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通过将一株野毒株与标准菌株PG2进行比较,验证抑制性消减杂交方法在无乳支原体中的有效性。

Validation of the suppressive subtractive hybridization method in Mycoplasma agalactiae species by the comparison of a field strain with the type strain PG2.

作者信息

Marenda Marc S, Vilei Edy M, Poumarat François, Frey Joachim, Berthelot Xavier

机构信息

UMR INRA-ENVT 1225, Ecole Nationale Vétérinaire de Toulouse, 23 chemin des Capelles, 31076 Toulouse, France.

出版信息

Vet Res. 2004 Mar-Apr;35(2):199-212. doi: 10.1051/vetres:2004006.

DOI:10.1051/vetres:2004006
PMID:15099496
Abstract

The subtractive suppressive hybridization (SSH), a method that allows the identification of sequences that are present in one genome (tester) but not in the other (driver), is a promising technique for the comparison of Mycoplasma agalactiae pathogenic strains. The optimal conditions for SSH were established by subtracting the M. agalactiae type strain PG2 DNA from the M. agalactiae strain 5632 DNA. Because these two strains possess different vpma gene repertoires, 5632-specific vpma sequences (and possibly other 5632-specific sequences) were predicted to be retrieved by SSH. The subtracted tester DNA was PCR-amplified and cloned into the pGEM-T easy E. coli vector. Two independent libraries were generated and used to prepare individual probes that were tested by Southern blot with genomic DNA from various field isolates and mycoplasma reference strains. Sequence analysis of two overlapping clones showed that they potentially code for a large carboxyterminal portion of a new vpma ORF. Several DNA fragments homologous to insertion sequences were also found in 5632 and related strains. These preliminary data suggest that SSH is a powerful method to investigate differences between mycoplasma strains, and may be applied to molecular epidemiology, diagnostic, and host specificity or pathogenicity determinant discovery.

摘要

消减抑制杂交(SSH)是一种能够鉴定存在于一个基因组(测试组)而不存在于另一个基因组(驱动组)中的序列的方法,是比较无乳支原体致病菌株的一种有前景的技术。通过从无乳支原体菌株5632 DNA中减去无乳支原体模式菌株PG2 DNA,确定了SSH的最佳条件。由于这两个菌株具有不同的vpma基因库,预计通过SSH可检索到5632特异性vpma序列(以及可能的其他5632特异性序列)。对消减后的测试组DNA进行PCR扩增,并克隆到pGEM-T easy大肠杆菌载体中。生成了两个独立的文库,并用于制备单个探针,通过Southern印迹法用来自各种田间分离株和支原体参考菌株的基因组DNA进行检测。对两个重叠克隆的序列分析表明,它们可能编码一个新的vpma开放阅读框的大部分羧基末端。在5632及相关菌株中还发现了几个与插入序列同源的DNA片段。这些初步数据表明,SSH是研究支原体菌株间差异的一种强大方法,可应用于分子流行病学、诊断以及宿主特异性或致病决定因素的发现。

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