GENERAL PART Flashcards

1
Q

Veterinarians can cause iatrogenic infections.

A

T

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2
Q

Arthropod borne infections are direct infections

A

F

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3
Q

Arthopod born infections are indirect infections

A

T

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4
Q

Arthropods can be involved in indirect infections.

A

T

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5
Q

Venereal infections is a direct infection

A

T

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6
Q

In the case of iatrogenic infections the infective agents are transmitted by the
veterinarian

A

T

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7
Q

Drinking water cannot transmit infective agents since it is hypoosmotic

A

F

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8
Q

In case of direct infection tissues of the infected animal are contacted with tissues of the
host

A

T

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9
Q

In the case of aerogenic infection the agents are transmitted with air.

A

T

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10
Q

Aerogenic infection is a form of direct infection.

A

F

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11
Q

In the case of aerogenic infection the agent is transmitted by the air

A

T

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12
Q

Infective agents cannot survive in the soil, so soil cannot be a source of infection.

A

F

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13
Q

In the case of iatrogenic infection the agent is transmitted by humans.

A

T

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14
Q

Direct infection happens when infected animals pass the infection with water.

A

F

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15
Q

If the arthropod is a true vector, if it brings the pathogen into a susceptible animal.

A

F

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16
Q

The arthropod is a true vector, if the pathogen also replicates in the susceptible animal.

A

T

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17
Q

The arthropod is a true vector, if it propagates the pathogen.

A

T

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18
Q

The arthropod is a true vector, if it can take the pathogen to a further distance

A

F

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19
Q

Infection cannot happen through water since bacteria and viruses are inactivated in
water.

A

F

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20
Q

Meat is never involved in transmission of infections since fermentation of meat kills
agents.

A

F

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21
Q

Some infective agents are transmitted with eggs.

A

T

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22
Q

Germinative infection is more frequent in birds than in mammals.

A

T

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23
Q

Germinative infection is very frequent in mammals

A

F

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24
Q

Germinative infection is seen in mammals

A

T

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25
Q

Mammals can infect their offspring through milk

A

T

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26
Q

New-born animals cannot be infected from the milk thanks to the colostral antibodies.

A

F

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27
Q

Intrauterine infection happens if the foetus is infected during pregnancy from the dam

A

T

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28
Q

Vertical infection does not occur in mammals

A

F

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29
Q

Horizontally infections happen only in birds

A

F

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30
Q

Germinative infection is frequent in mammals, it will result in malformation of the
foetuses.

A

F

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31
Q

Galactogen infection cannot happen when the animals receive colostrum, since the
antibodies in the colostrum prevent it.

A

F

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32
Q

In the case of horizontal infection animals in the same group infect each other.

A

T

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33
Q

Intra uterine infection can occur in pregnant animals.

A

T

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34
Q

Germinative infection can happen in birds.

A

T

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35
Q

Galactogen infection is a form of horizontal infections.

A

F

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36
Q

If the dam infects newborn animals, we speak about horizontal infection.

A

F

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37
Q

Germinative infection can occur mainly in mammals.

A

F

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38
Q

In the case of galactogen infection the agent is transmitted by milk.

A

T

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39
Q

In the case of horizontal infection the agent is spreading between animals of about the
same age.

A

T

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40
Q

Horizontal infection does not occur in mammals

A

F

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41
Q

Vertical infection does not occur in mammals.

A

F

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42
Q

Germinative infection does not occur in mammals.

A

F

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43
Q

Galactogen infection does not occur in mammals

A

F

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44
Q

In germinative infection, the placenta is infected by the mother during pregnancy.

A

F

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45
Q

Germinative infection is a rare form of horizontal infection.

A

F

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46
Q

In germinative infection, the newborn is infected through the milk.

A

F

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47
Q

Zoonotic agents can cause disease in animals and humans

A

T

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48
Q

In the case of cyclozoonoses arthropods are responsible for maintaining the infections

A

F

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49
Q

If agents are passed from animals to humans, we speak about zoonosis.

A

T

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50
Q

If humans infect animals we speak about metazoonoses.

A

F

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51
Q

Cyclozoonoses require an arthropod for transmission

A

T in File, F in written

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52
Q

In the case of zoonotic diseases animals and humans can infect each other.

A

T

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53
Q

In the case of saprozoonoses animals and humans are infected from the same source.

