Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pntd.0004406
Title: Comparative Transcriptomic Exploration Reveals Unique Molecular Adaptations of Neuropathogenic Trichobilharzia to Invade and Parasitize Its Avian Definitive Host
Authors: Leontovyč R.
Young N.D.
Korhonen P.K.
Hall R.S.
Tan P. 
Mikeš L.
Kašný M.
Horák P.
Gasser R.B.
Keywords: adaptation
amino acid metabolism
Article
bioinformatics
carbohydrate metabolism
cell adhesion
cercaria
cross reaction
human
neuropathology
nonhuman
proteomics
RNA isolation
RNA translation
schistosomulum
sequence analysis
signal transduction
transcriptomics
upregulation
animal
biology
DNA sequence
duck
gene expression profiling
genetics
growth, development and aging
host pathogen interaction
life cycle stage
metabolism
molecular genetics
parasitology
Schistosomatidae
Adaptation, Biological
Animals
Computational Biology
Ducks
Gene Expression Profiling
Host-Pathogen Interactions
Life Cycle Stages
Metabolic Networks and Pathways
Molecular Sequence Data
Schistosomatidae
Sequence Analysis, DNA
Issue Date: 2016
Citation: Leontovyč R., Young N.D., Korhonen P.K., Hall R.S., Tan P., Mikeš L., Kašný M., Horák P., Gasser R.B. (2016). Comparative Transcriptomic Exploration Reveals Unique Molecular Adaptations of Neuropathogenic Trichobilharzia to Invade and Parasitize Its Avian Definitive Host. PLoS Neglected Tropical Diseases 10 (2) : e0004406. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pntd.0004406
Rights: Attribution 4.0 International
Abstract: To date, most molecular investigations of schistosomatids have focused principally on blood flukes (schistosomes) of humans. Despite the clinical importance of cercarial dermatitis in humans caused by Trichobilharzia regenti and the serious neuropathologic disease that this parasite causes in its permissive avian hosts and accidental mammalian hosts, almost nothing is known about the molecular aspects of how this fluke invades its hosts, migrates in host tissues and how it interacts with its hosts? immune system. Here, we explored selected aspects using a transcriptomic-bioinformatic approach. To do this, we sequenced, assembled and annotated the transcriptome representing two consecutive life stages (cercariae and schistosomula) of T. regenti involved in the first phases of infection of the avian host. We identified key biological and metabolic pathways specific to each of these two developmental stages and also undertook comparative analyses using data available for taxonomically related blood flukes of the genus Schistosoma. Detailed comparative analyses revealed the unique involvement of carbohydrate metabolism, translation and amino acid metabolism, and calcium in T. regenti cercariae during their invasion and in growth and development, as well as the roles of cell adhesion molecules, microaerobic metabolism (citrate cycle and oxidative phosphorylation), peptidases (cathepsins) and other histolytic and lysozomal proteins in schistosomula during their particular migration in neural tissues of the avian host. In conclusion, the present transcriptomic exploration provides new and significant insights into the molecular biology of T. regenti, which should underpin future genomic and proteomic investigations of T. regenti and, importantly, provides a useful starting point for a range of comparative studies of schistosomatids and other trematodes. © 2016 Leontovyč et al.
Source Title: PLoS Neglected Tropical Diseases
URI: https://scholarbank.nus.edu.sg/handle/10635/161923
ISSN: 19352727
DOI: 10.1371/journal.pntd.0004406
Rights: Attribution 4.0 International
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