Ben's lecture Flashcards

1
Q

Were there any examples of leaks?

A

Anthrax leak in Russia, 1979
Foot and Mouth at the Pirbright in 2007
Smallpox keeps showing up

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2
Q

Rapidly draw the hierarchy at the UZH for biosafety

A

Researcher then PI, Biosafety Officer, and Institutional Biosafety Committee

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3
Q

Which offices rule over the UZH’s biosafety?

A
The AWEL, then
the BAFU (FOEN, ECOGEN)
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4
Q

What’s the AWEL purpose?

A

Overseeing the lab infrastructure, and doing regular inspections.

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5
Q

What’s the BAFU’s purpose?

A

Federal office, overseeing everything biotechnology wise.

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6
Q

FOEN is part of BAFU. What exactly does it do?

A

Does everything related to laws and guidelines, then advises the cantons on how to enforce it on a federal level. They’re also the ones ruling the recommendations for safety regarding the GMOs.

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7
Q

Before commencing a new activity, what are the steps to do?

A

First, carry a risk assesment.
Then, apply the safety measures to protect humans, animals and environment.
Record all the relevant information.
Determine if this activity must be registered with the relevant authorities.

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8
Q

What parameters go into a risk assesment?

A

What the damage to people and environment would do
How easily transmissible the disease is
If any genetic material (modified) can be passed on and spilled through the environment
Assess the probability of the damage.

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9
Q

Risk assessment requires a bit of a classification… What is it?

A

You assign the organism to a group.

You assign the activity to a class.

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10
Q

Sometimes, pathogen classifications vary between countries. Why ?

A

Well, regarding climate and occurrence of the pathogens in the environment. It’s a bit moronic to put a pathogen in class 4 when you are more likely to catch it outside the lab than inside.

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11
Q

Why are certain cell lines classified in higher groups than group 1?

A

Well, primary cell lines can contain some weird stuff that is not necessarily evident. Also, some cells have some viral sequences like SV40 promoters etc… Therefore group 2. Other cell lines, like our dear MT4 cells, are virus producing cells. So.. Cat 3.

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12
Q

Groups are not always clear cut. There’s the group 3**. What does it mean?

A

It means it has a quite limited risk of infection for employees. For example, HIV: it’s not aerosol, if you’re good enough at not stabbing yourself regularly, it’s hard to infect yourself. Also, the availability of a vaccine or a treatment can influence that.

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13
Q

What are the main differences between BSLII and III?

A
The lab must be isolated.
The room must be sealable.
A specific ventilation system is in place (pressurize, HEPA filters, and controlled ventilation).
The lab has an anteroom, with a shower.
The lab has a specific sewage system.
The lab has an autoclave.
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14
Q

What are the key differences between BSL3 and 4?

A

The airlock is the main one, with a shower.
The hoods can be class 3, or class 2 with the sealed respiratory equipment.
There is also need for monitoring equipment to be sure you’re not half dead on the ground for a few days.

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15
Q

What must you think about when you’re starting to work on a pathogen to assess its risk?

A

First of all, how pathogenic is it (specific dose to get sick)?
Then, evaluate the possible routes of transmission. How is it transmitted (aerosol?), is it stable in the environment, can it be transmitted by vectors present in the region, can it infect animals etc.
Also, have you modified it so it’s even more of a pain to work with?
Finally, is there availability of any treatments for the disease locally?

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16
Q

You’re working with a GMO pathogen. What do you have to think about?

A

First of all, did you just put in something novel (aka a nasty gene like oncogenes, toxins, hormones etc)?
Is the modification relevant to the pathogenicity of the virus? For example, did you attenuate the disease so much you can consider another group for the GMO-
Tropism.
Possibility of causing a cancer by integrating its genome where it doesn’t belong in your cells?

17
Q

Give me all the PPE you know of. And yes, gloves and lab coat no shit

A

Footwear - has to be closed toe to avoid getting foot flu
Goggles, protecting from impact and splashes.
Faceshields, the level up.
Respirators. Mostly used if you are working in the US and don’t know how to build a closed hood.

18
Q

When getting gloves for your work, what are the parameters you must be aware of?

A
  • How it’s impacted by certain chemicals you might use (it sucks if you get becomes more permeable, or the chemical goes through easily)
  • How thick is it? e.g. not ideal to have regular gloves if dealing with a rabid tiger
  • Suitability rating (wtf?)
19
Q

What are the labcoat requirements?

A

Must be autoclavable, and fit well.

20
Q

Give the requirements for Biosafety II lab building.

A
  • Lockable doors
  • Windows always closed during operation
  • Floors must be easily washable and not affected by all the chemicals
  • Autoclave within reach
  • BSCII hoods
  • Centrifuges with airtight buckets (lol we don’t have that)
  • Biohazard sign on the entrance
21
Q

Main differences between the BSC I, II and III ?

A
  • BSC I just protects you from what’s in the hood. The air goes up and through a HEPA filter.
  • BSC II protects also the product from your filthy breathing -> laminar flow. The air gets sucked down, goes through a HEPA filter, then gets pumped back in and out of the hood through more HEPA filters.
  • BSC III is sealed, so the airflow is pretty easy. Goes in from the top through a HEPA filter, then goes out through a double HEPA filter.
22
Q

What’s the difference between disinfection and sterilization?

A

Disinfection eleminates a bunch of the pathogenic microorganisms on objets.
Sterilisation destroys all microbial life, using chemical or physical methods.

23
Q

What’s a low level disinfectant?

A

Phenolics, aka soapy soap soaps

24
Q

What’s intermediate level disinfectants?

A

Alcohols (not 100% ethanol that’s just not working)

Hypochlorites (bleach)

25
Q

What’s high level disinfectants?

A

Hydrogen Peroxide at 35% to gas stuff at low temps. Not horrible for the environment.
Formaldehyde fuming or glutaraldehyde. Potent.

26
Q

Give 3 examples of phyiscal disinfectants.

A

Steam under pressure aka autoclaving.
Dry Heat
Ionizing radiation.

27
Q

Why is autoclaving so efficient? what are the essential conditions for it to work?

A

The bags must have an opening to have the steam come in. There must be an air pump to remove the air first, then an external steam generator to fill in all the stuff to autoclave.

28
Q

Why is steam so much better than dry air?

A

Steam carries more heat energy. Also, dry air will just set everything on fire and that’s not ideal.