Collection, Observation, and Analysis of Microorganisms in the human environment Introduction The necessity and value of collecting, identifying, and analyzing the various microbes regularly encountered in the daily human environment becomes quite apparent when one gains even a very basic knowledge of how diseases are acquired and spread. The purpose of this lab was to collect and observe microbes from environmental and human body samples by culturing them on the appropriate media using aseptic transfer techniques.Materials • Distilled water • Test tube • 6 Unopened packages of 1 sterile cotton swab • 2 sterile nutrient agar Petri dishes • 1 sterile blood agar Petri dish • Incubator • Refrigerator • Bunsen burner • Gas connection • Plastic tubing • Inoculating loop • 12 sterile glass slides • Wax pencil • Igniter • Crystal violet dye • Gram’s iodine • Ethyl alcohol • Safranin dye • Paper towels • Wire rack • Sink • Brightfield compound microscope • Lens paper • Immersion oil • Pen and paper Methods I. Collecting the environmental specimens: 1. Place some distilled water into the test tube. 2.Open one package of sterile cotton swabs by peeling apart the packaging at the top. Do not peel the package apart completely, just at the top.
3. Take out the cotton swab, dip it into the test tube of distilled water, and place it back into the original package with the cotton tip facing down. 4. Repeat the previous two steps for three more unopened packages of sterile cotton swabs. 5. Choose four locations from which environmental samples can be taken. (For example, use the bottom of a shoe, a light switch, or a sink handle). Write these locations down on a piece of paper and number them E1-E4 for later reference.
For example, E1 is the sink handle). 6. At each location, take out one of the wetted sterile cotton swabs and rub it against a small area of the surface being sampled.
Make sure to turn the swab as well to ensure that the sample is on all sides of the cotton swab. After swabbing, place each swab back into its original package, with the cotton tip facing downwards. Keep track of which swabs were used for which samples. Label them if necessary. II.
Collecting the throat and nose samples: 1. Place some distilled water into the test tube. 2.Open one package of sterile cotton swabs by peeling apart the packaging at the top. Do not peel the package apart completely, just at the top.
3. Take out the cotton swab, dip it into the test tube of distilled water, and place it back into the original package with the cotton tip facing down. 4. Repeat the previous two steps for one more unopened package with a sterile cotton swab. 5. Take one of the wetted sterile cotton swabs and rub it against the inside of one’s nose. Make sure to turn the swab as well to ensure that the sample is on all sides of the cotton swab.After swabbing, place the swab back into its original package, with the cotton tip facing downwards.
6. Repeat the previous step, but instead take a sample from the back of the throat. III. Aseptic transfer of the environmental specimens: 1. Take the two nutrient agar Petri dishes and turn them bottom side up. Then, using a wax pencil, draw a line down the middle of each dish. Label each of these four sections E1, E2, E3, E4 so that the origin of each sample is known for later.
2. Take out one cotton swab that was used on an environmental surface out of its packaging. Keep this swab in one hand. . With the other hand, open the lid of one sterile nutrient agar Petri dish slightly at an angle. 4. Take the cotton swab in the other hand and gently swab it against the appropriately labeled half of the nutrient agar’s surface evenly.
5. Close the lid of the nutrient agar Petri dish and place the cotton swab back into its packaging. Dispose of the cotton swab and package in the appropriate container. 6. Repeat the previous four steps for the other three cotton swabs used on the environmental surfaces. Make sure to use the appropriate swab for the appropriately labeled section of the Petri dish. . Place the two inoculated nutrient agar plates into the incubator in an inverted position, or with the lid facing downwards, to prevent condensation on the agar’s surface.
IV. Aseptic transfer of the nose and throat specimens: 1. Take the one blood agar Petri dish and turn it bottom side up. Then, using a wax pencil, draw a line down the middle of the dish. Label each of these two sections N and T so that the origin of each sample is known for later.
2. Take out the cotton swab that was used on the inside of the nose out of its packaging. Keep this swab in one hand. 3.With the other hand, open the lid of the sterile blood agar Petri dish slightly at an angle. 4. Take the cotton swab in the other hand and gently swab it against the appropriate half 5. Close the lid of the blood agar Petri dish and place the cotton swab back into its packaging.
Dispose of the cotton swab and package in the appropriate container. 6. Repeat the previous four steps for the other cotton swab used on the back of the throat. 7.Place the inoculated blood agar plate into the incubator in an inverted position, or with the lid facing downwards to prevent condensation on the agar’s surface. V. Making heat fixed bacterial smears of all the samples: 1.
