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SRX7175222: GSM4173863: mf_1_ES; Litomosoides sigmodontis; ncRNA-Seq
1 ILLUMINA (Illumina Genome Analyzer) run: 6.1M spots, 306M bases, 130.2Mb downloads

Submitted by: NCBI (GEO)
Study: Comparative analysis of small RNAs released by the filarial nematode Litomosoides sigmodontis in vitro and in vivo
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BACKGROUND: The release of small non-coding RNAs (sRNAs) has been reported in parasitic nematodes, trematodes and cestodes of medical and veterinary importance. However, little is known regarding the diversity and composition of sRNAs released by different lifecycle stages and the portion of sRNAs that persist in host tissues during filarial infection. This information is relevant to understanding potential roles of sRNAs in parasite-to-host communication, as well as to inform on the location within the host and time point at which they can be detected. METHODOLOGY & PRINCIPAL FINDINGS: We have used small RNA (sRNA) sequencing analysis to identify sRNAs in replicate samples of the excretory-secretory (ES) products of developmental stages of the filarial nematode Litomosoides sigmodontis in vitro and compare this to the parasite-derived sRNA detected in host tissues. We show that all L. sigmodontis developmental stages release RNAs in vitro, including ribosomal RNA fragments, 5'-derived tRNA fragments (5'-tRFs) and, to a lesser extent, microRNAs (miRNAs). The gravid adult females (gAF) produce the largest diversity and abundance of miRNAs in the ES compared to the adult males or microfilariae. Analysis of sRNAs detected in serum and macrophages from infected animals reveals that the class of parasite miRNAs are preferentially detected in vivo, compared to their low levels in the ES products, and identifies miR-92-3p and miR-71-5p as L. sigmodontis miRNAs that are stably detected in host cells in vivo. CONCLUSIONS: Our results suggest that gravid adult female worms secrete the largest diversity of extracellular sRNAs compared to adult males or microfilariae. We further show differences in the parasite sRNA biotype distribution detected in vitro versus in vivo. We identify macrophages as one reservoir for parasite sRNA during infection, and confirm the presence of parasite miRNAs and tRNAs in host serum during patent infection. Overall design: We examined the content of several tissues and in vitro Excretory/Secretory (ES) products by next generation DNA sequencing
Sample: mf_1_ES
SAMN13319697 • SRS5682007 • All experiments • All runs
Library:
Instrument: Illumina Genome Analyzer
Strategy: ncRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Small RNA libraries were prepared using TriLink small RNA library preparation kit (Illumina compatible), following manufacturer's recommendations.
Experiment attributes:
GEO Accession: GSM4173863
Links:
Runs: 1 run, 6.1M spots, 306M bases, 130.2Mb
Run# of Spots# of BasesSizePublished
SRR104856416,120,158306M130.2Mb2019-11-21

ID:
9424683

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