The Staphylococci
← Back 📖 Definitions 🏠 All Units
⭐⭐ HIGHEST YIELD ★★★
Pathogenic Bacteria · Unit 8 of 28

The Staphylococci

TMU Lecture 8 — Pathogenic Cocci, 57 slides (part 1 of 2) ⭐ Owns SPA (2020 term, 4 marks) AND the 2019 S. aureus brief answer (7 marks) — 11 marks across two papers The lecture's own summary slide sets both questions
01

The pyogenic cocci ★★★

Most cocci are not associated with human disease. A minority cause human infectious disease, and these are the pathogenic cocci. Because the diseases they cause usually belong to pyogenic infection — pus-generating — they are also called pyogenic cocci.

⭐ The five species — memorise this list

Gram-positive cocciGram-negative cocci
Staphylococcus aureusNeisseria meningitidis
Streptococcus pyogenesNeisseria gonorrhoeae
Streptococcus pneumoniae
⭐ The lecture sets this question itself
“Make a list of all the pyogenic cocci (5 species), and indicate the virulence factors and diseases which each one is often associated with.”TMU Lecture 8 summary slide
This is the parent of the 2019 Section III question on S. aureus, and it could equally be set on any of the other four. The five species are in the table above; this unit answers it for S. aureus and Unit 9 for the remaining four.

Note the qualifier in the lecture's own wording: “only the name of virulence factors and diseases”. Lists, not essays.
TMU Microbiology Lecture 8 — Pathogenic Cocci summary slide · 2019 Microbiology paper, Section III
Test yourself
  • Why are pathogenic cocci also called pyogenic cocci? → The diseases they cause are usually pyogenic — pus-generating
  • Name the five pyogenic cocci. → G+: Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae. G−: Neisseria meningitidis, Neisseria gonorrhoeae
02

Biological characteristics ★★★

The staphylococci exist widely in nature, and humans are the most common carriers — we carry them in the nose, throat and on the skin surface. Three species matter: S. aureus, S. epidermidis and S. saprophyticus.

FeatureDetail
Size0.5–1.5 µm in diameter
ShapeRound
ArrangementGrape-like clusters
StainingGram-positive
CultivationDetail
Nutrient requirementLow — grows very well in basic media
OxygenFacultative anaerobe
Conditions37 °C, pH 7.4
Colony1–2 mm, circular, smooth, shiny surface, opaque
PigmentVarious liposoluble pigments; S. aureus colonies appear golden yellow
On blood agarS. aureus usually forms complete haemolysis (β-haemolysis)

⭐ The catalase test

Catalase test: positive2H₂O₂ → 2H₂O + O₂. Its purpose is to differentiate the staphylococci (positive) from the streptococci (negative).

Resistance to the environment

Detail
Resistant toDrying · heat (60 °C for 1 h, 80 °C for 30 min) · high salt concentration (10–15%)more resistant than other non-spore-forming bacteria
Sensitive toBasic dyes (crystal violet) · antibiotics (penicillin, vancomycin)
MRSA — and why salt tolerance matters

In recent years more and more drug-resistant strains have emerged. MRSA (methicillin-resistant S. aureus) is the most common in nosocomial infection. Nosocomial infection was defined in Unit 6 §6 — hospital-acquired — and MRSA is its emblem.

The salt tolerance is not a laboratory curiosity either. Tolerating 10–15% NaCl is precisely what allows S. aureus to live on salty human skin, where sweat concentrates as it evaporates. It is also the basis of mannitol-salt agar, the selective medium that grows staphylococci while suppressing almost everything else — and, since S. aureus ferments mannitol and the other two do not, identifies the pathogen in the same step.

One environmental property; one ecological niche and one culture medium.

Test yourself
  • Describe staphylococcal morphology. → Gram-positive, round, 0.5–1.5 µm, in grape-like clusters
  • Culture characteristics? → Low nutrient requirement, facultative anaerobe, 37 °C, pH 7.4; 1–2 mm circular smooth shiny opaque colonies; S. aureus golden yellow with β-haemolysis
  • What does the catalase test distinguish? → Staphylococci (positive) from streptococci (negative)
  • What is S. aureus resistant to? → Drying, heat (60 °C/1 h, 80 °C/30 min), 10–15% salt — more than other non-spore formers
  • What is MRSA and why does it matter? → Methicillin-resistant S. aureus, the commonest organism in nosocomial infection
03

⭐ SPA — Staphylococcal Protein A ★★★

SPA (staphylococcal protein A) — the 2020 Section I term

A surface protein of Staphylococcus aureus, covalently bound to the peptidoglycan, which combines non-specifically with the Fc fragment of IgG.

