Occurrence of bovine ephemeral fever in Okinawa Prefecture, Japan, in 2012 and development of a reverse-transcription polymerase chain reaction assay to detect bovine ephemeral fever virus gene.

Tsuyoshi Niwa, Hiroaki Shirafuji, Kazufumi Ikemiyagi, Yoshiki Nitta, Moemi Suzuki, Tomoko Kato, Tohru Yanase
Author Information
  1. Tsuyoshi Niwa: Okinawa Prefectural Institute of Animal Health, 24-29 1-chome, Kohagura, Naha, Okinawa 900-0024, Japan.

Abstract

In September 2012, several cows and a calf showed decreased activity, anorexia and fever on Ishigaki Island, Okinawa Prefecture, Japan, and the cases were diagnosed as bovine ephemeral fever (BEF). We isolated BEF virus (BEFV) from one of the affected cows and then determined the complete genome sequence of the G gene, which encodes a class I transmembrane glycoprotein of BEFV. The BEFV isolate in this case, ON-3/E/12, was sorted into the same cluster as other BEFV isolates in Japan, Taiwan and China obtained in 1996-2004 and was most closely related to a 2002 Chinese isolate, JT02L, according to the phylogenetic analysis of the complete G gene. Since inactivated vaccines for BEF available in Japan are considered effective against the ON-3/E/12 isolate as well as other isolates in East Asia from 1996-2004, annual vaccination should be conducted to prevent BEF in Okinawa. Additionally, in this study, we developed an RT-PCR assay to detect the BEFV gene in Japan and neighboring countries. Our assay was able to amplify target sequences in all of the tested BEFV isolates, including 18 isolates in Japan and another isolate in Australia. The assay was found to be useful also for testing RNA samples extracted from bovine peripheral blood mononuclear cells, and the detection limit of the assay was 10 copies per tube. We believe that our assay would be an important tool for the screening of BEFV infection and the diagnosis of BEF.

References

  1. J Vet Diagn Invest. 2001 Nov;13(6):462-7 [PMID: 11724135]
  2. Aust Vet J. 1994 Feb;71(2):50-2 [PMID: 8166615]
  3. Nucleic Acids Res. 1994 Nov 11;22(22):4673-80 [PMID: 7984417]
  4. Microbiol Res. 1998 Nov;153(3):289-95 [PMID: 9880933]
  5. J Vet Med Sci. 2005 Apr;67(4):411-6 [PMID: 15876792]
  6. Curr Top Microbiol Immunol. 2005;292:57-80 [PMID: 15981468]
  7. Vet Microbiol. 2009 Jun 12;137(3-4):217-23 [PMID: 19201554]
  8. Aust Vet J. 2010 Aug;88(8):301-6 [PMID: 20633165]
  9. J Virol Methods. 2011 Jan;171(1):306-9 [PMID: 21093487]
  10. Mol Biol Evol. 2011 Oct;28(10):2731-9 [PMID: 21546353]
  11. Virol J. 2012;9:268 [PMID: 23150932]
  12. J Virol Methods. 2013 Aug;191(2):128-35 [PMID: 23623826]
  13. J Vet Med Sci. 2013 Nov;75(11):1511-4 [PMID: 23800972]
  14. Aust Vet J. 2014 Jan;92(1-2):24-7 [PMID: 24471878]
  15. Vet Microbiol. 2014 Oct 10;173(3-4):241-8 [PMID: 25175802]
  16. Transbound Emerg Dis. 2015 Oct;62(5):e66-70 [PMID: 24219124]

MeSH Term

Animals
Cattle
Ephemeral Fever
Ephemeral Fever Virus, Bovine
Female
Gene Expression Regulation, Viral
Japan
Phylogeny
Reverse Transcriptase Polymerase Chain Reaction
Viral Proteins

Chemicals

Viral Proteins

Word Cloud

Created with Highcharts 10.0.0BEFVJapanassayBEFfeverbovinegeneisolateisolatesOkinawaephemeral2012cowsPrefectureviruscompleteGON-3/E/121996-2004detectSeptemberseveralcalfshoweddecreasedactivityanorexiaIshigakiIslandcasesdiagnosedisolatedoneaffecteddeterminedgenomesequenceencodesclasstransmembraneglycoproteincasesortedclusterTaiwanChinaobtainedcloselyrelated2002ChineseJT02LaccordingphylogeneticanalysisSinceinactivatedvaccinesavailableconsideredeffectivewellEastAsiaannualvaccinationconductedpreventAdditionallystudydevelopedRT-PCRneighboringcountriesableamplifytargetsequencestestedincluding18anotherAustraliafoundusefulalsotestingRNAsamplesextractedperipheralbloodmononuclearcellsdetectionlimit10copiespertubebelieveimportanttoolscreeninginfectiondiagnosisOccurrencedevelopmentreverse-transcriptionpolymerasechainreaction

Similar Articles

Cited By