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The genome of Cryptosporidium hominis
Ping Xu1, Giovanni Widmer, Yingping Wang
1Center for the Study of Biological Complexity, Virginia Commonwealth University, Richmond, Virginia 23284-2030, USA.
Abstract:
Cryptosporidium species cause acute gastroenteritis and diarrhoea worldwide. They are members of the Apicomplexa--protozoan pathogens that invade host cells by using a specialized apical complex and are usually transmitted by an invertebrate vector or intermediate host. In contrast to other Apicomplexans, Cryptosporidium is transmitted by ingestion of oocysts and completes its life cycle in a single host. No therapy is available, and control focuses on eliminating oocysts in water supplies. Two species, C. hominis and C. parvum, which differ in host range, genotype and pathogenicity, are most relevant to humans. C. hominis is restricted to humans, whereas C. parvum also infects other mammals. Here we describe the eight-chromosome approximately 9.2-million-base genome of C. hominis. The complement of C. hominis protein-coding genes shows a striking concordance with the requirements imposed by the environmental niches the parasite inhabits. Energy metabolism is largely from glycolysis. Both aerobic and anaerobic metabolisms are available, the former requiring an alternative electron transport system in a simplified mitochondrion. Biosynthesis capabilities are limited, explaining an extensive array of transporters. Evidence of an apicoplast is absent, but genes associated with apical complex organelles are present. C. hominis and C. parvum exhibit very similar gene complements, and phenotypic differences between these parasites must be due to subtle sequence divergence.
Insights
The genome of Cryptosporidium hominis, a cause of gastroenteritis, reveals limited biosynthesis and adaptable energy metabolism. Phenotypic differences between C. hominis and C. parvum likely stem from subtle genetic variations.
Area of Science:
- Parasitology
- Genomics
- Infectious Diseases
Background:
- Cryptosporidium species are Apicomplexa protozoan pathogens causing global gastroenteritis.
- Unlike other Apicomplexans, Cryptosporidium is transmitted via oocysts and has a single-host life cycle.
- Two species, C. hominis and C. parvum, are significant human pathogens with distinct host ranges.
Purpose of the Study:
- To sequence and analyze the genome of Cryptosporidium hominis.
- To understand the genetic basis of C. hominis's parasitic lifestyle and host interactions.
- To compare the genetic makeup of C. hominis with C. parvum.
Main Methods:
- Whole-genome sequencing of the eight-chromosome C. hominis genome (approximately 9.2 million bases).
- Bioinformatic analysis of protein-coding genes to infer metabolic capabilities and organelle presence.
- Comparative genomics to assess gene complement similarity with C. parvum.
Main Results:
- The C. hominis genome exhibits gene content aligned with its parasitic niches, including limited biosynthesis capabilities and extensive transporters.
- Energy metabolism relies heavily on glycolysis, with both aerobic and anaerobic pathways present.
- Absence of apicoplast genes, but presence of genes for apical complex organelles.
- Gene complements of C. hominis and C. parvum are highly similar.
Conclusions:
- The C. hominis genome provides insights into its adaptation to host environments and parasitic strategies.
- Metabolic pathways and transporter systems are key features reflecting its lifestyle.
- Subtle genetic sequence divergence likely accounts for phenotypic differences between C. hominis and C. parvum.
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