Blooming Bacteria

Testing various surfaces to see how much bacteria was on them.
Lily Mitchell
Grade 8

Hypothesis

If I swab 10 different surfaces in the school, then I believe that the chromebook from the grade 8 cart will be the dirtiest because it is used the most and cleaned the least.
 

 

Research

Bacteria are microscopic single-celled organisms that serve a purpose in all organisms. Most bacteria are useful and serve a purpose within an organism, such as bifidobacteria, which help with digestion, infection prevention, and the production of compounds such as B vitamins. Then there are harmful bacteria that can weaken the immune system with viruses and are spread through contact with an infected surface. An example of harmful bacteria would be salmonella.

Bifidobacteria                                                          Salmonella

Bacteria thrive in moist, warm, and dark environments. This means that schools are great breeding grounds for thousands of different kinds of bacteria to reproduce. Bacteria reproduce asexually by mitosis or meiosis. Mitosis is when a cell duplicates itself completely and splits into 2 identical daughter cells. Meiosis is when a cell divides itself twice to produce 4 cells containing half the original amount of genetic information. Bacteria also reproduce using binary fission. Binary fission is nearly the same as mitosis, but mitosis is used for the growth of organisms, while binary fission is for reproduction. Binary fission is also simpler because it uses prokaryotic cells, instead of mitosis, which uses eukaryotic cells. This is because the cell structure of a prokaryotic cell is simpler than that of a eukaryotic cell. Prokaryotic cells are single-celled organisms that don't have a nucleus in comparison to eukaryotic cells which do contain a nucleus. 

Prokaryotic Cell                                                         Eukaryotic Cell

   

For these cells to reproduce, they must have the right environment to do so. I am creating that environment for the bacteria with nutrient agar which provides a rich environment for bacteria to grow. Nutrient agar is a cushion of nutrients for bacteria to grow on while not being a material that mold can eat through. Nutrient agar contains moisture and nutrients that fungi absorb when they grow on it.  

Bacteria are some  of the fastest-reproducing organisms in the world. Some species of bacteria can double in 4 to 20 minutes! These bacteria can grow to visible quantities within hours. This is only some species of bacteria under the right nutrient-rich conditions. 

 

  

        

Variables

Constant Variables

Day swabbed

Temp of petri dishes

Amount of nutrient agar

Type of swab 

Temp of agar when swabbed

Agar

Manipulated Variable

Location/Item Swabbed

Responding Variable

Amount of bacteria grown

Procedure

Procedure: Set-Up

  • Fill a large pot about halfway full with water
  • Boil the water
  • Once boiled, turn off the heat
  • Dip tongs into boiling water for about 10 seconds
  • Place all Petri dishes into the hot water 
  • Let them sit in the water for about 30 seconds
  • Take them out with the sterilized tongs and transfer them to a large ziplock bag
  • Leave the bag open somewhere safe so that they can dry

Procedure: Bacteria Collection

  • Get your 10 swabs
  • Label each tube with what you plan to swab
  • Collect sample by taking your swab and gliding it over a surface
  • DO NOT TOUCH THE SWAB 
  • Place your swab into the tube and close the lid tightly
  • Repeat step five nine more times to collect all of your samples

Procedure: Agar Prep 

  • Boil water in a small pot
  • Turn off the stove
  • Mix boiling water with agar
  • Stir until dissolved
  • Pour agar into Petri dishes (equal amount in each)
  • Let the agar cool in the Petri dishes
  • Once cool and solidified, glide your sample swab over the surface of the 
  • agar on the petri dish
  • Using tape and a sharpie write where the sample is from on the lid of the petri dish
  • Repeat step seven nine more times until all Petri dishes have bacteria on them
  • Place lids on all Petri dishes and place them somewhere dark
  • Daily, record how much has grown on each petri dish
     

PICTURES OF DAILY GROWTH: 11 TOTAL PICTURES RANGING FROM DECEMBER 15TH TO JANUARY 1ST

 

Observations

  • Most samples went from 0-100 within 3 days
  • Most samples plateaued 

Analysis

In my experiment, I swabbed 10 surfaces in my school and grew mold from them on agar petri dishes. I was shocked to find that the classroom door handle of room 18 was the dirtiest because I thought they were cleaned regularly. 

I was also surprised by how many different kinds of mold the desk sample grew. I was surprised because I know that the desks get cleaned every once in a while. I guess it just goes to show how much bacteria is on our hands.

I was not, however, shocked to see how little the bathroom stall grew, because I know that our bathrooms are cleaned regularly by the custodial staff. I think this is also because the upstairs plays host to fewer classes and so the bathroom I swabbed is used less than the ones on the main floor. 
 

Conclusion

My hypothesis was incorrect because I predicted that the Chromebook would grow the most mold, and while it did end up being 100% covered, so did many other samples. 

The sample that reached 100% coverage the fastest was the room 18 door handle. I think the experiment resulted this way because the door handles are not cleaned regularly and are touched by many people every day.
 

Application

As of March 8th, 2024, 4.2% of students at R.T. Alderman school have been reported sick. My project shows areas of the school that need to be sanitized more often to get that number down in the coming years. It also shows that no matter how old the students are, handwashing protocols and sanitizing protocols must stay the same. 

My next steps would be to swab the same items in different grade-level classrooms to determine which grades need to be reminded about cleaning protocols and which classrooms are in more dire need of sanitizing.  
 

Sources Of Error

My first source of error was the time between collecting the samples and swabbing them onto the agar plates. This may have caused the growth to be less than if the swabs were taken and then immediately placed onto the plates.

My second source of error is that I only tested each surface once, so I have no way of knowing if the results I received were an anomaly or if they were completely accurate. 
 

Acknowledgement

I would like to thank my mother for helping me with my experiment and letting me use her camera for pictures. I would also like to thank my friends Ally and Sophie for Setting up and presenting my trifold in my absence.