出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/10/24 21:28:48」(JST)[Wiki en表示]
|Human parainfluenza viruses (hPIV)|
|Group:||Group V ((-)ssRNA)|
|Genus:||Respirovirus & Rubalavirus|
|Human parainfluenza viruses|
|Classification and external resources|
|ICD-10||B34.8, J12.2, J20.4|
Human parainfluenza viruses (hPIVs) are the etiologic agents causing 'human parainfluenza.' hPIVs are a group of four distinct serotypes of enveloped single-stranded RNA viruses belonging to the paramyxovirus family. These viruses are closely associated with both human and veterinary disease. They are approximately 150-250 nm in size and composed of negative sense RNA with a genome encompassing ~15,000 nucleotides.
The viruses can be detected via cell culture, immunofluorescent microscopy, and PCR. hPIV remains the second main cause of hospitalisation in children under 5 years of age suffering from a respiratory illness (only respiratory syncytial virus causes more respiratory hospitalisations for this age group).
- 1 Classification
- 1.1 Viral structure and organisation
- 1.2 Viral entry and replication
- 1.3 Host range
- 2 Clinical significance
- 2.1 Airway inflammation
- 2.2 Immunology
- 3 Diagnosis
- 4 Morbidity and mortality
- 4.1 Risk factors
- 5 Prevention
- 6 Medication
- 7 Interactions with the environment
- 8 Economic burden
- 9 External reading
- 10 References
The first hPIV was discovered in the late 1950s. The taxonomic division is broadly based on antigenic and genetic characteristics, forming four major serotypes. These include:
- Human parainfluenza virus type 1 (hPIV-1) (most common cause of croup)
- Human parainfluenza virus type 2 (hPIV-2) (causes croup and other upper and lower respiratory tract illnesses)
- Human parainfluenza virus type 3 (hPIV-3) (associated with bronchiolitis and pneumonia)
- Human parainfluenza virus type 4 (hPIV-4) (includes subtypes 4a and 4b)
hPIV is closely related to a recently formed virus grouping, the 'megamyxoviruses' (Hendra and Nipah) and closely linked to the metapneumovirus. hPIV is divided within two genera: Respirovirus (hPIV-1 & hPIV-3) and the Rubulavirus (hPIV-2 & hPIV-4).
Viral structure and organisation
hPIV is characterised by being enveloped and containing single stranded negative sense RNA. Non-infectious virions have also been reported with positive RNA polarity. The genome has in the region of 15,000 nucleotides and this is used to encode six key structural proteins.
The structural gene sequence is believed to be as follows: 3′-NP-P-M-F-HN-L-5′ (the protein prefixes and further details are outlined in the table below).
|Hemagglutinin-neuraminidase (HN)||Envelope||Attachment and cell entry|
|Fusion Protein (F)||Envelope||Fusion and cell entry|
|Matrix Protein (M)||Within the envelope||Assembly|
|Nucleoprotein (NP)||Nucleocapsid||Forms a complex with the RNA genome|
|Phosphoprotein (P)||Nucleocapsid||Forms as part of RNA polymerase complex|
|Large Protein (L)||Nucleocapsid||Forms as part of RNA polymerase complex|
With the advent of reverse genetics, it has been found that the most efficient human parainfluenza viruses (in terms of replication and transcription) have a genome nucleotide total which is divisible by the number 6. This has led to the "rule of six" being coined. Exceptions to this rule have been found and its exact advantages are not fully understood.
Electrophoresis has shown that the molecular weight (MW) of the proteins for the four hPIV serotypes are similar (with the exception of the phosphoprotein, which shows significant variation). More information on the structural proteins can be found in the paramyxovirus protein section or here.
Viral entry and replication
Viral replication is initiated only after successful entry into a cell by attachment and fusion between the virus and the host cell lipid membrane. Viral RNA (vRNA) is initially associated with nucleoprotein (NP), phosphoprotein (P) and the large protein (L). The hemagglutinin-neuraminidase (HN) is involved with viral attachment and thus hemadsorption and hemagglutination. Furthermore, the fusion (F) protein is important in aiding the fusion of the host and viral cellular membranes, eventually forming syncytia.
