2020 taxonomic update for phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales (original) (raw)
Abstract
In March 2020, following the annual International Committee on Taxonomy of Viruses (ICTV) ratification vote on newly proposed taxa, the phylum Negarnaviricota was amended and emended. At the genus rank, 20 new genera were added, two were deleted, one was moved, and three were renamed. At the species rank, 160 species were added, four were deleted, ten were moved and renamed, and 30 species were renamed. This article presents the updated taxonomy of Negarnaviricota as now accepted by the ICTV.
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Introduction
Phylum Negarnaviricota was established in 2019 by the International Committee on Taxonomy of Viruses (ICTV) for negative-sense RNA viruses that can be connected evolutionarily through their encoded RNA-directed RNA polymerase (RdRp) core domains. The phylum includes two subphyla, Haploviricotina and Polyploviricotina, for negative-sense RNA viruses that encode large (L) proteins with or without mRNA capping activity, respectively. The two subphyla include four classes (Chunqiuviricetes, Milneviricetes, Monjiviricetes, and Yunchangviricetes) and two classes (Ellioviricetes and Insthoviricetes), respectively [56, 109, 136]. The vast majority of viruses that have been assigned to phylum Negarnaviricota belong to two orders: Mononegavirales (established in 1991 [92] and amended/emended in 1995 [16], 1997 [93], 2000 [94], 2005 [95], 2011 [32], 2016 [2], 2017 [7], March 2018 [8], October 2018 [66], and 2019 [9]) and Bunyavirales (established in 2017 and amended/emended in 2018 [64, 65] and 2019 [1]).
Here we present the changes that were proposed to the entire phylum Negarnaviricota via official ICTV taxonomic proposals (TaxoProps) in 2019 and that were accepted by the ICTV in March 2020 [128]. These changes are now part of the official ICTV taxonomy.
Taxonomic changes above the phylum rank
Until recently, Negarnaviricota, included in realm Riboviria (established in 2019 [127]), was the only established phylum in the ICTV framework. In 2020, virus taxonomy was amended to include Negarnaviricota in the new riboviriad kingdom Orthornavirae as one of five sister phyla [55] (TaxoProp 2019.006G.A.v1.Riboviria).
Taxonomic changes at the subphylum rank
No new subphyla were created.
Taxonomic changes at the class rank
No new classes were created.
Taxonomic changes at the order rank
No new orders were created.
Taxonomic changes within order Goujianvirales (Haploviricotina: Yunchangviricetes)
No changes were made.
Taxonomic changes within order Jingchuvirales (Haploviricotina: Monjiviricetes)
Family Chuviridae
One new species, Taiyuan mivirus, was added to genus Mivirus for Tàiyuán leafhopper virus (TYLeV) first discovered by high-throughput sequencing (HTS) in a leafhopper (Psammotettix alienus (Dahlbom, 1850)) sampled in Tàiyuán (太原), Shānxī Province (山西省), China [129] (TaxoProp 2019.018M.A.v2.1newsp_Taiyuan_mivirus).
Taxonomic changes within order Mononegavirales (Haploviricotina: Monjiviricetes)
Family Artoviridae
The family was expanded by one new genus, Hexartovirus, including one new species, Caligid hexartovirus, for Lepeophtheirus salmonis negative-stranded RNA virus 1 (LsNSRV-1) first discovered by HTS in salmon lice (Lepeophtheirus salmonis (Krøyer, 1837)) sampled on the west coast of Norway [81]. Species Barnacle peropuvirus was moved from genus Peropuvirus into genus Hexartovirus and renamed Barnacle hexartovirus (TaxoProp 2019.021M.A.v1.1newgenus_Hexartovirus).
Family Bornaviridae
No changes were made.
Family Filoviridae
The family was expanded by one genus, Dianlovirus, including a single new species, Mengla dianlovirus, for Měnglà virus (MLAV) discovered by HTS in a Rousettus sp. bat sampled in Měnglà County (勐腊县), Yúnnán Province (云南省), China [145, 146] (TaxoProp 2019.011M.A.v1.Mengla_dianlovirus).
One new species, Bombali ebolavirus, was created in genus Ebolavirus, for Bombali virus (BOMV) first discovered by consensus PCR and confirmed by HTS in little free-tailed bats (Chaerephon pumilus (Cretzschmar, 1830–1831)) and Angolan free-tailed bats (Mops condylurus (A. Smith, 1833)) sampled in Bombali District, Northern Province, Sierra Leone [37] (TaxoProp 2019.007M.A.v2.Bombali_ebolavirus).
Family Lispiviridae
No changes were made.
Family Mymonaviridae
A new genus, Hubramonavirus, was established for two new species: Hubei hubramonavirus for Húběi rhabdo-like virus 4 (HbRLV-4) discovered by HTS in an arthropod mix collected in Húběi Province (湖北省), China [106] and Lentinula hubramonavirus for Lentinula edodes negative-strand RNA virus 1 (LeNSRV-1) first detected by HTS in commercial shiitakes (Lentinula edodes (Berk.) Pegler (1976)) sampled in Japan [60] (TaxoProp 2019.001F.A.v1.Hubramonavirus_1gen).
Family Nyamiviridae
No changes were made.
Family Paramyxoviridae
The overlooked deletion of species Bat mumps orthorubulavirus and the overlooked renaming of species Synodus paramyxovirus to Synodus synodonvirus were corrected (TaxoProp 2019.016M.A.v1.Corrections).
The family was expanded by three new genera: genus Cynoglossusvirus for the already established species Cynoglossus paramyxovirus (now renamed Cynoglossus cynoglossusvirus); genus Hoplichthysvirus for the already established species Hoplichthys paramyxovirus (now renamed Hoplichthys hoplichthysvirus); and genus Scoliodonvirus for the already established species Scoliodon paramyxovirus (now renamed Scoliodon scoliodonvirus) (TaxoProp 2019.025M.A.v2.Paramyxoviridae_3gen5sp4rensp).
Genus Aquaparamyxovirus was expanded by one species, Oncorhynchus aquaparamyxovirus, for Pacific salmon paramyxovirus (PSPV) first isolated from Chinook salmon (Oncorhynchus tshawytscha (Walbaum, 1792)) in Oregon, USA [135]. Species Salmon aquaparamyxovirus was renamed Salmo aquaparamyxovirus (TaxoProp 2019.025M.A.v2.Paramyxoviridae_3gen5sp4rensp).
Genus Jeilongvirus was expanded by one species, Miniopteran jeilongvirus, for “bat paramyxovirus isolate Bat-ParaV/B16-40” (here renamed Shaan virus [ShaV]) first isolated from a Schreibers’s long-fingered bat (Miniopterus schreibersii (Kuhl, 1817)) feces sampled in Danyang County (단양군), North Chungcheong Province (충청북도), South Korea [79] (TaxoProp 2019.025M.A.v2.Paramyxoviridae_3gen5sp4rensp).
Genus Orthoavulavirus was expanded erroneously by two species, Avian orthoavulavirus 21 and Avian orthovulavirus 21 [sic], for the same virus, “avian paramyxovirus 17” (here renamed avian paramyxovirus 21 [APMV-21]) first isolated from bird feces collected in Seosan (서산시), South Chungcheong Province (충청남도), South Korea [48] (TaxoProps 2019.014M.A.v1.Avulavirus_1newsp and 2019.025M.A.v2.Paramyxoviridae_3gen5sp4rensp).
Genus Orthorubulavirus was expanded by one species, Mammalian orthorubulavirus 6, for Alston virus (AlsV) first isolated from pteropodid bat urine sampled in Alstonville, New South Wales, Australia [49] (TaxoProp 2019.025M.A.v2.Paramyxoviridae_3gen5sp4rensp).
Genus Pararubulavirus was expanded by one species, Hervey pararubulavirus, for Hervey virus (HerV) first isolated from pteropodid bat urine sampled in Hervey Bay, Queensland, Australia [11, 53]. (TaxoProp 2019.025M.A.v2.Paramyxoviridae_3gen5sp4rensp).
Genus Respirovirus was expanded by one species, Squirrel respirovirus, for giant squirrel virus (GSqV) first isolated from a Sri Lankan giant squirrel (Ratufa macroura (Pennant, 1769)) sampled in a German zoo [35] (TaxoProp 2019.019M.A.v2.1newsp_Squirrel_respirovirus).
Family Rhabdoviridae
Genus Almendravirus was expanded by one species, Menghai almendravirus, for Menghai rhabdovirus (MRV) first isolated from Asian tiger mosquitoes (Aedes albopictus (Skuse, 1894)) collected in Měnghǎi County (勐海县) in Yúnnán Province (云南省), China [113] (TaxoProp 2019.033M.N.v1.Menghai_almendravirus_1sp).
Genus Nucleorhabdovirus was split into three genera, Alphanucleorhabdovirus, Betanucleorhabdovirus, and Gammanucleorhabdovirus (TaxoProp 2019.031M.Ac.v1.Nucleorhabdovirus_splitgen). Established species Eggplant mottled dwarf nucleorhabdovirus, Maize Iranian mosaic nucleorhabdovirus, Maize mosaic nucleorhabdovirus, Potato yellow dwarf nucleorhabdovirus, Rice yellow stunt nucleorhabdovirus, and Taro vein chlorosis nucleorhabdovirus were assigned to genus Alphanucleorhabdovirus and renamed Eggplant mottled dwarf alphanucleorhabdovirus, Maize Iranian mosaic alphanucleorhabdovirus, Maize mosaic alphanucleorhabdovirus, Potato yellow dwarf alphanucleorhabdovirus, Rice yellow stunt alphanucleorhabdovirus, and Taro vein chlorosis alphanucleorhabdovirus, respectively. Established species Datura yellow vein nucleorhabdovirus, Sonchus yellow net nucleorhabdovirus, and Sowthistle yellow vein nucleorhabdovirus were assigned to genus Betanucleorhabdovirus and renamed Datura yellow vein betanucleorhabdovirus, Sonchus yellow net betanucleorhabdovirus, and Sowthistle yellow vein betanucleorhabdovirus, respectively. Established species Maize fine streak nucleorhabdovirus was assigned to genus Gammanucleorhabdovirus and renamed Maize fine streak gammanucleorhabdovirus (TaxoProp 2019.031M.Ac.v1.Nucleorhabdovirus_splitgen).
