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75 Cards in this Set
- Front
- Back
- Acute viral infection - Latent infection - Chronic/ persistent infection |
three characteristic clinical presentations: |
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Acute viral infection |
displaying evident signs and symptoms. |
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Latent infection |
has no visible signs and symptoms, but the virus is still present in the host cell in a lysogenic state (inserted into the host genome in a resting state) or maintained as a nuclear or cytoplasmic epi-some. |
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Chronic or persistent infection |
in which low levels of virus are detectable and the degree of visible signs or symptoms varies |
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mucosal site, “viremia” |
After viral infection at a local, often may occur viruses disseminated in peripheral blood |
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Secondary viremia |
may occur in a variety of tissues, such as the skin, salivary glands, kidneys, brain, and other central nervous system (CNS) tissues including the meninges. |
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herpesvirus group |
remain latent in host tissues with no observable signs or symptoms of disease. |
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Retroviruses |
establish a latent state after primary infection. During the latent state, the viral genome is often integrated into the host cell's chromosome and no viral replication occurs. |
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● Latent viruses |
can reactivate silently, resulting in viral replication and shedding but no clinical symptoms, or they can reactivate and cause symptomatic, even fatal, disease. |
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immune suppression |
Reactivation may accompany _______________, resulting in the recurrence of clinically apparent disease. |
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● Pathogenic viruses ● autoimmune pathogenesis |
_____________ stimulate an immune reaction that cross-reacts with antigenically similar components of the host tissues, resulting in impairment to host function. Is called ______________ |
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Autoimmune pathogenesis |
it occurs well after the acute viral infection has resolved and after antibodies are generated in response to viral antigens; this process takes several weeks to occur. |
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Transformation or immortalization |
ultimately resulting in dysregulation or uncontrolled cell proliferation. |
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oncogenic viruses |
Viruses with the ability to stimulate uncontrolled growth of host cells are referred to as |
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oncoviruses |
oncogenic viruses (also known as _____ ). |
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Human papillomaviruses (HSV) |
are oncogenic and are responsible for dysregulation of normal epithelial differentiation leading to cervical cancer. |
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- specific disease syndrome - viral agents suspected - time of year. |
Specimen selection depends on the (Code q: SDS - VAS - T) |
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Calcium alginate swabs |
interfere with PCR, the recovery of some enveloped viruses, and fluorescent-antibody tests and therefore should not be used. |
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centrifugation or filtration. |
Contaminants may be removed by concentrating the sample through what? this process may also result in removal of virus-infected cells and reduce the recovery of viral agents from the sample. |
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nasopharyngeal aspirates |
superior to throat |
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nasopharyngeal swabs |
for recovering viruses; |
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Throat swabs |
acceptable for the recovery of enteroviruses, adenoviruses, and HSY (EAH) |
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nasopharyngeal swab or aspirate |
specimens are preferred for the detection of RSV and influenza and parainfluenza viruses. (RIP) |
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Rhinovirus detection |
It requires a nasal specimen. |
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Dry sterile swab |
Throat specimens are collected with |
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inflamed, vesiculated, or purulent |
Throat specimens are collected with a dry, sterile swab by passing the swab over the ________, ________, _______ areas on the posterior pharynx. |
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touched to the tongue, buccal mucosa, teeth, or gums |
The swab should not be: |
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Nasopharyngeal Secretion Speciman |
Is collected by inserting a swab with a flexible shaft through the nostril into the nasopharynx or by washing and collecting the secretions by rinsing with a bulb syringe and 3 to 7 mL of buffered saline |
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Bronchoscopy |
are excellent specimens for detecting viruses that infect the lower respiratory tract, especially influenza viruses and adenoviruses. |
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Stool and rectal swabs |
used to detect rotavirus, enteric adenoviruses |
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- do not grow in cell culture - require PC or electron microscopy for detection |
agents of viral gastroenteritis. |
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rectal swab |
inserted 3 to 5 cm into the rectum and rotated against the mucosa to obtain feces. |
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stool specimens |
preferable to rectal swabs and should be required for rotavirus and enteric adenovirus testing. |
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diarrheal stool or stool |
