INVESTIGATING TEMPORAL STRAIN DIVERSITY IN HUMAN E. COLI · investigating temporal strain diversity...
Transcript of INVESTIGATING TEMPORAL STRAIN DIVERSITY IN HUMAN E. COLI · investigating temporal strain diversity...
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INVESTIGATING TEMPORAL STRAIN DIVERSITY IN HUMAN E. COLI
POPULATIONS USING PYROPRINTING:
A NOVEL STRAIN IDENTIFICATION METHOD
February 25, 2012 Emily Neal Michael Black Chris Kitts
Aldrin Montana Alex Dekhtyar
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Background
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Why E. coli?
Found in GI tract in many mammals,
birds, and reptiles
Indicator for fecal contamination Microbial Source Tracking
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Reproducibility Randomly amplified polymorphic DNA
(RAPD)
Repetitive extragenic palindromic PCR (rep-PCR)
Biochemical Profiling
Time Intensive/Laborious Pulsed-field gel electrophoresis (PFGE)
Ribotyping
CURRENT METHODS FOR STRAIN IDENTIFICATION HAVE PROBLEMS
Solution: Pyroprinting!
Expensive PFGE
Multilocus enzyme electrophoresis (MLEE)
Sensitivity Antibiotic resistance profiles (ARP)
Serotyping
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The Questions
How do E. coli populations vary over time in human individuals?
How many different strains are detected over the total
time period? How frequently are strains detected? How does population variation differ between
individual hosts?
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The Hypothesis
Hosts will carry the same 1-2 dominant strains
throughout the study Different minor strains will be detected throughout
the study
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Sampling PCR Pyroprinting Clustering
The Method
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Work Flow
E. coli collection & isolation
Colony PCR
Pyroprinting (Data Collection)
Match pyroprints = build strains
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E. coli Collection & Isolation
Collect & swab fecal samples 3 individuals 6 months 15 isolates (colonies)
once a month
Metabolic confirmation
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Colony PCR
ITS: Intergenic Transcribed Spacer Non-coding Increased accumulation of mutations
Ribosomal RNA Locus
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Colony PCR
Ribosomal RNA Locus x 7 copies in E. coli genome
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Colony PCR
Ribosomal RNA Locus
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Pyroprinting
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What is a Pyroprint?
Obtained through pyrosequencing Similar to a “fingerprint”
Used for identification— not information Creates a unique pattern of peaks based on
DNA sequences from all 7 ITS copies
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Data Output
Extract Peak Heights
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Data Processing
Sim(X, Y) = Pearson(X, Y)
X
Y
X
Y
MITS1[Hu-404, Hu-700] = Sim(X, Y) MITS2[Hu-404, Hu-700] = Sim(X, Y)
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If thr(Sim(X, Y)) >= α Sim(X, Y) := 1
If thr(Sim(X, Y)) < β Sim(X, Y) := 0
If SimITS1(XITS1, YITS1) and SimITS2(XITS2, YITS2) > 0 Sim(Cm, Cn) = Avg(SimITS1, SimITS2)
Data Processing
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Novel Clustering Algorithm
Aldrin Montana, Alexander Dekhtyar, Emily Neal, Michael Black, and Chris Kitts. 2011. Chronology-Sensitive Hierarchical Clustering of Pyrosequenced DNA Samples of E. coli: A Case Study. In Proceedings of the 2011 IEEE International Conference on Bioinformatics and Biomedicine (BIBM '11). IEEE Computer Society, Washington, DC, USA, 155-159.
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Clustering Approach
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Results
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Person A
Person B
Person C
# of Isolates
# of Isolates
# of Isolates
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# of Strains
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Conclusions
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What We Know So Far…
Strain discrimination with pyroprinting It’s possible! More sensitive than other methods
Hypothesis supported….partially
Variation is variable!
Population structures in different humans may vary in different ways
Change will occur
Supported by both this study and literature
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Future Work
More data to analyze! Building a database More temporal studies Broad human population studies
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Future Work
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Questions?
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Person A
Person B
Person C
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Person A
Person B
Person C
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Person A
Person B
Person C
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Clustering Approach