A Varied Thrush struck a window at Saanich, Vancouver Island, British Columbia, and was brought to BC SPCA Wild ARC, an animal rehabilitation centre for wildlife, located near Metchosin, B.C. Upon presentation, the thrush was thoroughly examined, and placed in a screened, outdoor enclosure which provided natural enrichment. After 18 d, the thrush was euthanized due to a fractured jaw and, at this time, an attached tick was found under the beak. Using super-fine, stainless steel forceps, wildlife rehabilitators removed the tick. The engorged tick was then put in a round-bottom, 8.5 mL polypropylene tube (15.7 mm ´ 75 mm) (Sarstedt, Montreal, Quebec) with a label specifying background information (host, geographic location, date collected, collector’s name). A 7-mm hole in the polyethylene push cap (15.7 mm) provided ventilation for the tick and, to prevent the tick from escaping, fine tulle netting was stretched over the mouth of the vial before the push cap was inserted. The vial, which contained the tick, was placed in a self-sealing, double-zipper, plastic bag with a slightly moistened paper towel. The live tick was sent directly to the laboratory (JDS), and identified using a taxonomic key [19] . Since the partially engorged tick had only been attached to the bird for 3 days, the tick was acquired onsite.

After identification, the tick was put in a 2 mL micro tube (Sarstedt, Montreal, Quebec) containing 94% ethyl alcohol, and sent by courier to the PCR amplification laboratory (JEF). DNA was extracted from the tick using an ammonium hydroxide technique as described previously [26] . Screening of the I. auritulus nymph for Borrelia species was performed using real-time PCR (TaqMan) as described previously [27] . We modified the protocol to use only the forward and reverse primers and the probe identified in that paper specific for B. burgdorferi s.s. (in silico analysis and/or unpublished data indicate that both primers are generic for borreliae; the probe has 100% homology to almost all B. burgdorferi s.l. genospecies). The reaction was run in a combined thermocycler/fluorometer (ABI Prism 7700, Applied Biosystems, Foster City, California). A water negative control was included in each run and, likewise, DNA from cultured strains of B. burgdorferi s.s. and B. bissettii were employed as positive controls. The sample was considered positive if it had a cycle threshold (CT) <40, and a characteristic amplification curve. A strongly PCR-positive sample with a CT <35 was evaluated using conventional PCR for the flagellin gene as described [28] , with modification to use GoTaq^â Green Master Mix (Promega, Madison, Wisconsin). Following PCR and agarose gel electrophoresis, DNA was purified from gels using a kit (QiaQuick, Qiagen, Valencia, California), and submitted for sequencing on a ABI 3730 sequencer (UC Davis Sequencing, Davis, California) using the forward PCR primer; DNA from this tick (15-5A94) underwent bidirectional sequencing (forward and reverse). Electropherograms were corrected by visual examination and end-read errors trimmed. The sequenced amplicon was evaluated by BLAST search of GenBank (NCBI; http://blast.ncbi.nlm.nih.govBlast.cgi). Alignment of various sequences from the database with the I. auritulus-derived sequence, and construction of a maximum likelihood phylogenetic tree, were completed using the program CLC Workbench (Aahus, Denmark).

In order to confirm the identity of the B. burgdorferi s.l. from Vancouver Island, we obtained and sequenced borrelial amplicons from the I. auritulus nymph (15-5A94). DNA sequences for B. americana Can94 were deposited in GenBank database, and the respective accession number is KX022979.

Migratory songbirds play a significant role in the wide dispersal of bird-feeding ticks in North America. Currently, we know that B. americana is present in southeastern United States and California, and now British

Columbia. Our study reveals that B. americana is now connected with I. auritulus, a tick species that is exclusively on birds. Since B. americana is associated with birds, it is likely that it has extensive distribution in North America and, to our knowledge, has not been detected by standard borrelial screening. When birds migrate, they have great capacity to fly hundreds of kilometres, and widely disperse bird-feeding ticks, including I. auritulus. Because the Pacific flyway and the Atlantic flyway converge in Central and South America, there is ample opportunity for a replete tick to drop off a passerine migrant at an overwintering tropical stopover, and moult to the next life stage, and then parasitize another migratory songbird that is connected with another flyway. In essence, B. americana-infected ticks, which are linked with one flyway, can switch to migratory songbirds associated with another flyway. Such transfers provide a way for ticks from southbound fall migrants from the East Coast to switch to northbound spring migrants destine for the West Coast, and vice versa.

On the other hand, domestic travel could have been the mode of transport of B. americana-infected ticks from coast to coast. For example, a dog, which was infested with B. americana-infected I. pacificus ticks, could have transported this borrelial genospecies from California to the East Coast during long-distance, vehicular or airplane travel. Upon arrival, these replete ticks dropped off the dog in a tick-conducive habitat, and moulted to the next life stage, and subsequently bite a suitable host, including humans. On the contrary, a dog infested with B. americana-infected I. scapularis could have transported engorged ticks from the southeastern United States to California via travel by automobile or airplane. Such epidemiological events provide alternate mechanisms for the transcontinental dispersal of B. americana.

