Morgan Q. Goulding

Morgan Q. Goulding

Oct 28, 2018

Group 6 Copy 154
4

Update: No exciting results

Snail genes targeted:

A: Nonmuscle Myosin II; C,D: MRCK; F: ROCK

Sunday 10/21

9pm: Single snails placed in 220ml well water in cups with ~1.3ml chow (mixture of heat-killed E. coli pellet + 1ml lettuce-steeped LB agar)

Tuesday 10/23

9am: Water turbid, presumably with bacterial growth. Chow has been mostly gnawed to shreds. Guesstimate 50% devoured. Snails transferred to new cups with 220ml fresh well water and chow made with pellets from duplicate cultures.

Wednesday 10/24

9am: Water getting turbid again. Discarded by decanting, replaced with 220ml fresh well water. One quarter-stick of chalk (RoseArt) placed in each cup.

Noon: One snail (C) has deposited an egg mass on the chalk! Removed from chalk, transferred to 100mm petri dish. No other egg masses seen at 4pm.

Thursday 10/25

Eggs (C) observed to have clouds of yolky material next to them. Almost every egg in the brood shows this. Explosion?

Friday 10/26

AM: Conditions look again like they did on Tuesday. Again, chow has been mostly gnawed to shreds, guesstimate 50% devoured. All dsRNA chow snails transferred to freshly washed cups, given lettuce and fresh chalk.

Saturday 10/27

Three more egg masses found, all on chalk pieces. One from D, one from F, and another from C. All transferred to 100mm petri dishes. Chalk sticks removed from all cups.

Sunday 10/28

All embryos seem to be developing normally. No new eggs seen at noon. All snails have been feeding on lettuce. Squirted into each cup ~1ml snail-conditioned water (from 1gal tank with many Biomphalaria) containing one adult Daphnia (for microbe population control).



4 comments

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  • Nicole Sharpe
    Nicole Sharpe
    Sometimes science is negative results, right?!
    Oct 31, 2018
  • Morgan Q. Goulding
    Morgan Q. GouldingResearcher
    Nicole, thanks for your comment. Science is often negative results. Negative results are good. The best kind of negative result allows us to confidently conclude: A does NOT cause B. You get this conclusion only with a carefully controlled experiment. Everything - every thing! - has to be constant, except for variable A, which is well-defined. (Of course, phenomenon B has to be well-defined too!) (To be extra sure, you need a 'positive control' where factor X should reliably cause phenomenon B. Just to make sure everything else is set up right.) If factor A has no effect on phenomenon B, then, hooray! you have falsified a hypothesis about how something works. A is not a cause of B. Move on to the next hypothesis about what causes B. Most new hypotheses are easily shown to be wrong. Keep going through the wrong ones until you find any that do not seem wrong. In the case of my first trial with the bacterial food and snails, we aren't talking about such a well-controlled experiment. Many variables are uncontrolled and/or undefined. Even observable effects are not very well defined. That's OK, because THIS IS NOT SCIENCE. This is, in fact, what we call ENGINEERING. This is the game where we are aiming at a desired practical GOAL, and not urgently caring about how everything works in between a design and its result. The earliest attempts at human flight, for example, failed to consider a lot of variables that have since been considered - and maybe more that have yet to be considered. But if a human got to fly a little bit (hopefully landing safely) it was considered a *positive* result - an approximation of the desired goal. And then the tinkering would go on to improve it. For the snail feeding RNAi project, the good news is that the first trial had some obvious flaws, and the second trial can easily fix these. Since this work is not being done in a well-equipped molecular lab, it will contain unanswered questions, such as: are the bacteria making any dsRNA, and if so, how much? Does this material survive the food-making process? How much of it gets eaten by snails? How much of the ingested material makes it into the snail's gut? How much of this gets transported to cells throughout the snail's body? This engineering project cares only about two questions. Are we producing dsRNA? and does it have an effect on the snails!
    Dec 18, 2018
  • Andy Goulding & Barbara Culp
    Andy Goulding & Barbara CulpBacker
    Helicopter parent.
    Oct 28, 2018
  • camille steen
    camille steenBacker
    Or dead snails?
    Oct 28, 2018
  • camille steen
    camille steenBacker
    What was the result we hoped.for? No eggs?
    Oct 28, 2018
  • Morgan Q. Goulding
    Morgan Q. GouldingResearcher
    The hope is to shut down the action of a gene that is essential for life. The expected results of this gene shutdown would be (a) embryos fail to develop; (b) adult snails cease to lay eggs; (c) adult snails die.
    Oct 28, 2018

About This Project

Schistosomiasis is a disease transmitted by snails, responsible for chronic illness of many millions of the world's poorest people, mainly in Africa. This project tests the efficacy of RNAi, a targeted genetic weapon, to kill the snails and thus curtail the spread of the disease. RNAi acts only on specific gene sequences, making it environmentally benign and preventing the evolution of resistance in snail populations. Importantly, this snail-killing material would be very cheap to produce.

Blast off!

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