Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic loci

<p>Abstract</p> <p>Background</p> <p><it>Cryptosporidium </it>is a protozoan parasite that causes diarrheal illness in a wide range of hosts including humans. Two species, <it>C. parvum </it>and <it>C. hominis </it>are of primary publ...

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Main Authors: Bouzid Maha, Tyler Kevin M, Christen Richard, Chalmers Rachel M, Elwin Kristin, Hunter Paul R
Format: Article
Language:English
Published: BMC 2010-08-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/10/213
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spelling doaj-633e8a09fd3d44d38c2f9fce07f5eb512020-11-24T22:12:57ZengBMCBMC Microbiology1471-21802010-08-0110121310.1186/1471-2180-10-213Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic lociBouzid MahaTyler Kevin MChristen RichardChalmers Rachel MElwin KristinHunter Paul R<p>Abstract</p> <p>Background</p> <p><it>Cryptosporidium </it>is a protozoan parasite that causes diarrheal illness in a wide range of hosts including humans. Two species, <it>C. parvum </it>and <it>C. hominis </it>are of primary public health relevance. Genome sequences of these two species are available and show only 3-5% sequence divergence. We investigated this sequence variability, which could correspond either to sequence gaps in the published genome sequences or to the presence of species-specific genes. Comparative genomic tools were used to identify putative species-specific genes and a subset of these genes was tested by PCR in a collection of <it>Cryptosporidium </it>clinical isolates and reference strains.</p> <p>Results</p> <p>The majority of the putative species-specific genes examined were in fact common to <it>C. parvum </it>and <it>C. hominis</it>. PCR product sequence analysis revealed interesting SNPs, the majority of which were species-specific. These genetic loci allowed us to construct a robust and multi-locus analysis. The Neighbour-Joining phylogenetic tree constructed clearly discriminated the previously described lineages of <it>Cryptosporidium </it>species and subtypes.</p> <p>Conclusions</p> <p>Most of the genes identified as being species specific during bioinformatics in <it>Cryptosporidium </it>sp. are in fact present in multiple species and only appear species specific because of gaps in published genome sequences. Nevertheless SNPs may offer a promising approach to studying the taxonomy of closely related species of Cryptosporidia.</p> http://www.biomedcentral.com/1471-2180/10/213
collection DOAJ
language English
format Article
sources DOAJ
author Bouzid Maha
Tyler Kevin M
Christen Richard
Chalmers Rachel M
Elwin Kristin
Hunter Paul R
spellingShingle Bouzid Maha
Tyler Kevin M
Christen Richard
Chalmers Rachel M
Elwin Kristin
Hunter Paul R
Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic loci
BMC Microbiology
author_facet Bouzid Maha
Tyler Kevin M
Christen Richard
Chalmers Rachel M
Elwin Kristin
Hunter Paul R
author_sort Bouzid Maha
title Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic loci
title_short Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic loci
title_full Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic loci
title_fullStr Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic loci
title_full_unstemmed Multi-locus analysis of human infective <it>Cryptosporidium </it>species and subtypes using ten novel genetic loci
title_sort multi-locus analysis of human infective <it>cryptosporidium </it>species and subtypes using ten novel genetic loci
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2010-08-01
description <p>Abstract</p> <p>Background</p> <p><it>Cryptosporidium </it>is a protozoan parasite that causes diarrheal illness in a wide range of hosts including humans. Two species, <it>C. parvum </it>and <it>C. hominis </it>are of primary public health relevance. Genome sequences of these two species are available and show only 3-5% sequence divergence. We investigated this sequence variability, which could correspond either to sequence gaps in the published genome sequences or to the presence of species-specific genes. Comparative genomic tools were used to identify putative species-specific genes and a subset of these genes was tested by PCR in a collection of <it>Cryptosporidium </it>clinical isolates and reference strains.</p> <p>Results</p> <p>The majority of the putative species-specific genes examined were in fact common to <it>C. parvum </it>and <it>C. hominis</it>. PCR product sequence analysis revealed interesting SNPs, the majority of which were species-specific. These genetic loci allowed us to construct a robust and multi-locus analysis. The Neighbour-Joining phylogenetic tree constructed clearly discriminated the previously described lineages of <it>Cryptosporidium </it>species and subtypes.</p> <p>Conclusions</p> <p>Most of the genes identified as being species specific during bioinformatics in <it>Cryptosporidium </it>sp. are in fact present in multiple species and only appear species specific because of gaps in published genome sequences. Nevertheless SNPs may offer a promising approach to studying the taxonomy of closely related species of Cryptosporidia.</p>
url http://www.biomedcentral.com/1471-2180/10/213
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