A

T

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54
Q

In case of secondary infection, a bacterium infects an individual, which is already infected with a pathogen

A

T

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55
Q

In case of secondary infection, a new pathogen infects an already cured animal.

A

F

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56
Q

In case of secondary infection, two pathogens infect the host simultaneously.

A

F

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57
Q

In case of secondary infection, one of the agents is always a virus.

A

F

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58
Q

Facultative pathogenic agents are helped by predisposing factors

A

T

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59
Q

Stenoxen agents have a wide host range.

A

F

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60
Q

Euryxen agents have a wide host range

A

T

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61
Q

An euryxen agent can infect several host species

A

T

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62
Q

There is no minimum number of agents necessary to infection, because they can replicate in the host

A

F

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63
Q

Mutations generally result decrease of the virulence.

A

T

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64
Q

Immunogenicity of the different agents is different

A

T

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65
Q

There is a minimum number of each agent that is necessary to infect animals

A

T

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66
Q

A minimum amount of bacteria or viruses is needed to a successful infection

A

T

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67
Q

Virulence of an agent can be characterized with its LD50 value

A

T

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68
Q

Pathogenicity means the ability of the agent to cause disease

A

T

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69
Q

Virulence means the level of pathogenicity.

A

T

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70
Q

The amount of the agent does not influence the outcome of the infection, since it can
replicate in the host.

A

F

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71
Q

In the case of optimal way of infection the least amount of agent can cause disease.

A

T

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72
Q

The virulence of the agents is connected to virulence factors.

A

T

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73
Q

Virulence is a stable characteristic of an agent.

A

F

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74
Q

the way of the infection (entrance of the agents) can influence its outcome.

A

T

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75
Q

Virulence of a bacterium or virus can be changed spontaneously

A

T

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76
Q

In case of a secondary infection the agent complicates a primary infection.

A

T

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77
Q

The virulence factors help the agents in causing disease.

A

T

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78
Q

Virulence variants can occur within a bacterium or virus species.

A

T

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79
Q

Species specific resistance can be overcome by increasing the number of agents.

A

F

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80
Q

Within a pathogenic species no avirulent strains can occur.

A

F

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81
Q

Foetuses can have active immune response.

A

T

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82
Q

Newborn animals have local immune response

A

T

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83
Q

Foetuses do not have immune reactions

A

F

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84
Q

the skin, mucous membranes and mucous are parts of the non specific resistance system of the host.

A

T

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85
Q

The normal microflora of the gut is essential for animals; they cannot live without it

A

F

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86
Q

Foetuses have no immune response; they appear only in 2-4 week old animals

A

F

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87
Q

The age of the animals does not influence their susceptibility to a certain agent

A

F

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88
Q

Susceptibility to a disease can be influenced by age.

A

T

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89
Q

Certain medicines and agents can decrease the protection of the hosts

A

T

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90
Q

Species specific resistance means that certain agents cannot infect certain hosts

A

T

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91
Q

Species related resistance means that certain agents cannot cause infection in resistant
host species.

A

T

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92
Q

Certain animal species are resistant against certain agents.

A

T

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93
Q

Chicken embryos are able to produce an immune response

A

T

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94
Q

Cellular immune response is very important in the case of viral diseases.

A

T

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95
Q

Gastric juice can protect the host from infections.

A

T

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96
Q

From 2nd trimester of pregnancy, the foetus produces an immune response against any antigen.

A

F

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97
Q

There is no immune response in the foetus, only from 4 weeks after birth.

A

F

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98
Q

Unfavourable environmental effects can predispose animals to diseases caused by facultative pathogenic agents.

A

T

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99
Q

Nutrition of the animals can influence the appearance of infectious diseases

A

T

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100
Q

Environmental effects can influence the survival of the agents in the environment

A

T

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101
Q

Mycotoxins can suppress the activity of the immune system

A

T

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102
Q

Overcrowding can help the spreading of several infectious diseases.

A

T

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103
Q

Deserts can inhibit the spreading of several infectious diseases.

A

T

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104
Q

Viruses causing generalised diseases generally replicate at the place of entry and in the regional lymph nodes.

A

T

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105
Q

The lesions are at the place of entry of the agent in the case of local infections.

