New Culicoides Vector Species for BTV Transmission in Central and Central West of Anatolia

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.

Study on mRNA expression of TNFRSF12 in peripheral blood leukocytes of SLE patients / 中国免疫学杂志

Objective:To explore whether the mRNA expression of TNFRSF12 in peripheral blood leukocytes of SLE patients is abnormal and to determine whether the TNFRSF12 gene is susceptibility gene to SLE.Methods:The level of mRNA expression of TNFRSF12 in peripheral blood leukocytes was detected by TaqMan one-step RT-PCR method.Results:The mRNA expression pattern in SLE patients is different to that of normal control.The mRNA in SLE consists of 2 types of isoforms of TNFRSF12,encoding membrane bound glycoprotein and potentially secreted molecules respectively,whereas only the latter in normal control.After PHA treatment,the mRNA expression pattern in normal control becomes the same as that of SLE patients.Overall TNFRSF12 mRNA expression was significantly decreased in active SLE group and significantly increased in lupus nephritis group.Conclusion:The results indicated that TNFRSF12 may play a role in the pathogenesis of SLE and was susceptibility gene to SLE.

RESEARCH ON THE TESTING OF PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME VIRUS BY NESTRT-PCR / 微生物学通报

Three primer were designed based on the consevered area of the genetic of the ATCC VR-2332 strain and LV strain. And the nest RT-PCR of testing porcine reproductive and respiratory syndrome virus were developed. The nest RT-PCR against ATCC VR-2332 strain, LV strain and B13 strain were done by this method.The DNA fragment were obtained specially from the three strains isolated from different region. The size were 430bp (430bp) , 410bp (413bp) and 410 bp (413bp) separately. But the DNA fragment were not obtained from HCV, PPV and PRV. Its sensitivity was 10-2 TCID50. It's sensitivity increased 10000 times than one step RT-PCR. It should make the method of testing porcine reproductive and respiratory syndrome virus more sensitive, fast and accurate.