Transient flora on hands as a vehicle of transmission to food for Staphylococcus aureus

1. Transient flora on hands as a vehicle of transmission to food for Staphylococcus aureus Elissa Redmiles and Lucy Erickson

2. Background History of food bourn illness Hypothesis

3. History of food borne illness Since the beginning of human history, food borne illness has been an issue Various food preservation methods have been employed over the years to slow down food spoilage by microbes and natural aging processes, some common prevention methods include: drying freezing freeze-drying salting curing canning pickling irradiation treating with sugar treating with inert gases (such as carbon dioxide) S

4. Transient flora found on human skin and hands plays an important role in food contamination When those involved in food preparation fail to observe hygienic methods

5. It is hypothesized that Staphylococcus aureus, a microbe occurring naturally on the hands of some people, would be found at various locations throughout the Microbiology building It was also hypothesized that many different types of bacteria would be isolated from the various locations tested

6. Hypothesis (cont.) The isolation of bacteria from the inside handle of the bathroom door particularly holds implications for food hygiene, as ideally it should only be touched by pristinely washed hands.

7. Protocol Design and Detailed Methods Overall approach and rationale for approach Detailed methods and rationale behind methods Expected results

8. Overall approach and rationale for approach There were 2 objectives for this experiment: To determine the number of different types of bacteria that live on each of 7 objects tested To identify on which objects Staphylococcus aureus is present

9. Overall approach and rationale for approach (cont.) To achieve these objectives a growth medium was required Both agar and broth were considered Agar was determined to be a more suitable growth medium since: It allows direct observation of different types of bacterial colonies It prohibits the number of bacteria on an object from being determined Broth was determined to be a less suitable growth medium because: It allows the number of bacteria on an object to be determined It does not allow direct observation of different types of bacterial colonies

10. To achieve the first objective a sampling technique was required Both saline wetted and dry sterile cotton swabs were considered: Wet cotton swabs were determined to be most effective for obtaining the largest sample of microorganisms Microorganisms adhere more readily to wet surfaces A swab and streak method was used to inoculate the agar plates Overall approach and rationale for approach (cont.)

11. To achieve the second objective a method of differentiating Staphylococcus aureus was needed: Differential mediums and assays were used: The gram stain was used to differentiate gram negative organisms from gram positive organisms The catalase assay was used to differentiate Staphylococci (positive result) from Streptococci (negative result) Blood Agar was used to differentiate S. aureus (positive result) from S. epidermis (negative result) Mannitol Salt Agar was used to differentiate S. aureus (positive result) from S. epidermis (negative result) The CoAgulase assay was used to differentiate S. aureus (positive result) from S. epidermis (negative result) Overall approach and rationale for approach (cont.)

12. Day 1 Made Mannitol Salt Agar Autoclaved and cooled medium Day 2 Poured Mannitol Salt Agar plates Day 3 Obtained Trypticase Soy Agar (TSA) plates Obtained a package of sterile cotton swabs, and a tube of diluted saline Swabbed 7 objects: Bathroom sink faucet (1st floor) Bathroom (interior) doorknob (1st floor) Micro bench sink faucet (Room x) Front door handle�Micro building Handicapped door button�Micro building Computer mouse in lab Stair rail (1st floor) Detailed Methods

13. Day 3 (cont.) Swabbing method used: Dipped tip of sterile swab into saline Swabbed 1 of 7 objects Struck inoculated swab on sterile agar plate with zigzag motion A new swab was used for each plate 4 plates (2 TSA and 2 Mannitol Salt Agar) were used for each object Discarded the swab Incubated all plates at 37�C for 48 hours Detailed Methods (cont.)

14. Day 4 Observed growth of different colony types on TSA plates Observed growth of colonies on Mannitol Salt Agar plates Observed fermentation Photographed certain colonized plates Counted and recorded different types of colonies Selected different types of colonies from each Mannitol Salt Agar plate Struck the selected colonies on (new) Mannitol Salt Agar plates, on (new) TSA plates, and on (new) Blood Agar plates Incubated all plates at 37�C for 24 hours Detailed Methods (cont.)

15. Day 5 Observed Mannitol Salt Agar plates Observed fermentation Observed TSA plates Observed Blood Agar plates Observed hemolysis Performed catalase assay on pure colonies isolated from Mannitol Salt Agar plates Performed gram stain on pure colonies isolated from Mannitol Salt Agar plates Performed CoAgulase assay on certain pure colonies isolated from Mannitol Salt Agar plates Bactistaph latex 150 test Photographed relevant results Day 6 Observed results from CoAgulase assay Detailed Methods (cont.)