Three new species were established in genus Alphanucleorhabdovirus:
- Morogoro maize-associated alphanucleorhabdovirus for Morogoro maize-associated virus (MMaV) first detected by HTS in maize (Zea mays L.) sampled in Morogoro, Morogoro Region, Tanzania [97];
- Physostegia chlorotic mottle alphanucleorhabdovirus for Physostegia chlorotic mottle virus (PhCMoV) first isolated from lionhearts (Physostegia sp.) in Austria [76]; and
- Wheat yellow striate alphanucleorhabdovirus for wheat yellow striate virus (WYSV) first isolated from common wheat (Triticum aestivum L.) sampled in Hánchéng (韩城), Shǎnxī/Shaanxi Province (陕西省), China [61] (TaxoProp 2019.031M.Ac.v1.Nucleorhabdovirus_splitgen).
Three new species were established in genus Betanucleorhabdovirus:
- Alfalfa betanucleorhabdovirus for alfalfa-associated nucleorhabdovirus (AaNV) first discovered by HTS in alfalfa (Medicago sativa L.) sampled in Stadl-Paura, Upper Austria (Oberösterreich), Austria [36];
- Blackcurrant betanucleorhabdovirus for blackcurrant-associated rhabdovirus (BCaRV) first discovered by HTS in blackcurrant (Ribes nigrum L.) sampled in Russia [138]; and
- Trefoil betanucleorhabdovirus for birds-foot trefoil-associated virus (BFTV) first discovered by HTS in Bird’s-foot trefoil (Lotus corniculatus L.) sampled in the Qínlǐng Mountains (秦岭山), Shǎnxī/Shaanxi Province (陕西省), China [26, 131] (TaxoProp 2019.031M.Ac.v1.Nucleorhabdovirus_splitgen).
One new genus, Arurhavirus, was established to include four species:
- Aruac arurhavirus for Aruac virus (ARUV) first isolated from mosquitoes (Trichoprosopon theobaldi Lane and Cerqueira, 1942) collected in Melaju Forest, Trinidad, Trinidad and Tobago [110, 126];
- Inhangapi arurhavirus for Inhangapi virus (INHV) first isolated from sandflies (Lutzomyia flaviscutellata (Mangabeira, 1942)) collected in Catu Forest, Belém, Pará State, Brazil [3, 126];
- Santabarbara arurhavirus for Santa Barbara virus (SBAV) first in mice sampled in Santa Bárbara do Pará, Pará State, Brazil [unpublished]; and
- Xiburema arurhavirus for Xiburema virus (XIBV) first isolated from mosquitoes (Sabethes intermedius (Lutz, 1904)) sampled in Sena Madureira, Acre State, Brazil [51, 132] (2019.006M.A.v1.Arurhavirus_1gen4sp).
One new genus, Barhavirus, was established to include two new species:
- Bahia barhavirus for Bahia Grande virus (BGV) first isolated from mosquitoes (Aedes, Culex, Anopheles, Psorophora spp.) collected in Texas, Louisiana, New Mexico, and North Dakota, USA [52, 126] and also for Harlingen virus (HARV) isolated from salt marsh mosquitoes (Culex salinarius Coquillett, 1904) sampled in Harlingen, Texas, USA [126].
- Muir barhavirus for Muir Springs virus (MSV) first isolated from mosquitoes (Aedes sp.) collected in Fort Morgan, Colorado, USA [52, 126] (TaxoProp 2019.012M.A.v1.Rhabdoviridae_5gen8sp1reasp).
One new genus, Lostrhavirus, was established to include new species Lonestar zarhavirus [sic] for lone star tick rhabdovirus (LSTRV) first detected by HTS in lone star ticks (Amblyomma americanum (Linnaeus, 1758)) collected in the USA [unpublished] (TaxoProp 2019.012M.A.v1.Rhabdoviridae_5gen8sp1reasp).
One new genus, Mousrhavirus, was established to include the previously established species Moussa virus (now renamed Moussa mousrhavirus) (TaxoProp 2019.012M.A.v1.Rhabdoviridae_5gen8sp1reasp).
One new genus, Ohlsrhavirus, was established to include five new species:
- Culex ohlsrhavirus for Culex rhabdo-like virus (CRLV) first discovered by HTS in southern house mosquitoes (Culex quinquefasciatus Say, 1823) collected near Perth, Western Australia, Australia [107];
- Northcreek ohlsrhavirus for North Creek virus (NORCV) first discovered by HTS in mosquitoes (Culex sitiens Wiedemann, 1828) collected in Ballina, New South Wales, Australia [23];
- Ohlsdorf ohlsrhavirus for Ohlsdorf virus (OHLDV) first discovered by HTS in mosquitoes (Ochlerotatus cantans (Meigen, 1818)) collected in Hamburg, Germany [105];
- Riverside ohlsrhavirus for riverside virus (RISV) first discovered by HTS in mosquitoes (Ochlerotatus sp.) collected in Gemenc, Gyékényes, and Drávaszabolcs, Hungary [98]; and
- Tongilchon ohlsrhavirus for Tongilchon virus 1 (TCHV-1) first detected in mosquitoes (Culex bitaeniorhynchus Giles, 1901) collected in Tongil-chon (통일촌), Gyeonggi Province (경기도), South Korea [39] (TaxoProp 2019.032M.N.v1.Ohlsrhavirus_1gen5sp).
One new genus, Sawgrhavirus, was established to include four new species:
- Connecticut sawgrhavirus for Connecticut virus (CNTV) first isolated from ticks (Ixodes dentatus Marx, 1899) taken from an eastern cottontail (Sylvilagus floridanus (J. A. Allen, 1890)) captured in Lyme, Connecticut, USA [67, 126];
- Island sawgrhavirus for Long Island tick rhabdovirus (LITRV) first detected by HTS in lone star ticks (Amblyomma americanum (Linnaeus, 1758)) collected on Long Island, New York, USA [119];
- Minto sawgrhavirus for New Minto virus (NMV) first isolated from rabbit ticks (Haemaphysalis leporispalustris Packard, 1869) sampled in New Minto, Alaska, USA [99, 126]; and
- Sawgrass sawgrhavirus for Sawgrass virus (SAWV) isolated from American dog ticks (Dermacentor variabilis (Say, 1821)) sampled at Sawgrass Lake, Tampa Bay, Florida, USA [102, 126] (TaxoProp 2019.012M.A.v1.Rhabdoviridae_5gen8sp1reasp).
One new genus, Sunrhavirus, was established to accommodate six novel species:
- Garba sunrhavirus for Garba virus (GARV) first isolated from a malachite kingfisher (Corythornis cristatus (Pallas, 1764)) trapped in Bangui, Central African Republic [51, 126];
- Harrison sunrhavirus for Harrison Dam virus (HARDV) first isolated from common banded mosquitoes (Culex annulirostris Skuse, 1889) collected at Beatrice Hill, Northern Territory, Australia [71];
- Kwatta sunrhavirus for Kwatta virus (KWAV) first isolated from mosquitoes (Culex sp.) collected near Paramaribo, Suriname [25, 126];
- Oakvale sunrhavirus for Oak Vale virus (OVV) first isolated from mosquitoes (Culex edwardsi Barraud, 1923) sampled in Peachester, Queensland, Australia [77, 96];
- Sunguru sunrhavirus for Sunguru virus (SUNV) first isolated from a domestic chicken (Gallus gallus domesticus (Linnaeus, 1758)) in Arua District, Northern Region, Uganda [58]; and
- Walkabout sunrhavirus for Walkabout Creek virus (WACV) first isolated from biting midges (Culicoides austropalpalis Lee and Reye, 1955) collected near Samford, Queensland, Australia [71] (2019.004M.A.v2.Sunrhavirus).
One new genus, Zarhavirus, was created for one new species, Zahedan zarhavirus, for Zahedan rhabdovirus (ZARV) first isolated from ticks (Hyalomma anatolicum anatolicum (Koch, 1844)) collected in Zâhedân , Sistan and Baluchestan Province , Iran [28] (TaxoProp 2019.012M.A.v1.Rhabdoviridae_5gen8sp1reasp).
One new species, Taiwan bat lyssavirus, was added to genus Lyssavirus for Taiwan bat lyssavirus (TWBLV) first isolated from a Japanese pipistrelle (Pipistrellus abramus (Temminck, 1838)) sampled in Taiwan [45] (TaxoProp 2019.001M.A.v1.Lyssavirus).
Genus Cytorhabdovirus was expanded by 12 species:
- Cabbage cytorhabdovirus for cabbage cytorhabdovirus 1 (CCyV-1) first discovered by HTS in cabbage (Brassica oleracea L.) sampled in the UK [89];
- Maize-associated cytorhabdovirus for maize-associated cytorhabdovirus (MaCV) first discovered by HTS in maize (Zea mays L.) collected in Lima, Peru [133];
- Maize yellow striate cytorhabdovirus for maize yellow striate virus (MYSV) first discovered by HTS in maize (Zea mays L.) and common wheat (Triticum aestivum L.) collected in Sinsacate, Córdoba Province, Argentina [70];
- Papaya cytorhabdovirus for papaya virus E (PpVE) first discovered by HTS in papaya (Carica papaya L.) sampled in Los Ríos Province, Ecuador [73];
- Persimmon cytorhabdovirus for persimmon virus A (PeVA) first discovered by HTS in Japanese persimmon (Diospyros kaki L.f.) sampled in Japan [47];
- Raspberry vein chlorosis cytorhabdovirus for raspberry vein chlorosis virus (RVCV) first discovered by HTS in red raspberries (Rubus idaeus L.) sampled in Dundee, Scotland, UK [50];
- Rice stripe mosaic cytorhabdovirus for rice stripe mosaic virus (RSMV) first discovered by HTS in rice (Oryza sativa L.) sampled in Luódìng (罗定), Guǎngdōng Province (广东省), China [147];
- Tomato yellow mottle-associated cytorhabdovirus for tomato yellow mottle-associated virus (TYMaV) first discovered by HTS in tomato (Solanum lycopersicum L.) sampled in Chóngqìng (重庆), China [141];
- Wuhan 4 insect cytorhabdovirus for Wuhan insect virus 4 (WuIV-4) first discovered by HTS in mealy plum aphids (Hyalopterus pruni (Geoffroy, 1762)) sampled in Wǔhàn (武汉), Húběi Province (湖北省), China [59];
- Wuhan 5 insect cytorhabdovirus for Wuhan insect virus 5 (WuIV-5) first discovered by HTS in mealy plum aphids (Hyalopterus pruni (Geoffroy, 1762)) sampled in Wǔhàn (武汉), Húběi Province (湖北省), China [59];
- Wuhan 6 insect cytorhabdovirus for Wuhan insect virus 6 (WuIV-6) first discovered by HTS in mealy plum aphids (Hyalopterus pruni (Geoffroy, 1762)) sampled in Wǔhàn (武汉), Húběi Province (湖北省), China [59]; and
- Yerba mate chlorosis-associated cytorhabdovirus for yerba mate chlorosis-associated virus (YmCaV) [12] first discovered by HTS in yerba mate (Ilex paraguariensis A. St.-Hil.) sampled in Cerro Azul, Misiones Province, Argentina (TaxoProps 2019.002M.A.v3.Cytorhabdovirus and 2019.030M.A.v1.Cytorhabovirus_12newsp).
