Applied Microbiology Flashcards

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1
Q

Normal flora

A

→The population of microorganisms that inhabit skin & mucous membranes of normal human body.

  1. Resident flora→ organisms regularly present in a particular area & when disturbed it re-establishes itself
  2. transient flora → both non-pathogenic & potentially pathogenic bacteria that inhibit the body surface or mucous membrane for a limited period.
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2
Q

Normal flora of the skin.

A
→ staph.epidermidis & diphtheroids
→ peptococcus
→ str. viridans
→ enterococcus
→ micrococcus
→ esch.coli
→ proteus
→ Candida albicans
→ pityrosporum orbiculare
→ propionibacterium acne
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3
Q

Normal flora of the conjunctiva

A

→ corynebacterium xerosis
→ staph.epidermidis
→ moraxella sp
→ non-haemolytic streptococci

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4
Q

Normal flora of the nose & nasopharynx.

A
Nose:
→ Diphtheroids
→ staphylococci
→ streptococci
→ Haemophilus sp
Nasopharynx:
→ pseudomonas aeruginosa
→ esch.coli
→ proteus
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5
Q

Normal flora of the mouth.

A
→ micrococci
→ gram +ve aerobic spore bearing bacilli
→ coliforms
→ proteus
→ lactobacilli
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6
Q

Normal flora of the URT

A

→ alpha haemolytic streptococci

→ similar flora of mouth

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7
Q

Normal flora of the GIT

A
Breast fed infants:
→ lactobacilli
→ enterococci
→ colon bacilli
→ staphylococci
Bottle fed infants:
→ leptotricha
→ anaerobic lactobacilli
→ colon bacilli
→ aerobic & anaerobic spore bearing organisms.
Adult:
→ lactobacilli
→ enterococci
→ bifidobacteria
→ anaerobic lactobacilli.
→ Bacteroides sp
→ anaerobic streptococci
→ clostridia
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8
Q

Normal flora of the GUT

A
→ mycobacterium smegmatis
→ strains of mycoplasma & ureaplasma
Penile urethra:
→ gardnerella vaginalis
→ Bacteroides sp
→ alpha haemolytic streptococci.
Female urethra:
→ staph. epidermidis
Vagina:
→Clostridia
→ anaerobic streptococci
→ Bacteroides sp
→ gardnerella vaginalis
→ diphtheroids
→ listeria
→ Candida albicans.
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9
Q

Normal flora of the external auditory meats.

A

→ staph.epidermidis

→ Diphtheroids

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10
Q

Usinary tract infections

A
→A disease caused by microbial invasion of the genitourinary tract that extends from the renal cortex of the kidney to the urethral meatus.
→causative organisms:
A. Gram -ve bacilli
     1. Escherichia coli
     2. Klebsiella sp
     3. Proteus mirabilis
     4. Enterobacter
     5. Pseudomonas aeruginosa
     6. Serratia
B. Gram + ve cocci
     1. Enterococci faecalis
     2. Staph. saprophyticus
     3. Staph. aureus
     4. Staph. epidermidis
C. Miscellaneous
     1. M. tuberculosis
     2. Citrobacter
     3. Salmonellae
     4. Str. pyogenes
     5. Str. agalactiae
     6. Gardnerella vaginalis
D. Fungus
     1. Candida albicans
→lab diagnosis:
1. Specimen- midstream urine specimen,catheter specimen
2.transport- minimum delay, refrigerate @4°c
3. Microscopy- pus cells, epithelial cells, erythrocytes & bacteria
4. Culture- blood agar & Mac conkey's agar @37°c for 24 hours
5. Other methods
      a) dip slides
      b) pour plate method
      c) Griess nitrite test
      d) triphenyltetrazolium chloride test
      e) catalase test
       f) gram staining
      g) glucose test paper
      h) polymorphonuclear neutrophils
        i) leucocyte esterase
        j) defection of lipopolysaccharide
6. Differentiation of UUTI & LUTI → antibody coated bacteria detected by immunofluorescence test indicates UUTI.
7. Antibody susceptibility testing.→ Stokes disc diffusion method
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11
Q