We provide the northernmost record of B. americana in North America. Prior to our study, the closest known location for B. americana was California. The B. americana strain, Can94, is 99% homologous to B. americana type strain SCW-41, and is well within the genetic proximity of this genospecies. In addition, Can94, only has 97% homology with B. burgdorferi s.s. strain B31 and, therefore, does not belong to the commonly occurring B. burgdorferi s.s. genospecies. Epidemiologically, the uncovering of the Borrelia variant, Can94, in an I. auritulus tick on Vancouver Island, B.C.’s a novel occurrence of B. americana in Canada.

In the present study, travel does not have any direct relationship with the B. americana-infected I. auritulus nymph because the Varied Thrush had been in a rehabilitation enclosure for 18 d before the nymph was collected. Any birds, which were previously in the rehabilitation compound, could have dropped fully engorged ticks and, these replete ticks would moult and, later, parasitize subsequent avian hosts. In late October, the day length is too short and the degree-days are insufficient for ticks to moult. Since the Varied Thrush was parasitized in the enclosure, the questing I. auritulus nymph must have entered the screen wall from the surrounding environs. This unique situation suggests that B. americana is cycling enzootically in the vicinity.

Scott et al. [21] found that 31% of the I. auritulus (larvae, nymphs, adults) collected along Vancouver Island’s South Coast were infected with B. burgdorferi s.l. Since borrelial genospecies characterization was not conducted in this particular study [21] , we do not know if any of the I. auritulus ticks were infected with B. americana. With respect to the distribution of I. auritulus along B.C.’s coast, tick researchers reported I. auritulus locally on the southern fringe of Vancouver Island and, also, unveiled the presence of this tick species at more northerly locations (i.e., Haida Gwaii) [21] [22] [24] [33] . Ecologically, whenever birds are heavily infested with ticks, they can start new Lyme disease foci [34] [35] . Based on earlier tick studies, established populations of I. auritulus are certainly present along southern Vancouver Island. In our particular case, knowing the travel history of the Varied Thrush, and whether it was a resident or a migrant, is not helpful in determining the source of B. americana. Perhaps, a bird, which was previously in rehabilitation, could have dropped a replete I. auritulus larva, and this tick crawled outside the enclosure to the surrounding vegetation, and moulted, and re-entered the enclosure as an unfed nymph. Since the B. americana-infected I. auritulus was acquired at the rehabilitation centre, there is substantial evidence to suggest that B. americana is established locally in this bioregion.

The presence of B. americana on both sides of North America is intriguing. In southeastern United States, B. americana has been isolated from I. minor immatures collected from ground-frequenting songbirds [7] and, in California, from I. pacificus adults [25] . Since Ixodes affinis Neumann, I. minor, and I. scapularis infest rodents and birds in southeastern United States, there is every likelihood that north-bound passerine migrants are transporting B. americana-infected ticks to central and eastern Canada. Similarly, I. auritulus, I. pacificus, and I. spinipalpis feed on birds in far-western North America, and widely disperse these Ixodes species. Because I. pacificus and I. spinipalpis feed both on birds and rodents, there is ample opportunity for B. americana to be maintained in Lyme disease foci in the Pacific Northwest by rodents and, ultimately, be dispersed by resident and long-distance avifauna.

In far-western North America, I. spinipalpis serves as a maintenance vector of B. burgdorferi s.l., and I. pacificus acts as a bridge vector to humans [7] . Likewise, in southeastern U.S.A., I. affinis and I. minor act as maintenance vectors in the enzootic cycle of B. burgdorferi s.l, and I. scapularis serves as a bridge vector to humans [36] . It is noteworthy that B. americana has been obtained from Ixodes ticks that have birds as hosts, and many of these avian hosts have long-range dispersal capabilities. Based on current epidemiological information, people residing on both the West Coast and East Coast can be exposed to B. americana.

During spring migration, several Ixodes ticks that originated from southern latitudes have been reported in Canada: an I. minor larva was collected from a Common Yellowthroat, Geothlypis trichas (Linnaeus) [37] , I. affinis immatures have be collected from both Common Yellowthroat and Swainson’s Thrushes, Catharus ustulatus (Nuttall) [22] [38] , and many I. scapularis immatures have been collected from migratory songbirds during spring migration [22] [24] [33] [39] - [41] . Since all of these tick species are songbird-transported ticks, they can be imported into Canada annually during northward spring migration. Since B. americana is associated with each of these bird-feeding ticks, we anticipate that this borrelial genospecies has wider distribution in Western Hemisphere than previously thought.

