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Streptococci (Gram
positive cocci)
Dr Marianne Mureithi
marianne@uonbi.ac.ke
: @docmureithi
2
3
Learning Objectives
4
By the end of this lecture, you will be able to:
•Classify Streptococci by hemolysis patterns and Lancefield
grouping
•Identify key pathogenic Streptococci species & describe their
disease associations.
•Explain the pathogenesis of Streptococcal infections
•Diagnose Streptococcal infections using a combination of
clinical presentation, laboratory diagnostics,
•Discuss treatment strategies and prevention including
antibiotic selection, resistance challenges, and the role of
vaccines in managing Streptococcal diseases.
Streptococci
• Morphology: Gram-positive cocci approximately 1µm in
diameter.
• Arrangement: Occur in chains or pairs.
• Capsule: Often encapsulated, contributing to virulence.
• Mobility: Non-motile.
• Spore Formation: Do not form spores.
• Respiration: Facultative anaerobes, can survive with or without
oxygen.
• Enzyme Activity: Catalase-negative; unlike Staphylococci,
they cannot decompose hydrogen peroxide.
Classification of Streptococci
• Streptococci can be classified according to:
– Serology (Lanciefield Classification)
– Hemolysis on Blood Agar (BA)
Serology: Lanciefield Classification
Streptococci
Group A
S. pyogenes
Group B
S. agalactiae
Group C
S. equisimitis
Group D
Enterococcus
Other groups
(E-U)
Lanciefield
classification
Hemolysis on Blood agar
-hemolysis
-hemolysis
-hemolysis
Classification of Streptococci Based
on Hemolysis on Blood Agar
Hemolysis on BA
– -hemolysis
Partial hemolysis
Green discoloration around the colonies- Iron oxidation
e.g. non-groupable streptococci (S. pneumoniae & S. viridans)
– -hemolysis
Complete hemolysis
Clear zone of hemolysis around the colonies
e.g. Group A & B (S. pyogenes & S. agalactiae)
– -hemolysis
No lysis
e.g. Group D (Enterococcus spp)
Streptococci
-hemolysis -hemolysis -hemolysis
10
Beta hemolytic Group A
Streptococcus
(GAS) 1
11
Group A Streptococci(GAS)
Streptococcus pyogenes:
• Basic Characteristics:
• Gram-positive cocci in chains or pairs.
• Epidemiology:
• Commonly found in the throat and on the skin.
• Can be carried asymptomatically.
• Pathogenicity:
• Produces a wide range of virulence factors, including M proteins, streptolysins, and
exotoxins.
• Causes both suppurative (pus-forming) and non-suppurative (post-infectious) diseases.
• Clinical Diseases:
• Suppurative: Pharyngitis (strep throat), impetigo, cellulitis, and necrotizing fasciitis.
• Non-suppurative: Rheumatic fever and acute glomerulonephritis following infection.
• Treatment and Management:
• Typically sensitive to penicillin; antibiotic treatment is effective for most acute infections.
• Post-infection sequelae require long-term management and can lead to chronic conditions.
• .
Data obtained from a Centers for Disease Control and Prevention Active Bacterial Core
Surveillance Report for group A streptococcal
Who is at Risk for Infection?
Clinical conditions
1. Pyogenic
– Pharyngitis, tonsillitis, peritonsillar abscess, sinusitis, otitis
media, impetigo, wound infection, osteomyelitis, septic arthritis,
puerperal sepsis, bacteraemia, acute bacterial endocarditis
2. Toxigenic(exotoxins)
– Scarlet fever
– Streptococcal toxic shock syndrome
3. Immune-mediated: non-suppurative
– Occurs after repeated infections
– AGN- Acute glomerulonephritis-follows skin
– ARF- Acute rheumatic fever. Cross reactivity of the antibodies
produced during streptococcal pharyngitis, cross react with
antigens in heart muscle
hemolytic streptococcal gangrene
Virulence factors
Strep throat
 - hemolytic - Group A (GAS) streptococci: S.
pyogenes
Droplet Transmission
Symptoms: Sore throat, high fever, coughing, otitis
media may also occur
Complications of Strep Throat
S. pyogenes causes two major autoimmune complications
(antibodies cross-react)
1. Acute rheumatic fever:
Short period of arthritis and fever followed in  50% of
affected by rheumatic heart disease
 heart valve damage  chronic valvular disease
(stenosis and/or incompetence)  heart failure and/or
subacute bacterial endocarditis
2. Acute poststreptococcal glomerulonephritis
19
Laboratory diagnosis
• Specimen: Throat swabs, pus swabs, blood, CSF
etc
• Direct Gram stain- Gram-positive cocci in chains,
pus cells
• Culture:
– BA, aerobically, 37°C for 18-24 hours
– Smooth circular colonies of 2-3 mm diameter, β-
haemolysis
• Gram-positive cocci in chains
• Catalase negative
• Bacitracin sensitive
Treatment and Prevention
Treatment
– Cephalosporins
– Tetracyclines
– Erythromycin
– Chloramphenicol
Prevention
– Infection control
– Treat pharyngitis as early as possible to prevent ARF
– No vaccine
VACCINES
• Research focuses on M protein-based, multivalent,
recombinant, and universal antigen vaccines for
broad immunity.
• Clinical trials underway; major challenges include
preventing autoimmune reactions and ensuring
global vaccine accessibility. 22
Group B Streptococci(GBS)
Streptococcus agalactiae
• Classification: Belongs to Group B of the Lancefield
classification.
• Morphology: Gram-positive cocci, usually in chains.
• Habitat: Colonizes the gastrointestinal and genitourinary
tracts of humans.
• Virulence Factors: Capsular polysaccharide, C5a peptidase,
hemolysins, and sialic acid-rich surface proteins contribute to
its evasion of the immune system and pathogenicity.
Clinical manifestations
• Pathogenicity:
• In Neonates: Leading cause of neonatal sepsis, meningitis, and
pneumonia.
• In Adults: Can cause urinary tract infections, skin and soft-tissue
infections, and, in pregnant women, chorioamnionitis and postpartum
infections.
Early onset neonatal disease(1st 7 days of life)-
– Vertical transmission in utero or at time of delivery
Late onset(7-90 days)- nosocomial/vertical
25
26
Lab diagnosis – Group B
Streptococci
• Specimens: CSF, blood, vaginal smears,
urine
• Microscopy :Gram stain - GPC in
chains
• Culture: BA - beta hemolytic colonies
• Identification tests
– Catalase negative
– Bacitracin resistance
– CAMP Test +
– Penicillin sensitive
P B
2
VACCINE
2
Group B streptococcal vaccine - This vaccine is currently under
development
30
Alpha hemolytic streptococci
Streptococcus pneumoniae
1
INTRODUCTION:
• Common name Pneumococcus.
• Has over 100 Serotypes
• Normal inhabitants of the upper respiratory tract of
human beings.
• Gram positive small(1μm), slightly elongated cocci,
with one end broad & other end pointed, presenting a
flame shaped or lanceolate appearance.
Disease:
1. Otitis media & sinusitis
2. Pneumonia
a. Lobar pneumonia
b. Bronchopneumonia
3. Tracheobronchitis
4. Meningitis
5. Other infections- empyema, pericarditis, conjunctivitis,
suppurative arthritis & peritonitis.
33
Marianne W. Mureithi, et al; T Cell Memory
Response to Pneumococcal Protein Antigens in an
Area of High Pneumococcal Carriage and
Disease, The Journal of Infectious Diseases, Volume
200, Issue 5, 1 September 2009, Pages 783–
793, https://doi.org/10.1086/605023
MOC Ota,, MW Mureithi, et al: Antibody and T-cell
responses during acute and convalescent stages of
invasive pneumococcal disease
Adam Finn, Marianne W. Mureithi, et al. Evolution
of Naturally Acquired T-Cell Immunity to
Pneumococcal Protein Antigens in Infants from an
Area of High Pneumococcal Carriage &
Disease. Infectious Diseases Society of America
(IDSA) 2008
Virulence
• Capsular polysaccharide- antiphagocytic
• IgA1 protease
• Pneumolysins
– Slows ciliary beating
– Toxic to pulmonary endothelial cells
– Spread of organism from alveoli into bloodstream
• Autolysin
– Breaks the peptide cross-linking of the cell wall peptides
leading to cell lysis
35
Lab diagnosis
• Specimen: CSF, blood, sputum, pus,
swabs
• Microscopy: Gram stain – GPC in
pairs, capsulated, lanceolate shaped
• Culture
– BA – alpha hemolytic colonies
• Identification tests
– Catalase –ve
– Optochin sensitive
– Bile solubility
– Quellung reaction
Optochin sensitivity: Sensitive.
Quellung( capsular swelling )
reaction
Bile Solubility
Treatment and Prevention
Treatment
• Penicillins, ampicillin- resistance increasing
• Ceftriaxone, cefotaxime, carbapenems,
fluoroquinolones, erythromycin, chloramphenicol,
vancomycin
Prevention
• Vaccine
Conjugate Vaccine
• A new generation of pneumococcal vaccines
• Coating removal of the capsular polysaccharide
• 7 (9, 11 or 13) types of saccharide is separately activated
and conjugated to protein carrier
• CDC recommended PVC vaccine schedule: 2mo, 4mo,
6mo, 12-15mo, 65years
LATEST NEWS
• FDA Approval: PREVNAR 20™, a 20-valent
pneumococcal conjugate vaccine by Pfizer, approved by the
U.S. FDA.
• Coverage: Provides protection against 20 serotypes of
pneumococcus responsible for most invasive pneumococcal
disease and pneumonia.
• Significance: Includes seven serotypes linked to 40% of
pneumococcal disease
• Advancement: Represents a significant advancement in
pneumococcal disease prevention, offering broader
protection than previously available vaccines.
40
Viridans Streptococci
Viridans Streptococci
• Normal flora of oral cavity, nasopharynx, genital
tract and skin
• S.mitis
• S.mutans
• S.milleri
• S.salivarius
• S.sanguis
unique ability to synthesize dextrans from glucose, which allows
them to adhere to fibrin-platelet aggregates at damaged heart valves.
extraction).
Clinical manifestations
• Dental caries
• Gingivitis, pyogenic oral infections
• Subacute bacterial endocarditis
• Brain abscesses, abdominal abscesses
Laboratory diagnosis
• Specimen: blood, pus
• Gram stain- Gram-positive cocci in chains
• Culture on BA
– Incubate in air at 37°C for 18-24 hours
• Biochemical tests
– Catalase negative
– Optochin resistant
– bile insoluble
• Molecular studies e.g. PCR
Treatment
• Prophylaxis to patient at risk during dental
surgery
• Penicillin and other β-lactam
• Ampicillin and Gentamicin
• Vancomycin- for penicillin allergies
ENTEROCOCCUS: STUDENT
REVIEW
47
Group D Streptococcus- Gamma Hemolytic
Normal flora in GIT, lower genital tract
Nosocomial / opportunistic pathogen
Enterococcus – 2 imp. species
E. fecalis
E. faecium
UTI, wound infection, endocarditis
Resistance to cephalosporins, even vancomycin
1
Points to Remember/Conclusion
• Diversity and Classification: Streptococci, a diverse genus of Gram-
positive bacteria, classified by hemolysis, Lancefield groups.
• Major Pathogens: Includes Group A (S. pyogenes) causing
rheumatic fever, and Group B (S. agalactiae) linked to neonatal sepsis.
• Virulence & Diseases: Equipped with virulence factors (e.g., M
protein, hyaluronic acid) causing diseases from pharyngitis to severe
infections.
• Diagnosis & Treatment: Diagnosed via culture, antigen detection;
treated with antibiotics, with emphasis on resistance management.
