Dunning Hotopp Julie C, Lin Mingqun, Madupu Ramana, Crabtree Jonathan, Angiuoli Samuel V, Eisen Jonathan A, Seshadri Rekha, Ren Qinghu, Wu Martin, Utterback Teresa R, Smith Shannon, Lewis Matthew, Khouri Hoda, Zhang Chunbin, Niu Hua, Lin Quan, Ohashi Norio, Zhi Ning, Nelson William, Brinkac Lauren M, Dodson Robert J, Rosovitz M J, Sundaram Jaideep, Daugherty Sean C, Davidsen Tanja, Durkin Anthony S, Gwinn Michelle, Haft Daniel H, Selengut Jeremy D, Sullivan Steven A, Zafar Nikhat, Zhou Liwei, Benahmed Faiza, Forberger Heather, Halpin Rebecca, Mulligan Stephanie, Robinson Jeffrey, White Owen, Rikihisa Yasuko, Tettelin Hervé
The Institute for Genomic Research, Rockville, Maryland, USA.
PLoS Genet. 2006 Feb;2(2):e21. doi: 10.1371/journal.pgen.0020021. Epub 2006 Feb 17.
Anaplasma (formerly Ehrlichia) phagocytophilum, Ehrlichia chaffeensis, and Neorickettsia (formerly Ehrlichia) sennetsu are intracellular vector-borne pathogens that cause human ehrlichiosis, an emerging infectious disease. We present the complete genome sequences of these organisms along with comparisons to other organisms in the Rickettsiales order. Ehrlichia spp. and Anaplasma spp. display a unique large expansion of immunodominant outer membrane proteins facilitating antigenic variation. All Rickettsiales have a diminished ability to synthesize amino acids compared to their closest free-living relatives. Unlike members of the Rickettsiaceae family, these pathogenic Anaplasmataceae are capable of making all major vitamins, cofactors, and nucleotides, which could confer a beneficial role in the invertebrate vector or the vertebrate host. Further analysis identified proteins potentially involved in vacuole confinement of the Anaplasmataceae, a life cycle involving a hematophagous vector, vertebrate pathogenesis, human pathogenesis, and lack of transovarial transmission. These discoveries provide significant insights into the biology of these obligate intracellular pathogens.
嗜吞噬细胞无形体(以前称为埃立克体)、查菲埃立克体和嗜人类新立克次体(以前称为埃立克体)是细胞内媒介传播的病原体,可引起人类埃立克体病,这是一种新出现的传染病。我们展示了这些生物体的完整基因组序列,并与立克次氏体目中的其他生物体进行了比较。埃立克体属和无形体属表现出免疫显性外膜蛋白的独特大量扩增,促进了抗原变异。与最接近的自由生活亲属相比,所有立克次氏体合成氨基酸的能力都有所下降。与立克次体科的成员不同,这些致病性无形体科能够合成所有主要维生素、辅因子和核苷酸,这可能在无脊椎动物媒介或脊椎动物宿主中发挥有益作用。进一步分析确定了可能参与无形体科液泡限制的蛋白质,这是一个涉及吸血媒介、脊椎动物发病机制、人类发病机制且缺乏经卵传播的生命周期。这些发现为这些专性细胞内病原体的生物学特性提供了重要见解。