Day 4
May 19, 2014
May 19, 2014
Today was the day we all
found out about our acceptance into the nursing program!! Lab began
with Dr. P teasing Elizabeth about her acceptance. She was afraid she
didn't get in and didn't want to get her letter from Dr. Miller but
in the end, we got her to smile with the good news.
Saturday night, Pete, Dr.
P, Mary Rose, Ben, and Adrianna went to the lab to take a culture of
Mary Rose's throat, thinking that she had strep. The plate with the
swab had incubated over two nights and we were ready to see the
results.
The plate had obvious
bacterial growth and as it turns out, Mary Rose tested positive for
strep. Pete had experimented with the strep by adding Penicillin,
cinnamon oil, and clove oil to the plate. We were able to link
lecture to lab by observing the changes in the bacteria. The cinnamon
oil killed RBC but did the best job of killing the strep. It did a
better job at this than Penicillin! Clove oil also did an incredible
job at killing the bacteria as did Penicillin. We were able to deduce
the bacteria's death due to clear rings around each of the three
substances on the plate.
Now we know! If you have
strep or a throat infection, take cinnamon and clove!!
Part 1: Thioglycolate
Practicing Ascetic
technique throughout the experiment, we took a loop and, taking a
culture of our unknown bacteria, we dipped it into a test tube filled
with thioglycolate. This substance was pink towards the top of the
tube and a yellowish color on the bottom. This was due to the
thioglycolate being oxygenated on the top and not the bottom. By
stabbing our bacteria into this tube, we will be able to see if our
bacteria is aerobic or anaerobic due to how it will grow in the
incubator overnight.
Upon receiving Dr. P's
permission, we repeated this procedure with Mary Rose's strep
culture. This too we put into the incubator.
Part 2: Stab to test
Motility
This we did by taking our
loop with our unknown bacteria and stabbing it into an agar deep
provided by Dr. Pathakamuri. We put it into the incubator and we'll
see what happens tomorrow!
Part 3: Inoculation of a
Slant Agar
Because our first slant
samples melted we had to redo the two agar slant samples we did
earlier last week. Taking our bacteria with a loop, and practicing
ascetic technique throughout, we used the snake method to spread the
bacteria on the surface of an agar slant. We'll see what happens to
the bacteria tomorrow!
Part 4: Testing the effects
of a virus on bacteria
We began this procedure by
spreading 50ml of group 1's, our group, broth onto a plate. This we
did by using a dispenser set to gather 50ml of the broth. Dr.
Pathakamuri gave each of the students a small amount of an unknown
virus and, taking a big tip, we each wrote something on the broth
with it. Our group chose to write Europe! We're excited to be going
officially now that we're in the program!
After that, we put the
plates the incubator for viral growth.
Taking a small sample of
our bacteria, we spread this on a plate. We then put the plate into
an anaerobic jar. This jar is used to test whether or not our
bacteria is anaerobic. This jar expels all traces of oxygen by the
use of hot gas packs in the air tight container. We also put an
indicator strip into the box. This will indicate the presence or lack
of oxygen. Pale white = no oxygen and blue = presence of oxygen.
Joanna Dawyot, Cassie Livingston, Mary Rose Capara
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