biochemical tests (2nd part)

76

Upload: aman-ullah

Post on 15-Jan-2017

506 views

Category:

Health & Medicine


0 download

TRANSCRIPT

Page 1: Biochemical tests (2nd part)
Page 2: Biochemical tests (2nd part)

PURPOSE

To determine the deaminase activity using the amino acids phenylalanine or tryptophan.

Only Proteus, Providencia and Morganella species possess the deaminase enzyme.

Page 3: Biochemical tests (2nd part)

PRINCIPLE

Deamination of the amino acid results in a colored compound with the addition of 10% ferric chloride

Phenylalanine ----------------PPA + 10% FeCl3 Phenylalanine deaminase green

Tryptophan-------------indole-pyruvic acid +10% FeCl3 Tryptophan deaminase brown

Page 4: Biochemical tests (2nd part)

INTERPRETATION

Positive deamination for phenylalanine – intense green color Positive deamination for tryptophan – brown color Negative – slant retains its original color after the addition of ferric chloride

Page 5: Biochemical tests (2nd part)

A. Negative – Escherichia coliB. Positive – Proteus vulgaris

A B

Phenylalanine deamination test

Page 6: Biochemical tests (2nd part)
Page 7: Biochemical tests (2nd part)

PURPOSE:

To determine the ability of the organism to deaminate lysine, decarboxylate lysine and produce H2S.

To identify Salmonella, Proteus, Providencia and Morganella.

Page 8: Biochemical tests (2nd part)

COMPOSITION

1. Proteins2. Sugar- Glucose3. Amino acid - Lysine4. Sulfur5. indicators a. ferric ammonium citrate – H2S production b. bromcresol purple – carbohydrate fermentation

Page 9: Biochemical tests (2nd part)

PRINCIPLE:

As glucose fermentation occurs, deep of the tube turns yellow.Lysine decarboxylation produces alkaline cadaverine and leads to reversion of the deep from yellow to purple.Lysine deaminatiion occurs in the presence of oxygen (on the slant) and results in the production of a red color.H2S production is noted by a black precipitate in the deep as H2S reacts with ferric ammonium citrate.

Page 10: Biochemical tests (2nd part)

INTERPRETATION

Lysine decarboxylation - butt Positive – purple Negative – yellow

Lysine deamination - slant Positive – red Negative –purple

Page 11: Biochemical tests (2nd part)

K/K alkaline slant/alkaline butt H2S(-) purple/ purple

Negative deaminationPositive decarboxylationNo blackening of the butt

Escherichia coli

Lysine iron agar

Page 12: Biochemical tests (2nd part)

K/K alkaline slant/alkaline butt H2S + purple/purple

Negative deamination Positive decarboxylationWith black precipitate in the butt

Salmonella typhimurium

Lysine iron agar

Page 13: Biochemical tests (2nd part)

K/A alkaline slant/acid butt H2S(-) (purple/yellow)

Negative deaminationNegative decarboxylationNo black precipitate in the butt

Shigella flexneri

Lysine iron agar

Page 14: Biochemical tests (2nd part)

R/A red slant/acid butt H2S(-) red/yellow

Positive deaminationNegative decarboxylationNo black precipitate in the butt

Proteus vulgaris

Lysine iron agar

Page 15: Biochemical tests (2nd part)
Page 16: Biochemical tests (2nd part)
Page 17: Biochemical tests (2nd part)

PURPOSE:

To determine if a member of the Enterobacteriaceae is capable of utilizing citrate as the sole source of carbon.

Useful in the identification of the lactose fermenting Enterobacteriaceae: Escherichia coli is citrate negative; Enterobacter and Klebsiella are positive

Page 18: Biochemical tests (2nd part)

PRINCIPLE

Sodium citrate is the only carbon source in Simmons citrate agar.If the organism can utilize citrate, the sodium citrate is converted to ammonia, which is then converted to ammonium hydroxide.The alkalinity of the compound formed raises the pH of the medium, and the bromthymol blue indicator takes on its alkaline color which is blue.

Page 19: Biochemical tests (2nd part)

INTERPRETATION

Positive – growth with an intense blue color on the slant or solely the presence of growth

Negative – absence of growth and no color change in the medium (remains green)

Page 20: Biochemical tests (2nd part)

Citrate Utilization test

A. Positive - Klebsiella pneumoniaeB. Negative - Escherichia coli

A B

Page 21: Biochemical tests (2nd part)
Page 22: Biochemical tests (2nd part)

PURPOSE

To determine the ability of an organism to use acetate as the sole source of carbon.

PRINCIPLE Breakdown of the sodium acetate causes the pH of the medium to shift toward the alkaline range, turning the indicator from green to blue.