Five to ten milliliters. collected in a diaper from young infants is sufficient and preferred for rotavirus and enteric adenovirus detection. |
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-CMV - Rubella - Adenoviruses - Measles - Mumps - Polyomaviruses |
can be detected in urine. (CODE: CRAMMP!!!) |
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processing multiple (two to three) specimens in parallel. |
Viral recovery may be increased by |
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clean-catch first-morning urine |
also known as first-void urine |
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urine pH and contaminating bacteria |
may interfere with viral replication. |
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centrifugation or filtering |
To remove contaminants and neutralizing the pH with a 7.5% solution of sodium bicarbonate. |
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7.5% solution of sodium bicarbonate. |
centrifugation or filtering to remove contaminants and neutralizing the pH with a |
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- Enteroviruses - HSV - VZV - CMV - Pox viruses |
can be detected in vesicular lesions of the skin and mucous membranes. (EHVCP ang code!) |
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HSV or VZV |
Collection of specimens from cutaneous vesicles for detecting |
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Tzanck smear |
may require if PCR testing is unavailable. |
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phosphate-buffered saline or viral support media (EMEM) |
added to the viral transport tube. If a tuberculin syringe is used. |
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glass microscope slide |
is pressed against the base of the ulcer. The slide is lifted, moved slightly, and pressed again. |
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laboratory for fixation and staining. |
The slides are sent to the |
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cytocentrifugation of fluid medium or PCR |
Smears can be prepared in the laboratory with |
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CSF Pericardial Pleural Fluid |
Sterile body fluids that may contain enteroviruses, HSV, VZV, influenza viruses, or CMV. |
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Physician |
specimens are collected aseptically by the _____ and sent to the laboratory for processing. |
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detect CMV |
Viral culture of blood is used primarily to |
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CMV Viremia |
is associated with peripheral blood leukocytes. |
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Heparinized citrated EDTA |
What anticoagulated blood is acceptable for CMV detection. |
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EDTA |
should be used for samples collected for nucleic acid testing |
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PCR Amplification |
EDTA should be used for samples collected for nucleic acid testing, because other anticoagulants may interfere with the enzyme functions required for |
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Serum |
may be used for serologic tests and nucleic acid assays. |
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sterile tube with anticoagulant. |
Bone marrow for virus detection should be added to |
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Aspiration |
Bone Marrow specimens are collected by |
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parvovirus B19 |
Except for ______ , most viruses are detected more readily from sites other than bone marrow. |
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lungs (CMV, influenza virus, adenovirus, sin nombre virus), brain (HSV), gastrointestinal tract (CMV). |
Tissue specimens are especially useful for detecting viruses that commonly infect the |
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Surgical procedures |
Tissue specimens are collected during |
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formalin fixed and paraffin-embedded tissue |
may be used after the removal of the paraffin (deparaffinization) and extraction. |
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HSV and human papillomavirus (HPV). |
Genital specimens often are required for the detection of |
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Genital swabs |
should be used for ulcerations and placed in appropriate viral transport media. |
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Swab/brush |
Cervical specimens may be collected using |
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● Acute specimens |
should be collected as soon as possible after the appearance of symptoms. |
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Serum for Antibody Testing |
Acute and convalescent serum specimens may be needed to detect antibodies to specific viruses. |
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Convalescent specimen |
collected in a minimum of 2 to 3 weeks after the acute specimen. |
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3 - 5 mL of serum collected by venipuncture |
Serum for antibody testing appropriate specimen is |
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4°C |
Storage up to 5 days, specimens are held at |
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-20°C, preferably -70°C. |
Storage for ≥ 6 days should be at |
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diluted or emulsified in viral transport medium. |
Specimens for freezing should first be |
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Swab |
Many types of specimens for the detection of viruses can be collected with |
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Cotton tips and Wooden shafts |
Swabs that are NOT ACCEPTABLE |
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viral serologic testing |
Blood for _______ should be transported to the laboratory in a sterile collection tube. |
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Serum |
stored for hours or days at 4°C or for weeks or months at -20°C or lower before testing. |