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OS16 - 2.P3.b Next Generation Sequencing Reveals New Southern African Territories Genotypes Bringing Us Closer to Understanding the History of FMD Virus in Africa - N. Knowles

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OS16 - 2.P3.b Next Generation Sequencing Reveals New Southern African Territories Genotypes Bringing Us Closer to Understanding the History of FMD Virus in Africa - N. Knowles

  1. 1. Next Generation Sequencing Reveals New Southern African Territories Genotypes Bringing Us Closer to Understanding the History of Foot-and-Mouth Disease Virus in Africa Lidia Lasecka-Dykes, Nick J. Knowles, Caroline F. Wright, Grace Logan, Toby Tuthill, Terry Jackson and Donald P. King
  2. 2. Foot-and-mouth disease virus (FMDV) • Genus Aphthovirus , family Picornaviridae; • Causes highly contagious disease of cloven-hoofed animals; • 7 serotypes: O, A, Asia1, C, SAT1-3; • African buffalo (Syncerus caffer) as ancestral reservoir of FMDV; • Biased sampling of true sequence diversity. VP1 O (58%) C (4%) A (20%) Asia1 (10%) SAT2 (3%) SAT1 (3%) SAT3 (1%)
  3. 3. SAT viruses with ‘non-SAT’ S-fragment ORF Mason et al. (2003) Virus Res; 91 [modified] What is the genetic basis of these unusual S-fragments?
  4. 4. SAT1,2,3 – ‘common’ SAT S-fragment SAT,1,2,3 – QEP (Queen Elizabeth Park) SAT1,2 – East Africa Serotype A Serotype O Serotype Asia 1 Serotype C 5’UTR of SAT viruses from Queen Elizabeth Park and East Africa show a distinct phylogenies S-fragment S-fragment Restof5’UTR VP1 SAT1 SAT2 SAT3 A Asia1 C O
  5. 5. SAT1,2,3 – ‘common’ SAT S-fragment SAT,1,2,3 – QEP (Queen Elizabeth Park) SAT1,2 – East Africa Serotype A Serotype O Serotype Asia 1 Serotype C Non-structural proteins of SAT viruses from Queen Elizabeth Park and East Africa also show distinct phylogenies Maximum likelihood trees suggest distinct evolutionary pathway of these viruses S-fragment 2B 2C 3C 3D
  6. 6. [Phylogenetic Signal Scan (SSE) - Toy Example] 1 10 20 30 40 Sgr A Sgr B Sgr C Sgr D Simmonds (2006) J Virol; 80 [modified] Method for identifying recombination
  7. 7. 5’UTR L VP4 VP2 VP3 VP1 2A 2B 2C 3A 3B1-3 3C 3D 3’UTR Genome positionTreeposition O C A Asia1 SAT2 SAT1 SAT3 Phylogenetic Signal Scan (SSE) (Bootstrap ≥ 70%) for 100 sequences and using 300 nts sliding window SSE: Simmonds (2012) BMC Research Notes; 20 Evidence of frequent recombination events in 5’UTR and NS region but not capsid
  8. 8. Genome positionTreeposition 5’UTR L VP4 VP2 VP3 VP1 2A 2B 2C 3A 3B1-3 3C 3D 3’UTR O C A Asia1 SAT2 SAT1 SAT3 East Africa QEP SEE: Simmonds (2012) BMC Research Notes; 20 Lack of recombination SAT viruses from East Africa and Queen Elizabeth Park suggests that these viruses evolved separately (e.g. parallel evolution?) Phylogenetic Signal Scan (SSE) (Bootstrap ≥ 70%) for 100 sequences and using 300 nts sliding window
  9. 9. “Common” SAT1/2/3 East Africa (SAT1/2) QEP (SAT1/2/3) Bayesian maximum clade credibility tree of 3C Cattle plague (Rinderpest) epidemic has influenced the genetic variability of SAT viruses currently found in Africa 1887 1889 1890 1892 Rinderpest spread according to Hutcheon (1897) Cattle distribution (present) Buffalo distribution (past) 1890 1890-92 1892 1893 Mar. 1896 Apr. 1896 Oct. 1896 1897 Feb. 1896 African Rinderpest Pandemic of 1887-1897
  10. 10. Historical Records: QENP
  11. 11. Acknowledgements The Pirbright Institute: Valerie Mioulet (samples) Graham Freimanis (“bioinformatics chat”) David King (“bioinformatics chat”) Nicolas strategic longer and larger grant Nic Stonehouse Dave Rowlands Sam Stephen Eleni-Anna Loundras Joseph Ward Martin Ryan Fiona Tulloch Garry Luke John Nicholson Angus Lamond Armel Nicolas Jürgen Haas Samantha Griffiths

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