties with chemistry or
instrumentation: check method and
calibrations
Antimicrobial Agents
 Inhibit growth (-static); e.g., bacteriostatic,
fungistatic
 Kill organisms (-cidal); e.g., bacteriocidal,
fungicidal, viricidal
 Antimicrobial agents are classified by:
1. static/-cidal
2. mode of action
3. chemical structure
Sites of Action of Antimicrobial
Agents
Mechanisms for Development of
Resistance to Antimicrobial Agents
 Enzymatic inactivation of agent
 Altered target
 Altered transport of agent in or out
 Acquisition of genetic factors from other
resistant organisms
Advantages of Molecular Detection of
Resistance to Antimicrobial Agents
 Mutated genes are strong evidence of
resistance
 Rapid detection without culturing
 Direct comparison of multiple isolates in
epidemiological investigations
Molecular Epidemiology
 Epidemic: rapidly spreading outbreak of
an infectious disease
 Pandemic: a disease that sweeps across
wide geographical areas
 Epidemiology: collection and analysis of
environmental, microbiological, and
clinical data
Molecular Epidemiology
 Phenotypic analysis measures biological
characteristics of organisms.
 Molecular epidemiology is a genotypic
analysis targeting genomic or plasmid
DNA.
 Species, strain, or type-specific DNA
sequences are the sources of genotype
information.
Pulsed-field Gel Electrophoresis
(PFGE)
M O 1 2 3 4 5 6
O = Outbreak strain
1-6 = Isolates
M O 1 2 3 4 5 6
= Changes from
outbreak strain
Criteria for PFGE Pattern
Interpretation: Rule of Three
Category Genetic Fragment Epidemiological
differences* differences* interpretation
Indistinguishable 0 0 Test isolate is the same
strain as the outbreak
strain.
Closely related 1 2–3 Test isolate is closely
related to the outbreak
strain.
Possibly related 2 4–6 Test isolate is possibly
related to the outbreak
strain.
Different >3 >6 Test isolate unrelated
to the outbreak.
*Compared to the outbreak strain.

Arbitrarily Primed PCR: Random
Amplification of Polymorphic DNA (RAPD)
MO
M = Molecular weight marker

O = Outbreak strain
Four isolates differ from the outbreak strain.
Interspersed Repetitive Elements
REP sequence inverted repeat ….GTGAATCCCCAGGAGCTTACATAAGTAAGTGACTGGGGTGAGCG….
ERIC sequence inverted repeat GCC G/T GATGNCG G/A CG C/T NNNNN G/A CG C/T CTTATC C/A GGCCTAC
PCR amplification priming outward from repetitive elements

generates strain-specific products.
Isolate A
Isolate B
M A B M A B U
Is the unknown (U) strain A or B?

Other Genotypic Methods Used to
Type Organisms
 Plasmid fingerprinting with restriction
enzymes
 RFLP analysis
 Amplified Fragment Length Polymorphism
(AFLP)
 Interspersed repetitive elements
 Ribotyping
 spa typing
 Multilocus sequence typing
Comparison of Molecular
Epidemiology Methods
Method Typing Discriminatory Reproducibility Ease of Ease of
capacity power use interpretation
Plasmid Good Good Good High Good
analysis
PFGE High High High Moderate Good
moderate
Genomic High Good Good High Moderate–
RFLP poor
Ribotyping High High High Good High
PCR-RFLP Good Moderate Good High High
RAPD High High Poor High Good–high
AFLP High High Good Moderate High
Repetitive Good Good High High High
elements
Sequencing High High High Moderate Good–high
Viruses
 “Classical methods” of detection include
antibody detection, antigen detection, or
culture.
 Molecular methods of detection include
target, probe, and signal amplification.
 Tests are designed for identification of
viruses, determination of viral load
(number of viruses per ml of fluid), and
genotyping by sequence analysis.
Test Performance Features for
Viral Load Measurement
Characteristic Description
Sensitivity Lowest level detected at least 95% of the time
Accuracy Ability to determine true value
Precision Reproducibility of independently determined test

results
Specificity Negative samples are always negative and positive
results are true positives
Linearity A serial dilution of standard curve closely
approximates a straight line
Flexibility Accuracy of measurement of virus regardless of
sequence variations
Viral Genotyping
 Viral genes mutate to overcome antiviral
agents.
 Gene mutations are detected by
sequencing.
 Primary resistance mutations affect drug
sensitivity but may slow viral growth.
 Secondary-resistance mutations
compensate for the primary-resistance
growth defects.
Summary
 Molecular-based methods offer sensitive and
direct detection of microorganisms.
 Due to high sensitivity and specificity, proper
quality control is critical for molecular testing.
 Several molecular methods are used to type
bacterial strains in epidemiological
investigations.
 Target, probe, or signal amplification
procedures are also used to determine viral
load.

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Chapter 12

Detection and Identification of Microorganisms

*Compared to the outbreak strain.

M = Molecular weight marker

PCR amplification priming outward from repetitive elements

Is the unknown (U) strain A or B?

Accuracy Ability to determine true value

Precision Reproducibility of independently determined test

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