One new species, Holmes hapavirus, was added to genus Hapavirus for Holmes Jungle virus (HOJV) first isolated from common banded mosquitoes (Culex annulirostris Skuse, 1889) collected near Darwin, Northern Territory, Australia [38] (2019.003M.A.v3.Hapavirus).
Three new species were added to genus Sripuvirus:
- Charleville sripuvirus for Charleville virus (CHVV) first isolated from sandflies (Phlebotomus sp.) collected in Charleville, Queensland, Australia [29, 123];
- Cuiaba sripuvirus for Cuiaba virus (CUIV) isolated from a cane toad (Rhinella marina (Linnaeus, 1758)) captured in Pará State, Brazil [51, 123]; and
- Hainan sripuvirus for Hainan black-spectacled toad rhabdovirus (HnBSTRV) first detected by HTS in an Asian common toad (Duttaphrynus melanostictus (Schneider, 1799)) sampled in Hǎinán Province (海南省), China [108] (TaxoProp 2019.013M.A.v1.Sripuvirus_3newsp).
Taxonomic changes within order Muvirales (Haploviricotina: Chunqiuviricetes)
No changes were made.
Taxonomic changes within order Serpentovirales (Haploviricotina: Milneviricetes)
No changes were made.
Taxonomic changes within order Articulavirales (Polyploviricotina: Insthoviricetes)
No changes were made.
Taxonomic changes within order Bunyavirales (Polyploviricotina: Ellioviricetes)
Family Arenaviridae
Genus Hartmanivirus was expanded by three species: Muikkunen hartmanivirus for Dante Muikkunen virus 1 (DaMV-1), Schoolhouse hartmanivirus for old schoolhouse viruses 1 and 2 (OScV-1/2), and Zurich hartmanivirus for veterinary pathology Zurich viruses 1 and 2 (VPZV-1/2), all first detected by HTS in captive boid snakes [44] (TaxoProp 2019.008M.A.v2.Hartmanivirus_3new sp).
Genus Mammarenavirus was expanded by four species:
- Alxa mammarenavirus for RtDs-AreV/IM2014 virus (here renamed Alxa virus [ALXV]) (TaxoProp 2019.020M.A.v2.1newsp_Alxa_mammarenavirus) first discovered by HTS in a Northern three-toed jerboa (Dipus sagitta (Pallas, 1773)) sampled in Alxa Left Banner (阿拉善左旗), Inner Mongolia Autonomous Region (内蒙古自治区), China [139, 140];
- Chevrier mammarenavirus for Lìjiāng virus (LIJV) first discovered by HTS in a Chevrier’s field mouse (Apodemus chevrieri (Milne-Edwards, 1868)) sampled around Lìjiāng (丽江), Yúnnán Province (云南省), China [unpublished] (TaxoProp 2019.009M.A.v2.Mammarenavirus_sp_LIJV);
- Planalto mammarenavirus for Aporé virus (APOV) first discovered by HTS in a Mato Grosso colilargo (Oligoryzomys mattogrossae (J. A. Allen, 1916)) sampled in Cassilândia, Mato Grosso do Sul State, Brazil (TaxoProp 2019.010M.A.v1.Mammarenavirus_sp_APOV) [34]; and
- Xapuri mammarenavirus for Xapuri virus (XAPV) first discovered by HTS in a Musser’s neacomys (Neacomys musseri Patton, da Silva, and Malcolm, 2000) sampled in Xapuri, Acre State, Brazil [33] (TaxoProp 2019.005M.A.v1.Mammarenavirus_sp_XAPV).
Family Fimoviridae
Genus Emaravirus was expanded by two species: Blackberry leaf mottle associated emaravirus for blackberry leaf mottle-associated virus (BLMaV) first discovered in blackberries (Rubus spp.) collected in various US states (TaxoProp 2019.010P.A.v1.Emaravirus_1sp) [41] and Pistacia emaravirus B for pistacia virus B (PiVB) discovered by HTS in pistachios (Pistacia vera L.) sampled in Turkey [18] (TaxoProp 2019.011P.A.v1.Emaravirus_1sp).
Family Hantaviridae
Genus Loanvirus was expanded by one species, Brno loanvirus, for Brno virus (BRNV) first discovered by HTS in a noctule (Nyctalus noctula (Schreber, 1774)) sampled in Brno, South Moravia Region (Jihomoravský kraj), Czech Republic [112] (TaxoProp 2019.017M.A.v3.1newsp_Brno_virus).
Family Peribunyaviridae
Genus Pacuvirus was expanded by two species: new species Caimito pacuvirus for Caimito virus (CAIV) first isolated from sandflies (Nyssomyia ylephiletor (Fairchild and Hertig, 1952)) sampled in El Aguacate, Panamá Province, Panama [46, 116] (TaxoProp 2019.022M.A.v2.2sp_Pacuvirus) and Chilibre pacuvirus (the former Chilibre phlebovirus, renamed and moved from genus Phlebovirus) (TaxoProps 2019.022M.A.v2.2sp_Pacuvirus and 2019.026M.A.v1.Phenuiviridae_4gen79sp).
Family Phasmaviridae
The previously established genus Inshuvirus and its included species Insect inshuvirus were both abolished due to insufficient member virus information (TaxoProp 2019.028M.A.v2.Phasmaviridae_1newsp_abol1gen3sp).
New species Anopheles orthophasmavirus was included in genus Orthophasmavirus for Anopheles triannulatus orthophasmavirus (AtOPV) first discovered by HTS in mosquitoes (Anopheles triannulatus (Neiva and Pinto, 1922)) sampled in Santa Bárbara Farm, Amapá State, Brazil [103]. Two species, Nome phantom orthophasmavirus and Seattle orthophasmavirus, were abolished (TaxoProp 2019.028M.A.v2.Phasmaviridae_1newsp_abol1gen3sp).
Family Phenuiviridae
The previously unassigned genus Coguvirus was included in family Phenuiviridae (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp). One new species, Coguvirus eburi, was created in the genus for citrus virus A (CiVA) first discovered by HTS in a sweet orange tree in Italy [78] (2019.004P.A.v1.Coguvirus_1sp).
Genus Banyangvirus and included species Huaiyangshan banyangvirus, Guertu banyangvirus, and Heartland banyangvirus were renamed Bandavirus, Dabie bandavirus, Guertu bandavirus, and Heartland bandavirus, respectively (TaxoProps 2019.015M.A.v1.Bandavirus and 2019.026M.A.v1.Phenuiviridae_4gen79sp). Four new bandavirus species were added to the genus:
- Bhanja bandavirus for Bhanja virus (BHAV) first isolated from flat-inner-spurred haemaphysalids (Haemaphysalis intermedia Warburton and Nuttall, 1909) sampled in Orissa State, India [27, 104];
- Hunter Island bandavirus for Hunter Island virus (HUIV) first isolated from ticks (Ixodes eudyptidis Maskell, 1885) sampled on Albatross Island, Tasmania, Australia [130];
- Kismaayo bandavirus for Kismaayo virus (KISV; name corrected from the previously circulating “Kismayo virus” and “Kisemayo virus”) first isolated from yellow back ticks (Rhipicephalus pulchellus (Gerstäcker, 1873)) sampled in Kismaayo, Lower Juba (Jubbada Hoose) Region, Somalia [149]; and
- Lone Star bandavirus [sic] for lone star virus (LSV) first isolated from lone star ticks (Amblyomma americanum (Linnaeus, 1758)) sampled in Kentucky, USA [54, 114] (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp).
Genus Entovirus was created for one new species, Entoleuca entovirus, for Entoleuca phenui-like virus 1 (EnPLV-1) first discovered by HTS in Entoleuca sp. fungi sampled in Málaga Province, Spain [124] (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp).
