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HIV (Human Immunodeficiency Virus)

Total questions: 29

Worksheet time: 58mins

Name
Class
Date
1.

Genus of HIV is

a)

Lentivirus

b)

Morbillivirus

c)

Rubivirus

d)

Orthoretrovirinae

2.

Subfamily of HIV is

a)

Lentivirus

b)

Orthoretrovirinae

c)

Retroviridae

d)

Paramyxovirinae

3.

Family of HIV is :

a)

Retroviridae

b)

Orthoretrovirinae

c)

Coronavirales

d)

Mononegavirales

4.

HIV is enveloped.

a)

True

b)

False

c)

It has not been proven scientifically.

d)

The virus is not enveloped in some cases.

5.

Possible treatments to delay HIV infection :

a)

Administration of anti-retroviral drugs (Combination of at least 3 drugs)

b)

Suppressing the replication of HIV

c)

Slowing the decline of CD4 T-cell count and progression of AIDS

d)

Using HAART

e)

Tenormin ® 50mg is mild to delay the effects of HIV infection

6.

HAART stands for :

(a)  

7.

What is HAART used for?

a)

to cure HIV infection by completely eradicating the number of viruses in the blood

b)

to prevent the HIV from making copies of itself, limit how much viral load should be in the blood and greatly reduce the chance of passing HIV to partners

c)

to weaken the viruses so that the patient cannot transmit HIV to other people through risky behaviors

d)

to strengthen the CD4 T-cells for fighting HIV as many as possible

8.

What is window period?

a)

The time between the infection and the revelation of detectable of HIV antibodies

b)

The incubation period of HIV, meaning the time between the entry of the HIV and the onset of symptoms

c)

The time when a patient receives treatment for HIV

d)

The time when an infected person transmits HIV to another person.

9.

How long is the window period of HIV?

a)

1 - 2 weeks

b)

6 weeks - 3 months

c)

1 - 2 years

d)

5 - 6 years

10.

Why can a person be HIV-positive while the test shows negative?

a)

He or she did the test during the window period, meaning HIV antibody is absent.

b)

His or her immune system may have eliminated HIV once, but they rise in bloodstream again right after their latent period

c)

HIV had been filtered by nephrons of the kidneys, thus they were excreted completely, but the person gets infected again. Subsequently, the kidneys lose their function to excrete the viruses.

d)

He or she is using HAART to suppress the viruses

11.

HIV infection is divided in

a)

2 stages

b)

3 stages

c)

4 stages

d)

5 stages

12.

Acute HIV infection is in

a)

Primary stage

b)

Secondary stage

c)

Tertiary stage

d)

Quaternary stage

13.

Chronic HIV infection or viral latency is in

a)

Primary stage

b)

Secondary stage

c)

Tertiary stage

d)

Quaternary stage

14.

AIDS appears in

a)

Primary stage

b)

Secondary stage

c)

Tertiary stage

d)

Quaternary stage

15.

Normal people have CD4 cell count of

a)

100 - 500

b)

500 - 1200

c)

700 - 1500

d)

1000 - 2000

16.

An HIV-infected person is at risk for opportunistic infections when his or her CD4 cell count drops below

a)

1000

b)

500

c)

200

d)

50

17.

An HIV-infected person gets advanced HIV infection when his or her CD4 cell count drops below

a)

1000

b)

500

c)

200

d)

50

18.

Most deaths of HIV infection occur when CD4 cell count drops below

a)

1000

b)

500

c)

200

d)

50

19.

Primary infection stage of HIV infection gives out some neglect-able symptoms such as

a)

Lymphadenopathy, fever, rash, headache, fatigue, sore throat, diarrhea, neurological manifestation, loss of appetite, weight loss

b)

Persistent herpes-zoster (Shingles), oral candidiasis, oral hairy leukoplekia, Kaposi's sarcoma

c)

Pneumocystis carinii pneumonia (PCP), Cryptococcal meningitis, toxoplasmosis

d)

Mycobacterium avium, cytomegalovirus infection, lymphoma

20.

In tertiary infection, predictive diseases of the progression of AIDS are

a)

Lymphadenopathy, fever, rash, headache, fatigue, sore throat, diarrhea, neurological manifestation, loss of appetite, weight loss

b)

Persistent herpes-zoster (Shingles), oral candidiasis, oral hairy leukoplekia, Kaposi's sarcoma

c)

Pneumocystis carinii pneumonia (PCP), Cryptococcal meningitis, toxoplasmosis

d)

Mycobacterium avium, cytomegalovirus infection, lymphoma

21.

Once the CD4 cell count of an HIV-infected person drops below 200, he or she is at risk for :

a)

Lymphadenopathy, fever, rash, headache, fatigue, sore throat, diarrhea, neurological manifestation, loss of appetite, weight loss

b)

Persistent herpes-zoster (Shingles), oral candidiasis, oral hairy leukoplekia, Kaposi's sarcoma

c)

Pneumocystis carinii pneumonia (PCP), Cryptococcal meningitis, toxoplasmosis

d)

Mycobacterium avium, cytomegalovirus infection, lymphoma

22.

Once the CD4 cell count of an HIV-infected person drops below 50, he or she is at risk for :

a)

Lymphadenopathy, fever, rash, headache, fatigue, sore throat, diarrhea, neurological manifestation, loss of appetite, weight loss

b)

Persistent herpes-zoster (Shingles), oral candidiasis, oral hairy leukoplekia, Kaposi's sarcoma

c)

Pneumocystis carinii pneumonia (PCP), Cryptococcal meningitis, toxoplasmosis

d)

Mycobacterium avium, cytomegalovirus infection, lymphoma

23.

Direct diagnosis for HIV :

a)

RT-PCR test for viral RNA

b)

Detection of HIV antigen p24

c)

Viral cultivation

d)

Western blot

e)

Detection of specific antibodies : IgM and IgG

24.

Indirect diagnosis for HIV :

a)

RT-PCR test for viral RNA

b)

Detection of HIV antigen p24

c)

CD4 cell count

d)

Western blot

e)

Detection of specific antibodies : IgM and IgG

25.

HIV 1 presents in :

a)

Sub-Saharan region and worldwide

b)

West Central Africa

c)

Part of Europe

d)

India

26.

HIV 2 presents in :

a)

Sub-Saharan region and worldwide

b)

West Central Africa

c)

Part of Europe

d)

India

27.

A group of HIV 1 that usually dominates the pandemics :

a)

Group M

b)

Group N

c)

Group O

d)

Group P

28.

HIV 1 is less easily transmissible and pathogenic than HIV 2.

a)

True

b)

False

c)

It has not been proven scientifically

d)

In some cases, HIV 2 is less easily transmissible and pathogenic.

29.

HIV transmission :

a)

Sexual contact with infected partner(s)

b)

Exposure of broken skin or wound to infected blood products

c)

Sharing contaminated needles (among IV drug abusers especially)

d)

Transplantation of infected tissues or organs

e)

Mother-to-fetus transmission (perinatal transmission, breastfeeding)