Literature DB >> 20600069

Re-description of Cryptosporidium cuniculus Inman and Takeuchi, 1979 (Apicomplexa: Cryptosporidiidae): morphology, biology and phylogeny.

Guy Robinson1, Steve Wright, Kristin Elwin, Stephen J Hadfield, Frank Katzer, Paul M Bartley, Paul R Hunter, Mintu Nath, Elisabeth A Innes, Rachel M Chalmers.   

Abstract

To provide re-description of Cryptosporidium cuniculus Inman and Takeuchi, 1979 (synonymous with rabbit genotype), a species closely related to Cryptosporidium hominis, the morphology, natural and experimental host specificity, and genetic characterisation were investigated. The morphology and diagnostic characteristics are typical of other intestinal species of Cryptosporidium, albeit with slightly larger oocysts (5.55-6.40×5.02-5.92 μm; mean 5.98×5.38 μm; length:width=1.1; n=50). Natural hosts appear to be European rabbits (Oryctolagus cuniculus) and humans (Homo sapiens). Experimental infections have been established in weanling rabbits (O. cuniculus), immunosuppressed Mongolian gerbils (Meriones unguiculatus) and immunosuppressed adult Porton strain mice (Mus musculus), but not in neonatal mice. Patterns of infection measured by oocyst shedding are significantly different compared with C. hominis, particularly in rabbits. Histological examination reveals endogenous stages in the brush border of the epithelium of the small intestinal villi, but clinical signs are absent. Inoculation of human HCT-8 cells results in discrete clusters of endogenous stages. A close relationship with C. hominis is inferred from molecular analyses at the ssrRNA, 70 kDa heat shock protein (HSP70), actin, Cryptosporidium oocyst wall protein (COWP), 60 kDa glycoprotein (GP60) genes and a region encoding a product of unknown function (LIB13). Sequences contained limited, consistent polymorphisms at the ssrRNA, HSP70 and actin genes, were identical at the COWP and LIB13 genes and demonstrated two unique families at the GP60 gene. Although genetically closely related, there are significant biological differences between C. cuniculus and C. hominis that support these protozoa being separate species. This is based on the current understanding of these organisms and relies on the assumption that mating between these species would not normally occur. If this is subsequently demonstrated their categorisation may need to be re-addressed.
Copyright © 2010 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20600069     DOI: 10.1016/j.ijpara.2010.05.010

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  25 in total

1.  Coevolution of Cryptosporidium tyzzeri and the house mouse (Mus musculus).

Authors:  Martin Kváč; John McEvoy; Martina Loudová; Brianna Stenger; Bohumil Sak; Dana Květoňová; Oleg Ditrich; Veronika Rašková; Elaine Moriarty; Michael Rost; Miloš Macholán; Jaroslav Piálek
Journal:  Int J Parasitol       Date:  2013-06-18       Impact factor: 3.981

2.  Detection and characterization of Cryptosporidium cuniculus by real-time PCR.

Authors:  Stephen J Hadfield; Rachel M Chalmers
Journal:  Parasitol Res       Date:  2012-03-06       Impact factor: 2.289

3.  Detection and differentiation of Cryptosporidium spp. in human clinical samples by use of real-time PCR.

Authors:  Stephen J Hadfield; Guy Robinson; Kristin Elwin; Rachel M Chalmers
Journal:  J Clin Microbiol       Date:  2010-12-22       Impact factor: 5.948

4.  Molecular epidemiology and spatial distribution of a waterborne cryptosporidiosis outbreak in Australia.

Authors:  Liette S Waldron; Belinda C Ferrari; Cristel Cheung-Kwok-Sang; Paul J Beggs; Nicola Stephens; Michelle L Power
Journal:  Appl Environ Microbiol       Date:  2011-09-09       Impact factor: 4.792

5.  Molecular epidemiology, spatiotemporal analysis, and ecology of sporadic human cryptosporidiosis in Australia.

Authors:  Liette S Waldron; Borce Dimeski; Paul J Beggs; Belinda C Ferrari; Michelle L Power
Journal:  Appl Environ Microbiol       Date:  2011-09-09       Impact factor: 4.792

Review 6.  Genomics and population biology of Cryptosporidium species.

Authors:  G Widmer; S Sullivan
Journal:  Parasite Immunol       Date:  2012 Feb-Mar       Impact factor: 2.280

7.  Multi-locus analysis of human infective Cryptosporidium species and subtypes using ten novel genetic loci.

Authors:  Maha Bouzid; Kevin M Tyler; Richard Christen; Rachel M Chalmers; Kristin Elwin; Paul R Hunter
Journal:  BMC Microbiol       Date:  2010-08-09       Impact factor: 3.605

8.  The Applicability of TaqMan-Based Quantitative Real-Time PCR Assays for Detecting and Enumerating Cryptosporidium spp. Oocysts in the Environment.

Authors:  Sarah E Staggs; Erin M Beckman; Scott P Keely; Reena Mackwan; Michael W Ware; Alan P Moyer; James A Ferretti; Abu Sayed; Lihua Xiao; Eric N Villegas
Journal:  PLoS One       Date:  2013-06-21       Impact factor: 3.240

9.  Molecular surveillance of Cryptosporidium spp., Giardia duodenalis, and Enterocytozoon bieneusi by genotyping and subtyping parasites in wastewater.

Authors:  Na Li; Lihua Xiao; Lin Wang; Shuming Zhao; Xukun Zhao; Liping Duan; Meijin Guo; Lili Liu; Yaoyu Feng
Journal:  PLoS Negl Trop Dis       Date:  2012-09-06

10.  Sporadic human cryptosporidiosis caused by Cryptosporidium cuniculus, United Kingdom, 2007-2008.

Authors:  Rachel M Chalmers; Kristin Elwin; Stephen J Hadfield; Guy Robinson
Journal:  Emerg Infect Dis       Date:  2011-03       Impact factor: 6.883

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