Center of Collecting, Welcome and Handling of Wild Animals (CRATAS), University of Trá s-os-Montes and Alto Douro, Vila Real, PortugalA total of 36 Escherichia coli and 31 enterococci isolates were recovered from 42 common buzzard faecal samples. The E. coli isolates showed high levels of resistance to streptomycin and tetracycline. The following resistance genes were detected: bla TEM (20 of 22 ampicillin-resistant isolates), tet(A) and/or tet(B) (16 of 27 tetracycline-resistant isolates), aadA1 (eight of 27 streptomycin-resistant isolates), cmlA (three of 15 chloramphenicol-resistant isolates), aac(3)-II with/without aac(3)-IV (all seven gentamicin-resistant isolates) and sul1 and/or sul2 and/or sul3 [all eight sulfamethoxazole/trimethoprim-resistant (SXT) isolates]. intI1 and intI2 genes were detected in four SXT-resistant isolates. The virulence-associated genes fimA (type 1 fimbriae), papC (P fimbriae) and aer (aerobactin) were detected in 61.1, 13.8 and 11.1 % of the isolates, respectively. The isolates belonged to phylogroups A (47.2 %), B1 (8.3 %), B2 (13.9 %) and D (30.5 %). For the enterococci isolates, Enterococcus faecium was the most prevalent species (48.4 %). High levels of tetracycline and erythromycin resistance were found among our isolates (87 and 81 %, respectively). Most of the tetracycline-resistant strains carried the tet(M) and/or tet(L) genes. The erm(B) gene was detected in 80 % of erythromycin-resistant isolates. The vat(D) and/or vat(E) genes were found in nine of the 17 quinupristin-dalfopristin-resistant isolates. The enterococcal isolates showing high-level resistance for kanamycin, gentamicin and streptomycin contained the aph(39)-IIIa, aac(69)-aph(20) and ant(6)-Ia genes, respectively. This report reveals that common buzzards seem to represent an important reservoir, or at least a source, of multiresistant E. coli and enterococci isolates, and consequently may represent a considerable hazard to human and animal health by transmission of these isolates to waterways and other environmental sources via their faecal deposits.

We report an investigation of antibodies to Toxoplasma gondii in 52 wild birds and 20 wild mammals from northern and central areas of Portugal by using the modified agglutination test. The birds comprised 26 common buzzards (Buteo buteo), five tawny owls (Strix aluco), four white storks (Ceconia ceconia), three Eurasian eagle owls (Bubo bubo), three northern goshawks (Accipiter gentilis), two booted eagles (Hieraaetus pennatus), two common barn owls (Tyto alba), two Eurasian sparrowhawks (Accipiter nisus), two short-toed eagles (Circaetus gallicus), one black kite (Milvus migrans), one Griffin vulture (Gyps fulvus), and one peregrine falcon (Falco peregrinus). The mammals were eight wild boars (Sus scrofa), six red foxes (Vulpes vulpes), two common genets (Genetta genetta), two European badgers (Meles meles), one European roe deer (Capreolus capreolus), and one Iberian wolf (Canis lupus signatus). Fifty percent of the wild birds and 90% of the wild mammals were seropositive; the overall seroprevalence of infection was 61.1%. When comparing the prevalence of antibodies in birds and mammals from northern Portugal, a significant difference was found, but the same was not true for birds and mammals from central Portugal. Seroprevalence levels were 30.0% in juvenile and 62.5% in adult birds (p=0.046), 0.0% in juvenile and 94.7% in adult mammals (p=0.100), 80.0% in female and 66.7% in male birds (p=1.000), and 81.8% in female and 100% in male mammals (p=0.479). This is the first study performed on T. gondii in birds of prey, white storks, and wild carnivores in Portugal.

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