By Julie Steenhuysen
CHICAGO (Reuters) – A single genetic change that occurred in 2013 may explain how Zika acquired the ability to attack fetal nerve cells, causing a severe birth defect in babies whose mothers were infected while pregnant, Chinese and U.S. researchers reported on Thursday.
Scientists have posited many theories about why Zika, a mosquito-borne virus that had been linked with only mild symptoms since its discovery in 1947, could suddenly be associated with thousands of cases of the birth defect known as microcephaly, as it was in Brazil in 2015.
That outbreak prompted the World Health Organization to declare Zika a public health emergency in 2016, and set off a scientific quest to determine whether Zika could cause microcephaly, a condition marked by small head size.
Several teams have already traced the virus circulating in Brazil and elsewhere in South America to a strain of Zika that had been quietly circulating in Southeast Asia for decades.
In the new study, published in Science, Ling Yuan of the Chinese Academy of Sciences and colleagues compared genetic changes in samples of the South American virus with one isolated in 2010 in Cambodia.
They created seven sample viruses, each with a single genetic difference from the Cambodian strain, and tested these in brains of fetal mice. Although the viruses caused some degree of damage in all, those infected with a virus that carried a single mutation in a structural protein called prM developed severe microcephaly. That strain also proved more lethal to fetal brain cells.
The team estimates the genetic change occurred in May 2013, just before a French Polynesian outbreak of Zika in which the first cases of microcephaly and Guillain-Barre, a rare neurological disorder, were noted.
“Our findings offer an explanation for the unexpected causal link of Zika to microcephaly, and will help understand how Zika evolved from an innocuous mosquito-borne virus to a congenital pathogen with global impact,” Yuan and…