Microbiology Flashcards

1
Q

Explain the use of gram staining to identify bacteria

A

pg 127 laz;s notes

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2
Q

Give the relevant immunological detail of a substance that is only present in gram negative bacteria

A

pg 128 Laz’s notes

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3
Q

List the different techniques following gram stain that may be used to distinguish between bacteria

A

pg 128 Laz’s notes

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4
Q

The majority of bacteria are harmless or beneficial (COMMENSAL), but some are pathogenic(True/False)

A

Laz’s notes, pg 128, True

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5
Q

Recall examples of gram positive and gram negative bacteria and mycobacteria

A

Laz’s notes,pg 128

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6
Q

To be a pathogen you need to be able to(name five requirements):

A

Laz’s notes , pg 129

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7
Q

Give examples of intra and extracellular bacteria

A

Laz’s notes, pg 129

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8
Q

A lot of gram negative bacteria do not use the same method for invading host cells as salmonella(T/F). Summarise a method for the Invasion of host cells by salmonella

A

Laz’s notes,PG 130, FALSE

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9
Q

Name Two related multi-protein machines required by Salmonella Motility and Invasion an that of d a large proportion of other gram negative bacteria that uses the same method:

A

Laz’s notes ,PG 130

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10
Q

Describe the functions of flagella and Type III Secretion System

A

Laz’s notes,pg 130

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11
Q

RECALL THE STRUCTURE OF THE TYPE 3 SECRETORY SYSTEM(the diagram)

A

Laz’s notes, pg 131

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12
Q

1)DESCRIBE AND THE EXPLAIN THE FUNCTION OF THE TYPE 3 SECRETIRY SYSTEM

A

Laz’s notes ,131

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13
Q

Describe and explain two examples of the manipulation of actin by bacteria, and identify the kind of bacteria that use such

A

Laz’s notes,131

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14
Q

State two methods bacteria may use to get into a host cell(129-130)

A

Laz’s notes,(129-130)

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15
Q

Describe the full details as to how structures as sophisticated as those involved in the invasion of host cells have evolved, include statistical evidence for these details?

A

Laz’s notes ,131

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16
Q

How many proteins do bacteria encode and how many be described as non-accessory or non-pathogenic)

A

Laz’s notes ,131

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17
Q
  • Name the Three Main Mechanisms for horizontal gene transmission:
A

Laz’s notes,132

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18
Q

State a major activity by bacteria associated with DNA that allows them to overcome our immune system

A

Laz’s notes,132

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19
Q
  • Describe the Three Main Mechanisms for horizontal gene transmission:
A

Laz’s notes ,132

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20
Q

Define PATHOGENICITY ISLAND

A

Laz’s notes,133

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21
Q

Verticacl gene transfer is the main drivers of evolution of bacterial pathogens and their origin is usually unknown. (T/F)

A

Laz’s notes,F,PATHOGENICITY ISLAND are the main drivers of evolution of bacterial pathogens and their origin is usually unknown

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22
Q

As they have access to a huge variety of DNA through horizontal gene transmission, bacteria occupy a huge component of the biodiversity in the world(true/false)

A

Laz’s notes, true,pg 144

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23
Q

Name the Intrinsic Sources of Bacterial infections and identify the sources where you would expect bacteria

A

Laz’s notes,134

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24
Q

the SMALL INTESTINE you get GRAM NEGATIVE BACTERIA and gram positive bacteria(True/False)

A

Laz’s notes ,F, the SMALL INTESTINE you only get GRAM NEGATIVE BACTERIA,134

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25
Q

Name the viruses and bacteria for Portal of Entry - Upper Respiratory Tract

A

Laz’s notes,134

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26
Q

Infections targeting the upper respiratory tract - usually extrinsically-acquired from respiratory tract droplets or airborne(T/F)

A

Laz’s notes,T,134

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27
Q

Hand transmission can act as an intermediate for Portal of Entry - Upper Respiratory Tract(True/False)

A

Laz’s notes ,T,134

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28
Q

Describe Consequences of bacterial infection acquired via the upper respiratory tract

A

Laz’s notes,135

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29
Q

For portal of Entry - Urogenital Tract,dissect the sources of bacteria and name the bacteria that go through these sources

A

Laz’s notes,135

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30
Q

What is needed to acquire an infection through the skin, give examples of causes of broken skin.

