Difference between revisions of "Tissue Sample Collection"

Revision as of 16:50, 13 May 2019

Statement of Purpose

These links and documents contain information about best practices for tissue sample collection

Introduction

Contributors

Major editor: Breda Zimkus. Original content generated during The American Society of Ichthyologists and Herpetologists (ASIH) Annual Joint Meeting - 2016, during an iDigBio sponsored workshop by the following individuals participating in the "Field to Database" Group of the aforementioned workshop: Breda Zimkus, Cesar Aguilar, Ben Frable, Meredith Mahoney, Zachary Randall, and David Wernecke.

Preparation

• Sterilization of all dissection equipment (including surface if not using disposable for surface)
• Weighing paper, scraps of thermal paper (left over from printing tags), parafilm, paper towels may be used as disposable surface covers, though none are sterile. Can use on top of cutting board.
• Gloves
• Field catalog to write additional notes (see Preparation)

Labeling and organizing vials

• Can pre-label vials (maybe include specimen tags inside)
• Alcohol-proof pen
• Scribe
• Paper inside vials not ideal because of possible contamination

- Pencil for inside labels, or rinse ink before inserting

• Organizing vials numerically in boxes is preferable to storage in bags (in case writing comes off vials)
• Tissue samples should be taken as soon after euthanization as possible

Vial Considerations

• Internally threaded fit more/box (100 vials/box versus 81 vials/box) but if overfilled can be difficult to open
• Silicone o-ring is vapor permeable (Stuart and Hogue, 2012)

Tissue Collection Methods

• Fill two sets of tissue vials in the field, one for current project and one for institutional collection (rather than subsampling one vial later).
• Label vial to indicate tissue type, one tissue type per vial

- Epigenetic studies require same tissue type for all samples in study (i.e. all muscle)

• Cut/slice up tissue sample, small size allows permeation by preservative
• Fresh preservative may be needed if in field for extended period of time
• Don’t over-fill vial with tissue, or tissue and preservative (expansion, can interfere with vial threads, etc.)
• NGS methods need reasonable sample size to yield lots of DNA, ~500 ng (my notes say 500 ng, but is that the tissue or the desired amount of DNA? I’m guessing DNA)
• Collect sample as soon after euthanasia as possible

Tissue Preservation Methods

• Immediate freezing without preservative
• Alcohols

- 95% ethanol recommended; above 95% is technically dried (to remove the residual water which at this point can hardly be removed by distillation) with low boiling benzines so not recommended

- 1:10 tissue:ethanol seems to be a good ratio, ethanol may need to be replaced after ~24 hrs to maintain concentration.

• RNAlater

- Fill vials no more than 80% because will expand upon freezing

- Only good for 10 days? at room temperature without freezing

Allprotect

• DMSO

- DMSO solution has the advantage of being stable at room temperature, non-toxic and non-flammable. It can be carried on airplanes without a permit. However, it is photosensitive and can easily penetrate skin.

• FTA cards/swabs
• Non-iodized salt (e.g. Kosher salt)

Preserving Tissue Quality

• Minimize exposure to heat, light, moisture, and other chemicals
• Maintain cold chain if samples are frozen

Discipline Specific Information

Herpetology

• Liver
• Toe clips
• Muscle
• Tail clipping (salamanders, tadpoles)

Ichthyology

• Take tissue clips from right side (as for all destructive samples)
• Fin
• Muscle (hypaxial)
• Gill
• Whole animal (e.g. larval fish)
• Eye (especially from larvae), from right side

References

Nagy, Z.T. A hands-on overview of tissue preservation methods for molecular genetic analyses. Gamble, T. Collecting and Preserving Genetic Material for Herpetological Collection