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Textbook
Introduction
1. Anatomy
2. Microbiology
2.1 General bacteriology
2.2 Introduction to systemic bacteriology
2.3 Gram positive cocci
2.4 Gram negative cocci
2.5 Gram positive bacilli
2.6 Gram negative bacilli
2.7 Other important bacteria
2.8 Virology
2.8.1 Overview
2.8.2 Herpesviruses
2.8.3 Poxviruses
2.8.4 Adenovirus
2.8.5 Papilloma and Polyoma viruses
2.8.6 Parvovirus
2.8.7 Orthomyxoviruses and Paramyxoviruses
2.8.8 Viruses causing diarrhea
2.8.9 Picornavirus
2.8.10 Hepatitis Viruses
2.8.11 Arboviruses
2.8.12 Retroviruses
2.8.13 Other important viruses
2.8.14 Additional information
2.9 Parasitology
2.10 Mycology
3. Physiology
4. Pathology
5. Pharmacology
6. Immunology
7. Biochemistry
8. Cell and molecular biology
9. Biostatistics and epidemiology
10. Genetics
11. Behavioral science
Wrapping up
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2.8.6 Parvovirus
Achievable USMLE/1
2. Microbiology
2.8. Virology

Parvovirus

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Parvovirus is the only single-stranded DNA virus. It’s transmitted by the respiratory route, transplacentally, or via blood. The virus replicates in the host cell nucleus.

Replication can occur only during the S phase of the cell cycle. For this reason, it doesn’t infect mature RBCs. Instead, it mainly infects erythroblasts and endothelial cells.

The virus requires the P blood antigen receptor (also known as globoside) to enter the cell. Rare individuals who lack the P antigen are immune to parvovirus B19 infection.

Deposition of immune complexes composed of virus particles and IgM or IgG occurs in endothelial cells and joints.

Clinical features: It causes erythema infectiosum, also called “slapped cheek disease.” It’s typically seen in children. It presents with fever, malaise, headache, myalgia, nausea, and rhinorrhea, followed by a bright red macular exanthem on the cheeks that’s often associated with circumoral pallor. A diffuse maculopapular rash can appear 1-4 days later and fade to a lacy erythematous rash, which may be pruritic and gradually spread toward the distal extremities.

Fifth disease rash
Fifth disease rash

Slapped cheek rash

In patients with hemoglobinopathies or hemolytic anemias, parvovirus may precipitate aplastic crisis. The bone marrow reveals an absence of erythroid precursors and the presence of striking giant pronormoblasts.

Cases of immune thrombocytopenic purpura, Henoch-Schönlein purpura, and hemophagocytic syndrome have been attributed to parvovirus B19. It may also cause polyarthropathy syndrome, mainly affecting the small joints of the hands and feet and mimicking rheumatoid arthritis.

Intrauterine infections may cause hydrops fetalis. This occurs when a nonimmune woman is infected, usually in the first 20 weeks of pregnancy. There is generalized swelling of the fetus from heart failure secondary to severe anemia from parvovirus infection.

Diagnosis of parvovirus infections: IgG and IgM antibodies can be detected by ELISA, RIA, or immunofluorescence. DNA hybridization or PCR can be used for viral detection. PCR of amniotic fluid can be done in fetal hydrops fetalis.

Virology and Transmission

  • Only single-stranded DNA virus
  • Transmission: respiratory, transplacental, blood
  • Replicates in host cell nucleus during S phase

Cellular Targets and Entry

  • Infects erythroblasts, endothelial cells (not mature RBCs)
  • Requires P blood antigen (globoside) for cell entry
    • Individuals lacking P antigen are immune

