Spatial spread and demographic expansion of Lyme borreliosis spirochaetes in Eurasia

Infection, Genetics and Evolution

Volumn 14, Issue 1, 2013, Pages 147-155

  Vollmer, Stephanie A ^a   Feil, Edward J ^a   Chu, Chen Yi ^b   Raper, Stephen L ^a   Cao, Wu Chun ^b   Kurtenbach, Klaus ^a   Margos, Gabriele ^c  

^a University of Bath   (United Kingdom)

^b BEIJING INSTITUTE OF MICROBIOLOGY AND EPIDEMIOLOGY   (China)

^c UNIVERSITY OF MUNICH   (Germany)

Author keywords

Borrelia afzelii; Borrelia garinii; Host; Population expansion

Indexed keywords

ARTICLE; ASIA; BACTERIAL TRANSMISSION; BIRD; BORRELIA; BORRELIA AFZELII; BORRELIA GARINII; BORRELIA VALAISIANA; CLPA GENE; CLPX GENE; EUROPE; GENETIC DISTANCE; GEOGRAPHIC DISTRIBUTION; HOST RANGE; HOUSEKEEPING GENE; LAST GLACIAL MAXIMUM; LYME DISEASE; MULTILOCUS SEQUENCE TYPING; NIFS GENE; NONHUMAN; PATHOGENESIS; PEPX GENE; PHYLOGENY; POPULATION ABUNDANCE; POPULATION GROWTH; PRIORITY JOURNAL; PYRG GENE; RECG GENE; RODENT; RP1B GENE; SEQUENCE ALIGNMENT; SPECIES DIFFERENCE; SPECIES DISTRIBUTION; SPIROCHETE; UVRA GENE;

ANIMALS; ASIA; BORRELIA; EUROPE; EVOLUTION, MOLECULAR; GENES, ESSENTIAL; HUMANS; LYME DISEASE; MULTILOCUS SEQUENCE TYPING; PHYLOGENY;

AVES; BORRELIA; BORRELIA AFZELII; BORRELIA GARINII; BORRELIA VALAISIANA; RODENTIA; SPIROCHAETES;

EID: 84872392245     PISSN: 15671348     EISSN: 15677257     Source Type: Journal    
DOI: 10.1016/j.meegid.2012.11.014     Document Type: Article

References (42)

