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Brief Report

Taxonomy of Phleboviruses, Emphasizing Those That Are Sandfly-Borne †

by
Charles H. Calisher
1,* and
Mattia Calzolari
2
1
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology and Pathology, College of Veterinary Medicine and Biological Sciences, 3195 Rampart Rd., Foothills Campus, Colorado State University, Fort Collins, CO 80523-1690, USA
2
Laboratorio Entomologia Sanitaria, Sede Territoriale di Reggio Emilia, Istituto Zooprofilattico Sperimentale della Lombardia e dell′Emilia Romagna “B. Ubertini” via Pitagora 2, 42124 Reggio Emilia, Italy
*
Author to whom correspondence should be addressed.
Intended for Special Issue of Viruses; edited by Mattia Calzolari and Charles H. Calisher.
Viruses 2021, 13(5), 918; https://doi.org/10.3390/v13050918
Submission received: 11 April 2021 / Revised: 27 April 2021 / Accepted: 6 May 2021 / Published: 15 May 2021
(This article belongs to the Special Issue Sand Fly-Borne Phleboviruses)

Abstract

:
Sandfly-borne phleboviruses (phylum Negarnavaricota, realm Riboviria, kingdom Orthornavirae, genus Phlebovirus) comprise three genome segments of ribonucleic acid (RNA) and which encode an RNA-dependent RNA polymerase, which they use to transcribe the viral RNA genome into messenger RNA and to replicate the genome. At least some of these viruses cause mild 3-day fevers in humans but some also have been associated with more severe illnesses in humans. The 67 recognized phleboviruses are listed here in a table composed by the authors from International Committee on Taxonomy of Viruses reports as well as the scientific literature.

