Nora Al-Kubaisi Gram’s +ve Cocci Irregular Clusters Tetrads Chains or Pairs Staphylococci Micrococci Streptococci.

Slides:



Advertisements
Similar presentations
Upper and Lower Respiratory Tract Infection
Advertisements

IDENTIFIKASI BAKTERI OLEHSUDRAJAT FMIPA UNMUL 2009.
طريقة تخطيط الاطباق Streak Plate Method
Lab. No Microscopical Appearance:(Gram’s Stain) Gram’s +ve Cocci Irregular ClustersChains or PairsTetrads Staphylococci MicrococciStreptococci.
Staphylococcus Gram + cocci In clumps.
Lab. No Microscopical Appearance:(Gram’s Stain) Gram’s +ve Cocci Irregular ClustersChains or PairsTetrads Staphylococci MicrococciStreptococci.
Isolation and Identification of Staphylococci
Lab 14 Goals and Objectives: Exercise 69: Staphylococci Identification Read and record results Exercise 70: Streptococci & Enterococci Identification Read.
Streptococci Characters of Streptococci Gram positive cocci
Micrococci Marphology: _ Gram +ve cocci Arrangement : Tetrades _ _ _ _ _ Non motile, non capsulated, non sporulated Habitat : May be normal present in.
Identification methods of gram positive and gram negative cocci
Streptococci Eva L. Dizon, M.D.,D.P.P.S Department of Microbiology.
Isolation and Identification of Gram Positive Cocci
Medical bacteriology:
PHT382 Lab. No.1.
Lab. No. 3. Gram’s +ve Bacilli Spore forming Non spore forming AerobicAnaerobic Bacillus Clostridium Corynebacterium.
Culture Media (Types, Preparation & Sterilization)
Staph and Strep.
Lab 23 Respiratory Microorganisms. Objectives Interpret hemolysis results Classify various Streptococcus species.
Streptococcus Basmah almaarik Lab # 6.
Identification of Strep and Staph and Isolating gram – pathogens Lab # 10 Medgar Evers College Prof. Santos.
Gram Positive Bacteria and Clinical Case Studies II
PHT 416 Lab 7. Steps Microscopic Morphology Growth Biochemical Tests Nutrient agar Blood agar Mannitol Salt Agar MacConkey’s agar.
Identification of Pathogenic Bacteria by Laboratory Methods M. Kent Froberg, MD.
Exercise 41: Multiple Test Media: Read and record results
Diagnosis of streptococci Compiled by Thamer Hamdan Compiled by Thamer Hamdan M.Sc. Clinical Microbiology and Immunology M.Sc. Clinical Microbiology and.
Streptococci.
Streptococcus Gram+ cocci In chains.
Streptococci. Introduction Pyogenic pathogens - nonmotile, catalase negative, Gram positive cocci in chains.
Lab 13- Bacterial cultivation
Identification of Staphylococci and Streptococci
PHT 313 Lab (1) Staphylococci.
STAPHYLOCICCI Lecture # 3. Staphylococcus sp.  Morphology:  Gram positive cocci.  In clusters  Culture:  Facultative anaerobes  Incubation 37ºC.
STAPHYLOCICCI Basmah almaarik
PHT 313 Lab (3) Streptococci. Staphylococci Streptococci Enterococci NeisseriaCorynbacterium Clostridum Bacillus Enterobacteriaceae Pseudomonas. Bacteria.
Types of Agar.
LAB 7: RESPIRATORY SYSTEM. RESPIRATORY SYSTEM: UPPER AND LOWER.
Prof. Jyotsna Agarwal Dept Microbiology KGMU
Lesson 3 WT Staphylococcal infections Diagnosis of staphylococcal infections Diagnostical model: abscess - pus, enterotoxicosis - food, osteomyelitis -
Clinical Microbiology ( MLCM- 201) Prof. Dr. Ebtisam.F. El Ghazzawi. Medical Research Institute (MRI) Alexandria University.
Lab. No. 6. I. Pseudomonas Most Important Strains: Most Important Strains:  Ps. aeruginosa which is opportunistic microorganism, causes UTI, wound.
PHT313 Lab. No. 4.
226 PHT Final Spots. Gram’s stain Results: Shape: Cocci Arrangment: irregular clusters Colour: Violet Gram’s reaction: Gram’s +ve Name of microorganism:
General Microbiology Laboratory Isolation and Identification of Gram Positive Cocci.
Lab. No. 3. Microscopical Appearance:(Gram’s Stain) Microscopical Appearance:(Gram’s Stain) Gram’s +ve Cocci Irregular ClustersChains or PairsTetrads.
COLLECTION OF SAMPLES FOR BACTERIOLOGICAL EXAMINATION
Selective and differential Media By : Mahmoud W. El-Hindi
Staphylococci DON XAVIER N.D.  Cocci.  Gram positive.  Non motile.  On NA they form pigmented colonies.  Haemolytic.  Enzyme production.  Ferment.
Medically Important Bacteria Gram Positive Cocci
Streptococcus IMPORTANT PROPERTIES 1-streptococci are spherical gram-positive cocci. 2-arranged in chain or pairs. 3-all streptococci are catalase negative.
PHT 313 Lab (1) Staphylococci.
Lab 14 Goals and Objectives: Exercise 69: Staphylococci Identification Read and record results Exercise 70: Streptococci & Enterococci Identification Read.
Media!.
Streptococcus agalactiae (GBS)
Bacterial Identification
Medically Important Bacteria Gram Positive Cocci.
Streptococcaceae family Classification - Includes 7 genera: –Streptococcus – a major cause of human infections –Enterococcus – frequent cause of human.
Exercise 39: Oxidation and Fermentation Tests (Catalase)
Staphylococcus.
PHT313 Lab. No. 3.
Revision.
Bacteriology 1 Lab 1.
STREPTOCOCCI By Eric S. Donkor.
Staphylococcus Streptococcus
Streptococci Basmah almaarik
Lab 3 streptococci.
طريقة تخطيط الاطباق Streak Plate Method
II- Streptococci Characters of Streptococci Gram positive cocci
Streptococcus pneumoniae
assist. Prof. Zainab Abdul jabar Aldhaher
Presentation transcript:

Nora Al-Kubaisi

Gram’s +ve Cocci Irregular Clusters Tetrads Chains or Pairs Staphylococci Micrococci Streptococci

– Gram positive cocci. –1μm in diameter. – Chains or pairs. –Usually capsulated. –Non motile. – Non spore forming. – Facultative anaerobes. –Fastidious. – Catalase negative (Staphylococci are catalase positive).

I DENTIFICATION OF S TERPTOCOCCI C hains

Oxygen requirements Anaerobic (Peptostreptococcus) Aerobic or facultative anaerobic (Streptococcus) Serology ( Lanciefield Classification). Hemolysis on Blood Agar (BA). 1. β-hemolytic Sterptococci. 2. α-hemolytic Sterptococci. 3.γ-hemolytic Sterptococci.

Gram’s +ve Cocci Irregular Clusters Tetrads Chains or Pairs Catalase +ve Catalase -ve

C ATALASE T EST Differentiative test ( separate Staphylococci and Micrococci which are catalase +ve from Sterptococci which are catalase –ve ). Principle : Procedure H2o2 H2o +O2 (gas) Catalse Air bubbles

C ATALASE T EST R ESULTS : Positive test : rapid appearance of gas bubbles. Catalase +ve Catalase –ve Staphylococci or MicrococciStreptococci

G ROWTH ON B LOOD A GAR Sterptococci are divided into three main groups accorging to its action on erythrocytes: 1.β-hemolytic Sterptococci. 2.α-hemolytic Sterptococci. 3.γ-hemolytic Sterptococci.

G ROWTH ON B LOOD A GAR Β - HEMOLYTIC S TERPTOCOCCI : It causes : complete hemolytic to RBCs leading to formation of clear zone around the colonies.

