G - Streptococcus
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Transcript of G - Streptococcus
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Streptococcus
J. Walter Sowell, R.Ph., Ph.D.
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G2
General Characteristics of Genus
Diverse group of gram-positive cocci which grow
in chains in broth or individually, in pairs, or as
short chains on solid media
Some Streptococcus have capsules
Streptococcus pyogenes
Streptococcus pneumoniae Most species are facultative anaerobes but a few
range from anaerobic to capnophilic (requires
carbon dioxide)
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G3
General Characteristics of Genus
Energy is derived by carbohydrate fermentation
with lactic acid production
Unlike Staphylococci, this genus is catalase
negative
Preliminary laboratory identification is based on
hemolytic reactions on 5% sheep blood agar plates
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G4
Beta-Hemolytic Streptococci
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G5
Serologic Classification for
Streptococcus species
Rebecca Lancefield (1933) developed technique
Based on immunoassay of group antigen in cell wall
Within cell wallGroup specific and Type-specific antigens
Group antigen = N-acetylglucosamine-Rhamnose
Group A Streptococci
Group antigen = Glucosamine polysaccharide-Rhamnose
Group B Streptococci
Group antigen = N-acetylgalactosamine ±Rhamnose
Group C Streptococci
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G6
Importance of Lancefield
Classification Rapid identification of pathogenGroup
antigen within the cell wall
Immunoassay from a throat
swabQuick way to identify
Streptococcus pyogenes as the
pathogen in pharyngitis
Often used in physician¶s offices or the
hospital to identify pathogen
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G7
Limitation of Lancefield
Classification
Many species of Streptococci lack a group
antigen Require other biochemical tests for
identification
Lancefield classification used for a few
species
Group A, B, C, F, and G
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G8
Streptococcus pyogenes (Group A)
General Characteristics/Classification
Possesses a specific carbohydrate antigen inthe cell wall called the C antigen.
This antigen is used to separate the various
species of Streptococcus into multiple groups:
A,B
, C, D, F, andG
Serological Classification ± Group A
Hemolytic Pattern ± Beta hemolytic
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G9
S. pyogenes
General Characteristics (cont¶)
M protein, a major surface antigen, is presenton the fimbriae of this pathogen
Subdivides Group A into multiple immunologic
types100+
Clinical importance?? Differ serotypes areassociated with causing disease. It is type specific.
Serves as a basis for preventing reinfection
Antiphagocytic
Immunity is type specific (based on M protein)
Important in epidemiological studies
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G10
S. pyogenes
Habitat ± lives on human skin and mucous
membranes Transmission
> Respiratory tract droplets from a carrier
> Fomites (pens, paper, drinking glasses)
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G11
S. pyogenes ± Virulence Factors
Structural Components
Capsule Some strains have a hyaluronic acid capsule
Nonimmunogenic and antiphagocytic
Hyaluronic acid is an important component of
connective tissue
Capsule is recognized as natural by the immune system
Encapsulated strains more likely to cause severe
systemic infections
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G12
S. pyogenes ± Virulence Factors
Structural Components (cont¶)
M Protein
The M protein on fimbriae serves as a major surface antigen and serves as the basis for thesubdivision within Streptococcus pyogenes
It is antiphagocytic and serves to degrade one of
the components of complement F Protein
May participate in tight binding of the pathogen tothe epithelial cells of the throat and skin
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G13
S. pyogenes ± Virulence Factors
Enzymes Secreted by the Pathogen
Streptolysin O (oxygen labile) Antigenic ± Antibodies formed against this
antigenhelpful when testing for a recent infection
by this pathogen
Antibodies against Streptolysin O (ASO) appear 3 to 4
weeks after initial infection and persist
Lyses blood cells (WBC, R BC, platelets)
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G14
S. pyogenes ± Virulence Factors
Enzymes Secreted by the Pathogen (cont¶)
Streptolysin S (oxygen stable) Nonantigenic
Lyses blood cells (WBC, R BC, platelets)
Streptokinase
Lyses blood clots Dissemination factor
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G15
S. pyogenes ± Virulence Factors
Enzymes Secreted by the Pathogen (cont¶)
DNases A
D Lyses DNA
Dissemination factor
Pus, which contains DNA, is more fluid with
Streptococcus infections in comparison toStaphylococcus infections
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G16
S. pyogenes ± Virulence Factors Streptococcal Pyrogenic Exotoxins
(previously called Erythrogenic Toxins)
Four types (Toxin A, B, C, and F)
Possibly responsible for clinical manifestations seen in
severe reactions
Rash in Scarlet fever
Necrotizing fasciitis
Streptococcal toxic shock syndrome
Phage mediated
Toxins are classified as a superantigen
Bridge Macrophages to Helper T cells
Hyper response of the immune system
shock, organfailure and death
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G17
Streptococcus pyogenes-CDC In 2005, CDC reports that 4700 cases of
invasive disease in the U.S.
