Looks like no one added any tags here yet for you.
genus staphylococcus
staphylococci
occur in cocci clusters
gram positive
part of normal flora of nasal membranes, hair follicles, skin, and perineum
pathogenic
at least 40 different species
staphylo
latin for bunch of grapes
what infections is staphylococcus is involved in
involved in acne, boils, UTI, Pneumonia, Endocarditis, septicemia
staphylococci pathogenic
post surgical infections and multi resistant forms
staphylococcus aureus
most common staphylococcus
catalase positive - separates it from enterococcus and streptococcus
pathogenic strains can produce unique enzymes
exotoxins
protein A
coagulase
exotoxin
toxic shock syndrome or enterotoxin
toxin that cause food poisoning
enzyme caused by pathogenic strains in staphylococcus
protein A
enzyme caused by pathogenic strains in staphylococcus
all S. aureus strains and can differentiate species
surface protein (antigen)
coagulase on cell surface via fibrin
enzyme caused by pathogenic strains in staphylococcus
undetectable by immune system
promotes clots
some species of staphylococcus dont produce it but are pathogenic like S. epidermidis
staphyloslide test
latex beads are coated with antibodies for protein A
if positive its S. aureus
if negative its other S. species
coagulase test
coagulase is an exoenzyme that causes fibrin of blood plasma to clot
coagulase positive = S. aureus
coagulase negative = S. epidermidis
Catalase test
Catalase is an enzyme that is responsible for breaking down hydrogen peroxide (H2O2) and releasing water and oxygen.
positive = rapid formation of bubbles.
This test allows the separation of Staphylococcus species from Streptococcus and Enterococcus species.
biochemical testing and identifying bacteria
reals information necessary to help identify bacteria within a sample
metabolism
used as an additional factor to identify bacteria because many of them share colony and cell morphology. bacteria produce enzymes that play a role in metabolic processes. the enzymes allow for identification through biochemical testing
biochemical testing agar
Simmons citrate agar and urea agar
Simmons citrate
differential
enzyme citrate lyase are able to use citrate as a carbon source
when citrate is used it becomes more alkaline
turns green to blue
Bromothymol Blue
the pH indictor in the medium for a Simmons citrate agar, changes medium from a green to blue color.
Uninoculated Simmons Citrate slant
pH 6.9 – 7.6, green agar slant, negative reaction
Inoculated Simmons Citrate slant
pH > 7.6, blue agar slant, positive reaction
urea agar
differential - only organisms with enzyme urease can break down urea
when ammonia (NH4) is freed from the agar it causes a pH change and the environment becomes more alkaline
urea
a waste product of protein digestion in most vertebrates and is excretes in the urine
pH indicator in urea agar
phenol red, changes color yellow to hot pink (fuchsia)
Uninoculated Urea agar slant
pH 6.8 – 8.0, yellow agar slant, negative reaction
Inoculated Urea agar slant
pH > 8.0, fuchsia agar slant, positive reaction
2 differential media
contains various nutrients that allow one to distinguish one bacterium from another by how they metabolize or change media with a waste product
mannitol salt agar
selective = contains a high salt concentration (only organism that are halophiles or halotolerant will grow)
differential = contains the sugar mannitol (looking for mannitol fermentation)
also contains pH indicator called phenol red
fermentation of mannitol
the medium will change from red to yellow due to the pH
pH color change for mannitol
pH >8.4 = pink
pH 6.9-8.4 = red
pH < 6.9 =
Microbiological Culture
method of multiplying microbial organisms by letting them reproduce in a predetermined culture media under controlled laboratory conditions
mixed culture
yellow, more than one type of organism
pure culture
pink, single type of organism, main idea is to dilute the original sample until the organism of interest is isolated and pure
ways to obtain pure culture
spread, pour, streak plate
details of methods of getting pure culture
they dilute or thin out a heavy population of bacteria across an agar surface. Once a pure culture is obtained it can be used to identify if the bacteria is sensitive or resistant to an antibiotic
spread plate
original culture is serially diluted then the final dilution is spread on the surface of the plate. surface colonies grow
pour plate
serial dilution than final dilution added to molten agar which is poured over an agar plate. surface and subsurface colonies grow
streak plate
original culture directly diluted across (agar) new plate with inoculating loop. 3 sections in a T pattern, in each section start with a line from the previous section
types of media
broth, agar
broth
liquid media; nutrients (used in motility experiment)
agar
jellylike substance derived from seaweed: thickening agent
why do we use agar
because microorganisms cannot digest agar. it’s a solid surface for microorganisms to grow and we can pick out individual colonies
all purpose/supportive media
contains nutrients that will support the growth of a large variety microorganisms
selective media
promote growth of some bacteria and/or limits growth of other bacteria
differential media
distinguish between different bacteria based on changes in colonies or changes in media
types of agar
tryptic soy agar, Eosin methylene blue agar
tryptic soy agar (TSA)
all-purpose/supportive medium used to grow most microorganisms
Eosin methylene blue agar (EMB)
selective media for gram negative organisms. inhibits the growth of gram-positive organisms due to the dye’s eosin Y and methylene Blue
lactose fermentation makes it a differential media. it causes precipitation of the dyes on the surface of the colonies resulting in different colors.
Lots of acid = green metallic sheen
small amount of acid = pink or blue center (fish eye)
no fermentation = colorless
aseptic transfer
conducting your work in a way that will not contaminate the culture itself, and also without contaminating your workspace to yourself with the specimen
keep the lid on the plate at all times, can come off to pick a colony and then immediately
how to achieve aseptic technique
disinfect work area
all tools that handle bacteria need to be sterile
loops/needles: flamed in the incinerator or Bunsen burner to sterilize
tubes, plates, etc: autoclaved
keep all cultures covered unless you are using it that second
if unaware if tools are sterile start over