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Das Seoul-Virus (auch Seoulvirus, SEOV oder SOUV, wissenschaftlich Seoul orthohantavirus, veraltet Seoul hantavirus) ist eine Spezies von RNA-Viren. Es zählt zum Genus (Gattung) Orthohantavirus aus der Familie Hantaviridae, Unterfamilie Mammantavirinae. Das Erregerreservoir ist die Wanderratte.[3]
Ein großer Teil der Hantavirus-Infektionen verläuft vermutlich asymptomatisch oder mit unspezifischen Symptomen. Hantaviren können aber auch schwere Krankheitsbilder hervorrufen. Asiatische und europäische Hantavirus-Stämme sind Auslöser des Hämorrhagischen Fiebers mit renalem Syndrom (HFRS).[3][4]
Der Nachweis von Hantaviren-Infektionen ist in Deutschland, Österreich und der Schweiz meldepflichtig bzw. anzeigepflichtig (siehe im Einzelnen unter Hantaviren).
SEOV ist wie alle anderen Hantaviren ein einzelsträngiges RNA-Virus negativer Polarität. Sein Genom hat drei verschiedene Segmente: S (klein, englisch small), M (mittel, en. medium) und L (groß, en. large).[5][6]
Das Virus ist pleomorph (d. h., es hat verschiedene Formen); oft ist jedoch eine kugelförmige Gestalt zu beobachten, wobei seine beiden Oberflächenglykoproteine in Reihen angeordnet sind. Innerhalb dieser Kugel befinden sich die drei zirkulären RNA-Segmente kreisförmig angeordnet. Die RNA ist mit dem N-Protein (Nukleokapsid-Protein) des Virus beschichtet und an das sog. L-Protein gebunden. Die 5'- und 3'-Enden der Genomsegmente stimmen überein, wodurch eine Pfannenstielstruktur entsteht. Diese Basenpaarung kommt bei allen Hantavirus-Spezies vor, wobei die genaue Pfannenstielstruktur und -sequenz für jede einzelne Spezies charakteristisch ist. Dabei gibt es allerdings Ähnlichkeiten und Überlappungen zwischen verschiedenen Spezies, einschließlich einer Konsensussequenz mit acht Nukleotiden.[7][5][6]
Das Seoul-Virus ist hauptsächlich in Asien verbreitet, wo dieses auch seinen Ursprung hat.
Das Virus soll über infizierte Wildratten über Schiffe nach Europa gelangt sein.[8]
Der Nachweis einer ersten Übertragung von einer Heimratte auf einen Menschen erfolgte in Deutschland im November 2020.[9][10] Eine Frau aus Niedersachsen musste mit Symptomen eines akuten Nierenversagens mehrere Tage intensivmedizinisch versorgt werden.[11][10][12][13][14]
Das Seoul-Virus (auch Seoulvirus, SEOV oder SOUV, wissenschaftlich Seoul orthohantavirus, veraltet Seoul hantavirus) ist eine Spezies von RNA-Viren. Es zählt zum Genus (Gattung) Orthohantavirus aus der Familie Hantaviridae, Unterfamilie Mammantavirinae. Das Erregerreservoir ist die Wanderratte.
Ein großer Teil der Hantavirus-Infektionen verläuft vermutlich asymptomatisch oder mit unspezifischen Symptomen. Hantaviren können aber auch schwere Krankheitsbilder hervorrufen. Asiatische und europäische Hantavirus-Stämme sind Auslöser des Hämorrhagischen Fiebers mit renalem Syndrom (HFRS).
Der Nachweis von Hantaviren-Infektionen ist in Deutschland, Österreich und der Schweiz meldepflichtig bzw. anzeigepflichtig (siehe im Einzelnen unter Hantaviren).
Seoul orthohantavirus (SEOV) is a member of the Orthohantavirus family of rodent-borne viruses and is one of the 4 hantaviruses that are known to be able to cause Hantavirus hemorrhagic fever with renal syndrome (HFRS).[1][2] It is an Old World hantavirus; a negative sense, single-stranded, tri-segmented RNA virus.
Seoul virus is found in Rattus species rats, most commonly Rattus norvegicus, but occasionally Rattus rattus.[3] The two distinct hantaviruses have been identified in Korea in 1976, from Apodemus agrarius, and in 1980, from Rattus norvegicus. In 1994, a genetically different hantavirus was identified from Apodemus peninsulae.[4] Rats do not show physiological symptoms when carrying the virus, but humans can be infected through exposure to infected rodent body fluids (blood, saliva, urine), exposure to aerosolized rat excrement, or bites from infected rats.[1] When rodent bedding or urine is stirred up by either natural causes or human-caused disturbances, small particles are made to be airborne. This can be breathed in and cause an infection in humans. There is currently no evidence of human-to-human transmission of SEOV, only rodent-human transmission.[5]
Seoul virus was first described by Dr. Lee Ho-Wang (Ho-Wang Lee), a Korean virologist. As the infection was first found in an apartment in Seoul, the virus was named "Seoul Virus".
