Huang Jinling, Mullapudi Nandita, Lancto Cheryl A, Scott Marla, Abrahamsen Mitchell S, Kissinger Jessica C
Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA 30602, USA.
Genome Biol. 2004;5(11):R88. doi: 10.1186/gb-2004-5-11-r88. Epub 2004 Oct 19.
The apicomplexan parasite Cryptosporidium parvum is an emerging pathogen capable of causing illness in humans and other animals and death in immunocompromised individuals. No effective treatment is available and the genome sequence has recently been completed. This parasite differs from other apicomplexans in its lack of a plastid organelle, the apicoplast. Gene transfer, either intracellular from an endosymbiont/donor organelle or horizontal from another organism, can provide evidence of a previous endosymbiotic relationship and/or alter the genetic repertoire of the host organism. Given the importance of gene transfers in eukaryotic evolution and the potential implications for chemotherapy, it is important to identify the complement of transferred genes in Cryptosporidium.
We have identified 31 genes of likely plastid/endosymbiont (n = 7) or prokaryotic (n = 24) origin using a phylogenomic approach. The findings support the hypothesis that Cryptosporidium evolved from a plastid-containing lineage and subsequently lost its apicoplast during evolution. Expression analyses of candidate genes of algal and eubacterial origin show that these genes are expressed and developmentally regulated during the life cycle of C. parvum.
Cryptosporidium is the recipient of a large number of transferred genes, many of which are not shared by other apicomplexan parasites. Genes transferred from distant phylogenetic sources, such as eubacteria, may be potential targets for therapeutic drugs owing to their phylogenetic distance or the lack of homologs in the host. The successful integration and expression of the transferred genes in this genome has changed the genetic and metabolic repertoire of the parasite.
顶复门寄生虫微小隐孢子虫是一种新出现的病原体,可导致人类和其他动物患病,并可导致免疫功能低下个体死亡。目前尚无有效的治疗方法,其基因组序列最近已完成。这种寄生虫与其他顶复门生物的不同之处在于它缺乏质体细胞器——顶质体。基因转移,无论是从内共生体/供体细胞器进行的细胞内转移,还是从另一种生物体进行的水平转移,都可以提供先前内共生关系的证据和/或改变宿主生物体的基因库。鉴于基因转移在真核生物进化中的重要性以及对化疗的潜在影响,确定隐孢子虫中转移基因的组成非常重要。
我们使用系统发育基因组学方法鉴定了31个可能起源于质体/内共生体(n = 7)或原核生物(n = 24)的基因。这些发现支持了这样一种假设,即隐孢子虫从一个含有质体的谱系进化而来,随后在进化过程中失去了其顶质体。对藻类和真细菌起源的候选基因的表达分析表明,这些基因在微小隐孢子虫的生命周期中表达并受到发育调控。
隐孢子虫是大量转移基因的受体,其中许多基因是其他顶复门寄生虫所没有的。从远缘系统发育来源转移而来的基因,如真细菌,由于其系统发育距离或宿主中缺乏同源物,可能是治疗药物的潜在靶点。这些转移基因在该基因组中的成功整合和表达改变了寄生虫的遗传和代谢库。