Abstract
The gastrointestinal parasitic nematode Strongyloides spp. has a unique life cycle that alternates between a parasitic generation that reproduces through mitotic parthenogenesis and a dioecious free-living sexually reproducing generation. Adult females from these two generations are genetically identical, making them an informative model to identify molecular differences between parasitic and free-living lifestyles and understand different reproductive strategies. We investigated the expression of small RNAs (sRNAs) that are either enriched for a 5' monophosphate modification (5'pN) or are 5' modification-independent, across five life cycle stages of the rodent parasite Strongyloides venezuelensis. We identified miRNAs and small-interfering RNAs expressed by S. venezuelensis that are predicted to target and regulate the expression of protein-coding genes and transposable elements (TEs). Three previously unreported classes of sRNA were identified: (1) 25Gs with a putative role in reproduction in adult females, (2) tRNA-derived 24-28 nt sRNAs (tsRNAs) which are predicted to target TEs in free-living females, and (3) 5'pN-enriched 26-29Cs with 5' CGAATCC and 3' TTT motifs expressed in parasitic females. We also confirmed that S. venezuelensis expresses the 27G class of sRNAs involved in TE regulation, which was previously identified in the rodent parasite Strongyloides ratti. Taken together, these results provide new insights into the role of sRNAs in reproductive biology and parasitism.
Original language | English |
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Article number | 20608 |
Journal | Scientific Reports |
Volume | 15 |
Issue number | 1 |
Early online date | 1 Jul 2025 |
DOIs | |
Publication status | Published - 1 Jul 2025 |
Data Availability Statement
All sequence data from the genome projects have been deposited at INSDC under the BioProject accession PRJDB13089.Acknowledgements
The authors thank all members of Parasite Systems Biology lab for their critical comments and technical supports. Computations were partially performed on the NIG supercomputer at ROIS National Institute of Genetics.Funding
VLH was funded by a Japanese Society for the Promotion of Science Fellowship (PE16024) and a Wellcome Trust Sir Henry Dale Fellowship (211227/Z/18/Z). TK was funded by Japan Society for the Promotion of Science (JSPS) KAKENHI Grant Numbers 19H03212 and 17KT0013, and JST CREST Grant Number JPMJCR18S7 and JPMJCR23B1. For the purpose of Open Access, the author has applied a CC BY public copyright licence to any Author Accepted Manuscript version arising from this submission.
Keywords
- Animals
- Strongyloides/genetics
- DNA Transposable Elements/genetics
- RNA, Small Untranslated/genetics
- Female
- Reproduction/genetics
- Life Cycle Stages/genetics
- RNA, Helminth/genetics
- MicroRNAs/genetics
- Gene Expression Regulation