SEOV, along with all other hantaviruses, is a negative sense, single-stranded RNA virus. Its genome has three different segments: S (small), M (medium), and L (large).[6] The virus is pleomorphic, having various shapes, but often is seen as spherical, with its two surface glycoproteins arranged in rows. Inside this sphere, the three RNA segments are arranged as circles, coated in the virus' N (nucleocapsid) protein and attached to the L protein. The 5' and 3' ends of the genome segments match up, creating a panhandle structure. This base pairing occurs in all hantavirus species, with the panhandle structure and sequence being unique to each particular species, of course with some similarities and overlap between species, including an eight nucleotide consensus sequence.[7][6]
There are four major viral proteins, the two surface glycoproteins (Gn and Gc), the nucleocapsid protein (N), and the viral polymerase (L).
The Gn and Gc proteins exist on the surface of the mature virus as spikes in highly ordered rows, with each spike having four Gn/Gc heterodimers.[6][8] Interactions between the spikes are thought to cause viral budding into the Golgi apparatus.[9] These surface glycoproteins are also responsible for the attachment of the virus to its target host cell. Gn and Gc spikes attach to β3 integrins and co-receptors on the target cell surface.[8][10]
The SEOV is transmitted among the rats rapidly and has been detected in rat populations that reside in port cities worldwide.[11]
There are no instances of SEOV transmission from human to human.
Most human infections are recorded in Asia.[5] Human infections account for ~25% of cases of hemorrhagic fever with renal syndrome in Asia.[12]
R. norvegicus rodents are found in urban areas worldwide, meaning that SEOV and HFRS are also found globally in human populations in urban areas.[3] As of 2015 the virus has been found in wild rats in the Netherlands, and in both rodents and humans in England, Wales, France, Belgium, and Sweden.[1] Rats in New York City are also known reservoirs.[13]
An outbreak of Seoul virus infected eleven people in the U.S. states of Illinois, Indiana and Wisconsin from December 2016 to February 2017. Individuals who operated a home-based rat-breeding facility in Wisconsin became ill and were hospitalized. The ill individuals had purchased rats from animal suppliers in Wisconsin and Illinois. Investigators traced the infection to two Illinois ratteries and identified six additional people who tested positive for Seoul virus. All these individuals recovered. Further investigation by the Centers for Disease Control and Prevention revealed that potentially infected rodents may have traveled to the states of Alabama, Arkansas, Colorado, Illinois, Indiana, Iowa, Louisiana, Michigan, Minnesota, Missouri, North Dakota, South Carolina, Tennessee, Utah, and Wisconsin.[14][5] Cases were also reported in Ontario in February 2016.[15] In 2017, the investigation further showed that there were 17 infected people and 31 infected ratteries in 11 states, which are Colorado, Georgia, Illinois, Iowa, Minnesota, Missouri, Pennsylvania, South Carolina, Tennessee, Utah, and Wisconsin. The infected rodents are found to be distributed from Colorado, Delaware, Georgia, Illinois, Idaho, Iowa, Minnesota, Missouri, New Jersey, Pennsylvania, South Carolina, Tennessee, Utah, and Wisconsin.[16]
Although rodents are known to be the main reservoir for the virus, there are studies that show that other wild animals such as cats, dogs, pigs, cattle, and deer can also work as a reservoir. The transmission between the rodents to listed animals also seems to be possible.[17]
The SEOV is transmitted to humans mainly from feces, body fluid, and excrete of rodents. It usually occurs in agricultural locations, but there were cases of the virus in the city. It may happen in laboratory environments as well. There are increase in the number of patients in late fall (October to November) and late spring (May to June). The main targeted age group is people in their 20s to 60s, as they are more active than the age group outside of the range.[18]
In humans, Seoul virus causes hemorrhagic fever with renal syndrome (HFRS), along with other Old World hantaviruses. Although New World hantaviruses typically cause hantavirus pulmonary syndrome (HPS), either disease can involve the patient's kidneys or lungs.[19][20] The virus can cause severe health issues and even death. HPS has a mortality rate of 38%.[21] The infection of the virus in humans can be tested through blood testing as the strain of the virus can be isolated.[22]
The patient will develop high grade fever, sweating, chills, abdominal pain, joint pain, red eye, nausea, vomiting, one or multiple rash(es) and/or a headache as early symptoms. After 4 to 10 days of initial symptoms, the patient may show late symptoms such as coughing and shortness of breath due to the lungs being filled up by liquid.[21]
The incubation period varies from 1–8 weeks. The symptoms can appear quickly, the majority of patients developing symptoms 1–2 weeks from the time of infection. The patient will develop severe symptoms which may lead to death. To prevent contracting this virus, avoid contact with wild rats and only adopt pet rats from trusted sources who have tested their rats by serology in order to confirm their colony does not carry this virus.
