Ohio (US):A new study has found how a small difference in the RNA sequence can allow the viral RNA to be packaged for replication, creating potential targets for future HIV treatments.
The study has been published in the 'Proceedings of the National Academy of Sciences'. The study found that HIV chose its viral RNA genome - the "source code" that is injected into healthy human cells to infect them - based on functions attributable to just two nucleotides.
"It's just this two-nucleotide difference that makes such a dramatic effect," said Karin Musier-Forsyth, senior author of the study, Ohio Eminent Scholar and a professor of chemistry and biochemistry at The Ohio State University.
"If we can prevent it from packaging its own genome, we can prevent it from spreading inside the body," she added. The study's authors, who also included researchers from the National Cancer Institute, hoped to answer a long-standing question in HIV biology research: How does the virus know to package its specific viral RNA to be copied in human cells? "Just like we need a genome encoded by DNA, viruses have their own genomic DNA or RNA - in the case of HIV it's RNA - and they have to package their genomic RNA and that's what this whole study is about," she said.
Also Read:Number of HIV positive patients increasing in Tripura
"It's an essential step for how we understand the replication of the virus," she added. RNA is a string of nucleotides, and it is present in some form or another in all living things, including viruses. In HIV, it carried the genetic information that allowed the virus to copy itself inside a host - the human body. HIV RNA comprised about 9,800 nucleotides.
"We have lots of types of RNA in our cells as humans, including messenger RNA (mRNA), which is very abundant - and which everyone has heard about now, thanks to COVID-19," Musier-Forsyth said.