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Comparative genomic analysis of the principal Cryptosporidium species that infect humans.
Arias-Agudelo, Laura M; Garcia-Montoya, Gisela; Cabarcas, Felipe; Galvan-Diaz, Ana L; Alzate, Juan F.
Afiliação
  • Arias-Agudelo LM; Centro Nacional de Secuenciación Genómica - CNSG, Sede de Investigación Universitaria - SIU, Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad de Antioquia, Medellin, Antioquia, Colombia.
  • Garcia-Montoya G; Centro Nacional de Secuenciación Genómica - CNSG, Sede de Investigación Universitaria - SIU, Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad de Antioquia, Medellin, Antioquia, Colombia.
  • Cabarcas F; Centro Nacional de Secuenciación Genómica - CNSG, Sede de Investigación Universitaria - SIU, Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad de Antioquia, Medellin, Antioquia, Colombia.
  • Galvan-Diaz AL; Grupo SISTEMIC, Departamento de Ingeniería Electrónica, Facultad de Ingeniería, Universidad de Antioquia, Medellin, Antioquia, Colombia.
  • Alzate JF; Grupo de Microbiología ambiental. Escuela de Microbiología, Universidad de Antioquia, Medellin, Antioquia, Colombia.
PeerJ ; 8: e10478, 2020.
Article em En | MEDLINE | ID: mdl-33344091
ABSTRACT
Cryptosporidium parasites are ubiquitous and can infect a broad range of vertebrates and are considered the most frequent protozoa associated with waterborne parasitic outbreaks. The intestine is the target of three of the species most frequently found in humans C. hominis, C. parvum, and. C. meleagridis. Despite the recent advance in genome sequencing projects for this apicomplexan, a broad genomic comparison including the three species most prevalent in humans have not been published so far. In this work, we downloaded raw NGS data, assembled it under normalized conditions, and compared 23 publicly available genomes of C. hominis, C. parvum, and C. meleagridis. Although few genomes showed highly fragmented assemblies, most of them had less than 500 scaffolds and mean coverage that ranged between 35X and 511X. Synonymous single nucleotide variants were the most common in C. hominis and C. meleagridis, while in C. parvum, they accounted for around 50% of the SNV observed. Furthermore, deleterious nucleotide substitutions common to all three species were more common in genes associated with DNA repair, recombination, and chromosome-associated proteins. Indel events were observed in the 23 studied isolates that spanned up to 500 bases. The highest number of deletions was observed in C. meleagridis, followed by C. hominis, with more than 60 species-specific deletions found in some isolates of these two species. Although several genes with indel events have been partially annotated, most of them remain to encode uncharacterized proteins.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article