Microbiology Flashcards

1
Q

describe the tolerogen effect in HBV

A

E antigen is a soluble form of HBV core antigen.
E antigen crosses the placenta.
This results in clonal detection of lymphocytes recognising epitopes shared with HBV core antigen.
HBV core is effectively recognised as self antigen.
This leads to chronic infection.

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2
Q

describe the usefulness of the markers used for HBV

A

see blood virus lecture part 1 - slide 18

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3
Q

what is the difference between e antigen positive and negative in HBV

A
e antigen positive:
• High grade infection
• High risk of onward transmission
• e.g. from needle stick 33% risk
• Likely to develop chronic active hepatitis, Cirrhosis and hepatocellular carcinoma
e antigen negative:
• Low grade infection
• Low risk of onward transmission
• e.g. from needle stick < 1% risk
• Not likely to develop clinical effects
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4
Q

what is the treatment of HBV

A

Lamivudine
• Aim is suppression rather than cure
- can develop resistance however

Interferon
• Aim is cure of high grade infection

Transplantation

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5
Q

Main route of transmission for HCV

A

IV drug use

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6
Q

Describe the usefulness of markers for HCV

A

See blood virus lecture 2 slide 6

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7
Q

describe treatment of HCV

A

Interferon and Ribavirin
• Aim is cure of high grade infection

Transplantation
• HCV recurs in graft

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8
Q

describe the mechanism of action of HIV

A

Retrovirus

  • Infects immune cells
  • CD4 Lymphocytes (TH cells)
  • Macrophages
  • Causes immunosuppression due to reduction in T cell function
  • 2 main subtypes (HIV1 & HIV2 and multiple genotypes)
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9
Q

describe some infections that may occur in aids

A

blood lecture 2 slide 14

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10
Q

describe treatment of HIV

A

Anti‐retroviral therapy (ART):
• Aim is suppression rather than cure
• 14 licenced drugs
- To combat development of resistance

Combination of drugs:
- From 3 main classes:
> Nucleoside Reverse transcriptase inhibitors
> Non‐nucleoside Reverse transcriptase inhibitors
> Protease inhibitors
- 3 drugs used together
- Very successful

Mother to baby transmission can be prevented:
- Caesarian section
• ART to mother and baby
• Avoidance of breast feeding
• Reduces transmission rate from 16% to 1%

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11
Q

overview of treatment for HBV HCV and HIV

A

slide 18 blood lecture 2

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12
Q

Name some key agents that cause bacterial diarrhoea

A
Campylobacter
• Salmonella
• Shigella
• E.coli – various pathogenic types
• Vibrio cholerae
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13
Q

name some key agents that cause GI infections from toxin ingestion

A

Clostridium perfringens
• Bacillus cereus
• Staphylococcus aureus
• Clostridium botulinum

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14
Q

name some key agents that cause antibiotic associated diarrhoea

A

• Clostridium difficile

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15
Q

name two viruses that cause go infections

A

Norovirus

• Rotavirus

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16
Q

name two parasites that cause GI infections

A
  • Cryptosporidium

* Giardia

17
Q

name some opportunistic bacteria in HIV/AIDS

A

Mycobacterium tuberculosis
Pneumocystis, Toxoplasmosis
Cytomegalovirus (CMV), Mycobacterium avium‐intracellulare

see slide 28 of immunodeficiency lecture

18
Q

name some fungi that cause infection in HIV

A

Pneumocystis
• Candida spp.
• Cryptococcus neoformans

19
Q

name some parasites that cause infection in HIV

A
  • Cerebral toxoplasmosis

* Cryptosporidiosis

20
Q

name some bacteria that cause infection in HIV

A

Mycobacterium avium intracellulare
Mycobacterium tuberculosis
Salmonella

21
Q

name some viruses that cause infection in HIV

A
  • CMV
  • Herpes simplex virus
  • Human HerpesVirus 8
22
Q

describe the diagnosis presentation and treatment of Pneumocystis pneumonia (PCP) in HIV patient

A

Diagnosis:
- Silver stain/monoclonal antibody detection in BAL or biopsy
• PCR on bronchial lavage

Presentation:
• Non productive cough, dyspnoea, fever
• Perihilar infiltrates
• May progress – severe respiratory distress
• Extrapulmonary infection

Treatment
• High dose cotrimoxazole
• ICU usually required

23
Q

cause of cerebral toxoplasmosis

A

T. gondii

24
Q

describe infection in healthy and advanced HIV for cerebral toxoplasmosis

A

Infection in Healthy hosts:
• Protozoal infection, usually asymptomatic (50% infected by middle age) or glandular fever‐like illness
• Zoonosis: from cats

Presentation in advanced HIV:
• Main cause of focal CNS lesions
• Note ring enhancement
• Pneumonitis and chorioretinitis also occur

25
Q

How are infections prevented in HIV

A

• CD4 count boosted by HAART (Highly Active AntiRetroviral Therapy) → fewer opportunistic infections

As CD4 count falls prophylaxis is offered for:
• Pneumocystis (co‐trimoxazole)
• Mycobacterium avium intracellulare (rifabutin)
• CMV (ganciclovir)

26
Q

name two opportunistic fungal infections in neutropenia

A
  • Aspergillus fumigatus

* Candida albicans

27
Q

Describe management of sepsis in neutropenia

A

Empirical therapy:
• Febrile neutropenics cannot await culture results
• URGENT bactericidal broad‐spectrum agents
• Anti‐pseudomonal penicillin + aminoglycoside
• Add vancomycin/teicoplanin (for resistant Gram‐positive bacteria), if no improvement
• Then antifungal if still no improvement
• Other supportive measures (oxygenation, circulatory support, etc.) are CRITICAL

28
Q

name two common infectious agents in burn patients

A
  • Infections with Pseudomonas aeruginosa and Staphylococcus aureus common
  • Can spread to bloodstream
29
Q

name two infections pregnant women are at more risk of

A
  1. Ascending UTI

2. Listeria monocytogenes (a Gram‐positive bacillus)