A

Laz’s notes,135

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31
Q
  • Name Infections Targeting Broken Skin, and describe where relevant of feature of these infections:
A

Laz’s notes,136

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32
Q
  • Describe the consequences** **of infection via broken skin
A

Laz’s notes ,136

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33
Q

What is the main cause of infection via broken skin)

A

136,Laz’s notes

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34
Q

Name the viruses,bacteria and the toxins for Portal of Entry: The Gastro-Intestinal Tract (‘faeco-oral route’)

A

Laz’s notes,136

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35
Q
  • Describe the** **Consequences of infection via the GI tract
A

Laz’s notes,136

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36
Q

What is significant about of the consequences of listeria infection via the GI tract

A

Laz’s notes,137

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37
Q

Define the following(pathogenicity, commensal, true pathogen, opportunistic pathogen,infectivity,virulence, infectious dose

A

Laz’s notes,137

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38
Q

List the factors involved in infectivity

A

Laz’s notes ,137

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39
Q

Analyse 3 examples of a pathogens that has a feature that increases it virulence

A

Laz’s notes ,137

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40
Q

List features that enhance virulence

A

Laz’s notes,137

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41
Q

List the features that infectious dose is affected by

A

Laz’s notes,138

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42
Q

Give** **Infectious Disease Examples and describe how they produce their infection by Portal of Entry

A

Laz’s notes,138

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43
Q

Reacall examples of gram positive and gram negative Opportunistic Bacterial Pathogens, and explain them

A

Laz’s notes,139

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44
Q

Define Bacteriostatic and bacteriocidAL

A

Laz’s notes,140

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45
Q

Define resistance , breakpoint and minimum inhibitory concentration

A

Laz’s notes,141

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46
Q

Explain the relationship between breakpoint and resistance

A

Laz’s notes ,141

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47
Q

Resistance to AB usually arises soon after the introduction of AB to clinical use in hospitals(T/F)

A

Laz’s notes ,T

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48
Q

Resistance to AB usually arises soon after the introduction of AB to clinical use in hospitals.(State two exceptions to this rule and explain one of these exceptions)

A

Laz’s notes,141

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49
Q

Recall Diseases caused by the drug resistant bacteria, identify whether they are gram positive and gram negative recall features of the diseases where relevant (i.e. portal of entry , consequences and drugs that are used in their treatment )

A

Laz’s notes

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50
Q

what is the common/ general mechanism for the role of antibiotics)

A

Laz’s notes,142

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51
Q

Describe the mechanism of action of seven antibiotic sub-groups

A

Laz’s notes,142

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52
Q

Name four mechanisms of antibiotic resistance:

A

Laz’s notes ,145

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53
Q

Explain how Altered Target Site can act as a mechanism for antibiotic resistance and give examples of when this can happen

A

Laz’s notes ,145

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54
Q

Explain how Inactivation of Antibiotic can act as a mechanism for antibiotic resistance and give examples of when this can happen

A

Laz’s notes,146

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55
Q

What would the term ‘broad spectrum’ mean?

A

Laz’s notes,146

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56
Q

Explain how altered metabolism can act as a mechanism for antibiotic resistance and give examples of when this can happen

A

Laz’s notes ,146

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57
Q

Explain how Decreased Drug Accumulation can act as a mechanism for antibiotic resistance and give examples of when this can happen

A

Laz’s notes ,146

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58
Q

Summarise five real life mechanism for resistance mechanisms, state the antibiotic or type of antibiotic they act on , and state the method of acquisition of the genes for this.

A

Laz’s notes,147

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59
Q

Recall what a transposon is

A

Laz’s notes,147

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60
Q

Recall the Sources of Antibiotic Resistance Genes

A

Laz’s notes,147

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61
Q

Horizontal gene transfer allows the rapid spread of antibiotic resistance (T/F)

A

Laz’s notes,149

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62
Q

State five reasons for treatment failure other than Antibiotic resistance

A

Laz’s notes ,148

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63
Q

Strong selective pressures in hospitals are due to the regular use of antibiotics(True/False )

A

Laz’s notes ,True

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64
Q

Name eight Hospital Acquired Infection Examples

A

Laz’s notes,148

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65
Q
  • Name seven** **Risk Factors for HAI:
A

Laz’s notes,,148

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66
Q

A doctor came up to me and said that he would like to find a way fof monitoring the amount of Streptococcus pyogenes in the nose, so that he can ensure amounts are kept within normal levels for patiets being treated in antibiotic . Explain why what the doctor is trying to do is useful?

A

Laz’s notes,148

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67
Q

Give examples of ways for preventing** **the emergence of drug resistance bacteria and nosocomial infections

A

Laz’s notes ,149

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68
Q

How main phyla does the fungi kingdom consist of and what are the names of these phyla

A

Laz’s notes,150

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69
Q

How many serious fungal infections of humans are there?)