Take the twelve sterile glass slides and label their corners using the wax pencil. Since a sample from two different colonies is going to be taken from each of the six tested locations, label them accordingly: E1C1 (environmental sample number one, colony number one), E1C2, E2C1, E2C2, E3C1, E3C2, E4C1, E4C2, NC1, NC2, TC1, TC2. 2. Place a drop of distilled water on the center of each slide. bbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbbb bbbbbbbbbbb incubator. Observe the intensity of growth and the number of colonies formed from each sample. Write these results on a piece of paper. 4.
Take out the Bunsen burner and connect it to the available gas source using the plastic tubing. Turn the gas on. 5. Use the igniter to ignite the Bunsen burner flame.
6. With one hand, take the inoculating loop and pass it through the flame until it is red- 7.With the other hand, open one of the Petri dishes slightly. 8. Take the sterilized inoculating loop and lightly touch it to one of the colonies on the agar’s surface.
9. Close the Petri dish lid and take the inoculating loop and gently smear it in the drop of water on the appropriately labeled slide so that it coincides with the sample you took from. Smear from side to side to create a thin film. Let this slide air-dry. 10. Pass the inoculating loop through the flame again until it is red-hot.
11. Repeat the previous eight steps for the rest of the samples and slides.Remember to take two samples from each of the six locations, each from a different colony. Also remember to place the colony samples on the appropriately labeled slide. 12. Once the twelve slides have dried, pass each one through the Bunsen burner flame once or twice. Do not hold the slide in the flame, as this will cause the sample on the slide to burn. 13.
If the nutrient agar and blood agar Petri dishes are going to be used again, place them in the refrigerator, if not, place them in the appropriate container. VI. Gram staining all of the samples: 1.Separate the twelve heat fixed slides into three groups of four. This makes it easier to apply the dyes to the slides for the appropriate amount of time. 2. Take one of the three groups of heat fixed slides and place them on the wire rack on top of the sink.
3. Take the crystal violet dye and apply it to the slides on the rack generously, making sure to cover the entire slide. Leave the crystal violet dye on the slides for thirty seconds. 4.
Rinse the crystal violet dye off of the slides with distilled water, and place the slides back onto the wire rack. 5.Place the Gram’s iodine generously onto only one of the slides and let it sit for ten seconds. Rinse the slide immediately with distilled water and return it to the wire rack. Repeat this step for the other three slides, making sure to do each slide individually to ensure that the Gram’s iodine does not stay on the slide for more than ten seconds. 6. Take one slide and hold it at an angle over the sink.
Take the ethyl alcohol and carefully place ten drops of it onto the slide, allowing it to slide off quickly. Immediately rinse the slide with distilled water and place it back on the wire rack.Repeat this step for the other three slides, making sure to do each slide individually to ensure that the ethyl alcohol does not stay on the slide for too long. 7.
Take the safranin dye and apply it to the slides on the rack generously, making sure to cover the entire slide. Leave the safranin dye on the slides for thirty seconds. 8. Rinse the safranin dye off of the slides with distilled water, and place the slides onto a paper towel to dry.
The excess water on the slides can be blotted off gently with another paper towel. 9. Repeat the previous seven steps for the other two groups of four slides.VII. Determining the morphology and the gram stain results of the samples: 1. Take out the brightfield compound microscope, plug it into an outlet, and turn the power switch on.
2. Use the lens paper to wipe off the objective and ocular lenses. 3. Take one of the gram stained slides and place it onto the stage of the microscope.
Use the stage slips to keep the slide in place. 4. Focus using the 10x low power objective lens by first using the coarse adjustment knob to bring the lens as close to the slide as possible. Focus by moving the coarse adjustment knob to move the lens away from the slide. 5.Use the knobs on the stage to move the slide up and down, and side to side to find a portion of the slide with a good amount of sample on it. 6.
Get the immersion oil and place a small drop of it onto the slide where the light is shining through it. 7. Switch into the 100x oil immersion objective lens and focus using only the fine adjustment knob. 8. If necessary, use the light source and the condenser to alter the illumination of the slide. 9.