Perhaps, 10 million cases of noninvasivedisease, mostly pharyngitis and pyoderma
Pharyngitis caused by Streptococcus
pyogenes is most often seen in children, ages
5 to 15 years, but certainly not limited to this
age range.
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G18
S. pyogenes ± Suppurative Diseases
Pharyngitis (³Strep Throat´)
Fever, sore throat, redness, and edema of the mucous
membranes, purulent exudates, and enlargement of the cervical lymph nodes
May extend to middle ear, mastoid, and meninges
Pyoderma (Impetigo) ± Vesicles Pustules (pus
filled) Rupture Crust
Puerperal Sepsis ± postpartum infection of uterus
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G19
S. pyogenes ± Suppurative Diseases
Cellulitis of skin
Involves deeper subcutaneous tissue withrapid spread
Often the result of damage to skin (burn or wound)
Post-surgical WoundI
nfection ± Onset of symptoms of infection occur rapidly (6-12hours), while 48 hours or longer withStaphylococcus aureus
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G20
S. pyogenes ± Suppurative Diseases Scarlet Fever
Complications of pharyngitis
Rash caused by pyrogenic exotoxins Within a couple of days after initial symptoms
of pharyngitis, a red rash appears on upper chest
and spreads to extremities
Erysipelas ± rash on skin as a complication of
pharyngitis
Pneumonia
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G21
S. pyogenes ± Suppurative Diseases Necrotizing fasciitis(Streptococcal gangrene)
An infection that occurs in the deep
subcutaneous tissue
Very rapid movement
³Flesh eating bacteria´ that causes death to
fascia and destruction to muscle and fat
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G22
S. pyogenes ± Suppurative Diseases
Streptococcal Toxic Shock Syndrome
Typically occurs in association withnecrotizing fasciitis or bacteremia
Rapidly progresses to shock and death due to
organ failure (kidneys, lungs, liver, heart)
See Clinical Case 22-1 of Textbook-Page 231(Note how rapidly this patient declined!!)
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G23
Erysipelas Necrotizing fasciitis
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G25
S. pyogenes ± Nonsuppurative Diseases
Acute Glomerulonephritis
Associated with untreated skin or respiratory tract
infections caused by nephritogenic strains of S. pyogenes, Group A
Onset of symptoms may be as short as one week after infection
Evidence strongly support a Type III hypersensitivity
reaction, where the antigen-antibody complex istrapped in the glomerular membranes
Symptoms include hypertension, edema, BUN, serum creatinine, blood and protein in urine
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G26
S. pyogenes ± Nonsuppurative Diseases
Acute Rheumatic Fever
Greatly reduced incidence in U.S. (only 112 cases in 1994)
Far more prevalent in developing countries
Associated with untreated upper respiratory tract infections,usually pharyngitis
Onset of symptoms 14 weeks post S. pyogenes infection
M protein of the pathogen shares some common structural
features with certain cardiac tissue. M protein serves as anantigen which induces antibody formation. A Type II
hypersensitivity reaction may occur with the antibody
binding to cardiac tissue, causing inflammation and cardiac
damage
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G27
S. pyogenes ± Diagnosis Rapid antigen detection from specimen
Release the C antigen by enzymatic or chemicalmeans
Detection of the C antigen with ELISA or latexagglutination
If rheumatic fever is suspected, high ASO titers(Antibody to Streptolysis O) would confirm arecent Streptococcus pyogenes infection
If acute glomerulonephritis is suspected, highanti-DNase B titers would confirm a recent
Streptococcus pyogenes skin infection
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G28
Streptococcus agalactiae (Group B) General Characteristics/Classification
Serological classification ± Group B
Hemolytic pattern ± beta hemolytic, but narrowzone
Growth pattern ± short chainslong chains
Habitat ± GI
and female genital tracts Transmission ± Can be transmitted to unborn,
in utero, or to newborn during birth
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G29
Streptococcus agalactiae (Cont¶d) Early-Onset Neonatal
Birth1st week of life
Bacteremia, pneumonia,
or meningitis Mortality rate-5% or so
Meningitis survival-
Significant neurological
effects (blindness,deafness, mental
retardation)
Late-Onset Neonatal
One week 3 months
Bacteremia with
meningitis
Neurological effects
high with meningitis
See Case 22-2-p 235
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G30
S. agalactiae - Diseases
Adults
After deliver, the pathogen can cause
endometritis . Pathogen may cause UTI
Older adults with compromised immunity
Bacteremia, bone and joint, skin and soft-tissue,
pneumonia Mortality rate fairly high