A

T

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106
Q

-

A

T

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107
Q

Lesions can be seen in different organs in the case of generalised diseases

A

T

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108
Q

Intra uterine infection can result immune tolerance in the case of some diseases

A

T

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109
Q

Intra uterine infection can result embryonic death in the case of some diseases

A

T

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110
Q

Intra uterine infection does not occur since the placenta protects the foetus

A

F

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111
Q

Fetuses cannot be infested since the placenta completely isolates them

A

F

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112
Q

The incubation time is the time between the appearance of the clinical signs and death
of the animal

A

F

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113
Q

The incubation time is the time between infection and the appearance of clinical signs.

A

T

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114
Q

-

A

T

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115
Q

Some infective agents have immunosuppressive effect

A

T

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116
Q

Some infective agents can cause malformation of fetuses.

A

T

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117
Q

Subacute diseases last one or 2 days.

A

F

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118
Q

Intra uterine infections does not occur in mammals since the agents cannot penetrate
the placenta.

A

F

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119
Q

In the case of local infections the lesions can be seen at the site of entry.

A

T

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120
Q

In the case of generalised infections the agent is generally spreading with blood.

A

T

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121
Q

In the case of generalised infections the placenta prevents the infection of the foetus.

A

F

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122
Q

Some agents can spread along the nerves.

A

T

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123
Q

The agent does not replicate in dead end hosts

A

F

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124
Q

Dead end hosts do not show clinical signs, they die without signs

A

F

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125
Q

In the case of latent infection the agents are continuously shed

A

F

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126
Q

Latent infection happens when the genome of the agent is integrated in the genome of
the host

A

T

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127
Q

-

A

F

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128
Q

In latent infection, there is no virus shedding.

A

T

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129
Q

Abortion is the main clinical sign of abortive infections

A

F

130
Q

The animals do not carry the agent after recovery from an infectious disease because the immune system eliminates it.

A

F

131
Q

Tolerated infections result in high level of immune reaction.

A

F

132
Q

Infection before self-recognition of the immune system can result tolerated infections

A

T

133
Q

Infected animals have a high level of antibodies in the case of tolerated infections

A

F

134
Q

The agent is not shed in the case of inapparent infections.

A

F

135
Q

Dead end hosts do not shed the agent.

A

T

136
Q

Asymptomatic infections can become manifest

A

T

137
Q

Formation of immune complexes can be a consequence of persistent viral infection

A

T

138
Q

When the clinical signs disappear, shedding the agent is finished

A

F

139
Q

In the case of an abortive infection no clinical signs will be seen

A

T

140
Q

In the case of latent infection only mild clinical signs will be seen

A

F

141
Q

Animals with tolerated infection shed the agent

A

T

142
Q

Only animals showing clinical signs can shed infective agents.

A

F

143
Q

In case of inapparent infections no clinical signs can be seen

A

T

144
Q

Latent infection is common in the case of Gram-positive bacteria.

A

F

145
Q

In the case of inapperent infections seropositivity can be seen.

A

T

146
Q

Inapparent infections cannot be detected in laboratory examinations.

A

F

147
Q

In case of abortive infection, the animal always aborts.

A

F

148
Q

In case of subclinical infection, the animals can shed the agent

A

T

149
Q

Tolerated infection can be demonstrated only by serology.

A

F

150
Q

Abortive infection can be demonstrated only by serology.

A

T

151
Q

During a tolerated infection the animals are seropositive

A

F

152
Q

In the case of latent infection no clinical signs can be seen.

A

T

153
Q

Asymptomatic infections cannot be manifest.

A

F

154
Q

Animals do not carry the agents after recovery from an infectious disease.

A

F

155
Q

Mortality shows the percentage of dead animals compared to the size of the herd.

A

T

156
Q

Mortality show what proportion of the diseased animals die.

A

F

157
Q

Lethality shows the percentage of dead animals compared to the number of diseased
ones.

A

T

158
Q

Lethality shows the number of died animals compared to the total number of the herd

A

F

159
Q

Prevalence shows the number of diseased animals compared to the total number of the
herd

A

F

160
Q

Mortality shows the proportion of dead animals compared to the number of diseases
ones.

A

F

161
Q

Monitoring is routine collection of data on a disease

A

T

162
Q

Monitoring is routine collection of data on a disease

A

T

163
Q

Pandemic diseases are fast spreading ones; they are fast transmitted between continents

A

T

164
Q

Pandemic diseases are spreading fast around the Earth.

A

T

165
Q

Pandemic disease occurs in large areas, continents.

A

T

166
Q

Endemic diseases occur in a small, limited area including a farm, some farms or a village.

