Skip to content
naulon

No retraction, correction or concern found when last checked on Oct 26, 2026.

Rapid host switching in generalist Campylobacter strains erodes the signal for tracing human infections

Bethany L Dearlove, Alison J Cody, Ben Pascoe and 3 more

The ISME Journal · 2015 · CC BY

doi:10.1038/ismej.2015.149

Abstract

Campylobacter jejuni and Campylobacter coli are the biggest causes of bacterial gastroenteritis in the developed world, with human infections typically arising from zoonotic transmission associated with infected meat. Because Campylobacter is not thought to survive well outside the gut, host-associated populations are genetically isolated to varying degrees. Therefore, the likely origin of most strains can be determined by host-associated variation in the genome. This is instructive for characterizing the source of human infection. However, some common strains, notably isolates belonging to the ST-21, ST-45 and ST-828 clonal complexes, appear to have broad host ranges, hindering source attribution. Here whole-genome sequencing has the potential to reveal fine-scale genetic structure associated with host specificity. We found that rates of zoonotic transmission among animal host species in these clonal complexes were so high that the signal of host association is all but obliterated, estimating one zoonotic transmission event every 1.6, 1.8 and 12 years in the ST-21, ST-45 and ST828 complexes, respectively. We attributed 89% of clinical cases to a chicken source, 10% to cattle and 1% to pig. Our results reveal that common strains of C. jejuni and C. coli infectious to humans are adapted to a generalist lifestyle, permitting rapid transmission between different hosts. Furthermore, they show that the weak signal of host association within these complexes presents a challenge for pinpointing the source of clinical infections, underlining the view that whole-genome sequencing, powerful though it is, cannot substitute for intensive sampling of suspected transmission reservoirs.

Full text

Its licence does not allow us to show the full text. Read it at PubMed Central:

Read at PubMed Central

References 47

  1. 1.

    Allos BM. (2001 ). Campylobacter jejuni infections: update on emerging issues and trends. Clin Infect Dis 32: 1201–1206.

    Not in our library10.1086/319760

  2. 2.
  3. 3.

    Cody AJ, McCarthy ND, Jansen van Rensburg M, Isinkaye T, Bentley SD, Parkhill J et al. (2013 ). Real-time genomic epidemiological evaluation of human Campylobacter isolates by use of whole-genome multilocus sequence typing. J Clin Microbiol 51: 2526–2534.

    Not in our library10.1128/jcm.00066-13

  4. 4.

    Didelot X, Bowden R, Wilson DJ, Peto TEA, Crook DW. (2012 ). Transforming clinical microbiology with bacterial genome sequencing. Nat Rev Genet 13: 601–612.

    Not in our library10.1038/nrg3226

  5. 5.

    Didelot X, Falush D. (2007 ). Inference of bacterial microevolution using multilocus sequence data. Genetics 175: 1251–1266.

    Not in our library10.1534/genetics.106.063305

  6. 6.
  7. 7.
  8. 8.

    Drummond AJ, Suchard MA, Xie D, Rambaut A. (2012 ). Bayesian phylogenetics with BEAUti and the BEAST 1.7. Mol Biol Evol 29: 1969–1973.

    Not in our library10.1093/molbev/mss075

  9. 9.

    Edgar RC. (2004 ). MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 32: 1792–1797.

    Not in our library10.1093/nar/gkh340

  10. 10.

    Engberg J, Gerner-Smidt P, Scheutz F, Møller Nielson E, On SLW, Mølbak K. (1998 ). Water-borne Campylobacter jejuni infection in a Danish town - a 6-week continuous source outbreak. Clin Microbiol Infect 4: 648–656.

    Not in our library10.1111/j.1469-0691.1998.tb00348.x

  11. 11.

    Eyre DW, Cule ML, Wilson DJ, Griffiths D, Vaughan A, O'Connor L et al. (2013 ). Diverse sources of C. difficile infection identified on whole-genome sequencing. N Engl J Med 369: 1195–1205.

    Not in our library10.1056/nejmoa1216064

  12. 12.

    Falush D, Kraft C, Taylor NS, Correa P, Fox JG, Achtman M et al. (2001 ). Recombination and mutation during long-term gastric colonization by Helicobacter pylori: estimates of clock rates, recombination size, and minimal age. Proc Natl Acad Sci USA 98: 15056–15061.

    Not in our library10.1073/pnas.251396098

  13. 13.

    Griekspoor P, Colles FM, McCarthy ND, Hansbro PM, Ashhurst-Smith C, Olsen B et al. (2013 ). Marked host specificity and lack of phylogeographic population structure of Campylobacter jejuni in wild birds. Mol Ecol 22: 1463–1472.

    Not in our library10.1111/mec.12144

  14. 14.

    Gripp E, Hlahla D, Didelot X, Kops F, Maurischat S, Tedin K et al. (2011 ). Closely related Campylobacter jejuni strains from different sources reveal a generalist rather than a specialist lifestyle. BMC Genomics 12: 584.

    Not in our library10.1186/1471-2164-12-584

  15. 15.

    Guindon S, Dufayard J-F, Lefort V, Anisimova M, Hordijk W, Gascuel O. (2010 ). New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol 59: 307–321.

    Not in our library10.1093/sysbio/syq010

  16. 16.
  17. 17.

