Analyze Diet
mBio2017; 8(5); doi: 10.1128/mBio.01613-17

Straight from the Horse’s “Mouth”: Genomic Epidemiology of an Icelandic Equine Epidemic.

Abstract: Despite tight biosecurity measures, an outbreak of respiratory disease rapidly spread across the Icelandic equine population in 2010. Horse transportation was brought to a halt in order to contain the spread of the infectious agent. In a recent article, Björnsdóttir and colleagues (S. Björnsdóttir et al., mBio 8:e00826-17, 2017, https://doi.org/10.1128/mBio.00826-17) employ the power and resolution of "genomic epidemiology," the combination of whole genomic sequencing and epidemiological approaches, to examine the source and spread of the outbreak. Intriguingly, the outbreak was not viral in origin, but linked to a bacterial "commensal" Streptococcus equi subsp. zooepidemicus infection. A national sampling strategy coupled with population genomics revealed that the outbreak was most likely driven by a S. equi subsp. zooepidemicus sequence type 209 (ST209) infection that spread nationally from a single source. This retrospective study demonstrates the power of genomics applied on a national scale to unravel the cause of a significant biosecurity threat.
Publication Date: 2017-10-10 PubMed ID: 29018124PubMed Central: PMC5635694DOI: 10.1128/mBio.01613-17Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Comment

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research article investigates a 2010 Icelandic horse respiratory disease outbreak using whole genome sequencing and epidemiological analysis. The study discovered that the disease was not virus-based, but was related to a bacterial infection, and demonstrated how genome sequencing on a national scale can help identify the origins of such outbreaks.

Genomic Epidemiology and the Icelandic Equine Epidemic

In 2010, a severe respiratory disease quickly spread among the horse population in Iceland, despite strict biosecurity precautions. The sudden outbreak led to a halt in horse transportation to prevent further spreading of the infectious agent. This research, conducted by Björnsdóttir and her colleagues, used “genomic epidemiology” – a technique that pairs whole genomic sequencing with epidemiological methods to examine the source and progression of the outbreak.

  • The team began by collecting samples nationwide, forming a comprehensive data set to allow for a thorough population genomic analysis.
  • Contrary to initial thoughts that the outbreak would be viral, the team discovered it was in fact bacterial, specifically, a “commensal” subsp. infection.
  • The results showed that the disease outbreak was likely caused by a subsp. sequence type 209 (ST209) infection. This is a type of bacterial infection, contradicting the initial viral hypothesis.
  • The analysis suggested that the infection had spread from a single source across the national horse population.

Significance of Genomic Epidemiology Techniques

This study illustrates the potential power of genomic epidemiology, especially when applied on a national scale, to uncover the causes of significant biosecurity threats.

  • By combining traditional epidemiological methods with advanced genomic sequencing techniques, researchers can more accurately identify the cause of outbreaks.
  • This approach allows for more effective strategies to combat the issue in the future.
  • The study’s results clarify the cause of the 2010 outbreak and provide valuable insights for future prevention and management strategies for equivalent infectious diseases.

Cite This Article

APA
Davies MR. (2017). Straight from the Horse’s “Mouth”: Genomic Epidemiology of an Icelandic Equine Epidemic. mBio, 8(5). https://doi.org/10.1128/mBio.01613-17

Publication

ISSN: 2150-7511
NlmUniqueID: 101519231
Country: United States
Language: English
Volume: 8
Issue: 5

Researcher Affiliations

Davies, Mark R
  • Department of Microbiology and Immunology, at the Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Victoria, Australia mark.davies1@unimelb.edu.au.

