Next Generation Panel Oriented Diagnostics The FilmArray Pathogen Identification System Idaho Technology.

Slides:



Advertisements
Similar presentations
Respiratory infection - 1
Advertisements

Enhanced Etiological Diagnosis Of Respiratory Virus Outbreaks Using Nucleic Acid Amplification Testing Against An Expanded Range Of Targets Sallene Wong.
1 HIV Drug Resistance Training Module 7: HIV Genotyping Assay Validation.
DCLS Influenza Laboratory Testing Denise M. Toney, Ph.D. Commonwealth of Virginia Division of Consolidated Laboratory Services H & M Panel – May 2009.
By Gracie Canales August 10, 2010
About these slides SPEC – Short Presentation in Emerging Concepts
Interpretation of Results
Which viruses can we detect? What is the appropriate specimen?
Recombinant Expression of PDI in E. coli
QIAGEN 2009 QIAgility ─ Pure Precision Andrea Tesoriero
DNA Microarray Jamie Mashek.
Virus discovery-454 sequencing
The relative importance of respiratory viruses in lower respiratory tract infections in primary care. [P1581] F. Coenjaerts 1, C. Lammens 2, M. Viveen.
Avian Influenza: Laboratory Issues Jill Taylor, Ph.D. Director, Clinical Virology Program Wadsworth Center.
Influenza Transmission Among Pediatric Patients and Family Contacts 1747 Citadel Plaza Suite 206 San Antonio, TX (210)
Wade K. Aldous, Ph.D. LTC, USA Edgie-Mark Co, Ph.D., M(ASCP), CPT, USA Edward Keen, Ph.D., M(ASCP), CPT USA.
Utilizing a Non-Commercial Real- Time PCR to Detect HIV-1 RNA in HIV Antibody Negative Diagnostic Sera Submitted to The Maryland Public Health Laboratory.
Pediatric Diagnosis of HIV-1 Infection Using Dried Blood Spots Chin-Yih Ou, PhD NCHSTP/DHAP Centers for Disease Control and Prevention.
and Respiratory Viruses in Multiple Specimen Types
 Molecular Laboratory must have an ongoing Bio-safety SOP and also quality improvement program to monitor and evaluate objectively and systematically.
Nucleic Acid Extraction Control in Real-Time PCR Assays Steve Hawkins Senior Global Product Manager Bioline.
Amplification and Detection of Nucleic Acid by the Real-Time RT-PCR Procedure Janice C. Pedersen, Microbiologist Avian Section Diagnostic Virology Laboratory.
DR. MOHAMMED ARIF ASSOCIATE PROFESSOR CONSULTANT VIROLOGIST HEAD OF THE VIROLOGY UNIT Viral infection of the respiratory tract
BioFire (FilmArray) Multiplex PCR Assays
Genomic DNA purification
Plant virus infections induce tremendous economic losses for agricultural production each year in the U.S. Accurate and reliable diagnosis of the pathogens.
New Monogram Biosciences Testing Capabilities: Influenza, RSV, Ebola and Other Respiratory and Enveloped Viruses.
HIV GENOTYPE ASSAY Anabelia Perez, MLT (ASCP) Molecular Technologist August 6, 2008.
Variants of PCR Lecture 4
FilmArray™ - Nested Multiplex PCR for Multi-pathogen Screening
A.Selvapandiyan LBPUA, OBRR, CBER, FDA, Bethesda, MD July Multiplex fluorescence-based PCR assay to detect pathogens in blood Multiplex fluorescence-based.
FilmArray: Automated PCR
Detection of parvovirus B19 and novel human parvoviruses in high-risk individuals Ashleigh Manning 1, Kate Templeton 2, Ed. Gomperts 3, Peter Simmonds.
Luciferase Based Plasmid Reporter System for the Detection and Quantification of Human Respiratory Syncytial Virus Group 14: Oral Report 2, 1/24/2008 Melanie.
Development and Validation of a Novel Real-Time RT-PCR Assay to Distinguish Porcine Reproductive and Respiratory Syndrome (PRRS) Virus Subtypes with High.
مصرف منطقی داروها در عفونت های تنفسی، عفونت های گوارشی و عفونت سیستم ادراری دکتر احمد رضا مبیّن متخصص بیماریهای عفونی MD-MPH.
Purification of DNA from a cell extract In addition to DNA, bacterial cell wall extract contain significant quantities of protein and RNA. A variety of.