Functions

As a virulence factorAs a reagent
Anti-phagocytosisCoagglutination test
Damages platelets
Activates B cells
Induces hypersensitivity and inflammation
⭐ The 2020 Section I term
“Staphylococcal Protein A (SPA)”4 marks, 2020 Section I
A surface protein of S. aureus, covalently bound to the peptidoglycan of the cell wall, which binds non-specifically to the Fc fragment of IgG.

Then the four functions for the remaining marks: it is a virulence factoranti-phagocytic, it damages platelets, activates B cells, and induces hypersensitivity and inflammation. And its laboratory use: the coagglutination test.

Do not stop at “a surface protein” — the Fc-binding and the anti-phagocytic consequence are what the four marks are for.
2020 Microbiology paper, Section I · TMU Microbiology Lecture 8 — Pathogenic Cocci
Binding IgG backwards is the whole trick

An antibody has two ends. The Fab arms grip the antigen; the Fc stem is the handle that a phagocyte's Fc receptor grabs in order to eat the target. That handle is what opsonisation means.

SPA binds the Fc end. So antibody coats S. aureus the wrong way round — Fab arms pointing outward into space, Fc stems buried against the bacterium. There is no handle left for the neutrophil to grab.

Hence anti-phagocytosis, and hence, in Unit 5's framework, mechanisms for escaping elimination by host defences.

The coagglutination test is the same property turned into a reagent: coat SPA-bearing staphylococci with an antiserum, the Fc ends stick to the bacteria and the Fab arms all point outward — a ready-made particle that clumps visibly the moment it meets its antigen. The bacterium's defence becomes the laboratory's tool.

Test yourself
  • Define SPA. → A surface protein of S. aureus, covalently bound to the peptidoglycan, binding non-specifically to the Fc fragment of IgG
  • Name its four functions as a virulence factor. → Anti-phagocytosis · damages platelets · activates B cells · induces hypersensitivity and inflammation
  • What is its laboratory use? → The coagglutination test
  • Why does Fc binding block phagocytosis? → It coats the organism with antibody the wrong way round, leaving no Fc handle for the phagocyte's Fc receptor
04

The three species compared ★★★

Classification is based on the pigments and chemical reactions — more than 30 species. Three matter clinically, and this table separates them.

PropertyS. aureusS. epidermidisS. saprophyticus
PigmentGold-yellowWhiteCitrine
Coagulase+
Mannitol+
Thermostable nuclease+
α-haemolysin+
SPA+
PathogenicityPotentWeakWeak

There is a second, simpler classification based on coagulase: coagulase-positive staphylococci — S. aureus; and coagulase-negative staphylococci — S. epidermidis and S. saprophyticus.

Test yourself
  • Name the three species and their pigments. → S. aureus gold-yellow · S. epidermidis white · S. saprophyticus citrine
  • Which five tests are positive only in S. aureus? → Coagulase, mannitol, thermostable nuclease, α-haemolysin, SPA
  • What is the coagulase-based classification? → Coagulase-positive (S. aureus) vs coagulase-negative (S. epidermidis, S. saprophyticus)
05

⭐ Virulence factors of S. aureus ★★★

Half of the 2019 seven-mark question. The lecture groups them in three: invasiveness — surface structures and enzymes — and toxins.

GroupFactors
Invasiveness — surface structureSPA, and others
Invasiveness — enzymesCoagulase · hyaluronidase · thermostable nuclease · staphylokinase
Toxins (exotoxins)Staphylolysin · leukocidin · staphylococcal enterotoxin · toxic shock syndrome toxin-1 (TSST-1) · exfoliatin

⭐ Coagulase — the most examinable enzyme

Coagulase

An enzyme that converts soluble fibrinogen into fibrin, causing coagulation of blood or plasma.