A

Laz’s notes,150

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70
Q

Describe the distribution of serious fungal infections of humans in terms of their phyla

A

Laz’s notes ,150

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71
Q

Describe how crytococci can get into the body, which cells may mop them up and where they can get to and why?

A

Laz’s notes,150

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72
Q

Summarise how fungi deal with their food source

A

Laz’s notes ,150

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73
Q

Describe spore** **dispersal in fungi

A

Laz’s notes ,150

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74
Q

Name** **Three Types of Illness caused by Fungi

A

Laz’s notes ,150

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75
Q

Recall examples of fungal allergies:

A

Laz’s notes ,151

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76
Q

Define Mycotoxicoses)

A

Laz’s notes,151

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77
Q

What are mycotoxins)

A

Laz’s notes,151

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78
Q
  • Recall symptoms of mycotoxicoses:
A

Laz’s notes

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79
Q

what is the treatment for mycotoxicosis

A

Laz’s notes,151

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80
Q

What produce aflatoxin , and what is special about it compared to other rcpmpounds, and give an example of its effect on the body

A

Laz’s notes,151

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81
Q

What is a mycose

A

Laz’s notes ,151

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82
Q

Describe what superficial mycoses are and give examples of them.

A

Laz’s notes,152

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83
Q

Describe what cutaneous mycoses are( double check info here) and give examples of them.

A

Laz’s notes,152

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84
Q

define subcutaneous mycoses

A

Laz’s notes ,153

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85
Q

what is a mycetoma

A

Laz’s notes,153

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86
Q
  • Give examples of deep / systemic mycoses
A

Laz’s notes,153

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87
Q

What is significant about the relation between fungal infections and transplant settings.give an example of a particular fungal infection

A

Laz’s notes,153

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88
Q

Describe and explain where relevant how Candida can interact with us under different circumstances

A

Laz’s notes ,154

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89
Q

DESCRIBE THE EPIDEMIOLOGY OF INVASIVE ASPERGILLOSIS

A

Laz’s notes,154

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90
Q

DESCRIBE THE METHOD OF Diagnosis of Fungal Infections

A

Laz’s notes,155

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91
Q

Three targets for treating fungal infection are:

A

Laz’s notes

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92
Q

Describe features of the targets for antifungal infection

A

Laz’s notes,155

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93
Q

Explain and Categorise the functions of antifungal treatment, include specific examples in your answer

A

Laz’s notes

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94
Q

Describe a procedure that can be used to check that a microorganism causes a disease and name this procedure.

A
95
Q

(Definition of a Virus

A
96
Q

Definition of Obligate)

A
97
Q

Describe the two main types of virus morphologies

A
98
Q

How can viruses be named( less important)

A
99
Q

RECALL THE FULL DETAILS OF THE MAIN WAY FOR CLASSIFYING VIRUSES. WHAT IS THE NAME GIVEN TO THIS

A
100
Q

Summarise the different ways of the joint process of transcription and translation in viruses

A
101
Q

Describe the defining feature of a retrovirus

A
102
Q

Recall two anti-herpes virus drugs and two anti-influenza virus drugs and a retroviral drug

A
103
Q

Summarise the consequences of the Viral Genome Type

A
104
Q

Recall the details of a generic virus replication cycle

A
105
Q

What is the difference between VIRUS AND A VIRION?

A
106
Q

Describe the the Replication Cycle of HIV-1

A
107
Q

Describe The Replication of Ebola Virus

A
108
Q

Describe how the action of viruses can be investigated in the labarotary and explain the usual results viewed once viruses are investigated.

A
109
Q

Describe and explain two different ways of investigating viral presence other than the use of plaques formation

A
110
Q

Describe and explain the Single Step Growth Kinetics of a Virus

A
110
Q

Summarise the different ways of Viral Diagnosis(not very important)

A
111
Q

Describe how antiviral vaccines can be formed

A
112
Q

Describe how to culture norovirus in the lab

A
113
Q

Define tropism and explain its determinant (using a definition of its determinants)

A
114
Q

Describe the receptor attachment involved in HIV

A
115
Q

How can people who exposed to HIV not be affected by the virus and describe how this can change in HIV replication

A
116
Q

Describe the measles virus receptor use, tropism and pathogenesis

A
117
Q

Give two examples of viruses whose tropism are determined by receptor use)

A
118
Q

(give an example of virus whose tropism is not determined by receptor use)

A
119
Q

Explain the determination of tropism of influenza

A
120
Q

What is the difference between the underlying dterminants influenza and HIV & measle