Genus Kabutovirus and included species Kabuto mountain kabutovirus and Huangpi kabutovirus were renamed Uukuvirus, Kabuto mountain uukuvirus, and Huangpi uukuvirus, respectively. The established species Uukuniemi phlebovirus was moved into genus Uukuvirus and renamed Uukuniemi uukuvirus. 14 new species were established in genus Uukuvirus:
- American dog uukuvirus for American dog tick virus (ADAV) first detected by HTS in American dog ticks (Dermacentor variabilis (Say, 1821)) sampled in Heckscher State Park, New York, USA [120];
- Dabieshan uukuvirus for Dàbiéshān tick virus (DbsTV) first discovered by HTS in Asian longhorned ticks (Haemaphysalis longicornis Neumann, 1901) collected in the Dàbié Mountains (大別山), China [59];
- Grand Arbaud uukuvirus for Grand Arbaud virus (GAV) first isolated from ticks (Argas reflexus (Fabricius, 1794)) sampled in Bouches-du-Rhône Department, France [40, 85];
- Kaisodi uukuvirus for Kaisodi virus (KASDV) first isolated from hard-bodied ticks (Haemaphysalis spinigera Neumann, 1897) sampled in Mysore State, India [14, 88, 144];
- Lihan uukuvirus for Lǐhán tick virus (LITV) first discovered by HTS in Asian blue ticks (Rhipicephalus microplus (Canestrini, 1888)) sampled in Lǐhán (李韩), Húběi Province (湖北省), China [59];
- Murre uukuvirus for murre virus (MURV) first isolated from common murres (Uria aalge (Pontoppidan, 1763)) sampled in Alaska, USA [85];
- Pacific coast uukuvirus for Pacific coast tick virus (PACTV) first discovered by HTS in Pacific coast ticks (Dermacentor occidentalis Marx, 1892) sampled in Mendocino County, California, USA [17];
- Precarious Point uukuvirus for Precarious Point virus (PPV) first isolated from seabird ticks (Ixodes uriae White, 1852) sampled on Macquarie Island, Tasmania, Australia [85, 111];
- Rukutama uukuvirus for Rukutama virus (RUKV) first isolated from seabird ticks (Ixodes uriae White, 1852) sampled on Tûlenij/Tyuleny Island (Ocтpoв Tюлeний), Sakhalin Oblast (Caxaлинcкaя oблacть), Russia [63, 150];
- Schmidt uukuvirus for EgAn 1825-61 virus (here renamed Nile warbler virus [NIWV]) first isolated from a willow warbler (Phylloscopus trochilus (Linnaeus, 1758)) sampled in Nile Delta, Egypt [85];
- Silverwater uukuvirus for Silverwater virus (SILV) first isolated from rabbit ticks (Haemaphysalis leporispalustris Packard, 1869) sampled near Powassan, Ontario, Canada [69, 72];
- Tacheng uukuvirus for Tǎchéng tick virus 2 (TcTV-2) first discovered by HTS in ticks (Dermacentor marginatus Sulzer, 1776) sampled in China [59];
- Yongjia uukuvirus for Yǒngjiā tick virus 1 (YjTV-1) first discovered by HTS in East Asian mountain haemaphysalids (Haemaphysalis hystricis Supino, 1897) in China [59]; and
- Zaliv Terpeniya uukuvirus for Zaliv Terpeniya virus (ZTV) first isolated from seabird ticks (Ixodes uriae White, 1852) sampled on Tyuleny Island (Tюлeний ocтpoв) in the Gulf of Patience (Зaлив Tepпeния), Sakhalin Oblast (Caxaлинcкaя oблacть) and Commander Islands (Кoмaндopcкиe ocтpoвa), Kamchatka Krai (Кaмчaтcкий кpaй), RSFSR, USSR [62, 151] (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp).
Genus Ixovirus was established for the three new species:
- Blackleg ixovirus for blacklegged tick phlebovirus 1, here renamed blacklegged tick virus 1 (BLTV-1), first discovered by HTS in deer ticks (Ixodes scapularis Say, 1821) sampled in Heckscher State Park, New York, USA [120];
- Norway ixovirus for Norway phlebovirus 1, here renamed Fairhair virus (FHAV), first discovered by HTS in castor bean ticks (Ixodes ricinus (Linnaeus, 1758)) sampled in Norway [91]; and
- Scapularis ixovirus for blacklegged tick phlebovirus 3, here renamed blacklegged tick virus 3 (BLTV-3), first discovered by HTS in deer ticks (Ixodes scapularis Say, 1821) sampled in Heckscher State Park, New York, USA [120] (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp).
Genus Lentinuvirus was created for one new species, Lentinula lentinuvirus, for Lentinula edodes negative-strand RNA virus 2 (LeNSRV-2) first discovered by HTS in shiitakes (Lentinula edodes (Berk.) Pegler (1976)) sampled in Japan [60] (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp).
In genus Phlebovirus, established species Sandfly fever Naples phlebovirus was renamed Naples phlebovirus. The genus was expanded by 53 new species (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp):
- Adana phlebovirus for Adana virus (ADAV) first isolated from Phlebotomus spp. sandflies sampled in Adana, Adana Province (Adana ili), Turkey [4];
- Aguacate phlebovirus for Aguacate virus (AGUV) first isolated from Lutzomyia spp. sandflies sampled in El Aguacate, Panamá Province, Panama [82, 116];
- Alcube phlebovirus for Alcube virus (ACBV) first isolated from sandflies (Phlebotomus perniciosus Newstead, 1911) sampled around Arrábida, Portugal [10];
- Alenquer phlebovirus for Alenquer virus (ALEV) first isolated from a human in Ramal das Pias, Alenquer, Pará State, Brazil [83, 122];
- Ambe phlebovirus for Ambe virus (ABEV) first isolated from psychodid sandflies sampled near Altamira, Pará State, Brazil [80, 118];
- Anhanga phlebovirus for Anhangá virus (ANHV) first isolated from a Linnaeus’s two-toed sloth (Choloepus didactylus (Linnaeus, 1758)) sampled in Castanhal Forest, Pará State, Brazil [80];
- Arumowot phlebovirus for Arumowot virus (AMTV) first isolated from mosquitoes (Culex antennatus (Becker, 1903)) sampled in Sudan [13, 84];
- _Buenaventura phleboviru_s for Buenaventura virus (BUEV) first isolated in 1984 from Lutzomyia sp. sandflies sampled in Rio Raposo, Valle del Cauca Department, Colombia [87, 116];
- Cacao phlebovirus for Cacao virus (CACV) first isolated from sandflies (Nyssomyia trapidoi (Fairchild and Hertig, 1952)) sampled in El Aguacate, Panamá Province, Panama [87, 116];
- Campana phlebovirus for Campana virus (CMAV) first isolated from phlebotomine sandflies sampled in El Aguacate, Panamá Province, Panama [87];
- Chagres phlebovirus for Chagres virus (CHGV) first isolated from a human sampled at Fort Sherman, Canal Zone/Cólon Province, Panama [90];
- Cocle phlebovirus for Coclé virus (CCLV) first isolated from a human sampled in Penonomé, Coclé Province, Panama [87];
- Dashli phlebovirus for Dāshlī virus (DASV) first isolated from Sergentomyia sp. sandflies sampled in Dāshlīborun , Golestān Province , Iran [6];
- Durania phlebovirus for Durania virus (DRNV) first isolated from sandflies sampled in 1986 near Durania, North Santander Department, Colombia [82, 118];
- Echarate phlebovirus for Echarate virus (ECHV) first isolated from a human sampled in Cusco, Peru [83];
- Gabek phlebovirus for Gabek Forest virus (GFV) first isolated from a northeast African spiny mouse (Acomys cahirinus (É. Geoffroy, 1803)) sampled in Gabek Forest, near Paloich, Sudan [86];
- Gordil phlebovirus for Gordil virus (GORV) first isolated from a typical lemniscomys (Lemniscomys striatus (Linnaeus, 1758)) sampled in Gordil, Vakaga Prefecture, Central African Republic [86];
- Icoaraci phlebovirus for Icoaraci virus (ICOV) first isolated from from an unidentified forest rat sampled in Belém, Pará State, Brazil [19, 142];
- Itaituba phlebovirus for Itaituba virus (ITAV) first isolated from a common opossum (Didelphis marsupialis Linnaeus, 1758) trapped at the Tapacurazinho stream, Itaituba, Pará State, Brazil [83, 122];
- Itaporanga phlebovirus for Itaporanga virus (ITPV) first isolated from a sentinel Swiss mouse collected in Itaporanga, São Paulo State, Brazil [46, 121];
- Ixcanal phlebovirus for Ixcanal virus (IXCV) first isolated from Lutzomyia sp. sandflies sampled in Aldea Ixcanal and Aldea Puerta, El Progreso Departmesp. sandflies innt, Guatemala [82, 118];
- Karimabad phlebovirus for Karimabad virus (KARV) first isolated from Phlebotomus sp. sandflies in Karīmābād , Khūzestān Province , Iran [86];
- La Gloria phlebovirus for La Gloria virus (LAGV) first discovered by HTS in phlebotomine sandflies sampled near La Gloria village, Panama Canal area, central Panama [68];
- Lara phlebovirus for GGP-2011a virus (here renamed Rio Claro virus [RICV]) first isolated from a sentinel hamster sampled in Venezuela [unpublished];
- Leticia phlebovirus for Leticia virus (LETV) first isolated from sandflies sampled in Leticia, Amazonas Department, Colombia [87];
- Maldonado phlebovirus for Maldonado virus (MLOV) first isolated from a human sampled in Puerto Maldonado, Madre de Dios Region, Peru [83];
- Massilia phlebovirus for Massilia virus (MASV) first isolated from sandflies (Phlebotomus perniciosus Newstead, 1911) sampled in Marseille and Nice, Provence-Alpes-Côte d’Azur, France [20, 86];
- Medjerda phlebovirus for Medjerda Valley virus (MVV) first isolated from phlebotomine sandflies sampled at an archaeological site in Bizerte Governorate, Tunisia [15];
- Mona Grita phlebovirus for Mona Grita virus (MOGV) first discovered by HTS in sandflies (Nyssomyia trapidoi (Fairchild and Hertig, 1952)) sampled on Isla Mona Grita, Panama Canal, central Panama [68];
- Munguba phlebovirus for Munguba virus (MUNV) first isolated from sandflies (Nyssomyia umbratilis (Ward and Fraiha, 1977)) sampled in Monte Dourado, Pará State, Brazil [80, 122];
- Nique phlebovirus for Nique virus (NIQV) first isolated from sandflies (Lutzomyia panamensis (Shannon, 1926)) sampled in Cerro Nique, Darién Province, Panama [83, 117];
- Ntepes phlebovirus for Ntepes virus (NTPV) first isolated from Sergentomyia sp. sandflies sampled near Ntepes village, Marigat District, Baringo County, Kenya [115];
