Pheasants, Phasianus colchicus L., constitute a major part of the ground-feeding avifauna of England and Wales and are important hosts to immature stages of Ixodes ricinus L., the principal tick vector of Lyme borreliosis spirochetes in Europe. Therefore, their competence as hosts for Borrelia burgdorferi Johnson, Schmid, Steigerwalt & Brenner sensu lato was investigated. One group of pheasants was inoculated by needle with 1 x 10(6) cultured B. burgdorferi s.s. organisms, and a 2nd group of birds was infested with I. ricinus nymphs collected from a focus of Lyme borreliosis in southern England. Both bird groups were subjected to xenodiagnoses using uninfected I. ricinus nymphs. All recovered engorged ticks, as well as pheasant skin biopsies, were analyzed by a nested polymerase chain reaction targeting the 5S-23S rRNA genes of B. burgdorferi s.l. Both groups proved to be infective for ticks. The birds that were infected by tick bites proved to be significantly more infective for ticks (23% of the xenodiagnostic ticks positive) than those infected by needle (5%). The results show that pheasants can be infected experimentally with B. burgdorferi s.l., that they can pass the spirochetes to ticks and that their infectivity for ticks may persist as long as 3 mo. We conclude that pheasants are reservoir competent for Lyme borreliosis spirochetes and potentially play an important role in the maintenance of B. burgdorferi s.l. in England and Wales.

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SUMMARYViruses isolated from ticks (Ixodes uriae) and a kittiwake (Rissa tridactyla) from a seabird colony at St. Abb's Head, Scotland, were shown by complement fixation tests (CFT) to be antigenically related to the Uukuniemi and Kemerovo serogroups. Electron microscopic examination of cell cultures infected with the Kemerovo group viruses revealed particles characteristic of orbiviruses, 72 _+ 3 nm in diam., with an inner core 37 _+ 3 nm in diam., in association with intracytoplasmic, densely staining granular areas, and with fibrillar and tubular structures. Cell cultures infected with the Uukuniemi group viruses revealed characteristic bunyavirus particles, 94 +_ 7 nm in diam., with a closely adherent envelope. Both orbi-and bunyaviruses were isolated from two tick pools and the kittiwake. A third tick pool contained an orbivirus which cross-reacted with the other isolates in CFT and fluorescent antibody tests, but was distinguished from them by neutralization tests.

Viruses were isolated from 2 tick species collected from the nesting areas of seabirds on Great Saltee Island, Eire. Bunyaviruses of the Uukuniemi serogroup were isolated from hard ticks (Ixodes uriae and I. rothschildi), bunyaviruses of the Hughes serogroup from soft ticks (Ornithodoros maritimus), and orbiviruses of the Kemerovo serogroup from I. uriae and O. maritimus. The results indicate that the bunyaviruses, but not the orbiviruses, show "tick specificity". Neutralising activity against members of all 3 serogroups was detected in sera from chicks in the nesting areas; neutralising antibodies were probably maternal.