Page 23: Biochemical tests (2nd part)

INTERPRETATION

Positive – Medium becomes alkalinized(blue) because of the growth of the organism

Negative – no growth or growth with no indicator change to blue

Page 24: Biochemical tests (2nd part)

A B

Acetate utilization test

A. Positive - Klebsiella pneumoniaeB. Negative – Escherichia coli

Page 25: Biochemical tests (2nd part)
Page 26: Biochemical tests (2nd part)

PURPOSE

To determine the ability of an organism to use acetamide as the sole source of carbon.

PRINCIPLE Bacteria that can grow on this medium deaminate acetamide to release ammonia. The production of ammonia results in a pH-driven color change of the medium from green to royal blue.

Page 27: Biochemical tests (2nd part)

INTERPRETATION

Positive – deamination of the acetamide resulting in a blue color

Negative – no color change

Page 28: Biochemical tests (2nd part)

Acetamide utilization test

A. Positive – Klebsiella pneumoniaeB. Negative – Escherichia coli

Page 29: Biochemical tests (2nd part)
Page 30: Biochemical tests (2nd part)
Page 31: Biochemical tests (2nd part)

PURPOSE:

To differentiate Micrococccus and Stomatococcus from Staphylococcus when combined with other procedures such as the modified oxidase test.

For presumptive identification of Group A streptococcus

Page 32: Biochemical tests (2nd part)

Bacitracin(0.04 units) inhibits the growth of Micrococcus and Stomatococcus and Group A streptococcus while having no effect on Staphylo- coccus which is resistant.

PRINCIPLE:

Page 33: Biochemical tests (2nd part)

INTERPRETATION

susceptible – zones of inhibition greater than or equal to 10 mm resistant – zones of inhibition less than or equal to 9 mm.

Page 34: Biochemical tests (2nd part)

A. Susceptible – Micrococcus and StomatococcusB. Resistant – Staphylococcus epidermidis

A B

Bacitracin susceptibility test

Page 35: Biochemical tests (2nd part)
Page 36: Biochemical tests (2nd part)

PURPOSE:

To identify the different species of Streptococcus especially Group A and Group B beta hemolytic streptococci.

Page 37: Biochemical tests (2nd part)

PRINCIPLE

Group A beta hemolytic streptococci (Streptococcus pyogenes) are susceptible to 0.04 units bacitracin but resistant to 1.25 ug sulfamethoxazole-trimethoprim (SXT)Group B beta hemolytic streptococci – resistant to both bacitracin and SXT

Page 38: Biochemical tests (2nd part)

INTERPRETATION

Susceptible: any zone of inhibition around either diskResistant: growth up to the disk(no zone of inhibition

Page 39: Biochemical tests (2nd part)

Organism Bacitracin SXT

Group A susceptible resistant Group B resistant resistant Group C,F,G resistant susceptible

Page 40: Biochemical tests (2nd part)
Page 41: Biochemical tests (2nd part)

PURPOSE

To differentiate the different species of coagulase negative staphylococci.

PRINCIPLE

After incubation with 5 ug of novobiocin, Staphylococcus saprophyticus is not inhibited by the antibiotic whereas Staphylococcus epidermidis are susceptible to novobiocin.

Page 42: Biochemical tests (2nd part)

INTERPRETATION:

susceptible – zone greater than 16 mm

resistant – zone diameter less than or equal to 16 mm

Page 43: Biochemical tests (2nd part)

A B

Novobiocin susceptibility test

A. Susceptible - Staphylococcus epidermidisB. Resistant - Staphylococcus saprophyticus

Page 44: Biochemical tests (2nd part)
Page 45: Biochemical tests (2nd part)

PURPOSE

To differentiate Pediococcus from other alpha hemolytic streptococcus.

PRINCIPLE

After incubation with 5 ug of vancomycin, Pediococcus is not inhibited by the antibiotic whereas Viridans streptococcus is susceptible to vancomycin.

Page 46: Biochemical tests (2nd part)

INTERPRETATION

Susceptible – zone of inhibition

Resistant – no zone of inhibition

Page 47: Biochemical tests (2nd part)

Vancomycin susceptibility test

A. Susceptible - Viridans streptococcus B. Resistant - Pediococcus

A B

Page 48: Biochemical tests (2nd part)
Page 49: Biochemical tests (2nd part)

PURPOSE

To determine an anaerobe’s inhibition that can be used for presumptive identification based on its characteristic susceptibility pattern to colistin (10 ug), vancomycin(5 ug) and kanamycin(1 mg).

