Differential tick burdens may explain differential Borrelia afzelii and Borrelia garinii infection rates among four, wild, rodent species in Hokkaido, Japan.

The ecologies of Lyme disease Borrelia spp. are very specific to location, as they are dependent upon the spirochete species and genotypes, the vectors and the host vertebrates present. In Hokkaido, Japan, where two human pathogenic, Lyme disease Borrelia spp. are present, and human cases are reported annually, the ecologies have been poorly studied. Our goal was to determine whether variation in borrelial infection rates among rodent species sharing an environment, is due to immunological or ecological differences. To this end, we examined the relationships between tick burden and borrelial infection, by including examination of agreement between nested PCR, as a test for infection, and serology, as a test for exposure. We collected 868 rodents, comprised of four species commonly found in Hokkaido, and tested for infection rates with Borrelia spp. using PCR for the borrelial flaB gene, seroprevalence of Borrelia afzelii and Borrelia garinii using ELISA, and attachment of ticks by direct counts. We noted a correlation between differential nymph and larval burdens and the borrelial infection rates found among the four rodent species. Furthermore, there was significant correlation between infection and seroprevalence of B. afzelii and B. garinii (P<0.01), between infection and Ixodes persulcatus nymph burden (P<0.01), and between seroprevalence and I. persulcatus nymph burden (P<0.01). The close agreement among rodent species seroprevalences with infection rates and tick burdens suggest the differences in infection rates of Borrelia spp. may largely be a direct consequence of differential exposure to vectors.

[1]  A. Takano,et al.  Borrelia miyamotoi infections among wild rodents show age and month independence and correlation with Ixodes persulcatus larval attachment in Hokkaido, Japan. , 2013, Vector borne and zoonotic diseases.

[2]  L. Råberg Infection intensity and infectivity of the tick‐borne pathogen Borrelia afzelii , 2012, Journal of evolutionary biology.

[3]  B. Allan,et al.  The Ecology of Fear: Host Foraging Behavior Varies with the Spatio-temporal Abundance of a Dominant Ectoparasite , 2012, EcoHealth.

[4]  Z. Hubálek,et al.  Absence of Lyme disease spirochetes in larval Ixodes ricinus ticks. , 2012, Vector borne and zoonotic diseases.

[5]  M. Marsot,et al.  Introduced Siberian Chipmunks (Tamias sibiricus barberi) Harbor More-Diverse Borrelia burgdorferi Sensu Lato Genospecies than Native Bank Voles (Myodes glareolus) , 2011, Applied and Environmental Microbiology.

[6]  Haruo Watanabe,et al.  Multilocus Sequence Typing Implicates Rodents as the Main Reservoir Host of Human-Pathogenic Borrelia garinii in Japan , 2011, Journal of Clinical Microbiology.

[7]  D. Hulínská,et al.  Molecular and serological evidence of Borrelia burgdorferi sensu lato in wild rodents in the Czech Republic. , 2008, Vector borne and zoonotic diseases.

[8]  R. Ostfeld,et al.  Multiple causes of variable tick burdens on small-mammal hosts. , 2008, Ecology.

[9]  M. Bhide,et al.  Anti-Borrelia antibodies in rodents: important hosts in ecology of Lyme disease. , 2004, Annals of agricultural and environmental medicine : AAEM.

[10]  R. Ostfeld,et al.  Infestation of Peromyscus leucopus and Tamias striatus by Ixodes scapularis (Acari: Ixodidae) in relation to the abundance of hosts and parasites. , 1999, Journal of medical entomology.

[11]  D. Rogers,et al.  Incidence from coincidence: patterns of tick infestations on rodents facilitate transmission of tick-borne encephalitis virus , 1999, Parasitology.

[12]  P. Humair,et al.  Transmission of Borrelia afzelii from Apodemus mice and Clethrionomys voles to Ixodes ricinus ticks: differential transmission pattern and overwintering maintenance , 1999, Parasitology.

[13]  S. Randolph,et al.  Serum Complement Sensitivity as a Key Factor in Lyme Disease Ecology , 1998, Infection and Immunity.

[14]  Y. Yanagihara,et al.  Lyme disease (Lyme borreliosis). , 1997, FEMS immunology and medical microbiology.

[15]  K. Kurtenbach,et al.  Clethrionomys glareolus, but not Apodemus flavicollis, acquires resistance to lxodes ricinus L, the main European vector of Borrelia burgdorferi , 1995, Parasite immunology.

[16]  U. Schaible,et al.  Differential immune responses to Borrelia burgdorferi in European wild rodent species influence spirochete transmission to Ixodes ricinus L. (Acari: Ixodidae) , 1994, Infection and immunity.

[17]  中尾 稔 Reservoir competence of the wood mouse, Apodemus speciosus ainu, for the Lyme disease spirochete, Borrelia burgdorferi, in Hokkaido, Japan , 1994 .

[18]  R. C. Johnson,et al.  Experimental Borrelia burgdorferi infection of outbred mice , 1992, Journal of clinical microbiology.

[19]  A. Spielman,et al.  Comparing the relative potential of rodents as reservoirs of the Lyme disease spirochete (Borrelia burgdorferi). , 1989, American journal of epidemiology.