    Harris N V, Weiss NS, Nolan CM. (1986 ). The role of poultry and meats in the etiology of Campylobacter jejuni/coli enteritis. Am J Public Health 76: 407–411.

    Not in our library10.2105/ajph.76.4.407

  18. 18.

    Harris SR, Feil EJ, Holden MTG, Quail MA, Nickerson EK, Chantratita N et al. (2010 ). Evolution of MRSA during hospital transmission and intercontinental spread. Science 327: 469–474.

    Not in our library10.1126/science.1182395

  19. 19.

    Hasegawa M, Kishino H, Yano T. (1985 ). Dating of the human-ape splitting by a molecular clock of mitochondrial DNA. J Mol Evol 22: 160–174.

    Not in our library10.1007/bf02101694

  20. 20.
  21. 21.
  22. 22.

    Lefébure T, Pavinski Bitar PD, Suzuki H, Stanhope MJ. (2010 ). Evolutionary dynamics of complete Campylobacter pan-genomes and the bacterial species concept. Genome Biol Evol 2: 646–655.

    Not in our library10.1093/gbe/evq048

  23. 23.
  24. 24.

    McCarthy ND, Colles FM, Dingle KE, Bagnall MC, Manning G, Maiden MCJ et al. (2007 ). Host-associated genetic import in Campylobacter jejuni. Emerg Infect Dis 13: 267–272.

    Not in our library10.3201/eid1302.060620

  25. 25.

    Minin VN, Suchard MA. (2008 a). Counting labeled transitions in continuous-time Markov models of evolution. J Math Biol 56: 391–412.

    Not in our library10.1007/s00285-007-0120-8

  26. 26.

    Minin VN, Suchard MA. (2008 b). Fast, accurate and simulation-free stochastic mapping. Phil Trans R Soc B 363: 3985–3995.

    Not in our library10.1098/rstb.2008.0176

  27. 27.

    Mullner P, Spencer SEF, Wilson DJ, Jones G, Noble AD, Midwinter AC et al. (2009 ). Assigning the source of human campylobacteriosis in New Zealand: a comparative genetic and epidemiological approach. Infect Genet Evol 9: 1311–1319.

    Not in our library10.1016/j.meegid.2009.09.003

  28. 28.

    Neimann J, Engberg J, Mølbak K, Wegener HC. (2003 ). A case-control study of risk factors for sporadic campylobacter infections in Denmark. Epidemiol Infect 130: 353–366.

    Not in our library10.1017/s0950268803008355

  29. 29.

    Palmer SR, Gully PR, White JM, Person AD, Suckling WG, Jones DM et al. (1983 ). Water-borne outbreak of Campylobacter gastroenteritis. Lancet 321: 287–290.

    Not in our library10.1016/s0140-6736(83)91698-7

  30. 30.

    Parkhill J, Wren BW, Mungall K, Ketley JM, Churcher C, Basham D et al. (2000 ). The genome sequence of the food-borne pathogen Campylobacter jejuni reveals hypervariable sequences. Nature 403: 665–668.

    Not in our library10.1038/35001088

  31. 31.

    Pebody RG, Ryan MJ, Wall PG. (1997 ). Outbreaks of campylobacter infection: rare events for a common pathogen. Commun Dis Rep Rev 7: R33–R37.

    Not in our library

  32. 32.

    Pérez-Losada M, Crandall KA, Zenilman J, Viscidi RP. (2007 ). Temporal trends in gonococcal population genetics in a high prevalence urban community. Infect Genet Evol 7: 271–278.

    Not in our library10.1016/j.meegid.2006.11.003

  33. 33.
  34. 34.

    Pupko T, Pe'er I, Shamir R, Graur D. (2000 ). A fast algorithm for joint reconstruction of ancestral amino acid sequences. Mol Biol Evol 17: 890–896.

    Not in our library10.1093/oxfordjournals.molbev.a026369

  35. 35.

    Sears A, Baker MG, Wilson N, Marshall J, Muellner P, Campbell DM et al. (2011 ). Marked Campylobacteriosis decline after interventions aimed at poultry, New Zealand. Emerg Infect Dis 17: 1007–1015.

    Not in our library10.3201/eid1706.101272

  36. 36.
  37. 37.

    Sheppard SK, Colles FM, McCarthy ND, Strachan NJC, Ogden ID, Forbes KJ et al. (2011 ). Niche segregation and genetic structure of Campylobacter jejuni populations from wild and agricultural host species. Mol Ecol 20: 3484–3490.

    Not in our library10.1111/j.1365-294x.2011.05179.x

  38. 38.

    Sheppard SK, Dallas JF, Strachan NJC, MacRae M, McCarthy ND, Wilson DJ et al. (2009 ). Campylobacter genotyping to determine the source of human infection. Clin Infect Dis 48: 1072–1078.

    Not in our library10.1086/597402

  39. 39.
  40. 40.

    Sheppard SK, Didelot X, Meric G, Torralbo A, Jolley KA, Kelly DJ et al. (2013 b). Genome-wide association study identifies vitamin B5 biosynthesis as a host specificity factor in Campylobacter. Proc Natl Acad Sci USA 110: 11923–11927.

    Not in our library10.1073/pnas.1305559110

All 47 references

Cited by papers we hold 3

Reads

Read by people on this page

None yet.

Checked or read by AI through naulon

None yet.

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.

Are you an author?

Is this your paper?

Claim it to add your note and be paid when agents cite it. Free.