Book contents
- Frontmatter
- Contents
- Preface
- Contributors
- Part I Clinical Syndromes – General
- Part II Clinical Syndromes – Head and Neck
- Part III Clinical Syndromes – Eye
- Part IV Clinical Syndromes – Skin and Lymph Nodes
- Part V Clinical Syndromes – Respiratory Tract
- Part VI Clinical Syndromes – Heart and Blood Vessels
- Part VII Clinical Syndromes – Gastrointestinal Tract, Liver, and Abdomen
- Part VIII Clinical Syndromes – Genitourinary Tract
- Part IX Clinical Syndromes – Musculoskeletal System
- Part X Clinical Syndromes – Neurologic System
- Part XI The Susceptible Host
- Part XII HIV
- Part XIII Nosocomial Infection
- Part XIV Infections Related to Surgery and Trauma
- Part XV Prevention of Infection
- Part XVI Travel and Recreation
- Part XVII Bioterrorism
- Part XVIII Specific Organisms – Bacteria
- Part XIX Specific Organisms – Spirochetes
- Part XX Specific Organisms – Mycoplasma and Chlamydia
- Part XXI Specific Organisms – Rickettsia, Ehrlichia, and Anaplasma
- Part XXII Specific Organisms – Fungi
- Part XXIII Specific Organisms – Viruses
- 180 Cytomegalovirus
- 181 Dengue and Dengue-Like Illness
- 182 Enteroviruses
- 183 Epstein–Barr Virus and Other Causes of the Mononucleosis Syndrome
- 184 Hantavirus Cardiopulmonary Syndrome in the Americas
- 185 Herpes Simplex Viruses 1 and 2
- 186 Human Herpesviruses 6, 7, and 8
- 187 Influenza
- 188 Papillomavirus
- 189 Acute and Chronic Parvovirus Infection
- 190 Rabies
- 191 Varicella-Zoster Virus
- 192 Viral Hemorrhagic Fevers
- Part XXIV Specific Organisms – Parasites
- Part XXV Antimicrobial Therapy – General Considerations
- Index
189 - Acute and Chronic Parvovirus Infection
from Part XXIII - Specific Organisms – Viruses
Published online by Cambridge University Press: 05 March 2013
- Frontmatter
- Contents
- Preface
- Contributors
- Part I Clinical Syndromes – General
- Part II Clinical Syndromes – Head and Neck
- Part III Clinical Syndromes – Eye
- Part IV Clinical Syndromes – Skin and Lymph Nodes
- Part V Clinical Syndromes – Respiratory Tract
- Part VI Clinical Syndromes – Heart and Blood Vessels
- Part VII Clinical Syndromes – Gastrointestinal Tract, Liver, and Abdomen
- Part VIII Clinical Syndromes – Genitourinary Tract
- Part IX Clinical Syndromes – Musculoskeletal System
- Part X Clinical Syndromes – Neurologic System
- Part XI The Susceptible Host
- Part XII HIV
- Part XIII Nosocomial Infection
- Part XIV Infections Related to Surgery and Trauma
- Part XV Prevention of Infection
- Part XVI Travel and Recreation
- Part XVII Bioterrorism
- Part XVIII Specific Organisms – Bacteria
- Part XIX Specific Organisms – Spirochetes
- Part XX Specific Organisms – Mycoplasma and Chlamydia
- Part XXI Specific Organisms – Rickettsia, Ehrlichia, and Anaplasma
- Part XXII Specific Organisms – Fungi
- Part XXIII Specific Organisms – Viruses
- 180 Cytomegalovirus
- 181 Dengue and Dengue-Like Illness
- 182 Enteroviruses
- 183 Epstein–Barr Virus and Other Causes of the Mononucleosis Syndrome
- 184 Hantavirus Cardiopulmonary Syndrome in the Americas
- 185 Herpes Simplex Viruses 1 and 2
- 186 Human Herpesviruses 6, 7, and 8
- 187 Influenza
- 188 Papillomavirus
- 189 Acute and Chronic Parvovirus Infection
- 190 Rabies
- 191 Varicella-Zoster Virus
- 192 Viral Hemorrhagic Fevers
- Part XXIV Specific Organisms – Parasites
- Part XXV Antimicrobial Therapy – General Considerations
- Index
Summary
B19 parvovirus is the only member of the Parvoviridae family known to cause diseases in humans. Parvoviruses are small viruses with unenveloped icosahedral capsids that contain a single-stranded DNA genome. These physical properties contribute to viral resistance to heat, solvents, and extreme chemical conditions. Because of their limited genome, parvoviral propagation depends on infection of mitotically active cells. In the taxonomy of the parvovirus family, B19 and closely related simian parvoviruses constitute the Erythrovirus genus, separated from autonomous animal parvoviruses, dependoviruses (which require coinfection with a second virus for efficient propagation in cell culture), and insect parvoviruses called densoviruses.
B19 parvovirus has extreme tropism for human erythroid progenitor cells, which are responsible for the generation of circulating erythrocytes. In tissue culture, B19 has been propagated only in bone marrow, fetal liver, peripheral blood, and rather inefficiently in a few leukemic cell lines. B19 replication in patients has been detected in blood and marrow. Specificity for erythroid cells follows from the cellular receptor for the virus, globoside or P antigen, a tetrohexoseceramide present on erythroid cells, megakaryocytes, endothelial cells, and some placental cell types, as well as fetal liver and heart. Parvovirus infection is terminated by host production of neutralizing antibodies. Failure to produce neutralizing antibodies can result in persistent infection. Recently, cellular immune responses to parvoviruses have been measured and some CD4 and CD8 T-cell epitopes defined.
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- Clinical Infectious Disease , pp. 1301 - 1304Publisher: Cambridge University PressPrint publication year: 2008