• Prevention & Research: Hygiene, antibiotics, pneumococcal
vaccines critical; ongoing research into GAS vaccines and new
treatments.
• Global Impact: significant health challenge, requiring ongoing
vigilance and innovative control strategies.
Hemolysis Patterns of
Streptococci

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Streptococci In medical microbiology and health

  • 1. 1 Streptococci (Gram positive cocci) Dr Marianne Mureithi marianne@uonbi.ac.ke : @docmureithi
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  • 4. Learning Objectives 4 By the end of this lecture, you will be able to: •Classify Streptococci by hemolysis patterns and Lancefield grouping •Identify key pathogenic Streptococci species & describe their disease associations. •Explain the pathogenesis of Streptococcal infections •Diagnose Streptococcal infections using a combination of clinical presentation, laboratory diagnostics, •Discuss treatment strategies and prevention including antibiotic selection, resistance challenges, and the role of vaccines in managing Streptococcal diseases.
  • 5. Streptococci • Morphology: Gram-positive cocci approximately 1µm in diameter. • Arrangement: Occur in chains or pairs. • Capsule: Often encapsulated, contributing to virulence. • Mobility: Non-motile. • Spore Formation: Do not form spores. • Respiration: Facultative anaerobes, can survive with or without oxygen. • Enzyme Activity: Catalase-negative; unlike Staphylococci, they cannot decompose hydrogen peroxide.
  • 6. Classification of Streptococci • Streptococci can be classified according to: – Serology (Lanciefield Classification) – Hemolysis on Blood Agar (BA)
  • 7. Serology: Lanciefield Classification Streptococci Group A S. pyogenes Group B S. agalactiae Group C S. equisimitis Group D Enterococcus Other groups (E-U) Lanciefield classification
  • 8. Hemolysis on Blood agar -hemolysis -hemolysis -hemolysis
  • 9. Classification of Streptococci Based on Hemolysis on Blood Agar Hemolysis on BA – -hemolysis Partial hemolysis Green discoloration around the colonies- Iron oxidation e.g. non-groupable streptococci (S. pneumoniae & S. viridans) – -hemolysis Complete hemolysis Clear zone of hemolysis around the colonies e.g. Group A & B (S. pyogenes & S. agalactiae) – -hemolysis No lysis e.g. Group D (Enterococcus spp) Streptococci -hemolysis -hemolysis -hemolysis
  • 10. 10 Beta hemolytic Group A Streptococcus (GAS) 1
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  • 12. Group A Streptococci(GAS) Streptococcus pyogenes: • Basic Characteristics: • Gram-positive cocci in chains or pairs. • Epidemiology: • Commonly found in the throat and on the skin. • Can be carried asymptomatically. • Pathogenicity: • Produces a wide range of virulence factors, including M proteins, streptolysins, and exotoxins. • Causes both suppurative (pus-forming) and non-suppurative (post-infectious) diseases. • Clinical Diseases: • Suppurative: Pharyngitis (strep throat), impetigo, cellulitis, and necrotizing fasciitis. • Non-suppurative: Rheumatic fever and acute glomerulonephritis following infection. • Treatment and Management: • Typically sensitive to penicillin; antibiotic treatment is effective for most acute infections. • Post-infection sequelae require long-term management and can lead to chronic conditions. • .
  • 13. Data obtained from a Centers for Disease Control and Prevention Active Bacterial Core Surveillance Report for group A streptococcal Who is at Risk for Infection?