Serum procalcitonin and C-reactive protein in children with community- acquired pneumonia K.Gogvadze, I.Guramishvili, I.Chkhaidze, K.Nemsadze, T.Maglakelidze.
Microarray Technology
DNA Chips Attach DNA to tiny spots on glass slides (i.e., chip). Hybridize fluorescently-labeled DNA probes to chip. Detect hybridization to different.
Risk factors, pathophysiology and causative agents of acute otitis media This teaching presentation for the ISOM website has been prepared by Tal Marom,
Twelve years‘ detection of respiratory viruses by immunofluorescence in hospitalised children: impact of the introduction of a new respiratory piconarvirus.
Influenza C in Alberta TARRANT Symposium 2012 Kanti Pabbaraju Lab Scientist ProvLab
Chronic Bronchitis Breathlessness, and Productive purulent cough, and Fever Chest X-ray for to exclude lung neoplasm,
RESPIRATORY INFECTIONS. World Lung Foundation
W W W. Q I A G E N. C O M Dirk Heckel, PhD Diagnostic Sample Preparation and Stabilization QIAGEN GmbH.
Biotechniques. DNA sequencing To determine the base sequence of DNA fragments. DNA replicated into smaller fragments incorporating fluorescent tags Fragments.
DISEASES OF THE RESPIRATORY SYSTEM
1 Common cold. 2 Background Heikkinen T and Järvinen A. Lancet 2003;361:51–59. Viral cause : rhinoviruses 30–50%, coronaviruses 10–15%, influenza viruses.
MCT = Molecular Colony Technique Alexander Chetverin Institute of Protein Research of the Russian Academy of Sciences References: NAR(10)2349 from 1993.
Bronchiolitis Abdullah M. Al-Olayan MBBS, SBP, ABP. Assistant Professor of Pediatrics. Pediatric Pulmonologist.
Point-of-Care PCR Testing for Respiratory pathogens:- Multiplexed Viral Panels David Squirrell, KTN Meeting September 2013.
MERS (Corona-EMC) JUNE 2013 CountryReports (deaths) France2 (1) Italy3 (0) Jordan2 (2) Katar2 (0) Saudi Arabia39 (24) Tunesia2 (0) Great Britain3 (2) United.
Bacterial and viral infections in patients requiring hospitalization : effect of mixed infections on clinical outcome J. Petitjean Lecherbonnier 1, F.
Antibiotics In Respiratory Infection To Use or Not to Use - that is the question. Dr. James Paton University of Glasgow.
Viro-chip Microarray Using a Pan-Viral Microarray Assay (Viro-chip) to Screen Clinical Samples for Viral Pathogens.
RT-PCR analysis 생화학 실험 2 조교 : 이 선 민 내선 7699, 첨단과학기술관 201-B 호 신과학원 S438 호.
Emerging Advances in Rapid Diagnostics of Respiratory Infections David R. Murdoch*, Lance C. Jennings, Niranjan Bhat, Trevor P. Anderson Department of.
Aim: To develop a new one-step RT-PCR assay to detect H1N1 by designing new primer to target NP gene Experimental approach: -nasopharyngeal swabs from.
Comparison of the Focus Diagnostics Simplexa™ Flu A/B & RSV Direct Assay with the Prodesse® ProFlu™ + Assay for Detection of Influenza A Virus (FluA),
Overview Wednesday Thursday Labs 12, 13 & 14 due March 7th
ASM 2017 Microbe Annual Meeting Sunday-507
Molecular screening of Respiratory pathogens
DNA EXTRACTION Protocol and notes 9/17/2018.
Syndromic Multiplex Panels – What’s New, How Will We Use Them and What is the Impact on the Microbiology Laboratory Nathan A Ledeboer Associate Professor.
Lecture 11 By Shumaila Azam
Reverse Complement PCR: fast, low cost amplicon based NGS
Luciferase Based Plasmid Reporter System for the Detection and Quantification of Human Respiratory Syncytial Virus Progress Report 1, 12/6/2007 Melanie.
توان بخشي ورزشي بيماران آسمي
Development of a Rapid Automated Influenza A, Influenza B, and Respiratory Syncytial Virus A/B Multiplex Real-Time RT-PCR Assay and Its Use during the.
Presentation transcript:

