Sample collection and shipping: what's important and why

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Sample Collection and Shipping What’s important ____and why___ Deb Miller 1,2 and Matt Gray 1 1 Center for Wildlife Health 2 College of Veterinary Medicine

Transcript of Sample collection and shipping: what's important and why

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Sample Collection and

Shipping

What’s important ____and why___

Deb Miller1,2 and Matt Gray1

1Center for Wildlife Health 2College of Veterinary Medicine

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Collecting Animals

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Enclosure (Pipe) Sampling

Count Number of Dips

Dip until No Larvae Captured after 10 dips

Is probability of transmission

affected?

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Co-housing Animals

Mean = 0.8 – 0.9 contacts/min for 40 tadpoles/m2

(10 tadpoles per 5-gal [19 L] bucket)

All should contact each other in 9 Minutes

10, 20, 40% X

15, 30, 60 min What about

gloves?

Ranavirus Example

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Methods: Cohousing 450 Total Animals

Cohouse in buckets for 15, 30, or 60 minutes; 10%, 20%, or 40% infected; 50 animals per treatment

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Results:  Cohousing

Unpublished  Figured  Deleted  

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Methods:  Glove  Change    (600  total  animals)

• Change  gloves  or  don’t  change  gloves  • Vary  density  of  infected  individuals  

5%  

40%  

10%  

20%  

100  animals  per  treatment  for  14  days  600  animals  total  

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Methods: Glove Change

Swab individual

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Results:  Glove  Changing

Unpublished  Figured  Deleted  

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Smokies Example Searching and Numbered Bags

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Isolating Animals

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Holding Containers One Individual per Container

Plastic Bags

1-L or 2-L Plastic Tubs

Mason Jars

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Processing Station

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Aseptic Processing Station

People that collect do

NOT process!!

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ID and Morphometrics: Stations 1 and 2

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Aseptic Processing Station Station 1

ID Rinsed & Labeled

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Weigh SVL

Aseptic Processing Station Station 2

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Swabbing: Station 3

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Type of swab: 1. Individually packaged. 2. Wire or plastic shaft (plastic often is designed with breaking point so no need for additional instrument to cut the shaft when placing in tube). NOTE: wood shafts may interfere with molecular testing 3. Microtip is easier for smaller species

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Swabbing Anurans Bd and Bsal Surveillance

Non-lethal Techniques: Brem et al. (2007)

Swabbing Preferred

Swab 5 times in 5 locations

A. Cressler, USGS

A. Cressler, USGS

•  Ventral feet

•  Inner thighs

•  Ventral Abdomen

Larvae: Swab Oral Cavity 5 times

Adults: if needed, lightly rinse with sterile water to remove any dirt/debris

Store:

1.  Dry swab (refrigerate or freeze)

2.  70% EtOH if you cannot dry the swab or keep it cool

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Swabbing Salamanders Bd and Bsal Surveillance

Ventral surfaces (all feet, belly, tail); 5 times each, often they will grab the swab and you can twirl it while they hold onto it.

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Photo courtesy Dale McGinnity , Nashville zoo

What if you see a lesion?

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https://www.youtube.com/watch?v=a5CtPrGOK8c

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Sample Storage Individual tubes (if shipping, USE SCREW TOP TUBES)

LABEL!! Use marker that will not come off with ethanol/alcohol

90% EtOH or keep cool

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Clipping: station 4

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Tail Clip

Aseptic Processing Station Station 4

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Sample Storage Individual tubes

LABEL!! Use marker that will not come off with Ethanol

90% EtOH or Dry Ice

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Data Recording!!!: Station 5

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Data Recording

Aseptic Processing Station Station 5

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Release: Station 6

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Aseptic Processing Station Station 6

Releasing or Collecting Individuals

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Whole animals

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Biosecurity

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Matt Gray, Debra Miller, and Amanda Duffus Diseases, Pathogens and Parasites Task Team

Biosecurity Precautions: Disinfecting Procedures

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Wear Disposable Gloves

Gloves Rinsed with Distilled H2O Greer et al. (2009)

Latex Vinyl

Nitrile

$12/box of 100

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Disinfecting Equipment Scrape Mud and Scrub

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Disinfecting Equipment Spray Bottle or Immersion

• Bleach >4% • EtOH >70% • Virkon >1%

• Nolvasan >0.75%

Johnson et al. (2003), Bryan et al. (2009), Gold et al. (2013)

$50/ bottle

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Amphibian Biosecurity References

www.separc.org

Dodd, C. K., editor. 2009. Amphibian Ecology and Conservation: A handbook of techniques. Oxford University Press, UK.

ISBN 9780199541188

Pessier, A.P. and J.R. Mendelson (eds.). 2010.

Miller et al. (2015)

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Shipping

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Debra Miller and Matt Gray Diseases, Pathogens and Parasites Task Team

Shipping Amphibians for Diagnostic Testing

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Transporting Amphibians

Most Diagnostic Labs Prefer Fresh Specimens if Possible

Tent Design

No Direct Contact with Dry Ice or Ice

Packs

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Preserving Animals

95% EtOH 10% neutral buffered formalin

Separate Containers for Each Specimen! DO NOT USE GLASS FOR SHIPPING

50 mL

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Shipping Animals

(1)  Call the Diagnostic Lab for Specific Instructions

(2) Follow Courier Guidelines

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Shipping Specimens Triple Packaging

First Layer

Label Each Layer!

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Shipping Specimens Triple Packaging

Second Layer Do not use Biohazard Bags

(unless known to be infected with a BSL-2 agent)

Absorbent Paper Towel

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Shipping Specimens Triple Packaging

Third Layer

ThermoSafe* Polar Pack

Place Cooler in Cardboard Box

Only Use Dry Ice for Frozen Samples

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List of Contents & MSDS if Needed

• Detailed list of all contents • Description and location of die-off

• Requested services

• Contact information of the shipper ▪ General Pathological Screening ▪ Specific Pathogen Testing

MSDS Required

▪ EtOH or Formalin

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Labeling University of Tennessee (Matthew J. Gray, Ph.D.) Department of Forestry, Wildlife and Fisheries Institute of Agriculture 274 Ellington Plant Sciences Building Knoxville, TN 37996-4563 USA

Debra L. Miller, D.V.M., Ph.D. Veterinary Diagnostic Laboratory The University of Georgia

43 Brighton Road

Tifton, GA 31793-1389

Contents: Exempt Animal Specimen (Refrigerate upon Arrival)

Phone: 229-386-3340

(5 lbs) (>1 L or 33.8 oz) (<500 mL, <30 mL Container)

Dangerous Goods Excepted Quantity Dangerous Goods in

Hazardous Quantity

No statement required for

environmental samples

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Excellent Example

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Why? �  Culture for pathogen (virus isolation or fungal

culture or if looking for the causative bacteria): often is not possible from autolysed tissues because of growth/contamination of postmortem organisms.

�  PCR: DNA becomes compromised and can be harder to extract and detect with autolysis, contamination (bacterial overgrowth).

�  Histology!! Huge difference in what can be seen under the microscope.

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Tadpole liver Necropsied approximately 12 hours after death

Tadpole liver Necropsied immediately after death

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Adult salamander liver Dead for greater than a day before fixing in alcohol & shipping

Adult salamander liver Necropsied immediately after death

Adult liver Fixed in ethanol shortly after death and then shipped

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Tadpole liver Collected fresh and shipped overnight with plenty of cold packs

Tadpole liver Collected fresh and shipped overnight with too few cold packs

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Questions?