Initially the F protein is in an inactive form (F0) but can be cleaved by proteolysis to form its active form, F1 and F2, linked by di-sulphide bonds. Once complete, this is followed by the hPIV nucleocapsid entering the cytoplasm of the cell. Subsequently, genomic transcription occurs using the viruses own 'viral RNA-dependant RNA polymerase' (L protein). The cells own ribosomes are then tasked with translation, forming the viral proteins from the viral mRNA.
Towards the end of the process, (after the formation of the viral proteins) the replication of the viral genome occurs. Initially this occurs with the formation of a positive-sense RNA (intermediate step necessary for producing progeny) and finally negative-sense RNA is formed which is then associated with the nucleoprotein. This may then be either packaged and released from the cell by budding or it can be used for subsequent rounds of transcription and replication.
The observable and morphological changes which can be seen in infected cells includes the enlargement of the cytoplasm, decreased mitotic activity and 'focal rounding,' with the potential formation of multi-nucleate cells.
The pathogenicity of hPIV is mutually dependant on the virus having the correct accessory proteins which are able to elicit anti-interferon properties. This is a major factor in the clinical significance of disease.
The main host remains the human. Despite this, infections have been induced in other animals (both under natural and experimental situations) although these were always asymptomatic.
In the USA it is estimated that there are 5 million children with lower respiratory infections (LRI) each year. Estimates have shown that hPIV-1, hPIV-2 and hPIV-3 have been linked with up to a third of these infections. Upper respiratory infections (URI) are also important in the context of hPIV, however are caused to a lesser extent by the virus. The highest rates of serious HPIV illnesses occur among young children and surveys have shown that about 75% of children aged 5 or older have antibodies to HPIV-1.
For infants and young children it has been estimated that ~25% will develop 'clinically significant disease.'
Repeated infection throughout the life of the host is not uncommon and symptoms of later breakouts include upper respiratory tract illness, such as cold and a sore throat. The incubation period for all four serotypes is 1 to 7 days. In immunosuppressed people, parainfluenza virus infections can cause severe pneumonia which can be fatal.
hPIV-1 and hPIV-2 have been demonstrated to be the principal causative agent behind croup (laryngotracheobronchitis) which is a viral disease of the upper airway and is mainly problematic in children aged 6–48 months of age. Biennial epidemics starting in Autumn are associated with both hPIV-1 and 2 however, hPIV-2 can also have yearly outbreaks. Additionally, HPIV-1 tends to cause biennial outbreaks of croup in the fall. In the United States, large peaks have presently been occurring during odd-numbered years.
hPIV-3 has been closely associated with bronchiolitis and pneumonia and principally targets those aged <1 year.
hPIV-4 remains infrequently detected. However, it is now believed to be more common than previously thought, but is less likely to cause severe disease. By the age of 10, the majority of children are sero-positive for hPIV-4 infection which may be indicative of a large proportion of asymptomatic or mild infections.
Important epidemiological factors that are associated with a higher risk of infection and mortality are those who are immuno-compromised and may be taken ill with more extreme forms of LRI. Associations between hPIV and neurologic disease are known, for example hospitalisation with certain types of hPIV has a strong association with febrile seizures. hPIV-4B has the strongest association (up to 62%) followed by hPIV-3 and 1.
hPIV has also been linked with rare cases of virally caused meningitis and Guillain-Barré syndrome.
HPIVs are spread person to person by contact with infected secretions through respiratory droplets or contaminated surfaces or objects. Infection can occur when infectious material contacts mucous membranes of the eyes, mouth, or nose, and possibly through the inhalation of droplets generated by a sneeze or cough. HPIVs can remain infectious in airborne droplets for over an hour.