16. Day 3 Saline was used: To maintain highest degree of sterility Since bacteria adhere more readily to wet surfaces than to dry surfaces In a diluted form so growth of non-salt tolerant organisms was uninhibited A new swab was used for each plate to reduce the risk of contamination by organisms not found on objects of interest TSA plates were used: As a control To determine the different types of organisms on objects of interest Detailed Rationale Behind Methods

17. Detailed Rationale (cont.) Day 3 (cont.) Mannitol Salt Agar plates were used: To isolate Staphylococcus aureus from objects of interest Staphylococcus aureus is a salt tolerant organism that grows on Mannitol Salt Agar while other non-salt tolerant organisms will not grow All plates were incubated at 37�C for 48 hours: 37�C is in the optimal growth temperature range for organisms that could be found on objects of interest 48 hours is in the optimal growth time range for organisms that could be found on objects of interest 4 plates (2 TSA and 2 Mannitol Salt Agar) were used: To safeguard from error If an error occurred with one �set� (1 TSA and 1 Mannitol Salt Agar plate) results could be obtained from another �set� (theoretically void of error)

18. Detailed Rationale (cont.) Day 4 Different colonies from each TSA plate were struck on (new) TSA plates to confirm that colonies selected were pure and different from other colonies on the plate Struck colonies from Mannitol Salt Agar on (new) Mannitol Salt Agar plates to isolate pure colonies for further tests and to confirm that colonies isolated were Staphylococcus aureus Staphylococcus aureus ferments Mannitol producing a yellow zone surrounding colony

19. Detailed Rationale (cont.) Day 4 (cont.) Struck colonies from Mannitol Salt Agar on (new) TSA plates as a control Isolated colonies were struck on Blood Agar to confirm that isolated colonies were Staphylococcus aureus Staphylococcus aureus has ?-hemolysis on Blood Agar

20. Detailed Rationale (cont.) Day 5 Catalase test was performed to: Confirm that cultures from Mannitol Salt Agar plates were Staphylococci (positive) not Streptococci (negative) Indicating that cultures were Staphylococcus aureus Gram stain was performed to: Confirm that cultures from Mannitol Salt Agar plates were gram positive not gram negative Indicating that cultures were Staphylococcus aureus Confirm that bacteria colonized on Mannitol Salt Agar plates formed clusters not chains Indicating that cultures were Staphylococcus aureus

21. Detailed Rationale (cont.) Day 5 (cont.) Bacti Staph Latex 150 test was performed to: Confirm that isolated colonies tested positive not negative for agglutination Indicating that the cultures were Staphylococcus aureus CoAgulase assay was performed to: Confirm that isolated colonies were CoAgulase positive not CoAgulase negative Indicating that the cultures were Staphylococcus aureus

22. Expected Results It was expected that: Numerous types of microorganisms would live on the tested objects Staphylococcus aureus is found on some human hands and would therefore be present on some of the tested objects

23. Results Findings Summary of Findings Relationship of findings to expectations

24. TSA plate 1 was inoculated with microorganisms from the bathroom sink faucet: 7 small white colonies grew 8 large white colonies grew TSA plate 2 was inoculated with microorganisms from the bathroom sink faucet: 16 small white colonies grew 31 large white colonies grew Mannitol Salt Agar plate 1 was inoculated with microorganisms from the bathroom sink faucet: 2 small white colonies grew Mannitol Salt Agar plate 2 was inoculated with microorganisms from the bathroom sink faucet: No growth Findings

25. TSA plate 1 was inoculated with microorganisms from the computer mouse: No growth TSA plate 2 was inoculated with microorganisms from the computer mouse: 1 small white colonies grew 1 medium white colonies grew Mannitol Salt Agar plate 1 was inoculated with microorganisms from the computer mouse: 2 small white colonies grew 3 large peaked colonies grew Mannitol Salt Agar plate 2 was inoculated with microorganisms from the computer mouse: No growth Findings (cont.)

26. TSA plate 1 was inoculated with microorganisms from the stair rail: No growth TSA plate 2 was inoculated with microorganisms from the stair rail: No growth Mannitol Salt Agar plate 1 was inoculated with microorganisms from the stair rail: 1 small white colony grew 1 large colony with yellow zone grew Mannitol Salt Agar plate 2 was inoculated with microorganisms from the stair rail: No growth Findings (cont.)