A
121
Q

Explain how influenza tropism can be extended

A
122
Q

Explain what determines the outcome of a virus infection

A
123
Q

Transmission Terminology

Define the following terms: latrogenic , nosocomial, vertical, horizontal, germ line

A
124
Q

Recall the difference bwetween vertical and horizontal DNA transmission

Vertical DNA transmission

A
125
Q

)Summarise how you can get Viral Rashes

A
126
Q

Define incubation period

A
127
Q

Describe and explain how the varicella zoster virus can act on a human from its initial infection over a lifetime(include details of the days events occur)

A
128
Q

Recall the ways of describing the patterns of viral infection, and what they mean

A
129
Q

2)Recall the classifation of the pattern of viral infection( pg 249 ibook to help)

A
130
Q

Describe Strategies of Viral Persistence

A
131
Q

Explain the concept of latency, using the example of the Herpes Simplex Virus to illustrate your answer

A
132
Q

Explain the how viruses may cause cancer

A
133
Q

How does papillomaviruses cause cancer

A
134
Q

how were Kaposi Sarcoma-Associated Herpes Virus (KSHV or HHV8) and Merkel Cell Polyoma first discovered

A
135
Q

what causes hepatocellular carcinoma

A
136
Q

HBV is a hepadnavirus (has a DNA genome) but it uses reverse transcriptase during a stage in its life cycle (T/F)

A

T

137
Q

There is a vaccine for HBV and HCV(T/F)

A

There is a vaccine for HBV and no vaccine for HCV

138
Q

1)Recall examples of diseases for the different patterns of viral infection

A
139
Q

HCV and HBV is a blood borne virus(T/F)

A

T

140
Q
  • 55% of us are infected with Epstein-Barr Virus(T/F)
A
  • 95% of us are infected with Epstein-Barr Virus(,F
141
Q

Postulate possible consequences of infections with EBV

A
142
Q

Which cell type does the Epstein Barr Virus most commonly affect, and what are symptoms-what is the genric name for the symtomes?

A
143
Q

Outcome of infection can vary depending on(state seven

A
144
Q

Explain how Viral Sequence may affect outcome of virus infection

A
145
Q

Explain how Viral Sequence may affect outcome of virus infection

A
146
Q

Using an example, illustrate how Viral Load may affect outcome of virus infection

A
147
Q

Use two examples to illustrate how Co-Infections

may affect outcome of virus infection

A
148
Q

Use two examples to illustrate how Genetic Resistance and Susceptibility may affect outcome of virus infection

A
149
Q

Recall Predisposing Co-morbidities and Conditions for viral infections

A
150
Q

Describe Host Defence against infectious agents

A
151
Q

Describe Non-immune mechanisms for host defence against infectious agents

A
152
Q

Describe immune mechanisms for host defence against infectious agents

A
153
Q

Describe the features of acquired immunity

A
154
Q

Vaccines are primarily aimed at eliciting acquired immunity which requires exposure to the infectious agent or its antigens(T/F).

A
155
Q

5)Catergorise the two different types of acquired immunity and give the details of these two different types

A
156
Q

Name an example of what humoral immunity would be important for

A
157
Q

Name an example of what Cell mediated immunity would be important for

A
158
Q

Define active and passive immunity and state the purpose of a vaccine

A
159
Q

List the properties of a good vaccine, and describe the features of two of these properties

A
160
Q

A good vaccine PROVIDES SUBSTANTIAL BENEFIT TO HEALTH AT LOW COST AND LOW RISK(True/False)

A

T

161
Q

Describe what happens in the four stages of vaccine clinical trials

A
162
Q

define vaccine efficacy

A
163
Q

where is vaccine efficacy determined

A
164
Q

How is vaccine efficacy calculated , and how is it usually expressed

A
165
Q

what is herd immunity)

A
166
Q

use a sentence to summarise how herd immunity carries out its function

A
167
Q

Toxoids will offer herd immunity_(T/F)_

A

F,

Toxoids will not offer herd immunity_(_

168
Q

(in what scenario would herd immunity be irrelevant

A
169
Q

Give an example to describe how herd immunity can be important

A
170
Q

What is the endemic state state

A
171
Q

There is a relationship between the basic reproduction number R0, vaccine effectiveness and coverag needed to reduce or eliminate disease(T/F)

A

T

172
Q

Recall the equation needed to determine the minimum proportion of the population that must be immunised at birth (or close to) in order for the infection to die out in the population

A
173
Q

Recall the equation for calculating the herd effect

A
174
Q

Explain what is included in Vaccine Formulations

A
175
Q

List and describe some of the features of the different categories of antigenic properties of vaccines(not sure about this one)

A
176
Q

Recall the different vaccine subcategories

A
177
Q

2)Describe what a live-attenuated vaccine is

A
178
Q

)state the advantages and disadvantages of live attenuated vaccines

A
179
Q

Give examples of attenuated vaccines

A
180
Q

Describe how the BCG vaccine is produces, and describe what is known about the effectiveness of the BCG vaccine and problem with evaluating effectiveness of the BCG vaccine

A
181
Q

State : the name of the pathogen that causes typhoid, how the pathogen is transmitted and how it causes disease. List the symptoms of typhoid fever.