Next Generation Panel Oriented Diagnostics The FilmArray Pathogen Identification System Idaho Technology

The FilmArray Today we get to introduce you to a new molecular diagnostic platform that we are very excited about at Idaho Technology – The FilmArray. Today, we’ll be talking about: what the FilmArray is how it works our new respiratory panel and, most importantly, what it can do for you Additionally, today, we are going to fire up the FilmArray and do a live demo so that you can see it action.

User-Friendly Multiplex PCR The FilmArray is… User-Friendly Multiplex PCR Automated Protocol Integrated Sample Prep Automated Results Analysis We set out to make the FilmArray the most user-friendly multiplex PCR platform available. It has: Completely automated protocol Integrated Sample Prep Automated Results Analysis Speed Massive multiplex PCR Let me tell you a little more… Multiplex PCR Speed

Run Set-up Load Pouch Inject pouch Hydration Solution Add sample to Sample Buffer

Run Set-up Inject sample Load pouch in FilmArray Enter pouch and sample ID, user info, then press go!

Automated Protocol We all know there is automated and then there’s automated. The FilmArray is automated. In a typical PCR reaction you start with a sample, take some reagents, some disposables and an DNA extraction robot and you extract the nucleic acids from the sample. You then transfer the nucleic acids, along with some additional reagents, to a thermal cycler instrument for PCR. If you are doing a deep multiplex analysis, you then transfer your amplified product, along with even more reagents, to analysis instrument which generates your results. With the FilmArray, you start with a sample add it to your sample buffer. You add your buffered sample and some rehydration solution to the FilmArray pouch, load the pouch on the FilmArray instrument, start the run and your done.

Start the run & walk away Automated Protocol 5 min of hands on time Start the run & walk away With the FilmArray, you can set up a run in 5 minutes or less. This hands on labor involves simply injecting sample and rehydration buffer into a FilmArray pouch, loading the pouch into the FilmArray instrument, and starting the run. All subsequent sample manipulations, reagent transfers, and results analysis are completely automated – once you start the run you are free to walk away. The automated protocol includes integrated sample prep…

Integrated Sample Prep One of the key aspects of our automated protocol that I want to emphasize is integrated sample prep. We have taken all the reagents, the instrument, and the disposables required to extract and purify nucleic acids from the patient specimen and integrated it all into the FilmArray. Integrated sample prep means less labor, less cost, less overhead, and less hassle for your lab. After the FilmArray extracts and purifies all the nucleic acids from the specimen, it automatically performs PCR analysis and reports the results.

Multiplex PCR Simultaneous detection of dozens of targets from one patient sample The FilmArray performs multiplex PCR – simultaneously detecting dozens of DNA targets from one patient sample. This is the ideal approach for getting the most possible work done for least possible effort. In one run, with 5 minutes of labor, you get dozens of results.

Automated Results Analysis Positive or negative call for each target The FilmArray analyzes real-time PCR curves, checks the results of the controls, and produces a positive or negative result for each target analyzed.

Automated Results Analysis Eliminate Subjectivity analysis.