Pathogenesis

  • Immune complexes (virus + IgM/IgG) deposit in endothelium, joints

Clinical Features

  • Erythema infectiosum (“slapped cheek disease”) in children
    • Initial: fever, malaise, headache, myalgia, nausea, rhinorrhea
    • Rash: bright red cheeks, circumoral pallor, lacy maculopapular rash spreading to extremities
  • Can cause aplastic crisis in hemoglobinopathies/hemolytic anemias
    • Bone marrow: absence of erythroid precursors, giant pronormoblasts
  • Associated syndromes: immune thrombocytopenic purpura, Henoch-Schönlein purpura, hemophagocytic syndrome, polyarthropathy (mimics rheumatoid arthritis)
  • In pregnancy: hydrops fetalis (fetal heart failure, severe anemia)

Diagnosis

  • Serology: IgG, IgM detection (ELISA, RIA, immunofluorescence)
  • Viral detection: DNA hybridization, PCR
    • PCR of amniotic fluid for hydrops fetalis

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Parvovirus

Parvovirus is the only single-stranded DNA virus. It’s transmitted by the respiratory route, transplacentally, or via blood. The virus replicates in the host cell nucleus.

Replication can occur only during the S phase of the cell cycle. For this reason, it doesn’t infect mature RBCs. Instead, it mainly infects erythroblasts and endothelial cells.

The virus requires the P blood antigen receptor (also known as globoside) to enter the cell. Rare individuals who lack the P antigen are immune to parvovirus B19 infection.

Deposition of immune complexes composed of virus particles and IgM or IgG occurs in endothelial cells and joints.

Clinical features: It causes erythema infectiosum, also called “slapped cheek disease.” It’s typically seen in children. It presents with fever, malaise, headache, myalgia, nausea, and rhinorrhea, followed by a bright red macular exanthem on the cheeks that’s often associated with circumoral pallor. A diffuse maculopapular rash can appear 1-4 days later and fade to a lacy erythematous rash, which may be pruritic and gradually spread toward the distal extremities.

Slapped cheek rash

In patients with hemoglobinopathies or hemolytic anemias, parvovirus may precipitate aplastic crisis. The bone marrow reveals an absence of erythroid precursors and the presence of striking giant pronormoblasts.

Cases of immune thrombocytopenic purpura, Henoch-Schönlein purpura, and hemophagocytic syndrome have been attributed to parvovirus B19. It may also cause polyarthropathy syndrome, mainly affecting the small joints of the hands and feet and mimicking rheumatoid arthritis.

Intrauterine infections may cause hydrops fetalis. This occurs when a nonimmune woman is infected, usually in the first 20 weeks of pregnancy. There is generalized swelling of the fetus from heart failure secondary to severe anemia from parvovirus infection.

Diagnosis of parvovirus infections: IgG and IgM antibodies can be detected by ELISA, RIA, or immunofluorescence. DNA hybridization or PCR can be used for viral detection. PCR of amniotic fluid can be done in fetal hydrops fetalis.

Key points

Virology and Transmission

  • Only single-stranded DNA virus
  • Transmission: respiratory, transplacental, blood
  • Replicates in host cell nucleus during S phase

Cellular Targets and Entry

  • Infects erythroblasts, endothelial cells (not mature RBCs)
  • Requires P blood antigen (globoside) for cell entry
    • Individuals lacking P antigen are immune

Pathogenesis

  • Immune complexes (virus + IgM/IgG) deposit in endothelium, joints

Clinical Features

  • Erythema infectiosum (“slapped cheek disease”) in children
    • Initial: fever, malaise, headache, myalgia, nausea, rhinorrhea
    • Rash: bright red cheeks, circumoral pallor, lacy maculopapular rash spreading to extremities
  • Can cause aplastic crisis in hemoglobinopathies/hemolytic anemias
    • Bone marrow: absence of erythroid precursors, giant pronormoblasts
  • Associated syndromes: immune thrombocytopenic purpura, Henoch-Schönlein purpura, hemophagocytic syndrome, polyarthropathy (mimics rheumatoid arthritis)
  • In pregnancy: hydrops fetalis (fetal heart failure, severe anemia)

Diagnosis

  • Serology: IgG, IgM detection (ELISA, RIA, immunofluorescence)
  • Viral detection: DNA hybridization, PCR
    • PCR of amniotic fluid for hydrops fetalis