European magpies (Pica pica) from southern France were tested for antibodies to West Nile virus (WNV) and viral shedding in feces during spring-autumn 2005. Results suggest that this peridomestic species may be a suitable sentinel species and a relevant target for additional investigations on WNV ecology in Europe. (WNV, Flaviviridae, Flavivirus) is an arbovirus that principally infects a wide range of bird species, but spillover infections may occur in mammals, including horses and humans. In southern France, WNV was fi rst reported during the 1960s in the Camargue, a wetland area with many types of birds. This virus was recently detected in the same area. It was responsible for 76 equine cases in 2000 and 32 equine cases in 2004. On the basis of ornithologic and epidemiologic data, several bird species were suggested as candidates for WNV amplifi cation and emergence in the Camargue (1). Among these species, corvids may be of particular interest because several species of the family Corvidae have experimentally been shown to be highly competent for WNV transmission (2,3).
W est Nile virusWe studied the European magpie or common magpie (Pica pica) because this species is territorial and abundant in both wet and dry areas. Pilot serologic investigations conducted in the 2000 and 2004 Camargue outbreaks in horses suggested a high WNV seroprevalence in magpies (4,5). Furthermore, WNV was isolated in 2004 from a yearling magpie near a farm with clinical equine cases (5). The aim of our study was to better assess WNV seroprevalence in magpies in the Camargue area and detect WNV circulation during the postepizootic year of 2005.
The StudyThe study was conducted from late spring to early autumn 2005. Multicatch magpie traps, i.e., circular traps that catch <4 birds simultaneously, were set 1 day per week from July to September in different places within 3 areas Flying birds were classifi ed as juveniles or adults by using plumage criteria (6). All magpies were ringed, sampled (blood and cloacal swab), and released. Serum samples were fi rst screened for immunoglobulin (Ig)G to WNV by using an indirect ELISA with horseradish peroxidase-conjugated anti-wild bird IgG (A140-110P; Bethyl Laboratories, Montgomery, TX, USA). Positive and doubtful samples were further tested by microneutralization by using the France 05.21/00 equine WNV strain (GenBank accession no. AY268132) and staining with crystal violet (5). Because the recapture rate of wild birds is usually low and WNV is excreted in feces of infected birds over a short period (2), we also tested for WNV RNA in feces of all 29 seropositive birds (i.e., 35 samples because some birds were captured several times) and 4 seronegative birds. Nucleic acid was extracted from cloacal swabs by using the QIAamp viral RNA mini kit (QIAGEN S.A., Courtaboeuf, France) and amplifi ed with WNV-specifi c primers (7).Of 271 magpies captured, 29 had WNV neutralizing antibodies at a titer >20, which confi rmed a relatively high WNV seroprevalence (10.7%, 95% binomial confi dence interval ...