Shaw E I, Dooley C A, Fischer E R, Scidmore M A, Fields K A, Hackstadt T
Host-Parasite Interactions Section, Laboratory of Intracellular Parasites, Hamilton, MT 59840, USA.
Mol Microbiol. 2000 Aug;37(4):913-25. doi: 10.1046/j.1365-2958.2000.02057.x.
The obligate intracellular bacterium Chlamydia trachomatis has a unique developmental cycle that involves functionally and morphologically distinct cell types adapted for extracellular survival and intracellular multiplication. Infection is initiated by an environmentally resistant cell type called an elementary body (EB). Over the first several hours of infection, EBs differentiate into a larger replicative form, termed the reticulate body (RB). Late in the infectious process, RBs asynchronously begin to differentiate back to EBs, which accumulate within the lumen of the inclusion until released from the host cell for subsequent rounds of infection. In an effort to characterize temporal gene expression in relation to the chlamydial developmental cycle, we have used quantitative-competitive polymerase chain reaction (QC-PCR) and reverse transcription (RT)-PCR techniques. These analyses demonstrate that C. trachomatis double their DNA content every 2-3 h, with synthesis beginning between 2 and 4 h after infection. We determined the onset of transcription of specific temporal classes of developmentally expressed genes. RT-PCR analysis was performed on several genes encoding key enzymes or components of essential biochemical pathways and functions. This comparison encompassed approximately 8% of open reading frames on the C. trachomatis genome. In analysis of total RNA samples harvested at 2, 6, 12 and 20 h after infection, using conditions under which a single chlamydial transcript per infected cell is detected, three major temporal classes of gene expression were resolved. Initiation of transcription appears to occur in three temporal classes which we have operationally defined as: early, which are detected by 2 h after infection during the germination of EBs to RBs; mid-cycle, which appear between 6 and 12 h after infection and represent transcripts expressed during the growth and multiplication of RBs; or late, which appear between 12 and 20 h after infection and represent those genes transcribed during the terminal differentiation of RBs to EBs. Collectively, the data suggest that chlamydial early gene functions are weighted toward initiation of macromolecular synthesis and the establishment of their intracellular niche by modification of the inclusion membrane. Surprisingly, representative enzymes of intermediary metabolism and structural proteins do not appear to be transcribed until 10-12 h after infection; coinciding with the onset of observed binary fission of RBs. Late gene functions appear to be predominately those associated with the terminal differentiation of RBs back to EBs.
专性细胞内细菌沙眼衣原体具有独特的发育周期,涉及功能和形态上不同的细胞类型,这些细胞类型适合细胞外生存和细胞内繁殖。感染由一种称为原体(EB)的具有环境抗性的细胞类型引发。在感染的最初几个小时内,原体分化为一种更大的复制形式,称为网状体(RB)。在感染过程后期,网状体开始异步分化回原体,原体在包涵体腔内积累,直至从宿主细胞释放,以进行后续轮次的感染。为了表征与衣原体发育周期相关的时间基因表达,我们使用了定量竞争聚合酶链反应(QC-PCR)和逆转录(RT)-PCR技术。这些分析表明,沙眼衣原体每2至3小时使其DNA含量加倍,合成在感染后2至4小时之间开始。我们确定了发育表达基因的特定时间类别的转录起始时间。对编码关键酶或基本生化途径及功能的几个基因进行了RT-PCR分析。这种比较涵盖了沙眼衣原体基因组上约8%的开放阅读框。在分析感染后2、6、12和20小时收获的总RNA样本时,在每个感染细胞检测到单个衣原体转录本的条件下,解析出了三个主要的基因表达时间类别。转录起始似乎发生在三个时间类别中,我们将其操作性地定义为:早期,在原体萌发为网状体的感染后2小时内检测到;中期,出现在感染后6至12小时之间,代表网状体生长和繁殖期间表达的转录本;或晚期,出现在感染后12至20小时之间,代表在网状体向原体的终末分化期间转录的那些基因。总体而言,数据表明衣原体早期基因功能倾向于通过修饰包涵体膜来启动大分子合成并建立其细胞内生态位。令人惊讶的是,中间代谢的代表性酶和结构蛋白似乎直到感染后10至12小时才转录;这与观察到的网状体二分裂开始时间一致。晚期基因功能似乎主要是那些与网状体分化回原体相关的功能。