Example: Strept. Pyogenes  group A  β-hemolytic Strept.

Α - HEMOLYTIC S TERPTOCOCCI : It causes: 1. Partial hemolysis to RBCs. 2. Act enzymatically on blood pigment leading to green discoloration around the colonies.

Example: Strept. Pneumonia viridans Streptococci.

β -hemolytic Sterptococci α-hemolytic Sterptococci :

Γ - HEMOLYTIC S TERPTOCOCCI : It has no effect on RBCs : ( Non hemolytic Sterptococci ) Example Enterococcus faecalis

γ-hemolytic Sterptococci. α-hemolytic Sterptococci. β-hemolytic Sterptococci.

Hemolysis on Blood agar

Definitive test to differentiate between ; S.Pyogenes & Non group A β-hemolytic Streptococci Principle: (Bacitracin Sensitivity Test) A low conc. of Bacitracin (0.04 units) will selectively inhibit the growth of S.pyogenes giving a zone of inhibition around the disc.

Bacitracin Sensitive S.Pyogenes

Group A streptococci Pathogenesis and Virulence Factors;  Structural components: M protein M Lipoteichoic acid & F protein Hyaluronic acid capsule, which acts to camouflage the bacteria  Enzymes Streptokinases Deoxynucleases C5a peptidase  Pyrogenic toxins Streptolysins Streptolysin O lyse red blood cells, white blood cells, and platelets Streptolysin S

Α - HEMOLYTIC S TREPTOCOCCI Definitive test to differentiate between S.Pneumoniae & Viridans Streptococci 1. Optochin Sensitivity Test: S.Pneumoniae is inhibited by less than 5 μg/ml Optochin reagent giving a zone of inhibition more than 15 mm in diameter.

α-hemolytic Sterptococci 1.Optochin Sensitivity Test: Procedure: 1. Inoculate blood agar plate with the test organism. 2. Aseptically apply Optochin disc onto the center of the streaked area. 3. Incubate the plate at 35oC for 18 hrs. 4. Accurately measure the diameter of the inhibition zone around the disc.

Α - HEMOLYTIC S TERPTOCOCCI 1. Optochin Sensitivity Test: Results: Positive test: inhibition zone more than 15 mm in diameter. Optochin sensitive S.pneumoniae Optochin resistant Viridans Streptococci

O PTOCHIN S USCEPTIBILITY T EST Optochin resistant S. viridans Optochin susceptible S. pneumoniae

Α - HEMOLYTIC S TREPTOCOCCI 2. Bile Solubility Test: Principle: S.Pneumoniae produce a self-lysing enzyme to depress the growth of old colonies. The presence of bile salt accelerate this process.

P ROCEDURE : 10 ml broth culture of the test organism Add 1 ml 10% bile salt solution Incubate at 37oC for 15 min. Observe for the visible clearing of the turbid culture.

Results: Positive test: Visible clearance of the turbid culture. Remain turbid Viridans Streptococci Visible clearance S.Pneumoniae

Γ - HEMOLYTIC S TERPTOCOCCI Definitive test for Enterococcus faecalis Growth on MacConkey’s agar. Principle: MacConkey’s agar is a selective medium for Gram’s –ve bacteria. It contains bile salt and crystal violet to inhibit the growth of Gram’s +ve bacteria. Enterococcus faecalis is the only Streptococcus species which can grow on MacConkey’s agar giving pink colonies.

Procedure: 1. Inoculate MacConkey’s agar plate with the test organism by streaking. Incubate the plate at 35oC for 24 hrs.

R ESULTS : pink colonies of Enterococcus faecalis

1.Gram’s Stain (spots) 2.Catalase test 3.Blood agar plate. 4.Bacitracin & Optochin Sensitivity. 5.MacConkey’s agar plate.

O UTLINE OF DIFFERENTIATION BETWEEN G RAM -P OSITIVE COCCI