首页> 外文会议>Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009 >Detection of Haplosporidium nelsoni in Oysters from China Coast
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Detection of Haplosporidium nelsoni in Oysters from China Coast

机译:中国海岸牡蛎牡蛎单核孢菌的检测

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Oysters of nineteen cities from China coast were investigated in our study. The localization of Haplosporidium nelsoni-like (MSX) Plasmodia was detected by light microscopy. In Situ hybridization of infected tissue section was conducted with the H.nelsoni-specific DNA probe MSX1347. DNA was extracted from the oysters Crassostrea gigas, Crassostrea plicatula, Crassostrea rivularis, Ostrea crenulifera for PCR amplification. MSX-A', MSX-B and Hap-F2, Hap-R2 were applied to amplify the MSX. PCR amplification of genomic DNA with primer pairs MSX-A'+B and HAP-F2+R2 yielded the expected products for 573 bp, 239 bp, respectively. These PCR products were sequenced and the similarities from C. gigas was 99% in the 16S-like rRNA region of H.nelsoni. Subsequently, MSX was identified in Crassostrea Plicatula. However, MSX was not detected in oysters, C. rivularis, O. crenulifera. Our study demonstrates H. nelsoni in oysters presents between 24 and 40 at north latitude in China. These results approved that H. nelsoni occured in China and the distribution of MSX could be relative to host and latitude.
机译:在我们的研究中,对中国沿海19个城市的牡蛎进行了调查。通过光学显微镜检测了单孢子虫(Haplosporidium)/奈氏球菌样(MSX)疟原虫的定位。用 nelsoni 特异性DNA探针MSX1347进行感染组织切片的 In 原位杂交。从牡蛎 Crassostrea gigas Crassostrea 复制子 Crassostrea rivularis Ostrea crenulifera 进行PCR扩增。应用MSX-A',MSX-B和Hap-F 2 ,Hap-R 2 来扩增MSX。用引物对MSX-A'+ B和HAP-F 2 + R 2 对基因组DNA进行PCR扩增,分别得到预期的产物,分别为573 bp和239 bp。对这些PCR产物进行测序,并且在H.nelsoni 的16S样rRNA区域中与C.gigas 的相似性为99%。随后,在 Crassostrea Plicatula 中鉴定出MSX。但是,在牡蛎 C。 河豚 O。 crenulifera 中未检测到MSX。我们的研究表明,在中国北纬24至40之间的牡蛎中,牡蛎中的 H。 nelsoni 。这些结果证明了 H。 nelsoni 在中国发生,MSX的分布可能与寄主和纬度有关。

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