Speed…. It’s really fast. Sample prep 1 hour RT-PCR Multiplex PCR Analysis Results And it’s really fast. The FilmArray Extracts and purifies nucleic acids from a patient specimen Converts and RNA into DNA via at Reverse Transcription step Performs a multiplex PCR Analyzes all the data And reports the results All in less than 1 hour! This allows you to do what you do best – get results to your customers in a more timely fashion. And the icing on the cake is that you don’t get just one result in one hour but…

The FilmArray How does it work?

Sample extraction & purification The FilmArray Pouch Reagent Storage Chemical Circuit Board 2 minutes The FilmArray pouch is made up of two sections: A series of reagent storage chambers A chemical circuit board All the necessary reagents required for sample preparation, RT-PCR, PCR, and detection are stored in the reagent storage chambers. The chemical circuit board is made up of 2 layers of thin plastic film which contains various compartments for each of the steps I just mentioned as well as channels between each compartment. The ability to store and manipulate these reagents in this pouch allows us to completely automate the entire process downstream of sample loading. Sample extraction & purification 1st stage multiplex PCR 2nd stage PCR

The FilmArray – How Does it Work? FilmArray Animation 2 minutes To further help you understand how the FilmArray works, here is an animated description.

Automated Protocol Bladders inflate over blisters to push liquid Air Channels Pistons close channels Pneumatically driven plungers in the FilmArray instrument are driven into the reagent storage chambers and delivers the appropriate reagents at the right time and the right place. The chemical circuit board is manipulated by pneumatically opening and closing the various reaction blisters as well as the channels between the reaction blisters. In this way, the FilmArray instrument is able to drive reagents left and right through the chemical circuit board. All of this allows us to provide you with a completely automated protocol. The FilmArray mixes all the appropriate reagents at the appropriate place and at the appropriate time – so that you don’t have to. Pneumatic Bladders

The FilmArray: Video analysis 2 minutes To further help you understand how the FilmArray works, here is a video showing how the reagents are moved around within the pouch. This is time-compressed actual footage of a FIlmArray run.

Integrated Sample Prep Once the patient specimen is injected into the pouch and run began, the specimen is bead beat to release all nucleic acids. Bead beating has been shown to be an effective and robust method for nucleic acid extraction for a variety of sample types. It’s like a micro-blender for cells and viruses. After the nucleic acids have been released they are bound by magnetic beads and then moved from the sample lysis blister to the purification blisters. Here the nucleic acids are washed 3 times to remove any remaining cellular and viral debris. The last sample prep step is to elute the nucleic acids from off the magnetic beads and move them to the PCR I blister. + + =

Nested MultiPlex PCR 3 minutes Next, the purified nucleic acids are moved to the PCR I blister. Here any RNA is converted into DNA via a reverse transcription step. Then a massive multiplex PCR reaction is performed – but only for a limited number of cycles. During the early cycles of PCR, reagents are plentiful and do not become a limiting factor until the later PCR cycles. So after a limited number of PCR cycles, before competitive effects become problematic, the FilmArray halts the PCR reaction. The products from PCR I are then diluted to functionally remove any remaining PCR I primers. The diluted PCR I products are then combined with a fresh primer free master mix. Aliquots of this solution are then distributed to each well of the array in the PCR II blister. Individual primer sets are pre-spotted in each well of this array. Each of these primer sets are nested primers designed to detect and amplify one of the PCR products generated in PCR I. Thus PCR II is performed in traditional single-plex fashion – so during the detection phase the later cycles of PCR, we eliminate the competitive effects common to multiplex PCR.

Automated Results Analysis 102 individual 2nd stage PCR wells Each well contains one reaction Fluorescent data is generated for each well During the PCR II phase, the FilmArray generates real time PCR curves for each well in the array.

Automated Results Analysis All targets tested in triplicate With so much real-estate in this array we are able to test all targets in duplicates or triplicates.