  • 14. Clinical conditions 1. Pyogenic – Pharyngitis, tonsillitis, peritonsillar abscess, sinusitis, otitis media, impetigo, wound infection, osteomyelitis, septic arthritis, puerperal sepsis, bacteraemia, acute bacterial endocarditis 2. Toxigenic(exotoxins) – Scarlet fever – Streptococcal toxic shock syndrome 3. Immune-mediated: non-suppurative – Occurs after repeated infections – AGN- Acute glomerulonephritis-follows skin – ARF- Acute rheumatic fever. Cross reactivity of the antibodies produced during streptococcal pharyngitis, cross react with antigens in heart muscle
  • 17. Strep throat  - hemolytic - Group A (GAS) streptococci: S. pyogenes Droplet Transmission Symptoms: Sore throat, high fever, coughing, otitis media may also occur
  • 18. Complications of Strep Throat S. pyogenes causes two major autoimmune complications (antibodies cross-react) 1. Acute rheumatic fever: Short period of arthritis and fever followed in  50% of affected by rheumatic heart disease  heart valve damage  chronic valvular disease (stenosis and/or incompetence)  heart failure and/or subacute bacterial endocarditis 2. Acute poststreptococcal glomerulonephritis
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  • 20. Laboratory diagnosis • Specimen: Throat swabs, pus swabs, blood, CSF etc • Direct Gram stain- Gram-positive cocci in chains, pus cells • Culture: – BA, aerobically, 37°C for 18-24 hours – Smooth circular colonies of 2-3 mm diameter, β- haemolysis • Gram-positive cocci in chains • Catalase negative • Bacitracin sensitive
  • 21. Treatment and Prevention Treatment – Cephalosporins – Tetracyclines – Erythromycin – Chloramphenicol Prevention – Infection control – Treat pharyngitis as early as possible to prevent ARF – No vaccine
  • 22. VACCINES • Research focuses on M protein-based, multivalent, recombinant, and universal antigen vaccines for broad immunity. • Clinical trials underway; major challenges include preventing autoimmune reactions and ensuring global vaccine accessibility. 22
  • 23. Group B Streptococci(GBS) Streptococcus agalactiae • Classification: Belongs to Group B of the Lancefield classification. • Morphology: Gram-positive cocci, usually in chains. • Habitat: Colonizes the gastrointestinal and genitourinary tracts of humans. • Virulence Factors: Capsular polysaccharide, C5a peptidase, hemolysins, and sialic acid-rich surface proteins contribute to its evasion of the immune system and pathogenicity.
  • 24. Clinical manifestations • Pathogenicity: • In Neonates: Leading cause of neonatal sepsis, meningitis, and pneumonia. • In Adults: Can cause urinary tract infections, skin and soft-tissue infections, and, in pregnant women, chorioamnionitis and postpartum infections. Early onset neonatal disease(1st 7 days of life)- – Vertical transmission in utero or at time of delivery Late onset(7-90 days)- nosocomial/vertical
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  • 27. Lab diagnosis – Group B Streptococci • Specimens: CSF, blood, vaginal smears, urine • Microscopy :Gram stain - GPC in chains • Culture: BA - beta hemolytic colonies • Identification tests – Catalase negative – Bacitracin resistance – CAMP Test + – Penicillin sensitive P B
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  • 29. VACCINE 2 Group B streptococcal vaccine - This vaccine is currently under development
  • 31. INTRODUCTION: • Common name Pneumococcus. • Has over 100 Serotypes • Normal inhabitants of the upper respiratory tract of human beings. • Gram positive small(1μm), slightly elongated cocci, with one end broad & other end pointed, presenting a flame shaped or lanceolate appearance.
  • 32. Disease: 1. Otitis media & sinusitis 2. Pneumonia a. Lobar pneumonia b. Bronchopneumonia 3. Tracheobronchitis 4. Meningitis 5. Other infections- empyema, pericarditis, conjunctivitis, suppurative arthritis & peritonitis.