Organisms causing diarrhoea

A
A. Bacteria
    1. Vibrios
         • vibrio cholerae
         • V. Parahaemolyticus
         • other halophitic vibrios
     2. Esch. coli ( ETEC, EPEC)
     3.salmonellae
          • S. enteritidis
          • S. Typhimurium
      4. Shigella sp
      5. Campylobacter jejuni
      6. Yersinia enterocolitica
      7. Clostridium perfringens
      8.C. difficile
B. Viruses
      1. Rotavirus
      2. Norwalk virus
      3. Adenovirus
      4. Astrovirus
      5. Calicivirus
C. Protozoa
      1. Entamoeba histolytica
      2. Giardia lamblia
      3. Cryptosporidium parvum
D. Fungus → Candida albicans.
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12
Q

Food poisoning.

A

→ an illness acquired through consumption of food or drink contaminated either with microorganisms, their toxins or chemical poisons.
1. Infective type: 8-24 hours, infected dose of microorganisms ingested with food. Eg. , Salmonella sp, vibrio parahaemolyticus, campylobacter jejuni.
2. Toxic type: 2-6 hours, preformed bacterial toxin ingested with food. Eg.staphylococcus aureus, bacillus cereus, clostridium botulinum.
3. Intermediate type: 6-12 hours, bacteria ingested with food release toxin in gut. Eg. Cl. Perfringens.
→lab diagnosis:
1. Specimen- food, vomitus, faeces,blood.
2. Demonstration of toxin- toxin-antitoxin neutralization test in mice
3. Demonstration of organisms- gram staining, culture on blood agar or cooked meat broth in anaerobic conditions.

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13
Q

Causes of acute pyogenic meningitis

A

In children & adults:

  1. Neisseria meningitidis
  2. Streptococcus pneumoniae
  3. Haemophilus influenzae
  4. Staphylococcus aureus.
  5. Listeria monocytogenes
  6. Esch. coli
  7. Proteus sp
  8. Klebsiella sp
  9. Citrobacter sp
  10. Enterobacter sp
  11. Serratia

In neonates & infants:

  1. Esch. col
  2. Group B streptococci
  3. Staphylococcus aureus
  4. Haemophilus influenzae
  5. Listeria monocytogenes
  6. Streptococcus pneumoniae
  7. Klebsiella sp
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14
Q

Lab diagnosis -acute pyogenic meningitis.

A
  1. Specimen -CSF
  2. Microscopy- gram staining → plenty of pus cells & few gram + ve / -ve organisms.
  3. Antigen detection - latex agglutination,countercurrent immunoelectrophoresis.
  4. Culture:
    a) CSF culture- blood agar, chocolate agar & cooked meat broth @ 37°c for 24 hours with 5-10% CO2
    b) blood culture- in meningitis due to N.meningitidis, H.influenzae & str. preumoniae
  5. Agglutination
  6. Demonstration of bacterial endotoxins- limulus lysate test → extract prepared from blood cells of the horse shoe crab is coagulated when mixed with blood containing endotoxins.
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15
Q

Tuberculous meningitis.

A

→ CSF shows moderate rise in cell count & predominant cells are lymphocytes.
→ moderate rise of total protein & sugar is reduced.
→ lab diagnosis:
1. Specimen- CSF shows cobweb appearance.
2. Microscopy-ZN staining shows lymphocytes with few acid-fast-bacilli.
3. Culture - Lowenstein-Jensen medium @37°c x 6-8 weeks.

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16
Q

Aseptic meningitis-causes.

