Host RNA incorporation linked to chronic hepatitis E infection

If the virus incorporates host genetic segments into its genome, the infection may become chronic.

Why does Hepatitis E become chronic in some patients, and why do medications not work? To find out, an international research team led by scientists from Bochum observed a patient with chronic Hepatitis E infection over a year. Repeated sequencing of the virus RNA showed that the virus incorporated various parts of the host's messenger RNA into its genome. This resulted in a replication advantage, which may have contributed to the infection becoming chronic.

The so-called insertion of host RNA can possibly predict the transition of an acute infection to a chronic condition." 

Dr. Daniel Todt, head of the Computational Virology research group, Department of Medical and Molecular Virology, Ruhr University Bochum, Germany

The researchers report in the journal Nature Communications on June 6, 2024.

Sequencing of the virus population

Around 20 million people worldwide contract Hepatitis E every year. Normally, the infection heals without consequences, but it can be life-threatening for pregnant women or people with suppressed immune systems. In some cases, it becomes chronic. There are no specific effective medications. The broad-spectrum antiviral drug Ribavirin is also used against Hepatitis E, but it does not always work.

How can the virus evade the immune system? Why does the infection become chronic and not heal? The researchers wanted to find out and analyzed for the first time all virus populations of a chronically infected patient over a period of more than a year. They examined more than 180 individual sequences from blood samples in detail.

Replication in cell culture benefits from host RNA

"The Hepatitis E virus has a so-called hypervariable region in its genetic information, into which it can incorporate various RNA sequences from host cells," describes Daniel Todt. His team was able to show that the composition of this region changed massively during the observation period. Additionally, many different compositions occurred simultaneously. In cell culture experiments, it was shown that incorporating host RNA provided a replication advantage: The altered viruses could replicate better than others. "We assume that this is partly responsible for the infection becoming chronic and the therapy failing," says Daniel Todt.

The researchers examined the composition of the host RNA incorporated into the virus to determine if there were any common features characterizing the gene segments. "However, we could not detect any meaningful similarities," says Todt. The incorporated gene sequences are predominantly those that are very common in host cells, indicating a random selection.

"Possibly, during Hepatitis E infection, a race between the virus and the immune system occurs in the body," speculates Daniel Todt. If the virus manages to incorporate host RNA before the immune system successfully combats the infection, it may lead to a chronic course. "Host RNA in the viral genome could, in any case, serve as a biomarker in the acute phase of an infection, indicating early on that it is likely to become chronic."

The researchers plan to expand their studies to larger cohorts of patients.


The work was funded by the Federal Ministry of Education and Research as part of the junior research group "VirBio" and by the German Research Foundation. Further funding came from the Federal Ministry of Health, the German Centre for Infection Research and the National Institutes of Health.

Journal reference:

Wißing, M. H., et al. (2024). Genetic determinants of host- and virus-derived insertions for hepatitis E virus replication. Nature Communications.


The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
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