Viruses of the genus Phlebovirus (realm Riboviria, kingdom Orthornaviridae, phylum Negarnavaricota, order Bunyavirales and family Phenuiviridae) comprise three genome segments of ribonucleic acid (RNA) which encode an RNA-dependent RNA polymerase, which they use to transcribe the viral RNA genome into messenger RNA and to replicate the genome [1]. Phleboviruses have a large (L) segment (6.4 kb) that codes for the RNA-dependent RNA polymerase (RdRp); a medium (M) segment (3.2 kb), which encodes for several polyproteins, obtained by leaky scanning and cleaved into several proteins (Nsm-GN, Nsm, NSm′, Gn and Gc); and a small (S) segment (1.7 kb) that encodes for two proteins (N and NSs) with an ambisense strategy (https://viralzone.expasy.org/252 accessed on 10 April 2021).
The genus name is derived from Phlebotominae, the taxon of vectors of member species sandfly fever Naples phlebovirus, from the Greek phlebos, meaning “vein”. Species in the genus were previously defined by serological cross reactivity. The detection of new phleboviruses, not often available for serological assays, prompted the change of classification rules. Now, viral species are defined by 95% or greater identity in the amino acid sequences of their RdRp [TaxoProp 2019.026M.A.v1.Phenuiviridae_4gen79sp]. The genus currently comprises 67 species, listed in Table 1. Phleboviruses mentioned in this Special Issue have not all been detected in sandflies. Those that have are noted in Table 1 with an asterisk. Some of these viruses have other hematophagous arthropods as their main vectors, such as mosquitoes for Rift Valley fever virus, while Mukawa virus has been isolated from ticks but remains in the genus Phlebovirus, despite the observations that most tick-borne viruses formerly included in the genus Phlebovirus are now included in the genus Uukuvirus. Some phleboviruses have been isolated from vertebrates, such as wild or sentinel rodents in the Americas, and in Africa, such as opossums or sloths. Other phleboviruses have been isolated from febrile patients in South America (Table 1). This variety of sources highlights the possible presence of diverse epidemiological cycles of these viruses. A high rate of vertical transmission of Toscana virus has been demonstrated in sandflies by experimental infections [2,3], suggesting that there is an amplifying role for vertebrate hosts but that maintenance in nature is mainly by sandflies.
“Sandfly” (or “sand fly”) is a colloquial name for members of any species or genus of flying, biting, blood-sucking dipteran encountered in sandy areas. In the United States, “sandfly” may refer to certain horse flies that are also known as “greenheads”, or to members of the family Ceratopogonidae. Outside the United States, “sandfly” may refer to members of the subfamily Phlebotominae within the Psychodidae. The three main genera are Lutzomyia (found in the New World) and Phlebotomus and Sergentomyia (both found in the Old World), the former two genera contain the more relevant species able to transmit viral pathogens [4]. Biting midges are sometimes called “sandflies” or “no-see-ums”. New Zealand sandflies are in the genus Austrosimulium, a type of black fly (https://en.wikipedia.org/wiki/Sandfly accessed on 10 April 2021).
Infections with many of these viruses cause mild 3-day fevers, also known as pappataci fevers or phlebotomus fevers [5]. These illnesses are influenza-like and are characterized by a rapid onset. The diseases occur commonly in endemic areas in summer months, especially in August during which sandflies are active. Toscana virus has been associated with benign meningitis and, occasionally, more severe meningitis in humans [6]. The most important phlebovirus is Rift Valley fever virus, which has been responsible for wide-spread epidemics and epizootics in livestock in Africa, most notably in Egypt [7]. However, it is transmitted principally by mosquitoes, and so it is not mentioned further here.
A diagnostically complicating feature of phlebovirus replication may be reassortant generation resulting from multiple simultaneous phlebovirus infections [8]. As with other segmented RNA viruses, the reassortment of RNA segments of phleboviruses is commonly observed. By this means, the RNA segments of different virus strains become mixed during replication, and the progeny viruses contain genome segments of the parental viruses. Thus, the progeny viruses have new combinations of these segments and possess novel properties and may be confused for one another due to the specificity of the testing procedures. Only complete genetic analyses can be used to definitively identify such progeny [9]. It has been argued that perhaps all available viruses in this virus family may be the most recent of long genetic lineages [8]. Undoubtedly, some (or all) of the viruses listed in Table 1 are reassortant phleboviruses, particularly those detected in Italy [10], possibly due to the co-circulation of multiple phleboviruses in arthropod vectors occurring in close proximity [11].
To assess possible reassortant phleboviruses, amino acid sequences of the RdRp and correspondent M segments have been retrieved from GenBank and aligned with MAFFT [12]. The percentage of identity has been evaluated with MegaX software, using p-distance with a pairwise deletion option [13]. A maximum likelihood phylogenetic tree was obtained with the RdRp aligned using IQtree software [14]. In this tree, in Figure 1, sequences with more than 95% identity, then ascribable to a single species, are highlighted in red.
The likely reassortant phleboviruses have different M segments (with the exception of Ponticelli II and Bregalaka, which are very similar). Reassortment events have been described for phleboviruses of the Candiru antigenic complex [15], among Massilia, Granada and Arrabida viruses [16,17], and likely produced Ponticelli I, Ponticelli II and Ponticelli III, which belong to the Adana phlebovirus species, according to the RdRp threshold. The possibility of reassortment involving the M segment would be a relevant phenomenon in the evolution of this group, as similarly reported for orthobunyaviruses [18]. The M segment is likely responsible for modifying the pathogenic potential of a virus, as has been reported for reassortant orthobunyaviruses [18,19].
Table 1. Viruses of the genus Phlebovirus, modified from [1].
Table 1. Viruses of the genus Phlebovirus, modified from [1].
Species 1Virus 2Abbreviation
Adana phlebovirusAdana virus *ADAV
Ponticelli I virus *
Ponticelli II virus *
Ponticelli III virus *
Bregalaka virus *
Aguacate phlebovirusAguacate virus *AGUV
Alcube phlebovirusAlcube virus *ACBV
Alenquer phlebovirusAlenquer virusALEV
Ambe phlebovirusAmbe virus *ABEV
Anhanga phlebovirusAnhangá virusANHV
Arumowot phlebovirusArumowot virusAMTV
Bogoria phlebovirusBogoria virusBGRV
Buenaventura phlebovirusBuenaventura virus *BUEV
Bujaru phlebovirusBujaru virusBUJV
Cacao phlebovirusCacao virus *CACV
Campana phlebovirusCampana virus *CMAV
Candiru phlebovirus 3
Ariquemes virusARQV
Candirú virusCDUV
Jacundá virusJCNV
Morumbi virusMRBV
Mucura virusMCRV
Serra Norte virusSRNV
Chagres phlebovirusChagres virus *CHGV
Cocle phlebovirusCoclé virusCCLV
Corfou phlebovirusCorfou virus *CFUV
Dashli phlebovirusDāshlī virus *DASV
Durania phlebovirusDurania virus *DRNV
Echarate phlebovirusEcharate virusECHV
Embossos phlebovirusEmbossos virus *EMBV
Gabek phlebovirusGabek forest virusGFV
Gordil phlebovirusGordil virusGORV
Icoaraci phlebovirusIcoaraci virusICOV
Itaituba phlebovirusItaituba virusITAV
Itaporanga phlebovirusItaporanga virusITPV
Ixcanal phlebovirusIxcanal virus *IXCV
Karimabad phlebovirusKarimabad virus *KARV
Kiborgoch phlebovirusKiborgoch virus *KBGV
La Gloria phlebovirusLa Gloria virus *LAGV
Lara phlebovirusRio Claro virusRICV
Leticia phlebovirusLeticia virus *LTCV
Maldonado phlebovirusMaldonado virusMLOV
Mariquita phlebovirusMariquita virus *MRQV
Massilia phlebovirusMassilia virus *MASV
Medjerda phlebovirusMedjerda Valley virus *MVV
Mona Grita phlebovirusMona Grita virus *MOGV
Mukawa phlebovirusMukawa virusMKWV
Munguba phlebovirusMunguba virus *MUNV
Naples phlebovirus 3
Arrabida virus *ARRV
Balkan virus *BALKV
Fermo virus *FERV
Granada virus *GRAV
Saddaguia virus *SADV
sandfy fever Naples virus *SFNV
Nique phlebovirusNique virus *NIQV
Ntepes phlebovirusNtepes virus *NTPV
Odrenisrou phlebovirusOdrénisrou virusODRV
Oriximina phlebovirusOriximiná virus *ORXV
Pena Blanca phlebovirusPeña Blanca virus *PEBV
Penshurt phlebovirusPenshurt virusPEHV
Perkerra phlebovirusPerkerra virusPKEV
Punique phlebovirusPunique virus*PUNV
Punta Toro phlebovirus 3
Buenaventura virus *BUEV
Capira virus *CAPIV
Punta Toro virus *PTV
Rift Valley fever phlebovirus 4Rift Valley fever virusRVFV
Hedi virus * [20]HEDV
Rio Grande phlebovirusRio Grande virusRGV
Saint Floris phlebovirusSaint-Floris virusSAFV
Salanga phlebovirusSalanga virusSLGV
Salehabad phlebovirus 3
Adria virus *ADRV
Arbia virus *ARBV
Olbia virus *OLBV
Salehabad virus *SALV
Zaba virus *ZABAV
Salobo phlebovirusSalobo virus *SLBOV
Sicilian phlebovirussandfy fever Sicilian virus *SFSV
Tapara phlebovirusTapará virus *TPRV
Tehran phlebovirusTehran virus *THEV
Tico phlebovirusTico virus *TICV
Toros phlebovirusToros virus *TORV
Toscana phlebovirusToscana virus *TOSV
Tres Almendras phlebovirusTres Almendras virus *TRAV
Turuna phlebovirusTuruna virus *TUAV
Uriurana phlebovirusUriurana virus *URIV
Urucuri phlebovirusUrucuri virusURUV
Viola phlebovirusViola virus *VIOV
Zerdali phlebovirusZerdali virus *ZERV
1 Taxon names are always italicized and always begin with a capital letter. Note that viruses are real objects that are assigned to concepts that are called taxa. Species, genera, subfamilies, families and orders are taxa; 2 virus names are not italicized and are not capitalized, except if the name or a name component is a proper noun. This column lists the virus names with their correct (including lack of) capitalization; 3 lists of viruses within a given species are provisional at this point and will likely be amended in the near future; 4 type of species; * detected in sandflies.

