TIGER * Biosensor for Emerging Infectious Disease Surveillance *Triangulation Identification for Genetic Evaluation of Risks Ranga Sampath David Ecker.

Slides:



Advertisements
Similar presentations
Recombinant DNA Technology
Advertisements

Dr. Thaweesak Tirawatnapong Chula Medical Research Center (Chula MRC)
Development of a Panel for Dengue Virus Maria Rios, PhD CBER/FDA Blood Products Advisory Committee Meeting December 14, 2010.
Virus discovery-454 sequencing
Office of Infectious Diseases Computational Challenges for Infectious Diseases Michael Shaw, PhD OID/Office of the Director.
PCR Polymerase Chain Reaction Mariam Cortes Tormo Miami Children’s Hospital Research institute 2013.
REAL TIME PCR ………A step forward in medicine
Recombinant DNA technology
Metabarcoding 16S RNA targeted sequencing
Next-generation sequencing
Molecular Diagnosis of Infectious Diseases. Why use a molecular test to diagnose an infectious disease? Need an accurate and timely diagnosis Important.
DNA Microarray: A Recombinant DNA Method. Basic Steps to Microarray: Obtain cells with genes that are needed for analysis. Isolate the mRNA using extraction.
Python Programming on PCR Primers Design
Real-Time Detection of Biological Pathogens in Urban Environments Laura Barry Hung Phan Gloria See Introduction to Biosensors Presentation 2 - 4/5/2011.
New Molecular Based Methods of Diagnosis
10 Genomics, Proteomics and Genetic Engineering. 2 Genomics and Proteomics The field of genomics deals with the DNA sequence, organization, function,
Data analytical issues with high-density oligonucleotide arrays A model for gene expression analysis and data quality assessment.
What Can You Do With qPCR?
Genomic DNA purification
Kamila Balušíková.  DNA – sequence of genes, repetitive sequence of noncoding regions  RNA  Proteins gene expression.
Variants of PCR Lecture 4
COBAS AmpliPrep/Cobas TaqMan HIV-1 Test
APPLICATIONS OF MOLECULAR BIOLOGY TECHNIQUES TO MEDICAL MICROBIOLOGY.
Laboratory Training for Field Epidemiologists Viral cultures Investigation strategies and methods May 2007.
Genetic and Molecular Epidemiology Lecture III: Molecular and Genetic Measures Jan 19, 2009 Joe Wiemels HD 274 (Mission Bay)
AP Biology: Chapter 14 DNA Technologies
Analyzing DNA Differences PHAR 308 March 2009 Dr. Tim Bloom.
PCR and Diagnostics Unique sequences of nucleotides if detectable can be used as definitive diagnostic determinants NA hybridisation is the basis for rapid.
From Genomic Sequence Data to Genotype: A Proposed Machine Learning Approach for Genotyping Hepatitis C Virus Genaro Hernandez Jr CMSC 601 Spring 2011.
Development and Evaluation of a Comprehensive Functional Gene array for Environmental Studies Zhili He 1,2, C. W. Schadt 2, T. Gentry 2, J. Liebich 3,
Polymerase Chain Reaction (PCR) What is PCR?: Use of DNA polymerase to selectively amplify a segment of DNA from a much larger sample. Xeroxing DNA, start.
Biotechnology and Genetic Engineering. Human Cloning-The Science In The News.
HCV PCR By Henrietta Orji July 31 st, 2010 Hepatitis C Virus by Polymerase Chain Reaction.
Chapter 18 Reading Quiz 1.Which viral reproductive cycle destroys the host cell? 2.A(n) ______ is a harmless variant or derivative of a pathogen that.
Molecular Techniques in Microbiology These include 9 techniques (1) Standard polymerase chain reaction Kary Mullis invented the PCR in 1983 (USA)Kary.
Molecular Testing and Clinical Diagnosis
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Human Genomics. Writing in RED indicates the SQA outcomes. Writing in BLACK explains these outcomes in depth.
DNA Amplification and PCR Technology
professor in microbiology
Chapter 10: Genetic Engineering- A Revolution in Molecular Biology.
ANALYSIS OF GENE EXPRESSION DATA. Gene expression data is a high-throughput data type (like DNA and protein sequences) that requires bioinformatic pattern.
Chapter 20 DNA Technology and Genomics. Biotechnology is the manipulation of organisms or their components to make useful products. Recombinant DNA is.
A Robust and Accurate Binning Algorithm for Metagenomic Sequences with Arbitrary Species Abundance Ratio Zainab Haydari Dr. Zelikovsky Summer 2011.
 Routine viral diagnostics: indirect and direct detection of viruses. ◦ Indirect detection: serological tests; ◦ Direct detection:  Viral antigens;
Unit 1 – Living Cells.  The study of the human genome  - involves sequencing DNA nucleotides  - and relating this to gene functions  In 2003, the.
Genotypic Microbiological Methods Can be used to determine genetic composition of organisms: Identify organisms (diagnostics) Identify distinct groups.
Viro-chip Microarray Using a Pan-Viral Microarray Assay (Viro-chip) to Screen Clinical Samples for Viral Pathogens.
What is PCR? : Why “Polymerase”?
The stroke size should be 0.25
Ch Epidemiology Microbiology.
Result Introduction Methods
COLLEGE OF VETERINARY MEDICINE
Polymerase Chain Reaction (PCR) and Its Applications
Gel electrophoresis analysis Automated DNA analyzer.
Workshop on the analysis of microbial sequence data using ARB
Human Cells Human genomics
DNA Tools & Biotechnology
Lecture 11 By Shumaila Azam
Polymerase Chain Reaction
PCR How does PCR work?: Separation of two strands
DNA Tools & Biotechnology
PCR–Electrospray Ionization Mass Spectrometry
Accurate genotyping of hepatitis C virus through nucleotide sequencing and identification of new HCV subtypes in China population  Y.-Q. Tong, B. Liu,
Bioinformatics for plant biosecurity and surveillance systems
Accurate genotyping of hepatitis C virus through nucleotide sequencing and identification of new HCV subtypes in China population  Y.-Q. Tong, B. Liu,
Identification of Bacteria BBT203 Ach
PCR–Electrospray Ionization Mass Spectrometry
This work is licensed under a Creative Commons Attribution 4
Marina Papaiakovou, D. Timothy J
Presentation transcript:

TIGER * Biosensor for Emerging Infectious Disease Surveillance *Triangulation Identification for Genetic Evaluation of Risks Ranga Sampath David Ecker Ibis Therapeutics

Chart 2 Infectious Disease Detection Today Culture techniques –Detects a subset of all pathogens Nucleic Acid Tests (NAT’s) –One test at a time (HIV, HCV, tuberculosis, etc.) –Need too many tests –Fail to detect newly emergent pathogens There is currently no good method to detect organisms that have never been seen before Nucleic acid tests (NAT’s)

Chart 3 Problems Addressed by TIGER Animal Reservoirs of Infectious Agents Environmental Surveillance of Public Places Clinical Diagnostics/ Biosurveillance Agricultural Diagnostics/ Biosurveillance

Chart 4 TIGER Process Part 1: Sample Preparation and Broad Range PCR

Chart 5 TIGER Process Part 2: Post PCR Spray and Analysis

Chart 6 Triangulation Using Multiple Primer Pairs Correlated information from multiple primer pairs add redundancy and resolving power

Chart 7 “Back-Ends” to PCR 1- 4 analyses per well Hybridization-based detection based upon selected probes Thousands of analyses in parallel Hybridization-based detection with selected probes Thousands of analyses in parallel Base composition detection without having to select probes Information rich results Taqman probes Chips

Chart 8 RNA Virus Families

Chart 9 Detection and Classification of Coronavirus Species RNA Virus Families

Chart 10 Coronavirus Phylogenetic Tree

Chart 11 Coronavirus Broad-range Primers RdRp Primer nsp11 Primer Multiple primers selected based on alignment of all available sequences in Genbank in March 2003 Primers target all known CoV species Specificity verified using electronic PCR

Chart 12 Primer Target Site in Polymerase

Chart 13 Ibis Chemically Modified Oligonucleotides

Chart 14 ESI-FTICR Two Strands of a PCR Product m/z (M-27H + )

Chart 15 A27 G19 C14 T28 A22 G22 C14 T30 A25 G24 C11 T28 Base Compositions from Mass Spectra MW (Da) SARS CoV HCoV OC HCoV 229E

Chart 16 Triangulation Identification Using Base Compositions

Chart 17 Base Compositions as Virus Classifier - Resolution across viral groups Base compositions are remarkably rich in information content –Corresponding regions from different viral families occupy distinct base composition space

Chart 18 SARS CoV [A27 G19 C14 T28] HCoV 229E [A25 G24 C11 T28] HCoV OC43 [A22 G22 C14 T30]  = [-2A, +5G, -3C, 0T]  = [-5A, +3G, 0C, +2T]  = [-3A, -2G, +3C, +2T] Rotate by T A C G Base Compositions as Virus Classifier - Resolution within a viral group RNA viruses mutate –Multiple isolates could vary in sequence and composition

Chart 19 Base Compositions as Virus Classifier - Resolution within a viral group HCV-1b (50 sequences X 6 regions) Training Set (40 sequences) Test Set (10 sequences) 95% sensitivity Estimate pairwise sequence variation Average “Cloud” Non HCV-1b (50 sequences) Derive probabilities for [A G C T] changes Species variations modeled on HCV sequences –>100 complete genomes; multiple subtypes –Multiple TIGER-like primer regions analyzed –Derived classification probabilities based on observed changes

Chart 20 Base Compositions as Virus Classifier - Resolution within a viral group RNA viruses mutate –Most of these variations are constrained and not random Species variations modeled on HCV sequences –>100 complete genomes; multiple subtypes –Multiple TIGER-like primer regions analyzed –Derived classification probabilities based on observed changes A C G [ ] A C G

Chart 21 The probability of mis- assigning an unknown 229E or OC43 variant as SARS is nearly zero Distribution of probabilities for HCoV 229E or OC43 variants SARS HCoV 229E A C HCoV OC43 G

Chart 22 SARS Classification Probabilities

Chart 23 Mixture sample of SARS, HCoV OC43, HCoV 229E SARS CoVHCoV OC43HCoV 229E MIX MW (Da) 26900

Chart 24 TIGER Sensitivity Maximum Achievable by PCR Genome Copies Probability of detection

Chart 25 Current Semi-Automated Process Collect Sample Suspend and/or Concentrate Lyse DNA Isolation PCR Preparation Mass. Spec. PCR Analyze Results Signal Processing Drill-down Cleanup

Chart 26 Future Automated Process Collect Sample Suspend and/or Concentrate Lyse Auto Signal Processing Drill-down

Chart 27 Conclusions TIGER is a new paradigm for broad detection of infectious disease causative agents Can detect and identify emerging infectious organisms Detections are broad yet highly information rich Sensitive to theoretical limit of PCR High throughput (1800 samples/day/instrument) Applications –Diagnosis of infectious agents in humans –Identification of animal reservoirs –Environmental surveillance of infectious agents

Chart 28 Exact Mass Measurements Facilitate Unambiguous Base Composition Determination ppm # comp pairs AWGXCYTZAWGXCYTZ TWCXGYAZTWCXGYAZ