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1.
Article | IMSEAR | ID: sea-187898

ABSTRACT

The aim of this study was to investigate the presence of BTV infection and possible vector species in different regions of Turkey. In the study, blood samples taken from 666 Akkaraman sheep were examined. 2000 Culicoides specimens were captured by light traps from the same provinces and 20 Culicoides spp. were identified. Blood sera samples were investigated by c-ELISA and SNT for detecting Abs to BTV. Sera samples were detected as positive 67 (10.06%) and 160 (24.02%) by SNT and ELISA, respectively. SN50 values of the 67 positive sera samples by SNT were detected between 1/2.38 and 1/200. All sheep blood samples and pools became Culicoides spp. samples were examined for BTV Ag presence by BTACE. Thirty six (5.40%) blood samples were detected as positive, but no from Culicoides pools. In the meantime, all sheep blood samples and Culicoides samples were directly investigated for BTV genome by one step RT-PCR. Fourteen (2.10%) blood samples and 7 (11.11%) Culicoides species were detected as positive. Also, the blood samples and the Culicoides samples were inoculated into Vero cell culture and passaged 5 times. Twenty nine (4.35%) blood samples cultured in Vero cell culture lines showed CPE but non CPE was observed in Culicoides samples. While 5 (17.24%) of 29 CPE positive isolates were identified as BTV by One Step RT-PCR. Total 26 samples (14 blood samples, 7 Culicoides samples and 5 supernatants) which detected BTV genome positive by One Step RT-PCR were serotyped. At the end of the study, while 23 of 26 samples were serotyped as BTV-9, two samples were serotyped as BTV-4. One sample (C. punctatus) from Culicoides was not serotyped as none of serotypes of BTV. In the present study, BTV was isolated for the first time from C. circumscriptus, C. kibunensis, and C. punctatus in Turkey.

2.
Indian Pediatr ; 2004 Jun; 41(6): 590-4
Article in English | IMSEAR | ID: sea-8531

ABSTRACT

We examined prospectively, stool specimens from 135 children, 0 to 3 years old, referred for fever, abdominal pain, vomiting and/or acute diarrhea. Rotavirus antigens were detected from fecal samples by latex agglutination (LA), ELISA and polyacrylamide gel electrophoresis (PAGE). Rotavirus antigen positivity by Latex, ELISA and PAGE were 15, 55%, 12.59% and 11.85%, respectively. With PAGE test as reference, the sensitivity and specificity of LA and ELISA tests was 93.75%, 94.96% and 100%, 99.16%, respectively, The positivity ratio between 13-24 months group was meaningful with all tests (P = 0.042 for LA; P = 0.05 for ELISA; P = 0.031 for PAGE). ELISA and LA use found to be as sensitive and specific as PAGE in the diagnosis of rotavirus diarrhea.


Subject(s)
Acute Disease , Child, Preschool , Electrophoresis, Polyacrylamide Gel , Enzyme-Linked Immunosorbent Assay , Female , Humans , Infant , Infant, Newborn , Latex Fixation Tests , Male , Predictive Value of Tests , Reproducibility of Results , Rotavirus Infections/diagnosis , Turkey
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