Author Contributions

Conceptualization, C.H.C.; data curation, C.H.C. and M.C.; writing—original draft preparation, C.H.C.; writing—review and editing, C.H.C. and M.C.; visualization, M.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Midpoint rooted maximum likelihood tree obtained with amino acid sequences of the RdRp of available phleboviruses. Sequences in red: ascribable to the same species according the 95% identity threshold. Bootstrap values >85% are shown over the branch.
Figure 1. Midpoint rooted maximum likelihood tree obtained with amino acid sequences of the RdRp of available phleboviruses. Sequences in red: ascribable to the same species according the 95% identity threshold. Bootstrap values >85% are shown over the branch.
Viruses 13 00918 g001
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Calisher, C.H.; Calzolari, M. Taxonomy of Phleboviruses, Emphasizing Those That Are Sandfly-Borne. Viruses 2021, 13, 918. https://doi.org/10.3390/v13050918

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Calisher CH, Calzolari M. Taxonomy of Phleboviruses, Emphasizing Those That Are Sandfly-Borne. Viruses. 2021; 13(5):918. https://doi.org/10.3390/v13050918

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Calisher, Charles H., and Mattia Calzolari. 2021. "Taxonomy of Phleboviruses, Emphasizing Those That Are Sandfly-Borne" Viruses 13, no. 5: 918. https://doi.org/10.3390/v13050918

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