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dc.contributor.authorSchwarz, Erich M.
dc.contributor.authorHu, Yan
dc.contributor.authorAntoshechkin, Igor
dc.contributor.authorMiller, Melanie M.
dc.contributor.authorSternberg, Paul W.
dc.contributor.authorAroian, Raffi V
dc.date2022-08-11T08:10:18.000
dc.date.accessioned2022-08-23T17:03:39Z
dc.date.available2022-08-23T17:03:39Z
dc.date.issued2015-04-01
dc.date.submitted2016-04-13
dc.identifier.citationNat Genet. 2015 Apr;47(4):416-22. doi: 10.1038/ng.3237. Epub 2015 Mar 2. <a href="http://dx.doi.org/10.1038/ng.3237">Link to article on publisher's site</a>
dc.identifier.issn1061-4036 (Linking)
dc.identifier.doi10.1038/ng.3237
dc.identifier.pmid25730766
dc.identifier.urihttp://hdl.handle.net/20.500.14038/44472
dc.description.abstractHookworms infect over 400 million people, stunting and impoverishing them. Sequencing hookworm genomes and finding which genes they express during infection should help in devising new drugs or vaccines against hookworms. Unlike other hookworms, Ancylostoma ceylanicum infects both humans and other mammals, providing a laboratory model for hookworm disease. We determined an A. ceylanicum genome sequence of 313 Mb, with transcriptomic data throughout infection showing expression of 30,738 genes. Approximately 900 genes were upregulated during early infection in vivo, including ASPRs, a cryptic subfamily of activation-associated secreted proteins (ASPs). Genes downregulated during early infection included ion channels and G protein-coupled receptors; this downregulation was observed in both parasitic and free-living nematodes. Later, at the onset of heavy blood feeding, C-lectin genes were upregulated along with genes for secreted clade V proteins (SCVPs), encoding a previously undescribed protein family. These findings provide new drug and vaccine targets and should help elucidate hookworm pathogenesis.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=25730766&dopt=Abstract">Link to Article in PubMed</a>
dc.rights<p>This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit <a href="http://creativecommons.org/licenses/by-nc-sa/3.0/">http://creativecommons.org/licenses/by-nc-sa/3.0/</a>..</p>
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/
dc.subjectAncylostoma
dc.subjectAncylostomatoidea
dc.subjectAncylostomiasis
dc.subjectAnimals
dc.subjectBase Sequence
dc.subjectFemale
dc.subject*Genome, Helminth
dc.subjectHumans
dc.subjectMale
dc.subjectMolecular Sequence Data
dc.subjectMultigene Family
dc.subjectPhylogeny
dc.subjectSpecies Specificity
dc.subject*Transcriptome
dc.subjectZoonoses
dc.subjectBioinformatics
dc.subjectComputational Biology
dc.subjectGenetics
dc.subjectGenomics
dc.subjectImmunology and Infectious Disease
dc.subjectMolecular Genetics
dc.titleThe genome and transcriptome of the zoonotic hookworm Ancylostoma ceylanicum identify infection-specific gene families
dc.typeJournal Article
dc.source.journaltitleNature genetics
dc.source.volume47
dc.source.issue4
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1065&amp;context=pmm_pp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/pmm_pp/66
dc.identifier.contextkey8471556
refterms.dateFOA2022-08-23T17:03:39Z
html.description.abstract<p>Hookworms infect over 400 million people, stunting and impoverishing them. Sequencing hookworm genomes and finding which genes they express during infection should help in devising new drugs or vaccines against hookworms. Unlike other hookworms, Ancylostoma ceylanicum infects both humans and other mammals, providing a laboratory model for hookworm disease. We determined an A. ceylanicum genome sequence of 313 Mb, with transcriptomic data throughout infection showing expression of 30,738 genes. Approximately 900 genes were upregulated during early infection in vivo, including ASPRs, a cryptic subfamily of activation-associated secreted proteins (ASPs). Genes downregulated during early infection included ion channels and G protein-coupled receptors; this downregulation was observed in both parasitic and free-living nematodes. Later, at the onset of heavy blood feeding, C-lectin genes were upregulated along with genes for secreted clade V proteins (SCVPs), encoding a previously undescribed protein family. These findings provide new drug and vaccine targets and should help elucidate hookworm pathogenesis.</p>
dc.identifier.submissionpathpmm_pp/66
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages416-22


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<p>This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit <a href="http://creativecommons.org/licenses/by-nc-sa/3.0/">http://creativecommons.org/licenses/by-nc-sa/3.0/</a>..</p>
Except where otherwise noted, this item's license is described as <p>This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit <a href="http://creativecommons.org/licenses/by-nc-sa/3.0/">http://creativecommons.org/licenses/by-nc-sa/3.0/</a>..</p>