A
1. Viruses
→ enterovirus( echo, coxsackie & polioviruses)
→ mumps virus
→ herpes simplex virus.
→ varicella zoster virus.
→ measles virus.
→ adenoviruses
→ arboviruses.
2. Bacteria.
→ M. tuberculosis.
→ leptospira interrogans
→ treponema pallidum
3. Fungi
→ cryptococcus neoformans
→ Candida albicans
4. Protozoa
→ acanthamoeba
→ naegleria
→ toxoplasma gondii
17
Q

Infective endocarditis.

A
1. Subacute endocarditis - infection on damaged or defective valve cusps & large firm vegetations comprising of dense fibrin, platelet aggregates with bacterial colonies are formed.
• bacteria:
    → streptococcus sanguis
    → str. mutans
    → str. mitis
    → enterococcus faecalis
    → staph. epidermidis
    →coxiella burnetii
    → chlamydia psittaci
• fungi:
     → Candida albicans
     → Aspergillus sp.
2. Acute endocarditis - vegetations are large & valve destruction is greater than in subacute endocarditis.
• causative agents:
     → staphylococcus aureus
     → streptococcus pneumoniae
     → str. pyogenes
     → str. agalactiae
3. Post -operative endocarditis- following cardiac surgery particularly in prosthetic valve replacement.
• causative agents:
    → staphylococcus epidermidis
    → staph. aureus
    → Candida albicans
4. Endocarditis associated with iv drug abuse
• causative agents:
    → staphylococcus aureus
    → Viridans group of streptococci
    → Candida sp
    → pseudomonas sp

→ predisposing factors:

  1. Rheumatic valvular disease
  2. Congenital valve deformities.
  3. Cardiac valve prosthesis
  4. Degenerative cardiac disease
  5. Drug abuse.

→ lab diagnosis:
1. Specimen -blood 3-6 samples
2. Culture- glucose broth @37°c x 3 weeks. Subcultures on blood agar & MacConckey’s agar.
3. Identification- colony morphology, gram staining, biochemical reactions & serological tests.
4. Antibiotic sensitivity test- minimum inhibitory concentration & minimum bacterial concentration of the antimicrobial for the isolated organism
5. Culture negative endocarditis due to:
→ recent antibiotic therapy
→ inadequate number of specimens
→ infection with coxiella burnetti or chlamydia sp.
6. Other tests:
→ total leukocyte count. -leucocytosis
→ erythrocytes sedimentation rate- elevated.
→ echocardiogram

18
Q

Fever of unknown origin

A
→ any febrile illness ( > 38°c) lasting 3 weeks or longer, without any obvious cause & failure to reach a diagnosis despite 1 week of inpatient investigations.
→ causes:
1. Bacterial infections.
    • enteric fever
    • UTI
    • lung abscess & other deep abscesses
    • septicaemia associated with pneumonia, infective endocarditis, etc.
    • tuberculosis
    • brucellosis
    • rheumatic fever
    • relapsing fever
    • leptospirosis
    • typhus fever
    • Q fever
2. Parasitic infections
     • malaria
     • hepatic amoebiasis or liver abscess
     • visceral leishmaniasis (kala-azar)
     • filariasis
     • toxoplasmosis
     • trypanosomiasis ( tropical Africa)
3. Viral infections
      • infectious mononucleosis
      • Cytomegalovirus infection
      • hepatitis A & B virus infection.
      • rubella & other infections fever without rash
      • HIV infection.
4. Fungal infections
     • histoplasmosis
     • coccidioidomycosis
5. Neoplasms
     • hodgkin's lymphoma
     • non-hodgkin's lymphoma
     • leukaemia
     • Hypernephroma
     • hepatoma
     • disseminated malignancy
6. Connective tissue disorders
     • systemic lupus erythematosus
     • polyarteritis nodosa
7. Granulomatous diseases
     • sarcoidosis
     • crohn's disease
8. Doug induced fever.