Overall, hPIV remains best known for its effects on the respiratory system and this appears to be where the majority of the focus has been upon.
The inflammation of the airway is a common attribute of hPIV infection. It is believed to occur due to the large scale up-regulation of inflammatory cytokines. Common cytokines which would be expected to be up-regulated include IFN–α, various other interleukins (IL–2, IL-6) and TNF–α. Various other chemokines and inflammatory proteins are also believed to be associated with the common symptoms of hPIV infection.
Recent evidence seems to suggest that viral specific antibodies (IgE) may be responsible for mediating large scale releases of histamine in the trachea which are believed to cause croup. More detail on the pathways and interactions can be found here.
The bodies primary defence against hPIV infection remains humoral immunity. This is mainly directed against surface proteins which can be found on the virus. In particular the proteins HN and F prove to be most immunogenic in terms of stimulating the immune system.
Recently the importance of the 'cell mediated immune system' has been scrutinised. Reports have shown that those with defective adaptive immune responses are at a higher risk of severe infection.
Diagnosis can be made in several ways, encompassing a range of multi-faceted techniques:
- Isolation and detection of the virus in cell culture.
- Detection of viral antigens directly within bodily respiratory tract secretions using immunofluorescence, enzyme immunoassays or fluroimmunoassays.
- Polymerase chain reaction (PCR).
- Analysis of specific IgG antibodies showing a subsequent rise in titre following infection (using paired serum specimens).
Because of the similarity in terms of the antigenic profile between the viruses, hemagglutination assay (HA) or hemadsorption inhibition (HAdI) processes are often used. Both complement fixation, neutralisation and enzyme linked immunosorbent assays – ELISA, can also be used to aid in the process of distinguishing between viral serotypes.
Morbidity and mortality
Mortality caused by hPIV in developed regions of the world remains rare. Where mortality has occurred, it is principally in the three core risk groups (very young, elderly and immuno-compromised). Long term changes can however be associated with airway remodelling and are believed to be a significant cause of morbidity. The exact associations between hPIV and diseases such as chronic obstructive pulmonary disease (COPD) are still being investigated.
In developing regions of the world, the highest risk group in terms of mortality remains pre-school children. Mortality may be as a consequence of primary viral infection or secondary problems such as bacterial infection. Predispositions, such as malnutrition and other deficiencies may further elevate the chances of mortality associated with infection.
Overall, LRI's cause approximately 25-30% of total deaths in pre-school children in the developing world. hPIV is believed to be associated with 10% of all LRI cases, thus remaining a significant cause of mortality.
Numerous factors have been suggested and linked to a higher risk of acquiring the infection, inclusive of malnutrition, vitamin A deficiency, absence of breastfeeding during the early stages of life, environmental pollution and overcrowding.
Despite decades of research, no vaccines currently exist.
Recombinant technology has however been used to target the formation of vaccines for hPIV-1, 2 and 3 serotypes and has taken the form of several live-attenuated intranasal vaccines. Two vaccines in particular were found to be immunogenic and well tolerated against hPIV-3 in phase I trials. hPIV 1 and 2 vaccine candidates remain less advanced.
Vaccine techniques which have been used against hPIV are not limited to intranasal forms, but also viruses attenuated by cold passage, host range attenuation, chimeric construct vaccines and also introducing mutations with the help of reverse genetics to achieve attenuation.
Maternal antibodies may offer some degree of protection against hPIV during the early stages of life via the colostrum in breast milk.
Ribavirin is one medication which has shown good potential for the treatment of hPIV-3 given recent in-vitro tests (in-vivo tests show mixed results). Ribavirin is a broadscale anti-viral and is currently being administered to those who are severely immuno-compromised, despite the lack of conclusive evidence for its use. Protein inhibitors and novel forms of medication have also been proposed to relieve the symptoms of infection.
Furthermore, antibiotics may be used if a secondary bacterial infection develops. Corticosteroid treatment and nebulizers and also a first line choice against croup if breathing difficulties ensue.
