Middendorf B, Gross R
Lehrstuhl für Mikrobiologie, Theodor-Boveri-Institut Biozentrum der Universität Würzburg, Germany.
Mol Gen Genet. 1999 Aug;262(1):189-98. doi: 10.1007/s004380051074.
Bordetella pertussis and B. bronchiseptica are genetically very closely related but differ significantly in their virulence properties. Using Representational Difference Analysis (RDA), 11 DNA fragments specific for B. pertussis Tohama I or B. bronchiseptica BB7865 were identified. All B. bronchiseptica BB7865-derived fragments also hybridized with chromosomal DNA from B. parapertussis but not from the B. pertussis strains Tohama I and W28, underlining the close phylogenetic relationship between B. bronchiseptica and B. parapertussis. The B. pertussis type strain BP18323 is a special case, as it contains DNA sequences characteristic for both B. pertussis and B. bronchiseptica. As demonstrated by pulsed-field gel electrophoresis, several of the BB7865-derived fragments are present on a single 30-kb XbaI fragment. Based on the sequences of putative coding regions, four of these fragments may code for proteins involved in carbohydrate metabolism or transport. In agreement with this notion, a mutant for one of these loci synthesizes a significantly altered lipopolysaccharide that lacks the O-specific side chains. The analysis of the corresponding genomic region in various Bordetella species showed that this locus is present in B. bronchiseptica and B. parapertussis but not in B. pertussis. This confirms that the RDA approach has identified a novel strain-specific LPS biosynthesis locus which accounts for the differences between the LPS structures elaborated by different Bordetella species.
百日咳博德特氏菌和支气管败血博德特氏菌在基因上密切相关,但毒力特性差异显著。利用代表性差异分析(RDA),鉴定出了11个百日咳博德特氏菌Tohama I或支气管败血博德特氏菌BB7865特有的DNA片段。所有源自支气管败血博德特氏菌BB7865的片段也能与副百日咳博德特氏菌的染色体DNA杂交,但不能与百日咳博德特氏菌菌株Tohama I和W28的染色体DNA杂交,这突出了支气管败血博德特氏菌和副百日咳博德特氏菌之间密切的系统发育关系。百日咳博德特氏菌模式菌株BP18323是一个特殊情况,因为它同时含有百日咳博德特氏菌和支气管败血博德特氏菌的特征性DNA序列。脉冲场凝胶电泳显示,几个源自BB7865的片段存在于一个单一的30 kb XbaI片段上。根据推定编码区的序列,其中四个片段可能编码参与碳水化合物代谢或转运的蛋白质。与此观点一致,其中一个基因座的突变体合成了一种显著改变的脂多糖,该脂多糖缺乏O特异性侧链。对不同博德特氏菌属物种中相应基因组区域的分析表明,该基因座存在于支气管败血博德特氏菌和副百日咳博德特氏菌中,但不存在于百日咳博德特氏菌中。这证实了RDA方法鉴定出了一个新的菌株特异性LPS生物合成基因座,该基因座解释了不同博德特氏菌属物种所产生的LPS结构之间的差异。