Worm Collection and DNA Extraction

· Data Collection

Ordering worms.

An order for worms was placed with Redworm Composting1. One pound each of two kinds of worms were ordered (using personal funds): “Eisenia fetida(the red wiggler worm) and Eisenia hortensis (the European nightcrawler)”. I note that we decided to use worms ordered from a common vermicomposting source so that the genomics work here was more likely to be of relevance to real world applications than might be the case for laboratory specimens of these taxa.

Worm arrival.

The worms arrived in two separate shipments delivered directly to UC Davis. Figure 1 shows one of the boxes that was delivered. The second box was similar to this one.

Shipment of Eisenia.


Bag of worms.

 Worm pictures and videos.

There was no information inside or out as to which worms these were and thus we referred initially to the two shipments as “Worm #1” and “Worm #2.” Photographs and videos were taken of some representatives of each of Worm #1 and Worm #2 (see Figures and YouTube Videos – Worm #1 and Worm #2).

Worm #1

Worm #2

Worm storage.

A sample of individuals of “Worm #1” and “Worm #2” were removed from the canvas bags and frozen in individual 50 ml tubes for further studies.

Freezing worms.

Not wasting extra worms.

The remaining worms were used to seed personal vermicomposting activities in multiple locations in Davis, CA.

Not wasting the leftover worms.

Worm identification.

Meanwhile, the vendor was contacted to attempt to identify which shipment corresponded to which worms but the vendor did not have tracking IDs for the separate shipments which came from different sources.Based upon appearance we were confident in identifying which shipment corresponded to which worm, but to double check we sent photographs to the vendor. It was confirmed that Worm #1 was supposed to be the European Nightcrawler (Eisenia hortensis) and Worm #2 the red wiggler worm (Eisenia fetida).

DNA extraction.

DNA was extracted by Qingyi (John) Zhang in the J. Eisen lab from small pieces of a single representative of each worm (i.e., worm #1 and worm #2). DNA was stored at -80 °C and then used for DNA sequencing. An aliquot of DNA was sent to the M. Eisen lab at UC Berkeley.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

%d bloggers like this: