Transcriptional patterns of sexual dimorphism and in host developmental programs in the model parasitic nematode Heligmosomoides bakeri, Parasites & Vectors

Por um escritor misterioso

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Background Heligmosomoides bakeri (often mistaken for Heligmosomoides polygyrus) is a promising model for parasitic nematodes with the key advantage of being amenable to study and manipulation within a controlled laboratory environment. While draft genome sequences are available for this worm, which allow for comparative genomic analyses between nematodes, there is a notable lack of information on its gene expression. Methods We generated biologically replicated RNA-seq datasets from samples taken throughout the parasitic life of H. bakeri. RNA from tissue-dwelling and lumen-dwelling worms, collected under a dissection microscope, was sequenced on an Illumina platform. Results We find extensive transcriptional sexual dimorphism throughout the fourth larval and adult stages of this parasite and identify alternative splicing, glycosylation, and ubiquitination as particularly important processes for establishing and/or maintaining sex-specific gene expression in this species. We find sex-linked differences in transcription related to aging and oxidative and osmotic stress responses. We observe a starvation-like signature among transcripts whose expression is consistently upregulated in males, which may reflect a higher energy expenditure by male worms. We detect evidence of increased importance for anaerobic respiration among the adult worms, which coincides with the parasite’s migration into the physiologically hypoxic environment of the intestinal lumen. Furthermore, we hypothesize that oxygen concentration may be an important driver of the worms encysting in the intestinal mucosa as larvae, which not only fully exposes the worms to their host’s immune system but also shapes many of the interactions between the host and parasite. We find stage- and sex-specific variation in the expression of immunomodulatory genes and in anthelmintic targets. Conclusions We examine how different the male and female worms are at the molecular level and describe major developmental events that occur in the worm, which extend our understanding of the interactions between this parasite and its host. In addition to generating new hypotheses for follow-up experiments into the worm’s behavior, physiology, and metabolism, our datasets enable future more in-depth comparisons between nematodes to better define the utility of H. bakeri as a model for parasitic nematodes in general. Graphical Abstract
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
Exosomes secreted by nematode parasites transfer small RNAs to
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
Transcriptional patterns of sexual dimorphism and in host
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
Dictyocaulus viviparus genome, variome and transcriptome
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
Dictyocaulus viviparus genome, variome and transcriptome elucidate
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
Parasite burden and fitness in SPF and GF mice. (A) Number of
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
PDF) Trickle infection with Heligmosomoides polygyrus results in
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
PDF) Estimation of C. elegans cell- and tissue volumes
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
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Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
PDF) The production of excretory-secretory molecules from
Transcriptional patterns of sexual dimorphism and in host developmental  programs in the model parasitic nematode Heligmosomoides bakeri, Parasites  & Vectors
Exosomes secreted by nematode parasites transfer small RNAs to
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