- Odrenisrou phlebovirus for Odrénisrou virus (ODRV) first isolated from mosquitoes (Culex albiventris Edwards, 1922) collected in the forest of Taï National Park, Côte d’Ivoire [84];
- Oriximina phlebovirus for Oriximiná virus (ORXV) first isolated from Lutzomyia sp. sandflies sampled in Saracazinho, Pará State, Brazil [83, 122];
- Pena Blanca phlebovirus for Peña Blanca virus (PEBV) first discovered by HTS in sandflies sampled on Peña Blanca peninsula, Panama Canal, central Panama [68];
- Punique phlebovirus for Punique virus (PUNV) first isolated from sandflies (Phlebotomus perniciosus Newstead, 1911 and Phlebotomus longicuspis Nitzulescu, 1930) sampled in Tunis, Tunisia [86];
- Rio Grande phlebovirus for Rio Grande virus (RGV) first isolated from a Southern Plains woodrat (Neotoma micropus Baird, 1855) sampled in Texas, USA [46];
- Saint Floris phlebovirus for Saint-Floris virus (SAFV) first isolated from a gerbil sampled in Gordil, Vakaga Prefecture, Central African Republic [86];
- Salanga phlebovirus for Salanga virus (SLGV) first isolated from a Hinde’s aethomys (Aethomys hindei (Thomas, 1902)) collected in Salanga, Ombella-M’Poko Prefecture, Central African Republic [51, 148];
- Salobo phlabovirus [sic] for Salobo virus (SLBOV) first isolated from a Guyenne spiny-rat (Proechimys guyannensis (E. Geoffroy, 1803)) in Pará State, Brazil [142];
- Sicilian phlebovirus for sandfly fever Sicilian virus (SFSV) first isolated from a human sampled in Palermo Province, Sicily Region, Italy [101, 137];
- Tapara phlebovirus for Tapará virus (TPRV) first isolated from phlebotomine sandflies in Altamira, Pará State, Brazil [80];
- Tehran phlebovirus for Tehran virus (THEV) first isolated from sandflies (Phlebotomus papatasi (Scopoli, 1786)) sampled in Tehran, Iran [86];
- Tico phebovirus [sic] for Tico virus (TICV) discovered by HTS in sandflies sampled in Panama Canal area, central Panama [68];
- Toros phlebovirus for Toros virus (TORV) first discovered by HTS in sandflies sampled in Damyeri, Adana Province (Adana ili), Turkey [5];
- Toscana phlebovirus for Toscana virus (TOSV) first isolated from sandflies (Phlebotomus perniciosus Newstead, 1911) in Toscany, Italy [86, 125];
- Tres Almendras phlebovirus for Tres Almendras virus (TRAV) first discovered by HTS in sandflies (Psychodopygus panamensis (Shannon, 1926)) sampled on Tres Almendras Islands, Panama Canal area, central Panama [68];
- Turuna phlebovirus for Turuna virus (TUAV) first isolated from Lutzomyia sp. sandflies sampled in Cachoeira Porteira, Pará State, Brazil [83, 122];
- Uriurana phlebovirus for Uriurana virus (URIV) first isolated from phlebotomine sandflies in Tucuruí, Pará State, Brazil [80];
- Urucuri phlebovirus for Urucuri virus (URUV) first isolated from a Guyenne spiny-rat (Proechimys guyannensis (E. Geoffroy, 1803)) in Utinga Forest, Belém, Pará State, Brazil [80, 122];
- Viola phlebovirus for viola virus (VIOV) first discovered by HTS in sandflies (Lutzomyia longipalpis (Lutz and Neiva, 1912)) sampled in Pirizal, Mato Grosso State, Brazil [24]; and
- Zerdali phlebovirus for Zerdali virus (ZERV) first discovered by HTS in sandflies sampled in Zerdali, Adana Province (Adana ili), Turkey [5].
Genus Rubodvirus was created for the two new species Apple rubodvirus 1 and 2 to accommodate apple rubbery wood viruses 1 and 2 (ARWV-1/2), respectively, first discovered using HTS in apple trees (Malus sp.) sampled in Germany and USA [100] (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp).
One new species, Melon tenuivirus, was added to genus Tenuivirus for melon chlorotic spot virus (MeCSV) first isolated from muskmelon (Cucumis melo L.) sampled in Provence-Alpes-Côte d’Azur Region, France [57].
Genus Wubeivirus was abolished and its two species, Fly wubeivirus and Dipteran wubeivirus, were moved into genus Phasivirus and renamed Fly phasivirus and Dipteran phasivirus, respectively (TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp).
Family Tospoviridae
The overlooked adjustment of 12 tospovirid species names to correct non-Latinized binomials was implemented (TaxoProp 2019.016M.A.v1.Corrections).
Eight new species were created in genus Orthotospovirus:
- Alstroemeria necrotic streak orthotospovirus for Alstroemeria necrotic streak virus (ANSV) first isolated from ornamental crops (Alstroemeria sp.) sampled in Colombia [42];
- Alstroemeria yellow spot orthotospovirus for Alstroemeria yellow spot virus (AYSV) first isolated from ornamental crops (Alstroemeria sp.) imported to and sampled in the Netherlands [43];
- Groundnut chlorotic fan spot orthotospovirus for groundnut chlorotic fan-spot virus (GCFSV) first isolated from peanut (Arachis hypogaea L.) sampled in Taiwan [21];
- Hippeastrum chlorotic ringspot orthotospovirus for Hippeastrum chlorotic spot virus (HCRV) first isolated from amaryllis (Hippeastrum sp.) and spider lily (Hymenocallis littoralis (Jacq.) Salisb.) sampled in southwestern China [31, 143];
- Mulberry vein banding associated orthotospovirus for mulberry vein banding-associated virus (MVBaV) discovered first by HTS in mulberry (Morus alba L.) sampled in Guǎngxī Zhuàng Autonomous Region (广西壮族自治区), China in 2011 [74, 75];
- Pepper chlorotic spot orthotospovirus for pepper chlorotic spot virus (PCSV) first isolated from sweet pepper (Capsicum annuum L.) in Taiwan [22];
- Tomato yellow ring orthotospovirus for tomato yellow ring virus (TYRV) first isolated from tomato (Solanum lycopersicum L.) in Iran [134]; and
- Tomato zonate spot orthotospovirus for tomato zonate spot virus (TZSV) first isolated from tomato (Solanum lycopersicum L.) and chili pepper (Capsicum annuum L.) sampled in Yúnnán Province (云南省), China [30] (TaxoProp 2019.006P.A.v1.Orthotospovirus_8sp).
SUMMARY
A summary of the current, ICTV-accepted taxonomy of the phylum Negarnaviricota is presented in Table 1 (Goujianvirales), Table 2 (Jingchuvirales), Table 3 (Mononegavirales), Table 4 (Muvirales), Table 5 (Serpentovirales), Table 6 (Articulavirales), and Table 7 (Bunyavirales).
Table 1 ICTV-accepted taxonomy of the order Goujianvirales (Negarnaviricota: Haploviricotina: Yunchangviricetes) as of March 2020
Table 2 ICTV-accepted taxonomy of the order Jingchuvirales (Negarnaviricota: Haploviricotina: Monjiviricetes) as of March 2020
Table 3 ICTV-accepted taxonomy of the order Mononegavirales (Negarnaviricota: Haploviricotina: Monjiviricetes) as of March 2020
Table 4 ICTV-accepted taxonomy of the order Muvirales (Negarnaviricota: Haploviricotina: Chunqiuviricetes) as of March 2020
Table 5 ICTV-accepted taxonomy of the order Serpentovirales (Negarnaviricota: Haploviricotina: Milneviricetes) as of March 2020
Table 6 ICTV-accepted taxonomy of the order Articulavirales (Negarnaviricota: Polyploviricotina: Insthoviricetes) as of March 2020
Table 7 ICTV-accepted taxonomy of the order Bunyavirales (Negarnaviricota: Polyploviricotina: Ellioviricetes) as of March 2020
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Acknowledgements
We thank W. Ian Lipkin and Rafal Tokarz (Columbia University Irving Medical Center, New York, New York, USA) for providing/approving new names for “blacklegged tick phleboviruses 1 and 3” and Edward Holmes (University of Sydney, Australia) for providing/approving a new name for “Norway phlebovirus”. Many authors are current members of 2017-2020 International Committee on Taxonomy of Viruses (ICTV) Study Groups: Arenaviridae (Jens H. Kuhn, Michael J. Buchmeier, Rémi N. Charrel, J. Christopher S. Clegg, Juan Carlos de la Torre, Jean-Paul J. Gonzalez, Stephan Günther, Mark D. Stenglein, Jussi Hepojoki, Manuela Sironi, Igor S. Lukashevich, Sheli R. Radoshitzky, Víctor Romanowski, Maria S. Salvato), Artoviridae (Jens H. Kuhn, Ralf G. Dietzgen, Dàohóng Jiāng, Nikos Vasilakis), Aspiviridae (John V. da Graça, Elena Dal Bó, Selma Gago-Zachert, María Laura García, John Hammond, Tomohide Natsuaki, José A. Navarro, Vicente Pallás, Carina A. Reyes, Gabriel Robles Luna, Takahide Sasaya, Ioannis Tzanetakis, Anna Maria Vaira, Martin Verbeek), Bornaviridae (Jens H. Kuhn, Thomas Briese, Ralf Dürrwald, Masayuki Horie, Timothy H. Hyndman, Norbert Nowotny, Susan Payne, Dennis Rubbenstroth, Mark D. Stenglein, Keizō Tomonaga), Bunyavirales (Jens H. Kuhn, Scott Adkins, Juan Carlos de la Torre, Sandra Junglen, Amy J. Lambert, Piet Maes, Marco Marklewitz, Gustavo Palacios, Takahide Sasaya, Yong-Zhen Zhang), Filoviridae (Jens H. Kuhn, Gaya K. Amarasinghe, Christopher Basler, Sina Bavari, Alexander Bukreyev, Kartik Chandran, Ian Crozier, Olga Dolnik, John M. Dye, Pierre B. H. Formenty, Anthony Griffiths, Roger Hewson, Gary Kobinger, Eric M. Leroy, Elke Mühlberger, Sergey V. Netesov, Gustavo Palacios, Bernadett Pályi, Janusz T. Pawęska, Sophie Smither, Ayato Takada, Jonathan S. Towner, Victoria Wahl), Fimoviridae (Michele Digiaro, Toufic Elbeaino, Giovanni P. Martelli, Nicole Mielke-Ehret, Hans-Peter Mühlbach), Hantaviridae (Steven Bradfute, Charles H. Calisher, Boris Klempa, Jonas Klingström, Lies Laenen, Piet Maes, Jin-Won Song, Yong-Zhen Zhang), Jingchuvirales (Nicholas Di Paola), Monjiviricetes (Jens H. Kuhn, Ralf G. Dietzgen, W. Paul Duprex, Dàohóng Jiāng, Piet Maes, Janusz T. Pawęska, Bertus K. Rima, Dennis Rubbenstroth, Peter J. Walker, Yong-Zhen Zhang), Mymonaviridae (María A. Ayllón, Dàohóng Jiāng, Shin-Yi L. Marzano), Nairoviridae (Jens H. Kuhn, Sergey V. Alkhovsky, Tatjana Avšič-Županc, Dennis A. Bente, Éric Bergeron, Felicity Burt, Nicholas Di Paola, Koray Ergünay, Aura R. Garrison, Roger Hewson, Ali Mirazimi, Gustavo Palacios, Anna Papa, Amadou Alpha Sall, Jessica R. Spengler), Negarnaviricota (Jens H. Kuhn, Eugene