Automated Results Analysis For some organisms we target multiple genes – each tested in triplicate Software generates an automated call for each organism And some organisms, we look at multiple genes – each in triplicate. At the completion of PCR II, the FilmArray software analyzes the data from each well – including several controls. The software performs a complex meta analysis of the data for each replicate of each target for each organism. Based on this analysis the FilmArray reports a positive or negative result for each organism.

The FilmArray Respiratory Panel Viral Adenovirus Bocavirus Coronavirus 229E Coronavirus HKU1 Coronavirus OC43 Coronavirus NL63 Entero Virus Influenza A Influenza A H1 Influenza A H1 2009 Influenza A H3 Bacterial Bordetella pertussis Chlamydophila pneumoniae Mycoplasma pneumoniae Influenza B Metapneumovirus Parainfluenza 1 Parainfluenza 2 Parainfluenza 3 Parainfluenza 4 Respiratory Syncytial Virus Rhinovirus

Nested Multiplex PCR

Comparison of Multiplex PCR Blue Graph - 5000 x LOD* C. burnetti Red Graph - 0.1x LOD* B. anthracis (100 ul of a 100 CFU/ml BA sample) *LOD = 1000 cfu/ml 25

Robust Multiplex PCR

Triple Infection Bocavirus – black PIV2 – blue Human Rhinovirus - green Bocavirus – black PIV2 – blue Human Rhinovirus - green 27

Simultaneous Detection of 12 Organisms Flu A H1 Flu A H3 Flu B RSV Para Flu 1 Para Flu 2 Para Flu 3 Adeno Human Meta Pneumo Rhino Boca S. pneumoniae 1 minute This experiment was run using our Bio-Threat panel. In this experiment 5 low-copy targets were spiked with 1 high copy target into one sample. As you can see the FilmArray was able to detect all 5 low-copy targets at their limit of detection.

System Controls

Internal pouch Controls Controls currently in the pouch: RNA Process mRNA from freeze-dried S. pombe Pouch pass/fail is set on this control 1st Stage PCR synthetic oligos in PCR1 2nd Stage PCR synthetic oligos in PCR2 Useful for understanding failure modes Human mRNA assay for human mRNA in sample We are collecting data

Location of the controls PCR2 control (spotted with PCR2 primers) 2 minutes The FilmArray pouch is made up of two sections: A series of reagent storage chambers A chemical circuit board All the necessary reagents required for sample preparation, RT-PCR, PCR, and detection are stored in the reagent storage chambers. The chemical circuit board is made up of 2 layers of thin plastic film which contains various compartments for each of the steps I just mentioned as well as channels between each compartment. The ability to store and manipulate these reagents in this pouch allows us to completely automate the entire process downstream of sample loading. Yeast control Freeze dried into sample well PCR1 control Freeze-dried with Primer Pellet

Comparative Data

The FilmArray – Data FilmArray vs DFA in 387 Pediatric NPAs Pediatric NPA samples were tested by DFA (blue) and by FilmArray (maroon).

82% of 387 pediatric NPA samples tested positive by FilmArray analysis 2 minutes Getting back to the data from our collaboration with Primary Children’s Medical Center…. In this collaboration we tested 387 pediatric NPAs and compared the results to DFA. As you can see the FilmArray has a much higher rate of positive calls vs. DFA. 82% of the samples tested on the FilmArray were positive versus only 47% positive tested via DFA. Of course on the FilmArray we are able to test for more organisms than DFA. Most of the positives we saw were due to a few major contributors : Rhino Virus, Adeno Virus, RSV, and Influenza A Virus.

32% tested positive for 2 or more pathogens by FilmArray analysis 1 minute One of the more interesting observations from this data set is the rate of multiple positives detected on the FIlmArray. 32% of the 387 pediatric NPAs we tested in collaboration with PCMC tested positive for 2 or more pathogens – compared to only 2.1% by DFA. What are the clinical implications of this? Great question. We don’t know. But isn’t exciting to finally have the tools to address that question.

Future Developments Product Development (Beyond RP) Sepsis/Meningitis Panel Enteric Pathogens Panel STD Panel Biothreat Panel

Questions