Dr. Ashutosh Verma, BVSc, MVSc, PhD, DipACVM, Professor of Microbiology, Richard A. Gillespie College of Veterinary Medicine, Lincoln Memorial University, Harrogate, TN
The material used in this presentation has been obtained from different sources including books, published papers and online resources. It is intended only for educational purposes.
Books referenced
Veterinary Microbiology and Microbial Diseases, Quinn et al., 2nd ed.
Veterinary Microbiology, Songer and Post
Clinical Veterinary Microbiology, Markey et al., 2nd ed.
Infectious Diseases of the Dog and Cat, Greene, 4th ed.
Veterinary Microbiology, Hirsh et al., 2nd ed.
Learning Objectives
Discuss skin defenses and how they work to protect
Explain, with examples, the differences between primary and secondary skin infections
Explain differences between resident and transient skin flora and give some examples for each category
Explain the differences between colonization and infection with reference to skin
Describe predisposing factors for secondary bacterial infections of skin
Discuss considerations for collection and diagnosis of clinical samples for skin infections
Describe classification of pyodermas
Skin – a natural defense
Physical barriers
Hair/fur – prevent direct skin contact
Stratum corneum – inert and impermeable layer
Temperature and pH – too cold/unfavorable pH for optimal growth of many
Chemical barriers
Fatty acids – bacteriostatic
Inorganic salts – High salt conc.
Transferrins – bind iron needed for bacterial growth
Immunological defense
Site for interactions between immune cells and antigens
Prevent deeper invasion
Normal flora
Bacteria and fungi
Protective
Factors affecting number and species of normal flora
Hydration
General health
Physical and chemical environment – salt, transferrin
Other bacteria – nutrients, antibiotic production
Types of normal flora
Resident flora
Transient flora
Resident flora
Live and multiply on the skin (obligate parasites)
Form a permanent population
Cannot be eliminated
Normally are harmless
Examples – Coagulase-negative Staphylococcus, alpha-hemolytic Streptococcus, Micrococcus spp., etc.
Transient flora
Acquired from environment or mucous membranes
Most do NOT multiply efficiently on skin - just there
Are transient - CAN be removed or eliminated
May be involved in pathologic processes
Examples – Coagulase-positive Staphylococcus, E. coli, Proteus, etc.
Types of bacterial skin infections
Primary infections
Secondary infections
Primary skin infections
Bacteria initiate and cause most of the pathology
Occur in otherwise "healthy" skin - predisposing factor, if any, is minor
Antibacterial therapy is effective - underlying problem is less significant
Primary bacterial skin infections
Greasy pig disease caused by Staphylococcus hyicus
Dermatophilosis caused by Dermatophilus congolensis
Secondary skin infections
Bacterial infections associated with other infection(s) and/or condition(s)
Predisposing conditions for secondary skin infections: Skin infected with parasites, viruses, fungi, etc.; Other local predisposing factors - moisture, skin folds, etc.; Systemic disease resulting in skin pathology - hypothyroidism, Cushing's disease; Physical or chemical trauma - surgical incision, catheter placement, etc.; Immunosuppression - e.g., corticosteroid therapy
Colonization
Present, but not causing disease
Infection
Present, associated with pathology
Identification of bacteria in primary and secondary infection is useful if also consider the presence of normal flora
Isolation of Staphylococcus pseudintermedius alone is not enough to determine if it is a bacterial infection (and is significant)
Diagnosis of bacterial skin infections
1. Correlate history, clinical signs, and bacterial isolates
2. Bacterial culture to distinguish colonization and infection
3. Direct smears: Gram's and Wright's stains
4. Histopathology and surgical biopsy
Sampling for bacterial culture
Do NOT sample open tracts or erosions (use unopened pustule)
Punch biopsy of lesion- NOT into formalin for culture
Direct smears: Gram's and Wright's stains
Gram's stain (numbers and types bacteria; presumptive ID; initiation of therapy)
Wright's stain (e.g., Diff-Quik)- presence/type inflammatory cell; degenerate neutrophils with bacteria within the cells is indicative of infection
Histopathology and surgical biopsy
When to biopsy- Any dermatosis that is unresponsive to the treatment for 3 weeks or any recurrent dermatosis
Advantages of early biopsy- Avoids nonspecific, masking, and misleading changes of chronicity; allows rapid institution of specific therapy
What to biopsy- Intact pustules; take multiple biopsies; try to obtain primary lesions (avoid those marred by excoriation and chronicity)
Classification of Skin infections (pyodermas)
Surface pyoderma
Superficial pyoderma
Deep pyoderma
Surface pyoderma
Involves epidermis only
Often sequelae to self-trauma or allergic skin disease
Examples include hot spots and early skin fold dermatitis
Superficial pyoderma
Involves skin down to and including intact hair follicles (folliculitis)
Pustules are present – mini abscesses
Often secondary to other diseases (hormonal, metabolic or parasitic)
Recurrence is common and long-term management may be difficult
Deep pyoderma
Involves tissues deeper than hair follicles
Almost ALWAYS secondary to other contributing factors
Not common, but VERY difficult to treat
Clinical case from the first lecture
10 yr. old Spayed Pekingese, 4.8 Kg, 6-day history of Pyrexia, Anorexia, Depression, Multiple non-pruritic erythematous skin nodules
The skin lesions began on the abdomen and extended to the neck, axilla and perianal region
Atopic dermatitis at 2 years of age, pruritus, responded to corticosteroid (prednisone) therapy, owner continued to treat pruritus with prednisone intermittently
Prior to referral, dog was treated with antibiotic enrofloxacin and corticosteroid prednisone, but clinical signs did not resolve