| Literature DB >> 35496684 |
Abstract
As educators, we strive to provide the best delivery method to improve our students' learning experience. The Covid-19 shutdown posed an incredible challenge by forcing us to redesign the way we teach with no time to prepare. Bringing the laboratory curriculum outside the lab was one of the most challenging tasks. Instructors got creative, adopting safe, at-home laboratory experiments, at-home kits bought from distributors, and relying on online simulations. Now that we are returning to face-to-face meetings, the experience gained during the lockdown can be harnessed and used as extra tools available for our students' learning experience. Online simulations gained attention during the lockdown and turned out to be of great value, with different studies reporting on improved students' experiences following the use of simulations. This paper outlines how to incorporate Labster simulations in an in-person microbiology semester for undergraduate students.Entities:
Keywords: curriculum; microbiology; online learning; pedagogy; simulations
Year: 2022 PMID: 35496684 PMCID: PMC9053027 DOI: 10.1128/jmbe.00269-21
Source DB: PubMed Journal: J Microbiol Biol Educ ISSN: 1935-7877
FIG 1Snapshot of part of the Gram staining simulation. Students control the hands of the scientist with their mouse. On the bottom left, the lab pad is available to students during the entire simulation. Students record the data on the lab pad and can access the information on the theory behind the lab through it.
FIG 2Distribution of student ratings of the online simulations. 91 students, who were distributed in 4 different online lab sections in the Fall semester 2020, responded to the following question: “from 1 to 10 (1 being the lowest), how much did you like the Labster simulation as a learning tool?” On the
Descriptive statistic of the distribution of student’s rating
| Analysis variable: scores | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| N | Mean | Std dev | Lower 95% | Upper 95% | Mode | Median | Lower quartile | Upper quartile | |||||
| 91 | 8.1868132 | 1.8373416 | 7.8041683 | 8.5694581 | 10.0000000 | 8.0000000 | 7.0000000 | 10.0000000 | |||||
The mean is 8.19 (SD = 1.84), the median was 8 (Q1 = 7 and Q3 = 10), and the mode 10.
Prelab online simulation and corresponding laboratory activities for an 11 weeks laboratory class
| Topic | Learning outcome for the laboratory simulation | Techniques applied |
|---|---|---|
|
Wear the correct clothing to work in the lab. Describe the do’s and don’ts in a laboratory Correctly use the lab safety equipment React in an emergency situation Understand how a Biosafety containment level III laboratory is constructed Understand the basic safety rules of a Biosafety containment level III laboratory Handle microorganisms in a Biosafety containment level III laboratory |
Students go through the simulation for laboratory safety and bio safety before coming to in person lab. The biosafety laboratory simulation is more advanced and can be skipped based on instructor needs. | |
|
Understand the principles of aseptic technique for the prevention of infection and contamination Create and maintain a sterile work area Use sterile equipment and consumables correctly State potential sources of microbial contamination Assess whether a sample was contaminated |
Aseptic technique Culturing | |
|
Explain how and why microbial colonization occurs Recognize potential sources of contamination. Describe the consequences of unregulated population growth. Describe the ideal environments for microbial growth and how they can be manipulated. Appreciate different levels of selective toxicity Describe modes of microorganism growth control. Define selective toxicity and what it means for host organisms. Differentiate between disinfectants, antiseptics, and antimicrobials. Explain the utility of antimicrobial agents Appreciate why different antimicrobials are effective against different infections. Select an appropriate antimicrobial to target a given microorganism. Compare the effectiveness of different antimicrobial compounds. |
Diffusion disk assays Decontamination methods Sterilization techniques | |
|
Describe the structure of the Gram-positive and Gram-negative bacteria Appreciate theoretical and technical aspects of the Gram staining procedure Know the most commonly made mistakes in Gram staining Critically interpret the results of a Gram staining expt using a light microscope |
prepn of bacterial smears The Gram stain technique Light microscopy | |
|
Explain why micropipettes are used in laboratory settings Choose the correct pipettor for a given use case Describe how to correctly use of the two stops on a micropipette plunger Explain the visualization and separation of nucleic acid molecules through gel electrophoresis Summarize how nucleic acid molecules migrate through an agarose gel Explain the principles behind size separation and direction of migration Analyze and interpret a nucleic acid gel by using a DNA ladder and controls |
Pipetting Gel electrophoresis | |
|
Distinguish vertical gene transfer from horizontal gene transfer Understand the concept of genetic variability and survivability in bacteria Describe the concept of horizontal gene transfer Identify genetic elements and cell machinery required for DNA transfer Outline the main events that occur during conjugation, transformation, and transduction Discuss the outcome and barrier of genetic transfer in bacteria |
MEGA-Plate setup Basic agar plate setup Bacteria morphology examination | |
|
Explain the function of DNA polymerase in DNA replication and synthesis Perform a PCR expt using DNA from a blood sample as the template Carry out a gel electrophoresis that separates DNA according to its size Interpret the unique signature of the human genome and the use of tandem repeated regions (TRR) in DNA profiling |
Polymerase Chain Reaction (PCR) Gel electrophoresis DNA profiling | |
|
Understand molecular cloning techniques: DNA extraction and prepn, ligation, transformation, plate streaking and antibiotic selection Understand inducible gene expression regulation Understand the use of GFP as a reporter gene Understand DNA damage and DNA repair system |
DNA extraction Transformation Colony screening Cloning | |
|
Describe the basics of CRISPR-Cas technique Design a guide RNA construct for knock-out strategies Evaluate CRISPR-Cas9 results |
Immunofluorescence CRISPR-Cas9 | |
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Discuss the fundamental need for the immune system Identify physical and chemical barriers against pathogen invasion Describe mechanisms of immune evasion by pathogens Predict the outcome of scenarios of immune deficiency Summarize the key features of innate and adaptive immune responses Describe antigen-antibody interactions Classify immune cell types by their role in responses Define immunological memory and its importance Explain the importance of lymphocyte clonal selection & deletion processes Explain the concept of diagnostic serology Identify common features and principles of serological methods Compare the applications for serological methods in biomedical research and healthcare |
Serological investigation Enzyme-linked immunoassay | |
|
Explain the principle of different ELISA techniques Apply sandwich ELISA to quantify protein samples Analyze the standard curve of ELISA expt Understand the function of reagents and equipment used in ELISA Describe the basic troubleshooting process of ELISA |
Sandwich ELISA | |
|
Understand the structure and function of antibodies Understand the formation of the antibody-antigen complex |
Blood typing |
The online simulations are assigned ahead of the in-person laboratory meeting. The length of the online simulation is listed in column one in minutes. Learning outcome of the online simulations as reported from the Labster website, is listed in column two. Column contents from https://www.labster.com/. Simulations available on the Labster website, https://www.labster.com/. In-person lab activities. Link to kit is available in Appendix 1.