  • 33. 33 Marianne W. Mureithi, et al; T Cell Memory Response to Pneumococcal Protein Antigens in an Area of High Pneumococcal Carriage and Disease, The Journal of Infectious Diseases, Volume 200, Issue 5, 1 September 2009, Pages 783– 793, https://doi.org/10.1086/605023 MOC Ota,, MW Mureithi, et al: Antibody and T-cell responses during acute and convalescent stages of invasive pneumococcal disease Adam Finn, Marianne W. Mureithi, et al. Evolution of Naturally Acquired T-Cell Immunity to Pneumococcal Protein Antigens in Infants from an Area of High Pneumococcal Carriage & Disease. Infectious Diseases Society of America (IDSA) 2008
  • 34. Virulence • Capsular polysaccharide- antiphagocytic • IgA1 protease • Pneumolysins – Slows ciliary beating – Toxic to pulmonary endothelial cells – Spread of organism from alveoli into bloodstream • Autolysin – Breaks the peptide cross-linking of the cell wall peptides leading to cell lysis
  • 35. 35 Lab diagnosis • Specimen: CSF, blood, sputum, pus, swabs • Microscopy: Gram stain – GPC in pairs, capsulated, lanceolate shaped • Culture – BA – alpha hemolytic colonies • Identification tests – Catalase –ve – Optochin sensitive – Bile solubility – Quellung reaction
  • 36. Optochin sensitivity: Sensitive. Quellung( capsular swelling ) reaction Bile Solubility
  • 37. Treatment and Prevention Treatment • Penicillins, ampicillin- resistance increasing • Ceftriaxone, cefotaxime, carbapenems, fluoroquinolones, erythromycin, chloramphenicol, vancomycin Prevention • Vaccine
  • 38. Conjugate Vaccine • A new generation of pneumococcal vaccines • Coating removal of the capsular polysaccharide • 7 (9, 11 or 13) types of saccharide is separately activated and conjugated to protein carrier • CDC recommended PVC vaccine schedule: 2mo, 4mo, 6mo, 12-15mo, 65years
  • 39. LATEST NEWS • FDA Approval: PREVNAR 20™, a 20-valent pneumococcal conjugate vaccine by Pfizer, approved by the U.S. FDA. • Coverage: Provides protection against 20 serotypes of pneumococcus responsible for most invasive pneumococcal disease and pneumonia. • Significance: Includes seven serotypes linked to 40% of pneumococcal disease • Advancement: Represents a significant advancement in pneumococcal disease prevention, offering broader protection than previously available vaccines. 40
  • 41. Viridans Streptococci • Normal flora of oral cavity, nasopharynx, genital tract and skin • S.mitis • S.mutans • S.milleri • S.salivarius • S.sanguis unique ability to synthesize dextrans from glucose, which allows them to adhere to fibrin-platelet aggregates at damaged heart valves. extraction).
  • 42. Clinical manifestations • Dental caries • Gingivitis, pyogenic oral infections • Subacute bacterial endocarditis • Brain abscesses, abdominal abscesses
  • 43. Laboratory diagnosis • Specimen: blood, pus • Gram stain- Gram-positive cocci in chains • Culture on BA – Incubate in air at 37°C for 18-24 hours • Biochemical tests – Catalase negative – Optochin resistant – bile insoluble • Molecular studies e.g. PCR
  • 44. Treatment • Prophylaxis to patient at risk during dental surgery • Penicillin and other β-lactam • Ampicillin and Gentamicin • Vancomycin- for penicillin allergies
  • 46. 47 Group D Streptococcus- Gamma Hemolytic Normal flora in GIT, lower genital tract Nosocomial / opportunistic pathogen Enterococcus – 2 imp. species E. fecalis E. faecium UTI, wound infection, endocarditis Resistance to cephalosporins, even vancomycin 1
  • 47. Points to Remember/Conclusion • Diversity and Classification: Streptococci, a diverse genus of Gram- positive bacteria, classified by hemolysis, Lancefield groups. • Major Pathogens: Includes Group A (S. pyogenes) causing rheumatic fever, and Group B (S. agalactiae) linked to neonatal sepsis. • Virulence & Diseases: Equipped with virulence factors (e.g., M protein, hyaluronic acid) causing diseases from pharyngitis to severe infections. • Diagnosis & Treatment: Diagnosed via culture, antigen detection; treated with antibiotics, with emphasis on resistance management. • Prevention & Research: Hygiene, antibiotics, pneumococcal vaccines critical; ongoing research into GAS vaccines and new treatments. • Global Impact: significant health challenge, requiring ongoing vigilance and innovative control strategies.