Staphylococcus and Micrococcus Flashcards

In taxonomy, the term "aureus" is derived from Latin and means "golden."

1
Q

Briefly describe important characteristics of the Staphylococcus genus.

A

◾ Gram positive cocci arranged in irregular grapelike clusters
◾ Commensals on the skin and mucous membranes of humans
◾ Catalase-positive

[Image 1] [Image 2]

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2
Q

How are Staphylococci clinically grouped?

A

Staphylococci are clinically grouped into two categories:
(i) Coagulase positive Staphylococci
(ii) Coagulase negative Staphylococci

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3
Q

Name one coagulase positive species of Staphylococcus.

A

Staphylococcus aureus

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4
Q

Name two coagulase negative Staphylococcus species.

A

S. epidermidis and S. saprophyticus

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5
Q

How is S. aureus transmitted from person to person?

A

direct contact, fomites

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6
Q

List pyrogenic exotoxins produced by S. aureus.

A

◾ Enterotoxins (A-F)
◾ Toxic shock syndrome toxin-1 (TSST-1)
◾ Epidermolytic toxins A and B

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7
Q

Briefly discuss how the following contribute to pathogenicity of S. aureus.
(a) Protein A
(b) Teichoic acids
(c) Capsule

A

(a) Protein A: binds to the Fc region of immunoglobulin G (IgG) antibodies. It thus prevents opsonization and phagocytosis.
(b) Teichoic acids: Teichoic acids can trigger an immune response in the host, leading to inflammation. They are also capable of producing septic shock, contributing to the severity of infections caused by S. aureus.
(c) Capsule: it is antiphagocytic

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8
Q

Briefly discuss 7 enzymes that facilitate invasiveness of S. aureus.

A

(a) coagulase: converts fibrinogen to fibrin, leading to clot formation. The clots enable S. aureus to evade the host immune system by creating a protective barrier around the bacteria, preventing phagocytosis and immune detection.

(b) haemolysins: these lyse red blood cells. The lysis of red blood cells results in release of nutrients such as iron, which are essential for bacterial growth.

(c) leukocidin: targets and destroys white blood cells.

(d) fibrinolysin [aka. staphylokinase]: dissolves fibrin clots. This allows S. aureus to spread from the initial site of infection to other parts of the host.

(e) lipase: breaks down lipids. This enables S. aureus to colonize and invade fatty tissues such as the skin and sebaceous glands.

(f) hyaluronidase: breaks down hyaluronic acid, a component of the extracellular matrix. This facilitates the spread of S. aureus through connective tissues.

(g) β-Lactamase: breaks down β-lactam antibiotics, such as penicillin.

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9
Q

Explain how the following contribute to the pathogenicity of staphylococcus aureus.
(a) biofilms
(b) small-colony variants
(c) chemotaxis inhibitory protein

A

(a) biofilms: these are structured communities of bacteria encased in a self produced extracellular matrix. They protect S. aureus from host defenses and antimicrobial agents, making infections difficult to treat.
(b) small-colony variants: these are a subpopulation of bacteria with a slow-growing phenotype. SCVs are associated with persistent and recurrent infections. They can survive in hostile environments, such as within host cells, and are often less susceptible to antibiotics, contributing to the chronic nature of some S. aureus infections.
(c) chemotaxis inhibitory protein: inhibits the chemotaxis of immune cells, such as neutrophils, to the site of infection

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10
Q

Outline clinical features of Staphylococcal infection.

A

(1) Pyogenic diseases
Local lesions of skin: impetigo, furuncles (boils) and carbuncles (boils clustered together), folliculitis, eyelid infection (styes)
Deep infections: septicemia, endocarditis, osteomyelitis, arthritis, post-surgical wound infections

(2) Toxin-mediated diseases
(a) Gastroenteritis
Due to ingestion of preformed toxin in food.
Patients present with vomiting and water non-bloody diarrhea which resolves within 24 hours.

(b) Toxic shock syndrome
Mediated by TSST-1.
Characterised by fever, erythematous skin rash, desquamation of the palms of the hands and the soles of the feet and shock.

(c) Staphylococcal scalded skin syndrome (SSSS)
Mediated by exfoliative or epidermolytic toxin-characterized by fever, and large erythematous rash that sloughs off the body.

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11
Q

What specimens are used in the laboratory testing of S. aureus infection?

A

Pus and swabs from infected sites, sputum, blood, nasal swabs from carriers

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12
Q

What is the clonal morphology when S. aureus is cultured on:
(a) blood agar
(b) mannitol salt agar

A

(a) blood agar: Golden-yellow colonies with beta-hemolysis (clear zones around the colonies) [Image 1]
(b) mannitol salt agar: yellow colonies [Image 2]

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13
Q

Explain what would be observed if MacConkay agar is inoculated with S. aureus.

A

Colonies of S. aureus would not be observed.
Reason: MacConkey agar is selective for Gram-negative bacteria and inhibits the growth of Gram-positive bacteria

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14
Q

What are the appropriate growth conditions when culturing S. aureus?

A

Temperature: 37°C
Duration: 12 - 18 hours
Incubate in air.

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15
Q

What is one advantage of using mannitol salt agar over blood agar in the culturing of S. aureus?

A

Mannitol salt agar contains a high concentration of salt (7.5% NaCl), which inhibits the growth of most bacteria except for staphylocci. This makes it highly selective for S. aureus.