A
182
Q

What is the name of the typhoid vaccine- describe how it is produced

A
183
Q

Describe the features of the typhoidvaccine itself and its administration that allows a smooth treatment using the vaccine

A
184
Q

Describe the features of a killed whole cell vaccine

A
185
Q

State the advantages and disadvantages of Killed Whole Cell Vaccines. Recall example of such vaccine

A
186
Q

Describe the features of the antigens for the different vaccine subcategories.

A
187
Q

Recall features of the tetanus and diphtheria toxin, and how the toxoid used for them is produced.

A
188
Q

Describe what conjugate vaccines are)

12)List the advantages of using conjugate vaccines

A
189
Q

Describe how conjugate vaccines can be prepared

A
190
Q

How do conjugate vaccines work

A
191
Q

describe the role of adjuvants)

A
192
Q

Explain the role of adjuvant immune response

A
193
Q

Explain the general categorisation of adjuvants

A
194
Q

Define prophylaxis and therapy

A
195
Q

Name two examples of successful virus vaccination and describe why one of them is successful

A
196
Q

Describe the features of toxoid vaccines, the advantages of using them, and recall examples of diseases that they vaccinate against

A
197
Q

Describe the different types of viral vaccines

A
198
Q

Recall examples Human Virus Vaccines and the category they come under(less important)

A
199
Q

Describe the process of Attenuation of Viruses to make Live Virus Vaccines

A
200
Q

Recall Pros and cons of live vs inactivated viral vaccines

A
201
Q

RECALL Examples of viruses for which both live and inactivated vaccines are available AND THE DETAILS EACH TYPE FOR THE VIRUSES(1)

A
202
Q
  • What is involved in the new strategy for influenza vaccination in children(2)
A
203
Q

why must influenza vaccine be regularly updated)

A
204
Q

who is the influenza vaccine given to)

A
205
Q
  • influenza evolves fast(why must influenza vaccine be regularly updated)
A
206
Q

Describe in what cases you would each type of polio virus vaccine and why(3)

A
207
Q

Describe the process of Making recombinant attenuated virus vaccines

A
208
Q

What is Rotavirus Vaccine called , what type of vaccine is it , how is it used and why

A
209
Q

Recall examples ofSubunit Vaccines

A
210
Q

Describe the features of the Shingles Vaccine, how it is used and why

A
211
Q
  • The live attenuated vaccine is similar but distinct from the chicken pox vaccine given to children in some countries(T/F)
A

T

211
Q

DESCRIBE THE ACTION OF INTERFERONS IN ANTIVIRAL TREATMENT HOW IT USED in healthcare AND WHY

A
212
Q

Explain how viruses are targeted in general.

A
213
Q

EXPLAIN THE ACTION OF Nucleoside Analogues IN VIRAL TREATMENT

A
214
Q

DESCRIBE THE ACTION OF ACYCLOVIR IN VIRAL TREATMENT

A
215
Q

Explain the TWO Strategies to Inhibit Influenza

A
215
Q
  • What is involved in the new strategy for influenza vaccination in children(2)
A
216
Q

RECALL THE DIFFERENT TYPES OF HIV Treatment

A
217
Q

Recall the different methods that can be used for

Hepatitis C Treatment

A
218
Q

Why do viruses evolve fast)

A
219
Q

explain what a quasi species is

A
220
Q

Describe the impact of some of the mutations of viruses in human circulation0

A
221
Q

How can the evolution of human viruses during human circulation be observed

A
222
Q

Explain the purpose of using Highly Active Anti-Retroviral Therapy

A
223
Q

List how new viruses may emerge

A
224
Q

Explain the concept of antigenic drift

A
225
Q

call Global influences of emerging viral infections

A
226
Q

Define the terms zoonosis and host range, and explain its consequences

A
227
Q

Explain how viruses emerge and re-emerge using named examples, including influenza virus antigenic shift and drift, HIV, West Nile Virus, SARS and noroviruses.

A
228
Q

Explain the principles of the evolution of drug resistant variants of viruses

A
229
Q

Explain the process of antibody dependent enhancement of the infection in dengue fever

A
230
Q
A