Systems-Based Analysis of the Sarcocystis neurona Genome Identifies Pathways That Contribute to a Heteroxenous Life Cycle

Author:

Blazejewski Tomasz1,Nursimulu Nirvana12,Pszenny Viviana3,Dangoudoubiyam Sriveny4,Namasivayam Sivaranjani5,Chiasson Melissa A.3,Chessman Kyle12,Tonkin Michelle6,Swapna Lakshmipuram S.1,Hung Stacy S.17,Bridgers Joshua5,Ricklefs Stacy M.8,Boulanger Martin J.6,Dubey Jitender P.8,Porcella Stephen F.9,Kissinger Jessica C.51011,Howe Daniel K.4,Grigg Michael E.3,Parkinson John1712

Affiliation:

1. Program in Molecular Structure and Function, Hospital for Sick Children, Toronto, Ontario, Canada

2. Department of Computer Science, University of Toronto, Toronto, Ontario, Canada

3. Molecular Parasitology Section, Laboratory of Parasitic Diseases, NIAID, National Institutes of Health, Bethesda, Maryland, USA

4. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, Kentucky, USA

5. Department of Genetics, University of Georgia, Athens, Georgia, USA

6. Department of Biochemistry and Microbiology, University of Victoria, Victoria, British Columbia, Canada

7. Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada

8. U.S. Department of Agriculture, Animal Parasitic Diseases Laboratory, Beltsville Agricultural Research Center, Agricultural Research Service, Beltsville, Maryland, USA

9. Genomics Unit, Research Technologies Section, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, Hamilton, Montana, USA

10. Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, Georgia, USA

11. Institute of Bioinformatics, University of Georgia, Athens, Georgia, USA

12. Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada

Abstract

ABSTRACT Sarcocystis neurona is a member of the coccidia, a clade of single-celled parasites of medical and veterinary importance including Eimeria , Sarcocystis , Neospora , and Toxoplasma. Unlike Eimeria , a single-host enteric pathogen, Sarcocystis , Neospora , and Toxoplasma are two-host parasites that infect and produce infectious tissue cysts in a wide range of intermediate hosts. As a genus, Sarcocystis is one of the most successful protozoan parasites; all vertebrates, including birds, reptiles, fish, and mammals are hosts to at least one Sarcocystis species. Here we sequenced Sarcocystis neurona , the causal agent of fatal equine protozoal myeloencephalitis. The S. neurona genome is 127 Mbp, more than twice the size of other sequenced coccidian genomes. Comparative analyses identified conservation of the invasion machinery among the coccidia. However, many dense-granule and rhoptry kinase genes, responsible for altering host effector pathways in Toxoplasma and Neospora , are absent from S. neurona. Further, S. neurona has a divergent repertoire of SRS proteins, previously implicated in tissue cyst formation in Toxoplasma. Systems-based analyses identified a series of metabolic innovations, including the ability to exploit alternative sources of energy. Finally, we present an S. neurona model detailing conserved molecular innovations that promote the transition from a purely enteric lifestyle ( Eimeria ) to a heteroxenous parasite capable of infecting a wide range of intermediate hosts. IMPORTANCE Sarcocystis neurona is a member of the coccidia, a clade of single-celled apicomplexan parasites responsible for major economic and health care burdens worldwide. A cousin of Plasmodium, Cryptosporidium, Theileria , and Eimeria , Sarcocystis is one of the most successful parasite genera; it is capable of infecting all vertebrates (fish, reptiles, birds, and mammals—including humans). The past decade has witnessed an increasing number of human outbreaks of clinical significance associated with acute sarcocystosis. Among Sarcocystis species, S. neurona has a wide host range and causes fatal encephalitis in horses, marine mammals, and several other mammals. To provide insights into the transition from a purely enteric parasite (e.g., Eimeria ) to one that forms tissue cysts (Toxoplasma), we present the first genome sequence of S. neurona. Comparisons with other coccidian genomes highlight the molecular innovations that drive its distinct life cycle strategies.

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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