Interactions with the environment
Parainfluenza viruses last only a few hours in the environment and are inactivated by soap and water. Furthermore, the virus can also be easily destroyed using common hygiene techniques and detergents, disinfectants and antiseptics.
Environmental factors which are important for hPIV survival are pH, humidity, temperature and the medium the virus in found within. The optimal pH is around the physiologic pH values (7.4 to 8.0), whilst at high temperatures (above 37°C) and low humidity, infectivity reduces.
The majority of transmission has been linked to close contact, especially in nosocomial infections. Chronic care facilities and doctors surgery's are also known to be transmission 'hotspots' with transmission occurring via aerosols, large droplets and also fomites (contaminated surfaces).
The exact infectious dose remains unknown.
In the poorest regions of the world, hPIV infection can be measured in terms of mortality. In the developed world where mortality remains rare, the economic costs of the infection can be estimated. Estimates from the USA are suggestive of a cost (based on extrapolation) in the region of $200 million per annum.
Parainfluenza Clinical Microbiology Review
Clinical Features of Human Parainfluenza Viruses (hPIVs)
- Vainionpää R, Hyypiä T (April 1994). "Biology of parainfluenza viruses". Clin. Microbiol. Rev. 7 (2): 265–75. doi:10.1128/CMR.7.2.265. PMC 358320. PMID 8055470.
- Henrickson, KJ (2003 Apr). "Parainfluenza viruses". Clinical Microbiology Reviews 16 (2): 242–64. doi:10.1128/CMR.16.2.242-264.2003. PMC 153148. PMID 12692097.
- "Human Parainfluenza Viruses". Centers for Disease Control and Prevention (2011). Retrieved 21 March 2012.
- Schmidt,, Alexander; Anne Schaap-Nutt, Emmalene J Bartlett, Henrick Schomacker, Jim Boonyaratanakornkit, Ruth A Karron and Peter L Collins (1 February 2011). "Acknowledgements". Expert Review of Respiratory Medicine 5 (1): 137–137. doi:10.1586/ers.11.3. Retrieved 21 March 2012.
- "Parainfluenza Viruses". Retrieved 2009-03-15.
- Hunt, Dr. Margaret. "PARAINFLUENZA, RESPIRATORY SYNCYTIAL AND ADENO VIRUSES". Reference.MD. Retrieved 21 March 2012.
- Vulliémoz, D; Roux, L (2001 May). ""Rule of six": how does the Sendai virus RNA polymerase keep count?". Journal of Virology 75 (10): 4506–18. doi:10.1128/JVI.75.10.4506-4518.2001. PMC 114204. PMID 11312321.
- Moscona, A (2005 Jul). "Entry of parainfluenza virus into cells as a target for interrupting childhood respiratory disease". The Journal of Clinical Investigation 115 (7): 1688–98. doi:10.1172/JCI25669. PMC 1159152. PMID 16007245.
- Chambers,; Raychel, Takimoto, Toru (March 2011). "Parainfluenza Viruses". ELS.
- "Parainfluenza Virus: Epidemiology". eMedicine. Retrieved 21 March 2012.
- "HUMAN PARAINFLUENZA VIRUS". Public Health Agency of Canada. Retrieved 21 March 2012.
- Henrickson, KJ; Kuhn, SM, Savatski, LL (1994 May). "Epidemiology and cost of infection with human parainfluenza virus types 1 and 2 in young children". Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 18 (5): 770–9. doi:10.1093/clinids/18.5.770. PMID 8075269.
- Denny, FW; Clyde WA, Jr (1986 May). "Acute lower respiratory tract infections in nonhospitalized children". The Journal of pediatrics 108 (5 Pt 1): 635–46. doi:10.1016/S0022-3476(86)81034-4. PMID 3009769.
- "Acute Respiratory Infections". WHO. Retrieved 21 March 2012.
