dc.contributor.author
Ebner, Friederike
dc.contributor.author
Kuhring, Mathias
dc.contributor.author
Radonic, Aleksandar
dc.contributor.author
Midha, Ankur
dc.contributor.author
Renard, Bernhard Y.
dc.contributor.author
Hartmann, Susanne
dc.date.accessioned
2018-09-12T08:01:46Z
dc.date.available
2018-09-12T08:01:46Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/22835
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-634
dc.description.abstract
Gastrointestinal nematodes are among the most prevalent parasites infecting humans and livestock worldwide. Infective larvae of the soil-transmitted nematode Ascaris spp. enter the host and start tissue migration by crossing the intestinal epithelial barrier. The initial interaction of the intestinal epithelium with the parasite, however, has received little attention. In a time-resolved interaction model of porcine intestinal epithelial cells (IPEC-J2) and infective Ascaris suum larvae, we addressed the early transcriptional changes occurring simultaneously in both organisms using dual-species RNA-Seq. Functional analysis of the host response revealed an overall induction of metabolic activity, without induction of immune responsive genes or immune signaling pathways and showing suppression of chemotactic genes like CXCL8/IL-8 or CHI3L1. Ascaris larvae, when getting in contact with the epithelium, showed induction of genes that orchestrate motor activity and larval development, such as myosin, troponin, myoglobin, and protein disulfide isomerase 2 (PDI-2). In addition, excretory-secretory products that likely facilitate parasite invasion were increased, among them, aspartic protease 6 or hyaluronidase. Integration of host and pathogen data in an interspecies gene co-expression network indicated links between nematode fatty acid biosynthesis and host ribosome assembly/protein synthesis. In summary, our study provides new molecular insights into the early factors of parasite invasion, while at the same time revealing host immunological unresponsiveness. Reproducible software for dual RNA-Seq analysis of non-model organisms is available at https://gitlab.com/mkuhring/project_asuum and can be applied to similar studies.
en
dc.format.extent
15 Seiten
de
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
de
dc.subject
host–pathogen
en
dc.subject
parasitic nematode
en
dc.subject
Ascaris suum
en
dc.subject
dual-species
en
dc.subject
RNA sequencing
en
dc.subject
transcriptomics
en
dc.subject
epithelial communication
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::630 Landwirtschaft::636 Viehwirtschaft
de
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::578 Naturgeschichte von Organismen
de
dc.title
Silent Witness: Dual-Species Transcriptomics Reveals Epithelial Immunological Quiescence to Helminth Larval Encounter and Fostered Larval Development
de
dc.type
Wissenschaftlicher Artikel
de
dcterms.bibliographicCitation.articlenumber
1868
dcterms.bibliographicCitation.doi
10.3389/fimmu.2018.01868
dcterms.bibliographicCitation.journaltitle
Frontiers in Immunology
dcterms.bibliographicCitation.volume
9
dcterms.bibliographicCitation.url
https://doi.org/10.3389/fimmu.2018.01868
de
refubium.affiliation
Veterinärmedizin
de
refubium.affiliation.other
Institut für Immunologie
de
refubium.funding
Institutional Participation
refubium.funding.id
Frontiers
refubium.note.author
Der Artikel wurde in einer reinen Open-Access-Zeitschrift publiziert.
de
refubium.resourceType.isindependentpub
no
de
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
1664-3224