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Printable Handouts
Navigable Slide Index
- Introduction
- The short version
- The researcher’s needs
- Part one: Microbial quality
- Microbial quality: example
- Microbial quality: specifics
- Rederivation
- Embryo transfer
- Barrier systems
- Bioexclusion
- Traditional barrier
- BioBubble: clean rooms
- History of microisolation (1)
- History of microisolation (2)
- Microisolation
- Germ-free mice: cage-autonomous method
- Isolators
- Isolators: different materials and designs
- Isolators: larger facilities
- Monitoring microbial quality
- Part two: Genetic quality
- Genetic quality
- Genetic quality (Definitions)
- Breeding management
- Breeding management: Outbred Lines
- Breeding management: Inbreeding
- Documentation
- Breeding management: tracking errors
- Breeding management: Backcrossing
- Monitoring genetic quality
- Phenotype assisted “genetic” monitoring
- Monitor phenotype: diet and genes
- Genetic monitoring
- Genetic monitoring: SNP's
- SNP’s (1)
- SNP’s (2)
- Part three: Tools applied in animal production
- Speed congenics
- Transgenic model generation
- Embryology
- Embryology: IVF
- Embryology: ICSI
- Revisiting embryo transfer
- Embryo transfer: non-surgical (1)
- Embryo transfer: non-surgical (2)
- Summary
- Thank you & contact details
Topics Covered
- Ensuring microbial quality (Complex processes and Bioexclusion)
- Ensuring genetic quality (Breeding management and molecular testing solutions)
- Molecular methods and embryology applied to generate & breed complex models
Talk Citation
Toft, M. (2015, February 11). Modern production of laboratory animals [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/JRTP3593.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Martin Toft has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Series: Animal Models in Biomedical Research
Transcript
Please wait while the transcript is being prepared...
0:00
Welcome to this lecture
on Modern Production Methodologies
of Laboratory Animals.
My name is Martin Fitzner Toft, and
I have over 10 years of experience
in large-scale commercial
breeding of mice and rats.
0:13
Looking at breeding
mice and rats, it should
be fairly simple, as depicted here.
So the short version is that you
bring a male and female together,
you turn off the light,
and something happens.
And all of a sudden,
you have a lot of pups.
But that's only the short version.
0:29
If we're looking at how
laboratory animals are used,
they are very complex machines
actually, or equipment.
So if we're looking at
the researchers' needs
in a more generic way,
what are they looking for?
They're looking for
correction and exact results,
reproducible results.
They would like to have high
sensitivity and specificity.
It should be a documented
technique, or methodology.
And they want predictive results.
And if you're looking at that--
and that's actually regardless
of the species used--
those are highly
influenced by microbial
and genetic quality
when using laboratory animals.
So that's what I will spend some
time on during this lecture.
Naturally, with my
background, it's highly
focused on mine and rats,
which are also the species
most commonly used for research.
But, many of the aspects
that I mentioned here
is also applicable to
other laboratory species
to varying degrees.
1:34
If we're starting with first
looking at the microbial quality,
this is just an example.
This is mouse hepatitis
virus, also known as MHV.
It's coronavirus.
And on the left, you see some
histopathological changes
as a result of MHV.
But those are only the direct
effects on the animals.
If we're looking at other areas
where mouse hepatitis virus might
interfere with research,
it is known that it
severely effects the
immune system, resulting
in a chronic immunodepression.
It also alters the hepatic
enzyme activity, which naturally,
if you're looking at
pharmical metabolomics,
you have a problem if the
enzyme activity is not normal.
You can see procoagulant
activity, anemia,
leukopenia, and thrombocytopenia.
It also increases the susceptibility
to other pathogens as a result
of the chronic immunodepression.
It even can cause a rejection
of xenograft tumors.
But it can actually
also be a disease model.
So it's very important that, when
you're looking at microbial quality
in the animals, that you
know which agents are there
and how they might
affect your research.