→ lab diagnosis:
1.specimens -blood, urine, sputum, pus.
2. Culture.
a) blood- glucose broth & taurocholate broth @ 37°c for 24 hours, subculture on blood agar & MacConckey’s agar @ 37°c for 24 hours.
b) urine- blood agar & MacConckey’s agar. LJ medium in case of renal TB
c) sputum-blood agar & MacConckey’s agar. LJ medium in case of TB
d) pus- glucose broth, blood agar & MacConckey’s agar. LJ medium in case of TB
3. Identification- colony morphology, gram staining, biochemical reactions & agglutination. ZN staining in case of TB
4. Serology
5. Parasitic infections- stained peripheral blood smears.
6.viral infections- tissue culture, serology.
7.fungal infections- culture on SDA or brain-heart infusion agar
8. Other tests:
a) skin tests
•mantoux test
•skin tests for histoplasmosis, coccidioidomycosis, sarcoidosis.
b) haematology
• total leukocyte count
• differential leukocyte count.
c) immunologic tests- LE cell phenomenon & antinuclear antibody test in SLE
d) biopsy- lymph node or other tissues.

19
Q

Nosocomial infections

A

→ infection developing in patients after admission to the hospital, which was neither present nor in the incubation period at the time of hospitalisation.
→ factors:
1.susceptible patients.
2. Hospital environment
3. Diagnostic or therapeutic procedures
4. Drug resistance.
5. Transfusion
6. Advances in Medical progress.
→ modes of transmission.
1. Contact
• hands or clothing
• inanimate objects.
2. Airborne
• droplets
• dust
• aerosols
3. Oral route
4. Parental route
→ common infections.
1. UTI ( cauti ) - Esch.coli, klebsiella, proteus, serratia, pseudomonas…
2. Respiratory infection ( vap) - staph.aureus, krebsiella, enterobacter, serratia, proteus…
3. Wound & skin sepsis-staph.aureus, pseudomonas aeruginosa, Esch.coli, proteus, enterococci…
4. GIT infections- salmonella, shigella sonnei & viruses
5. Burns-staph.aureus, pseudomonas aeruginosa, acinetobacter & str. pyogenes.
6. Bacteraemia & septicaemia-gram -ve bacilli

20
Q

MMR vaccine

A

→ Live attenuated vaccine
→ measles, mumps, rubella vaccine
→ 1st dose- 9-12 months, 0.5 ml subcutaneous.
→ 2nd dose- 16-24 months, 0.5 ml subcutaneous.

21
Q

Methods of antibiotic sensitivity testing.

A
  1. Dilution method
    a) broth dilution-microbroth (petri plates), macrobroth ( test tubes).
    b) agar dilution.
  2. Disc diffusion method.
    a) Kirby Bauer disc diffusion.
    b) Stokes method.
  3. E test ( epsilometer)
22
Q

Molecular diagnostic methods.

A

A. Amplified methods.
1. Polymerase chain reaction
2. Transcription mediated amplification
3. Nucleic acid sequence based amplification
4. Ligase chain reaction.
B. Non-amplified method ⇒ nucleic acid probes.

23
Q

Bacteriological examination of drinking water.

A
  1. Collection of water samples.
    a) sampling from a tap or pump outlet.
    b) sampling from a reservoir
    c) sampling from a ding well.
  2. Transport- wrapped in a Kraft paper, keep in ice box if delay.
  3. Methods of analysis.
    a) presumptive coliform count
    b) differential coliform count
    c) detection of faecal streptococci & clostridium perfringens
    d) membrane filtration test
  4. Examination for specific pathogens
24
Q

Categories of biomedical waste.

A
Category No. 1- Human anatomical waste
Category No.2- animal waste
Category No. 3- microbiology & biotechnology waste & other laboratory waste
Category No. 4- waste sharps.
Category No. 5- discarded medicines & cytotoxic drugs.
Category No. 6- solid waste.
Category No. 7- infections solid waste.
Category No. 8- chemical waste.