1. Booth W., Montgomery W.I., Prodohl P.A. Spatial genetic structuring in a vagile species, the European wood mouse (Apodemus sylvaticus). J. Zool. 2009, 279:219-228.
2. Canica M.M., Nato F., du Merle L., Mazie J.C., Baranton G., Postic D. Monoclonal antibodies for identification of Borrelia afzelii sp. nov., associated with late cutaneous manifestations of Lyme borreliosis. Scand. J. Infect. Dis. 1993, 25:441-448.
3. Chu C.Y., Liu W., Jiang B.G., Wang D.M., Jiang W.J., Zhao Q.M., Zhang P.H., Wang Z.X., Tang G.P., Yang H., Cao W.C. Novel genospecies of Borrelia burgdorferi sensu lato from rodents and ticks in Southwestern China. J. Clin. Microbiol. 2008, 46:3130-3133.
4. Cockerham C.C., Weir B.S. Covariances of relatives stemming from a population undergoing mixed self and random mating. Biometrics 1984, 40:157-164.
5. Comstedt P., Asokliene L., Eliasson I., Olsen B., Wallensten A., Bunikis J., Bergstrom S. Complex population structure of Lyme borreliosis group spirochete Borrelia garinii in subarctic Eurasia. PLoS One 2009, 4:e5841.
6. Edgar R.C. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 2004, 32:1792-1797.
7. Etti S., Hails R., Schafer S.M., De Michelis S., Sewell H.S., Bormane A., Donaghy M., Kurtenbach K. Habitat-specific diversity of Borrelia burgdorferi sensu lato in Europe, exemplified by data from Latvia. Appl. Environ. Microbiol. 2003, 69:3008-3010.
8. Excoffier L., Laval G., Schneider S. Arlequin (version 3.0): an integrated software package for population genetics data analysis. Evol. Bioinf. Online 2005, 1:47-50.
9. Excoffier L., Smouse P.E., Quattro J.M. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 1992, 131:479-491.
10. Falco R.C., Fish D. Horizontal movement of adult Ixodes dammini (Acari: Ixodidae) attracted to CO2-baited traps. J. Med. Entomol. 1991, 28:726-729.
11. Fumagalli L., Hausser J., Taberlet P., Gielly L., Stewart D.T. Phylogenetic structures of the Holarctic Sorex araneus group and its relationships with S. samniticus, as inferred from netDNA sequences. Hereditas 1996, 125:191-199.
12. Gomez-Diaz E., Boulinier T., Sertour N., Cornet M., Ferquel E., McCoy K.D. Genetic structure of marine Borrelia garinii and population admixture with the terrestrial cycle of Lyme borreliosis. Environ. Microbiol. 2011, 13:2453-2467.
13. Guindon S., Gascuel O. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst. Biol. 2003, 52:696-704.
14. Harr B., Musolf K., Gerlach G. Characterization and isolation of DNA microsatellite primers in wood mice (Apodemus sylvaticus, Rodentia). Mol. Ecol. 2000, 9:1664-1665.
15. Heckel G., Burri R., Fink S., Desmet J.F., Excoffier L. Genetic structure and colonization processes in European populations of the common vole, Microtus arvalis. Evolution 2005, 59:2231-2242.
16. Hewitt G.M. Post-glacial re-colonization of European biota. Biol. J. Linn. Soc. 1999, 68:87-112.
17. Hoen A.G., Margos G., Bent S.J., Diuk-Wasser M.A., Barbour A., Kurtenbach K., Fish D. Phylogeography of Borrelia burgdorferi in the eastern United States reflects multiple independent Lyme disease emergence events. Proc. Nat. Acad. Sci. USA 2009, 106:15013-15018.
18. IUCN, 2010. IUCN red list of threatened species, in: IUCN (Ed.). International Union for Conservation of Nature and Natural Resources, Cambridge.
19. Kumar S., Tamura K., Nei M. MEGA3: integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief Bioinf. 2004, 5:150-163.
20. Kurtenbach K., De Michelis S., Sewell H.S., Etti S., Schafer S.M., Hails R., Collares-Pereira M., Santos-Reis M., Hanincova K., Labuda M., Bormane A., Donaghy M. Distinct combinations of Borrelia burgdorferi sensu lato genospecies found in individual questing ticks from Europe. Appl. Environ. Microbiol. 2001, 67:4926-4929.
21. Kurtenbach K., Hanincova K., Tsao J.I., Margos G., Fish D., Ogden N.H. Fundamental processes in the evolutionary ecology of Lyme borreliosis. Nat. Rev. Microbiol. 2006, 4:660-669.
22. Librado P., Rozas J. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics 2009, 25:1451-1452.
23. Margos G., Gatewood A.G., Aanensen D.M., Hanincova K., Terekhova D., Vollmer S.A., Cornet M., Piesman J., Donaghy M., Bormane A., Hurn M.A., Feil E.J., Fish D., Casjens S., Wormser G.P., Schwartz I., Kurtenbach K. MLST of housekeeping genes captures geographic population structure and suggests a European origin of Borrelia burgdorferi. Proc. Nat. Acad. Sci. USA 2008, 105:8730-8735.
