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. 2015 Sep 10;3(5):e00921-15. doi: 10.1128/genomeA.00921-15

Consensus Sequence of 27 African Horse Sickness Virus Genomes from Viruses Collected over a 76-Year Period (1933 to 2009)

A Christiaan Potgieter a,b,*,, Isabella M Wright a,*, Alberdina A van Dijk b
PMCID: PMC4566168  PMID: 26358586

Abstract

We announce the complete consensus genome sequence of 27 African horse sickness viruses, representing all nine African horse sickness virus (AHSV) serotypes from historical and recent isolates collected over a 76-year period (1933 to 2009). The data set includes the sequence of the virulent Office International des Epizooties AHSV reference strains which are not adapted to cell culture.

GENOME ANNOUNCEMENT

African horse sickness (AHS) was first identified as a disease in horses in South Africa in 1891 and the viral nature of its etiological agent, African horse sickness virus (AHSV), was established in 1900 (1). The virus is transmitted by hematophagous Culicoides midges (2, 3) and can cause mortalities in up to 95% of fully susceptible horses. AHS is endemic in most of sub-Saharan Africa, occurs sporadically in North Africa, Mediterranean countries, and the Middle East, and a few outbreaks have been recorded in India and Pakistan. AHSV is a double-stranded RNA (dsRNA) virus with ten genome segments that belongs to the genus Orbivirus, family Reoviridae. Nine serotypes of the virus have been distinguished (4, 5).

Currently, the AHSV reference strains of the Office International des Epizooties (OIE) used at the ARC-Onderstepoort Veterinary Institute (OVI), South Africa, consist of at least one pathogenic isolate of each serotype from AHS outbreaks between 1955 and 1963 (6). These virulent reference viruses are used as challenge viruses during vaccine trials. Tissue culture–adapted progeny of these viruses and guinea pig sera raised against them are widely used as diagnostic reagents for serotyping AHSV isolates and to determine the immunity status of horses before and after vaccination (6).

The histories of the viruses used in this study (Table 1) were compiled from ARC-OVI specimen collection records from 1958 to 2009, records of vaccine trials in horses, personal communication with B. J. Erasmus, and the literature (4, 68). For this project, the virulent OIE reference strains and neurotropic vaccines were propagated by intracerebral injection of 2-day-old Swiss white mice, and the recent field isolates of AHSV were propagated in either BHK-21 or Vero cells. Extraction and purification of dsRNA, sequence-independent genome amplification, Roche 454 sequencing, and de novo sequence assembly were done as described previously (9).

TABLE 1.

History of 27 AHSV isolates from a 76-year period (1933–2009)

AHSV serotype Original isolate Isolate no. or yr of isolation Passage levela Origin Accession no.
History of the current OIE reference strains of African horse sickness virus used at ARC-OVI
    1 HS 61/61b HS 29/62c 2S Nelspruit, South Africa KF859986KF859995
    2 Unknown HS 82/61c 3S South Africa KF859996KF860005
    3 HS 13/63c 4S Malmesbury, South Africa KM886354KM886363
    4 HS 47/58 (Specimen 341) HS 32/62c 1S Zimbabwe KM609465KM609474
    5 FR (Fourie) HS 30/62c 2S South Africa KM886344KM886353
    6 HS 09/58 (Mule 3858) HS 39/63 1S Kaalplaas, South Africa KF860006KF860015
    6 HS 02/75c 4S South Africa KP009741KP009750
    7 HS 59/61 HS 31/62c 2S Kaalplaas, South Africa KF860016KF860025
    8 HS 10/62c 2S Kenya KF860026KF860035
    9 HS 90/61 4S Chad (Fort Lamy) KF860036KF860045
History of recent field isolates of African horse sickness virus
    1 HS 21/07 Unknown South Africa KP009621KP009630
    2 HS 90/07 2Vero South Africa KP009631KP009640
    3 HS 73/08 Unknown South Africa KP009641KP009650
    4 HS 128/06 1Vero South Africa KP009651KP009660
    5 HS 28/08 Unknown South Africa KP009661KP009670
    6 HS 04/08 Unknown South Africa KP009671KP009680
    7 HS 23/08 Unknown South Africa KP009681KP009690
    8 HS 29/00 1S,5BHK South Africa KP009691KP009700
    8 HS 83/04 3Vero,1BHK South Africa KP009721KP009730
    9 HS 27/08 Unknown South Africa KP009701KP009710
    9 HS 72/08 Unknown South Africa KP009731KP009740
    9 HS145/09 Unknown South Africa KP033466KP033475
History of the historic neurotropic strains of African horse sickness virus
    1 1180 1933 100+ in adult mice South Africa KP009711KP009720
    3 L 1940 100+ in adult mice Ladysmith, South Africa KP009761KP009770
    4 Vryheid 1938 100+ in adult mice Vryheid, South Africa KP009771KP009780
    5 Westerman 1936 100+ in adult mice South Africa KP009781KP009790
    7 Karen 1952 100+ in adult mice Kabete, Kenya KP009751KP009760
a

The passage level refers to the final passage number before dsRNA extraction and sequencing.

b

The number after the / indicates the year of the original isolate and the number before the / indicates the number of the isolate during the particular year.

c

Virulent strains used to develop attenuated vaccines by serial passage in BHK-21 and selection of genetically stable large plaques on Vero cells (6, 7).

