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USAMRIID Development, Comparison, and Use of Nucleic Acid-Based Diagnostics to Detect Arboviruses in the Field LTC Monica O’Guinn and Dr. John Lee US Army.

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Presentation on theme: "USAMRIID Development, Comparison, and Use of Nucleic Acid-Based Diagnostics to Detect Arboviruses in the Field LTC Monica O’Guinn and Dr. John Lee US Army."— Presentation transcript:

1 USAMRIID Development, Comparison, and Use of Nucleic Acid-Based Diagnostics to Detect Arboviruses in the Field LTC Monica O’Guinn and Dr. John Lee US Army Medical Research Institute of Infectious Disease, Fort Detrick, Frederick, Maryland

2 Overview Confirmation Detection Sequence Analysis
Other Assays Pool Triturate Extract RNA Sequence Analysis TRIzol DNAzol DNA cDNA PCR Ready-To-Go™ Blast Search on GenBank Detection Remaining PCR Product Phylogenetic Tree PCR Clean Up Sequencing

3 Mosquito Trapping

4 Human Landing Collections

5 Use of Sentinal Animals

6 Setting Traps During Daylight

7 Setting Traps at Night

8 Reluctant Mosquito Bait

9 Eager to help . . .

10 Early Morning Collecting

11 A Single Trap’s Catch

12 Mosquito Identification
Culex Anopheles Aedes Ochlerotatus Psorophora Mansonia Uranotaenia Wyomeyia Coquilletidia

13 Mosquito Preparation Pool mosquitoes by species
Triturate mosquitoes in PBS/media Add 250 ul of mosquito suspension to 750 ul of TRIzol® LS Use of BBs to triturate-decreases contamination

14 RNA Extraction Followed by Reverse Transcription
RNA Extraction - Trizol LS Reverse transcription - formation of cDNA Cold chain limited to chopped ice

15 Equipment Thermocycler Transilluminator Electrophoresis unit
Microscope Centrifuge Camera RT reagents PCR reagents Ice chest/cold block Pipettors

16 Equipment Upgrades Refrigerated centrifuge 96-well thermocycler
E-gel™ system

17 Field Gels

18 RAPID Real-Time Cycler
Ruggedized Advanced Pathogen Identification Device

19 RAPID Cycler Reactions can be monitored using
hybridization probes or double-strand DNA specific dyes, such as SYBR Green

20 Lightcycler Features STEP #1 Freeze-dried reagents in foil pack
STEP #2 Reconstitute with liquid sample or water STEP #3 Load in to R.A.P.I.D STEP #4 Run and read results

21 New Technology - MiniOpticon
Benefits: Light weight - 7 kg 48 Samples Plastic tubes Conventional PCR Real-Time PCR

22 Field Use of the MiniOpticon Real-Time Thermocycler

23 Conventional PCR Pros Well established technology
Product amenable to direct sequencing Can visualize band intensity and size Literature contains multiple references Present in the Army inventory 96-well block Cons Requires gels Longer time

24 Real-Time PCR - RAPID Advantages
Rapid heating of sample - shorter run times Present in the Army inventory Disadvantages Glass capillaries and 32-reactions per run Heavy - difficult as checked baggage Expensive - fluorescently labeled probes No automatic memory after power failure

25 Real-Time PCR - MiniOpticon
Advantages Plastic tubes and Lightweight instrument Dual use for real-time and conventional Disadvantages Overheats easily Sun glare sensitive No automatic memory

26 From Mosquitoes to PCR Products
Hands-On Demonstration From Mosquitoes to PCR Products


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