RAPID COMMUNICATION
A novel Bluetongue virus serotype 3 strain in Tunisia,
November 2016
S. Sghaier
1†
| A. Lorusso
2†
| O. Portanti
2
| M. Marcacci
2
| M. Orsini
2
|
M. E. Barbria
3
| A. S. Mahmoud
2-4
| S. Hammami
5
| A. Petrini
2
| G. Savini
2
1
Institut de la Recherche V et erinaire de
Tunisie, Laboratoire de virologie, Univ ersit e
de Tunis El Manar, Tunis, Tunisia
2
OIE Reference Laboratory for Bluetongue,
Istituto Zooprofilattico Sperimentale
dell’Abruzzo e del Molise (IZSAM), Teramo,
Italy
3
CRDA-Commissariats R egionaux au
D eveloppement Agricole, Menzel Bouzelfa,
Tunisia
4
Dipartimento di Scienze Veterinarie,
Universit a degli Studi di Pisa, Pisa, Italy
5
Ecole Nationale de M edecine V et erinaire
de Sidi Thabet, Tunis, Tunisia
Correspondence
A. Lorusso, OIE Reference Laboratory for
Bluetongue, Istituto Zooprofilattico
Sperimentale dell’Abruzzo e del Molise
(IZSAM), Teramo, Italy.
Email: a.lorusso@izs.it
Funding information
Italian Ministry of Health
Summary
Since 1998, southern Europe has experienced multiple incursions of different sero-
types and topotypes of Bluetongue virus, a vector-borne transmitted virus, the cau-
sative agent of Bluetongue (BT), a major disease of ruminants. Some of these
incursions originated from northern Africa, likely because of wind-blown dissemina-
tion of infected midges. In this report, we describe the detection and whole genome
characterization of a novel BTV-3 strain identified in a symptomatic sheep in Tuni-
sia. Sequences were immediately deposited with the GenBank Database under
Accession Nos KY432369-KY432378. Alert and preparedness are requested to face
the next vector seasons in northern Africa and the potential incursion of this novel
strain in southern Europe.
KEYWORDS
Bluetongue serotype 3, whole genome sequencing, Tunisia
1 | INTRODUCTION
Bluetongue virus (BTV), the type species of the genus Orbivirus
within the family Reoviridae, is the causative agent of Bluetongue
(BT), one of the OIE-listed major diseases of ruminants. Bluetongue
virus is an arbovirus that generally spreads between mammalian
hosts by competent species of biting midges (Culicoides spp.). The
BTV genome consists of ten segments (Seg-1–Seg-10) of linear
dsRNA and it codes for structural (VP1-VP7) and non-structural
(NS1-NS5) proteins. VP2 and VP5 (encoded by Seg-2 and Seg-6,
respectively) are the most variable BTV proteins (Schwartz-Cornil
et al., 2008). They form the outer capsid, representing a target for
neutralizing antibodies (particularly VP2), and determine virus sero-
type. This virus exists into multiple serotypes (potentially 28, Sun
et al., 2016) and two major geographic groups of BTVs have been
identified and designated as eastern (e) or western (w) topotype.
They include viruses from Australia and the Middle/Far East, or
Africa and the Americas, respectively (Maan et al., 2008). Moreover,
the Seg-2 and Seg-6 sequences of reference strains of the different
BTV serotypes are classified so far as a number of distinct evolution-
ary lineages (nucleotypes). As for Seg-2, 12 nucleotypes (A–L) have
been so far defined and they also may reflect the serological rela-
tionships. As for Seg-6, 11 putative nucleotypes (A–K) are potentially
designated but its sequence variation does not show an absolute
correlation with serotype (Maan et al., 2015; Schulz et al., 2016; Sun
et al., 2016). Importantly, a characteristic of BTV is the ability to “re-
assort” genomic segments with related members of the same species
(Lorusso, Costessi et al., 2013; Lorusso, Sghaier et al., 2013; Nomi-
kou et al., 2015). BTV strains derived from modified live-attenuated
vaccines (MLVs) have also been used for BT prevention and isolated
in the field (Batten, Maan, Shaw, Maan, & Mertens, 2008; Ferrari
et al., 2005; Savini et al., 2014). Although still used in northern †
These authors equally contributed to this manuscript
Received: 13 January 2017
DOI: 10.1111/tbed.12640
Transbound Emerg Dis. 2017;1–7. wileyonlinelibrary.com/journal/tbed © 2017 Blackwell Verlag GmbH
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