Blood agar supports the growth of a wide range of bacteria, making it less selective.

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16
Q

What biochemical tests can be used in the identification of S. aureus?

A

(a) Catalase test: This test will differentiate Staphylococcus species from Streptococcus species. Staphylococcus species produce catalase (catalase positive), while Streptococcus species do not.
[Procedure & Observation: Place a drop of hydrogen peroxide on a glass slide. Using a sterile loop, transfer a small amount of the bacterial colony to the drop. Immediate bubling indicates a positive catalase test, confirming the presence of Staphylococcus species.]

(b) Coagulase test: Differentiates S. aureus from other Staphylococcus species. Coagulase is an enzyme produced by S. aureus that converts fibrinogen to fibrin, causing clotting.
[Procedure & Observation: Mix a small amount of bacterial colony with a drop of plasma on a slide. Clumping within a few seconds indicates a positive result. OR Mix the bacterial colony with plasma in a test tube and incubate at 37°C for 4 hours. Clot formation indicates a positive result.]

17
Q

Briefly discuss antimicrobial suseptibility of Staphylococcus aureus.

A

🦠 Most strains are resistant to penicillin due to the production of beta-lactamase, an enzyme that breaks down penicillin.
🦠 Methicillin-Resistant Staphylococcus aureus (MRSA) strains are resistant to methicillin and other beta-lactam antibiotics, including penicillins and cephalosporins.
🦠 Vancomycin-Resistant Staphylococcus aureus (VRSA) and Vancomycin-Intermediate Staphylococcus aureus (VISA)

18
Q

MRSA strains are treated with ____(3)____.

A

vancomycin, daptomycin, linezolid

19
Q

VRSA and VISA strains are treated with ____(3)____.

A

linezolid, daptomycin, tigecycline

20
Q

For localized skin infections, topical antibiotics like ________ are effective.

A

muciprocin

21
Q

Outline important characteristics of coagulase negative staphylococci.

A

◾ Gram-positive cocci
◾ Non-hemolytic on blood agar
◾ Catalase positive
◾ Coagulase negative
◾ Do not ferment mannitol
◾ Resistant to polymyxin B

22
Q

How can S. epidermidis and S. saprophyticus be differentiated based on their susceptibitily to novobiocin?

A

S. saprophyticus is resistant to novobiocin while S. epidermidis is susceptible.

23
Q

What is the normal habitat of Staphylococcus epidermidis?

A

S. epidermidis is a common inhabitant of the skin and mucous membranes. It is part of the normal human microbiota and usually harmless in healthy individuals.

24
Q

What is the role of glycocalyx in Staphylococcus epidermidis?

A

S. epidermidis produces a glycocalyx, a sticky extracellular polysaccharide matrix that allows it to adhere to surfaces, such as indwelling medical devices like catheters and prosthetic joints. This biofilm formation is a key factor in its pathogenicity.

25
Q

What infections can Staphylococcus epidermidis cause?

A

S. epidermidis can cause endocarditis, bacteremia, sepsis in neonates, and peritonitis in patients undergoing peritoneal dialysis.

26
Q

What is the significance of beta-lactamase production in Staphylococcus epidermidis?

A

S. epidermidis is highly resistant to many antibiotics due to the production of beta-lactamase, an enzyme that breaks down beta-lactam antibiotics like penicillin.

27
Q

What are the treatment options for infections caused by Staphylococcus epidermidis?

A

Infections caused by S. epidermidis are often treated with a combination of antibiotics. Vancomycin is commonly used, often in combination with rifampin or an aminoglycoside.

Further notes:
Aminoglycosides work by binding to the bacterial ribosome, specifically the 30S subunit, which interferes with protein synthesis.

Rifampin binds to the beta subunit of bacterial DNA-dependent RNA polymerase. This binding prevents the enzyme from synthesizing RNA, which is essential for bacterial protein synthesis and replication.

28
Q

Where does Staphylococcus saprophyticus typically inhabit?

A

S. saprophyticus inhabits the skin surrounding the genitourinary tract. It is part of the normal flora of the perineum, rectum, urethra, cervix, and gastrointestinal tract.

29
Q

What is the significance of Staphylococcus saprophyticus in urinary tract infections (UTIs)?

A

It is the second most common cause of community-acquired UTIs in sexually active young women, after Escherichia coli.

30
Q

What other infections can Staphylococcus saprophyticus cause besides UTIs?

A

endocarditis, bacteremia, meningitis, and peritonitis.

31
Q

How are UTIs caused by Staphylococcus saprophyticus typically treated?

A

UTIs caused by S. saprophyticus are typically treated with quinolones (such as norfloxacin) or trimethoprim-sulfamethoxazole.

32
Q

Outline important characteristics of Micrococcus spp.

A

◾ Gram-positive cocci
◾ Form pairs, tetrads or irregular clusters
◾ Catalase positive
◾ Coagulase negative
◾ Form part of the transient flora on exposed skin of the face, arms, hands and legs

33
Q

Outline associated infections of Micrococcus spp.

A

◾ Pulmonary infections [esp. in immunocompromised patients]
◾ Recurrent bacteremia
◾ Septic shock
◾ Septic arthritis
◾ Endocarditis
◾ Menengitis