Seoul virus is known to be found primarily in Rattus norvegicus (Norway Rat), but has also been seen in Rattus rattus (Black Rat) populations.[3] Traditionally, it has been thought that each virus in the hantavirus genus is highly specific to a single rodent host species,[23][24] but this idea is being challenged.[25][26]
Rattus species rodents do not show symptoms of infection with SEOV.[27]
The best way to prevent the transmission of the virus is to limit the human-rodent interaction.[28]
The treatment of HPS has been developed and is proved to be effective, as it shortens the course of illness and reduces the mortality rate. The vaccination of the virus has also been out in the market for over two decades, but the effectiveness has not been clearly supported.[29]
Seoul orthohantavirus (SEOV) is a member of the Orthohantavirus family of rodent-borne viruses and is one of the 4 hantaviruses that are known to be able to cause Hantavirus hemorrhagic fever with renal syndrome (HFRS). It is an Old World hantavirus; a negative sense, single-stranded, tri-segmented RNA virus.
Seoul virus is found in Rattus species rats, most commonly Rattus norvegicus, but occasionally Rattus rattus. The two distinct hantaviruses have been identified in Korea in 1976, from Apodemus agrarius, and in 1980, from Rattus norvegicus. In 1994, a genetically different hantavirus was identified from Apodemus peninsulae. Rats do not show physiological symptoms when carrying the virus, but humans can be infected through exposure to infected rodent body fluids (blood, saliva, urine), exposure to aerosolized rat excrement, or bites from infected rats. When rodent bedding or urine is stirred up by either natural causes or human-caused disturbances, small particles are made to be airborne. This can be breathed in and cause an infection in humans. There is currently no evidence of human-to-human transmission of SEOV, only rodent-human transmission.
Seoul virus was first described by Dr. Lee Ho-Wang (Ho-Wang Lee), a Korean virologist. As the infection was first found in an apartment in Seoul, the virus was named "Seoul Virus".
El Virus Seoul (SEOV) es un virus del género Hantavirus,[1] de la familia Hantaviridae, grupo V, es un Hantavirus que puede causar una forma de fiebre hemorrágica
Datos: Q29002561
Especies: Seoul orthohantavirus
El Virus Seoul (SEOV) es un virus del género Hantavirus, de la familia Hantaviridae, grupo V, es un Hantavirus que puede causar una forma de fiebre hemorrágica
Seoul orthohantavirus
Синонимы Группа по Балтимору
Вирус Сеул[4] (англ. Seoul orthohantavirus, ранее Seoul virus) относится к семейству Hantaviridae порядка Bunyavirales. Является вторым по распространённости на территории Южной Кореи после вируса Хантаан. Случаи заражения вирусом также зафиксированы в Китае, на Дальнем Востоке России и в Японии[5]. По данным исследований, вирус Сеул вызывает до 25 % всех случаев геморрагической лихорадки с почечным синдромом в Азии[6].
В 2004 году впервые был зафиксирован случай заболевания вирусом Сеул на территории Франции. До этого случая учёным было известно, что крысы в Европе давали положительный ответ на антитела к вирусу, но никогда прежде в Старом Свете заражения вирусом не происходило[7]. В 2017 году в связи с выделением порядка Bunyavirales и ревизией рода Hantavirus научное название вида изменено, как и у большинства других относящихся к порядку таксонов[2].
В отличие от своего ближайшего родственника, вируса Хантаан, симптомы после заражения вирусом Сеул проходят значительно мягче. Так, расстройство почек проходит в более лёгкой форме, кроме того, фиксируется меньшее количество повреждений кровеносных сосудов и, как следствие, меньше кровотечений. В то же время, отдельные органы страдают сильнее, например, поражение клеток печени проходит в более серьёзной форме[8].
Естественным переносчиком вируса являются чёрная крыса и серая крыса. Чаще всего заражения вирусом происходит в летний период[8].
Вирус Сеул (англ. Seoul orthohantavirus, ранее Seoul virus) относится к семейству Hantaviridae порядка Bunyavirales. Является вторым по распространённости на территории Южной Кореи после вируса Хантаан. Случаи заражения вирусом также зафиксированы в Китае, на Дальнем Востоке России и в Японии. По данным исследований, вирус Сеул вызывает до 25 % всех случаев геморрагической лихорадки с почечным синдромом в Азии.
В 2004 году впервые был зафиксирован случай заболевания вирусом Сеул на территории Франции. До этого случая учёным было известно, что крысы в Европе давали положительный ответ на антитела к вирусу, но никогда прежде в Старом Свете заражения вирусом не происходило. В 2017 году в связи с выделением порядка Bunyavirales и ревизией рода Hantavirus научное название вида изменено, как и у большинства других относящихся к порядку таксонов.
В отличие от своего ближайшего родственника, вируса Хантаан, симптомы после заражения вирусом Сеул проходят значительно мягче. Так, расстройство почек проходит в более лёгкой форме, кроме того, фиксируется меньшее количество повреждений кровеносных сосудов и, как следствие, меньше кровотечений. В то же время, отдельные органы страдают сильнее, например, поражение клеток печени проходит в более серьёзной форме.
Естественным переносчиком вируса являются чёрная крыса и серая крыса. Чаще всего заражения вирусом происходит в летний период.