Songbirds are known to harbour B. burgdorferi s.l. in their bodies and, subsequently, transmit Lyme disease spirochetes to feeding ticks [42] . Based on a host competency study involving spirochete-free I. scapularis larvae, Richter et al. [43] revealed that the American Robin, Turdus migratorius Linnaeus, is a competent reservoir of B. burgdorferi s.l. As well, Hamer et al. [44] , found that the Swainson’s Thrush, which is another member of the thrush family, is a reservoir-competent host. With respect to the I. scapularis, there is no transovarial transmission of B. burgdorferi s.l. from eggs to larvae, and any fed larvae that are infected with B. burgdorferi s.l. after a blood meal must have acquired spirochetes from the host [45] . Analogous to the present study, B. americana spirochetes could either have come directly from the host bird (Varied Thrush), or indirectly from the I. auritulus larva that had fed on a B. americana-infected bird. Previous studies with I. auritulus reveal that there is transstadial transmission of spirochetes from larvae to nymphs and, similarly, from nymphs to adults [21] [22] ; however, there is no evidence to suggest transovarial transmission of B. burgdorferi s.l. from eggs to larvae.

Anderson et al. [42] cultured B. burgdorferi s.l. from the liver of a Veery, Catharus fuscescens (Stephens), and, likewise, isolated Lyme disease spirochetes from the blood of the American Robin and Common Yellowthroat and, additionally, from attached larvae [34] . As well, Durden et al. [46] detected B. burgdorferi s.l. in skin biopsies from songbirds which suggests that certain birds are competent reservoir hosts. Further studies along Canada’s West Coast have reported B. burgdorferi s.l. infected I. auritulus larvae from birds (Passeriformes, Accipitriformes) which suggests that several species of avifauna can be spirochetemic, and act as competent reservoirs [20] [24] [37] . In far-western Canada, there is substantive evidence that birds are the spirochetal reservoir of B. americana.

When a B. americana-infected I. auritulus tick parasitizes a bird, it can start a chain of events that leads to human infection. The spirochetemic bird now becomes a reservoir of B. americana for other bird-feeding ticks. If an I. pacificus larva bites this infected bird, it can acquire B. americana, and moult to a nymph in 5 - 8 weeks. Then the B. americana-infected I. pacificus nymph can transmit spirochetal infection to dogs, cats, and humans. When people become infected, they will normally exhibit symptoms associated with Lyme disease. Because these patients are infected with B. americana, they will likely be seronegative, and may not be able to obtain therapeutic treatment.

The presence of B. americana in Lyme disease vector ticks has important medical significance. Using PCR amplification, Clark et al. [12] detected B. americana in the blood and skin tissue of patients residing in Florida. Although these patients were seronegative and culture-negative (BSK II culture medium), the PCR results were positive for B. americana using the flagellin gene. The patients displayed a wide array of clinical symptoms, including fatigue, headache, vertigo, chills, and rashes (single and multiple). Interestingly, these symptomatic patients were treated with standard courses of antibiotics, and symptoms improved for a while, but then returned after treatment was halted. These febrile, clinical manifestations indicate that B. americana can evade the immune system, and sequester in deep-seated tissue, and develop into persistent Lyme disease. Even though patients are infected with B. americana, they can be seronegative and, regrettably, may be misdiagnosed, and not be able to get proper treatment. Many Lyme disease infections are undiagnosed and neglected, particularly if they do not have the characteristic skin rash or do not remember a tick bite. Furthermore, inconsistent or negative serological results might be connected to the use of B. burgdorferi s.s. as the antigen during serological testing. Moreover, a co-infection of B. burgdorferi s.l. strains or associated tick-borne pathogens will normally induce a diverse spectrum of clinical manifestations [31] [47] . Currently, patients will have to obtain PCR testing and DNA sequencing to obtain definitive proof of B. americana infection. Because B. americana is pathogenic to humans, medical practitioners must be aware that patients can have Lyme disease without having a typical rash, or exhibiting positive serology, or traveling to an endemic area. Our findings suggest that B. americana in ticks in British Columbia is one of the reasons why some patients are seronegative using standard 2-tiered Lyme disease serology.

In conclusion, we demonstrate the presence of B. americana in I. auritulus in Canada for the first time. This discovery highlights the northernmost documentation of B. americana in North America, and the first record of this B. burgdorferi s.l. genospecies in Canada. The flagellin amplicon in the present study is genetically consistent with other B. americana isolates collected previously in California and southeastern United States. The presence of B. americana along coastal B.C. provides further evidence that there is considerable genetic heterogeneity among B. burgdorferi s.l. in far-western Canada. Because migratory songbirds widely disperse Lyme disease vector ticks, dogs, cats, and people can be bitten by B. americana-infected ticks throughout much of the Western Hemisphere. Since B. americana is pathogenic to humans, health-care providers should be aware that B. americana infection will cause Lyme disease in patients.