A

T

167
Q

Epidemic diseases are fast spreading; they are fast transmitted between continents

A

F

168
Q

Pandemic diseases have no tendency to spread.

A

F

169
Q

Epidemic diseases are spreading in a larger geographical area e.g. in several countries.

A

T

170
Q

Contagious diseases are spreading from one animal to the other.

A

T

171
Q

Lethality shows the ratio of dead animals and the total stock.

A

F

172
Q

Hemagglutination inhibition test is used for the detection of antigens of certain agents.

A

F

173
Q

Genome of agents is detected with PCR

A

T

174
Q

Antigens of certain agents can be detected using PCR

A

F

175
Q

Surface antigens of certain agents are detected with ELIZA or PCR

A

F

176
Q

Infective agents can be detected 2-3days after infection using serological tests

A

F

177
Q

Virus Neutralisation test is used for the detection of antigens of the virus

A

F

178
Q

Serological tests are used for the detection of antibodies

A

T

179
Q

MATSA is used in laboratory diagnosis

A

T

180
Q

MATSA is a form of disease

A

F

181
Q

Microscopic detection of agents is not used in diagnostic work anymore

A

F

182
Q

If an animal is infected laboratory tests always detect the agent.

A

F

183
Q

The phase of the pathogenicity can influence the sensitivity of the laboratory tests.

A

F

184
Q

Using serological tests, we detect the antibodies produced against the agent.

A

T

185
Q

Using virus neutralization test we detect the antibodies produced against the agent.

A

T

186
Q

Polymerase chain reaction is used for the detection of antigens of the agent.

A

F

187
Q

Post mortem lesions help in setting up a preliminary diagnosis.

A

T

188
Q

Epidemiological data help in setting up a preliminary diagnosis.

A

T

189
Q

Antibacterial treatment is forbidden in the EU in the case of viral diseases.

A

F

190
Q

Individual and mass treatment can be combined in the case of some infectious diseases.

A

T

191
Q

Hyperimmune serum can be used for aetiological treatment of certain diseases

A

T

192
Q

No aetiological treatment is available in the case of viral diseases

A

F

193
Q

Mass treatment using antibiotics is not allowed in the EU.

A

F

194
Q

Antibiotics can be used for the aetiological treatment in case of bacterial disease

A

T

195
Q

All bacterial agents can be eradicated with antibiotic treatment

A

F

196
Q

Antibacterial treatment is used in the case of viral diseases in order to prevent bacterial
complications

A

T

197
Q

Antibiotics are used for the treatment of some viral diseases to prevent secondary
infections

A

T

198
Q

Antibiotics are generally used to the aetiological treatment of diseases caused by
bacteria.

A

T

199
Q

Use of antibiotics in the case of diseases caused by viruses is not allowed because of
antibiotic resistance.

A

F

200
Q

Treatment of certain infectious diseases is prohibited.

A

T

201
Q

Symptomatic treatment is recommended because it can support healing of the diseased
animals.

A

T

202
Q

In case of viral diseases, no antibiotics are given.

A

F

203
Q

Antibiotics may be used only until the disappearance of the clinical signs.

A

F

204
Q

Only diseased animals have to be treated with antibiotics to prevent resistance.

A

F

205
Q

There is no anti-viral therapy.

A

F

206
Q

Aetiological treatment with anti-bacterial is done, in the case of bacterial diseases.

A

T

207
Q

Using hyperimmune sera is usually not justifiable.

A

T

208
Q

In case of import of animals into a farm, animals in the quarantine must be tested for infections

A

T

209
Q

In case of import of animals into a farm, animals in the quarantine must only be observed, there is nothing to do with them if they do not show clinical signs

A

F

210
Q

Only eggs from the same flock are allowed to be hatches in one hatching machine

A

T

211
Q

Eggs of different species can be hatched together; they cannot infect each other thanks
to the different hatching time.

A

F

212
Q

All-in-all-out is an important principle in prevention of infectious diseases.

A

T

213
Q

Isolation of age groups is an important way of prevention of infectious diseases

A

T

214
Q

Isolated keeping of different age groups of the same species cannot prevent spreading
of infectious diseases since all animals of the same species are susceptible to the same
agents.

A

F

215
Q

Day-old birds cannot be infected in the hatchery because they are protected by yolk
Immunity.

