Non-parasite genome-encoded virus-like RNAs reprogramthe pathogenicity of human blood flukes
- Jan 11
- 2 min read
Written by: Farah Doctor
Reference Paper: https://www.nature.com/articles/s41467-025-67822-1

This paper by Nature investigates the virus-like RNAs (also called ngRNAs) that are found not in
viruses but encoded outside of a parasite’s own genome, in a parasite known as Schistosoma
japonicum. It is a type of blood fluke (parasitic flatworm) that causes a serious disease called
schistosomiasis. These ngRNAs resemble viruses as they can replicate the RNA and encode
viral-like enzymes.
Blood flukes (parasitic worms) infect millions of people around the globe and cause chronic
illness. The symptoms are itchy skin, high fever, headaches, stomach aches and joint pain,
lethargy, coughing and diarrhoea. These symptoms come from the eggs produced by the
parasite, not adult worms. Parasites often interact with viruses but the focus of this study is the
virus-like RNAs. Scientists have been studying the parasite’s biology for many years, but little
was known about the role of the virus-like RNAs in the parasite and how it impacted the
development and disease severity.
Researchers have used RNA sequencing, single-cell analysis and experimentation to detect the
presence of these ngRNAs and study them in Schistosoma japonicum. They examined the
locations of these ngRNAs throughout the parasite and their impact on its biological processes.
The researchers found that the ngRNAs were mainly present in germ cells, the cells responsible
for reproduction (oogenesis and egg production) of the parasite. The ngRNAs also encode an
enzyme called RNA-dependent RNA polymerase (RdRp), which helps copy RNA inside the
parasite itself. The activity of the ngRNAs influences and governs embryo viability (potential to
develop) and egg production, which are crucial for the life cycle of the parasite, helping it cause
disease in humans. These eggs produced trigger the disease symptoms people see, and
therefore, ngRNAs affect the severity of infection of the parasite. Similar virus-like RNAs have
also been found in another planarian (free-living flatworm) species, Duegesia japonica,
suggesting that this mechanism could be common in other organisms that are also parasitic.
This study matters as it suggests that virus-like RNAs (when they are not part of a virus but
behave similarly to one) can shape the severity of disease caused by parasites. Virus-like
molecules are able to cause diseases without being actual viruses. Using this information,
scientists may be able to find new treatments for schistosomiasis that reduce egg production
rather than killing the parasite or be able to control the spread of the disease, opening
possibilities for new drug targets.
In conclusion, the non-parasite genome-encoded virus-like RNAs exist inside blood flukes and regulate reproduction and development. By targeting the ngRNAs, researchers can reduce the impact of the schistosomiasis disease and also control the spread of the disease better.
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