Gram-positive cocci Staphylococci and Streptococcia

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Medical microbiology Laboratory Lab 8 Gram-positive cocci Staphylococci and Streptococcia Lecturer Maysam A Mezher

Gram positive cocci 1-Staphylococcus. 2-Streptococcus. 3-Micrococcus The medically important genera, are: Staphylococci and Streptococci. Both of them are non motile and do not form spores. They are distinguished by two main criteria: Microscopically: staphylococci appear in grape like clusters where as streptococci are in chains. Biochemically: staphylococci produce catalase which brakes down hydrogen peroxide, where as streptococci do not.

Staphylococci

Important properties : Gram-positive cocci, arranged in grape-like clusters Non spore-forming, non motile and capsule formation is variable. Aerobic and facultative anaerobic, grow readily on usual culture media, has large,raised, opaque colonies with smooth entire margin. Salt tolerant: allows them to tolerate the salt present on human skin.

Clinically important species: Staphylococcus aureus: most virulent species. It is responsible for awide range of medical illnesses extending from mild localized skin infection to life threatening septicemia. Staphylococcuse pidermidis: it is normal flora of the skin and mucous membranes, Staphylococcus saprophyticus: it is free living, common cause of UTI in women

Staphylococcus aureus General features Coagulase positive Produces golden yellow pigment

Lab diagnosis S. aureus Specimens: wound swab, pus, sputum, blood, urine CSF. Culture BA: beta hemolysis MSA: ferment mannitol (yellow colonies). Microscopy: Gram stain- Blood agar

Biochemical tests: Catalse : to differentiate staphylococci from streptococci. This enzyme break down H2O2 to Oxygen and water. Coagulase: to differentiate S. aureus frorm other staphylococci. Slide method: for detection of clumping factor. Tube method: for detection of plasma coagulase, Novobiocin disc: to differentiate S. saprophyticus which is resistant, whereas, other are sensitive.

Coagulase test

Streptococci

General characteristics: 1.Gram-positive cocci,arranged in chains or pairs. 2.Non motile, non spore forming. 3.Some strains are capsulated, which are important in pathogenicity. 4.Catalase-negative. 5.Majority are facultative anaerobes, few are obligate anaerobes. 6.They are fastidious microorganisms grow on enriched media such as blood agar,have small, pinhead, opaque, circular colonies. 7.Sensitive to drying, heat, and disinfectant.

Classification: 1- Hemolysis: ẞ-hemolysis: complete destruction of RBCs. e.g. S. pyogenes α-hemolysis: partial destruction of RBCs e.g. S. mutans, S. pneumoniae. γ-hemolysis: non-hemolysis.

2- Serology (Lancefield grouping): Streptococci Lancefield classification There are differences in the polysaccharide antigens of the cell wall. Depending on these specific polysaccharide antigens, streptococci are named as groups from A-U. Group A S. pyogenes Group B S. agalactiae Group C S. equisimitis Group D Enterococcus Other groups (E-U)

HUMAN STREPTOCOCCAL PATHOGENS S. pyogenes S. agalactiae Viridans streptococci S. pneumoniae Human streptococcal patohogens: - B -hemolytic Group A streptococci - S. pyogenes: Most serious streptococcal pathogen In habits throat, nasopharynx And occasionally skin.

Lab diagnosis Strep. Pyogenes Specimens: throat swab, pus, blood Microscopy :Gram stain -GPC in chains Culture: BA -beta hemolytic colonies Identification tests- Catalase Negative Bacitracin sensitive

Bacitracin sensitivity Principle: Bacitracin test Is used for presumptive identification of groupa To distinguish between S.pyogenes (susceptible to B) & non group A such as S.agalactiae (Resistant to B) Bacitracin will inhibit the growth of gp AStrep. Pyogenes giving zone of inhibition around the disk Procedure: Inoculate blood agar with heavy suspension of tested organism After incubation, any zone of inhibition around the disk is considered as susceptible

B -hemolytic :Group B streptococci- S. agalactiae: Normal flora of female vaginal tract and cause neonatal meningitis. Bacitracin resistant CAMP test+ve (Christie, Atkins, Munch-Peterson) hydrolize sodium hipurate and give+ve response in this test

- Alpha hemolytic streptococci Streptococcus pneumoniae (Pneumococcus) General features: Causes 60-70% of all bacterial pneumonias Small, lancet-shaped cells arranged in pairs and short chains Culture requires blood or chocolate agar, Growth improved by 5-10%CO2 50% of all people carry it as normal flora in the nasopharynx ; infections are usually endogenousvirulence

Lab. diagnosis: Gram stain: GPC arranged in pairs. (lancet-shaped diplococci) Rapid diagnostic test: Quellung test or capsular swelling reaction for S. pneumoniae: is a Rapid diagnostic test on sputum or culture. By mixing S. pneumoniae with specific antipolysaccharide (capsule component) on microscopic slide. The capsule swells due Ag-Ab reaction. Culture: BA-α-hemolytic Biochemical test: -optochin sensitivity: sensitive

Optochin Susceptibility Test Principle: Optochin(OP) test is presumptive test that is used to identify S. pneumoniae S. pneumoniae is inhibited by Optochin reagent (<5 µg/ml) giving a inhibition zone 14 mm in diameter. Procedure: BAP inoculated with organism to be tested OP disk is placed on the center of inoculated BAP After incubation at 37oC for 18 hrs, accurately measure the diameter of the inhibition zone by the ruler 14mm zone of inhibition around the disk is considered as positive and 13 mm is considered negative S. pneumoniae is positive (S) while S. viridansis