Ohashi Norio, Zhi Ning, Lin Quan, Rikihisa Yasuko
Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, Ohio 43210-1093, USA.
Infect Immun. 2002 Apr;70(4):2128-38. doi: 10.1128/IAI.70.4.2128-2138.2002.
Anaplasma (Ehrlichia) phagocytophila and Ehrlichia chaffeensis, the etiologic agents of granulocytic and monocytic ehrlichioses, respectively, are obligatory intracellular bacteria that cause febrile systemic illness in humans. We identified and characterized clusters of genes for a type IV secretion machinery in these two bacteria, and analyzed their gene expression in cell culture and mammalian hosts. Eight virB and virD genes were found in each bacterial genome, and all of the genes were transcribed in cell culture. Although the gene order and orientation were similar to those found in other bacteria, the eight virB and virD genes were clustered at two separate loci in each genome. Five of the genes (virB8, virB9, virB10, virB11, and virD4) were located downstream from a ribA gene. These five genes in both A. phagocytophila and E. chaffeensis were polycistronically transcribed and controlled through at least two tandem promoters located upstream of the virB8 gene in human leukemia cell lines. The virB9 gene of A. phagocytophila was transcriptionally active in peripheral blood leukocytes from human ehrlichiosis patients and experimentally infected animals. Three of the remaining genes (virB3, virB4, and virB6) of both A. phagocytophila and E. chaffeensis were arranged downstream from a sodB gene and cotranscribed with the sodB gene through one or more sodB promoters in human leukocytes. This suggests that transcription of the three virB genes in these two Anaplasma and Ehrlichia spp. is regulated by factors that influence the sodB gene expression. This unique regulation of gene expression for the type IV secretion system may be associated with intracellular survival and replication of Anaplasma and Ehrlichia spp. in granulocytes or monocytes.
嗜吞噬细胞无形体(埃立克体)和查菲埃立克体分别是粒细胞性埃立克体病和单核细胞性埃立克体病的病原体,它们是 obligatory intracellular bacteria,可导致人类发热性全身性疾病。我们鉴定并表征了这两种细菌中IV型分泌机制的基因簇,并分析了它们在细胞培养和哺乳动物宿主中的基因表达。在每个细菌基因组中发现了8个virB和virD基因,所有这些基因在细胞培养中均被转录。尽管基因顺序和方向与其他细菌中的相似,但这8个virB和virD基因在每个基因组中的两个独立位点上成簇。其中5个基因(virB8、virB9、virB10、virB11和virD4)位于ribA基因的下游。嗜吞噬细胞无形体和查菲埃立克体中的这5个基因通过位于人类白血病细胞系中virB8基因上游的至少两个串联启动子进行多顺反子转录和调控。嗜吞噬细胞无形体的virB9基因在人类埃立克体病患者和实验感染动物的外周血白细胞中具有转录活性。嗜吞噬细胞无形体和查菲埃立克体中其余3个基因(virB3、virB4和virB6)位于sodB基因的下游,并通过人类白细胞中的一个或多个sodB启动子与sodB基因共转录。这表明这两种无形体和埃立克体属中3个virB基因的转录受影响sodB基因表达的因素调控。IV型分泌系统这种独特的基因表达调控可能与无形体和埃立克体属在粒细胞或单核细胞中的细胞内存活和复制有关。