Observe the color shown on the slide and determine if it is pink or purple. If it is purple, it is gram positive, if it is pink, it is gram negative. Record these results on a piece of paper. 0. Observe the shape of the cells on the slide. If they are spherical in shape, they are cocci, if they are rod-like in shape, then they are bacilli. Record these results on a piece of paper 11. Remove the slide from the stage.
12. Use the lens paper to wipe of the oil on the slide and the lenses. 13. Repeat the previous ten steps for the remaining eleven slides.
14. After viewing all of the specimens, set the microscope onto the scanning power 4x objective lens and retract the lens as far away as possible from the stage using the coarse adjustment knob. 15. Give the ocular and objective lenses a final wipe down with the lens paper.
6. Construct all of the results into a chart or graph. Results |Source of specimen |Intensity of growth |Number of different |Gram reaction of 2 colony|Microscopic Morphology of 2 | | |(1-5) |colony types |types |colony types | |Nose (N) |3 |3 |C1: gram + purple C2: |C1: cocci clusters C2: bacilli | | | | |gram + purple |clusters | |Throat (T) |3. |4 |C1: gram – pink C2: gram |C1: cocci clusters C2: cocci | | | | |- pink |chains | |Bathroom door (E1) |4. |7 |C1: gram – pink C2: gram |C1: bacilli chains C2: cocci | | | | |+ purple |cluster | |Shoe bottom (E2) |5 |14 |C1: gram – pink C2: gram |C1: cocci clusters C2: bacilli | | | | |- pink |chains | |Bathroom sink handle |2 |5 |C1: gram + purple C2: |C1: small bacilli C2: cocci | |(E3) | | |gram + purple |clusters | |Light switch (E4) |1 |2 |C1: gram – pink C2: gram |C1: cocci clusters C2: large | | | | |- pink |bacilli | Discussion During the collection of the samples, a series of expectations were developed regarding the relative amount, type and characteristics of the microbes based on the locations they were collected.In terms of colony growth, it was originally expected that the most intense growth would be from environment two since the shoe bottom has probably come into contact with the most substances, however the results illustrated that this wa not the case.
What was surprising however, was the sparse growth of colonies from environment four. The low number of colonies formed was not as surprising as how small the colonies were in size. One reason to explain this could be that the sampled light switch was in an inconspicuous area, where it experienced minimal contact with human hands. The similar growth of colonies among the nose and throat samples could indicate that these areas may have shared some of the same microbes or bacteria. This could be an indication of why nose infections and throat infections often occur together.However, their differing gram test results could suggest that the throat may have had more pathogenic bacteria than the nose.
This is because gram-negative bacteria have a higher measure of virulence or pathogenicity due to the lipopolysaccharide layer present in their cell walls. The samples collected at the bathroom door were consistent with the original expectations in that gram negative rods (bacilli) were found, which is consistent with E-Coli, a microbe found in the human digestive tract always found in great quantities in feces. However, additional tests would need to be performed to confirm beyond a doubt that these were in-fact E-Coli.The fact that these gram negative rods were found on the door knob, so very far from the toilet bowl, where these microbes would likely first have been deposited, provides a good indication of how easily microbes can be spread from one area to another.
This also provides a good indication of the necessity of hand-washing after using the bathroom, and especially before eating anything, since the microbes were found on the door handle and would likely be picked up upon exiting, after hand-washing was complete. This can even be taken a step further in pointing out the importance of doctors scrubbing up before performing any surgical procedure as a way of minimizing patient exposure to any potentially harmful microbes the surgical team may have come in contact with.Not only for doctors and health care workers is it important to have an awareness of the pervasive, ever-present nature of potentially pathogenic (disease-causing) microbes in the human environment and the ease at which they can be distributed and spread from one person or location to another, but also for anyone who handles or prepares food for others, and basically anyone who is concerned with how best maintain good health and minimize exposure to anything that may compromise that good health.
Conclusion The results seen in this experiment proved to be fairly consistent with what was expected. The environmental samples showed different types of microorganisms on their culture media in the form of numerous colonies.Upon observation, the relatively large number of varying cell morphologies and sizes for the limited sample population provided an indication of the vast numbers and types of microorganisms that are ever-present and regularly encountered in the human environment. The process of collecting and transferring the microbes from the environment to the culture media for observation and rate in which they multiplied once in the incubator illustrated how easy it can be for certain diseases to spread, and how fast they can develop once acquired if left unchecked. This is all further confirmation of how essential it is to take the necessary precautions to keep the chance of exposure to an absolute minimum.