V. Koonin, Mart Krupovic, Yuri I. Wolf), Nyamiviridae (Jens H. Kuhn, Ralf G. Dietzgen, Dàohóng Jiāng, Nikos Vasilakis), Orthomyxoviridae (Justin Bahl, Inmaculada Casas, Adolfo García-Sastre, Seiji Hongo, Sergio H. Marshall, John W. McCauley, Gabriele Neumann, Colin R. Parrish, Daniel R. Pérez, Jonathan A. Runstadler, Martin Schwemmle), Paramyxoviridae (Anne Balkema-Buschmann, William G. Dundon, W. Paul Duprex, Andrew J. Easton, Ron Fouchier, Gael Kurath, Benhur Lee, Bertus K. Rima, Paul Rota, Lin-Fa Wang, Robobert A. Lamb), Peribunyaviridae (Scott Adkins, Sergey V. Alkhovsky, Martin Beer, Carol D. Blair, Charles H. Calisher, Michael A. Drebot, Holly R. Hughes, Amy J. Lambert, William Marciel de Souza, Marco Marklewitz, Márcio R. T. Nunes, Xiǎohóng Shí), Phasmaviridae (Matthew J. Ballinger, Roy A. Hall, Sandra Junglen, Stanley L. Langevin, Alex Pauvolid-Corrêa), Phenuiviridae (Thomas Briese, Rémi N. Charrel, Xavier De Lamballerie, Hideki Ebihara, George Fú Gāo, Martin H. Groschup, Márcio R. T. Nunes, Gustavo Palacios, Takahide Sasaya, Jin-Won Song), Pneumoviridae (Paul A. Brown, Ursula J. Buchholz, Rik L. de Swart, Jan Felix Drexler, W. Paul Duprex, Andrew J. Easton, Jiànróng Lǐ, Kirsten Spann, Natalie J. Thornburg, Bernadette van den Hoogen, John V. Williams), Rhabdoviridae (Kim R. Blasdell, Rachel Breyta, Ralf G. Dietzgen, Anthony R. Fooks, Juliana Freitas-Astúa, Hideki Kondō, Gael Kurath, Ivan V. Kuzmin, David M. Stone, Robert B. Tesh, Noël Tordo, Nikos Vasilakis, Peter J. Walker, Anna E. Whitfield), Sunviridae (Timothy H. Hyndman, Gael Kurath), Tenuivirus (Il-Ryong Choi, Gilda B. Jonson, Takahide Sasaya, Yukio Shirako, Tàiyún Wèi, Xueping Zhou), and Tospoviridae (Scott Adkins, Amy J. Lambert, Rayapati Naidu, Renato O. Resende, Massimo Turina, Anna E. Whitfield); or are ICTV Executive Committee Members: the 2017–2020 ICTV Chair of the Fungal and Protist Viruses Subcommittee (Peter Simmonds), the 2018–2020 ICTV Proposal Secretary (Peter J. Walker), the 2017–2020 ICTV Chair of the Plant Viruses Subcommittee (F. Murilo Zerbini), the 2017–2020 ICTV Chair of the Animal dsRNA and ssRNA- Viruses Subcommittee (Jens H. Kuhn), and 2017–2020 Elected Members (Sead Sabanadzovic, Arvind Varsani). We would like to thank Anya Crane (NIH/NIAID/DCR/IRF-Frederick) for critically editing the manuscript.
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Author notes
- Giovanni P. Martelli: Deceased.
Authors and Affiliations
- Integrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Fort Detrick, Frederick, MD, USA
Jens H. Kuhn - United States Department of Agriculture, Agricultural Research Service, US Horticultural Research Laboratory, Fort Pierce, FL, USA
Scott Adkins - Dipartimento di Agraria, Università degli Studi di Napoli Federico II, Portici, Italy
Daniela Alioto & Maria Minutolo - D.I. Ivanovsky Institute of Virology of N.F. Gamaleya National Center on Epidemiology and Microbiology of Ministry of Health of Russian Federation, Moscow, Russia
Sergey V. Alkhovsky - Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA
Gaya K. Amarasinghe - Mailman School of Public Health, Columbia University, New York, NY, USA
Simon J. Anthony - EcoHealth Alliance, New York, NY, USA
Simon J. Anthony - Ljubljana Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia
Tatjana Avšič-Županc - Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid-Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Campus de Montegancedo, Pozuelo de Alarcón, Madrid, Spain
María A. Ayllón - Departamento de Biotecnología-Biología Vegetal, Escuela Técnica Superior de Ingeniería Agronómica, Alimentaria y de Biosistemas, Universidad Politécnica de Madrid, Madrid, Spain
María A. Ayllón - Department of Infectious Diseases, Department of Epidemiology and Biostatistics, Institute of Bioinformatics, Center for Ecology of Infectious Diseases, University of Georgia, Athens, GA, USA
Justin Bahl - Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Novel and Emerging Infectious Diseases, Greifswald-Insel Riems, Germany
Anne Balkema-Buschmann & Martin H. Groschup - Department of Biological Sciences, Mississippi State University, Mississippi State, MS, USA
Matthew J. Ballinger - Department of Botany and Zoology, Masaryk University, Brno, Czech Republic
Tomáš Bartonička - Center for Microbial Pathogenesis, Institute for Biomedical Sciences, Georgia State University, Atlanta, GA, USA
Christopher Basler - Edge BioInnovation Consulting and Mgt, Frederick, MD, USA
Sina Bavari - Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany
Martin Beer, Leonie F. Forth, Florian Pfaff & Dennis Rubbenstroth - Galveston National Laboratory, The University of Texas, Medical Branch at Galveston, Galveston, TX, USA
Dennis A. Bente & Alexander Bukreyev - Viral Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA
Éric Bergeron, Jessica R. Spengler & Jonathan S. Towner - School of Veterinary Medicine, One Health Institute, University of California, Davis, CA, USA
Brian H. Bird - Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA
Carol Blair - Commonwealth Scientific and Industrial Research Organisation (CSIRO), Australian Centre for Disease Preparedness, Geelong, VIC, Australia
Kim R. Blasdell - University of New Mexico Health Sciences Center, Albuquerque, NM, USA
Steven B. Bradfute - US Geological Survey, Western Fisheries Research Center, Seattle, WA, USA
Rachel Breyta - Department of Epidemiology, Mailman School of Public Health, Center for Infection and Immunity, Columbia University, New York, NY, USA
Thomas Briese - Laboratory of Ploufragan-Plouzané-Niort, French Agency for Food, Environmental and Occupational Heath Safety ANSES, Ploufragan, France
Paul A. Brown - RNA Viruses Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA
Ursula J. Buchholz - Department of Molecular Biology and Biochemistry, University of California, Irvine, CA, USA
Michael J. Buchmeier - Department of Pathology, The University of Texas Medical Branch, Galveston, TX, USA
Alexander Bukreyev, Robert B. Tesh & Nikos Vasilakis - Division of Virology, National Health Laboratory Service, University of the Free State, Bloemfontein, Republic of South Africa
Felicity Burt - Department of Plant Protection, Faculty of Agriculture, Kahramanmaras Sütçü Imam University, Avsar Campus, 46060, Kahramanmaras, Turkey
Nihal Buzkan - Colorado State University, Fort Collins, CO, USA
Charles H. Calisher - National Citrus Engineering Research Center, Citrus Research Institute, Southwest University, Chongqing, 400712, China
Mengji Cao - Academy of Agricultural Sciences, Southwest University, Chongqing, 400715, China
Mengji Cao - Respiratory Virus and Influenza Unit, National Microbiology Center, Instituto de Salud Carlos III, Madrid, Spain
Inmaculada Casas - Virology and Pathogenesis Group, National Infection Service, Public Health England, Porton Down, UK
John Chamberlain - Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, USA
Kartik Chandran - Unité des Virus Emergents (Aix-Marseille Univ-IRD 190-Inserm 1207-IHU Méditerranée Infection), Marseille, France
Rémi N. Charrel & Xavier de Lamballerie - Guangdong Province Key Laboratory of Microbial Signals and Disease Control, College of Agriculture, South China Agricultural University, Guangdong, China
Biao Chen, Xin Yang, Tong Zhang & Guohui Zhou - Istituto per la Protezione Sostenibile delle Piante-Consiglio Nazionale delle ricerche (Institute for Sustainable Plant Protection-National Research Council), Bari, Italy
Michela Chiumenti, Francesco Di Serio, Angelantonio Minafra & Beatriz Navarro - Plant Breeding Genetics and Biotechnology Division, International Rice Research Institute, Los Baños, Philippines
Il-Ryong Choi - Les Mandinaux, Le Grand Madieu, France
J. Christopher S. Clegg - Clinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD, USA
Ian Crozier - Texas A&M University-Kingsville Citrus Center, Weslaco, TX, USA
John V. da Graça - CIDEFI. Facultad de Ciencias Agrarias y Forestales, Universidad de La Plata, La Plata, Argentina
Elena Dal Bó - Laboratório de Biologia Computacional e Sistemas, Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil
Alberto M. R. Dávila & Rodrigo Jardim - Department of Immunology and Microbiology IMM-6, The Scripps Research Institute, La Jolla, CA, USA
Juan Carlos de la Torre - Department Viroscience, Erasmus MC University Medical Centre Rotterdam, Rotterdam, The Netherlands
Rik L. de Swart & Ron A. M. Fouchier - Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR, 97331, USA
Patrick L. Di Bello - United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD, USA
Nicholas Di Paola, John M. Dye, Aura R. Garrison, Gustavo Palacios & Sheli R. Radoshitzky - Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, St. Lucia, QLD, Australia
Ralf G. Dietzgen - CIHEAM, Istituto Agronomico Mediterraneo di Bari, Valenzano, Italy
Michele Digiaro - Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR, USA
Valerian V. Dolja - Institute of Virology, Philipps University Marburg, Marburg, Germany
Olga Dolnik - Zoonotic Diseases and Special Pathogens, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB, Canada
Michael A. Drebot - Institute of Virology, Charité-Universitätsmedizin Berlin, corporate member of Free University Berlin, Humboldt-University Berlin, and Berlin Institute of Health, Berlin, Germany
Jan Felix Drexler, Sandra Junglen & Marco Marklewitz - Robert Koch Institut, Berlin, Germany
Ralf Dürrwald - Veterinary Research Institute, Brno, Czech Republic