Page 50: Biochemical tests (2nd part)

PRINCIPLE Most anaerobes have a characteristic susceptibility pattern to colistin(10 ug), vancomycin( 5 ug), and kanamycin(1 mg) disks.

kanamycin – inhibits facultative gram-negative bacilli vancomycin- inhibits facultative and obligate gram-positive bacteria colistin- inhibits facultative gram-negative bacilli

Page 51: Biochemical tests (2nd part)

K Va

Co

INTERPRETATION

Susceptible – zone greater than 10 mmResistant – zone of 10 mm. or less

Antibiotic Disks for the Presumptive Identification of Anaerobes

Page 52: Biochemical tests (2nd part)
Page 53: Biochemical tests (2nd part)
Page 54: Biochemical tests (2nd part)
Page 55: Biochemical tests (2nd part)

PURPOSE

To classify bacteria based on their ability to grow in the presence of 6.5% NaCl, a characteristic of certain species of gram positive and gram negative bacilli.

To differentiate the Group D(salt tolerant) from the nonenterococci(intolerant).

Page 56: Biochemical tests (2nd part)

PRINCIPLE

Nutrient broth or 6.5%NaClTrypticase broth-salt free medium

Positive equal equal

Negative good very weak

Page 57: Biochemical tests (2nd part)

INTERPRETATION

Positive – if growth is equivalent to both media – tolerant of salt

Negative- growth on the salt containing medium is very weak or absent growth in the salt free medium is good - intolerant of salt

Indicator: bromcresol purple Positive: medium turns yellow from purple or the appearance of growth

Page 58: Biochemical tests (2nd part)

SALT TOLERANCE TEST

A. Positive - Enterococcus faecalis ( salt tolerant)B. Negative - Streptococcus bovis(salt intolerant)

Page 59: Biochemical tests (2nd part)
Page 60: Biochemical tests (2nd part)

To distinguish Group D streptococci and Enterococcus species from other Lancefield group of streptococci

based on the organisms ability to grow in 40% bile and to hydrolyze esculin to produce esculitin Esculin reacts with ferric citrate to form a brown black precipitate.

PURPOSE

PRINCIPLE

Page 61: Biochemical tests (2nd part)

INTERPRETATION

Positive growth indicates tolerance to 40% bile(40% oxygall) blackening indicates hydrolysis of esculin

Negative lack of growth indicates inability to grow in 40% bile lack of color change indicates inability to hydrolyze esculin

Page 62: Biochemical tests (2nd part)

A. Positive - Enterococcus faecalisB. Negative - Streptococcus viridans

Bile esculin agar

A B

Page 63: Biochemical tests (2nd part)
Page 64: Biochemical tests (2nd part)

PURPOSE

To differentiate Streptococcus pneumoniae from other alpha hemolytic streptococci

PRINCIPLE In the presence of optochin, colonies of Strepto- coccus pneumoniae are selectively lysed indicated by a zone of inhibition after incubation under increased CO2. Other alpha hemolytic streptococci are resistant to optochin.

Page 65: Biochemical tests (2nd part)

Positive – zone of inhibition at least 14 mm. in diameter using a 10 ug P disk and at least 10 mm. using a 6 mg P disk

Negative – growth up to the disk or a zone of inhibition less than 14 mm with a 10 ug P disk or less than 10 mm. with a 6 ug P disk

INTERPRETATION

Page 66: Biochemical tests (2nd part)

Optochin susceptibility test

A. Positive – Streptococcus pneumoniaeB. Negative – Viridans streptococci

A B

Page 67: Biochemical tests (2nd part)
Page 68: Biochemical tests (2nd part)

PURPOSE

To differentiate Streptococcus pneumoniae(positive) from other alpha hemolytic streptococci.

Page 69: Biochemical tests (2nd part)

PRINCIPLE

Pneumococcal colonies are rapidly lysed by bile or a solution of a bile salt such as sodium deoxycholate. Lysis depends on the presence of an intracellular autolytic enzyme. Bile salts lower the surface tension between the bacterial cell membrane and the medium thus accelerating the organism’s natural autolytic process.

Page 70: Biochemical tests (2nd part)

INTERPRETATION

Positive – colony disintegrates; an imprint of the lysed colony may remain within the zone

Negative – intact colonies

Page 71: Biochemical tests (2nd part)

BA

Bile solubility test

A. Positive – Streptococcus pneumoniaeB. Negative – Viridans Streptococci

Page 72: Biochemical tests (2nd part)
Page 73: Biochemical tests (2nd part)

PURPOSE

to demonstrate the phenomena of synergistic hemolysis between group B streptococcus and beta hemolytic Staphylococcus aureus

PRINCIPLE

a characteristic “arrowhead” hemolytic pattern results when the organism is streaked perpen- dicular to beta hemolytic Staphylococcus aureus

Page 74: Biochemical tests (2nd part)

INTERPRETATION

Positive – a zone of enhanced hemolysis given by an arrowhead appearance at the junction of the Staphylococcus and Streptococcus – indicative of Group B streptococcus

Negative – no zone of enhanced hemolysis- not indicative of Group B streptococcus

Page 75: Biochemical tests (2nd part)

CAMP REACTION

A. Positive - Streptococcus agalactiae B. Negative - Streptococcus bovis

A B

Page 76: Biochemical tests (2nd part)