Teaching Under the
Microscope
by Christine Dunnington
Fenton M.Sc.
Member of the New Zealand
Microbiological Society
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The most favoured practical lesson
for Microbiology must be environmental
sampling. You know the one, open
agar plates on the windowsill, swabs
taken from all sorts of places then
smeared on a plate. Incubate, and
then look at all the pretty colonies.
Yes, it allows students to 'see'
the unseen - all the microbe life
from supposedly clean surfaces and
the fuzzy bits that we breathe in.
But is it good Science and more
importantly, is it safe? Can concentrating
unknown microorganisms and exposing
the plates for inspection by inexperienced
and curious students be wise?
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I personally have known
a fourth form boy ask which colonies should
he lick so he can get a day off school!
A horrifying thought. The normal environmental
sample could concentrate pathogens and
other nuisance organisms in enormously
high numbers. For instance Serratia
marcescens has known carcinogenic
properties and has red to pink colonies
- very attractive.
Mucor, Penicillium
and Aspergillus moulds are fascinating
and they grow very easily on bread but
can affect people with asthma and allergies.
Any of which could be present on an environmental
sample.
"The Guidance Manual for
NZ Schools" (Safety and Biotechnology
Education, Ministry of Education), recommends
that you NEVER work with unknown living
materials.
Rather than doing the typical
environmental sample you purchase known
microorganisms to work with. Bakers' yeast
(Saccharomyces cerevisiae ) and
yoghurt bacteria from commercial home
yoghurt packs can be used safely. Another
alternative is to use laminated colour
photographs of the cultures grown on petri
dishes or a web
camera with the display piped
through the computer onto a monitor in
the classroom.
However, I feel like the
traditional environmental sample can still
be done safely by following these precautions:
NEVER sample from
body fluids. This includes swabs taken
from the mouth, nose or sneezing and
coughing directly onto plates.
NEVER sample from
sinks, toilets, rubbish bins and taps.
ALWAYS use sterile
swabs to take samples with. Clean or
new does NOT mean sterile.
Once you have exposed
your petri dish plates then seal them
with "parafilm" or sellotape or even
glad wrap so that the lid cannot be
removed.
ALWAYS incubate
at room temperature. Be aware that this
is not a "safe" temperature
- some pathogens can grow at
temperatures below 37o C - they just
reproduce at a slower rate.
ALWAYS adequately
destroy plates after examination. Do
not just thrown in the bin! (yes, this
happens). Either pressure cook the plates
at 15 lbs pressure for 15 minutes then
discard or bag the plates up and microwave
until the plastic melts, then discard.
Alternatively you can incinerate or
soak in 10% bleach (NOTE: household
bleach is only 3% sodium hypo-chlorite)
for 3 days. Anything else is unacceptable
and unwise.
Presenting Microbiology
to the students in an interesting way
to spark the interest of budding young
Geneticists and Microbiologists is of
course very important. But for many the
lab practicals done at High School will
be the only time they are exposed to life
under the microscope so let's keep it
as safe as possible.