Brinig Mary M, Cummings Craig A, Sanden Gary N, Stefanelli Paola, Lawrence Andrew, Relman David A
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305, USA.
J Bacteriol. 2006 Apr;188(7):2375-82. doi: 10.1128/JB.188.7.2375-2382.2006.
Bordetella pertussis, an obligate human pathogen and the agent of whooping cough, is a clonal species, despite the dynamic selection pressures imposed by host immunity and vaccine usage. Because the generation of variation is critical for species evolution, we employed a variety of approaches to examine features of B. pertussis genetic variation. We found a high level of conservation of gene content among 137 B. pertussis strains with different geographical, temporal, and epidemiological associations, using comparative genomic hybridization. The limited number of regions of difference were frequently located adjacent to copies of the insertion element IS481, which is present in high numbers in the B. pertussis chromosome. This repeated sequence appears to provide targets for homologous recombination, resulting in deletion of intervening sequences. Using subtractive hybridization, we searched for previously undetected genes in diverse clinical isolates but did not detect any new genes, indicating that gene acquisition is rare in B. pertussis. In contrast, we found evidence of altered gene order in the several strains that were examined and again found an association of IS481 with sites of rearrangement. Finally, we compared whole-genome expression profiles of different strains and found significant changes in transcript abundance, even in the same strain after as few as 12 laboratory passages. This combination of approaches provides a detailed picture of a pathogenic species with little gene loss or gain but with the capacity to generate variation by rearranging its chromosome and altering gene expression. These findings have broad implications for host adaptation by microbial pathogens.
百日咳博德特氏菌是一种专性人类病原体,也是百日咳的病原体,尽管宿主免疫和疫苗使用带来了动态选择压力,但它仍是一个克隆物种。由于变异的产生对物种进化至关重要,我们采用了多种方法来研究百日咳博德特氏菌遗传变异的特征。通过比较基因组杂交,我们发现137株具有不同地理、时间和流行病学关联的百日咳博德特氏菌菌株之间基因含量高度保守。有限数量的差异区域经常位于插入元件IS481的拷贝附近,IS481在百日咳博德特氏菌染色体中大量存在。这种重复序列似乎为同源重组提供了靶点,导致中间序列缺失。利用消减杂交技术,我们在多种临床分离株中寻找以前未检测到的基因,但未检测到任何新基因,这表明百日咳博德特氏菌中基因获得的情况很少见。相比之下,我们在检测的几株菌株中发现了基因顺序改变的证据,并且再次发现IS481与重排位点有关联。最后,我们比较了不同菌株的全基因组表达谱,发现转录本丰度有显著变化,即使在同一菌株经过仅12次实验室传代后也是如此。这些方法的结合提供了一个致病物种的详细情况,该物种基因丢失或获得很少,但有能力通过重排其染色体和改变基因表达来产生变异。这些发现对微生物病原体的宿主适应性具有广泛影响。