27. TSA plate 1 was inoculated with microorganisms from the handicapped button: 1 small yellow colony grew TSA plate 2 was inoculated with microorganisms from the handicapped button: 1 small white colony grew Mannitol Salt Agar plate 1 was inoculated with microorganisms from the handicapped button: No growth Mannitol Salt Agar plate 2 was inoculated with microorganisms from the handicapped button: No growth Findings (cont.)

28. TSA plate 1 was inoculated with microorganisms from front door knob: 33 small yellow colonies grew 1 medium white colony grew TSA plate 2 was inoculated with microorganisms from the front door knob: 1 small white colony grew Mannitol Salt Agar plate 1 was inoculated with microorganisms from the front door knob: No growth Mannitol Salt Agar plate 2 was inoculated with microorganisms from the front door knob: No growth Findings (cont.)

29. TSA plate 1 was inoculated with microorganisms from bathroom door knob: 3 small yellow colonies grew 1 small white colony grew 1 medium white colony grew TSA plate 2 was inoculated with microorganisms from the bathroom door knob: 7 small white colonies grew 9 large white colonies grew Mannitol Salt Agar plate 1 was inoculated with microorganisms from the bathroom door knob: 2 medium colonies with yellow zones grew 2 large peaked colonies grew Mannitol Salt Agar plate 2 was inoculated with microorganisms from the bathroom door knob: No growth Findings (cont.)

30. TSA plate 1 was inoculated with microorganisms from lab sink: No growth TSA plate 2 was inoculated with microorganisms from the bathroom door knob: No growth Mannitol Salt Agar plate 1 was inoculated with microorganisms from the bathroom door knob: 1 small white colony grew Mannitol Salt Agar plate 2 was inoculated with microorganisms from the bathroom door knob: No growth Findings (cont.)

31. A Mannitol Salt Agar plate was inoculated with microorganisms from the bathroom door handle: Growth and fermentation on Mannitol plate Gram positive rods Snapping replication was observed Catalase positive A Mannitol Salt Agar plate was inoculated with microorganisms from the bathroom sink: Growth and fermentation on Mannitol plate Gram positive cocci organized in grape like clusters Catalase positive Findings (cont.)

32. A Mannitol Salt Agar plate was inoculated with microorganisms from the stair rail: Growth and fermentation on Mannitol plate Gram positive rods Snapping replication was observed Catalase negative A Mannitol Salt Agar plate was inoculated with microorganisms from the computer mouse: Growth and fermentation on Mannitol plate Gram positive rods Snapping replication was observed Catalase positive Findings (cont.)

33. A Blood Agar plate was inoculated with microorganisms from the bathroom door handle: Growth on Blood Agar �-hemolysis A Blood Agar plate was inoculated with microorganisms from the bathroom sink: Growth on Blood Agar � -hemolysis A Blood Agar plate was inoculated with microorganisms from the stair rail: Growth on Blood Agar �-hemolysis A Blood Agar plate was inoculated with microorganisms from the computer mouse: Growth on Blood Agar a-hemolysis Findings (cont.)

34. Microorganisms isolated from the objects exhibited a variety of phenotypes when grown on TSA plates: Small white bacterial colonies Small yellow bacterial colonies Medium white bacterial colonies Large white bacterial colonies The phenotypes above indicate that a very diverse bacterial population is present on the tested objects This data supports the first hypothesis that numerous types of microorganisms would live on tested objects Summary of Findings

35. Microorganisms isolated from the: Stair rail Computer mouse Bathroom door handle Are suspected to be Cornyebacteria since: They undergo snapping replication Form �Chinese letters� Are gram positive rods This was not hypothesized Summary of Findings (cont.)

36. Microorganisms isolated from the bathroom sink are suspected to be Staphylococcus aureus The samples are strongly suspected to be Staphylococcus aureus since: They are gram positive cocci seen in grape-like clusters Are catalase and CoAgulase positive Have �-hemolysis Ferment Mannitol These phenotypes are identical to those exhibited by Staphylococcus aureus This supports the second hypothesis: Staphylococcus aureus is found on human hands and would therefore be present on some of the tested objects Summary of Findings (cont.)

37. Discussion Description of Staphylococcus aureus Why Staphylococcus aureus was expected to be found Incidence of disease Virulence of Staphylococcus aureus Comments on protocol Comments on results Comments on overall significance of project

38. Description of Staphylococcus aureus

39. Habitat Air Dust Sewage Environmental surfaces 50% of humans (higher in health professionals) Foods Poultry and egg products Egg, tuna, potato, and chicken salads Milk and dairy products Description of Staphylococcus aureus (cont.)

