Title: Molecular Identification Methods
1(No Transcript)
2Molecular Identification Methods
- Confirmation of identity for commonly used
laboratory strains should ideally be done at the
level of genotypic analysis... Pharmacopeial
Forum, Volume 30 (5) 2004 Microbiological Best
Laboratory Practices, Page 1717)
3Overview
- Current phenotypic methods/ Problems
- Molecular case studies in industry
- PCR/Sequencing techniques
- Species level ID and Commercial systems
- Strain level ID and Commercial system
4Phenotypic Methods
- Morphology
- Growth Characteristics
- Serotyping
- Phage typing
- Bacteriocin
- Biochemical Characteristics
- phenol red carbohydrate, catalase production,
oxidase production, tests, methyl red test,
nitrate reduction,starch hydrolysis, tryptophan
hydrolysis, hydrogen sulfide production, citrate
utilization, and litmus milk
5Microbiological Analyses
Create microbe on plate
Streak on fresh plate
Biolog
Vitek
Gram Stain
6Problems With Microbiological Testing in QA
Laboratories
- Gram staining, messy, time consuming
- Biolog/Vitek time consuming 2-3 days
- Large amount of isolates unidentifiable
- Only identifiable to genus, species level
- Some non-specific, moulds take 2-3 weeks, many
repeats
7Microbiological Testing in IndustryHow can
Molecular Methods Improve Testing?
- Sterility testing
- Environmental testing
- Raw material testing
- Water testing
- Personnel monitoring
8When Genotyping Necessary?
- Sterility Test positive
- Requires
- Investigation, corrective and preventative action
(best case)
9Pharmaceutical Case Study Investigation 1
10Pharmaceutical Case Study Investigation 1 PFGE
- The PFGE results showed identical banding
patterns by not1 digest and are the same strain
of Bacillus pumilus
11Pharmaceutical Case Study Investigation 2
12Pharmaceutical Case Study Investigation 2 BoxAIR
13PCR
14Sequencing Method
15Automatic Sequencing
16Species Level ID
Sequencing rRNA Genes
411 completed bacterial genomes
Structural Conserved regions Universal Not
laterally transferred
17How is Ribosomal DNA Sequencing Carried Out?
- Ribosomal 18S/16S or 28S/23S
18Commercial Systems Species level ID
- Species Level IDs
- Microseq Applied Biosystems
- Sherlock (DNA) Midi Inc.
- Riboprinter (strain level?) DuPont Qualicon
- Bax (food pathogens, 0157 etc. ) DuPont
Qualicon -
19Microseq and Sherlock-DNA
- 3 Databases
- Fungal D2 region of large rRNA subunit
- Bacterial 16S full sequence (1500bp), 16S
partial sequence (500bp) - Microseq Software and Database adheres to good
manufacturing practice (CGMP) regulations (21 CFR
part 11 for audit trails)
20Strain Level IDs
- Sequencing ITS region
- - Strain level identification
- RFLP Restriction Fragment Length Polymorphism
- Identification and differentiation
- PFGE Pulse Field Gel Electrophoresis
- Epidemiological studies
- BoxAIR-PCR BoxA Inverse Repeat PCR
- Identification and differentiation
- Commercial System
- Ribotytping
- -RFLP principle
21Sequencing to Strain Level Identification
- ITS (Internal transcribed spacer regions)
- between 18S and 28S
- Or 16S and 23S
22RFLP
- RFLP (Restriction Fragment Length Polymorphism)
- Restriction digest of
- direct extracted DNA
- amplified selected genes via PCR
23Example of a PFGE Analysis on Staphylococcus
aureus.
24PFGE
Figur
e 2. Example of a real PFGE drug resistant
Staphylococcus aureus. The molecular weight
markers are digested lambda phage (?) and are
given in kb. See the CDC web page with the
original data .
25BOXAIR-PCR
- BOX-PCR (Amplification of BOX-cassettes)
- Rapid detection method with high reproducibility.
26Commercial System - Strain level ID
adheres to good manufacturing practice (CGMP)
regulations (21 CFR part 11 for audit trails)
Riboprinter
27Ribotyping
28Riboprinter Batch System Report
29Summary
- Species Level ID
- Sequencing 16S/5S/23S genes (bacteria)
- Sequencing 18S/5.8S/28S (fungal)
- Strain Level ID
- Sequencing ITS region
- PFGE Pulse Field Gel Electrophoresis
- RFLP Restriction Fragment Length Polymorphism
- BoxAIR-PCR BoxA Inverse Repeat PCR
- Ribotytping