SARS-CoV-2 genomes rapidly decreases after the first few months of evolution in humans. CpG numbers in virus genomes have been linked to host-switching, the efficiency of virus replication, immune evasion and the ability of a virus to cause disease. “Zinc-finger antiviral protein (ZAP) is a host protein that can bind to CpG-rich regions in SARS-CoV-2, the causative agent of the Covid-19 pandemic, and recruits other host proteins to degrade the viral RNA," Vivekanandan Perumal from the Kusuma School of Biological Sciences, IIT Delhi was quoted as saying by news agency PTI. "Several viruses including HIV-1, Influenza A virus and SARS-CoV-2 prefer to reduce their CpG content (by losing CpGs) to minimise the host immune response, thus allowing better virus replication and survival," Perumal added.
He informed that the researchers analysed over 1.4 million full-length SARS-CoV-2 sequences from across the world. They found that the rate of CpG depletion from SARS-CoV-2 genomes rapidly decreases after the first few months of evolution in humans. "Furthermore, most SARS-CoV-2 variants of concern had lower CpG content.
This work highlights the existence of selection pressures apart from ZAP that may lead to CpG depletion in SARS-CoV-2 genomes," he said.
SARS-CoV-2 has a uracil-rich (uracil is one of the four building blocks of RNA) genome. The researchers have identified how uracils adjacent to CpGs contribute to the accelerated loss of CpGs from SARS-CoV-2 genomes. "Our results lay the necessary groundwork for future studies on understanding the intricacies of virus-host interactions leading to CpG depletion," IIT Delhi professor Manoj Menon said.