Romano Julia D, de Beaumont Catherine, Carrasco Jose A, Ehrenman Karen, Bavoil Patrik M, Coppens Isabelle
Department of Molecular Microbiology and Immunology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, 21205, USA.
Cell Microbiol. 2013 Apr;15(4):619-46. doi: 10.1111/cmi.12060. Epub 2012 Nov 27.
Toxoplasma and Chlamydia trachomatis are obligate intracellular pathogens that have evolved analogous strategies to replicate within mammalian cells. Both pathogens are known to extensively remodel the cytoskeleton, and to recruit endocytic and exocytic organelles to their respective vacuoles. However, how important these activities are for infectivity by either pathogen remains elusive. Here, we have developed a novel co-infection system to gain insights into the developmental cycles of Toxoplasma and C. trachomatis by infecting human cells with both pathogens, and examining their respective ability to replicate and scavenge nutrients. We hypothesize that the common strategies used by Toxoplasma and Chlamydia to achieve development results in direct competition of the two pathogens for the same pool of nutrients. We show that a single human cell can harbour Chlamydia and Toxoplasma. In co-infected cells, Toxoplasma is able to divert the content of host organelles, such as cholesterol. Consequently, the infectious cycle of Toxoplasma progresses unimpeded. In contrast, Chlamydia's ability to scavenge selected nutrients is diminished, and the bacterium shifts to a stress-induced persistent growth. Parasite killing engenders an ordered return to normal chlamydial development. We demonstrate that C. trachomatis enters a stress-induced persistence phenotype as a direct result from being barred from its normal nutrient supplies as addition of excess nutrients, e.g. amino acids, leads to substantial recovery of Chlamydia growth and infectivity. Co-infection of C. trachomatis with slow growing strains of Toxoplasma or a mutant impaired in nutrient acquisition does not restrict chlamydial development. Conversely, Toxoplasma growth is halted in cells infected with the highly virulent Chlamydia psittaci. This study illustrates the key role that cellular remodelling plays in the exploitation of host intracellular resources by Toxoplasma and Chlamydia. It further highlights the delicate balance between success and failure of infection by intracellular pathogens in a co-infection system at the cellular level.
弓形虫和沙眼衣原体是专性细胞内病原体,它们进化出了类似的策略在哺乳动物细胞内进行复制。已知这两种病原体都会广泛重塑细胞骨架,并将内吞和外排细胞器募集到各自的液泡中。然而,这些活动对这两种病原体的感染性有多重要仍不清楚。在这里,我们开发了一种新型共感染系统,通过用这两种病原体感染人类细胞,并检查它们各自的复制和获取营养的能力,来深入了解弓形虫和沙眼衣原体的发育周期。我们假设弓形虫和衣原体用于实现发育的共同策略导致这两种病原体对同一营养库的直接竞争。我们发现单个人类细胞可以同时容纳衣原体和弓形虫。在共感染的细胞中,弓形虫能够转移宿主细胞器的内容物,如胆固醇。因此,弓形虫的感染周期不受阻碍地进行。相比之下,衣原体获取特定营养的能力下降,细菌转变为应激诱导的持续生长。杀死寄生虫会使衣原体有序恢复正常发育。我们证明,沙眼衣原体进入应激诱导的持续表型是由于其正常营养供应被阻断的直接结果,因为添加过量营养物质,如氨基酸,会导致衣原体生长和感染性大幅恢复。沙眼衣原体与生长缓慢的弓形虫菌株或营养获取受损的突变体共感染不会限制衣原体的发育。相反,在感染高毒力鹦鹉热衣原体的细胞中,弓形虫的生长会停止。这项研究说明了细胞重塑在弓形虫和衣原体利用宿主细胞内资源方面所起的关键作用。它进一步突出了在细胞水平的共感染系统中,细胞内病原体感染成败之间的微妙平衡。