Lucie Dufkova, Daniel Ruzek, Jiří Salát, Jana Širmarová & Petra Straková - Animal Production and Health Laboratory, Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture, Department of Nuclear Sciences and Applications, International Atomic Energy Agency, Vienna, Austria
William G. Dundon - School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA
W. Paul Duprex & John V. Williams - School of Life Sciences, University of Warwick, Coventry, UK
Andrew J. Easton - Department of Molecular Medicine, Mayo Clinic, Rochester, MN, USA
Hideki Ebihara - Istituto Agronomico Mediterraneo di Bari, Valenzano, Italy
Toufic Elbeaino - Virology Unit, Department of Medical Microbiology, Faculty of Medicine, Hacettepe University, Ankara, Turkey
Koray Ergünay - Animal and Plant Health Agency, Weybridge, Surrey, UK
Anthony R. Fooks - World Health Organization, Geneva, Switzerland
Pierre B. H. Formenty - Embrapa Cassava and Fruits, Cruz das Almas, Bahia, Brazil
Juliana Freitas-Astúa - Institute of Biochemistry and Biotechnology, Martin Luther University Halle-Wittenberg, Halle/Saale, Germany
Selma Gago-Zachert - Department of Molecular Signal Processing, Leibniz Institute of Plant Biochemistry, Halle/Saale, Germany
Selma Gago-Zachert - National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China
George Fú Gāo & Dexin Li - Instituto de Biotecnología y Biología Molecular, Facultad de Ciencias Exactas, CONICET UNLP, La Plata, Argentina
María Laura García - Icahn School of Medicine at Mount Sinai, New York, NY, USA
Adolfo García-Sastre - Metabiota, Inc. Sierra Leone, Freetown, Sierra Leone
Aiah Gbakima - One Health Institute, Karen C. Drayer Wildlife Health Center, School of Veterinary Medicine, University of California, Davis, CA, USA
Tracey Goldstein - Department of Microbiology and Immunology, Division of Biomedical Graduate Research Organization, School of Medicine, Georgetown University, Washington, DC, 20057, USA
Jean-Paul J. Gonzalez - Centaurus Biotechnologies, CTP, Manassas, VA, USA
Jean-Paul J. Gonzalez - Department of Microbiology and National Emerging Infectious Diseases Laboratories, Boston University School of Medicine, Boston, MA, USA
Anthony Griffiths & Elke Mühlberger - Department of Virology, Bernhard-Nocht Institute for Tropical Medicine, WHO Collaborating Centre for Arboviruses and Hemorrhagic Fever Reference and Research, Hamburg, Germany
Stephan Günther - Australian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Australia
Roy A. Hall - United States Department of Agriculture, Agricultural Research Service, USNA, Floral and Nursery Plants Research Unit, Beltsville, MD, USA
John Hammond - Department of Agricultural Botany, Faculty of Agriculture, Fayoum University, Fayoum, Egypt
Mohamed Hassan - Department of Virology, University of Helsinki, Medicum, Helsinki, Finland
Jussi Hepojoki, Satu Hepojoki & Teemu Smura - Vetsuisse Faculty, Institute of Veterinary Pathology, University of Zurich, Zurich, Switzerland
Jussi Hepojoki - Mobidiag Ltd, Espoo, Finland
Satu Hepojoki - Institute of Veterinary Pathology, University of Zuerich, Zurich, Switzerland
Udo Hetzel - Public Health England, Porton Down, Salisbury, Wiltshire, UK
Roger Hewson - Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany
Bernd Hoffmann & Dirk Höper - Department of Infectious Diseases, Faculty of Medicine, Yamagata University, Yamagata, Japan
Seiji Hongo - Hakubi Center for Advanced Research, Kyoto University, Kyoto, Japan
Masayuki Horie - School of Veterinary Medicine, Murdoch University, Murdoch, WA, Australia
Timothy H. Hyndman - Ministry of Health and Sanitation, Freetown, Sierra Leone
Amara Jambai - State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, Hubei, China
Dàohóng Jiāng - Ministry of Health Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
Qi Jin - Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou, China
Qi Jin - Department of Agricultural Biotechnology, Center for Fungal Pathogenesis, College of Agriculture and Life Sciences, Seoul National University, Seoul, South Korea
Gilda B. Jonson & Piet Maes - Republic Of Turkey Ministry Of Agriculture And Forestry, Pistachio Research Institute, Gaziantep, Turkey
Serpil Karadağ - United States Department of Agriculture, Agricultural Research Service, Horticulture Crops Research Unit, Corvallis, OR, USA
Karen E. Keller - Institute of Virology, Biomedical Research Center, Slovak Academy of Sciences, Bratislava, Slovakia
Boris Klempa - Department of Medicine Huddinge, Center for Infectious Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden
Jonas Klingström - Department of Microbiology, Immunology and Infectious Diseases, Université Laval, Quebec City, Canada
Gary Kobinger - Institute of Plant Science and Resources, Okayama University, Kurashiki, Japan
Hideki Kondō - National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA
Eugene V. Koonin, Yuri I. Wolf & Natalya Yutin - Archaeal Virology Unit, Institut Pasteur, Paris, France
Mart Krupovic - US Geological Survey Western Fisheries Research Center, Seattle, WA, USA
Gael Kurath - US Department of Agriculture, Animal and Plant Health Inspection, National Veterinary Services Laboratories, Diagnostic Virology Laboratory, Ames, USA
Ivan V. Kuzmin - Zoonotic Infectious Diseases Unit, KU Leuven, Rega Institute, Leuven, Belgium
Lies Laenen - Department of Laboratory Medicine, University Hospitals Leuven, Leuven, Belgium
Lies Laenen - Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA
Robert A. Lamb - Howard Hughes Medical Institute, Northwestern University, Evanston, IL, USA
Robert A. Lamb - Department of Microbiology, University of Washington, Washington, USA
Stanley L. Langevin - Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA
Benhur Lee - MIVEGEC (IRD-CNRS-Montpellier university) Unit, French National Research Institute for Sustainable Development (IRD), Montpellier, France
Eric M. Leroy - Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH, USA
Jiànróng Lǐ - Key Laboratory for Medical Virology, NHFPC, National Institute for Viral Disease Control and Prevention, Beijing, China
Mifang Liang - State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China
Wénwén Liú, Yàn Liú, Hui Wang, Xifeng Wang & Xueping Zhou - Department of Pharmacology and Toxicology, School of Medicine, The Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, University of Louisville, Louisville, KY, USA
Igor S. Lukashevich - Virology Research Center, University of São Paulo, Ribeirão Preto, Brazil
William Marciel de Souza - German Center for Infection Research (DZIF), Berlin, Germany
Sandra Junglen & Marco Marklewitz - Pontificia Universidad Católica de Valparaíso, Campus Curauma, Valparaíso, Chile
Sergio H. Marshall - Department of Plant, Soil and Food Sciences, University “Aldo Moro”, Bari, Italy
Giovanni P. Martelli - United States Department of Agriculture, Horticultural Crops Research Unit, Corvallis, OR, USA
Robert R. Martin - Department of Biology and Microbiology, Department of Plant Sciences, South Dakota State University, Brookings, SD, USA
Shin-Yi L. Marzano - Gembloux Agro-Bio Tech, TERRA, Plant Pathology Laboratory, Liège University, Liège, Belgium
Sébastien Massart - Worldwide Influenza Centre, Francis Crick Institute, London, UK
John W. McCauley - Biocentre Klein Flottbek, University of Hamburg, Hamburg, Germany
Nicole Mielke-Ehret & Hans-Peter Mühlbach - Folkhalsomyndigheten, Stockholm, Sweden
Ali Mirazimi - Department of Plant Pathology, Irrigated Agricultural Research and Extension Center, Washington State University, Prosser, WA, USA
Rayapati Naidu - School of Agriculture, Utsunomiya University, Utsunomiya, Tochigi, Japan
Tomohide Natsuaki - Instituto de Biología Molecular y Celular de Plantas, Universitat Politècnica de València-Consejo Superior de Investigaciones Científicas, Valencia, Spain
José A. Navarro - Novosibirsk State University, Novosibirsk, Novosibirsk Oblast, Russia
Sergey V. Netesov - Department of Pathobiological Sciences, Influenza Research Institute, University of Wisconsin-Madison, Madison, USA
Gabriele Neumann - Institute of Virology, University of Veterinary Medicine Vienna, Vienna, Austria
Norbert Nowotny - College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates
Norbert Nowotny - Evandro Chagas Institute, Ministry of Health, Pará, Brazil
Márcio R. T. Nunes - Fish Disease Research Group, Department of Biological Sciences, University of Bergen, Bergen, Norway
Are Nylund & Arnfinn L. Økland - Instituto de Biología Molecular y Celular de Plantas (IBMCP), Consejo Superior de Investigaciones Cientificas-Universidad Politécnica de Valencia, Valencia, Spain
Vicente Pallas - National Biosafety Laboratory, National Public Health Center, Budapest, Hungary
Bernadett Pályi - National Reference Centre for Arboviruses and Haemorrhagic Fever Viruses, Department of Microbiology, Medical School, Aristotle University of Thessaloniki, Thessaloníki, Greece
Anna Papa - College of Veterinary Medicine, Baker Institute for Animal Health, Cornell University, Ithaca, NY, USA
Colin R. Parrish - Department of Veterinary Integrated Biosciences and Department of Entomology, Texas A&M University, College Station, USA
Alex Pauvolid-Corrêa - Center for Emerging Zoonotic and Parasitic Diseases, National Institute for Communicable Diseases of the National Health Laboratory Service, Sandringham-Johannesburg, Gauteng, South Africa
Janusz T. Pawęska - Department of Veterinary Pathobiology, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, TX, USA
Susan Payne - Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA, USA
Daniel R. Pérez - Institute of Microbiology, University of Veterinary and Animal Sciences, Lahore, Pakistan