Detail
ClassificationFree coagulase — an extracellular enzyme · bound coagulase — bound to the surface of cells
RolesFibrin-coated bacteria and bacterial clumps inhibit phagocytosis and reduce the damage from antibacterial substances in the body · form a limited abscess
Laboratory useThe major criterion for differentiating potentially pathogenic staphylococci

The other enzymes

EnzymeAction
HyaluronidaseHydrolyses hyaluronic acid
Thermostable nucleaseDegrades DNA
StaphylokinaseDissolves fibrin clots

The five toxins

ToxinRole
StaphylolysinDamages host cell membranes; cytotoxic to phagocytes and tissue cells. Several kinds — α-lysin is the main pathogenic substance and causes the haemolysis ring around the colony; also β, γ and δ
LeukocidinLyses neutrophils and macrophages by damaging cell membranes
Staphylococcal enterotoxinProtein, heat-stable (100 °C for 30 min), resistant to proteolytic enzymes. Causes staphylococcal food poisoning and colitis with severe vomiting and diarrhoea, by acting on the CNS vomiting-control centre. Acts as a superantigen
TSST-1Causes toxic shock syndromea multisystem disease with high fever, shock and multi-organ failure. Increases the host's sensitivity to endotoxin. Death from profound shock, respiratory failure and DIC
ExfoliatinCauses blistering of the skin, associated with SSSS (staphylococcal scalded skin syndrome) in infants and young children. Erythema → denuding of skin. Mortality is low
Coagulase and staphylokinase do opposite things — deliberately

One enzyme makes fibrin; another dissolves it. That is not sloppiness, it is sequence.

Coagulase first. Clotting the plasma around itself walls the organism off from neutrophils and from antibiotics, and the result is the characteristic staphylococcal lesion: a localised abscess with thick pus. This is why staphylococcal infection is a boil, sharply demarcated, rather than the spreading cellulitis of a streptococcus — which, as Unit 9 shows, makes streptokinase and hyaluronidase instead.

Staphylokinase later. Having built the abscess and multiplied inside it, the organism dissolves the fibrin and escapes to seed elsewhere — osteomyelitis, endocarditis, septicaemia.

Build the fortress, then break out of it. Two enzymes, one strategy.

Test yourself
  • Name the three groups of S. aureus virulence factors. → Surface structures (SPA) · enzymes · toxins
  • Name the four enzymes. → Coagulase, hyaluronidase, thermostable nuclease, staphylokinase
  • Define coagulase and state its roles. → Converts soluble fibrinogen to fibrin; free and bound forms; fibrin coating inhibits phagocytosis and forms a limited abscess; the major criterion for identifying pathogenic staphylococci
  • Name the five toxins. → Staphylolysin, leukocidin, enterotoxin, TSST-1, exfoliatin
  • Which toxin is heat-stable, and what does it cause? → Staphylococcal enterotoxin (100 °C for 30 min); food poisoning and colitis with severe vomiting and diarrhoea, by acting on the CNS vomiting centre; a superantigen
  • What does TSST-1 do? → Causes toxic shock syndrome — high fever, shock, multi-organ failure; increases sensitivity to endotoxin; death from shock, respiratory failure and DIC
06

⭐ Diseases of S. aureus ★★★

The other half of the 2019 question. The lecture divides them in two, and that division is itself worth a mark.

GroupDiseases
Invasive / pyogenic infectioncharacterised by abscess formationLocal (skin) infectionhair folliculitis · boil (furuncle) · carbuncle · impetigo. Characteristics of the local abscess: thick pus, limited local area — related to the action of coagulases
Organ infectionpneumonia, meningitis
Systemic infectionsepticaemia
Toxin-associated diseaseFood poisoning (enterotoxin) · TSS — toxic shock syndrome (TSST-1) · SSSS — staphylococcal scalded skin syndrome (exfoliatin)
⭐ The 2019 Section III brief answer, assembled
“Please describe the virulence factors and the diseases caused by Staphylococcus aureus.” (7 marks, 2019 Section III)
Answer in two halves, each as a labelled list.

Virulence factors. Surface structureSPA (binds IgG Fc, anti-phagocytic). Enzymescoagulase (fibrinogen → fibrin, anti-phagocytic, localises the abscess), hyaluronidase, thermostable nuclease, staphylokinase. Toxinsstaphylolysin (α-lysin the main one), leukocidin, enterotoxin, TSST-1, exfoliatin.

