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During the period 2000-2003, patients hospitalized for suspected tick-borne encephalitis in the Czech Republic were screened for possible A. phagocytophilum co-infection. Blood samples taken at admission were tested for the presence of A. phagocytophilum DNA by nested PCR using a modified target sequence as an internal control, and sera were tested for the presence of antibodies by indirect immunofluorescence and western blotting methods using cell-culture-derived antigens. To verify the assay specificity, a set of 45 sera of Patagonian residents served as a non-tick-exposed control group, and a set of 14 B. henselae-positive sera was used to check cross-reactivity. Of 809 patients hospitalized, 80 (9.9

作者:Petr, Zeman;Petr, Pazdiora;Vaclav, Chmelik;Jiri, Januska;Karel, Sedivy;Alberto A, Guglielmone;Jorge A, Iriarte;Zuzana, Medkova

来源:Wiener klinische Wochenschrift 2007 年 119卷 17-18期

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作者:
Petr, Zeman;Petr, Pazdiora;Vaclav, Chmelik;Jiri, Januska;Karel, Sedivy;Alberto A, Guglielmone;Jorge A, Iriarte;Zuzana, Medkova
来源:
Wiener klinische Wochenschrift 2007 年 119卷 17-18期
During the period 2000-2003, patients hospitalized for suspected tick-borne encephalitis in the Czech Republic were screened for possible A. phagocytophilum co-infection. Blood samples taken at admission were tested for the presence of A. phagocytophilum DNA by nested PCR using a modified target sequence as an internal control, and sera were tested for the presence of antibodies by indirect immunofluorescence and western blotting methods using cell-culture-derived antigens. To verify the assay specificity, a set of 45 sera of Patagonian residents served as a non-tick-exposed control group, and a set of 14 B. henselae-positive sera was used to check cross-reactivity. Of 809 patients hospitalized, 80 (9.9