A

F

216
Q

The immunoglobulin content of the colostrum is continuously decreasing after farrowing

A

T

217
Q

Maternal antibodies can inhibit the active immune response.

A

T

218
Q

There is no maternal protection in birds.

A

F

219
Q

Maternal protection occurs only in mammals.

A

F

220
Q

Colostrum is the main way of maternal protection in the case of animals with
epitheliochorial placenta.

A

T

221
Q

The half-life of the heterologous hyperimmune serum is about 7-10 days.

A

T

222
Q

The half-life of the heterologous hyperimmune serum is about 2-3 weeks

A

F

223
Q

Animals having epitheliochorial placenta receive maternal antibodies only through the
placenta

A

F

224
Q

Animals having epitheliochorial placenta receive maternal antibodies only through the
colostrum

A

T

225
Q

Enteral lymphocytes of the dam can be transferred to the offspring in colostrum

A

T

226
Q

The immunoglobulin content of the colostrum is influenced by the nutrition of the dam

A

T

227
Q

The protein and antibody content of the colostrum is stable in the first week after
calving

A

F

228
Q

Absorption of maternal antibodies from the colostrum in the first three days is not
changing

A

F

229
Q

Colostrum is not important in protection of calves since the antibodies can go through
the placenta

A

F

230
Q

Colostrum is the only way of receiving maternal protection in calves.

A

T

231
Q

The immunoglobulin content of the colostrum is not changed in the first week after
birth.

A

F

232
Q

Calves can absorb maternal antibodies for a week after birth

A

F

233
Q

Maternal antibodies can inhibit certain immunization.

A

T

234
Q

New-born animals cannot be infected from the milk thanks to the colostral antibodies.

A

F

235
Q

The colostrum contains maternal lymphocytes.

A

T

236
Q

The protein content of the colostrum remains high for the first two weeks after giving
birth.

A

F

237
Q

The immune globulin content of the colostrum remains high for the first week after
giving birth

A

F

238
Q

The enteral absorption of immune globulins is decreasing after birth.

A

T

239
Q

Maternal antibodies can decrease the efficacy of vaccination.

A

T

240
Q

The immune globulin concentration of the colostrum decreases sharply after birth.

A

T

241
Q

The enteral absorption of immunoglobulins is about the same for a week after birth.

A

F

242
Q

The maternal antibodies can decrease the immune response against vaccines.

A

T

243
Q

Enteral lymphocytes can get from the dam to the newborn animal with colostrum.

A

T

244
Q

Animals with epitheliochorial placenta have maternal immunity only from colostrum.

A

T

245
Q

The endotheliochorial placenta prevents to transport of immunoglobulins to the foetus

A

F

246
Q

Homologous hyperimmune serum can provide about a year-long protection.

A

F

247
Q

Strains used in marker vaccines can be differentiated from the field strains.

A

T

248
Q

Avirulent strains can be used in live vaccines

A

T

249
Q

The health state of the vaccinated animals can influence the efficacy of the vaccination

A

T

250
Q

Adjuvants in vaccines increase the shelf life of vaccines

A

F

251
Q

Inactivated vaccines contain inactivated bacterial toxins

A

T

252
Q

The method of vaccination has no effect on the efficacy of the vaccination

A

F

253
Q

Adjuvants in vaccines increase the efficacy of vaccines.

A

T

254
Q

Attenuated strains can be used in live vaccines.

A

T

255
Q

Deletion vaccines can only be used as live vaccines.

A

F

256
Q

In the case of marker vaccines, the field strains and the vaccine strains can be
differentiated

A

T

257
Q

Inactivated vaccines can contain the whole agents or their components

A

T

258
Q

The colostral immunoglobulins have no effect on the vaccination of the new born
animals

A

F

259
Q

DIVA principle can only be used if the animals are vaccinated with deletion vaccines

A

F

260
Q

According to DIVA principle, infected and vaccinated animals can be differentiated.

A

T

261
Q

Subunit vaccines contain only antigens of the agents

A

T

262
Q

Certain parts of the genome are missing from deletion vaccine strains

A

T

263
Q

Some genes are missing from the strains included in deletion vaccines

A

T

264
Q

For safety reasons only inactivated vaccines are used

A

F

265
Q

Live vaccines can contain strains with lower virulence.

A

T

266
Q

Live vaccines always contain avirulent agents.

A

F

267
Q

Live vaccines can contain attenuated strains.

