Here is a comprehensive set of General Microbiology Questions and Answers for BPT Students, covering all major topics:
🦠 General Microbiology - BPT Question Bank
SECTION 1: Bacterial Structure & Classification
Q1. What are the four basic shapes of bacteria?
A.
| Shape | Term | Example |
|---|
| Spherical | Coccus | Staphylococcus, Streptococcus |
| Rod-shaped | Bacillus | E. coli, Clostridium |
| Spiral/curved | Spirillum / Vibrio | Vibrio cholerae, Treponema |
| Comma-shaped | Vibrio | Vibrio cholerae |
Q2. What is the difference between Gram-positive and Gram-negative bacteria?
A.
| Feature | Gram-Positive | Gram-Negative |
|---|
| Cell wall peptidoglycan | Thick (multilayer) | Thin (single layer) |
| Outer membrane | Absent | Present |
| Lipopolysaccharide (LPS/endotoxin) | Absent | Present |
| Color after Gram stain | Purple/Violet | Pink/Red |
| Periplasmic space | Absent/narrow | Present |
| Examples | Staph, Strep, Bacillus | E. coli, Pseudomonas, Salmonella |
- Medical Microbiology 9e, "Bacterial Structure"
Q3. What is peptidoglycan and why is it medically important?
A. Peptidoglycan (murein) is the rigid structural layer of the bacterial cell wall. It:
- Maintains cell shape and prevents osmotic lysis
- Is the target of beta-lactam antibiotics (penicillin, cephalosporins) which inhibit its cross-linking
- Is thicker in Gram-positive bacteria
- Is absent in human cells - making it an ideal antibiotic target
Q4. Name the structures found ONLY in bacteria (not in human cells).
A.
- Cell wall (peptidoglycan)
- 70S ribosomes (human cells have 80S)
- Pili (fimbriae)
- Flagella with unique basal body structure
- Plasmids
- Endospores (in some species)
- Capsule (in some species)
Q5. What is the function of the bacterial capsule?
A. The capsule:
- Protects bacteria from phagocytosis (main virulence factor)
- Helps in adherence to host tissues and surfaces
- Protects against desiccation
- Detected by the Quellung reaction (capsular swelling with specific antibody)
- Examples of encapsulated bacteria: Streptococcus pneumoniae, Klebsiella, Haemophilus influenzae, Neisseria meningitidis
Q6. What are endospores? Which bacteria produce them?
A. Endospores are dormant, highly resistant survival structures formed under adverse conditions (nutrient depletion).
- One cell forms one spore (sporulation), and the spore is liberated when the mother cell undergoes autolysis
- Can survive for centuries, resistant to heat, drying, radiation, and many chemicals
- All medically important spore-formers are Gram-positive rods
- Examples: Clostridium tetani (tetanus), C. botulinum (botulism), C. difficile (pseudomembranous colitis), Bacillus anthracis (anthrax)
- Autoclave at 121°C for 15 min is required to destroy spores
SECTION 2: Staining Techniques
Q7. Describe the steps of the Gram Stain.
A.
| Step | Reagent | Gram+ result | Gram- result |
|---|
| 1 | Crystal violet (primary stain) | Purple | Purple |
| 2 | Gram's iodine (mordant) | Purple-black | Purple-black |
| 3 | Alcohol/acetone (decolorizer) | Retains purple | Decolorized |
| 4 | Safranin (counterstain) | Purple | Pink/Red |
Mechanism: Gram-positive cells have a thick peptidoglycan wall that traps the crystal violet-iodine complex on decolorization. Gram-negative cells lose it due to dissolution of the thin lipid-containing outer membrane.
Q8. What is the Ziehl-Neelsen (ZN) stain used for?
A. ZN stain (acid-fast stain) is used for Mycobacteria (TB, leprosy) and Nocardia.
- Primary stain: Carbol fuchsin (red) - requires heat to penetrate the waxy mycolic acid wall
- Decolorizer: Acid-alcohol
- Counterstain: Methylene blue
- Result: Acid-fast organisms stain red/pink (AFB+), others stain blue
SECTION 3: Sterilization & Disinfection
Q9. Define and distinguish: Sterilization, Disinfection, Antisepsis, Asepsis.
A.
| Term | Definition | Kills spores? |
|---|
| Sterilization | Complete destruction of ALL microorganisms including spores | Yes |
| Disinfection | Destruction of most pathogens (not necessarily spores) | No |
| Antisepsis | Disinfection applied to living tissue (skin, mucous membranes) | No |
| Asepsis | Prevention of microbial contamination (technique) | N/A |
| Bactericidal | Kills bacteria | - |
| Bacteriostatic | Inhibits bacterial growth (doesn't kill) | - |
Q10. What are the methods of sterilization?
A.
Physical Methods:
| Method | Temp/Details | Use |
|---|
| Autoclave (moist heat) | 121°C, 15 min, 15 psi | Most reliable; kills spores |
| Dry heat (hot air oven) | 160°C, 60 min | Glassware, oils, powders |
| Boiling | 100°C, 20 min | Does NOT kill spores |
| Pasteurization | 72°C, 15 sec (HTST) | Milk; kills pathogens, not spores |
| UV radiation | 260 nm | Air, surfaces |
| Ionizing radiation (gamma) | - | Disposable syringes |
| Filtration | 0.22 µm membrane | Heat-sensitive liquids (sera, vaccines) |
Chemical Methods:
- Ethylene oxide - heat-sensitive instruments
- Formaldehyde, glutaraldehyde - endoscopes
- Chlorine, hypochlorite - water, surfaces
Key point for BPT: Autoclave is the gold standard for sterilizing surgical instruments and physiotherapy equipment.