Aziz-ul Rahman & Muhammad Z. Shabbir - Laboratório de Biologia Molecular Aplicada, Instituto Biológico, São Paulo, SP, Brazil
Pedro L. Ramos-González - Departamento de Biologia Celular, Universidade de Brasília, Brasília, Brazil
Renato O. Resende - Instituto de Biotecnología y Biología Molecular, CCT-La Plata, CONICET-UNLP, La Plata, Buenos Aires, Argentina
Carina A. Reyes & Gabriel Robles Luna - Centre for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, The Queen’s University of Belfast, Belfast, Northern Ireland, UK
Bertus K. Rima - Instituto de Biotecnología y Biología Molecular, Centro Cientifico Technológico-La Plata, Consejo Nacional de Investigaciones Científico Tecnológico-Universidad Nacional de La Plata, La Plata, Argentina
Víctor Romanowski - National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
Paul Rota - Department of Infectious Disease and Global Health, Tufts University Cummings School of Veterinary Medicine, 200 Westboro Road, North Grafton, MA, 01536, USA
Jonathan A. Runstadler - Institute of Parasitology, Biology Centre of the Czech Academy of Sciences, Branisovska 31, 37005, Ceske Budejovice, Czech Republic
Daniel Ruzek & Jiří Salát - Department of Biochemistry, Molecular Biology, Entomology and Plant Pathology, Mississippi State University, Mississippi State, MS, USA
Sead Sabanadzovic - Institut Pasteur de Dakar, Dakar, Senegal
Amadou Alpha Sall - Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA
Maria S. Salvato - Department of Forestry Engineering, Faculty of Forestry, Karabuk University (UNIKA), Karabük, Turkey
Kamil Sarpkaya - Western Region Agricultural Research Center, National Agriculture and Food Research Organization, Fukuyama, Japan
Takahide Sasaya - Faculty of Medicine, University Medical Center-University Freiburg, Freiburg, Germany
Martin Schwemmle - MRC-University of Glasgow Centre for Virus Research, Glasgow, Scotland, UK
Xiǎohóng Shí - CAS Key Laboratory of Special Pathogens, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, People’s Republic of China
Zhènglì Shí & Xīnglóu Yáng - Asian Center for Bioresources and Environmental Sciences, University of Tokyo, Tokyo, Japan
Yukio Shirako - Nuffield Department of Medicine, University of Oxford, Oxford, UK
Peter Simmonds - Bioinformatics Unit, Scientific Institute IRCCS “E. Medea”, Bosisio Parini, Italy
Manuela Sironi - CBR Division, Dstl, Porton Down, Salisbury, Wiltshire, UK
Sophie Smither - Department of Microbiology, College of Medicine, Korea University, Seoul, Republic of Korea
Jin-Won Song - School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia
Kirsten M. Spann - Department of Microbiology, Immunology, and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA
Mark D. Stenglein - Centre for Environment, Fisheries and Aquaculture Science, Weymouth, Dorset, UK
David M. Stone - Division of Global Epidemiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan
Ayato Takada - Centers for Disease Control and Prevention, Atlanta, GA, USA
Natalie J. Thornburg - Institute for Frontier Life and Medical Sciences (inFront), Kyoto University, Kyoto, Japan
Keizō Tomonaga - Institut Pasteur, Unité des Stratégies Antivirales, WHO Collaborative Centre for Viral Haemorrhagic Fevers and Arboviruses, OIE Reference Laboratory for RVFV and CCHFV, Paris, France
Noël Tordo - Institut Pasteur de Guinée, Conakry, Guinea
Noël Tordo - Institute for Sustainable Plant Protection, National Research Council of Italy (CNR), Strada delle Cacce 73, 10135, Turin, Italy
Massimo Turina - Division of Agriculture, Department of Entomology and Plant Pathology, University of Arkansas System, Fayetteville, AR, 72701, USA
Ioannis Tzanetakis - Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Institute of Novel and Emerging Infectious Diseases, Südufer 10, 17493, Greifswald-Insel Riems, Germany
Rainer G. Ulrich - German Center of Infection Research (DZIF), Partner site Hamburg-Lübeck-Borstel-Insel Riems, Greifswald-Insel Riems, Germany
Rainer G. Ulrich - Institute for Sustainable Plant Protection, National Research Council of Italy (IPSP-CNR), 73 Strada delle Cacce, 10135, Turin, Italy
Anna Maria Vaira - Department of Viroscience, Erasmus MC University Medical Centre Rotterdam, Rotterdam, The Netherlands
Bernadette van den Hoogen - The Biodesign Center for Fundamental and Applied Microbiomics, Center for Evolution and Medicine School of Life Sciences, Arizona State University, Tempe, AZ, USA
Arvind Varsani - Structural Biology Research Unit, Department of Clinical Laboratory Sciences, University of Cape Town, Observatory, Cape Town, South Africa
Arvind Varsani - Wageningen University and Research, Biointeractions and Plant Health, Wageningen, The Netherlands
Martin Verbeek - National Biodefense Analysis and Countermeasures Center, Fort Detrick, Frederick, MD, USA
Victoria Wahl - NHC Key Laboratory of Systems Biology of Pathogens and Christophe Mérieux Laboratory, IPB-Fondation Mérieux, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China
Jianwei Wang - Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore
Lin-Fa Wang - Fujian Province Key Laboratory of Plant Virology, Institute of Plant Virology, Fujian Agriculture and Forestry University, Fuzhou, Fujian, China
Tàiyún Wèi - Mailman School of Public Health, Center for Infection and Immunity, Columbia University, New York, USA
Heather Wells - Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, USA
Anna E. Whitfield - MOH Key Laboratory of Systems Biology of Pathogens, IPB, CAMS, Beijing, China
Zhìqiáng Wú - Wuhan University School of Health Sciences, Wuhan, China
Xuejie Yu - Departamento de Fitopatologia, Instituto de Biotecnologia Aplicada à Agropecuária, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil
F. Murilo Zerbini - National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Changping, Beijing, China
Yong-Zhen Zhang - Shanghai Public Health Clinical Center, Institutes of Biomedical Sciences, Fudan University, Shanghai, China
Yong-Zhen Zhang - Centers for Disease Control and Prevention, Fort Collins, CO, USA
Holly R. Hughes & Amy J. Lambert - Laboratório de Hantaviroses e Rickettsioses, Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Rio de Janeiro, RJ, Brasil
Jorlan Fernandes, Alexandro Guterres, Elba R. S. Lemos & Renata C. Oliveira - School of Biological Sciences, University of Queensland, St. Lucia, Queensland, Australia
Peter J. Walker
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Corresponding author
Correspondence toJens H. Kuhn.
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The views and conclusions contained in this document are those of the authors and should not be interpreted as necessarily representing the official policies, either expressed or implied, of the US Department of the Army, the US Department of Defense, the US Department of Health and Human Services, the US Department of Homeland Security (DHS) Science and Technology Directorate (S&T), or of the institutions and companies affiliated with the authors. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government. In no event shall any of these entities have any responsibility or liability for any use, misuse, inability to use, or reliance upon the information contained herein. The US departments do not endorse any products or commercial services mentioned in this publication. The US Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains a non-exclusive, paid up, irrevocable, world-wide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes.
Funding
This work was supported in part through Laulima Government Solutions, LLC prime contract with the US National Institute of Allergy and Infectious Diseases (NIAID) under Contract No. HHSN272201800013C. J.H.K. performed this work as an employee of Tunnell Government Services (TGS), a subcontractor of Laulima Government Solutions, LLC under Contract No. HHSN272201800013C. This project has been funded in whole or in part with federal funds from the National Cancer Institute (NCI), National Institutes of Health (NIH), under Contract No. 75N91019D00024, Task Order No. 75N91019F00130 to I.C., who was supported by the Clinical Monitoring Research Program Directorate, Frederick National Lab for Cancer Research, sponsored by NCI. This work was also funded in part by Contract No. HSHQDC-15-C-00064 awarded by the US Department of Homeland Security (DHS) Science and Technology Directorate (S&T) for the management and operation of The National Biodefense Analysis and Countermeasures Center (NBACC), a federally funded research and development center operated by the Battelle National Biodefense Institute (V.W.); and NIH contract HHSN272201000040I/HHSN27200004/D04 and grant R24AI120942 (N.V., R.B.T.). S.S. acknowledges partial support from the Special Research Initiative of Mississippi Agricultural and Forestry Experiment Station (MAFES), Mississippi State University, and the National Institute of Food and Agriculture, US Department of Agriculture, Hatch Project 1021494.
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The authors declare no conflicts of interest.
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Kuhn, J.H., Adkins, S., Alioto, D. et al. 2020 taxonomic update for phylum Negarnaviricota (Riboviria: Orthornavirae), including the large orders Bunyavirales and Mononegavirales.Arch Virol 165, 3023–3072 (2020). https://doi.org/10.1007/s00705-020-04731-2
- Received: 15 June 2020
- Accepted: 04 July 2020
- Published: 04 September 2020
- Issue Date: December 2020
- DOI: https://doi.org/10.1007/s00705-020-04731-2