40. Expected to find Staphylococcus aureus various surfaces throughout the microbiology building where the transient flora from many peoples� hands has been transferred. One of the places swabbed was the inside bathroom door handle, where hopefully only people with freshly washed hands are touching. Unfortunately, this is not always the case, and a diverse population of bacteria were isolated from the door handle. Someone who fails to wash his or her hands upon exiting the restroom is unlikely to remember to wash them before eating or preparing food for another person. Thus, if S. aureus were found on the locations tested it could hold strong ramifications for general human cleanliness, and subsequently, health. Why Staphylococcus aureus was expected to be found

41. Staphylococcus aureus is a component of the normal flora for 50% of all people Carriers of Staphylococcus aureus transfer the bacteria to every touched object Regardless of hand washing In proper growth conditions the bacteria will propagate on objects such as those tested As Staphylococcus aureus contaminated objects are used, bacteria are transferred to a users transient flora Staphylococcus aureus was isolated on tested objects Thus, hand washing does not preclude the transfer of Staphylococcus aureus to food Why finding Staphylococcus aureus was probable

42. The incidence of illness is difficult to pinpoint due to a number of reasons Poor response from victims during interviews Misdiagnosis (symptoms are very similar to those of Bacillus cereus toxin) Inadequate collection of lab samples Improper lab examination Incidence of disease

43. Causes staphyloenterotoxicosis (food poisoning) Operates by toxin, not colonization ID50 � 1.0 microgram Onset of illness is rapid and varies based on: Amount of food ingested Amount of toxin present in food Individual susceptibility General health of victim Virulence of Staphylococcus aureus

44. Symptoms: Nausea Vomiting Abdominal cramping Headache Changes in pressure and blood rates Average recovery time for mild case: 2-3 days Virulence of Staphylococcus aureus (cont.)

45. Treatment Rest Fluids Medicines to calm stomach Hospitalization/Intravenous therapy for more severe cases (usually elderly or infants) Virulence of Staphylococcus aureus (cont.)

46. Prevention Wash hands and under nails vigorously and often Do not prepare food with an eye or nose infection Do not serve food to others with open wounds Keep food preparation areas sanitary Store cooked food in wide, shallow containers and refrigerate Do not leave food out for long periods of time Keep hot foods hot (above 140 degrees F) Keep cold foods cold (40 degrees F or lower) Virulence of Staphylococcus aureus (cont.)

47. Comments on Protocol Method of multiple plate inoculation was successful By using 4 plates for each object tested it allowed for confirmation of results Saline wetted swab and streak inoculation method was successful: Isolated colony growth occurred Testing and differential media: Catalase CoAgulase Mannitol Blood

48. Comments on Results Comments on Results Found numerous colonies resembling Corynebacteria, a Gram-Positive rod generally found in soil Methylene blue staining did not reveal metachromatic granules, however not all species exhibit this trait This finding is consistent with concept of bacteria found on unwashed hands Unable to identify specific strain of Corynebacteria isolated, since many of the organisms can not be typed easily. Although there have been significant advances in PCR technology, this technology was not available. Isolate from bathroom sink faucet is indicated by tests to be Staphylococcus aureus

49. Comments on overall significance of project This project aims to raise public awareness that pathogenic microorganisms are present on numerous objects touched prior to and after hand washing

50. References Boyce, J., Pittet, D. (2002). �Guideline for Hand Hygiene in Health-Care Settings� 1 April 2006. Morbidity and Mortality Weekly Report, 51-RR16. 1-44 <http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5116a1.htm> CDC. Outbreak of community-associated methicillin-resistant Staphylococcus aureus skin infections---Los Angeles County, California, 2002--2003. Morbidity and Mortality Weekly Report 2006;52:88. <http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5512a1.htm> U.S. Food and Drug Administration. �Staphylococcus aureus.� 1992. Food borne Pathogenic Microorganisms and Natural Toxins Handbook. <http://www.cfsan.fda.gov/~mow/chap3.html>

51. References Rollins, David M. "Corynebacterium Summary." BSCI 424 � Pathogenic Microbiology. Aug. 2000. Dept. of Cell Bio. & Molecular Genetics, UMD. 2 May 2006 <http://www.life.umd.edu/classroom/bsci424/PathogenDescriptions/Corynebacterium.htm>. Madigan, Michael T., and John M. Martinko. Brock Biology of Microorganisms. 11th ed. London: Pearson Prentice Hall, 2006. 386-387. Sneath, Peter H., James T. Staley, and Stanley T. Williams, eds. Bergey's Manual of Systematic Bacteriology. Vol. 2. Baltimore: William and Wilkins, 1986. 1266-1280.