SECTION 4: Bacterial Growth & Reproduction
Q11. What are the four phases of the bacterial growth curve?
A.
| Phase | What happens |
|---|
| Lag | Adaptation period; no increase in cell number |
| Log (Exponential) | Rapid division; cells double every generation (2^n); most antibiotic-sensitive phase |
| Stationary | Nutrients depleted/toxins accumulate; birth rate = death rate |
| Decline (Death) | Death > division; persister cells may remain antibiotic-resistant |
Q12. What is binary fission?
A. Binary fission is the asexual reproduction method of bacteria:
- DNA replicates
- Cell wall and membrane extend
- Septum forms in the middle
- Cell divides into two identical daughter cells
- E. coli doubles every ~20 minutes; M. tuberculosis every ~18-24 hours (explains why TB treatment takes months).
SECTION 5: Infection & Immunity
Q13. What is the difference between innate and adaptive immunity?
A.
| Feature | Innate Immunity | Adaptive Immunity |
|---|
| Speed | Immediate (minutes-hours) | Slow (days-weeks) |
| Specificity | Non-specific | Highly specific |
| Memory | No | Yes (key feature) |
| Components | Skin, neutrophils, macrophages, NK cells, complement | T cells, B cells, antibodies |
| Response to 2nd exposure | Same | Faster and stronger (memory) |
Q14. What are the five classes of immunoglobulins (antibodies)?
A.
| Class | Key Feature |
|---|
| IgG | Most abundant; crosses placenta; secondary response |
| IgM | First antibody produced (primary response); pentamer |
| IgA | Found in secretions (saliva, breast milk, tears, mucosa) |
| IgE | Involved in allergy and parasitic infections |
| IgD | B cell surface receptor; function less clear |
Q15. What is the chain of infection?
A. Six essential links:
- Infectious agent (pathogen)
- Reservoir (human, animal, environment)
- Portal of exit (respiratory tract, blood, feces)
- Mode of transmission (droplet, contact, airborne, vector, fecal-oral)
- Portal of entry (skin, respiratory, GI, urogenital)
- Susceptible host
Breaking any link prevents infection - critical concept for physiotherapists in infection control.
SECTION 6: Viruses, Fungi & Parasites (Brief)
Q16. How do viruses differ from bacteria?
A.
| Feature | Bacteria | Virus |
|---|
| Cell structure | Prokaryotic cell | Not a cell (acellular) |
| Nucleic acid | Both DNA & RNA | Either DNA or RNA |
| Ribosomes | Yes (70S) | No |
| Reproduction | Binary fission | Replication inside host cell |
| Antibiotic sensitivity | Yes (most) | No |
| Size | 1-10 µm | 20-300 nm (smaller) |
Q17. What is MRSA? Why is it important in physiotherapy settings?
A. MRSA = Methicillin-Resistant Staphylococcus aureus
- Resistant to all beta-lactam antibiotics due to altered penicillin-binding protein (PBP2a)
- Spreads via direct contact and contaminated surfaces/equipment
- BPT relevance: Physiotherapy equipment (mats, ultrasound probes, hydrotherapy pools), close patient contact, and hospital wards are common transmission sites
- Prevention: Hand hygiene, gloves, surface disinfection, isolating infected patients
SECTION 7: Hospital-Acquired Infections (HAI) - High Yield for BPT
Q18. What is a nosocomial (hospital-acquired) infection?
A. An infection acquired in a healthcare setting, not present at the time of admission (develops after 48 hours of hospitalization).
- Common sites: UTI (most common), pneumonia, surgical site, bloodstream
- Common pathogens: E. coli, Klebsiella, Pseudomonas, Staph aureus, Candida
- BPT students must know: Physiotherapists are at risk of transmitting HAIs through hands, equipment, and close contact. Hand washing (WHO 5 moments) is the single most effective prevention.
Q19. What is the significance of biofilm in microbiology?
A. Biofilms are communities of bacteria adhering to surfaces, enclosed in a self-secreted polysaccharide matrix.
- Up to 1000x more resistant to antibiotics than planktonic (free-floating) bacteria
- Form on medical devices: catheters, prosthetic joints, endoscopes
- Highly relevant in chronic wound infections - a major physiotherapy concern
- Examples: Pseudomonas aeruginosa in chronic lung infections, dental plaque (Streptococcus mutans)
QUICK REVISION TABLE - One-Liners
| Topic | Key Fact |
|---|
| Smallest bacteria | Mycoplasma (no cell wall) |
| Largest bacteria | Thiomargarita |
| Obligate intracellular | Chlamydia, Rickettsia, viruses |
| Commonest cause of UTI | E. coli |
| Spore-forming anaerobe | Clostridium |
| Atypical pneumonia | Mycoplasma pneumoniae |
| Gram stain inventor | Hans Christian Gram (1884) |
| Autoclave temperature | 121°C, 15 psi, 15 min |
| Primary antibody response | IgM first, then IgG |
| Rabies virus shape | Bullet-shaped (rhabdovirus) |
Sources: Medical Microbiology 9e; Jawetz, Melnick & Adelberg's Medical Microbiology 28e; Sherris & Ryan's Medical Microbiology 8e
Tip for BPT exams: Focus especially on infection control (sterilization, HAIs, chain of infection) and common pathogens in wound/respiratory infections, as these are most clinically relevant for physiotherapy practice. Would you like detailed questions on any specific topic?