A

T

268
Q

Live vaccines are less effective than the inactivated ones.

A

F

269
Q

Live vaccines are dangerous, they are not on the market any more.

A

F

270
Q

Live vaccines are not used in Europe any more.

A

F

271
Q

Live vaccines do not provide good immunity.

A

F

272
Q

Marker vaccines are used to mark the site of vaccination.

A

F

273
Q

It is not allowed to use inactivated deletion vaccines in the EU.

A

F

274
Q

Live vaccines contain attenuated or avirulent agents.

A

T

275
Q

The agent in a vaccine can influence the level of the immune response of vaccinated
animals.

A

T

276
Q

If deletion vaccines are used, vaccinated and infected animals can be differentiated.

A

T

277
Q

Using marker vaccines, vaccinated and infected animals can be differentiated.

A

T

278
Q

Use of marker vaccines can be combined with “test and remove” eradication.

A

T

279
Q

Marker vaccines are marked with dyes

A

F

280
Q

The immune response produced by an attenuated vaccine is low.

A

F

281
Q

Some attenuated vaccine strains can be immunosuppressive.

A

T

282
Q

Attenuated vaccines induced a quick immune response.

A

T

283
Q

Vaccines containing attenuated strains are not used anymore

A

F

284
Q

The amount of antigen in the vaccine has no effect on the efficacy of the vaccine.

A

F

285
Q

Eradication with selection method is not done nowadays

A

F

286
Q

Newborn animals must be kept isolated when eradication with generation shift is used

A

T

287
Q

Eradication with generation shift cannot be used if the level of infection is high in the
herd

A

F

288
Q

Eradication using generation shift method is mainly used in Poultry

A

F

289
Q

Implantation of washed embryos from a non infected dam into infected one is a way of
eradication

A

F

290
Q

Implantation of washed embryos from a infected dam into non-infected one is a way of
eradication

A

T

291
Q

Eradication using the generation shift method is mainly used in pig herds

A

F

292
Q

In the case of generation shift the infected animals must be slaughtered at the beginning
of the eradication procedure.

A

F

293
Q

Eradication using selection method can be combined with vaccination

A

T

294
Q

In the case of generation shift the young animals must be isolated from the dam at the
age of 1-3 days

A

T

295
Q

Eradication using the selection method is generally implemented in case of low level of
infection

A

T

296
Q

When eradication is made with selection method, the infected animals are removed
from the herd

A

T

297
Q

Selection, generation shift and herd replacement can be used for eradication

A

T

298
Q

Eradication using generation shift can be used in cattle herds

A

T

299
Q

Caesarean section is the only way of birth when eradication is carried out using the SPF
method

A

F

300
Q

Certain diseases can be eradicated with generation shift

A

T

301
Q

Herd replacement is the cheapest way of eradication of a disease

A

F

302
Q

Selection (test and slaughter) is a method of eradiation of a disease

A

T

303
Q

Selection method can be used for eradication of infectious diseases, when we remove
infected animals.

A

T

304
Q

In the case of generation shift, newborn animals are separated from the dam and kept isolated.

A

T

305
Q

Embryo transfer cannot be used for eradication, since the embryo can be infected.

A

F

306
Q

The selection method cannot be combined vaccination.

A

F

307
Q

Test and slaughter as an eradication method can be used in case of low level of
infection

A

T

308
Q

There is no agent which can be eradicated by antibiotic treatment.

A

T

309
Q

In the case of generation shift newborn animals have to be kept isolated from the parent animals

A

T

310
Q

In the case of herd replacement, the herd is replaced with infection-free animals.

A

T

311
Q

In the case of selection method of eradication the infected animals are taken out of the herd.

A

T

312
Q

If eradication is made by selection method, vaccination is forbidden

A

F

313
Q

Early weaning is necessary if generation shift method of eradication is used.

A

T

314
Q

Generation shift is a frequently used eradication method in swine.

A

F

315
Q

Generation shift is a method of eradication of a disease.

A

T

316
Q

In eradication by selective breeding, the seropositive animals are eliminated.

A

T

317
Q

In eradication by selective breeding, only the animals shedding the bacteria are
eliminated.

A

F

318
Q

In eradication by selective breeding, vaccination cannot be used.

A

F

319
Q

Eradication by selective breeding is not used anymore.

A

F

320
Q

Selection (test and remove) is not used to eradicate a disease anymore

A

F