029 Viral Infections on Respiration Flashcards

1
Q

What are aerosols?

A

Light particles that are airborne, which can cause transmission of virus.

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2
Q

What are fomites?

A

Inanimate objects that can harbor pathogens e.g. door handles.

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3
Q

What is the most important respiratory pathogen of childhood, causing annual winter epidemics and hospital outbreaks?

A

RSV is most important, causing the common cold (rhinitis).

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4
Q

What are the characteristics of RSV?

A

It is a paramyxorvirus and envelopes RNA. It is very close to the human metaphneumovirus. It has a syncytial cytopathic effect, so under light micrograph of virus infected cells in culture, you will see several cells fused together.

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5
Q

What are common diseases for the upper respiratory tract and their virus causes?

A

Rhinitis (common cold) – caused by RSV, adenovirus, corona viruses, pharyngitis (sore throat) – caused by influenza, parainfluenza, adenoviruses, Laryngotracheobronchitis (croup) – RSV, influenza, human metapneumovirus.

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6
Q

What are common diseases for the lower respiratory tract and their virus causes?

A

Bronchiolitis, Bronchitis, Pneumonia – RSV, influenza, parainfluenza

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7
Q

What is malaise?

A

Malaise refers to general feeling of illness.

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8
Q

What is myalgia?

A

Myalgia refers to muscle pain.

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9
Q

What type of genetic material do influenza envelope and how many segments is it split into?

A

Influenza envelope SS viral –ve sense RNA and it is split into 8 segments.

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10
Q

What is the incubation period for influenza?

A

1-3 days

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11
Q

What is the period of infectivity of influenza?

A

3-5 days after illness onset

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12
Q

Describe some complications for influenza?

A

Primary viral pneumonia, Secondary bacterial pneumonia, Reyes syndrome. Reyes syndrome is the inflammation and swelling of liver and brain in children, usually caused by the intake of aspirin. It is quite rare, but is associated with fits, oedema, coma, and altered mental state.

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13
Q

What is the difference between primary viral pneumonia and secondary bacteria pneumonia?

A

Primary viral pneumonia occurs by the influenza virus penetrating the alveoli. It is very rare and is associated with rapid deterioration and death due to cyanosis etc. Secondary bacteria pneumonia is caused by the disruption in mucosal immunity caused by the influenza, allowing opportunistic bacterial infections to occur. This is normally caused by streptococcus pneumonia or Staphylococcus aureus.

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14
Q

On histology slides, what do the small purple dots represent?

A

Neutrophils – you will extensive neutrophils in secondary bacterial pneumonia but less in primary viral pneumonia.

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15
Q

What is the difference between latency and incubation?

A

Latency is the time period between infection and communicability. Incubation is time period between infection and onset of symptoms.

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16
Q

How is the influenza classified, and which is the result of antigenic shifts?

A

Influenza is classified into flu A, B, C. Flu A is the most severe and is the result of antigenic shifts. Flu B presents with more mild symptoms. Flu C is not present in man.

17
Q

What is the difference between antigenic shift and antigenic drift?

A

Antigenic drift is caused by single point mutations that are not corrected by RNA polymerase. There are lots of slow changes accumulated over time, and eventually the virus changes enough to cause an epidemic as humans will be partially immune. Antigenic shift is where reassortment occurs as the coinfection of two viruses will swap from their 8 sections, causing 256 variations. This forms an entirely new virus. Genetic reassortment can also occur. This normally causes epidemics and pandemics.

18
Q

What are the two antigens and the variations on the influenze?

A

Haemagglutinin – there is H1 – H3 on humans for flu A but H1-H15 for all species. Neuraminidase – there is N1, N2 in humans for flu B but N1-N9 for other species. Flu B only has one HA and NA subtype.

19
Q

What is the role of haemagglutinin?

A

HA attaches to sialic acid on cells, causing fusion and endocytosis to the influenza envelope.

20
Q

What is the role of neuraminidase?

A

NA cleaves the sialic acid off from the HA, allowing the newly formed virus to be released from the cell surface.

21
Q

What is the M2 (Matrix -2) protein ion channel and what is it specific to?

A

M2 protein ion channel is found in flu A strains. When HA binds to sialic acid on the cell surface in an acid environment, protons enter virus via the M2 protein ion transport channel allowing uncoating of viral nucleic acid.

22
Q

How would you write a vaccination classification?

A

Virus type / place of origin / strain number / year of isolation (subtype)

23
Q

How would you clinically diagnose the influenza?

A

The quickest way would be to use the nasopharyngeal aspirates and immunofluorescence tests of epithelial cells to detect antigens. Host antibody response can be tested, by taking serum samples from patient 10-14 days apart to see if it has response to the antibody. Reverse PCR can be used to determine the nucleic acid for identification and possible isolation. For vaccination, isolation for strains can occur.

24
Q

Why does RSV reinfection often occur in children?

A

They have poor mucosal immunity

25
Q

What is the incubation period of RSV, and how long do symptoms last?

A

1-4 days but symptoms can last to up to 2 weeks later.

26
Q

Which receptor on the influenza is the main target for neutralization?

A

Haemagglutinin

27
Q

What is the use of amantadine? Which flu can this treat?

A

Amantadine is used to block M2 channels, to prevent the acid environment allowing protons to uncoated the viral RNA when inside the cell. It can be used to treat flu A.

28
Q

What do neuraminidase inhibitors do?

A

Inhibit neuraminidase from cleaving the HA off the saliac acid.

29
Q

Which treatment is mainly used and for what purpose?

A

Neuraminidase is normally used to reduce side effects because viruses develop resistance much more slowly. It can be used against both flu A and flue B. Amantadine also has CNS side effects.

30
Q

Which strain of flu broke out in Hong Kong 1997? How did the city respond to this?

A

H5N1, city responded by slaying 1.5 million chickens. There were 18 cases in humans.

31
Q

Why is H5N1 able to cause multi-organ disease?

A

An enzyme is needed to cleave the haemagglutinin before it is able to attach to other host cells. This enzyme is normally found only in the respiratory tract, causing localization. H5N1 haemagglutinin can be cleaved elsewhere and can be activated by enzymes in cells throughout the body, causing multi-organ disease.

32
Q

When did H1N1 break out and what was the epidemiology of this?

A

2005, mostly young people developed this because there was a similar outbreak in the 1918’s and 1977s, which made older people immune.