MeSH Terms

  • Animals
  • Genomics
  • Horse Diseases
  • Horses
  • Iceland
  • Mouth
  • Retrospective Studies
  • Streptococcal Infections

References

This article includes 20 references
  1. Neumann G, Noda T, Kawaoka Y. Emergence and pandemic potential of swine-origin H1N1 influenza virus. Nature 459:931–939.
    doi: 10.1038/nature08157pmc: PMC2873852pubmed: 19525932google scholar: lookup
  2. Chen Y, Liang W, Yang S, Wu N, Gao H, Sheng J, Yao H, Wo J, Fang Q, Cui D, Li Y, Yao X, Zhang Y, Wu H, Zheng S, Diao H, Xia S, Zhang Y, Chan KH, Tsoi HW, Teng JL, Song W, Wang P, Lau SY, Zheng M, Chan JF, To KK, Chen H, Li L, Yuen KY. Human infections with the emerging avian influenza A H7N9 virus from wet market poultry: clinical analysis and characterisation of viral genome. Lancet 381:1916–1925.
  3. Björnsdóttir S, Harris SR, Svansson V, Gunnarsson E, Sigurðardóttir ÓG, Gammeljord K, Steward KF, Newton JR, Robinson C, Charbonneau ARL, Parkhill J, Holden MTG, Waller AS. Genomic dissection of an Icelandic epidemic of respiratory disease in horses and associated zoonotic cases. mBio 8:e00826-17.
    doi: 10.1128/mBio.00826-17pmc: PMC5539424pubmed: 28765219google scholar: lookup
  4. Fulde M, Valentin-Weigand P. Epidemiology and pathogenicity of zoonotic streptococci. Curr Top Microbiol Immunol 368:49–81.
    doi: 10.1007/82_2012_277pubmed: 23192319google scholar: lookup
  5. Velineni S, Desoutter D, Perchec AM, Timoney JF. Characterization of a mucoid clone of Streptococcus zooepidemicus from an epizootic of equine respiratory disease in New Caledonia. Vet J 200:82–87.
    doi: 10.1016/j.tvjl.2014.01.014pubmed: 24618399google scholar: lookup
  6. Lindahl SB, Aspán A, Båverud V, Paillot R, Pringle J, Rash NL, Söderlund R, Waller AS. Outbreak of upper respiratory disease in horses caused by Streptococcus equi subsp. zooepidemicus ST-24. Vet Microbiol 166:281–285.
    doi: 10.1016/j.vetmic.2013.05.006pubmed: 23773239google scholar: lookup
  7. Chalker VJ, Waller A, Webb K, Spearing E, Crosse P, Brownlie J, Erles K. Genetic diversity of Streptococcus equi subsp. zooepidemicus and doxycycline resistance in kennelled dogs. J Clin Microbiol 50:2134–2136.
    doi: 10.1128/JCM.00719-12pmc: PMC3372135pubmed: 22495558google scholar: lookup
  8. Pesavento PA, Hurley KF, Bannasch MJ, Artiushin S, Timoney JF. A clonal outbreak of acute fatal hemorrhagic pneumonia in intensively housed (shelter) dogs caused by Streptococcus equi subsp. zooepidemicus. Vet Pathol 45:51–53.
    doi: 10.1354/vp.45-1-51pubmed: 18192575google scholar: lookup
  9. Salasia SI, Wibawan IW, Pasaribu FH, Abdulmawjood A, Lammler C. Persistent occurrence of a single Streptococcus equi subsp. zooepidemicus clone in the pig and monkey population in Indonesia. J Vet Sci 5:263–265.
    pubmed: 15365243
  10. Luheshi LM, Raza S, Peacock SJ. Moving pathogen genomics out of the lab and into the clinic: what will it take?. Genome Med 7:132.
    doi: 10.1186/s13073-015-0254-zpmc: PMC4697326pubmed: 26719100google scholar: lookup
  11. Walker MJ, Beatson SA. Epidemiology. Outsmarting outbreaks. Science 338:1161–1162.
    doi: 10.1126/science.1232327pubmed: 23197523google scholar: lookup