Here we announce the first complete consensus genome sequence of each of the nine original pathogenic OIE reference strains of AHSV prior to the adaptation of the viruses to cell culture (10), some of the neurotropic AHSV vaccine strains (4, 11), and recent isolates of all nine AHSV serotypes made at the ARC-OVI from 1998 to 2009 (Table 1). In all, we sequenced 10 OIE reference strains (including HS2/75 used for attenuation of AHSV6), 5 neurotropic historic vaccine strains, and 12 recent field isolates. This sequence data set of 27 AHSV strains is the first representing all nine AHSV serotypes from both historical and recent isolates collected over a long period of 76 years (1933 to 2009). These genome sequence sets should be useful for comparison with sequences from live vaccine strains that were derived from them and published sequences from cloned genome segments that are mostly incorrect due to cloning biases, such as the genome segment 2 (VP2) sequence set of all nine AHSV serotypes (12). The consensus genome sequence data set of this announcement has already allowed the development of group- and serotype-specific real-time RT-PCRs (13) and, more importantly, has been used to rescue AHSVs of all nine serotypes by reverse genetics, which verifies their correctness (14).

Nucleotide sequence accession numbers.

The nucleotide sequences have been deposited in GenBank under the accession numbers listed in Table 1.

ACKNOWLEDGMENTS

This work was funded by the South African Department of Agriculture, Forestry and Fisheries (DAFF) as project number 21.1.1/6AH-10/OVI.

We acknowledge Baltus J. Erasmus for insightful discussions and contributing important historical information.

Footnotes

Citation Potgieter AC, Wright IM, van Dijk AA. 2015. Consensus sequence of 27 African horse sickness virus genomes from viruses collected over a 76-year period (1933 to 2009). Genome Announc 3(5):e00921-15. doi:10.1128/genomeA.00921-15.

REFERENCES

  • 1.Verwoerd DW. 2012. History of orbivirus research in South Africa. J S Afr Vet Assoc 83:532. [DOI] [PubMed] [Google Scholar]
  • 2.Du Toit RM. 1944. The transmission of bluetongue and horsesickness by Culicoides. Onderstepoort J Vet Sci Anim Ind 19:7–16. [Google Scholar]
  • 3.Meiswinkel R, Paweska JT. 2003. Evidence for a new field Culicoides vector of African horse sickness in South Africa. Prev Vet Med 60:243–253. doi: 10.1016/S0167-5877(02)00231-3. [DOI] [PubMed] [Google Scholar]
  • 4.McIntosh BM. 1958. Immunological types of horsesickness virus and their significance in immunization. Onderstepoort J Vet Res 27:465–539. [Google Scholar]
  • 5.Howell PG. 1962. The isolation and identification of further antigenic types of African horsesickness virus. Onderstepoort J Vet Res 29:139–149. [Google Scholar]
  • 6.Erasmus BJ. 1965. The attenuation of viscerotropic horsesickness virus in tissue culture. Bull Off Int Epizoot 64:697–702. [PubMed] [Google Scholar]
  • 7.Erasmus BJ. 1973. The pathogenesis of African horsesickness, p. 1–11. In Bryans JT, Gerber H (ed), Proceedings of the third international conference on equine infectious diseases, vol. III Karger, Basel, Switzerland. [Google Scholar]
  • 8.Erasmus BJ. 1978. A new approach to polyvalent immunization against African horsesickness, p. 401–403. In Bryans JT, Gerber H (ed), Proceedings of the third international conference on equine infectious diseases. Veterinary Publications, Princeton, NJ. [Google Scholar]
  • 9.Potgieter AC, Page NA, Liebenberg J, Wright IM, Landt O, van Dijk AA. 2009. Improved strategies for sequence-independent amplification and sequencing of viral double-stranded RNA genomes. J Gen Virol 90:1423–1432. doi: 10.1099/vir.0.009381-0. [DOI] [PubMed] [Google Scholar]
  • 10.Erasmus BJ. 1963. Cultivation of horsesickness virus in tissue culture. Nature 200:716. doi: 10.1038/200716a0. [DOI] [PubMed] [Google Scholar]
  • 11.Alexander RA. 1935. Studies on the neurotropic virus of horsesickness III: The intracerebral protection test and its application to the study of immunity. Onderstepoort J Vet Sci Anim Ind 4:349–377. [Google Scholar]
  • 12.Potgieter AC, Cloete M, Pretorius PJ, van Dijk AA. 2003. A first full outer capsid protein sequence data-set in the Orbivirus genus (family Reoviridae): cloning, sequencing, expression and analysis of a complete set of full-length outer capsid VP2 genes of the nine African horsesickness virus serotypes. J Gen Virol 84:1317–1326. doi: 10.1099/vir.0.18919-0. [DOI] [PubMed] [Google Scholar]
  • 13.Bachanek-Bankowska K, Maan S, Castillo-Olivares J, Manning NM, Maan NS, Potgieter AC, Di Nardo A, Sutton G, Batten C, Mertens PP. 2014. Real time RT-PCR assays for detection and typing of African horse sickness virus. PLoS One 9:e93758. doi: 10.1371/journal.pone.0093758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Van de Water SGP, van Gennip RGP, Potgieter CA, Wright IM, van Rijn PA. 2015. VP2 exchange and NS3/NS3a deletion in African horsesickness virus (AHSV) towards AHS disabled infectious single animal (DISA) vaccine candidates. J Virol 2015 Sep 1; 89(17):8764–8772. doi: 10.1128/JVI.01052-15 [Epub ahead of print.] [DOI] [PMC free article] [PubMed] [Google Scholar]

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