24. Margos G., Hojgaard A., Lane R.S., Cornet M., Fingerle V., Rudenko N., Ogden N., Aanensen D.M., Fish D., Piesman J. Multilocus sequence analysis of Borrelia bissettii strains from North America reveals a new Borrelia species, Borrelia kurtenbachii. Ticks Tick Borne Dis. 2010, 1:151-158.
25. Margos G., Vollmer S.A., Cornet M., Garnier M., Fingerle V., Wilske B., Bormane A., Vitorino L., Collares-Pereira M., Drancourt M., Kurtenbach K. A new Borrelia species defined by multilocus sequence analysis of housekeeping genes. Appl. Environ. Microbiol. 2009, 75:5410-5416.
26. Masuzawa T. Terrestrial distribution of the Lyme borreliosis agent Borrelia burgdorferi sensu lato in East Asia. Jpn. J. Infect. Dis. 2004, 57:229-235.
27. Ornstein K., Berglund J., Nilsson I., Norrby R., Bergstrom S. Characterization of Lyme borreliosis isolates from patients with erythema migrans and neuroborreliosis in Southern Sweden. J. Clin. Microbiol. 2001, 39:1294-1298.
28. Piesman J., Gern L. Lyme borreliosis in Europe and North America. Parasitology 2004, 129(Suppl):S191-S220.
29. Purse B.V., Mellor P.S., Rogers D.J., Samuel A.R., Mertens P.P., Baylis M. Climate change and the recent emergence of bluetongue in Europe. Nat. Rev. Microbiol. 2005, 3:171-181.
30. Rijpkema S.G., Tazelaar D.J., Molkenboer M.J., Noordhoek G.T., Plantinga G., Schouls L.M., Schellekens J.F. Detection of Borrelia afzelii, Borrelia burgdorferi sensu stricto, Borrelia garinii and group VS116 by PCR in skin biopsies of patients with erythema migrans and acrodermatitis chronica atrophicans. Clin. Microbiol. Infect. 1997, 3:109-116.
31. Rogers A.R., Harpending H. Population growth makes waves in the distribution of pairwise genetic differences. Mol. Biol. Evol. 1992, 9:552-569.
32. Rudenko N., Golovchenko M., Grubhoffer L., Oliver J.H. Borrelia carolinensis sp. nov., a new (14th) member of the Borrelia burgdorferi sensu lato complex from the southeastern region of the United States. J. Clin. Microbiol. 2009, 47:134-141.
33. Rudenko N., Golovchenko M., Lin T., Gao L., Grubhoffer L., Oliver J.H. Delineation of a new species of the Borrelia burgdorferi sensu lato complex, Borrelia americana sp. nov. J. Clin. Microbiol. 2009, 47:3875-3880.
34. Ruzic-Sabljic E., Lotric-Furlan S., Maraspin V., Cimperman J., Pleterski-Rigler D., Strle F. Analysis of Borrelia burgdorferi sensu lato isolated from cerebrospinal fluid. APMIS 2001, 109:707-713.
35. Taberlet P., Bouvet J. Mitochondrial DNA polymorphism, phylogeography, and conservation genetics of the brown bear Ursus arctos in Europe. Proc. Biol. Sci. 1994, 255:195-200.
36. Taberlet P., Fumagalli L., Hausser J. Chromosomal versus mitochondria1 DNA evolution: tracking thc cvolutiotrary history of the southwestern European populations of the Sow arunm group (Mammalia, Insectivora). Evolution 1994, 48:623-636.
37. Takano A., Nakao M., Masuzawa T., Takada N., Yano Y., Ishiguro F., Fujita H., Ito T., Ma X., Oikawa Y., Kawamori F., Kumagai K., Mikami T., Hanaoka N., Ando S., Honda N., Taylor K., Tsubota T., Konnai S., Watanabe H., Ohnishi M., Kawabata H. Multilocus sequence typing implicates rodents as the main reservoir host of human-pathogenic Borrelia garinii in Japan. J. Clin. Microbiol. 2011, 49:2035-2039.
38. Tao, N., Richardson, R., Bruno, W., Kuiken, C. 2009. FindModel. HIV Sequence Database, Los Alamos.
39. Trizio I., Crestanello B., Galbusera P., Wauters L.A., Tosi G., Matthysen E., Hauffe H.C. Geographical distance and physical barriers shape the genetic structure of Eurasian red squirrels (Sciurus vulgaris) in the Italian Alps. Mol. Ecol. 2005, 14:469-481.
40. Urwin R., Maiden M.C. Multi-locus sequence typing: a tool for global epidemiology. Trends Microbiol. 2003, 11:479-487.
41. Vollmer S.A., Bormane A., Dinnis R.E., Seelig F., Dobson A.D., Aanensen D.M., James M.C., Donaghy M., Randolph S.E., Feil E.J., Kurtenbach K., Margos G. Host migration impacts on the phylogeography of Lyme borreliosis spirochaete species in Europe. Environ. Microbiol. 2011, 13:184-192.
42. Wang G., van Dam A.P., Schwartz I., Dankert J. Molecular typing of Borrelia burgdorferi sensu lato: taxonomic, epidemiological, and clinical implications. Clin. Microbiol. Rev. 1999, 12:633-653.