Describe your study design and sample. 2) Will your findings be generalizable? Why or why not? 3) How does this exercise inform your interpretation of published research?.
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Using the clinical question --"Does antibacterial foam decrease bacteria count on hands as much as hand washing with soap and water.”
Question
1) Describe your study design and sample.
2) Will your findings be generalizable? Why or why not?
3) How does this exercise inform your interpretation of published research?.
Step by step
Solved in 3 steps
- In An Aseptic Technique, what are the uses of bunsen burners in the working area when performing a microbiological experiment? What equipment is used to accelerate the growth of microorganisms in the experiment? (b) What is the setting of the equipment and explain briefly the reason behind the setting?(1) why can't we say "sterile" technique (2) how are aseptic technique similar and different in the lab and Healthcare field?Be specific and explain at least 2 differences and two similarities. (3) You are asked to develop a method of transfer an unknown organism from a liquid broth to a solid petri dish.list each step that you would have to take .be specificKoch's postulates include all of the following EXCEPT O 1) Isolate the organism in pure culture. The symptoms of the test animal may vary from the symptoms seen in the O 2) patient. O 3) Inoculate a test animal with the isolated organism. 4) The organism must be isolated from the test animal in pure culture. 5) The organism isolated from the test animal must match the organism isolated from the patient.
- Explain why culture based biochemical and genetic testing would not be the ideal method to identify the microbe.Samples from an ill patient were collected by a physician for testing. A bacterial infection is suspected. Using the unknown flowcharts, a microbiologist conducted various tests to determine the identity of the unknown bacterial isolate. The resulting data is included in this presentation. Identify each test.1) based on the difference in appearance between mixed culture streak plates and broth culture plates, what would lead you to believe that you have created a pure culture when you inoculated the broths? 2) when using the loop dilution technique to produce pour plates, did all the plates produce isolated colonies? If your goal was to ultimately create pure cultures of E. coli, M. luteus, and S. morcescens, which plate or which dilution would you use, and why would you use this plate? 3) What are the advantages and disadvantages of streak plating compared with pour plating?
- What are the advantages and disadvantages of culture-dependent and culture-independent methods in microbiology, respectively.What will pose an ethical issue in these procedures are performed - mutilation, sterilization?You have learned many different techniques so far this semester that allow us to identify pathogenic microbes in the clinical setting. Why do you think rapid methods are so helpful? Why are traditional tests such as metabolic tests not always used to ID clinically important microbes?
- Using your fingers, you are asked to aseptically touch the surface of a sterile agar plate. Illustrate the possible result from this step if your fingers are (a) unwashed – touched various things prior to placing on agar surface, and (b) washed with soap or disinfected with 70% alcohol. Describe the relative abundance of microbial growth observed on the plates. List and draw the possible characteristics of an isolated bacterial colony that can be observed based on type of (a) margin, (b) elevation, (c) texture, and (d) optical property.Your instructor asks you to isolate and identify the organisms in an unknown culture. You find that the culture contains two gramnegative bacilli that produce swarming colonies. What biochemical test would you use to identify the bacilli? Justify your answer.Given the scenario, compute for the total volume of the culture media solution (milliliter or liter) and dehydrated media (grams). Scenario: The students of a Microbiology class were tasked to transfer or subculture a pure culture of Escherichia coli bacterium in five 7 mL nutrient broth and five petri dishes of nutrient agar with 20 mL capacity each. Based on the instruction bottles for nutrient broth and nutrient agar, preparation of the culture media is as follows. Nutrient broth: 8 g/liter Nutrient agar: 28 g/liter Formula: C1V1 = C2V2 *Concentration *Volume Computation: What are the answers to the following. Weight in grams of nutrient broth: _________ Distilled water in mL for nutrient broth: __________ Weight in grams of nutrient agar __________ Distilled water in mL for nutrient agar: ____________