Monnerat M P, Thiaucourt F, Poveda J B, Nicolet J, Frey J
Institute for Veterinary Bacteriology, University of Berne, CH-3012 Berne, Switzerland.
Clin Diagn Lab Immunol. 1999 Mar;6(2):224-30. doi: 10.1128/CDLI.6.2.224-230.1999.
The genes encoding the 62-kDa lipoproteins from the Mycoplasma mycoides subsp. mycoides large-colony type (LC) strain Y-goat and the M. mycoides subsp. capri strain PG3 were cloned and analyzed by sequencing. These two lipoproteins have been named LppA[MmymyLC] and LppA[Mmyca], and their corresponding genes have been named lppA[MmymyLC] and lppA[Mmyca], respectively. The nucleotide and deduced amino acid sequences of these two lipoproteins showed a very high degree of similarity between these two mycoplasmas. Given the sequence data, LppA seems to fulfill the same structural functions as the previously described major lipoproteins P72 of M. mycoides subsp. mycoides small-colony type and P67 of the Mycoplasma species bovine group 7. Based on lppA gene sequences of M. mycoides subsp. mycoides LC and M. mycoides subsp. capri type strains, a specific PCR assay was developed so that it amplified this gene in all field strains of the two species analyzed in this study but not in the other members of the M. mycoides cluster. Analysis of the PCR-amplified lppA genes with frequently cutting restriction enzymes showed a certain degree of genetic variability which, however, did not cluster the two subspecies. This PCR therefore allows a rapid identification of M. mycoides subsp. mycoides LC and M. mycoides subsp. capri but does not distinguish between these two closely related subspecies. LppA was expressed in Escherichia coli K-12 and used for the production of polyclonal mouse antiserum. Antibodies against recombinant LppA[MmymyLC] reacted with a 62-kDa protein in all M. mycoides subsp. mycoides LC and M. mycoides subsp. capri type strains and field strains tested but not with the other members of the M. mycoides cluster, thus showing the antigenic specificity of LppA and further supporting the concept that a close relationship exists between these two mycoplasmas.
对来自丝状支原体丝状亚种大菌落型(LC)Y - 山羊株和丝状支原体山羊亚种PG3株的编码62 kDa脂蛋白的基因进行了克隆,并通过测序进行分析。这两种脂蛋白分别命名为LppA[MmymyLC]和LppA[Mmyca],其相应基因分别命名为lppA[MmymyLC]和lppA[Mmyca]。这两种脂蛋白的核苷酸和推导的氨基酸序列在这两种支原体之间显示出非常高的相似性。根据序列数据,LppA似乎履行与先前描述的丝状支原体丝状亚种小菌落型的主要脂蛋白P72和支原体牛群7的P67相同的结构功能。基于丝状支原体丝状亚种LC和丝状支原体山羊亚种典型菌株的lppA基因序列,开发了一种特异性PCR检测方法,该方法能在本研究分析的两个物种的所有田间菌株中扩增该基因,但在丝状支原体群的其他成员中不扩增。用常用的限制性内切酶对PCR扩增的lppA基因进行分析,显示出一定程度的遗传变异性,然而,这并没有将两个亚种聚类。因此,这种PCR方法可以快速鉴定丝状支原体丝状亚种LC和丝状支原体山羊亚种,但不能区分这两个密切相关的亚种。LppA在大肠杆菌K - 12中表达,并用于制备多克隆小鼠抗血清。针对重组LppA[MmymyLC]的抗体与所有测试的丝状支原体丝状亚种LC和丝状支原体山羊亚种典型菌株及田间菌株中的一种62 kDa蛋白发生反应,但与丝状支原体群的其他成员不发生反应,从而显示出LppA的抗原特异性,并进一步支持了这两种支原体之间存在密切关系的概念。