- Durbin, AP; Karron, RA (2003 Dec 15). "Progress in the development of respiratory syncytial virus and parainfluenza virus vaccines". Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 37 (12): 1668–77. doi:10.1086/379775. PMID 14689350.
- "General information: human parainfluenza viruses". Health Protection Agency. Retrieved 21 March 2012.
- Sable CA, Hayden FG (December 1995). "Orthomyxoviral and paramyxoviral infections in transplant patients". Infect. Dis. Clin. North Am. 9 (4): 987–1003. PMID 8747776.
- "CDC - Human Parainfluenza Viruses: Common cold and croup". Retrieved 2009-03-15.
- "Croup Background". Medscape Reference.
- "Parainfluenza Virus Review". Medscape. Retrieved 21 March 2012.
- Stephen B Greenberg, Robert L Atmar. "Parainfluenza Viruses—New Epidemiology and Vaccine Developments". Touch Infectious Disease. Retrieved 21 March 2012.
- Arguedas, A; Stutman, HR, Blanding, JG (1990 Mar). "Parainfluenza type 3 meningitis. Report of two cases and review of the literature". Clinical pediatrics 29 (3): 175–8. doi:10.1177/000992289002900307. PMID 2155085.
- Dimopoulos, G; Lerikou, M, Tsiodras, S, Chranioti, A, Perros, E, Anagnostopoulou, U, Armaganidis, A, Karakitsos, P (2012 Feb). "Viral epidemiology of acute exacerbations of chronic obstructive pulmonary disease". Pulmonary pharmacology & therapeutics 25 (1): 12–8. doi:10.1016/j.pupt.2011.08.004. PMID 21983132.
- Beckham, JD; Cadena, A, Lin, J, Piedra, PA, Glezen, WP, Greenberg, SB, Atmar, RL (2005 May). "Respiratory viral infections in patients with chronic, obstructive pulmonary disease". The Journal of infection 50 (4): 322–30. doi:10.1016/j.jinf.2004.07.011. PMID 15845430.
- Berman, S (1991 May-Jun). "Epidemiology of acute respiratory infections in children of developing countries". Reviews of infectious diseases. 13 Suppl 6: S454–62. PMID 1862276.
- Sato M, Wright PF (October 2008). "Current status of vaccines for parainfluenza virus infections". Pediatr. Infect. Dis. J. 27 (10 Suppl): S123–5. doi:10.1097/INF.0b013e318168b76f. PMID 18820572.
- "Parainfluenza Viruses". eLS. Retrieved 21 March 2012.
- "Definition of Human parainfluenza virus". MedicineNet. Retrieved 21 March 2012.
- HAMBLING, MH (1964 Dec). "SURVIVAL OF THE RESPIRATORY SYNCYTIAL VIRUS DURING STORAGE UNDER VARIOUS CONDITIONS". British journal of experimental pathology 45 (6): 647–55. PMC 2093680. PMID 14245166.
- "Common Cold, Croup and Human Parainfluenza Viruses: Symptoms and Prevention.". NewsFlu. Retrieved 21 March 2012.
- There are four types of parainfluenza virus, all of which can cause upper respiratory infections or lower respiratory infections (pneumonia) in adults and children. The virus can cause croup, bronchiolitis, bronchitis and ...
- Parainfluenza viruses (PIVs) are paramyxoviruses of the order Mononegavirales, the family Paramyxoviridae, and the subfamily Paramyxovirinae. Human PIVs (HPIVs) are currently divided into 5 serotypes—HPIV-1, HPIV ...
|拡張検索||「human parainfluenza virus 3」「human parainfluenza virus 4」「parainfluenza virus type 2」「bovine parainfluenza virus 3」「parainfluenza viruses」|
- parainfluenza virus
- I型 ：喉頭炎。秋。
- II型 ：喉頭炎。秋。軽い。
- III型 ：肺炎。 春。幼児。
- IV型 ：上気道炎。散発的。
- computer virus