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Comparative genomics of the apicomplexan parasites Toxoplasma gondii and neospora caninum: Coccidia differing in host range and transmission strategy
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نویسنده
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reid a.j. ,vermont s.j. ,cotton j.a. ,harris d. ,hill-cawthorne g.a. ,könen-waisman s. ,latham s.m. ,mourier t. ,norton r. ,quail m.a. ,sanders m. ,shanmugam d. ,sohal a. ,wasmuth j.d. ,brunk b. ,grigg m.e. ,howard j.c. ,parkinson j. ,roos d.s. ,trees a.j. ,berriman m. ,pain a. ,wastling j.m.
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منبع
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plos pathogens - 2012 - دوره : 8 - شماره : 3
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چکیده
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Toxoplasma gondii is a zoonotic protozoan parasite which infects nearly one third of the human population and is found in an extraordinary range of vertebrate hosts. its epidemiology depends heavily on horizontal transmission,especially between rodents and its definitive host,the cat. neospora caninum is a recently discovered close relative of toxoplasma,whose definitive host is the dog. both species are tissue-dwelling coccidia and members of the phylum apicomplexa; they share many common features,but neospora neither infects humans nor shares the same wide host range as toxoplasma,rather it shows a striking preference for highly efficient vertical transmission in cattle. these species therefore provide a remarkable opportunity to investigate mechanisms of host restriction,transmission strategies,virulence and zoonotic potential. we sequenced the genome of n. caninum and transcriptomes of the invasive stage of both species,undertaking an extensive comparative genomics and transcriptomics analysis. we estimate that these organisms diverged from their common ancestor around 28 million years ago and find that both genomes and gene expression are remarkably conserved. however,in n. caninum we identified an unexpected expansion of surface antigen gene families and the divergence of secreted virulence factors,including rhoptry kinases. specifically we show that the rhoptry kinase rop18 is pseudogenised in n. caninum and that,as a possible consequence,neospora is unable to phosphorylate host immunity-related gtpases,as toxoplasma does. this defense strategy is thought to be key to virulence in toxoplasma. we conclude that the ecological niches occupied by these species are influenced by a relatively small number of gene products which operate at the host-parasite interface and that the dominance of vertical transmission in n. caninum may be associated with the evolution of reduced virulence in this species.
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آدرس
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wellcome trust sanger institute,hinxton,cambridgshire, United Kingdom, institute of infection and global health and school of veterinary science,faculty of health and life sciences,university of liverpool,liverpool,merseyside, United Kingdom, wellcome trust sanger institute,hinxton,cambridgshire, United Kingdom, wellcome trust sanger institute,hinxton,cambridgshire, United Kingdom, king abdullah university of science and technology,thuwal,jeddah, Saudi Arabia, institute for genetics,university of cologne,cologne,north rhine-westphalia, Germany, institute of infection and global health and school of veterinary science,faculty of health and life sciences,university of liverpool,liverpool,merseyside, United Kingdom, centre for geogenetics,natural history museum of denmark,university of copenhagen,copenhagen, Denmark, institute of infection and global health and school of veterinary science,faculty of health and life sciences,university of liverpool,liverpool,merseyside, United Kingdom, wellcome trust sanger institute,hinxton,cambridgshire, United Kingdom, wellcome trust sanger institute,hinxton,cambridgshire, United Kingdom, department of biology,university of pennsylvania,philadelphia,pa, United States, wellcome trust sanger institute,hinxton,cambridgshire, United Kingdom, program in molecular structure and function,hospital for sick children and departments of biochemistry and molecular genetics,university of toronto,toronto,on,canada,laboratory of parasitic diseases,national institutes of health,national institute of allergy and infectious diseases (niaid),bethesda,md, United States, department of biology,university of pennsylvania,philadelphia,pa, United States, laboratory of parasitic diseases,national institutes of health,national institute of allergy and infectious diseases (niaid),bethesda,md, United States, institute for genetics,university of cologne,cologne,north rhine-westphalia, Germany, program in molecular structure and function,hospital for sick children and departments of biochemistry and molecular genetics,university of toronto,toronto,on, Canada, department of biology,university of pennsylvania,philadelphia,pa, United States, institute of infection and global health and school of veterinary science,faculty of health and life sciences,university of liverpool,liverpool,merseyside, United Kingdom, wellcome trust sanger institute,hinxton,cambridgshire, United Kingdom, wellcome trust sanger institute,hinxton,cambridgshire,united kingdom,king abdullah university of science and technology,thuwal,jeddah, Saudi Arabia, institute of infection and global health and school of veterinary science,faculty of health and life sciences,university of liverpool,liverpool,merseyside, United Kingdom
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Authors
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