Diseases, in two groups. Invasive/pyogenic, with abscess formationlocal: folliculitis, boil, carbuncle, impetigo; organ: pneumonia, meningitis; systemic: septicaemia. Toxin-associatedfood poisoning (enterotoxin), toxic shock syndrome (TSST-1), scalded skin syndrome (exfoliatin).

Pair each toxin-associated disease with its toxin in brackets. That single habit shows the examiner you know which factor causes which disease, rather than having memorised two separate lists.
2019 Microbiology paper, Section III · TMU Microbiology Lecture 8 — Pathogenic Cocci
Test yourself
  • How are S. aureus diseases divided? → Invasive/pyogenic (abscess-forming) and toxin-associated
  • Name four local skin infections. → Hair folliculitis, boil (furuncle), carbuncle, impetigo
  • What characterises the local abscess, and why? → Thick pus in a limited local area — due to coagulase
  • Name the three toxin-associated diseases and their toxins. → Food poisoning (enterotoxin), toxic shock syndrome (TSST-1), scalded skin syndrome (exfoliatin)
07

Laboratory diagnosis and control ★★

StepDetail
SpecimenDirect smear and Gram stain
IsolationBlood agargold-yellow pigmentation, β-haemolysis
IdentificationCoagulase test · catalase test
ThenAntibiotic susceptibility tests
ControlDetail
TreatmentAntibiotics, based on the drug sensitivity test
PreventionProper personal hygiene, sanitary procedures and aseptic measures · identifying and treating carriers as soon as possible
Test yourself
  • Outline the laboratory diagnosis of S. aureus. → Direct smear and Gram stain → isolation on blood agar (gold-yellow pigment, β-haemolysis) → coagulase and catalase tests → antibiotic susceptibility test
  • How is it controlled? → Antibiotics guided by sensitivity testing; personal hygiene, sanitary and aseptic measures; identifying and treating carriers early
08

Revision

The two tests that decide everything

TestSeparates
CatalaseStaphylococci (+) from streptococci (−)
CoagulaseS. aureus (+) from the coagulase-negative staphylococci (−)

The whole unit on one screen

QuestionAnswer
Five pyogenic cocci?S. aureus · S. pyogenes · S. pneumoniae · N. meningitidis · N. gonorrhoeae
Morphology?G+, round, 0.5–1.5 µm, grape-like clusters
Colony?1–2 mm, circular, smooth, shiny, opaque; gold-yellow, β-haemolysis
Resistance?Drying · 60 °C/1 h, 80 °C/30 min · 10–15% salt
⭐ SPA?Surface protein bound to peptidoglycan, binds IgG Fc; anti-phagocytic, damages platelets, activates B cells, induces hypersensitivity; coagglutination test
Enzymes?Coagulase · hyaluronidase · thermostable nuclease · staphylokinase
Toxins?Staphylolysin (α main) · leukocidin · enterotoxin · TSST-1 · exfoliatin
Pyogenic diseases?Folliculitis, boil, carbuncle, impetigo · pneumonia, meningitis · septicaemia
Toxin diseases?Food poisoning · TSS · SSSS
MRSA?Methicillin-resistant S. aureus — commonest in nosocomial infection
Test yourself — the whole unit
  • Answer the 2019 question in full. → Virulence: SPA; coagulase, hyaluronidase, thermostable nuclease, staphylokinase; staphylolysin, leukocidin, enterotoxin, TSST-1, exfoliatin. Diseases: pyogenic (folliculitis, boil, carbuncle, impetigo; pneumonia, meningitis; septicaemia) and toxin-associated (food poisoning, TSS, SSSS)
  • Define SPA for 4 marks. → Surface protein of S. aureus covalently bound to peptidoglycan, binding non-specifically to the Fc fragment of IgG; anti-phagocytic, damages platelets, activates B cells, induces hypersensitivity; used in the coagglutination test
  • Which two tests identify S. aureus? → Catalase (staph vs strep) and coagulase (S. aureus vs the coagulase-negative species)
  • Why does S. aureus form a localised abscess? → Coagulase converts fibrinogen to fibrin, walling the lesion off and inhibiting phagocytosis