Rift Valley Fever
Classification according to ICD-10 | |
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A92.4 | Rift Valley Fever |
ICD-10 online (WHO version 2019) |
The Rift Valley fever ( English Rift valley fever , RVF) is a by phleboviruses ( Family Phenuiviridae ) evoked haemorrhagic fever in ruminants . The illness can cause a flu-like illness in humans , which can rarely be fatal. The Rift Valley fever is therefore a zoonosis . It is notifiable.
Occurrence
Rift valley fever was first described as a disease in the valley of the same name ( Rift Valley ) in Kenya in 1913. 1931 there was a first major epidemic and since then the disease has throughout Africa south of the Sahara spread. When it first appeared on the Arabian Peninsula in 2000, more than 160 people died.
The disease has not yet been observed in Europe.
The World Health Organization provides information on current cases .
Pathogen
Rift Valley Fever Virus | ||||||||||||||||||||
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Rift valley fever viruses under the electron microscope (source: CDC ) |
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Systematics | ||||||||||||||||||||
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Taxonomic characteristics | ||||||||||||||||||||
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Scientific name | ||||||||||||||||||||
Rift Valley fever phlebovirus | ||||||||||||||||||||
Short name | ||||||||||||||||||||
RVFV | ||||||||||||||||||||
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The causative agents of Rift Valley fever are viruses of the species Rift Valley fever phlebovirus (RVFV, Rift Valley Fever Virus ) from the genus Phlebovirus of the family Phenuiviridae in the order Bunyavirales . These are single-stranded RNA - viruses . Your genome is segmented into three parts (tripartite). While it is commonly referred to as negative polarity classified Indeed, the situation is complicated, however: The L and M segment have both negative polarity ( English negative-sense ), but the S-segment (and thus the entire genome) is ambisense . The three genome segments code for 6 main proteins :
- The viral polymerase : L-protein
- two glycoproteins : G (N) and G (C)
- other non-structural proteins: NSs and NSm
As with all bunyaviruses, the virus particles ( virions ) of RVFV have an outer lipid envelope (with the two glycoproteins - G (N) and G (C)). These are required for entry into the host cell, because they fuse the virus envelope with its endosomal membrane and thus bring the viral genome into the host cell.
The G (C) protein has a structure like the class II membrane fusion proteins of the flaviviruses and alphaviruses . This structural similarity suggests a possible common ancestry.
The virus originally caused a ruminant disease ( sheep , goats , cattle , camels , antelopes ), but it can also be transmitted to humans by various mosquitoes (especially Culex and Aedes species).
Clinical picture in ruminants
In young animals the disease is mostly dramatic with high fever , anorexia , weakness and ends in 70% of the animals fatal. Occasionally, nasal discharge and bloody diarrhea also occur. Adult animals show less pronounced courses. In pregnant animals, it usually comes to miscarriage . The disease is milder in cattle than in sheep.
Severe necrosis of the liver is typical of the disease.
Clinic in humans
Infections in humans mostly occur in connection with animal epidemics. The virus can be transmitted both through the air and through direct contact with infected animals, for example when slaughtered. The incubation period is between three and 12 days; Serological determination of the virus is possible from the fourth day of illness .
Symptoms of the disease include high fever , headache and muscle pain, and rarely hepatitis . About 1% of patients develop a pronounced hemorrhagic fever with hepatitis and often fatal outcome after a few days . After the fever has subsided, some patients develop a usually fatal inflammation of the meninges (meningitis) or inflammation of the retina (retinitis), which can lead to blindness .
A curative treatment option for Rift Valley fever does not yet exist (possibly ribavirin , which is effective in animal studies), so preventive protection ( exposure prophylaxis ) against insect bites in endemic areas is urgently recommended. Effective and well-tolerated vaccines are available for both humans and animals. However, they are not yet approved in Germany.
Combat
According to the IfSG , illnesses and deaths from Rift Valley fever must be reported. According to the ordinance on notifiable animal diseases (TierSeuchAnzV), a disease in animals is a notifiable animal disease .
Web links
- Rift Valley fever, Fact Sheet WHO (English)
Individual evidence
- ↑ Arabian Peninsula Primed for Rift Valley Fever NASA Earthobservatory (English)
- ^ WHO: Global Alert and Response - Rift Valley fever
- ↑ ICTV Master Species List 2018b v1 MSL # 34, Feb. 2019
- ↑ a b ICTV: ICTV Taxonomy history: Akabane orthobunyavirus , EC 51, Berlin, Germany, July 2019; Email ratification March 2020 (MSL # 35)
- ↑ a b ViralZone: Phlebovirus . Retrieved September 14, 2016.
- ^ Dessau M, Modis Y: Crystal structure of glycoprotein C from Rift Valley fever virus . In: Proceedings of the National Academy of Sciences of the United States of America . 110, No. 5, January 2013, pp. 1696-701. bibcode : 2013PNAS..110.1696D . doi : 10.1073 / pnas.1217780110 . PMID 23319635 . PMC 3562824 (free full text).
- ↑ Robert Koch Institute: Epidemiological Bulletin No. 3/2007 of January 19, 2007, p. 19