Treatment FAQ

what was the control treatment in the mice and bacteria experiment?

by Zakary Goldner Published 3 years ago Updated 2 years ago
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Four nonabsorbable antibiotics (streptomycin, neomycin, bacitracin, and amphotericin B) and a germicidal dip solution (Zephiran chloride/water) were used to eliminate all the detectable bacteria from conventional AKR mice. Control mice were not decontaminated and were used as such.

In control experiments mice that were infected with encapsulated virulent Type S pneumococci (serotype I) died and SI bacteria were recovered from the dead animals. By contrast, injected heat-killed SI bacteria did not cause death and no bacteria were detected in sacrificed animals.

Full Answer

What was the result of the experiment with the dead mice?

As a result, the mice died and he found colonies of encapsulated bacteria in the dead mice and isolated them from the mice. Second, he injected the mice with dead encapsulated or smooth (S) bacteria. The mice were alive and he found no colonies from the mice.

What is the Griffith experiment in microbiology?

Griffith experiment: gene transformation in bacteria. Frederick Griffith (England) in 1928 took an experiment to vaccinate mice against pneumonia by injecting the mice with heat-killed bacteria of encapsulated strain. For this purpose, he worked with two strains of Streptococcus pneumonia.

How are antibiotic-decontaminated mice treated for spontaneous lymphatic leukemia?

When antibiotic-decontaminated and control mice developed clinical manifestations of spontaneous lymphatic leukemia, each was treated for the disease with an antitumor drug (cyclophosphamide [CP]) at weekly intervals.

What do scientists do with mice in germ-free conditions?

In one experiment, scientists raised mice in germ-free conditions so the mice lacked intestinal microbes. The mice were fed a low-fat diet rich in the complex plant polysaccharides, such as cellulose, that are often called fiber.

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Which bacteria killed the mice in Griffith's experiment?

Frederick Griffith performed an experiment where mice were killed when injected with a mixture of heat-killed S-type Streptococcus (HKS) and live R-type Streptococcus (LRS) but not with HKS or LRS separately. Mice were killed because.

What is the purpose of Griffith's experiment 3?

Research question: The original purpose of Griffith's experiment was to test whether or not the bacteria synthesized their own polysaccharide capsule. He eventually answered how non-capsulated strains of Pneumococcus bacteria became virulent by providing them with capsular material from another strain.

What was the unique in Griffith experiment?

Griffith observed that in the blood of dead mice, both R and S type of bacteria were present. He thus concluded that heat-killed smooth type bacterial caused a transformation of the living rough type bacteria. This experiment suggested that DNA and not proteins are the genetic material.

Why do you think that the mix of heat killed and rough bacteria killed the fourth mouse?

2. Why did Griffith need to show that the heat-killed bacteria didn't make the mouse die? Because the heat-killed bacteria mixed with the rough bacteria were lethal to the mouse, Griffith concluded that something from the heat-killed bacteria “transformed” the rough bacteria and made them lethal.

What is the conclusion of Griffith experiment?

Griffith concluded that the R-strain bacteria must have taken up what he called a "transforming principle" from the heat-killed S bacteria, which allowed them to "transform" into smooth-coated bacteria and become virulent.

What was the purpose of Griffith's experiment 2 in which he injected a mouse with live S cells?

In this experiment, Griffith mixed the living non-virulent bacteria with a heat inactivated virulent form. He subsequently infected mice with this mixture and much to his surprise, the mice developed pneumonia and died. Furthermore, he was able to isolate colonies of the virulent strain from these mice.

How could you treat dead smooth bacteria with these enzymes?

How would you treat dead smooth bacteria with these enzymes to determine whether DNA, RNA or proteins are the material that was passed on to the rough bacteria to make them pathogenic? You could take Proteases and mix the heat-killed smooth strain with it, breaking down all the proteins in the strain.

What were the main outcomes of the experiments performed by Griffith 1928 )?

What were the main outcomes of the experiments performed by Griffith (1928)? He found that a mixture of living rough-type and dead smooth-type bacteria killed mice. He found that living smooth-type bacteria killed mice.

What happened when the samples of bacteria were injected into the mice select all that apply?

- When live, harmless bacteria were injected, the mice did not die. - When heat-killed, disease-causing bacteria and harmless bacteria were injected together, the mice were killed.

What happened when Griffith injected the R strain bacteria into the healthy mouse?

Griffith's Experiments When Griffith injected mice with disease-causing bacteria, the mice developed pneumonia and died.

What happened when Griffith injected mice with a mixture of heat killed?

Experiment 4: Griffith mixed his heat-killed, disease-causing bacteria with live, harmless bacteria and injected the mixture into the mice. The mice developed pneumonia and died.

What happened when the mice were injected with a mix of dead S strain and live R strain?

In the critical experiment, Frederick Griffith (1928) mixed heat-killed S with live R and injected the combination into mice: the mouse died. The dead mouse's tissues were found to contain live bacteria with smooth coats like S.

What was Griffith's experiment?

Griffith experiment: gene transformation in bacteria. Frederick Griffith (England) in 1928 took an experiment to vaccinate mice against pneumonia by injecting the mice with heat-killed bacteria of encapsulated strain. For this purpose, he worked with two strains of Streptococcus pneumonia. One is virulent (pathogenic) and other is avirulent.

Who performed the transformation experiment?

In the United States three scientists Oswald T. Avery, Colin M. MacLeod and Maclyn McCarty in 1944 performed an experiment for the molecular explanation of transformation.

What did the mice eat?

The mice were fed a low-fat diet rich in the complex plant polysaccharides, such as cellulose, that are often called fiber. When the mice were 12 weeks old, the scientists transplanted the microbial community from the intestine of a single "donor" mouse into all of the germ-free mice.

What are autotrophs and heterotrophs?

Autotrophs (literally "self-feeders") require only an inorganic substance, such as carbon dioxide, as their carbon source; heterotrophs (literally "other-feeders") require at least one organic nutrient as their carbon source. Nice work! You just studied 21 terms! Now up your study game with Learn mode.

Why are Azotobacter pink?

They are shaped like rods. Azotobacter is a genus of rod-shaped bacteria (bacilli). After Gram staining, bacteria in this genus appear pink due to the thin peptidoglycan layer in their cell wall.

Why do Gram negative bacteria appear red?

Gram-negative bacteria appear red or pink because the alcohol rinse washes away the crystal violet dye.

Why do Gram positive bacteria turn purple?

Gram-positive bacteria appear purple because the alcohol rinse does not wash away the crystal violet dye. Click again to see term 👆. Tap again to see term 👆. Label the diagram below to show the relationship between nutritional modes of bacteria. Drag the labels to their appropriate locations on the diagram.

What is the carbon source of an autotroph?

Autotrophs (literally "self-feeders") require only an inorganic substance, such as carbon dioxide, as their carbon source; heterotrophs (literally "other-feeders") require at least one organic nutrient as their carbon source.

Do obese mice have more energy?

The scientists hypothesized that the microbial community of obese mice is more efficient at extracting energy from food, thu s providing more calories to the host, and that it promotes more fat deposition than does the microbial community of lean mice.

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