  12. Anzai T, Walker JA, Blair MB, Chambers TM, Timoney JF. Comparison of the phenotypes of Streptococcus zooepidemicus isolated from tonsils of healthy horses and specimens obtained from foals and donkeys with pneumonia. Am J Vet Res 61:162–166.
    doi: 10.2460/ajvr.2000.61.162pubmed: 10685688google scholar: lookup
  13. Loman NJ, Constantinidou C, Christner M, Rohde H, Chan JZ, Quick J, Weir JC, Quince C, Smith GP, Betley JR, Aepfelbacher M, Pallen MJ. A culture-independent sequence-based metagenomics approach to the investigation of an outbreak of Shiga-toxigenic. Escherichia coli O104:H4. JAMA 309:1502–1510.
    doi: 10.1001/jama.2013.3231pubmed: 23571589google scholar: lookup
  14. Olm MR, Brown CT, Brooks B, Firek B, Baker R, Burstein D, Soenjoyo K, Thomas BC, Morowitz M, Banfield JF. Identical bacterial populations colonize premature infant gut, skin, and oral microbiomes and exhibit different in situ growth rates. Genome Res 27:601–612.
    doi: 10.1101/gr.213256.116pmc: PMC5378178pubmed: 28073918google scholar: lookup
  15. Davies MR, Holden MT, Coupland P, Chen JH, Venturini C, Barnett TC, Zakour NL, Tse H, Dougan G, Yuen KY, Walker MJ. Emergence of scarlet fever Streptococcus pyogenes emm12 clones in Hong Kong is associated with toxin acquisition and multidrug resistance. Nat Genet 47:84–87.
    doi: 10.1038/ng.3147pubmed: 25401300google scholar: lookup
  16. Gonçalves da Silva A, Baines SL, Carter GP, Heffernan H, French NP, Ren X, Seemann T, Bulach D, Kwong J, Stinear TP, Howden BP, Williamson DA. A phylogenomic framework for assessing the global emergence and evolution of clonal complex 398 methicillin-resistant Staphylococcus aureus. Microb Genom 3:e000105.
    doi: 10.1099/mgen.0.000105pmc: PMC5361625pubmed: 28348878google scholar: lookup
  17. Lowder BV, Guinane CM, Ben Zakour NL, Weinert LA, Conway-Morris A, Cartwright RA, Simpson AJ, Rambaut A, Nübel U, Fitzgerald JR. Recent human-to-poultry host jump, adaptation, and pandemic spread of Staphylococcus aureus. Proc Natl Acad Sci U S A 106:19545–19550.
    doi: 10.1073/pnas.0909285106pmc: PMC2780746pubmed: 19884497google scholar: lookup
  18. Mather AE, Reid SW, Maskell DJ, Parkhill J, Fookes MC, Harris SR, Brown DJ, Coia JE, Mulvey MR, Gilmour MW, Petrovska L, de Pinna E, Kuroda M, Akiba M, Izumiya H, Connor TR, Suchard MA, Lemey P, Mellor DJ, Haydon DT, Thomson NR. Distinguishable epidemics of multidrug-resistant Salmonella Typhimurium DT104 in different hosts. Science 341:1514–1517.
    doi: 10.1126/science.1240578pmc: PMC4012302pubmed: 24030491google scholar: lookup
  19. Ben Zakour NL, Davies MR, You Y, Chen JH, Forde BM, Stanton-Cook M, Yang R, Cui Y, Barnett TC, Venturini C, Ong CL, Tse H, Dougan G, Zhang J, Yuen KY, Beatson SA, Walker MJ. Transfer of scarlet fever-associated elements into the group A Streptococcus M1T1 clone. Sci Rep 5:15877.
    doi: 10.1038/srep15877pmc: PMC4629146pubmed: 26522788google scholar: lookup
  20. Zozaya-Valdés E, Porter JL, Coventry J, Fyfe JAM, Carter GP, Gonçalves da Silva A, Schultz MB, Seemann T, Johnson PDR, Stewardson AJ, Bastian I, Roberts SA, Howden BP, Williamson DA, Stinear TP. Target-specific assay for rapid and quantitative detection of Mycobacterium chimaera DNA. J Clin Microbiol 55:1847–1856.
    doi: 10.1128/JCM.00197-17pmc: PMC5442541pubmed: 28381604google scholar: lookup

Citations

This article has been cited 0 times.